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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   chronic myeloproliferative disease
  

Disease ID 441
Disease chronic myeloproliferative disease
Definition
Conditions which cause proliferation of hemopoietically active tissue or of tissue which has embryonic hemopoietic potential. They all involve dysregulation of multipotent MYELOID PROGENITOR CELLS, most often caused by a mutation in the JAK2 PROTEIN TYROSINE KINASE.
Synonym
chronic myeloproliferative disease (morphologic abnormality)
disease myeloproliferative
diseases myeloproliferative
disorder myeloproliferative
disorder, myeloproliferative
disorders myeloproliferative
disorders, myeloproliferative
myeloproliferative dis
myeloproliferative disease
myeloproliferative disease (morphologic abnormality)
myeloproliferative disease, no icd-o subtype
myeloproliferative disease, no icd-o subtype (morphologic abnormality)
myeloproliferative disease, nos
myeloproliferative disorder
myeloproliferative disorder (disorder)
myeloproliferative disorder (morphologic abnormality)
myeloproliferative disorders
myeloproliferative disorders (incl. cml)
myeloproliferative disorders [disease/finding]
myeloproliferative neoplasm
myeloproliferative neoplasms
proliferation of myeloid cells
Orphanet
DOID
ICD10
UMLS
C0027022
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:67)
C0040053  |  thrombosis  |  20
C0001815  |  myelofibrosis  |  13
C0836924  |  thrombocytosis  |  9
C0001815  |  primary myelofibrosis  |  7
C0020538  |  hypertension  |  5
C0032463  |  polycythemia vera  |  5
C0020542  |  pulmonary hypertension  |  4
C0023418  |  leukemia  |  4
C0001815  |  bone marrow fibrosis  |  3
C0002871  |  anemia  |  3
C0032461  |  polycythemia  |  3
C0836924  |  thrombocythemia  |  2
C0023448  |  lymphocytic leukemia  |  2
C0856761  |  budd-chiari syndrome  |  2
C0013080  |  trisomy 21  |  2
C0040028  |  essential thrombocythemia  |  2
C0023434  |  chronic lymphocytic leukemia  |  2
C0221013  |  systemic mastocytosis  |  2
C0020541  |  portal hypertension  |  2
C0018799  |  cardiac disorders  |  1
C0023467  |  acute myeloid leukemia  |  1
C0021053  |  immune disease  |  1
C0028326  |  noonan syndrome  |  1
C0022658  |  kidney disease  |  1
C1527249  |  colorectal cancers  |  1
C0024899  |  mastocytosis  |  1
C0029464  |  osteosclerosis  |  1
C0021390  |  inflammatory bowel disease  |  1
C0026986  |  myelodysplastic syndrome  |  1
C0040034  |  thrombocytopenia  |  1
C0042847  |  vitamin b12 deficiency  |  1
C0023470  |  myeloid leukemia  |  1
C0836924  |  thrombocythaemia  |  1
C0007114  |  skin cancer  |  1
C1279296  |  chronic leukemia  |  1
C0015499  |  factor v deficiency  |  1
C0024314  |  lymphoproliferative disorder  |  1
C0022661  |  chronic kidney disease  |  1
C0040028  |  essential thrombocytosis  |  1
C0085669  |  acute leukemia  |  1
C0009402  |  colorectal cancer  |  1
C1561644  |  chronic kidney disease (ckd)  |  1
C0013080  |  trisomy 21 syndrome  |  1
C0023418  |  leukemias  |  1
C1275081  |  cardio-facio-cutaneous syndrome  |  1
C0023418  |  leukaemia  |  1
C0042373  |  vascular disease  |  1
C0152276  |  myeloid sarcoma  |  1
C0024299  |  lymphomas  |  1
C0020532  |  hypersplenism  |  1
C0024299  |  lymphoma  |  1
C0392525  |  nephrolithiasis  |  1
C0007114  |  skin cancers  |  1
C0023462  |  acute megakaryoblastic leukaemia  |  1
C0740394  |  hyperuricemia  |  1
C0699893  |  non-melanoma skin cancer  |  1
C0021831  |  bowel disease  |  1
C0007113  |  rectal cancer  |  1
C0079744  |  diffuse large b-cell lymphoma  |  1
C0040028  |  essential thrombocythaemia  |  1
C0042847  |  vitamin b12 defic  |  1
C1261473  |  sarcoma  |  1
C0023473  |  chronic myeloid leukaemia  |  1
C0155773  |  portal vein thrombosis  |  1
C0010072  |  coronary thrombosis  |  1
C0026986  |  myelodysplastic syndromes  |  1
C0079731  |  b-cell lymphoma  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:12)
2260  |  FGFR1  |  CTD_human
613  |  BCR  |  CTD_human
3717  |  JAK2  |  CTD_human;GHR
4352  |  MPL  |  GHR
5159  |  PDGFRB  |  UNIPROT
54790  |  TET2  |  GHR
7066  |  THPO  |  GHR
55102  |  ATG2B  |  CTD_human
26127  |  FGFR1OP2  |  CTD_human
7750  |  ZMYM2  |  CTD_human
811  |  CALR  |  GHR
51527  |  GSKIP  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:10)
3717  |  JAK2  |  CIPHER;CTD_human
4352  |  MPL  |  CIPHER
171023  |  ASXL1  |  CIPHER
54790  |  TET2  |  CIPHER
613  |  BCR  |  CTD_human
26127  |  FGFR1OP2  |  CTD_human
7750  |  ZMYM2  |  CTD_human
51527  |  GSKIP  |  CTD_human
2260  |  FGFR1  |  CTD_human
55102  |  ATG2B  |  CTD_human
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:136)
25  |  ABL1  |  5.652  |  DISEASES
367  |  AR  |  1.637  |  DISEASES
10425  |  ARIH2  |  1.656  |  DISEASES
171023  |  ASXL1  |  5.083  |  DISEASES
10018  |  BCL2L11  |  1.158  |  DISEASES
664  |  BNIP3  |  1.205  |  DISEASES
665  |  BNIP3L  |  1.322  |  DISEASES
669  |  BPGM  |  1.774  |  DISEASES
801  |  CALM1  |  1.606  |  DISEASES
811  |  CALR  |  6.538  |  DISEASES
25901  |  CCDC28A  |  2.07  |  DISEASES
440193  |  CCDC88C  |  1.381  |  DISEASES
57126  |  CD177  |  5.26  |  DISEASES
966  |  CD59  |  1.241  |  DISEASES
1050  |  CEBPA  |  1.066  |  DISEASES
387119  |  CEP85L  |  2.844  |  DISEASES
1154  |  CISH  |  2.231  |  DISEASES
8738  |  CRADD  |  1.228  |  DISEASES
1441  |  CSF3R  |  3.343  |  DISEASES
8813  |  DPM1  |  6.301  |  DISEASES
1859  |  DYRK1A  |  1.238  |  DISEASES
64641  |  EBF2  |  1.037  |  DISEASES
56478  |  EIF4ENIF1  |  2.907  |  DISEASES
2022  |  ENG  |  1.336  |  DISEASES
2120  |  ETV6  |  3.566  |  DISEASES
2131  |  EXT1  |  1.551  |  DISEASES
2145  |  EZH1  |  1.352  |  DISEASES
2152  |  F3  |  2.306  |  DISEASES
55179  |  FAIM  |  1.664  |  DISEASES
55120  |  FANCL  |  1.003  |  DISEASES
100302740  |  FAS-AS1  |  3.436  |  DISEASES
54620  |  FBXL19  |  1.576  |  DISEASES
286151  |  FBXO43  |  2.717  |  DISEASES
2214  |  FCGR3A  |  1.048  |  DISEASES
2260  |  FGFR1  |  4.245  |  DISEASES
11116  |  FGFR1OP  |  1.58  |  DISEASES
2268  |  FGR  |  1.09  |  DISEASES
81608  |  FIP1L1  |  4.117  |  DISEASES
2298  |  FOXD4  |  1.829  |  DISEASES
2617  |  GARS  |  1.441  |  DISEASES
2623  |  GATA1  |  5.945  |  DISEASES
2624  |  GATA2  |  1.036  |  DISEASES
2634  |  GBP2  |  1.302  |  DISEASES
149775  |  GNAS-AS1  |  1.981  |  DISEASES
2811  |  GP1BA  |  3.035  |  DISEASES
493869  |  GPX8  |  1.899  |  DISEASES
2958  |  GTF2A2  |  2.257  |  DISEASES
2993  |  GYPA  |  2.354  |  DISEASES
10614  |  HEXIM1  |  1.254  |  DISEASES
8091  |  HMGA2  |  2.156  |  DISEASES
3149  |  HMGB3  |  1.355  |  DISEASES
3205  |  HOXA9  |  1.521  |  DISEASES
3418  |  IDH2  |  3.375  |  DISEASES
3440  |  IFNA2  |  3.427  |  DISEASES
10320  |  IKZF1  |  2.704  |  DISEASES
259307  |  IL4I1  |  1.151  |  DISEASES
3612  |  IMPA1  |  1.793  |  DISEASES
3633  |  INPP5B  |  1.083  |  DISEASES
3684  |  ITGAM  |  2.332  |  DISEASES
3716  |  JAK1  |  4.664  |  DISEASES
3717  |  JAK2  |  7.993  |  DISEASES
3718  |  JAK3  |  2.337  |  DISEASES
3720  |  JARID2  |  2.43  |  DISEASES
23189  |  KANK1  |  1.045  |  DISEASES
3767  |  KCNJ11  |  1.558  |  DISEASES
27040  |  LAT  |  1.713  |  DISEASES
26524  |  LATS2  |  1.233  |  DISEASES
9355  |  LHX2  |  1.009  |  DISEASES
4067  |  LYN  |  2.236  |  DISEASES
23764  |  MAFF  |  1.021  |  DISEASES
11184  |  MAP4K1  |  1.288  |  DISEASES
4146  |  MATN1  |  1.519  |  DISEASES
55796  |  MBNL3  |  1.43  |  DISEASES
57591  |  MKL1  |  1.044  |  DISEASES
4300  |  MLLT3  |  1.589  |  DISEASES
8777  |  MPDZ  |  1.075  |  DISEASES
4352  |  MPL  |  5.956  |  DISEASES
2475  |  MTOR  |  1.049  |  DISEASES
4602  |  MYB  |  1.018  |  DISEASES
4609  |  MYC  |  1.034  |  DISEASES
4638  |  MYLK  |  1.436  |  DISEASES
399687  |  MYO18A  |  1.756  |  DISEASES
4763  |  NF1  |  1.606  |  DISEASES
4893  |  NRAS  |  2.671  |  DISEASES
143  |  PARP4  |  1.12  |  DISEASES
9659  |  PDE4DIP  |  1.418  |  DISEASES
11040  |  PIM2  |  1.194  |  DISEASES
5493  |  PPL  |  1.09  |  DISEASES
5494  |  PPM1A  |  1.188  |  DISEASES
23532  |  PRAME  |  1.936  |  DISEASES
5688  |  PSMA7  |  2.389  |  DISEASES
9050  |  PSTPIP2  |  1.301  |  DISEASES
5742  |  PTGS1  |  1.448  |  DISEASES
5781  |  PTPN11  |  3.908  |  DISEASES
5777  |  PTPN6  |  1.34  |  DISEASES
5788  |  PTPRC  |  1.167  |  DISEASES
89941  |  RHOT2  |  1.601  |  DISEASES
60485  |  SAV1  |  1.96  |  DISEASES
462  |  SERPINC1  |  1.536  |  DISEASES
5345  |  SERPINF2  |  1.001  |  DISEASES
29072  |  SETD2  |  2.492  |  DISEASES
10019  |  SH2B3  |  4.049  |  DISEASES
116085  |  SLC22A12  |  1.617  |  DISEASES
83650  |  SLC35G5  |  2.389  |  DISEASES
26806  |  SNORD44  |  1.172  |  DISEASES
26788  |  SNORD60  |  2.215  |  DISEASES
8651  |  SOCS1  |  2.486  |  DISEASES
8835  |  SOCS2  |  2.384  |  DISEASES
9021  |  SOCS3  |  2.625  |  DISEASES
6693  |  SPN  |  1.655  |  DISEASES
6711  |  SPTBN1  |  1.316  |  DISEASES
6714  |  SRC  |  1.524  |  DISEASES
6427  |  SRSF2  |  3.643  |  DISEASES
23635  |  SSBP2  |  1.218  |  DISEASES
6776  |  STAT5A  |  4.315  |  DISEASES
8428  |  STK24  |  1.763  |  DISEASES
10494  |  STK25  |  2.038  |  DISEASES
6818  |  SULT1A3  |  1.931  |  DISEASES
445329  |  SULT1A4  |  1.956  |  DISEASES
54790  |  TET2  |  4.949  |  DISEASES
7056  |  THBD  |  2.735  |  DISEASES
7075  |  TIE1  |  1.065  |  DISEASES
85019  |  TMEM241  |  2.669  |  DISEASES
55504  |  TNFRSF19  |  1.061  |  DISEASES
116447  |  TOP1MT  |  1.729  |  DISEASES
8725  |  URI1  |  1.546  |  DISEASES
7404  |  UTY  |  1.134  |  DISEASES
7409  |  VAV1  |  2.068  |  DISEASES
7422  |  VEGFA  |  1.434  |  DISEASES
23038  |  WDTC1  |  3  |  DISEASES
7490  |  WT1  |  1.072  |  DISEASES
643836  |  ZFP62  |  2.621  |  DISEASES
7750  |  ZMYM2  |  4.061  |  DISEASES
7718  |  ZNF165  |  1.462  |  DISEASES
100293516  |  ZNF587B  |  2.442  |  DISEASES
79027  |  ZNF655  |  1.827  |  DISEASES
Locus(Waiting for update.)
