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Validation and Genomic Interrogation of the MET Variant rs11762213 as a Predictor of Adverse Outcomes in Clear Cell Renal Cell Carcinoma
BACKGROUND: The exonic single nucleotide variant rs11762213 located in the MET oncogene has recently been identified as a prognostic marker in clear cell renal cell carcinoma (ccRCC). We validated this finding using the Cancer Genome Atlas cohort and explored the biologic implications. METHODS: Geno...
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| Publicat a: | Cancer |
|---|---|
| Autors principals: | , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4803437/ https://ncbi.nlm.nih.gov/pubmed/26505625 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cncr.29765 |
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