Disease | nephroblastoma |
Comorbidity | C1261473|sarcoma |
Sentences | 3 |
PubMedID- 24624323 | This translocation fuses the ewing sarcoma gene (ews) with the wilms' tumor suppressor gene (wt1) to create a gene that likely acts as a transcriptional activator for pro-tumorigenic genes (fang et al., 2008). |
PubMedID- 23922674 | The hallmark of this disease is a ews-wt1 translocation resulting from apposition of the ewing's sarcoma (ews) gene with the wilms' tumor (wt1) gene. |
PubMedID- 22439159 | Extraocular retinoblastoma with central nervous system involvement, high-risk ewing's sarcoma family of tumors, high-risk relapsed wilm's tumor compared to conventional therapy (all three low strength). |
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