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Neoplasia (New York, N.Y.)|March 4, 2016
Nephron Progenitor But Not Stromal Progenitor Cells Give Rise to Wilms Tumors in Mouse Models with β-Catenin Activation or Wt1 Ablation and Igf2 UpregulationLe Huang, Sharada Mokkapati, Qianghua Hu, et al.
Genes, Chromosomes & Cancer|March 12, 2005
Genome-wide loss of heterozygosity analysis of WT1-wild-type and WT1-mutant Wilms tumorsE Cristy Ruteshouser, Brett W Hendrickson, Stefano Colella, et al.
Development (Cambridge, England)|April 12, 2008
Wt1 negatively regulates beta-catenin signaling during testis developmentHao Chang, Fei Gao, Florian Guillou, et al.
Journal of Medical Genetics|November 15, 2015
Identification of germline DICER1 mutations and loss of heterozygosity in familial Wilms tumourTimothy Blake Palculict, E Cristy Ruteshouser, Yu Fan, et al.
Translational Oncology|June 28, 2014
Characterization of the inflammatory microenvironment and identification of potential therapeutic targets in wilms tumorsParamahamsa Maturu, Willem W Overwijk, John Hicks, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
Twenty-four new cases of WT1 germline mutations and review of the literature: genotype/phenotype correlations for Wilms tumor developmentBrigitte Royer-Pokora, Manfred Beier, Markus Henzler, et al.
Human Molecular Genetics|September 7, 2013
Wt1 functions in ovarian follicle development by regulating granulosa cell differentiationFei Gao, Jun Zhang, Xiaona Wang, et al.
Plos One|December 14, 2018
A unique subset of low-risk Wilms tumors is characterized by loss of function of TRIM28 (KAP1), a gene critical in early renal development: A Children's Oncology Group studyAmy E Armstrong, Samantha Gadd, Vicki Huff, et al.
Cancer Research|May 23, 2014
β-catenin activation in a novel liver progenitor cell type is sufficient to cause hepatocellular carcinoma and hepatoblastomaSharada Mokkapati, Katharina Niopek, Le Huang, et al.
Molecular and Cellular Biology|October 29, 2004
The Wt1+/R394W mouse displays glomerulosclerosis and early-onset renal failure characteristic of human Denys-Drash syndromeFei Gao, Sourindra Maiti, Guizhi Sun, et al.
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