WT1

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WT1

A gene on chromosome 11p13 that encodes a transcription factor with a central role in urogenital development. WT1 displays complex tissue-specific and polymorphic imprinting pattern, with biallelic and monoallelic expression from the maternal and paternal alleles in different tissues. WT1 mRNA undergoes RNA editing, a tissue-restricted and developmentally regulated process.

Molecular pathology
WT1 is mutated in a small subset of patients with Wilm's tumours.
References in periodicals archive ?
Using Beyer, Peacock's earlier type 120328 drawing as a basis, Mills, now Chief Mechanical Engineer at the WAGR workshops, designed and supervised construction of the ASG engine.
Organised by Emirates Golf Federation, the 54-hole WAGR qualifying tournament is open to amateur men with an 18 or less handicap.
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Page 66: International WAGR Syndrome Association; Annie Prusakiewicz, Chairperson; 313-381-4302, telephone.
To be included in the WAGR index stocks must pass multiple screens, including for capitalization, float, exchange listing, share price and turnover.
In Ella's case, her aniridia results from a rare chromosome disorder called WAGR syndrome that affects one in 800,000 babies.
org 1,6 ANGIO-OSTEOHYPERTROPHY SYNDROME See: Klippel-Trenaunay Syndrome ANGIOKERATOMA CORPORIS DIFFUSUM See: Fabry Disease ANGIOMATOSIS RETINA See: Von Hippel-Lindau Syndrome ANIRIDIA See also: Visual Impairments, WAGR Syndrome Anradia Network PO Box 6444 Colchester C04 3XU UK (+44) 0777989624 * hannah@aniridia.
Three-year-old Ella Chapple has no irises, a condition called aniridia which, in her case, results from a chromosome disorder called WAGR syndrome that affects one in 800,000 babies.
ca /cass 1,2,3,5,6,9; French materials ANGIO-OSTEOHYPERTROPHY SYNDROME See: Klippel-Trenaunay Syndrome ANGIOKERATOMA CORPORIS DIFFUSUM See: Fabry Disease ANGIOMATOSlS RETINA See: Von Hippel-Lindau Syndrome ANIRIDIA See also: Visual Impairments, WAGR Syndrome The Canadian Foundation for Aniridia Research 3780 Verdun Ave.