Inherited WT1 mutation in Denys-Drash syndrome

scientific article published on November 1, 1992

Inherited WT1 mutation in Denys-Drash syndrome is …
instance of (P31):
scholarly articleQ13442814

External links are
P953full work available at URLhttp://cancerres.aacrjournals.org/cgi/content/abstract/52/21/6125
P698PubMed publication ID1327525

P2093author name stringHiguchi M
Balfe JW
Coppes MJ
Williams BR
Zinn AB
Liefers GJ
P433issue21
P407language of work or nameEnglishQ1860
P921main subjecthuman chromosome 11Q847096
P304page(s)6125-6128
P577publication date1992-11-01
P1433published inCancer ResearchQ326097
P1476titleInherited WT1 mutation in Denys-Drash syndrome
P478volume52

Reverse relations

cites work (P2860)
Q44252486A familial WT1 mutation associated with incomplete Denys-Drash syndrome
Q39431426Abnormal gonadal differentiation in two subjects with ambiguous genitalia, Mullerian structures, and normally developed testes: evidence for a defect in gonadal ridge development
Q33942505Critical windows of exposure for children's health: cancer in human epidemiological studies and neoplasms in experimental animal models
Q38307463DNA recognition by splicing variants of the Wilms' tumor suppressor, WT1
Q51458849Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome.
Q51726467Effects on kidney disease, fertility and development in mice inheriting a protein-truncating Denys-Drash syndrome allele (Wt1tmT396).
Q82887206Evolutive study of children with diffuse mesangial sclerosis
Q47861655Hereditary Podocytopathies in Adults: The Next Generation.
Q36106284Homozygous somatic Wt1 point mutations in sporadic unilateral Wilms tumor
Q34385164Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database
Q30482686In silico regulatory analysis for exploring human disease progression
Q35632404Metanephric adenofibroma in a 10-year-old boy: report of a case and review of the literature
Q35977161Molecular epidemiology studies of cancer in families
Q35979181Molecular genetic analysis of chromosome 11p in familial Wilms tumour
Q34041473Molecular genetics of Müllerian duct formation, regression and differentiation
Q33595792Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalities
Q38995226Recent findings on the genetics of disorders of sex development
Q35279994Reprogramming of Sertoli cells to fetal-like Leydig cells by Wt1 ablation
Q34647004Software and database for the analysis of mutations in the human WT1 gene
Q28247154The Denys-Drash syndrome
Q37598789The Wt1+/R394W mouse displays glomerulosclerosis and early-onset renal failure characteristic of human Denys-Drash syndrome
Q40596042The genetic contribution to the phenotype
Q36028194Towards an understanding of Wilms' tumour.
Q28259503WT1 and glomerular diseases
Q62810883WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele origin

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