Disease ID 441
Disease chronic myeloproliferative disease
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:50)
HP:0011974  |  Myelofibrosis  |  13
HP:0001894  |  Thrombocytosis  |  10
HP:0001880  |  Eosinophilia  |  8
HP:0030247  |  Blood clot in splanchnic vein  |  7
HP:0001744  |  Splenomegaly  |  5
HP:0000822  |  Hypertension  |  5
HP:0001909  |  Leukemia  |  4
HP:0002092  |  Pulmonary artery hypertension  |  4
HP:0001907  |  Thromboembolic disease  |  4
HP:0002664  |  Neoplasia  |  3
HP:0001903  |  Anemia  |  3
HP:0001901  |  Abnormally shaped erythrocytes  |  3
HP:0001978  |  Extramedullary hematopoiesis  |  3
HP:0004936  |  Blood clot in vein  |  2
HP:0002639  |  Budd-Chiari syndrome  |  2
HP:0005550  |  Chronic lymphatic leukemia  |  2
HP:0005305  |  Cerebral vein thrombosis  |  2
HP:0001971  |  Hypersplenism  |  1
HP:0100242  |  Sarcoma  |  1
HP:0003418  |  Back pain  |  1
HP:0001974  |  Leukocytosis  |  1
HP:0011001  |  Increased bone mineral density  |  1
HP:0011874  |  Heparin-induced thrombocytopenia  |  1
HP:0002488  |  Acute leukemias  |  1
HP:0012531  |  Pain  |  1
HP:0000787  |  Renal calculi  |  1
HP:0012324  |  Myeloid leukemia  |  1
HP:0100502  |  Vitamin B12 deficiency  |  1
HP:0100495  |  Mastocytosis  |  1
HP:0001873  |  Low platelet count  |  1
HP:0000752  |  Hyperactive behavior  |  1
HP:0002960  |  Autoimmune condition  |  1
HP:0100665  |  Angiooedema  |  1
HP:0003419  |  Low back pain  |  1
HP:0001409  |  Portal hypertension  |  1
HP:0012191  |  B-cell lymphoma  |  1
HP:0003256  |  Coagulopathy  |  1
HP:0012622  |  Chronic kidney disease  |  1
HP:0002149  |  Hyperuricemia  |  1
HP:0030242  |  Blood clot in portal vein  |  1
HP:0004808  |  Acute myelogenous leukemia  |  1
HP:0002665  |  Lymphoma  |  1
HP:0010972  |  Anemia of inadequate production  |  1
HP:0005523  |  Lymphoproliferative disorder  |  1
HP:0012190  |  T cell lymphoma  |  1
HP:0005505  |  Refractory anemia  |  1
HP:0005558  |  Chronic leukemia  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0100827  |  Lymphocytosis  |  1
HP:0002105  |  Hemoptysis  |  1
Disease ID 441
Disease chronic myeloproliferative disease
Manually Symptom
UMLS  | Name(Total Manually Symptoms:6)
C2613439  |  extramedullary hematopoiesis
C0836924  |  thrombocytosis
C0836924  |  thrombocythaemia
C0343888  |  cutaneous cryptococcosis
C0235604  |  thrombocytopathy
C0005699  |  blast crises
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:14)
C0040053  |  thrombosis  |  14
C0836924  |  thrombocythemia  |  4
C0020542  |  pulmonary hypertension  |  3
C0836924  |  thrombocytosis  |  2
C0001815  |  myelofibrosis  |  2
C1516669  |  clonal evolution  |  2
C0010072  |  coronary thrombosis  |  1
C0272285  |  heparin-induced thrombocytopenia  |  1
C0014804  |  erythromelalgia  |  1
C0029464  |  osteosclerosis  |  1
C0040028  |  essential thrombocythemia  |  1
C0018952  |  extramedullary hematopoiesis  |  1
C0005779  |  coagulopathy  |  1
C0856761  |  budd-chiari syndrome  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:337)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs10974944204224153717JAK2umls:C0027022GAD[The G allele of the JAK2 rs10974944 SNP, part of JAK2 46/1 haplotype, is strongly associated with JAK2 V617F-positive myeloproliferative neoplasms.]0.3516606542010JAK2;INSL695070831CG
rs121913615184641144352MPLumls:C0027022BeFreeTo investigate its prevalence in Chinese patients with MPD, we introduced allele-specific PCR (AS-PCR) combined with sequence analysis to simultaneously screen MPL W515L and JAK2 V617F mutations in 190 MPD patients.0.0366335162008MPL143349338GT
rs121913615184641146646SOAT1umls:C0027022BeFreeAs JAK2 V617F, MPL W515L is a novel acquired mutation that induces constitutive cytokine-independent activation of the JAK-STAT pathway in myeloproliferative disorders (MPD).0.0021715352008MPL143349338GT
rs121913615184641143717JAK2umls:C0027022BeFreeAs JAK2 V617F, MPL W515L is a novel acquired mutation that induces constitutive cytokine-independent activation of the JAK-STAT pathway in myeloproliferative disorders (MPD).0.3516606542008MPL143349338GT
rs121913615196434763717JAK2umls:C0027022BeFreeScanning of JAK2 exons 12-25 and MPL exon 10 revealed the presence of JAK2 alterations in six and MPL W515L/K mutations in five of 34 patients with myeloproliferative disorders.0.3516606542010MPL143349338GT
rs121913616191944674352MPLumls:C0027022BeFreeThe thrombopoietin receptor gene (MPL) is expressed in megakaryocytes and exhibits the gain of function point mutation W515K/L in approximately 5% of patients with primary myelofibrosis/idiopathic myelofibrosis (PMF) representing one subtype of the chronic myeloproliferative disorders (myeloproliferative neoplasm).0.0366335162009NANANANANA
rs121918464163713685781PTPN11umls:C0027022BeFreeOur results showed that SHP-2 E76K mutation caused myeloproliferative disease in mice, while overexpression of WT SHP-2 decreased hematopoietic potential of the transduced cells in recipient animals.0.0021715352006PTPN1112112450406GA,C
rs17849241197354889021SOCS3umls:C0027022BeFreeInterestingly, the SOCS3(F136L) mutation was detected in a Japanese myeloproliferative disorder patient cohort at double the frequency of healthy controls.0.0010857672009SOCS3;LOC1019286741778358688GT
rs386626619214351893717JAK2umls:C0027022BeFreeThe prevalence of overt MPN and that of JAK2 V617F were lower in Korean patients with SVT than in previous reports.0.3516606542011NANANANANA
rs386626619255594613717JAK2umls:C0027022BeFreeThe JAK2 V617F mutational status and allele burden may be related with the risk of venous thromboembolic events in patients with Philadelphia-negative myeloproliferative neoplasms.0.3516606542014NANANANANA
rs386626619250129142264FGFR4umls:C0027022BeFreeDiscovery of the protein tyrosine kinase JAK2 V617F allele contributed to better understanding of the pathogenetic mechanisms of MPNs.0.0005428842014NANANANANA
rs386626619233918443717JAK2umls:C0027022BeFreeIn contrast, this same mutation has been detected in only 4 patients with CNL to date, suggesting that the JAK2 V617F mutation is a rare event in patients with atypical MPD.0.3516606542013NANANANANA
rs386626619164563753717JAK2umls:C0027022BeFreeThe major incentives for this review have been the recent description of an activating JAK2 tyrosine kinase mutation (JAK2 (V617F)) in essential thrombocythemia, related myeloproliferative disorders, and the impact on clinical practice from the publication of a major treatment trial.0.3516606542006NANANANANA
rs386626619180328833717JAK2umls:C0027022BeFreePresence of JAK2(V617F) in bone marrow might therefore increase the risk of future MPD development, just as monoclonal gammopathy of undetermined significance (MGUS) increases the risk of multiple myeloma.0.3516606542007NANANANANA
rs386626619183365413717JAK2umls:C0027022BeFreeThe JAK2-V617F mutation can be frequently detected in the Taiwanese patients with MPD disorders and therefore should be incorporated into the initial evaluation of patients suspected of MPD.0.3516606542008NANANANANA
rs386626619221327293717JAK2umls:C0027022BeFreeRecent studies have identified a recurrent somatic activating mutation (JAK2 V617F) in majority of patients with myeloproliferative disorders (MPDs).0.3516606542012NANANANANA
rs386626619233009954953ODC1umls:C0027022BeFreeCritical roles of Myc-ODC axis in the cellular transformation induced by myeloproliferative neoplasm-associated JAK2 V617F mutant.0.0002714422013NANANANANA
rs386626619209665446776STAT5Aumls:C0027022BeFreeRecently, a single gain-of-function point mutation of JAK2 was described in myeloproliferative diseases leading to constitutive Jak2 kinase activity, subsequent Stat5a/b activation and involvement of V617F Jak2 in the pathogenesis of myeloproliferative disorders.0.0008143262010NANANANANA
rs386626619176875553717JAK2umls:C0027022BeFreeJAK2(V617F) positive early stage myeloproliferative disease (essential thrombocythemia) as the cause of portal vein thrombosis in two middle-aged women: therapeutic implications in view of the literature.0.3516606542007NANANANANA
rs386626619168106092056EPOumls:C0027022BeFreeMPD-specific markers such as serum EPO, endogenous erythroid colony formation (EEC), and JAK2 V617F have high specificities, but the sensitivities are not high enough to detect the early stages of the MPDs, ET, PV, and prefibrotic CIMF.0.0008143262006NANANANANA
rs386626619225797133717JAK2umls:C0027022BeFreeThe HDAC inhibitor Givinostat modulates the hematopoietic transcription factors NFE2 and C-MYB in JAK2(V617F) myeloproliferative neoplasm cells.0.3516606542012NANANANANA
rs386626619250129142046EPHA8umls:C0027022BeFreeDiscovery of the protein tyrosine kinase JAK2 V617F allele contributed to better understanding of the pathogenetic mechanisms of MPNs.0.0005428842014NANANANANA
rs386626619169989403717JAK2umls:C0027022BeFreeJAK2 (V617F) as an acquired somatic mutation and a secondary genetic event associated with disease progression in familial myeloproliferative disorders.0.3516606542006NANANANANA
rs386626619165025903717JAK2umls:C0027022BeFreeMethods for the detection of the JAK2 V617F mutation in human myeloproliferative disorders.0.3516606542006NANANANANA
rs386626619262352143717JAK2umls:C0027022BeFreeMicrofluidics-based assays can reduce the assay time and sample/reagent consumption and enhance the reaction efficiency; however, no current assay has integrated isothermal amplification for point-of-care MPN JAK2 V617F mutation testing with a microchip.0.3516606542015NANANANANA
rs386626619207284373717JAK2umls:C0027022BeFreeWe studied the sensitivity and reproducibility of LightScanner™ platform in the detection of JAK2 V617F mutation and the availability for diagnostic use in MPN.0.3516606542010NANANANANA
rs386626619254797525688PSMA7umls:C0027022BeFreeIn mice, tamoxifen treatment blocked development of JAK2(V617F)-induced myeloproliferative neoplasm in vivo, induced apoptosis of human JAK2(V617F+) HSPCs in a xenograft model, and sensitized MLL-AF9(+) leukemias to chemotherapy.0.0002714422014NANANANANA
rs386626619182455403717JAK2umls:C0027022BeFreeThe discovery of an activating somatic mutation in codon 617 of the gene encoding the Janus kinase (JAK)-2 (JAK2 V617F) in patients with myeloproliferative disorders has opened new avenues for the development of targeted therapies for these malignancies.0.3516606542008NANANANANA
rs386626619160816843717JAK2umls:C0027022BeFreeAltered gene expression in myeloproliferative disorders correlates with activation of signaling by the V617F mutation of Jak2.0.3516606542005NANANANANA
rs3866266191622565125ABL1umls:C0027022BeFreeAn association between an activating JAK2 mutation (JAK2(V617F)) and BCR/ABL-negative myeloproliferative disorders was recently reported in multiple simultaneous publications.0.017372282005NANANANANA
rs38662661919466975613BCRumls:C0027022BeFreeData on angiogenesis in the bone marrow of BCR-ABL1-negative myeloproliferative neoplasm (MPN) patients suggest an increase of the microvessel density (MVD) and vascular endothelial growth factor (VEGF) expression, but relations to the JAK2-V617F status remain controversial.0.1281531882009NANANANANA
rs386626619191357733717JAK2umls:C0027022BeFreeMyeloproliferative disorders (MPDs) are often associated with the presence of the JAK2-V617F mutation in hematopoietic cells.0.3516606542009NANANANANA
rs386626619248584123717JAK2umls:C0027022BeFreeAssociation between thromboembolic events and the JAK2 V617F mutation in myeloproliferative neoplasms.0.3516606542015NANANANANA
rs3866266191800393510148EBI3umls:C0027022BeFreeFinally, we show that IL-27R can functionally replace a homodimeric type I cytokine receptor in the activation of JAK2-V617F, a critical JAK2 mutation in various myeloproliferative disorders (MPDs).0.0005428842007NANANANANA
rs386626619250129143717JAK2umls:C0027022BeFreeDiscovery of the protein tyrosine kinase JAK2 V617F allele contributed to better understanding of the pathogenetic mechanisms of MPNs.0.3516606542014NANANANANA
rs386626619260714743717JAK2umls:C0027022BeFreeIn the current study, mutations of JAK2 V617F, JAK2 exon 12, MPL exon 10, and CALR exon 9 were analyzed in 929 Chinese patients with BCR-ABL1-negative MPN, including 234 cases of polycythemia vera (PV), 428 ETs, 187 PMFs, and 80 unclassifiable MPNs (MPN-Us).0.3516606542015NANANANANA
rs386626619200289726777STAT5Bumls:C0027022BeFreeSTAT5 activation is critical for the transformation mediated by myeloproliferative disorder-associated JAK2 V617F mutant.0.0005428842010NANANANANA
rs386626619168106103717JAK2umls:C0027022BeFreeNew insights into the pathogenesis of JAK2 V617F-positive myeloproliferative disorders and consequences for the management of patients.0.3516606542006NANANANANA
rs386626619174081063717JAK2umls:C0027022BeFreeA new mutation (V617F) affecting the JAK2 gene has been recently described as acquired in patients with myeloproliferative disorders and other myeloid malignancies.0.3516606542006NANANANANA
rs386626619252596263717JAK2umls:C0027022BeFreeThe classical Philadelphia chromosome-negative myeloproliferative neoplasms consist of three main pathological and clinical entities with the recurrent JAK2 V617F mutation present in ∼98% of patients with polycythemia vera and ∼50% of patients with essential thrombocythemia (ET) and primary myelofibrosis (PMF).0.3516606542015NANANANANA
