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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 21, 2004
Familial Wilms tumorE Cristy Ruteshouser, Vicki HuffExperimental Cell Research|January 8, 2013
Ubiquitin specific protease 18 (Usp18) is a WT1 transcriptional targetMohammad Shahidul Makki, E Cristy Ruteshouser, Vicki HuffGenes, Chromosomes & Cancer|March 4, 2008
Wilms tumor genetics: mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumorsE Cristy Ruteshouser, Stephen M Robinson, Vicki HuffDifferentiation; Research in Biological Diversity|June 28, 2024
Generation of a Wt1 conditional deletion, nuclear red fluorescent protein reporter allele in the mouseJace A Aloway, E Cristy Ruteshouser, Vicki Huff, et al.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.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.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.The Journal of Clinical Investigation|December 3, 2010
Wt1 ablation and Igf2 upregulation in mice result in Wilms tumors with elevated ERK1/2 phosphorylationQianghua Hu, Fei Gao, Weihua Tian, et al.Proceedings of the National Academy of Sciences of the United States of America|February 22, 2013
Rare variant detection using family-based sequencing analysisGang Peng, Yu Fan, Timothy B Palculict, et al.Pageof 6