113 related articles for article (PubMed ID: 8188285)
21. Malignant melanoma is genetically distinct from clear cell sarcoma of tendons and aponeurosis (malignant melanoma of soft parts).
Langezaal SM; Graadt van Roggen JF; Cleton-Jansen AM; Baelde JJ; Hogendoorn PC
Br J Cancer; 2001 Feb; 84(4):535-8. PubMed ID: 11207050
[TBL] [Abstract][Full Text] [Related]
22. Allelotype of pediatric rhabdomyosarcoma.
Visser M; Sijmons C; Bras J; Arceci RJ; Godfried M; Valentijn LJ; Voûte PA; Baas F
Oncogene; 1997 Sep; 15(11):1309-14. PubMed ID: 9315099
[TBL] [Abstract][Full Text] [Related]
23. Establishment of a rhabdoid tumor cell line with a specific chromosomal abnormality, 46,XY,t(11;22)(p15.5;q11.23).
Karnes PS; Tran TN; Cui MY; Bogenmann E; Shimada H; Ying KL
Cancer Genet Cytogenet; 1991 Oct; 56(1):31-8. PubMed ID: 1747867
[TBL] [Abstract][Full Text] [Related]
24. An integrated 5-Mb physical, genetic, and radiation hybrid map of a 1p36.1 region implicated in neuroblastoma pathogenesis.
Spieker N; Beitsma M; van Sluis P; Roobeek I; den Dunnen JT; Speleman F; Caron H; Versteeg R
Genes Chromosomes Cancer; 2000 Feb; 27(2):143-52. PubMed ID: 10612802
[TBL] [Abstract][Full Text] [Related]
25. The t(6;16)(p21;q22) chromosome translocation in the LNCaP prostate carcinoma cell line results in a tpc/hpr fusion gene.
Veronese ML; Bullrich F; Negrini M; Croce CM
Cancer Res; 1996 Feb; 56(4):728-32. PubMed ID: 8631004
[TBL] [Abstract][Full Text] [Related]
26. Expression profiling of t(12;22) positive clear cell sarcoma of soft tissue cell lines reveals characteristic up-regulation of potential new marker genes including ERBB3.
Schaefer KL; Brachwitz K; Wai DH; Braun Y; Diallo R; Korsching E; Eisenacher M; Voss R; Van Valen F; Baer C; Selle B; Spahn L; Liao SK; Lee KA; Hogendoorn PC; Reifenberger G; Gabbert HE; Poremba C
Cancer Res; 2004 May; 64(10):3395-405. PubMed ID: 15150091
[TBL] [Abstract][Full Text] [Related]
27. Microdissection of chromosome band 11p15.5: characterization of probes mapping distal to the HBBC locus.
Newsham I; Claussen U; Lüdecke HJ; Mason M; Senger G; Horsthemke B; Cavenee W
Genes Chromosomes Cancer; 1991 Mar; 3(2):108-16. PubMed ID: 1676905
[TBL] [Abstract][Full Text] [Related]
28. A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22).
Nimmakayalu MA; Gotter AL; Shaikh TH; Emanuel BS
Hum Mol Genet; 2003 Nov; 12(21):2817-25. PubMed ID: 12952865
[TBL] [Abstract][Full Text] [Related]
29. Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalities.
Reynolds PA; Powlesland RM; Keen TJ; Inglehearn CF; Cunningham AF; Green ED; Brown KW
Genes Chromosomes Cancer; 1996 Nov; 17(3):151-5. PubMed ID: 8946193
[TBL] [Abstract][Full Text] [Related]
30. Localization of the t(2;13) breakpoint of alveolar rhabdomyosarcoma on a physical map of chromosome 2.
Barr FG; Holick J; Nycum L; Biegel JA; Emanuel BS
Genomics; 1992 Aug; 13(4):1150-6. PubMed ID: 1505949
[TBL] [Abstract][Full Text] [Related]
31. Chromosomal sublocalization of the 2;13 translocation breakpoint in alveolar rhabdomyosarcoma.
Shapiro DN; Valentine MB; Sublett JE; Sinclair AE; Tereba AM; Scheffer H; Buys CH; Look AT
Genes Chromosomes Cancer; 1992 Apr; 4(3):241-9. PubMed ID: 1382566
[TBL] [Abstract][Full Text] [Related]
32. Assignment of the human fast skeletal troponin T gene (TNNT3) to chromosome 11p15.5: evidence for the presence of 11pter in a monochromosome 9 somatic cell hybrid in NIGMS mapping panel 2.
Mao C; Baumgartner AP; Jha PK; Huang TH; Sarkar S
Genomics; 1996 Feb; 31(3):385-8. PubMed ID: 8838323
[TBL] [Abstract][Full Text] [Related]
33. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
Sinclair P; Harrison CJ; Jarosová M; Foroni L
Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
[TBL] [Abstract][Full Text] [Related]
34. Evidence for two tumor suppressor loci associated with proximal chromosome 9p to q and distal chromosome 9q in bladder cancer and the initial screening for GAS1 and PTC mutations.
Simoneau AR; Spruck CH; Gonzalez-Zulueta M; Gonzalgo ML; Chan MF; Tsai YC; Dean M; Steven K; Horn T; Jones PA
Cancer Res; 1996 Nov; 56(21):5039-43. PubMed ID: 8895761
[TBL] [Abstract][Full Text] [Related]
35. Characterization of a familial t(16;22) balanced translocation associated with congenital cataract leads to identification of a novel gene, TMEM114, expressed in the lens and disrupted by the translocation.
Jamieson RV; Farrar N; Stewart K; Perveen R; Mihelec M; Carette M; Grigg JR; McAvoy JW; Lovicu FJ; Tam PP; Scambler P; Lloyd IC; Donnai D; Black GC
Hum Mutat; 2007 Oct; 28(10):968-77. PubMed ID: 17492639
[TBL] [Abstract][Full Text] [Related]
36. Molecular characterization of the genomic breakpoint junction in a t(11;22) translocation in Ewing sarcoma.
Obata K; Hiraga H; Nojima T; Yoshida MC; Abe S
Genes Chromosomes Cancer; 1999 May; 25(1):6-15. PubMed ID: 10221334
[TBL] [Abstract][Full Text] [Related]
37. Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma.
Barr FG; Galili N; Holick J; Biegel JA; Rovera G; Emanuel BS
Nat Genet; 1993 Feb; 3(2):113-7. PubMed ID: 8098985
[TBL] [Abstract][Full Text] [Related]
38. Characterization of the translocation between chromosomes X and 18 in human synovial sarcomas.
Reeves BR; Smith S; Fisher C; Warren W; Knight J; Martin C; Chan AM; Gusterson BA; Westbury G; Cooper CS
Oncogene; 1989 Mar; 4(3):373-8. PubMed ID: 2704557
[TBL] [Abstract][Full Text] [Related]
39. Narrowing the critical region for a rhabdoid tumor locus in 22q11.
Biegel JA; Allen CS; Kawasaki K; Shimizu N; Budarf ML; Bell CJ
Genes Chromosomes Cancer; 1996 Jun; 16(2):94-105. PubMed ID: 8818656
[TBL] [Abstract][Full Text] [Related]
40. Localization of the rhabdomyosarcoma t(2;13) breakpoint on a physical map of chromosome 13.
Barr FG; Sellinger B; Emanuel BS
Genomics; 1991 Dec; 11(4):941-7. PubMed ID: 1783402
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
