Two cases of isolated diffuse mesangial sclerosis with WT1 mutations. - Wikidata - awgldk - TriplyDB

Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.

Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.

http://www.wikidata.org/entity/Q37323778

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A novel WT1 gene mutation in a three-generation family with progressive isolated focal segmental glomerulosclerosis.Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations.Atypical clinical presentation of a WT1-related syndrome associated with a novel exon 6 gene mutation.Recent findings on the genetics of disorders of sex development.Genetics of kidney development: pathogenesis of renal anomalies.Clinical Aspects of WT1 and the Kidney.Refining the Diagnosis of Congenital Nephrotic Syndrome on Long-term Stored Tissue: c.1097G>A (p.(Arg366His)) WT1 Mutation Causing Denys Drash Syndrome.Genotype-phenotype analysis of pediatric patients with WT1 glomerulopathy.A novel WT1 gene mutation in a patient with Wilms' tumor and 46, XY gonadal dysgenesis.

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P2860

Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.

http://www.wikidata.org/entity/Q37323778

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

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scientific article published on February 2006

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.

@en

Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.

@nl

type

label

Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.

@en

Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.

@nl

prefLabel

Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.

@en

Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.

@nl

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P356

JKMS.2006.21.1.160

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Journal of Korean Medical Science

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Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.

@en

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Hae Il Cheong

http://www.w3.org/2001/XMLSchema#string

Han Wook You

http://www.w3.org/2001/XMLSchema#string

Hyewon Hahn

http://www.w3.org/2001/XMLSchema#string

Young Mi Cho

http://www.w3.org/2001/XMLSchema#string

Young Seo Park

http://www.w3.org/2001/XMLSchema#string

P2860

YAC complementation shows a requirement for Wt1 in the development of epicardium, adrenal gland and throughout nephrogenesis

WT1 is a key regulator of podocyte function: reduced expression levels cause crescentic glomerulonephritis and mesangial sclerosis

Association of an anatomo-pathological syndrome of male pseudohermaphroditism, Wilms' tumor, parenchymatous nephropathy and XX/XY mosaicism

A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease

WT-1 is required for early kidney development

Sex determination and the Y chromosome.

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database

A clinical overview of WT1 gene mutations.

The Wilms tumor suppressor WT1 regulates early gonad development by activation of Sf1.

Clinicopathologic review of twelve children with nephropathy, Wilms tumor, and genital abnormalities (Drash syndrome).

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160-164

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scholarly article

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10.3346/JKMS.2006.21.1.160

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