(Q45149880)

10 December 2017

title

Variants in the Wilms' tumor gene are associated with focal segmental glomerulosclerosis in the African American population (English)

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focal segmental glomerulosclerosis

10 December 2017

main subject

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12

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19

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10 December 2017

Sudha K Iyengar

2

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David Vlahov

13

object named as

David Vlahov

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3

Cheryl A Winkler

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10 December 2017

Mohammed S Orloff

1

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10 December 2017

Katrina A B Goddard

4

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10 December 2017

Richard A Dart

5

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10 December 2017

Tejinder S Ahuja

6

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Michele Mokrzycki

7

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10 December 2017

William A Briggs

8

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10 December 2017

Stephen M Korbet

9

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10 December 2017

Paul L Kimmel

10

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10 December 2017

Eric E Simon

11

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10 December 2017

Donna M Michel

14

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10 December 2017

Jeffrey S Berns

15

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10 December 2017

Michael C Smith

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10 December 2017

Jeffrey R Schelling

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John R Sedor

18

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10 December 2017

publication date

1 February 2005

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10 December 2017

published in

Physiological Genomics

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10 December 2017

volume

21

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10 December 2017

issue

2

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10 December 2017

page(s)

212-221

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Donor splice-site mutations in WT1 are responsible for Frasier syndrome

10 December 2017

cites work

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

RNA binding by the Wilms tumor suppressor zinc finger proteins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Fine mapping functional sites or regions from case-control data using haplotypes of multiple linked SNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Genomic control for association studies

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Molecular cloning and functional analysis of the adenovirus E1A-associated 300-kD protein (p300) reveals a protein with properties of a transcriptional adaptor

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Incorporating genotypes of relatives into a test of linkage disequilibrium

21 January 2018

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https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

The genomic organization and expression of the WT1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Alternative splicing and genomic structure of the Wilms tumor gene WT1

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Two splice variants of the Wilms' tumor 1 gene have distinct functions during sex determination and nephron formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Estimation of linkage disequilibrium in randomly mating populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Tissue, developmental, and tumor-specific expression of divergent transcripts in Wilms tumor

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Trends in the epidemiology of focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

WT-1 is required for early kidney development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Subnuclear localization of WT1 in splicing or transcription factor domains is regulated by alternative splicing

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

The Wilms' tumour protein (WT1) shuttles between nucleus and cytoplasm and is present in functional polysomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Murine Denys-Drash syndrome: evidence of podocyte de-differentiation and systemic mediation of glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

A zinc finger truncation of murine WT1 results in the characteristic urogenital abnormalities of Denys-Drash syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

The candidate Wilms' tumour gene is involved in genitourinary development

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

DNA-binding properties of the E1A-associated 300-kilodalton protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

CD2AP localizes to the slit diaphragm and binds to nephrin via a novel C-terminal domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

A haplotype-based 'haplotype relative risk' approach to detecting allelic associations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

21 January 2018

The complex life of WT1

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Analysis with specific polyclonal antiserum indicates that the E1A-associated 300-kDa product is a stable nuclear phosphoprotein that undergoes cell cycle phase-specific modification

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

Adenoviral ElA-associated protein p300 as a functional homologue of the transcriptional co-activator CBP

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00201.2004

10.1152/PHYSIOLGENOMICS.00201.2004

21 January 2018

Identifiers

DOI

1 reference

10 December 2017

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