203 related articles for article (PubMed ID: 9674708)
1. Loss of heterozygosity at chromosome 11p15 in Wilms tumors: identification of two independent regions.
Karnik P; Chen P; Paris M; Yeger H; Williams BR
Oncogene; 1998 Jul; 17(2):237-40. PubMed ID: 9674708
[TBL] [Abstract][Full Text] [Related]
2. Clinicopathologic correlates of loss of heterozygosity in Wilm's tumor: a preliminary analysis.
Grundy P; Telzerow P; Moksness J; Breslow NE
Med Pediatr Oncol; 1996 Nov; 27(5):429-33. PubMed ID: 8926924
[TBL] [Abstract][Full Text] [Related]
3. Genome-wide loss of heterozygosity analysis of WT1-wild-type and WT1-mutant Wilms tumors.
Ruteshouser EC; Hendrickson BW; Colella S; Krahe R; Pinto L; Huff V
Genes Chromosomes Cancer; 2005 Jun; 43(2):172-80. PubMed ID: 15761866
[TBL] [Abstract][Full Text] [Related]
4. Loss of heterozygosity at chromosome regions 22q11-12 and 11p15.5 in renal rhabdoid tumors.
Schofield DE; Beckwith JB; Sklar J
Genes Chromosomes Cancer; 1996 Jan; 15(1):10-7. PubMed ID: 8824720
[TBL] [Abstract][Full Text] [Related]
5. Clonality and loss of heterozygosity of WT genes are early events in the pathogenesis of nephroblastomas.
Guertl B; Ratschek M; Harms D; Jaenig U; Leuschner I; Poremba C; Hoefler G
Hum Pathol; 2003 Mar; 34(3):278-81. PubMed ID: 12673563
[TBL] [Abstract][Full Text] [Related]
6. High-density marker analysis of 11p15.5 in non-small cell lung carcinomas reveals allelic deletion of one shared and one distinct region when compared to breast carcinomas.
Tran YK; Newsham IF
Cancer Res; 1996 Jul; 56(13):2916-21. PubMed ID: 8674040
[TBL] [Abstract][Full Text] [Related]
7. Identification of a minimal region of loss on the short arm of chromosome 1 in Wilms tumor.
Tamimi Y; Ziebart K; Desaulniers N; Dietrich K; Grundy P
Genes Chromosomes Cancer; 2007 Apr; 46(4):327-35. PubMed ID: 17243164
[TBL] [Abstract][Full Text] [Related]
8. Frequency and timing of loss of imprinting at 11p13 and 11p15 in Wilms' tumor development.
Brown KW; Power F; Moore B; Charles AK; Malik KT
Mol Cancer Res; 2008 Jul; 6(7):1114-23. PubMed ID: 18644976
[TBL] [Abstract][Full Text] [Related]
9. Two distinct tumor suppressor loci within chromosome 11p15 implicated in breast cancer progression and metastasis.
Karnik P; Paris M; Williams BR; Casey G; Crowe J; Chen P
Hum Mol Genet; 1998 May; 7(5):895-903. PubMed ID: 9536095
[TBL] [Abstract][Full Text] [Related]
10. Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11.
Mannens M; Devilee P; Bliek J; Mandjes I; de Kraker J; Heyting C; Slater RM; Westerveld A
Cancer Res; 1990 Jun; 50(11):3279-83. PubMed ID: 2159377
[TBL] [Abstract][Full Text] [Related]
11. Loss of methylation at chromosome 11p15.5 is common in human adult tumors.
Scelfo RA; Schwienbacher C; Veronese A; Gramantieri L; Bolondi L; Querzoli P; Nenci I; Calin GA; Angioni A; Barbanti-Brodano G; Negrini M
Oncogene; 2002 Apr; 21(16):2564-72. PubMed ID: 11971191
[TBL] [Abstract][Full Text] [Related]
12. Genomic profiling maps loss of heterozygosity and defines the timing and stage dependence of epigenetic and genetic events in Wilms' tumors.
Yuan E; Li CM; Yamashiro DJ; Kandel J; Thaker H; Murty VV; Tycko B
Mol Cancer Res; 2005 Sep; 3(9):493-502. PubMed ID: 16179496
[TBL] [Abstract][Full Text] [Related]
13. Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour.
Grundy RG; Pritchard J; Scambler P; Cowell JK
Oncogene; 1998 Jul; 17(3):395-400. PubMed ID: 9690521
[TBL] [Abstract][Full Text] [Related]
14. Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours.
Satoh Y; Nakadate H; Nakagawachi T; Higashimoto K; Joh K; Masaki Z; Uozumi J; Kaneko Y; Mukai T; Soejima H
Br J Cancer; 2006 Aug; 95(4):541-7. PubMed ID: 16909133
[TBL] [Abstract][Full Text] [Related]
15. Mapping of a putative tumor suppressor locus to proximal 7p in Wilms tumors.
Miozzo M; Perotti D; Minoletti F; Mondini P; Pilotti S; Luksch R; Fossati-Bellani F; Pierotti MA; Sozzi G; Radice P
Genomics; 1996 Nov; 37(3):310-5. PubMed ID: 8938443
[TBL] [Abstract][Full Text] [Related]
16. Association of 11q loss, trisomy 12, and possible 16q loss with loss of imprinting of insulin-like growth factor-II in Wilms tumor.
Watanabe N; Nakadate H; Haruta M; Sugawara W; Sasaki F; Tsunematsu Y; Kikuta A; Fukuzawa M; Okita H; Hata J; Soejima H; Kaneko Y
Genes Chromosomes Cancer; 2006 Jun; 45(6):592-601. PubMed ID: 16518847
[TBL] [Abstract][Full Text] [Related]
17. Novel transcribed sequences within the BWS/WT2 region in 11p15.5: tissue-specific expression correlates with cancer type.
Crider-Miller SJ; Reid LH; Higgins MJ; Nowak NJ; Shows TB; Futreal PA; Weissman BE
Genomics; 1997 Dec; 46(3):355-63. PubMed ID: 9441738
[TBL] [Abstract][Full Text] [Related]
18. Allelotype of pediatric rhabdomyosarcoma.
Visser M; Sijmons C; Bras J; Arceci RJ; Godfried M; Valentijn LJ; Voƻte PA; Baas F
Oncogene; 1997 Sep; 15(11):1309-14. PubMed ID: 9315099
[TBL] [Abstract][Full Text] [Related]
19. p57K1P2 is expressed in Wilms' tumor with LOH of 11p15.5.
Overall ML; Spencer J; Bakker M; Dziadek M; Smith PJ
Genes Chromosomes Cancer; 1996 Sep; 17(1):56-9. PubMed ID: 8889507
[TBL] [Abstract][Full Text] [Related]
20. Loss of heterozygosity for chromosome 11 in adenocarcinoma of the stomach.
Baffa R; Negrini M; Mandes B; Rugge M; Ranzani GN; Hirohashi S; Croce CM
Cancer Res; 1996 Jan; 56(2):268-72. PubMed ID: 8542579
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]