rs386626619188151963717JAK2umls:C0027022BeFreeSOCS3 transcript levels were highest in patients with polycythemia vera and other JAK2 V617F positive myeloproliferative disorders, consistent with SOCS3 being a target gene of JAK2/STAT5 signaling.0.3516606542008NANANANANA
rs386626619169016563717JAK2umls:C0027022BeFreeThe first international meeting on V617F JAK2 mutation and its relevance in Philadelphia-negative myeloproliferative disorders.0.3516606542007NANANANANA
rs386626619240661273717JAK2umls:C0027022BeFreeHeterozygous and homozygous JAK2(V617F) states modeled by induced pluripotent stem cells from myeloproliferative neoplasm patients.0.3516606542013NANANANANA
rs386626619198777613717JAK2umls:C0027022BeFreeThe JAK2 V617F mutation has been implicated in a variety of diseases mainly related to myeloproliferative disorders including polycythemia vera, essential thrombocythemia, and idiopathic myelofibrosis with an increased demand for testing using molecular techniques.0.3516606542010NANANANANA
rs3866266192330099589874SLC25A21umls:C0027022BeFreeCritical roles of Myc-ODC axis in the cellular transformation induced by myeloproliferative neoplasm-associated JAK2 V617F mutant.0.0002714422013NANANANANA
rs386626619194824423717JAK2umls:C0027022BeFreeThe JAK2 [V617F] mutation has recently been recognised as critical to the pathogenesis of the myeloproliferative disorders (MPDs).0.3516606542009NANANANANA
rs386626619204343003717JAK2umls:C0027022BeFreeA recent novel mutation in the Janus activated kinase 2 gene involving a gain-of-function substitute of valine to phenylalanine at position 617 (JAK2 V617F) has been discovered to be prevalent in patients with mesenteric vein thrombosis and myeloproliferative disorders.0.3516606542010NANANANANA
rs386626619182459483717JAK2umls:C0027022BeFreeIn 2005, a point mutation in JAK2 (JAK2-V617F) was identified in a number of neoplastic myeloproliferative disorders, ushering in a new era of JAK2 research.0.3516606542008NANANANANA
rs386626619190463163717JAK2umls:C0027022BeFreeThe JAK2(V617F) tyrosine kinase mutation identifies clinically latent myeloproliferative disorders in patients presenting with hepatic or portal vein thrombosis.0.3516606542008NANANANANA
rs386626619165378033717JAK2umls:C0027022BeFreeGenetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders.0.3516606542006NANANANANA
rs386626619163304463717JAK2umls:C0027022BeFreeAlthough the V617F JAK2 mutation has been described by several groups to be associated with classical myeloproliferative disorders (MPD), this same mutation has been detected with a low incidence in atypical MPD, such as CNL.0.3516606542005NANANANANA
rs386626619187962513717JAK2umls:C0027022BeFreeAccordingly, it seems that the investigation for the V617F mutation of the JAK2 gene is not mandatory in all Mexican mestizo patients with unexplained thrombophilia and that this genetic study should be reserved for special cases, such as patients with thrombosis in uncommon sites or patients with cell counts suggesting the presence of an underlying MPD.0.3516606542008NANANANANA
rs386626619171787223717JAK2umls:C0027022BeFreeThese data suggest that erlotinib may be used for treatment of JAK2(V617F)-positive PV and other myeloproliferative disorders.0.3516606542007NANANANANA
rs386626619250156343717JAK2umls:C0027022BeFreeJAK2 V617F mutation is a molecular marker for myeloproliferative neoplasms (MPNs).0.3516606542015NANANANANA
rs386626619211983213717JAK2umls:C0027022BeFreeJAK2 V617F gene mutation in the laboratory work-up of myeloproliferative disorders: experience of a major referral center in Lebanon.0.3516606542011NANANANANA
rs38662661918723264947CD34umls:C0027022BeFreeWe conclude that the extent of JAK2(V617F) CD34(+) cell clonal dominance is associated with disease phenotype within the MPD and, in PV, is associated with extramedullary disease, leukocytosis, and disease duration.0.0024429772008NANANANANA
rs386626619213315933717JAK2umls:C0027022BeFreeA molecular fingerprint distinguishes JAK2(V617F)-positive MPN patients without response to HU treatment, with overexpression of JAK2, MAPK14, PIK3CA, and SFK genes.0.3516606542011NANANANANA
rs386626619249635933717JAK2umls:C0027022BeFreeThe JAK2 V617F mutation is highly prevalent in patients with myeloproliferative neoplasms (MPN).0.3516606542014NANANANANA
rs386626619164080983717JAK2umls:C0027022BeFreeJAK2 V617F tyrosine kinase mutation in cell lines derived from myeloproliferative disorders.0.3516606542006NANANANANA
rs386626619162938803717JAK2umls:C0027022BeFreeThe nature of the specific oncogenic mutation(s) is currently being unraveled with the recent discovery of an association between a somatic point mutation of JAK2 tyrosine kinase (V617F) and bcr/abl-negative myeloproliferative disorders, including MMM.0.3516606542005NANANANANA
rs386626619168850513717JAK2umls:C0027022BeFreeThe acquired mutation Val617Phe in the tyrosine kinase JAK2 was recently identified in most but not all patients with classical myeloproliferative disorders.0.3516606542006NANANANANA
rs386626619181606703717JAK2umls:C0027022BeFreeAn acquired somatic mutation in the JAK2 gene (JAK2-V617F) is present in the majority of patients with myeloproliferative disorders (MPDs).0.3516606542008NANANANANA
rs386626619225797134778NFE2umls:C0027022BeFreeThe HDAC inhibitor Givinostat modulates the hematopoietic transcription factors NFE2 and C-MYB in JAK2(V617F) myeloproliferative neoplasm cells.0.0005428842012NANANANANA
rs386626619166757103717JAK2umls:C0027022BeFreeAcquisition of the V617F mutation of JAK2 is a late genetic event in a subset of patients with myeloproliferative disorders.0.3516606542006NANANANANA
rs386626619192168433717JAK2umls:C0027022BeFreeAlthough the Jak2-V617F mutation has generated strong awareness because of its causative role in myeloproliferative disorders, reports of Jak2 gene aberrations linked to hematologic malignancies have preceded those of V617F by nearly a decade.0.3516606542009NANANANANA
rs386626619185286463717JAK2umls:C0027022BeFreeA single mutation 1849G>T in the JAK2 gene (V617F) has recently been described in classical myeloproliferative disorders (MPD).0.3516606542008NANANANANA
rs386626619194669753717JAK2umls:C0027022BeFreeIn addition, it provides evidence that despite the fact that angiogenesis is generally independent of the JAK2-V617F status in MPN, new vessel formation might be linked to Jak2 effects in some cases with high JAK2-V617F mutant allele burden.0.3516606542009NANANANANA
rs386626619172513343717JAK2umls:C0027022BeFreeHowever, the recent identification of a V617F mutation in the JH2 domain of the JAK2 gene in a high proportion of patients suffering from MPDs may provide confirmation of a diagnosis.0.3516606542007NANANANANA
rs386626619180039353717JAK2umls:C0027022BeFreeFinally, we show that IL-27R can functionally replace a homodimeric type I cytokine receptor in the activation of JAK2-V617F, a critical JAK2 mutation in various myeloproliferative disorders (MPDs).0.3516606542007NANANANANA
rs386626619182162973717JAK2umls:C0027022BeFreeThe V617F activating point mutation in Jak2 is associated with a proportion of myeloproliferative disorders.0.3516606542008NANANANANA
rs386626619180559833717JAK2umls:C0027022BeFreeFour novel JAK2 mutant alleles have recently been described in patients with V617F-negative myeloproliferative disorders presenting with erythrocytosis.0.3516606542007NANANANANA
rs386626619183007583717JAK2umls:C0027022BeFreeThe high prevalence of the V617F mutation of Janus kinase 2 and associated mutations in myeloproliferative disorders (> 95% in polycythemia vera and about half of patients with essential thrombocythemia and primary myelofibrosis) has led the World Health Organization to alter the diagnostic criteria for these myeloproliferative disorders, and these changes are reviewed.0.3516606542008NANANANANA
rs3866266191719466325ABL1umls:C0027022BeFreeDiscovery of a constitutively activating point mutation of the Janus kinase 2 (JAK2) receptor-associated tyrosine kinase in patients with polycythemia vera (PV) and other BCR/ABL-negative myeloproliferative disorders prompted many groups around the world to examine diverse subsets of patients with myeloid diseases for the prevalence of the JAK2 V617F mutation and its clinical and pathological associations.0.017372282006NANANANANA
rs386626619173078383717JAK2umls:C0027022BeFreeIn patients with SVT, screening for the JAK2 V617F mutation may be useful in recognising patients who should be carefully observed for the subsequent development of overt MPD.0.3516606542007NANANANANA
rs386626619249514233717JAK2umls:C0027022BeFreeJAK2(V617F), the main mutation involved in MPN, is considered as a risk factor for thrombosis, although the direct link between the mutation and hemostatic disorders is not strictly established.0.3516606542015NANANANANA
rs386626619234690883717JAK2umls:C0027022BeFreeNon-reactive platelet counts elevation occurs mainly in myeloproliferative disorders (MPDs), which have been reported to be closely associated with JAK2 V617F mutation.0.3516606542013NANANANANA
rs386626619183967503717JAK2umls:C0027022BeFreeWe report two cases of patient with portal vein thrombosis of unknown origin in whom the presence of the V617F mutation of the Janus Kinase 2 gene lead to the diagnosis of primary myeloproliferative disorder, confirmed on bone marrow examination.0.3516606542008NANANANANA
rs386626619168106094597MVDumls:C0027022BeFreeBone marrow histopathology in addition to clinical, laboratory, biological, and molecular markers, including the JAK2 V617 PCR test, serum EPO, PRV-1, EEC, LAP score, peripheral blood parameters, and spleen size on echogram will detect the early stages of MPD and allows diagnostic differentiation of the three primary MPDs (ET, PV, and CIMF) in both JAK2 V617F-positive and JAK2 wild-type MPD patients.0.0024429772006NANANANANA
rs386626619173790693717JAK2umls:C0027022BeFreeHowever, several unanswered questions regarding the essential role of JAK2(V617F) arose as 1) it is not a dominant mutation, 2) it is not PV-specific as it is found in several myeloproliferative disorders, and 3) some ( approximately 20%) PV patients lack the JAK2(V617F) mutation.0.3516606542007NANANANANA
rs386626619190040763717JAK2umls:C0027022BeFreeThe role of screening for the JAK2 V617F mutation in patients presenting with thrombosis without overt MPD is unclear, but appears justified in cases of idiopathic splanchnic vein thrombosis.0.3516606542008NANANANANA
rs3866266191667026625ABL1umls:C0027022BeFreeA JAK2(V617F) mutation is frequently found in several BCR/ABL-negative myeloproliferative disorders.0.017372282006NANANANANA
rs386626619253455903717JAK2umls:C0027022BeFreeThe acquired JAK2 V617F mutation is common in patients with myeloproliferative neoplasms.0.3516606542014NANANANANA
rs386626619233009953717JAK2umls:C0027022BeFreeCritical roles of Myc-ODC axis in the cellular transformation induced by myeloproliferative neoplasm-associated JAK2 V617F mutant.0.3516606542013NANANANANA
rs386626619181885943717JAK2umls:C0027022BeFreeThe diagnosis of a myeloproliferative disease could be corroborated by demonstration of the V617F mutation of JAK2.0.3516606542008NANANANANA
rs386626619162850063717JAK2umls:C0027022BeFreeThe V617F JAK2 mutation and the myeloproliferative disorders.0.3516606542005NANANANANA
rs386626619199395823717JAK2umls:C0027022BeFreeJAK2-V617F mutation in Moroccan patients with myeloproliferative disorders: contribution, diagnosis and therapeutic prospects.0.3516606542011NANANANANA
rs386626619166272723717JAK2umls:C0027022BeFreeDNA from 161 samples was isolated from peripheral blood granulocytes and formalin-fixed bone marrow clot sections in patients with CMPDs and without myeloproliferative disorders previously genotyped for the JAK2 V617F (G-->T) mutation, which included 114 wild types (GG) and 47 mutants (GT and TT).0.3516606542006NANANANANA
rs386626619184641146646SOAT1umls:C0027022BeFreeAs JAK2 V617F, MPL W515L is a novel acquired mutation that induces constitutive cytokine-independent activation of the JAK-STAT pathway in myeloproliferative disorders (MPD).0.0021715352008NANANANANA
rs386626619166702663717JAK2umls:C0027022BeFreeQuestions remain regarding the exact contribution of JAK2(V617F) in other myeloproliferative disorders.0.3516606542006NANANANANA
rs386626619179343513717JAK2umls:C0027022BeFreeA general theme is that JAK2 V617F is variably associated with thrombosis and, more consistently, associated with elevations in blood counts relative to mutation-negative myeloproliferative disorders; future preclinical research should focus on the pathophysiology of thrombosis in myeloproliferative disorders, particularly in terms of the relationship between dysregulated Janus kinase 2 and elevated blood counts.0.3516606542007NANANANANA
rs3866266192607147483886PRSS27umls:C0027022BeFreeIn the current study, mutations of JAK2 V617F, JAK2 exon 12, MPL exon 10, and CALR exon 9 were analyzed in 929 Chinese patients with BCR-ABL1-negative MPN, including 234 cases of polycythemia vera (PV), 428 ETs, 187 PMFs, and 80 unclassifiable MPNs (MPN-Us).0.0010857672015NANANANANA
