Ruteshouser EC - Search Results

1

Identification of germline DICER1 mutations and loss of heterozygosity in familial Wilms tumour.

Palculict TB, Ruteshouser EC, Fan Y, Wang W, Strong L, Huff V. Palculict TB, et al. Among authors: ruteshouser ec. J Med Genet. 2016 Jun;53(6):385-8. doi: 10.1136/jmedgenet-2015-103311. Epub 2015 Nov 13. J Med Genet. 2016. PMID: 26566882 Free PMC article.

2

Familial Wilms tumor.

Ruteshouser EC, Huff V. Ruteshouser EC, et al. Am J Med Genet C Semin Med Genet. 2004 Aug 15;129C(1):29-34. doi: 10.1002/ajmg.c.30025. Am J Med Genet C Semin Med Genet. 2004. PMID: 15264270 Review.

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. Ruteshouser EC, et al. Genes Chromosomes Cancer. 2005 Jun;43(2):172-80. doi: 10.1002/gcc.20169. Genes Chromosomes Cancer. 2005. PMID: 15761866

4

Wilms tumor genetics: mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors.

Ruteshouser EC, Robinson SM, Huff V. Ruteshouser EC, et al. Genes Chromosomes Cancer. 2008 Jun;47(6):461-70. doi: 10.1002/gcc.20553. Genes Chromosomes Cancer. 2008. PMID: 18311776 Free PMC article.

5

Wt1 ablation and Igf2 upregulation in mice result in Wilms tumors with elevated ERK1/2 phosphorylation.

Hu Q, Gao F, Tian W, Ruteshouser EC, Wang Y, Lazar A, Stewart J, Strong LC, Behringer RR, Huff V. Hu Q, et al. Among authors: ruteshouser ec. J Clin Invest. 2011 Jan;121(1):174-83. doi: 10.1172/JCI43772. Epub 2010 Dec 1. J Clin Invest. 2011. PMID: 21123950 Free PMC article.

6

Rare variant detection using family-based sequencing analysis.

Peng G, Fan Y, Palculict TB, Shen P, Ruteshouser EC, Chi AK, Davis RW, Huff V, Scharfe C, Wang W. Peng G, et al. Among authors: ruteshouser ec. Proc Natl Acad Sci U S A. 2013 Mar 5;110(10):3985-90. doi: 10.1073/pnas.1222158110. Epub 2013 Feb 20. Proc Natl Acad Sci U S A. 2013. PMID: 23426633 Free PMC article.

7

Nephron Progenitor But Not Stromal Progenitor Cells Give Rise to Wilms Tumors in Mouse Models with β-Catenin Activation or Wt1 Ablation and Igf2 Upregulation.

Huang L, Mokkapati S, Hu Q, Ruteshouser EC, Hicks MJ, Huff V. Huang L, et al. Among authors: ruteshouser ec. Neoplasia. 2016 Feb;18(2):71-81. doi: 10.1016/j.neo.2015.12.001. Neoplasia. 2016. PMID: 26936393 Free PMC article.

8

WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequences.

Huff V, Jaffe N, Saunders GF, Strong LC, Villalba F, Ruteshouser EC. Huff V, et al. Among authors: ruteshouser ec. Am J Hum Genet. 1995 Jan;56(1):84-90. Am J Hum Genet. 1995. PMID: 7825606 Free PMC article.

9

Absence of PPP2R1A mutations in Wilms tumor.

Ruteshouser EC, Ashworth LK, Huff V. Ruteshouser EC, et al. Oncogene. 2001 Apr 12;20(16):2050-4. doi: 10.1038/sj.onc.1204301. Oncogene. 2001. PMID: 11360189

10

Loss of heterozygosity at 2q37 in sporadic Wilms' tumor: putative role for miR-562.

Drake KM, Ruteshouser EC, Natrajan R, Harbor P, Wegert J, Gessler M, Pritchard-Jones K, Grundy P, Dome J, Huff V, Jones C, Aldred MA. Drake KM, et al. Among authors: ruteshouser ec. Clin Cancer Res. 2009 Oct 1;15(19):5985-92. doi: 10.1158/1078-0432.CCR-09-1065. Epub 2009 Sep 29. Clin Cancer Res. 2009. PMID: 19789318 Free PMC article.

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