129 related articles for article (PubMed ID: 8527383)
1. Distinct Xp11.2 breakpoints in two renal cell carcinomas exhibiting X;autosome translocations.
Dijkhuizen T; van den Berg E; Wilbrink M; Weterman M; Geurts van Kessel A; Störkel S; Folkers RP; Braam A; de Jong B
Genes Chromosomes Cancer; 1995 Sep; 14(1):43-50. PubMed ID: 8527383
[TBL] [Abstract][Full Text] [Related]
2. Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2.
Suijkerbuijk RF; Meloni AM; Sinke RJ; de Leeuw B; Wilbrink M; Janssen HA; Geraghty MT; Monaco AP; Sandberg AA; Geurts van Kessel A
Cancer Genet Cytogenet; 1993 Dec; 71(2):164-9. PubMed ID: 8281521
[TBL] [Abstract][Full Text] [Related]
3. Mapping the X chromosome breakpoint in two papillary renal cell carcinoma cell lines with a t(X;1)(p11.2;q21.2) and the first report of a female case.
Shipley JM; Birdsall S; Clark J; Crew J; Gill S; Linehan M; Gnarra J; Fisher S; Craig IW; Cooper CS
Cytogenet Cell Genet; 1995; 71(3):280-4. PubMed ID: 7587394
[TBL] [Abstract][Full Text] [Related]
4. TFE3 break-apart FISH has a higher sensitivity for Xp11.2 translocation-associated renal cell carcinoma compared with TFE3 or cathepsin K immunohistochemical staining alone: expanding the morphologic spectrum.
Rao Q; Williamson SR; Zhang S; Eble JN; Grignon DJ; Wang M; Zhou XJ; Huang W; Tan PH; Maclennan GT; Cheng L
Am J Surg Pathol; 2013 Jun; 37(6):804-15. PubMed ID: 23598965
[TBL] [Abstract][Full Text] [Related]
5. Validation and utilization of a TFE3 break-apart FISH assay for Xp11.2 translocation renal cell carcinoma and alveolar soft part sarcoma.
Pradhan D; Roy S; Quiroga-Garza G; Cieply K; Mahaffey AL; Bastacky S; Dhir R; Parwani AV
Diagn Pathol; 2015 Sep; 10():179. PubMed ID: 26415891
[TBL] [Abstract][Full Text] [Related]
6. Renal cell carcinoma with translocation (X;1). Further evidence for a cytogenetically defined subtype.
Tonk V; Wilson KS; Timmons CF; Schneider NR; Tomlinson GE
Cancer Genet Cytogenet; 1995 May; 81(1):72-5. PubMed ID: 7773963
[TBL] [Abstract][Full Text] [Related]
7. Utilization of a TFE3 break-apart FISH assay in a renal tumor consultation service.
Green WM; Yonescu R; Morsberger L; Morris K; Netto GJ; Epstein JI; Illei PB; Allaf M; Ladanyi M; Griffin CA; Argani P
Am J Surg Pathol; 2013 Aug; 37(8):1150-63. PubMed ID: 23715164
[TBL] [Abstract][Full Text] [Related]
8. Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint.
Weterman MA; Wilbrink M; Janssen I; Janssen HA; van den Berg E; Fisher SE; Craig I; Geurts van Kessel A
Cytogenet Cell Genet; 1996; 75(1):2-6. PubMed ID: 8995477
[TBL] [Abstract][Full Text] [Related]
9. Two new cases of papillary renal cell carcinoma with t(X;1)(p11;q21) in females.
Pérot C; Bougaran J; Boccon-Gibod L; Störkel S; Leverger G; van den Akker J; Taillemite JL; Couturier J
Cancer Genet Cytogenet; 1999 Apr; 110(1):54-6. PubMed ID: 10198623
[TBL] [Abstract][Full Text] [Related]