rs386626619166324703717JAK2umls:C0027022BeFreeThe V617F activating point mutation in Jak2 has recently been associated with myeloproliferative disorders.0.3516606542006NANANANANA
rs386626619197975253717JAK2umls:C0027022BeFreeMultiple iPS cell lines were also generated from peripheral blood CD34(+) cells of 2 patients with myeloproliferative disorders (MPDs) who acquired the JAK2-V617F somatic mutation in their blood cells.0.3516606542009NANANANANA
rs386626619230575173717JAK2umls:C0027022BeFreeMolecular genetic assays for the detection of the JAK2 V617F (c.1849G>T) and other pathogenetic mutations within JAK2 exon 12 and MPL exon 10 are part of the routine diagnostic workup for patients presenting with erythrocytosis, thrombocytosis or otherwise suspected to have a myeloproliferative neoplasm.0.3516606542013NANANANANA
rs386626619187814013717JAK2umls:C0027022BeFreeThe JAK2 V617F mutation has been implicated in a variety of diseases mainly related to myeloproliferative disorders including polycythemia Vera, essential thrombocythemia, and idiopathic Myelofibrosis but has not been previously described in Thalassemia patients.0.3516606542009NANANANANA
rs38662661925912019947CD34umls:C0027022BeFreeBMS-911543 is a JAK2-selective inhibitor that induces apoptosis in JAK2-dependent cell lines and inhibits the growth of CD34(+) progenitor cells from patients with JAK2(V617F)-positive MPN.0.0024429772015NANANANANA
rs386626619183287923717JAK2umls:C0027022BeFreeA sensitive assay for the JAK2 V617F mutation has the potential to diagnose atypical MPDs in multiple undiagnosed cases of intra-abdominal thrombosis and therefore alter the management and prognosis of these patients.0.3516606542008NANANANANA
rs386626619190169163717JAK2umls:C0027022BeFreeThe discovery of JAK2 V617F mutation has shed light on understanding of the molecular pathways involved in the pathogenesis of the myeloproliferative disorders.0.3516606542010NANANANANA
rs386626619173637313717JAK2umls:C0027022BeFreeLeukemic blasts in transformed JAK2-V617F-positive myeloproliferative disorders are frequently negative for the JAK2-V617F mutation.0.3516606542007NANANANANA
rs386626619219330043717JAK2umls:C0027022BeFreeJanus kinase 2 (JAK2) V617F mutation testing has revolutionized the classification of myeloproliferative disorders, for which several tests have been introduced for qualitative and quantitative diagnostics including the MutaScreen and MutaQuant kits by IPSOGEN.0.3516606542012NANANANANA
rs386626619201535053717JAK2umls:C0027022BeFreeWe conclude that JAK2 V617F mutation is uncommon in the 3q21q26 syndrome and that its presence may indicate an unusual coexistence of a myeloproliferative neoplasm.0.3516606542010NANANANANA
rs386626619259120193717JAK2umls:C0027022BeFreeLimited efficacy of BMS-911543 in a murine model of Janus kinase 2 V617F myeloproliferative neoplasm.0.3516606542015NANANANANA
rs386626619194744263717JAK2umls:C0027022BeFreeTET2 defects were present in hematopoietic stem cells and preceded the JAK2 V617F mutation in the five samples from patients with myeloproliferative disorders that we analyzed.0.3516606542009NANANANANA
rs386626619198160063717JAK2umls:C0027022BeFreeOur results seem to confirm that CLL cases are negative for JAK2(V617F) mutation in B- and T-lymphocyte populations.Presence of JAK2(V617F) mutation in subjects without myeloproliferative diseases could indicate an increased risk of a future myeloproliferative neoplasm development.0.3516606542009NANANANANA
rs386626619257463033717JAK2umls:C0027022BeFreeWe studied 1088 Chinese with diverse myeloproliferative neoplasms including ET (N=234) and PMF (N=50) without JAK2(V617F) or MPL exon 10 mutations.0.3516606542015NANANANANA
rs386626619226969083717JAK2umls:C0027022BeFreeAll idiopathic IAVT patients must be screened for JAK2(V617F) mutation to detect latent MPD.0.3516606542011NANANANANA
rs386626619196936453717JAK2umls:C0027022BeFreeMesenteric venous thrombosis secondary to an unsuspected JAK2 V617F-positive myeloproliferative disorder.0.3516606542012NANANANANA
rs386626619175961373717JAK2umls:C0027022BeFreeThe JAK2 V617F mutation is associated with platelet activation, as measured by elevated sP-selectin levels, in MPD.0.3516606542007NANANANANA
rs386626619173842213717JAK2umls:C0027022BeFreeAn acquired mutation in Janus kinase 2 (JAK2), V617F, has recently been identified in human myeloproliferative disorders.0.3516606542007NANANANANA
rs386626619169167243717JAK2umls:C0027022BeFreeWe aimed to determine the relative sensitivity of four separate molecular assays used to detect the presence of the JAK2 V617F mutation in peripheral blood from patients with essential thrombocythaemia and related myeloproliferative disorders.0.3516606542006NANANANANA
rs386626619194784803717JAK2umls:C0027022BeFreeJAK2 V617F-positive latent essential thrombocythemia and splanchnic vein thrombosis: the role of bone marrow biopsy for the diagnosis of myeloproliferative disease.0.3516606542009NANANANANA
rs386626619173842173717JAK2umls:C0027022BeFreeQuantitative determination of JAK2 V617F by TaqMan: An absolute measure of averaged copies per cell that may be associated with the different types of myeloproliferative disorders.0.3516606542007NANANANANA
rs386626619186000993717JAK2umls:C0027022BeFreeThe discovery of the Janus kinase 2 Val617Phe mutation has brought new insights into the development of myeloproliferative disorders; however, the pathogenesis of essential thrombocythemia and its related thrombotic complications has not been completely understood.0.3516606542008NANANANANA
rs386626619195213233717JAK2umls:C0027022BeFreeThe discovery that many patients with polycythemia vera, essential thrombocythemia, and primary myelofibrosis express a mutation in the Janus Kinase 2 gene (JAK2 V617F), a kinase essential for the normal development of erythrocytes, granulocytes, and platelets, provided a molecular explanation for the unregulated hematopoiesis typical of these disorders, a diagnostic test that distinguishes them from other types of myeloproliferative disorders, and an opportunity to develop targeted therapy that could potentially avoid the toxicities associated with the conventional chemotherapeutic agents currently employed in their treatment.0.3516606542009NANANANANA
rs386626619158606613717JAK2umls:C0027022BeFreeThe JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both atypical myeloproliferative disorders and myelodysplastic syndromes.0.3516606542005NANANANANA
rs386626619170594293717JAK2umls:C0027022BeFreeDetermination of the JAK2 V617F mutation may contribute to the search for genetic determinants of PMVT and may be useful to recognize patients who should be carefully observed for the subsequent development of overt MPDs.0.3516606542007NANANANANA
rs386626619180594843717JAK2umls:C0027022BeFreeSuch HLA-G5-mediated inhibition constitutes a new parameter to be considered in the design of future approaches aimed at treating JAK2 V617F-positive myeloproliferative disorders.0.3516606542008NANANANANA
rs386626619172660613717JAK2umls:C0027022BeFreeAnalysis of JAK2(V617F) mutation in Chinese patients with myeloproliferative disorders.0.3516606542007NANANANANA
rs386626619180039358809IL18R1umls:C0027022BeFreeFinally, we show that IL-27R can functionally replace a homodimeric type I cytokine receptor in the activation of JAK2-V617F, a critical JAK2 mutation in various myeloproliferative disorders (MPDs).0.0005428842007NANANANANA
rs386626619182940663717JAK2umls:C0027022BeFreeBecause of the clinical importance of this mutation in diagnosing myeloproliferative disorders and its relevance for disease progression, we have developed a tetra-primer polymerase chain reaction (PCR) assay to detect JAK2 p.V617F.0.3516606542007NANANANANA
rs386626619235882643717JAK2umls:C0027022BeFreeThe identification of Jak2(V617F) mutations in more than 90% of patients with polycythemia vera (PV) has greatly improved the diagnostic accuracy for this uncommon myeloproliferative disorder.0.3516606542013NANANANANA
rs386626619211183873717JAK2umls:C0027022BeFreeLaboratory testing for the presence of the V617F mutation in JAK2 has taken on great importance in the diagnosis of myeloproliferative disorders.0.3516606542011NANANANANA
rs386626619169463053717JAK2umls:C0027022BeFreeThe data suggest that the JAK2(V617F) mutation is apparently much more common than MPDs.0.3516606542007NANANANANA
rs386626619166757073717JAK2umls:C0027022BeFreeRecent information regarding disease pathogenesis, including a contribution to the myeloproliferative disorder phenotype by a gain-of-function JAK2 mutation (JAK2(V617F)), has revived the prospect of targeted therapeutics as well as molecular monitoring of treatment response.0.3516606542006NANANANANA
rs386626619189480493717JAK2umls:C0027022BeFreeMore recently, we demonstrated that constitutive phosphorylation of Lu/BCAM is also involved in abnormal RBC adhesion to endothelium in patients with polycythemia vera (PV), a frequent myeloproliferative disorders associated with the V617F mutation of the tyrosine kinase JAK2 leading to continuous stimulation of erythropoiesis.0.3516606542008NANANANANA
rs386626619260714745542PRB1umls:C0027022BeFreeIn the current study, mutations of JAK2 V617F, JAK2 exon 12, MPL exon 10, and CALR exon 9 were analyzed in 929 Chinese patients with BCR-ABL1-negative MPN, including 234 cases of polycythemia vera (PV), 428 ETs, 187 PMFs, and 80 unclassifiable MPNs (MPN-Us).0.0005428842015NANANANANA
rs386626619235585263717JAK2umls:C0027022BeFreeA role for reactive oxygen species in JAK2 V617F myeloproliferative neoplasm progression.0.3516606542013NANANANANA
rs386626619170069613717JAK2umls:C0027022BeFreeBecause of the clinical importance of this mutation (JAK2 V617F) in diagnosing myeloproliferative disorders and its relevance for disease progression, we developed a semi-quantitative real-time PCR test to detect JAK2 V617F.0.3516606542006NANANANANA
rs386626619225797134602MYBumls:C0027022BeFreeThe HDAC inhibitor Givinostat modulates the hematopoietic transcription factors NFE2 and C-MYB in JAK2(V617F) myeloproliferative neoplasm cells.0.0029957922012NANANANANA
rs3866266191946697525ABL1umls:C0027022BeFreeData on angiogenesis in the bone marrow of BCR-ABL1-negative myeloproliferative neoplasm (MPN) patients suggest an increase of the microvessel density (MVD) and vascular endothelial growth factor (VEGF) expression, but relations to the JAK2-V617F status remain controversial.0.017372282009NANANANANA
rs386626619187232643717JAK2umls:C0027022BeFreeWe conclude that the extent of JAK2(V617F) CD34(+) cell clonal dominance is associated with disease phenotype within the MPD and, in PV, is associated with extramedullary disease, leukocytosis, and disease duration.0.3516606542008NANANANANA
rs386626619188432873717JAK2umls:C0027022BeFreeThese results establish a role for JunB in normal erythropoiesis and indicate that JunB may play a major role in the development of JAK2 V617F myeloproliferative disorders.0.3516606542009NANANANANA
rs386626619184641143717JAK2umls:C0027022BeFreeAs JAK2 V617F, MPL W515L is a novel acquired mutation that induces constitutive cytokine-independent activation of the JAK-STAT pathway in myeloproliferative disorders (MPD).0.3516606542008NANANANANA
rs386626619167814783717JAK2umls:C0027022BeFreeIn addition, Bcr/Abl-negative classic myeloproliferative disorders are characterized by recurrent JAK2(V617F) mutations, whereas other mutations affecting the RAS signaling pathway molecules have been associated with juvenile myelomonocytic leukemia.0.3516606542006NANANANANA
rs386626619171458593717JAK2umls:C0027022BeFreeWe show that transplantation of JAK2(V617F)-transduced bone marrow into BALB/c mice induces MPD reminiscent of human PV, characterized by erythrocytosis, granulocytosis, extramedullary hematopoiesis, and bone marrow fibrosis, but not thrombocytosis.0.3516606542006NANANANANA
rs386626619257463034352MPLumls:C0027022BeFreeWe studied 1088 Chinese with diverse myeloproliferative neoplasms including ET (N=234) and PMF (N=50) without JAK2(V617F) or MPL exon 10 mutations.0.0366335162015NANANANANA
rs386626619224692363717JAK2umls:C0027022BeFreeIn this retrospective cohort study, patients with cerebral venous thrombosis were tested for the JAK2 V617F mutation and were followed until the development of a myeloproliferative neoplasm or censored at the end of follow-up.0.3516606542012NANANANANA
rs386626619168106093717JAK2umls:C0027022BeFreeMPD-specific markers such as serum EPO, endogenous erythroid colony formation (EEC), and JAK2 V617F have high specificities, but the sensitivities are not high enough to detect the early stages of the MPDs, ET, PV, and prefibrotic CIMF.0.3516606542006NANANANANA
rs386626619163736573717JAK2umls:C0027022BeFreeRelation between JAK2 (V617F) mutation status, granulocyte activation, and constitutive mobilization of CD34+ cells into peripheral blood in myeloproliferative disorders.0.3516606542006NANANANANA
rs38662661916373657947CD34umls:C0027022BeFreeWe studied the relationship between granulocyte JAK2 (V617F) mutation status, circulating CD34(+) cells, and granulocyte activation in myeloproliferative disorders.0.0024429772006NANANANANA
