Suggestions

Du même auteur

Germline mutation in the NBR1 gene involved in autophagy detected in a family with renal tumors

Archive ouverte | Adolphe, Florine | CCSD

International audience

Integrative analysis of dysregulated microRNAs and mRNAs in multiple recurrent synchronized renal tumors from patients with von Hippel-Lindau disease

Archive ouverte | Gattolliat, Charles-Henry | CCSD

International audience. Von Hippel-Lindau (VHL) disease is a rare autosomal dominant syndrome that is the main cause of inherited clear-cell renal cell carcinoma (ccRCC), which generally occurs in the form of multip...

Renal Cell Carcinoma Programmed Death-ligand 1, a New Direct Target of Hypoxia-inducible Factor-2 Alpha, is Regulated by von Hippel-Lindau Gene Mutation Status

Archive ouverte | Messai, Yosra | CCSD

International audience. BACKGROUND: Clear cell renal cell carcinomas (ccRCC) frequently display a loss of function of the von Hippel-Lindau (VHL) gene. OBJECTIVE: To elucidate the putative relationship between VHL m...

Chargement des enrichissements...