271 related articles for article (PubMed ID: 31943436)
1. Characterization of renal cell carcinoma-associated constitutional chromosome abnormalities by genome sequencing.
Smith PS; Whitworth J; West H; Cook J; Gardiner C; Lim DHK; Morrison PJ; Hislop RG; Murray E; ; Tischkowitz M; Warren AY; Woodward ER; Maher ER
Genes Chromosomes Cancer; 2020 Jun; 59(6):333-347. PubMed ID: 31943436
[TBL] [Abstract][Full Text] [Related]
2. Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocation.
Kato T; Franconi CP; Sheridan MB; Hacker AM; Inagakai H; Glover TW; Arlt MF; Drabkin HA; Gemmill RM; Kurahashi H; Emanuel BS
Cancer Genet; 2014 Apr; 207(4):133-40. PubMed ID: 24813807
[TBL] [Abstract][Full Text] [Related]
3. A constitutional balanced t(3;8)(p14;q24.1) translocation results in disruption of the TRC8 gene and predisposition to clear cell renal cell carcinoma.
Poland KS; Azim M; Folsom M; Goldfarb R; Naeem R; Korch C; Drabkin HA; Gemmill RM; Plon SE
Genes Chromosomes Cancer; 2007 Sep; 46(9):805-12. PubMed ID: 17539022
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. FHIT gene and the FRA3B region are not involved in the genetics of renal cell carcinomas.
Bugert P; Wilhelm M; Kovacs G
Genes Chromosomes Cancer; 1997 Sep; 20(1):9-15. PubMed ID: 9290948
[TBL] [Abstract][Full Text] [Related]
6. About the origin and development of hereditary conventional renal cell carcinoma in a four-generation t(3;8)(p14.1;q24.23) family.
Valle L; Cascón A; Melchor L; Otero I; Rodríguez-Perales S; Sánchez L; Cruz Cigudosa J; Robledo M; Weber B; Urioste M; Benítez J
Eur J Hum Genet; 2005 May; 13(5):570-8. PubMed ID: 15756303
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Characterization of a 3;6 translocation associated with renal cell carcinoma.
Foster RE; Abdulrahman M; Morris MR; Prigmore E; Gribble S; Ng B; Gentle D; Ready S; Weston PM; Wiesener MS; Kishida T; Yao M; Davison V; Barbero JL; Chu C; Carter NP; Latif F; Maher ER
Genes Chromosomes Cancer; 2007 Apr; 46(4):311-7. PubMed ID: 17205537
[TBL] [Abstract][Full Text] [Related]
9. Familial non-VHL clear cell (conventional) renal cell carcinoma: clinical features, segregation analysis, and mutation analysis of FLCN.
Woodward ER; Ricketts C; Killick P; Gad S; Morris MR; Kavalier F; Hodgson SV; Giraud S; Bressac-de Paillerets B; Chapman C; Escudier B; Latif F; Richard S; Maher ER
Clin Cancer Res; 2008 Sep; 14(18):5925-30. PubMed ID: 18794106
[TBL] [Abstract][Full Text] [Related]
10. Epigenetic inactivation of the RASSF1A 3p21.3 tumor suppressor gene in both clear cell and papillary renal cell carcinoma.
Morrissey C; Martinez A; Zatyka M; Agathanggelou A; Honorio S; Astuti D; Morgan NV; Moch H; Richards FM; Kishida T; Yao M; Schraml P; Latif F; Maher ER
Cancer Res; 2001 Oct; 61(19):7277-81. PubMed ID: 11585766
[TBL] [Abstract][Full Text] [Related]
11. Physical and functional mapping of a tumor suppressor locus for renal cell carcinoma within chromosome 3p12.
Lott ST; Lovell M; Naylor SL; Killary AM
Cancer Res; 1998 Aug; 58(16):3533-7. PubMed ID: 9721855
[TBL] [Abstract][Full Text] [Related]
12. UBE2QL1 is disrupted by a constitutional translocation associated with renal tumor predisposition and is a novel candidate renal tumor suppressor gene.
Wake NC; Ricketts CJ; Morris MR; Prigmore E; Gribble SM; Skytte AB; Brown M; Clarke N; Banks RE; Hodgson S; Turnell AS; Maher ER; Woodward ER
Hum Mutat; 2013 Dec; 34(12):1650-61. PubMed ID: 24000165
[TBL] [Abstract][Full Text] [Related]
13. The tumor suppressor gene FBXW7 is disrupted by a constitutional t(3;4)(q21;q31) in a patient with renal cell cancer.
Kuiper RP; Vreede L; Venkatachalam R; Ricketts C; Kamping E; Verwiel E; Govaerts L; Debiec-Rychter M; Lerut E; van Erp F; Hoogerbrugge N; van Kempen L; Schoenmakers EF; Bonne A; Maher ER; Geurts van Kessel A
Cancer Genet Cytogenet; 2009 Dec; 195(2):105-11. PubMed ID: 19963109
[TBL] [Abstract][Full Text] [Related]
14. [Development of human renal cell carcinoma (RCC)--the responsible genes for the development of hereditary and sporadic human RCCs].
Shuin T; Kamata M; Ashida S
Gan To Kagaku Ryoho; 2002 Oct; 29(10):1719-25. PubMed ID: 12402420
[TBL] [Abstract][Full Text] [Related]
15. Distinctive expression patterns of glycoprotein non-metastatic B and folliculin in renal tumors in patients with Birt-Hogg-Dubé syndrome.
Furuya M; Hong SB; Tanaka R; Kuroda N; Nagashima Y; Nagahama K; Suyama T; Yao M; Nakatani Y
Cancer Sci; 2015 Mar; 106(3):315-23. PubMed ID: 25594584
[TBL] [Abstract][Full Text] [Related]
16. Investigation of tumor suppressor genes apart from VHL on 3p by deletion mapping in sporadic clear cell renal cell carcinoma (cRCC).
Singh RB; Amare Kadam PS
Urol Oncol; 2013 Oct; 31(7):1333-42. PubMed ID: 21962529
[TBL] [Abstract][Full Text] [Related]
17. Association of a novel constitutional translocation t(1q;3q) with familial renal cell carcinoma.
Kanayama H; Lui WO; Takahashi M; Naroda T; Kedra D; Wong FK; Kuroki Y; Nakahori Y; Larsson C; Kagawa S; Teh BT
J Med Genet; 2001 Mar; 38(3):165-70. PubMed ID: 11238683
[TBL] [Abstract][Full Text] [Related]
18. Genome-Wide Uniparental Disomy and Copy Number Variations in Renal Cell Carcinomas Associated with Birt-Hogg-Dubé Syndrome.
Iribe Y; Yao M; Tanaka R; Kuroda N; Nagashima Y; Nakatani Y; Furuya M
Am J Pathol; 2016 Feb; 186(2):337-46. PubMed ID: 26776076
[TBL] [Abstract][Full Text] [Related]
19. Mapping of 29 YAC clones and identification of 3 YACs spanning the translocation t(3;8)(p14.2;q24.1) breakpoint at 8q24.1 in hereditary renal cell carcinoma.
Shi G; Cannizzaro LA
Cytogenet Cell Genet; 1996; 75(2-3):180-5. PubMed ID: 9040788
[TBL] [Abstract][Full Text] [Related]
20. Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene.
Slade I; Stephens P; Douglas J; Barker K; Stebbings L; Abbaszadeh F; Pritchard-Jones K; ; Cole R; Pizer B; Stiller C; Vujanic G; Scott RH; Stratton MR; Rahman N
J Med Genet; 2010 May; 47(5):342-7. PubMed ID: 19948536
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]