rs3866266191857504925ABL1umls:C0027022BeFreeBecause JAK2 V617F is specific for myeloid neoplasms, and because it can be detected in peripheral blood granulocytes, it offers a powerful tool that facilitates the diagnosis of these BCR-ABL negative myeloproLiferative disorders.0.017372282008NANANANANA
rs386626619173178613717JAK2umls:C0027022BeFreeThe myeloproliferative disorder-associated JAK2 V617F mutant escapes negative regulation by suppressor of cytokine signaling 3.0.3516606542007NANANANANA
rs386626619201338983717JAK2umls:C0027022BeFreeSince variability in the JAK2(V617F) allele burden is partly responsible for the distinct phenotypes seen in the myeloproliferative disorders, the objective of this study was to identify modifiers of the allele burden.0.3516606542010NANANANANA
rs386626619168106143717JAK2umls:C0027022BeFreeThe main conclusion is that JAK2 V617F is a 100% specific clue to a new distinct clonal myeloproliferative disorder.0.3516606542006NANANANANA
rs38662661919797525947CD34umls:C0027022BeFreeMultiple iPS cell lines were also generated from peripheral blood CD34(+) cells of 2 patients with myeloproliferative disorders (MPDs) who acquired the JAK2-V617F somatic mutation in their blood cells.0.0024429772009NANANANANA
rs386626619176981913717JAK2umls:C0027022BeFreeA new MALDI-TOF-based assay for monitoring JAK2 V617F mutation level in patients undergoing allogeneic stem cell transplantation (allo SCT) for classic myeloproliferative disorders (MPD).0.3516606542008NANANANANA
rs386626619234201503717JAK2umls:C0027022BeFreeThe JAK2 46/1 haplotype has recently been described as a major contributing factor to the development of myeloproliferative neoplasm, whether positive or negative forthe JAK2 V617F mutation.0.3516606542012NANANANANA
rs386626619254797523717JAK2umls:C0027022BeFreeIn mice, tamoxifen treatment blocked development of JAK2(V617F)-induced myeloproliferative neoplasm in vivo, induced apoptosis of human JAK2(V617F+) HSPCs in a xenograft model, and sensitized MLL-AF9(+) leukemias to chemotherapy.0.3516606542014NANANANANA
rs386626619200289723717JAK2umls:C0027022BeFreeSTAT5 activation is critical for the transformation mediated by myeloproliferative disorder-associated JAK2 V617F mutant.0.3516606542010NANANANANA
rs386626619171946633717JAK2umls:C0027022BeFreeDiscovery of a constitutively activating point mutation of the Janus kinase 2 (JAK2) receptor-associated tyrosine kinase in patients with polycythemia vera (PV) and other BCR/ABL-negative myeloproliferative disorders prompted many groups around the world to examine diverse subsets of patients with myeloid diseases for the prevalence of the JAK2 V617F mutation and its clinical and pathological associations.0.3516606542006NANANANANA
rs386626619191769883717JAK2umls:C0027022BeFreeA clear link appears to exist between leukocytosis, JAK2(V617F), and the hemostatic system activation in patients with Bcl-negative myeloproliferative disorders.0.3516606542008NANANANANA
rs3866266191947442654790TET2umls:C0027022BeFreeTET2 defects were present in hematopoietic stem cells and preceded the JAK2 V617F mutation in the five samples from patients with myeloproliferative disorders that we analyzed.0.0121825472009NANANANANA
rs386626619168310573717JAK2umls:C0027022BeFreeDetection of the JAK2(V617F) mutation in myeloproliferative disorders by melting curve analysis using the LightCycler system.0.3516606542006NANANANANA
rs386626619255380803717JAK2umls:C0027022BeFreeThus, targeting the pathway mediated by JAK and its downstream substrate, signal transducer and activator of transcription (STAT), may yield clinical benefit for patients with MPNs containing the JAK2(V617F) mutation.0.3516606542015NANANANANA
rs386626619179843123717JAK2umls:C0027022BeFreeSomatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders.0.3516606542008NANANANANA
rs386626619180546343717JAK2umls:C0027022BeFreeConventional diagnostic criteria for myeloproliferative disorders and the JAK2 V617F mutation (which is strongly associated with myeloproliferative disorders) were assessed in RVO patients showing EECs.0.3516606542007NANANANANA
rs386626619258345193717JAK2umls:C0027022BeFreeWe report a case of a 62-year-old black man with progressive abdominal swelling and features of decompensated chronic liver disease found to have SVT-portal vein thrombosis and how JAK2 V617F was useful in unmasking an underlying myeloproliferative neoplasm.0.3516606542015NANANANANA
rs386626619203061563717JAK2umls:C0027022BeFreeRecently, Janus kinase-2 (JAK2) V617F mutation has an important role in the diagnosis of myeloproliferative disorders, especially in polycythemia vera (PV).0.3516606542010NANANANANA
rs386626619230575174352MPLumls:C0027022BeFreeMolecular genetic assays for the detection of the JAK2 V617F (c.1849G>T) and other pathogenetic mutations within JAK2 exon 12 and MPL exon 10 are part of the routine diagnostic workup for patients presenting with erythrocytosis, thrombocytosis or otherwise suspected to have a myeloproliferative neoplasm.0.0366335162013NANANANANA
rs386626619162256513717JAK2umls:C0027022BeFreeAn association between an activating JAK2 mutation (JAK2(V617F)) and BCR/ABL-negative myeloproliferative disorders was recently reported in multiple simultaneous publications.0.3516606542005NANANANANA
rs386626619195646373717JAK2umls:C0027022BeFreeThe JAK2(V617F) mutation does not elucidate the phenotypic variability observed in myeloproliferative neoplasm (MPN) families.0.3516606542009NANANANANA
rs386626619252887763717JAK2umls:C0027022BeFreeThe V617F mutation in the JAK2 non-receptor tyrosine kinase (JAK2V617F) is present as an early somatic event in most patients with myeloproliferative neoplasms (MPNs), and the study of these chronic myeloid malignancies provides an experimentally tractable approach to understanding early tumorigenesis.0.3516606542015NANANANANA
rs386626619170226943717JAK2umls:C0027022BeFreeDetection of acquired Janus kinase 2 V617F mutation in myeloproliferative disorders by fluorescence melting curve analysis.0.3516606542006NANANANANA
rs386626619188151968651SOCS1umls:C0027022BeFreeSOCS1 expression was raised in myeloproliferative disorder granulocytes but the level was independent of JAK2 V617F status.0.0065344682008NANANANANA
rs386626619190476813717JAK2umls:C0027022BeFreeWe developed a real-time copy number polymerase chain reaction assay for deletions on chromosome 20q (del20q), screened peripheral blood granulocytes from 664 patients with myeloproliferative disorders, and identified 19 patients with del20q (2.9%), of which 14 (74%) were also positive for JAK2-V617F.0.3516606542009NANANANANA
rs386626619209665443717JAK2umls:C0027022BeFreeRecently, a single gain-of-function point mutation of JAK2 was described in myeloproliferative diseases leading to constitutive Jak2 kinase activity, subsequent Stat5a/b activation and involvement of V617F Jak2 in the pathogenesis of myeloproliferative disorders.0.3516606542010NANANANANA
rs386626619170456483717JAK2umls:C0027022BeFreeCorrelations of JAK2-V617F mutation with clinical and laboratory findings in patients with myeloproliferative disorders.0.3516606542007NANANANANA
rs386626619204890533717JAK2umls:C0027022BeFreeThe JAK2 V617F mutation is found in most patients with a myeloproliferative neoplasm and is sufficient to produce a myeloproliferative phenotype in murine retroviral transplantation or transgenic models.0.3516606542010NANANANANA
rs386626619204253353717JAK2umls:C0027022BeFreeThe JAK2(V617F) tyrosine kinase mutation in myeloproliferative disorders: Summary of published literature and a perspective.0.3516606542006NANANANANA
rs386626619175749703717JAK2umls:C0027022BeFreeIn an MPD with t(9;12)(q13 approximately q21;q22) and JAK2 V617F mutation, array comparative genomic hybridization delineated a deletion of about 3 Mb at 9q13 approximately q21 and a deletion of about 2 Mb at 12q22 containing SOCS2.0.3516606542007NANANANANA
rs386626619200289726776STAT5Aumls:C0027022BeFreeSTAT5 activation is critical for the transformation mediated by myeloproliferative disorder-associated JAK2 V617F mutant.0.0008143262010NANANANANA
rs386626619231110673717JAK2umls:C0027022BeFreeGivinostat and hydroxyurea synergize in vitro to induce apoptosis of cells from JAK2(V617F) myeloproliferative neoplasm patients.0.3516606542013NANANANANA
rs4495487222517093717JAK2umls:C0027022BeFreeThe C allele of JAK2 rs4495487 is an additional candidate locus that contributes to myeloproliferative neoplasm predisposition in the Japanese population.0.3516606542012JAK2;INSL695072798TC
rs77375493172660613717JAK2umls:C0027022BeFreeAnalysis of JAK2(V617F) mutation in Chinese patients with myeloproliferative disorders.0.3516606542007JAK2;INSL695073770GA,T
rs77375493252887763717JAK2umls:C0027022BeFreeThe V617F mutation in the JAK2 non-receptor tyrosine kinase (JAK2V617F) is present as an early somatic event in most patients with myeloproliferative neoplasms (MPNs), and the study of these chronic myeloid malignancies provides an experimentally tractable approach to understanding early tumorigenesis.0.3516606542015JAK2;INSL695073770GA,T
rs77375493198160063717JAK2umls:C0027022BeFreeOur results seem to confirm that CLL cases are negative for JAK2(V617F) mutation in B- and T-lymphocyte populations.Presence of JAK2(V617F) mutation in subjects without myeloproliferative diseases could indicate an increased risk of a future myeloproliferative neoplasm development.0.3516606542009JAK2;INSL695073770GA,T
rs77375493187962513717JAK2umls:C0027022BeFreeAccordingly, it seems that the investigation for the V617F mutation of the JAK2 gene is not mandatory in all Mexican mestizo patients with unexplained thrombophilia and that this genetic study should be reserved for special cases, such as patients with thrombosis in uncommon sites or patients with cell counts suggesting the presence of an underlying MPD.0.3516606542008JAK2;INSL695073770GA,T
rs77375493226969083717JAK2umls:C0027022BeFreeAll idiopathic IAVT patients must be screened for JAK2(V617F) mutation to detect latent MPD.0.3516606542011JAK2;INSL695073770GA,T
rs77375493233009954953ODC1umls:C0027022BeFreeCritical roles of Myc-ODC axis in the cellular transformation induced by myeloproliferative neoplasm-associated JAK2 V617F mutant.0.0002714422013JAK2;INSL695073770GA,T
rs77375493209665443717JAK2umls:C0027022BeFreeRecently, a single gain-of-function point mutation of JAK2 was described in myeloproliferative diseases leading to constitutive Jak2 kinase activity, subsequent Stat5a/b activation and involvement of V617F Jak2 in the pathogenesis of myeloproliferative disorders.0.3516606542010JAK2;INSL695073770GA,T
rs77375493201535053717JAK2umls:C0027022BeFreeWe conclude that JAK2 V617F mutation is uncommon in the 3q21q26 syndrome and that its presence may indicate an unusual coexistence of a myeloproliferative neoplasm.0.3516606542010JAK2;INSL695073770GA,T
rs77375493231110673717JAK2umls:C0027022BeFreeGivinostat and hydroxyurea synergize in vitro to induce apoptosis of cells from JAK2(V617F) myeloproliferative neoplasm patients.0.3516606542013JAK2;INSL695073770GA,T
rs77375493169989403717JAK2umls:C0027022BeFreeJAK2 (V617F) as an acquired somatic mutation and a secondary genetic event associated with disease progression in familial myeloproliferative disorders.0.3516606542006JAK2;INSL695073770GA,T
rs77375493260714743717JAK2umls:C0027022BeFreeIn the current study, mutations of JAK2 V617F, JAK2 exon 12, MPL exon 10, and CALR exon 9 were analyzed in 929 Chinese patients with BCR-ABL1-negative MPN, including 234 cases of polycythemia vera (PV), 428 ETs, 187 PMFs, and 80 unclassifiable MPNs (MPN-Us).0.3516606542015JAK2;INSL695073770GA,T
rs77375493169463053717JAK2umls:C0027022BeFreeThe data suggest that the JAK2(V617F) mutation is apparently much more common than MPDs.0.3516606542007JAK2;INSL695073770GA,T
rs7737549318723264947CD34umls:C0027022BeFreeWe conclude that the extent of JAK2(V617F) CD34(+) cell clonal dominance is associated with disease phenotype within the MPD and, in PV, is associated with extramedullary disease, leukocytosis, and disease duration.0.0024429772008JAK2;INSL695073770GA,T
rs77375493233009953717JAK2umls:C0027022BeFreeCritical roles of Myc-ODC axis in the cellular transformation induced by myeloproliferative neoplasm-associated JAK2 V617F mutant.0.3516606542013JAK2;INSL695073770GA,T
rs77375493170226943717JAK2umls:C0027022BeFreeDetection of acquired Janus kinase 2 V617F mutation in myeloproliferative disorders by fluorescence melting curve analysis.0.3516606542006JAK2;INSL695073770GA,T
rs77375493230575174352MPLumls:C0027022BeFreeMolecular genetic assays for the detection of the JAK2 V617F (c.1849G>T) and other pathogenetic mutations within JAK2 exon 12 and MPL exon 10 are part of the routine diagnostic workup for patients presenting with erythrocytosis, thrombocytosis or otherwise suspected to have a myeloproliferative neoplasm.0.0366335162013JAK2;INSL695073770GA,T
rs77375493190169163717JAK2umls:C0027022BeFreeThe discovery of JAK2 V617F mutation has shed light on understanding of the molecular pathways involved in the pathogenesis of the myeloproliferative disorders.0.3516606542010JAK2;INSL695073770GA,T
rs77375493183287923717JAK2umls:C0027022BeFreeA sensitive assay for the JAK2 V617F mutation has the potential to diagnose atypical MPDs in multiple undiagnosed cases of intra-abdominal thrombosis and therefore alter the management and prognosis of these patients.0.3516606542008JAK2;INSL695073770GA,T