10. Molecular cytogenetics of t(X;1)(p11.2;q21) with complex rearrangements in a renal cell carcinoma.
Zattara-Cannoni H; Daniel L; Roll P; Coulange C; Vagner-Capodano A
Cancer Genet Cytogenet; 2000 Nov; 123(1):61-4. PubMed ID: 11120337
[TBL] [Abstract][Full Text] [Related]
11. Comparative study of renal cell carcinoma by CGH, multicolor-FISH and conventional cytogenic banding analysis.
Sanjmyatav J; Schubert J; Junker K
Oncol Rep; 2005 Nov; 14(5):1183-7. PubMed ID: 16211283
[TBL] [Abstract][Full Text] [Related]
12. Cytogenetics of a renal cell carcinoma in a 17-month-old child. Evidence for Xp11.2 as a recurring breakpoint.
Tomlinson GE; Nisen PD; Timmons CF; Schneider NR
Cancer Genet Cytogenet; 1991 Nov; 57(1):11-7. PubMed ID: 1684532
[TBL] [Abstract][Full Text] [Related]
13. Validation of a TFE3 break-apart FISH assay for Xp11.2 translocation renal cell carcinomas.
Mosquera JM; Dal Cin P; Mertz KD; Perner S; Davis IJ; Fisher DE; Rubin MA; Hirsch MS
Diagn Mol Pathol; 2011 Sep; 20(3):129-37. PubMed ID: 21817901
[TBL] [Abstract][Full Text] [Related]
14. Translocation (X;1) associated with a nonpapillary carcinoma in a young woman: a new definition for an Xp11.2 RCC subtype.
Désangles F; Camparo P; Fouet C; Houlgatte A; Arborio M
Cancer Genet Cytogenet; 1999 Sep; 113(2):141-4. PubMed ID: 10484980
[TBL] [Abstract][Full Text] [Related]
15. [Cytogenetic alterations in renal tumors. Applications for comparative genomic hybridization and fluorescence in situ hybridization].
Mertz KD; Tchinda J; Küfer R; Möller P; Rubin MA; Moch H; Perner S
Urologe A; 2006 Mar; 45(3):316-8, 320-2. PubMed ID: 16465524
[TBL] [Abstract][Full Text] [Related]
16. Translocation (X;1) in papillary renal cell carcinoma. A new cytogenetic subtype.
Meloni AM; Dobbs RM; Pontes JE; Sandberg AA
Cancer Genet Cytogenet; 1993 Jan; 65(1):1-6. PubMed ID: 8431910
[TBL] [Abstract][Full Text] [Related]
17. Xp11 translocation renal cell carcinoma in adults: expanded clinical, pathologic, and genetic spectrum.
Argani P; Olgac S; Tickoo SK; Goldfischer M; Moch H; Chan DY; Eble JN; Bonsib SM; Jimeno M; Lloreta J; Billis A; Hicks J; De Marzo AM; Reuter VE; Ladanyi M
Am J Surg Pathol; 2007 Aug; 31(8):1149-60. PubMed ID: 17667536
[TBL] [Abstract][Full Text] [Related]
18. A novel case of t(X;1)(p11.2;p34) in a renal cell carcinoma with TFE3 rearrangement and favorable outcome in a 57-year-old patient.
Haudebourg J; Hoch B; Fabas T; Burel-Vandenbos F; Carpentier X; Amiel J; Cardot-Leccia N; Michiels JF; Pedeutour F
Cancer Genet Cytogenet; 2010 Jul; 200(2):75-8. PubMed ID: 20620589
[TBL] [Abstract][Full Text] [Related]
19. Translocation (X;1) reveals metastasis 31 years after renal cell carcinoma.
Dal Cin P; Stas M; Sciot R; De Wever I; Van Damme B; Van den Berghe H
Cancer Genet Cytogenet; 1998 Feb; 101(1):58-61. PubMed ID: 9460502
[TBL] [Abstract][Full Text] [Related]
20. Five new cases of juvenile renal cell carcinoma with translocations involving Xp11.2: a cytogenetic and morphologic study.
Pérot C; Boccon-Gibod L; Bouvier R; Doz F; Fournet JC; Fréneaux P; Vieillefond A; Couturier J
Cancer Genet Cytogenet; 2003 Jun; 143(2):93-9. PubMed ID: 12781442
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
