These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
10. The Microphthalmia-Associated Transcription Factor p.E318K Mutation Does Not Play a Major Role in Sporadic Renal Cell Tumors from Caucasian Patients. Stoehr CG; Walter B; Denzinger S; Ghiorzo P; Sturm RA; Hinze R; Moch H; Junker K; Hartmann A; Stoehr R Pathobiology; 2016; 83(4):165-9. PubMed ID: 26999813 [TBL] [Abstract][Full Text] [Related]
11. Imaging for Screening and Surveillance of Patients with Hereditary Forms of Renal Cell Carcinoma. Freifeld Y; Ananthakrishnan L; Margulis V Curr Urol Rep; 2018 Aug; 19(10):82. PubMed ID: 30116909 [TBL] [Abstract][Full Text] [Related]
12. BAP1 Syndrome - Predisposition to Malignant Mesothelioma, Skin and Uveal Melanoma, Renal and Other Cancers. Foretová L; Navrátilová M; Svoboda M; Házová J; Vašíčková P; Sťahlová EH; Fabian P; Schneiderová M; Macháčková E Klin Onkol; 2019; 32(Supplementum2):118-122. PubMed ID: 31409087 [TBL] [Abstract][Full Text] [Related]
13. Clinical and Molecular Characterization of Microphthalmia-associated Transcription Factor (MITF)-related Renal Cell Carcinoma. Lang M; Vocke CD; Ricketts CJ; Metwalli AR; Ball MW; Schmidt LS; Linehan WM Urology; 2021 Mar; 149():89-97. PubMed ID: 33242557 [TBL] [Abstract][Full Text] [Related]
14. [Heredity in renal and prostatic neoplasia]. Prayer Galetti T; D'Arrigo L; De Zorzi L; Patarnello T Arch Ital Urol Androl; 1997 Sep; 69(4):241-6. PubMed ID: 9417296 [TBL] [Abstract][Full Text] [Related]
15. Inactivation of the von Hippel-Lindau (VHL) tumour suppressor gene and allelic losses at chromosome arm 3p in primary renal cell carcinoma: evidence for a VHL-independent pathway in clear cell renal tumourigenesis. Clifford SC; Prowse AH; Affara NA; Buys CH; Maher ER Genes Chromosomes Cancer; 1998 Jul; 22(3):200-9. PubMed ID: 9624531 [TBL] [Abstract][Full Text] [Related]
16. Familial Kidney Cancer: Implications of New Syndromes and Molecular Insights. Carlo MI; Hakimi AA; Stewart GD; Bratslavsky G; Brugarolas J; Chen YB; Linehan WM; Maher ER; Merino MJ; Offit K; Reuter VE; Shuch B; Coleman JA Eur Urol; 2019 Dec; 76(6):754-764. PubMed ID: 31326218 [TBL] [Abstract][Full Text] [Related]
17. Molecular study of a new family with hereditary renal cell carcinoma and a translocation t(3;8)(p13;q24.1). Meléndez B; Rodríguez-Perales S; Martínez-Delgado B; Otero I; Robledo M; Martínez-Ramírez A; Ruiz-Llorente S; Urioste M; Cigudosa JC; Benítez J Hum Genet; 2003 Feb; 112(2):178-85. PubMed ID: 12522559 [TBL] [Abstract][Full Text] [Related]
18. PBRM1 and BAP1 as novel targets for renal cell carcinoma. Brugarolas J Cancer J; 2013; 19(4):324-32. PubMed ID: 23867514 [TBL] [Abstract][Full Text] [Related]
19. Genetic kidney cancer syndromes. Ho TH; Jonasch E J Natl Compr Canc Netw; 2014 Sep; 12(9):1347-55. PubMed ID: 25190700 [TBL] [Abstract][Full Text] [Related]