rs77375493253455903717JAK2umls:C0027022BeFreeThe acquired JAK2 V617F mutation is common in patients with myeloproliferative neoplasms.0.3516606542014JAK2;INSL695073770GA,T
rs77375493168106094597MVDumls:C0027022BeFreeBone marrow histopathology in addition to clinical, laboratory, biological, and molecular markers, including the JAK2 V617 PCR test, serum EPO, PRV-1, EEC, LAP score, peripheral blood parameters, and spleen size on echogram will detect the early stages of MPD and allows diagnostic differentiation of the three primary MPDs (ET, PV, and CIMF) in both JAK2 V617F-positive and JAK2 wild-type MPD patients.0.0024429772006JAK2;INSL695073770GA,T
rs77375493249514233717JAK2umls:C0027022BeFreeJAK2(V617F), the main mutation involved in MPN, is considered as a risk factor for thrombosis, although the direct link between the mutation and hemostatic disorders is not strictly established.0.3516606542015JAK2;INSL695073770GA,T
rs77375493194824423717JAK2umls:C0027022BeFreeThe JAK2 [V617F] mutation has recently been recognised as critical to the pathogenesis of the myeloproliferative disorders (MPDs).0.3516606542009JAK2;INSL695073770GA,T
rs77375493164563753717JAK2umls:C0027022BeFreeThe major incentives for this review have been the recent description of an activating JAK2 tyrosine kinase mutation (JAK2 (V617F)) in essential thrombocythemia, related myeloproliferative disorders, and the impact on clinical practice from the publication of a major treatment trial.0.3516606542006JAK2;INSL695073770GA,T
rs77375493250129142046EPHA8umls:C0027022BeFreeDiscovery of the protein tyrosine kinase JAK2 V617F allele contributed to better understanding of the pathogenetic mechanisms of MPNs.0.0005428842014JAK2;INSL695073770GA,T
rs77375493200289726777STAT5Bumls:C0027022BeFreeSTAT5 activation is critical for the transformation mediated by myeloproliferative disorder-associated JAK2 V617F mutant.0.0005428842010JAK2;INSL695073770GA,T
rs7737549316373657947CD34umls:C0027022BeFreeWe studied the relationship between granulocyte JAK2 (V617F) mutation status, circulating CD34(+) cells, and granulocyte activation in myeloproliferative disorders.0.0024429772006JAK2;INSL695073770GA,T
rs77375493169167243717JAK2umls:C0027022BeFreeWe aimed to determine the relative sensitivity of four separate molecular assays used to detect the presence of the JAK2 V617F mutation in peripheral blood from patients with essential thrombocythaemia and related myeloproliferative disorders.0.3516606542006JAK2;INSL695073770GA,T
rs77375493196936453717JAK2umls:C0027022BeFreeMesenteric venous thrombosis secondary to an unsuspected JAK2 V617F-positive myeloproliferative disorder.0.3516606542012JAK2;INSL695073770GA,T
rs77375493170069613717JAK2umls:C0027022BeFreeBecause of the clinical importance of this mutation (JAK2 V617F) in diagnosing myeloproliferative disorders and its relevance for disease progression, we developed a semi-quantitative real-time PCR test to detect JAK2 V617F.0.3516606542006JAK2;INSL695073770GA,T
rs77375493160816843717JAK2umls:C0027022BeFreeAltered gene expression in myeloproliferative disorders correlates with activation of signaling by the V617F mutation of Jak2.0.3516606542005JAK2;INSL695073770GA,T
rs77375493173842173717JAK2umls:C0027022BeFreeQuantitative determination of JAK2 V617F by TaqMan: An absolute measure of averaged copies per cell that may be associated with the different types of myeloproliferative disorders.0.3516606542007JAK2;INSL695073770GA,T
rs773754931800393510148EBI3umls:C0027022BeFreeFinally, we show that IL-27R can functionally replace a homodimeric type I cytokine receptor in the activation of JAK2-V617F, a critical JAK2 mutation in various myeloproliferative disorders (MPDs).0.0005428842007JAK2;INSL695073770GA,T
rs77375493183365413717JAK2umls:C0027022BeFreeThe JAK2-V617F mutation can be frequently detected in the Taiwanese patients with MPD disorders and therefore should be incorporated into the initial evaluation of patients suspected of MPD.0.3516606542008JAK2;INSL695073770GA,T
rs77375493200289726776STAT5Aumls:C0027022BeFreeSTAT5 activation is critical for the transformation mediated by myeloproliferative disorder-associated JAK2 V617F mutant.0.0008143262010JAK2;INSL695073770GA,T
rs77375493190476813717JAK2umls:C0027022BeFreeWe developed a real-time copy number polymerase chain reaction assay for deletions on chromosome 20q (del20q), screened peripheral blood granulocytes from 664 patients with myeloproliferative disorders, and identified 19 patients with del20q (2.9%), of which 14 (74%) were also positive for JAK2-V617F.0.3516606542009JAK2;INSL695073770GA,T
rs77375493173842213717JAK2umls:C0027022BeFreeAn acquired mutation in Janus kinase 2 (JAK2), V617F, has recently been identified in human myeloproliferative disorders.0.3516606542007JAK2;INSL695073770GA,T
rs77375493180546343717JAK2umls:C0027022BeFreeConventional diagnostic criteria for myeloproliferative disorders and the JAK2 V617F mutation (which is strongly associated with myeloproliferative disorders) were assessed in RVO patients showing EECs.0.3516606542007JAK2;INSL695073770GA,T
rs77375493209665446776STAT5Aumls:C0027022BeFreeRecently, a single gain-of-function point mutation of JAK2 was described in myeloproliferative diseases leading to constitutive Jak2 kinase activity, subsequent Stat5a/b activation and involvement of V617F Jak2 in the pathogenesis of myeloproliferative disorders.0.0008143262010JAK2;INSL695073770GA,T
rs7737549319797525947CD34umls:C0027022BeFreeMultiple iPS cell lines were also generated from peripheral blood CD34(+) cells of 2 patients with myeloproliferative disorders (MPDs) who acquired the JAK2-V617F somatic mutation in their blood cells.0.0024429772009JAK2;INSL695073770GA,T
rs77375493190040763717JAK2umls:C0027022BeFreeThe role of screening for the JAK2 V617F mutation in patients presenting with thrombosis without overt MPD is unclear, but appears justified in cases of idiopathic splanchnic vein thrombosis.0.3516606542008JAK2;INSL695073770GA,T
rs77375493168106143717JAK2umls:C0027022BeFreeThe main conclusion is that JAK2 V617F is a 100% specific clue to a new distinct clonal myeloproliferative disorder.0.3516606542006JAK2;INSL695073770GA,T
rs77375493174081063717JAK2umls:C0027022BeFreeA new mutation (V617F) affecting the JAK2 gene has been recently described as acquired in patients with myeloproliferative disorders and other myeloid malignancies.0.3516606542006JAK2;INSL695073770GA,T
rs77375493199395823717JAK2umls:C0027022BeFreeJAK2-V617F mutation in Moroccan patients with myeloproliferative disorders: contribution, diagnosis and therapeutic prospects.0.3516606542011JAK2;INSL695073770GA,T
rs7737549319466975613BCRumls:C0027022BeFreeData on angiogenesis in the bone marrow of BCR-ABL1-negative myeloproliferative neoplasm (MPN) patients suggest an increase of the microvessel density (MVD) and vascular endothelial growth factor (VEGF) expression, but relations to the JAK2-V617F status remain controversial.0.1281531882009JAK2;INSL695073770GA,T
rs77375493185286463717JAK2umls:C0027022BeFreeA single mutation 1849G>T in the JAK2 gene (V617F) has recently been described in classical myeloproliferative disorders (MPD).0.3516606542008JAK2;INSL695073770GA,T
rs77375493257463033717JAK2umls:C0027022BeFreeWe studied 1088 Chinese with diverse myeloproliferative neoplasms including ET (N=234) and PMF (N=50) without JAK2(V617F) or MPL exon 10 mutations.0.3516606542015JAK2;INSL695073770GA,T
rs77375493181606703717JAK2umls:C0027022BeFreeAn acquired somatic mutation in the JAK2 gene (JAK2-V617F) is present in the majority of patients with myeloproliferative disorders (MPDs).0.3516606542008JAK2;INSL695073770GA,T
rs77375493162256513717JAK2umls:C0027022BeFreeAn association between an activating JAK2 mutation (JAK2(V617F)) and BCR/ABL-negative myeloproliferative disorders was recently reported in multiple simultaneous publications.0.3516606542005JAK2;INSL695073770GA,T
rs77375493195646373717JAK2umls:C0027022BeFreeThe JAK2(V617F) mutation does not elucidate the phenotypic variability observed in myeloproliferative neoplasm (MPN) families.0.3516606542009JAK2;INSL695073770GA,T
rs77375493164080983717JAK2umls:C0027022BeFreeJAK2 V617F tyrosine kinase mutation in cell lines derived from myeloproliferative disorders.0.3516606542006JAK2;INSL695073770GA,T
rs77375493192168433717JAK2umls:C0027022BeFreeAlthough the Jak2-V617F mutation has generated strong awareness because of its causative role in myeloproliferative disorders, reports of Jak2 gene aberrations linked to hematologic malignancies have preceded those of V617F by nearly a decade.0.3516606542009JAK2;INSL695073770GA,T
rs77375493211983213717JAK2umls:C0027022BeFreeJAK2 V617F gene mutation in the laboratory work-up of myeloproliferative disorders: experience of a major referral center in Lebanon.0.3516606542011JAK2;INSL695073770GA,T
rs77375493170594293717JAK2umls:C0027022BeFreeDetermination of the JAK2 V617F mutation may contribute to the search for genetic determinants of PMVT and may be useful to recognize patients who should be carefully observed for the subsequent development of overt MPDs.0.3516606542007JAK2;INSL695073770GA,T
rs77375493233918443717JAK2umls:C0027022BeFreeIn contrast, this same mutation has been detected in only 4 patients with CNL to date, suggesting that the JAK2 V617F mutation is a rare event in patients with atypical MPD.0.3516606542013JAK2;INSL695073770GA,T
rs77375493168106093717JAK2umls:C0027022BeFreeMPD-specific markers such as serum EPO, endogenous erythroid colony formation (EEC), and JAK2 V617F have high specificities, but the sensitivities are not high enough to detect the early stages of the MPDs, ET, PV, and prefibrotic CIMF.0.3516606542006JAK2;INSL695073770GA,T
rs77375493173637313717JAK2umls:C0027022BeFreeLeukemic blasts in transformed JAK2-V617F-positive myeloproliferative disorders are frequently negative for the JAK2-V617F mutation.0.3516606542007JAK2;INSL695073770GA,T
rs77375493195213233717JAK2umls:C0027022BeFreeThe discovery that many patients with polycythemia vera, essential thrombocythemia, and primary myelofibrosis express a mutation in the Janus Kinase 2 gene (JAK2 V617F), a kinase essential for the normal development of erythrocytes, granulocytes, and platelets, provided a molecular explanation for the unregulated hematopoiesis typical of these disorders, a diagnostic test that distinguishes them from other types of myeloproliferative disorders, and an opportunity to develop targeted therapy that could potentially avoid the toxicities associated with the conventional chemotherapeutic agents currently employed in their treatment.0.3516606542009JAK2;INSL695073770GA,T
rs77375493214351893717JAK2umls:C0027022BeFreeThe prevalence of overt MPN and that of JAK2 V617F were lower in Korean patients with SVT than in previous reports.0.3516606542011JAK2;INSL695073770GA,T
rs77375493176875553717JAK2umls:C0027022BeFreeJAK2(V617F) positive early stage myeloproliferative disease (essential thrombocythemia) as the cause of portal vein thrombosis in two middle-aged women: therapeutic implications in view of the literature.0.3516606542007JAK2;INSL695073770GA,T
rs77375493166757073717JAK2umls:C0027022BeFreeRecent information regarding disease pathogenesis, including a contribution to the myeloproliferative disorder phenotype by a gain-of-function JAK2 mutation (JAK2(V617F)), has revived the prospect of targeted therapeutics as well as molecular monitoring of treatment response.0.3516606542006JAK2;INSL695073770GA,T
rs77375493172513343717JAK2umls:C0027022BeFreeHowever, the recent identification of a V617F mutation in the JH2 domain of the JAK2 gene in a high proportion of patients suffering from MPDs may provide confirmation of a diagnosis.0.3516606542007JAK2;INSL695073770GA,T
rs77375493219330043717JAK2umls:C0027022BeFreeJanus kinase 2 (JAK2) V617F mutation testing has revolutionized the classification of myeloproliferative disorders, for which several tests have been introduced for qualitative and quantitative diagnostics including the MutaScreen and MutaQuant kits by IPSOGEN.0.3516606542012JAK2;INSL695073770GA,T
rs77375493180559833717JAK2umls:C0027022BeFreeFour novel JAK2 mutant alleles have recently been described in patients with V617F-negative myeloproliferative disorders presenting with erythrocytosis.0.3516606542007JAK2;INSL695073770GA,T
rs77375493194744263717JAK2umls:C0027022BeFreeTET2 defects were present in hematopoietic stem cells and preceded the JAK2 V617F mutation in the five samples from patients with myeloproliferative disorders that we analyzed.0.3516606542009JAK2;INSL695073770GA,T
rs773754931857504925ABL1umls:C0027022BeFreeBecause JAK2 V617F is specific for myeloid neoplasms, and because it can be detected in peripheral blood granulocytes, it offers a powerful tool that facilitates the diagnosis of these BCR-ABL negative myeloproLiferative disorders.0.017372282008JAK2;INSL695073770GA,T
rs7737549325912019947CD34umls:C0027022BeFreeBMS-911543 is a JAK2-selective inhibitor that induces apoptosis in JAK2-dependent cell lines and inhibits the growth of CD34(+) progenitor cells from patients with JAK2(V617F)-positive MPN.0.0024429772015JAK2;INSL695073770GA,T
