Wilms tumor genetics: Mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors
作者： E. Cristy Ruteshouser , Stephen M. Robinson , Vicki Huff
DOI: 10.1002/GCC.20553
关键词:
摘要: … WTX mutations occur with similar frequency, that they partially overlap in Wilms tumors, and that mutations in WT1, WTX, and CTNNB1 underlie the genetic basis of about one‐third of …
sci-hub.se 参考文章(27)
Vicki D Huff, G. F. Saunders, F. Villalba, Louise C Strong, N. Jaffe, E. C. Ruteshouser, WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequences. American Journal of Human Genetics. ,vol. 56, pp. 84- 90 ,(1995)
Beatrice Lampkin, Sheng Wang-Wuu, Kevin Bove, Betsy Gotwals, Shirley Soukup, Chromosome Analysis of 31 Wilms' Tumors Cancer Research. ,vol. 50, pp. 2786- 2793 ,(1990)
Perry E. Telzerow, Andrew P. Feinberg, Michael R. Eccles, Paul E. Grundy, Marion A. Maw, Roseanne S. Dunn, Robert I. Richards, Malcolm C. Paterson, Lynn J. Millow, Anthony E. Reeve, Andrew D. Thompson, David F. Callen, Dave J. Law, Peter J. Smith, A Third Wilms' Tumor Locus on Chromosome 16q Cancer Research. ,vol. 52, pp. 3094- 3098 ,(1992)
C Heyting, M Mannens, J Bliek, A Westerveld, J de Kraker, R M Slater, I Mandjes, P Devilee, Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11 Cancer Research. ,vol. 50, pp. 3279- 3283 ,(1990)
David Virshup, Edwin C. Douglass, Vicki D Huff, Louise C Strong, Ross Fisher, J. Matthew McDonald, Carl E. Krill, Clementina F. Geiser, Linkage of Familial Wilms' Tumor Predisposition to Chromosome 19 and a Two-Locus Model for the Etiology of Familial Tumors Cancer Research. ,vol. 58, pp. 1387- 1390 ,(1998)
Stephen T. Sherry, Minghong Ward, Karl Sirotkin, dbSNP-database for single nucleotide polymorphisms and other classes of minor genetic variation. Genome Research. ,vol. 9, pp. 677- 679 ,(1999) , 10.1101/GR.9.8.677
E. Cristy Ruteshouser, Brett W. Hendrickson, Stefano Colella, Ralf Krahe, Lancelot Pinto, Vicki Huff, Genome-wide loss of heterozygosity analysis of WT1-wild-type and WT1-mutant Wilms tumors. Genes, Chromosomes and Cancer. ,vol. 43, pp. 172- 180 ,(2005) , 10.1002/GCC.20169
Y Satoh, H Nakadate, T Nakagawachi, K Higashimoto, K Joh, Z Masaki, J Uozumi, Y Kaneko, T Mukai, H Soejima, Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours British Journal of Cancer. ,vol. 95, pp. 541- 547 ,(2006) , 10.1038/SJ.BJC.6603302
Nazneen Rahman, Laura Arbour, Patricia Tonin, Jane Renshaw, Jerry Pelletier, Sylvain Baruchel, Kathryn Pritchard-Jones, Michael R. Stratton, Steven A. Narod, Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12-q21 Nature Genetics. ,vol. 13, pp. 461- 463 ,(1996) , 10.1038/NG0896-461
E. Cristy Ruteshouser, Vicki Huff, Familial Wilms tumor American Journal of Medical Genetics. ,vol. 129C, pp. 29- 34 ,(2004) , 10.1002/AJMG.C.30025