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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 15756303)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Cloning of a new familial t(3;8) translocation associated with conventional renal cell carcinoma reveals a 5 kb microdeletion and no gene involved in the rearrangement.
    Rodríguez-Perales S; Meléndez B; Gribble SM; Valle L; Carter NP; Santamaría I; Conde L; Urioste M; Benítez J; Cigudosa JC
    Hum Mol Genet; 2004 May; 13(9):983-90. PubMed ID: 15016767
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular cytogenetic characterization of early and late renal cell carcinomas in von Hippel-Lindau disease.
    Phillips JL; Ghadimi BM; Wangsa D; Padilla-Nash H; Worrell R; Hewitt S; Walther M; Linehan WM; Klausner RD; Ried T
    Genes Chromosomes Cancer; 2001 May; 31(1):1-9. PubMed ID: 11284029
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular genetic evidence for the independent origin of multifocal papillary tumors in patients with papillary renal cell carcinomas.
    Jones TD; Eble JN; Wang M; MacLennan GT; Delahunt B; Brunelli M; Martignoni G; Lopez-Beltran A; Bonsib SM; Ulbright TM; Zhang S; Nigro K; Cheng L
    Clin Cancer Res; 2005 Oct; 11(20):7226-33. PubMed ID: 16243792
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detailed genetic and physical map of the 3p chromosome region surrounding the familial renal cell carcinoma chromosome translocation, t(3;8)(p14.2;q24.1).
    LaForgia S; Lasota J; Latif F; Boghosian-Sell L; Kastury K; Ohta M; Druck T; Atchison L; Cannizzaro LA; Barnea G
    Cancer Res; 1993 Jul; 53(13):3118-24. PubMed ID: 8319219
    [TBL] [Abstract][Full Text] [Related]  

  • 8. VHL and FHIT locus loss of heterozygosity is common in all renal cancer morphotypes but differs in pattern and prognostic significance.
    Velickovic M; Delahunt B; Störkel S; Grebem SK
    Cancer Res; 2001 Jun; 61(12):4815-9. PubMed ID: 11406557
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15).
    Eleveld MJ; Bodmer D; Merkx G; Siepman A; Sprenger SH; Weterman MA; Ligtenberg MJ; Kamp J; Stapper W; Jeuken JW; Smeets D; Smits A; Geurts Van Kessel A
    Genes Chromosomes Cancer; 2001 May; 31(1):23-32. PubMed ID: 11284032
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Copy number profiling in von Hippel-Lindau disease renal cell carcinoma.
    Shuib S; Wei W; Sur H; Morris MR; McMullan D; Rattenberry E; Meyer E; Maxwell PH; Kishida T; Yao M; Latif F; Maher ER
    Genes Chromosomes Cancer; 2011 Jul; 50(7):479-88. PubMed ID: 21456047
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Loss of heterozygosity at 3p14.2 in clear cell renal cell carcinoma is an early event and is highly localized to the FHIT gene locus.
    Velickovic M; Delahunt B; Grebe SK
    Cancer Res; 1999 Mar; 59(6):1323-6. PubMed ID: 10096566
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mapping of constitutional translocation breakpoints in renal cell cancer patients: identification of KCNIP4 as a candidate gene.
    Bonne A; Vreede L; Kuiper RP; Bodmer D; Jansen C; Eleveld M; van Erp F; Arkesteijn G; Hoogerbrugge N; van Ravenswaaij C; Schoenmakers EF; Geurts van Kessel A
    Cancer Genet Cytogenet; 2007 Nov; 179(1):11-8. PubMed ID: 17981209
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mechanism of tumorigenesis of renal carcinomas associated with the constitutional chromosome 3;8 translocation.
    Schmidt L; Li F; Brown RS; Berg S; Chen F; Wei MH; Tory K; Lerman I; Zbar B
    Cancer J Sci Am; 1995; 1(3):191-5. PubMed ID: 9166475
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular analysis of germline t(3;6) and t(3;12) associated with conventional renal cell carcinomas indicates their rate-limiting role and supports the three-hit model of carcinogenesis.
    Yusenko MV; Nagy A; Kovacs G
    Cancer Genet Cytogenet; 2010 Aug; 201(1):15-23. PubMed ID: 20633763
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cytogenetic studies of 24 renal epithelial tumors with von Hippel-Lindau and fragile histidine triad protein expression correlation.
    Gayrard N; Cacheux V; Iborra F; Mourad G; Argilés A
    Arch Pathol Lab Med; 2008 Jun; 132(6):965-73. PubMed ID: 18517280
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A combination of molecular cytogenetic analyses reveals complex genetic alterations in conventional renal cell carcinoma.
    Strefford JC; Stasevich I; Lane TM; Lu YJ; Oliver T; Young BD
    Cancer Genet Cytogenet; 2005 May; 159(1):1-9. PubMed ID: 15860350
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Major role for a 3p21 region and lack of involvement of the t(3;8) breakpoint region in the development of renal cell carcinoma suggested by loss of heterozygosity analysis.
    van den Berg A; Hulsbeek MF; de Jong D; Kok K; Veldhuis PM; Roche J; Buys CH
    Genes Chromosomes Cancer; 1996 Jan; 15(1):64-72. PubMed ID: 8824727
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [Genetics of renal tumors].
    Oláh E; Jakab Z; Balogh E
    Orv Hetil; 2001 Jul; 142(26):1367-73. PubMed ID: 11478032
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.