rs77375493257463034352MPLumls:C0027022BeFreeWe studied 1088 Chinese with diverse myeloproliferative neoplasms including ET (N=234) and PMF (N=50) without JAK2(V617F) or MPL exon 10 mutations.0.0366335162015JAK2;INSL695073770GA,T
rs77375493168310573717JAK2umls:C0027022BeFreeDetection of the JAK2(V617F) mutation in myeloproliferative disorders by melting curve analysis using the LightCycler system.0.3516606542006JAK2;INSL695073770GA,T
rs77375493188151963717JAK2umls:C0027022BeFreeSOCS3 transcript levels were highest in patients with polycythemia vera and other JAK2 V617F positive myeloproliferative disorders, consistent with SOCS3 being a target gene of JAK2/STAT5 signaling.0.3516606542008JAK2;INSL695073770GA,T
rs77375493184641143717JAK2umls:C0027022BeFreeAs JAK2 V617F, MPL W515L is a novel acquired mutation that induces constitutive cytokine-independent activation of the JAK-STAT pathway in myeloproliferative disorders (MPD).0.3516606542008JAK2;INSL695073770GA,T
rs77375493191769883717JAK2umls:C0027022BeFreeA clear link appears to exist between leukocytosis, JAK2(V617F), and the hemostatic system activation in patients with Bcl-negative myeloproliferative disorders.0.3516606542008JAK2;INSL695073770GA,T
rs77375493182459483717JAK2umls:C0027022BeFreeIn 2005, a point mutation in JAK2 (JAK2-V617F) was identified in a number of neoplastic myeloproliferative disorders, ushering in a new era of JAK2 research.0.3516606542008JAK2;INSL695073770GA,T
rs77375493179843123717JAK2umls:C0027022BeFreeSomatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders.0.3516606542008JAK2;INSL695073770GA,T
rs77375493201338983717JAK2umls:C0027022BeFreeSince variability in the JAK2(V617F) allele burden is partly responsible for the distinct phenotypes seen in the myeloproliferative disorders, the objective of this study was to identify modifiers of the allele burden.0.3516606542010JAK2;INSL695073770GA,T
rs77375493186000993717JAK2umls:C0027022BeFreeThe discovery of the Janus kinase 2 Val617Phe mutation has brought new insights into the development of myeloproliferative disorders; however, the pathogenesis of essential thrombocythemia and its related thrombotic complications has not been completely understood.0.3516606542008JAK2;INSL695073770GA,T
rs77375493182455403717JAK2umls:C0027022BeFreeThe discovery of an activating somatic mutation in codon 617 of the gene encoding the Janus kinase (JAK)-2 (JAK2 V617F) in patients with myeloproliferative disorders has opened new avenues for the development of targeted therapies for these malignancies.0.3516606542008JAK2;INSL695073770GA,T
rs77375493225797134778NFE2umls:C0027022BeFreeThe HDAC inhibitor Givinostat modulates the hematopoietic transcription factors NFE2 and C-MYB in JAK2(V617F) myeloproliferative neoplasm cells.0.0005428842012JAK2;INSL695073770GA,T
rs77375493248584123717JAK2umls:C0027022BeFreeAssociation between thromboembolic events and the JAK2 V617F mutation in myeloproliferative neoplasms.0.3516606542015JAK2;INSL695073770GA,T
rs77375493173178613717JAK2umls:C0027022BeFreeThe myeloproliferative disorder-associated JAK2 V617F mutant escapes negative regulation by suppressor of cytokine signaling 3.0.3516606542007JAK2;INSL695073770GA,T
rs77375493194669753717JAK2umls:C0027022BeFreeIn addition, it provides evidence that despite the fact that angiogenesis is generally independent of the JAK2-V617F status in MPN, new vessel formation might be linked to Jak2 effects in some cases with high JAK2-V617F mutant allele burden.0.3516606542009JAK2;INSL695073770GA,T
rs77375493170456483717JAK2umls:C0027022BeFreeCorrelations of JAK2-V617F mutation with clinical and laboratory findings in patients with myeloproliferative disorders.0.3516606542007JAK2;INSL695073770GA,T
rs77375493163736573717JAK2umls:C0027022BeFreeRelation between JAK2 (V617F) mutation status, granulocyte activation, and constitutive mobilization of CD34+ cells into peripheral blood in myeloproliferative disorders.0.3516606542006JAK2;INSL695073770GA,T
rs77375493171458593717JAK2umls:C0027022BeFreeWe show that transplantation of JAK2(V617F)-transduced bone marrow into BALB/c mice induces MPD reminiscent of human PV, characterized by erythrocytosis, granulocytosis, extramedullary hematopoiesis, and bone marrow fibrosis, but not thrombocytosis.0.3516606542006JAK2;INSL695073770GA,T
rs77375493254797525688PSMA7umls:C0027022BeFreeIn mice, tamoxifen treatment blocked development of JAK2(V617F)-induced myeloproliferative neoplasm in vivo, induced apoptosis of human JAK2(V617F+) HSPCs in a xenograft model, and sensitized MLL-AF9(+) leukemias to chemotherapy.0.0002714422014JAK2;INSL695073770GA,T
rs77375493183007583717JAK2umls:C0027022BeFreeThe high prevalence of the V617F mutation of Janus kinase 2 and associated mutations in myeloproliferative disorders (> 95% in polycythemia vera and about half of patients with essential thrombocythemia and primary myelofibrosis) has led the World Health Organization to alter the diagnostic criteria for these myeloproliferative disorders, and these changes are reviewed.0.3516606542008JAK2;INSL695073770GA,T
rs77375493249635933717JAK2umls:C0027022BeFreeThe JAK2 V617F mutation is highly prevalent in patients with myeloproliferative neoplasms (MPN).0.3516606542014JAK2;INSL695073770GA,T
rs77375493168106092056EPOumls:C0027022BeFreeMPD-specific markers such as serum EPO, endogenous erythroid colony formation (EEC), and JAK2 V617F have high specificities, but the sensitivities are not high enough to detect the early stages of the MPDs, ET, PV, and prefibrotic CIMF.0.0008143262006JAK2;INSL695073770GA,T
rs77375493171787223717JAK2umls:C0027022BeFreeThese data suggest that erlotinib may be used for treatment of JAK2(V617F)-positive PV and other myeloproliferative disorders.0.3516606542007JAK2;INSL695073770GA,T
rs77375493225797133717JAK2umls:C0027022BeFreeThe HDAC inhibitor Givinostat modulates the hematopoietic transcription factors NFE2 and C-MYB in JAK2(V617F) myeloproliferative neoplasm cells.0.3516606542012JAK2;INSL695073770GA,T
rs77375493254797523717JAK2umls:C0027022BeFreeIn mice, tamoxifen treatment blocked development of JAK2(V617F)-induced myeloproliferative neoplasm in vivo, induced apoptosis of human JAK2(V617F+) HSPCs in a xenograft model, and sensitized MLL-AF9(+) leukemias to chemotherapy.0.3516606542014JAK2;INSL695073770GA,T
rs77375493255594613717JAK2umls:C0027022BeFreeThe JAK2 V617F mutational status and allele burden may be related with the risk of venous thromboembolic events in patients with Philadelphia-negative myeloproliferative neoplasms.0.3516606542014JAK2;INSL695073770GA,T
rs77375493258345193717JAK2umls:C0027022BeFreeWe report a case of a 62-year-old black man with progressive abdominal swelling and features of decompensated chronic liver disease found to have SVT-portal vein thrombosis and how JAK2 V617F was useful in unmasking an underlying myeloproliferative neoplasm.0.3516606542015JAK2;INSL695073770GA,T
rs77375493259120193717JAK2umls:C0027022BeFreeLimited efficacy of BMS-911543 in a murine model of Janus kinase 2 V617F myeloproliferative neoplasm.0.3516606542015JAK2;INSL695073770GA,T
rs77375493188432873717JAK2umls:C0027022BeFreeThese results establish a role for JunB in normal erythropoiesis and indicate that JunB may play a major role in the development of JAK2 V617F myeloproliferative disorders.0.3516606542009JAK2;INSL695073770GA,T
rs77375493255380803717JAK2umls:C0027022BeFreeThus, targeting the pathway mediated by JAK and its downstream substrate, signal transducer and activator of transcription (STAT), may yield clinical benefit for patients with MPNs containing the JAK2(V617F) mutation.0.3516606542015JAK2;INSL695073770GA,T
rs77375493250129143717JAK2umls:C0027022BeFreeDiscovery of the protein tyrosine kinase JAK2 V617F allele contributed to better understanding of the pathogenetic mechanisms of MPNs.0.3516606542014JAK2;INSL695073770GA,T
rs77375493221327293717JAK2umls:C0027022BeFreeRecent studies have identified a recurrent somatic activating mutation (JAK2 V617F) in majority of patients with myeloproliferative disorders (MPDs).0.3516606542012JAK2;INSL695073770GA,T
rs77375493225797134602MYBumls:C0027022BeFreeThe HDAC inhibitor Givinostat modulates the hematopoietic transcription factors NFE2 and C-MYB in JAK2(V617F) myeloproliferative neoplasm cells.0.0029957922012JAK2;INSL695073770GA,T
rs77375493162850063717JAK2umls:C0027022BeFreeThe V617F JAK2 mutation and the myeloproliferative disorders.0.3516606542005JAK2;INSL695073770GA,T
rs77375493180328833717JAK2umls:C0027022BeFreePresence of JAK2(V617F) in bone marrow might therefore increase the risk of future MPD development, just as monoclonal gammopathy of undetermined significance (MGUS) increases the risk of multiple myeloma.0.3516606542007JAK2;INSL695073770GA,T
rs77375493204890533717JAK2umls:C0027022BeFreeThe JAK2 V617F mutation is found in most patients with a myeloproliferative neoplasm and is sufficient to produce a myeloproliferative phenotype in murine retroviral transplantation or transgenic models.0.3516606542010JAK2;INSL695073770GA,T
rs77375493252596263717JAK2umls:C0027022BeFreeThe classical Philadelphia chromosome-negative myeloproliferative neoplasms consist of three main pathological and clinical entities with the recurrent JAK2 V617F mutation present in ∼98% of patients with polycythemia vera and ∼50% of patients with essential thrombocythemia (ET) and primary myelofibrosis (PMF).0.3516606542015JAK2;INSL695073770GA,T
rs77375493211183873717JAK2umls:C0027022BeFreeLaboratory testing for the presence of the V617F mutation in JAK2 has taken on great importance in the diagnosis of myeloproliferative disorders.0.3516606542011JAK2;INSL695073770GA,T
rs77375493207284373717JAK2umls:C0027022BeFreeWe studied the sensitivity and reproducibility of LightScanner™ platform in the detection of JAK2 V617F mutation and the availability for diagnostic use in MPN.0.3516606542010JAK2;INSL695073770GA,T
rs77375493230575173717JAK2umls:C0027022BeFreeMolecular genetic assays for the detection of the JAK2 V617F (c.1849G>T) and other pathogenetic mutations within JAK2 exon 12 and MPL exon 10 are part of the routine diagnostic workup for patients presenting with erythrocytosis, thrombocytosis or otherwise suspected to have a myeloproliferative neoplasm.0.3516606542013JAK2;INSL695073770GA,T
rs77375493235882643717JAK2umls:C0027022BeFreeThe identification of Jak2(V617F) mutations in more than 90% of patients with polycythemia vera (PV) has greatly improved the diagnostic accuracy for this uncommon myeloproliferative disorder.0.3516606542013JAK2;INSL695073770GA,T
rs773754932330099589874SLC25A21umls:C0027022BeFreeCritical roles of Myc-ODC axis in the cellular transformation induced by myeloproliferative neoplasm-associated JAK2 V617F mutant.0.0002714422013JAK2;INSL695073770GA,T
rs77375493250156343717JAK2umls:C0027022BeFreeJAK2 V617F mutation is a molecular marker for myeloproliferative neoplasms (MPNs).0.3516606542015JAK2;INSL695073770GA,T
rs77375493182162973717JAK2umls:C0027022BeFreeThe V617F activating point mutation in Jak2 is associated with a proportion of myeloproliferative disorders.0.3516606542008JAK2;INSL695073770GA,T
rs77375493184641146646SOAT1umls:C0027022BeFreeAs JAK2 V617F, MPL W515L is a novel acquired mutation that induces constitutive cytokine-independent activation of the JAK-STAT pathway in myeloproliferative disorders (MPD).0.0021715352008JAK2;INSL695073770GA,T
rs77375493262352143717JAK2umls:C0027022BeFreeMicrofluidics-based assays can reduce the assay time and sample/reagent consumption and enhance the reaction efficiency; however, no current assay has integrated isothermal amplification for point-of-care MPN JAK2 V617F mutation testing with a microchip.0.3516606542015JAK2;INSL695073770GA,T
rs77375493187814013717JAK2umls:C0027022BeFreeThe JAK2 V617F mutation has been implicated in a variety of diseases mainly related to myeloproliferative disorders including polycythemia Vera, essential thrombocythemia, and idiopathic Myelofibrosis but has not been previously described in Thalassemia patients.0.3516606542009JAK2;INSL695073770GA,T
rs77375493198777613717JAK2umls:C0027022BeFreeThe JAK2 V617F mutation has been implicated in a variety of diseases mainly related to myeloproliferative disorders including polycythemia vera, essential thrombocythemia, and idiopathic myelofibrosis with an increased demand for testing using molecular techniques.0.3516606542010JAK2;INSL695073770GA,T
rs77375493165378033717JAK2umls:C0027022BeFreeGenetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders.0.3516606542006JAK2;INSL695073770GA,T
rs77375493213315933717JAK2umls:C0027022BeFreeA molecular fingerprint distinguishes JAK2(V617F)-positive MPN patients without response to HU treatment, with overexpression of JAK2, MAPK14, PIK3CA, and SFK genes.0.3516606542011JAK2;INSL695073770GA,T
rs773754931946697525ABL1umls:C0027022BeFreeData on angiogenesis in the bone marrow of BCR-ABL1-negative myeloproliferative neoplasm (MPN) patients suggest an increase of the microvessel density (MVD) and vascular endothelial growth factor (VEGF) expression, but relations to the JAK2-V617F status remain controversial.0.017372282009JAK2;INSL695073770GA,T
