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5. Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour. Ogawa O; Eccles MR; Szeto J; McNoe LA; Yun K; Maw MA; Smith PJ; Reeve AE Nature; 1993 Apr; 362(6422):749-51. PubMed ID: 8097018 [TBL] [Abstract][Full Text] [Related]
6. Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor. Prawitt D; Enklaar T; Gärtner-Rupprecht B; Spangenberg C; Oswald M; Lausch E; Schmidtke P; Reutzel D; Fees S; Lucito R; Korzon M; Brozek I; Limon J; Housman DE; Pelletier J; Zabel B Proc Natl Acad Sci U S A; 2005 Mar; 102(11):4085-90. PubMed ID: 15743916 [TBL] [Abstract][Full Text] [Related]
7. Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome. Kubota T; Saitoh S; Matsumoto T; Narahara K; Fukushima Y; Jinno Y; Niikawa N Am J Med Genet; 1994 Feb; 49(4):378-83. PubMed ID: 7909196 [TBL] [Abstract][Full Text] [Related]
8. Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11. Grundy P; Koufos A; Morgan K; Li FP; Meadows AT; Cavenee WK Nature; 1988 Nov; 336(6197):374-6. PubMed ID: 2848199 [TBL] [Abstract][Full Text] [Related]
9. Aberrant imprinting of the insulin-like growth factor II receptor gene in Wilms' tumor. Xu YQ; Grundy P; Polychronakos C Oncogene; 1997 Mar; 14(9):1041-6. PubMed ID: 9070652 [TBL] [Abstract][Full Text] [Related]
10. Molecular biology of Beckwith-Wiedemann syndrome. Weksberg R; Squire JA Med Pediatr Oncol; 1996 Nov; 27(5):462-9. PubMed ID: 8827075 [TBL] [Abstract][Full Text] [Related]
11. 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]
14. 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]
15. Mosaic allelic insulin-like growth factor 2 expression patterns reveal a link between Wilms' tumorigenesis and epigenetic heterogeneity. Ohlsson R; Cui H; He L; Pfeifer S; Malmikumpu H; Jiang S; Feinberg AP; Hedborg F Cancer Res; 1999 Aug; 59(16):3889-92. PubMed ID: 10463576 [TBL] [Abstract][Full Text] [Related]
16. Identification of novel regions of deletion in familial Wilms' tumor by comparative genomic hybridization. Altura RA; Valentine M; Li H; Boyett JM; Shearer P; Grundy P; Shapiro DN; Look AT Cancer Res; 1996 Aug; 56(16):3837-41. PubMed ID: 8706032 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Duplication of HRAS1, INS, and IGF2 is not a common event in Beckwith-Wiedemann syndrome. Henry I; Jeanpierre M; Barichard F; Serre JL; Mallet J; Turleau C; de Grouchy J; Junien C Ann Genet; 1988; 31(4):216-20. PubMed ID: 2905880 [TBL] [Abstract][Full Text] [Related]
19. Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour. Cerrato F; Sparago A; Verde G; De Crescenzo A; Citro V; Cubellis MV; Rinaldi MM; Boccuto L; Neri G; Magnani C; D'Angelo P; Collini P; Perotti D; Sebastio G; Maher ER; Riccio A Hum Mol Genet; 2008 May; 17(10):1427-35. PubMed ID: 18245780 [TBL] [Abstract][Full Text] [Related]
20. Molecular and cellular biology of Wilms' tumour. Maitland NJ; Brown KW; Poirier V; Shaw AP; Williams J Anticancer Res; 1989; 9(5):1417-26. PubMed ID: 2556071 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]