rs77375493187232643717JAK2umls:C0027022BeFreeWe conclude that the extent of JAK2(V617F) CD34(+) cell clonal dominance is associated with disease phenotype within the MPD and, in PV, is associated with extramedullary disease, leukocytosis, and disease duration.0.3516606542008JAK2;INSL695073770GA,T
rs77375493175961373717JAK2umls:C0027022BeFreeThe JAK2 V617F mutation is associated with platelet activation, as measured by elevated sP-selectin levels, in MPD.0.3516606542007JAK2;INSL695073770GA,T
rs77375493180039358809IL18R1umls:C0027022BeFreeFinally, we show that IL-27R can functionally replace a homodimeric type I cytokine receptor in the activation of JAK2-V617F, a critical JAK2 mutation in various myeloproliferative disorders (MPDs).0.0005428842007JAK2;INSL695073770GA,T
rs77375493224692363717JAK2umls:C0027022BeFreeIn this retrospective cohort study, patients with cerebral venous thrombosis were tested for the JAK2 V617F mutation and were followed until the development of a myeloproliferative neoplasm or censored at the end of follow-up.0.3516606542012JAK2;INSL695073770GA,T
rs77375493190463163717JAK2umls:C0027022BeFreeThe JAK2(V617F) tyrosine kinase mutation identifies clinically latent myeloproliferative disorders in patients presenting with hepatic or portal vein thrombosis.0.3516606542008JAK2;INSL695073770GA,T
rs773754931622565125ABL1umls:C0027022BeFreeAn association between an activating JAK2 mutation (JAK2(V617F)) and BCR/ABL-negative myeloproliferative disorders was recently reported in multiple simultaneous publications.0.017372282005JAK2;INSL695073770GA,T
rs77375493235585263717JAK2umls:C0027022BeFreeA role for reactive oxygen species in JAK2 V617F myeloproliferative neoplasm progression.0.3516606542013JAK2;INSL695073770GA,T
rs773754931719466325ABL1umls:C0027022BeFreeDiscovery of a constitutively activating point mutation of the Janus kinase 2 (JAK2) receptor-associated tyrosine kinase in patients with polycythemia vera (PV) and other BCR/ABL-negative myeloproliferative disorders prompted many groups around the world to examine diverse subsets of patients with myeloid diseases for the prevalence of the JAK2 V617F mutation and its clinical and pathological associations.0.017372282006JAK2;INSL695073770GA,T
rs77375493240661273717JAK2umls:C0027022BeFreeHeterozygous and homozygous JAK2(V617F) states modeled by induced pluripotent stem cells from myeloproliferative neoplasm patients.0.3516606542013JAK2;INSL695073770GA,T
rs77375493162938803717JAK2umls:C0027022BeFreeThe nature of the specific oncogenic mutation(s) is currently being unraveled with the recent discovery of an association between a somatic point mutation of JAK2 tyrosine kinase (V617F) and bcr/abl-negative myeloproliferative disorders, including MMM.0.3516606542005JAK2;INSL695073770GA,T
rs77375493165025903717JAK2umls:C0027022BeFreeMethods for the detection of the JAK2 V617F mutation in human myeloproliferative disorders.0.3516606542006JAK2;INSL695073770GA,T
rs77375493166702663717JAK2umls:C0027022BeFreeQuestions remain regarding the exact contribution of JAK2(V617F) in other myeloproliferative disorders.0.3516606542006JAK2;INSL695073770GA,T
rs77375493260714745542PRB1umls:C0027022BeFreeIn the current study, mutations of JAK2 V617F, JAK2 exon 12, MPL exon 10, and CALR exon 9 were analyzed in 929 Chinese patients with BCR-ABL1-negative MPN, including 234 cases of polycythemia vera (PV), 428 ETs, 187 PMFs, and 80 unclassifiable MPNs (MPN-Us).0.0005428842015JAK2;INSL695073770GA,T
rs77375493158606613717JAK2umls:C0027022BeFreeThe JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both atypical myeloproliferative disorders and myelodysplastic syndromes.0.3516606542005JAK2;INSL695073770GA,T
rs77375493167814783717JAK2umls:C0027022BeFreeIn addition, Bcr/Abl-negative classic myeloproliferative disorders are characterized by recurrent JAK2(V617F) mutations, whereas other mutations affecting the RAS signaling pathway molecules have been associated with juvenile myelomonocytic leukemia.0.3516606542006JAK2;INSL695073770GA,T
rs77375493176981913717JAK2umls:C0027022BeFreeA new MALDI-TOF-based assay for monitoring JAK2 V617F mutation level in patients undergoing allogeneic stem cell transplantation (allo SCT) for classic myeloproliferative disorders (MPD).0.3516606542008JAK2;INSL695073770GA,T
rs77375493168850513717JAK2umls:C0027022BeFreeThe acquired mutation Val617Phe in the tyrosine kinase JAK2 was recently identified in most but not all patients with classical myeloproliferative disorders.0.3516606542006JAK2;INSL695073770GA,T
rs77375493234690883717JAK2umls:C0027022BeFreeNon-reactive platelet counts elevation occurs mainly in myeloproliferative disorders (MPDs), which have been reported to be closely associated with JAK2 V617F mutation.0.3516606542013JAK2;INSL695073770GA,T
rs77375493163304463717JAK2umls:C0027022BeFreeAlthough the V617F JAK2 mutation has been described by several groups to be associated with classical myeloproliferative disorders (MPD), this same mutation has been detected with a low incidence in atypical MPD, such as CNL.0.3516606542005JAK2;INSL695073770GA,T
rs77375493200289723717JAK2umls:C0027022BeFreeSTAT5 activation is critical for the transformation mediated by myeloproliferative disorder-associated JAK2 V617F mutant.0.3516606542010JAK2;INSL695073770GA,T
rs77375493181885943717JAK2umls:C0027022BeFreeThe diagnosis of a myeloproliferative disease could be corroborated by demonstration of the V617F mutation of JAK2.0.3516606542008JAK2;INSL695073770GA,T
rs77375493203061563717JAK2umls:C0027022BeFreeRecently, Janus kinase-2 (JAK2) V617F mutation has an important role in the diagnosis of myeloproliferative disorders, especially in polycythemia vera (PV).0.3516606542010JAK2;INSL695073770GA,T
rs77375493168106103717JAK2umls:C0027022BeFreeNew insights into the pathogenesis of JAK2 V617F-positive myeloproliferative disorders and consequences for the management of patients.0.3516606542006JAK2;INSL695073770GA,T
rs77375493188151968651SOCS1umls:C0027022BeFreeSOCS1 expression was raised in myeloproliferative disorder granulocytes but the level was independent of JAK2 V617F status.0.0065344682008JAK2;INSL695073770GA,T
rs77375493171946633717JAK2umls:C0027022BeFreeDiscovery of a constitutively activating point mutation of the Janus kinase 2 (JAK2) receptor-associated tyrosine kinase in patients with polycythemia vera (PV) and other BCR/ABL-negative myeloproliferative disorders prompted many groups around the world to examine diverse subsets of patients with myeloid diseases for the prevalence of the JAK2 V617F mutation and its clinical and pathological associations.0.3516606542006JAK2;INSL695073770GA,T
rs77375493180039353717JAK2umls:C0027022BeFreeFinally, we show that IL-27R can functionally replace a homodimeric type I cytokine receptor in the activation of JAK2-V617F, a critical JAK2 mutation in various myeloproliferative disorders (MPDs).0.3516606542007JAK2;INSL695073770GA,T
rs77375493191357733717JAK2umls:C0027022BeFreeMyeloproliferative disorders (MPDs) are often associated with the presence of the JAK2-V617F mutation in hematopoietic cells.0.3516606542009JAK2;INSL695073770GA,T
rs77375493194784803717JAK2umls:C0027022BeFreeJAK2 V617F-positive latent essential thrombocythemia and splanchnic vein thrombosis: the role of bone marrow biopsy for the diagnosis of myeloproliferative disease.0.3516606542009JAK2;INSL695073770GA,T
rs77375493173078383717JAK2umls:C0027022BeFreeIn patients with SVT, screening for the JAK2 V617F mutation may be useful in recognising patients who should be carefully observed for the subsequent development of overt MPD.0.3516606542007JAK2;INSL695073770GA,T
rs77375493179343513717JAK2umls:C0027022BeFreeA general theme is that JAK2 V617F is variably associated with thrombosis and, more consistently, associated with elevations in blood counts relative to mutation-negative myeloproliferative disorders; future preclinical research should focus on the pathophysiology of thrombosis in myeloproliferative disorders, particularly in terms of the relationship between dysregulated Janus kinase 2 and elevated blood counts.0.3516606542007JAK2;INSL695073770GA,T
rs77375493189480493717JAK2umls:C0027022BeFreeMore recently, we demonstrated that constitutive phosphorylation of Lu/BCAM is also involved in abnormal RBC adhesion to endothelium in patients with polycythemia vera (PV), a frequent myeloproliferative disorders associated with the V617F mutation of the tyrosine kinase JAK2 leading to continuous stimulation of erythropoiesis.0.3516606542008JAK2;INSL695073770GA,T
rs77375493180594843717JAK2umls:C0027022BeFreeSuch HLA-G5-mediated inhibition constitutes a new parameter to be considered in the design of future approaches aimed at treating JAK2 V617F-positive myeloproliferative disorders.0.3516606542008JAK2;INSL695073770GA,T
rs773754931947442654790TET2umls:C0027022BeFreeTET2 defects were present in hematopoietic stem cells and preceded the JAK2 V617F mutation in the five samples from patients with myeloproliferative disorders that we analyzed.0.0121825472009JAK2;INSL695073770GA,T
rs77375493183967503717JAK2umls:C0027022BeFreeWe report two cases of patient with portal vein thrombosis of unknown origin in whom the presence of the V617F mutation of the Janus Kinase 2 gene lead to the diagnosis of primary myeloproliferative disorder, confirmed on bone marrow examination.0.3516606542008JAK2;INSL695073770GA,T
rs77375493204253353717JAK2umls:C0027022BeFreeThe JAK2(V617F) tyrosine kinase mutation in myeloproliferative disorders: Summary of published literature and a perspective.0.3516606542006JAK2;INSL695073770GA,T
rs77375493173790693717JAK2umls:C0027022BeFreeHowever, several unanswered questions regarding the essential role of JAK2(V617F) arose as 1) it is not a dominant mutation, 2) it is not PV-specific as it is found in several myeloproliferative disorders, and 3) some ( approximately 20%) PV patients lack the JAK2(V617F) mutation.0.3516606542007JAK2;INSL695073770GA,T
rs77375493204343003717JAK2umls:C0027022BeFreeA recent novel mutation in the Janus activated kinase 2 gene involving a gain-of-function substitute of valine to phenylalanine at position 617 (JAK2 V617F) has been discovered to be prevalent in patients with mesenteric vein thrombosis and myeloproliferative disorders.0.3516606542010JAK2;INSL695073770GA,T
rs77375493175749703717JAK2umls:C0027022BeFreeIn an MPD with t(9;12)(q13 approximately q21;q22) and JAK2 V617F mutation, array comparative genomic hybridization delineated a deletion of about 3 Mb at 9q13 approximately q21 and a deletion of about 2 Mb at 12q22 containing SOCS2.0.3516606542007JAK2;INSL695073770GA,T
rs77375493250129142264FGFR4umls:C0027022BeFreeDiscovery of the protein tyrosine kinase JAK2 V617F allele contributed to better understanding of the pathogenetic mechanisms of MPNs.0.0005428842014JAK2;INSL695073770GA,T
rs77375493169016563717JAK2umls:C0027022BeFreeThe first international meeting on V617F JAK2 mutation and its relevance in Philadelphia-negative myeloproliferative disorders.0.3516606542007JAK2;INSL695073770GA,T
rs77375493166324703717JAK2umls:C0027022BeFreeThe V617F activating point mutation in Jak2 has recently been associated with myeloproliferative disorders.0.3516606542006JAK2;INSL695073770GA,T
rs77375493166272723717JAK2umls:C0027022BeFreeDNA from 161 samples was isolated from peripheral blood granulocytes and formalin-fixed bone marrow clot sections in patients with CMPDs and without myeloproliferative disorders previously genotyped for the JAK2 V617F (G-->T) mutation, which included 114 wild types (GG) and 47 mutants (GT and TT).0.3516606542006JAK2;INSL695073770GA,T
rs773754932607147483886PRSS27umls:C0027022BeFreeIn the current study, mutations of JAK2 V617F, JAK2 exon 12, MPL exon 10, and CALR exon 9 were analyzed in 929 Chinese patients with BCR-ABL1-negative MPN, including 234 cases of polycythemia vera (PV), 428 ETs, 187 PMFs, and 80 unclassifiable MPNs (MPN-Us).0.0010857672015JAK2;INSL695073770GA,T
rs77375493197975253717JAK2umls:C0027022BeFreeMultiple iPS cell lines were also generated from peripheral blood CD34(+) cells of 2 patients with myeloproliferative disorders (MPDs) who acquired the JAK2-V617F somatic mutation in their blood cells.0.3516606542009JAK2;INSL695073770GA,T
rs77375493182940663717JAK2umls:C0027022BeFreeBecause of the clinical importance of this mutation in diagnosing myeloproliferative disorders and its relevance for disease progression, we have developed a tetra-primer polymerase chain reaction (PCR) assay to detect JAK2 p.V617F.0.3516606542007JAK2;INSL695073770GA,T
rs77375493166757103717JAK2umls:C0027022BeFreeAcquisition of the V617F mutation of JAK2 is a late genetic event in a subset of patients with myeloproliferative disorders.0.3516606542006JAK2;INSL695073770GA,T
rs773754931667026625ABL1umls:C0027022BeFreeA JAK2(V617F) mutation is frequently found in several BCR/ABL-negative myeloproliferative disorders.0.017372282006JAK2;INSL695073770GA,T
rs77375493234201503717JAK2umls:C0027022BeFreeThe JAK2 46/1 haplotype has recently been described as a major contributing factor to the development of myeloproliferative neoplasm, whether positive or negative forthe JAK2 V617F mutation.0.3516606542012JAK2;INSL695073770GA,T
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Disease ID 441
Disease chronic myeloproliferative disease
Case(Waiting for update.)