WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis (Q35754616)

10 August 2017

title

WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis (English)

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10 August 2017

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Y Yang

1

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10 August 2017

C Jeanpierre

2

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10 August 2017

G R Dressler

3

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10 August 2017

M Lacoste

4

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10 August 2017

P Niaudet

5

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10 August 2017

M C Gubler

6

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10 August 2017

language of work or name

English

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publication date

1 January 1999

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The American Journal of Pathology

10 August 2017

published in

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10 August 2017

volume

154

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10 August 2017

issue

1

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10 August 2017

page(s)

181-192

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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

10 August 2017

cites work

1 reference

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Software and database for the analysis of mutations in the human WT1 gene

2 October 2017

1 reference

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Expression of the Wilms' tumour gene WT1 in the developing human and in paediatric renal tumours: an immunohistochemical study

2 October 2017

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A clinical overview of WT1 gene mutations

2 October 2017

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Identification of nuclear localization signals within the zinc fingers of the WT1 tumor suppressor gene product

2 October 2017

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The paired-box transcription factor, PAX2, positively modulates expression of the Wilms' tumor suppressor gene (WT1)

2 October 2017

1 reference

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The expression pattern of Wilms' tumour gene (WT1) product in normal tissues and paediatric renal tumours

2 October 2017

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The PAX2 tanscription factor is expressed in cystic and hyperproliferative dysplastic epithelia in human kidney malformations

2 October 2017

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RNA binding by the Wilms tumor suppressor zinc finger proteins.

2 October 2017

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Identification of novel Pax-2 binding sites by chromatin precipitation

2 October 2017

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Regulation of nov by WT1: a potential role for nov in nephrogenesis

2 October 2017

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Truncated WT1 mutants alter the subnuclear localization of the wild-type protein

2 October 2017

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Pax-2 controls multiple steps of urogenital development

2 October 2017

1 reference

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The Wilms' tumor gene product WT1 activates or suppresses transcription through separate functional domains

2 October 2017

1 reference

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WT-1 is required for early kidney development

2 October 2017

1 reference

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The WT1 Wilms tumor gene product: a developmentally regulated transcription factor in the kidney that functions as a tumor suppressor

2 October 2017

1 reference

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Diffuse mesangial sclerosis: a congenital glomerulopathy with nephrotic syndrome.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Nuclear localization of the protein encoded by the Wilms' tumor gene WT1 in embryonic and adult tissues

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Repression of the transforming growth factor-beta 1 gene by the Wilms' tumor suppressor WT1 gene product

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Comparative in situ hybridization analysis of PAX2, PAX8, and WT1 gene transcription in human fetal kidney and Wilms' tumors

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

WT1-mediated transcriptional activation is inhibited by dominant negative mutant proteins.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Repression of Pax-2 by WT1 during normal kidney development

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Antagonism of WT1 activity by protein self-association.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Early organogenesis of the kidney

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

The candidate Wilms' tumour gene is involved in genitourinary development

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney development

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Alternative splicing and genomic structure of the Wilms tumor gene WT1

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

The genomic organization and expression of the WT1 gene

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Expression of the PAX2 gene in human fetal kidney and Wilms' tumor

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Human platelet-derived growth factor A chain is transcriptionally repressed by the Wilms tumor suppressor WT1

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Pax-2 is a DNA-binding protein expressed in embryonic kidney and Wilms tumor

2 October 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Role of extracellular matrix, growth factors and proto-oncogenes in metanephric development

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Products of alternatively spliced transcripts of the Wilms' tumor suppressor gene, wt1, have altered DNA binding specificity and regulate transcription in different ways.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Pax2, a new murine paired-box-containing gene and its expression in the developing excretory system.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Congenital glomerulosclerosis and nephrotic syndrome in two infants. Speculations and pathogenesis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Deregulation of Pax-2 expression in transgenic mice generates severe kidney abnormalities.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1853439

Evidence that WT1 mutations in Denys — Drash syndrome patients may act in a dominant-negative fashion

25 September 2018

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965264-9

DNA binding capacity of the WT1 protein is abolished by Denys—Drash syndrome WT1 point mutations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965264-9

Repression of the insulin-like growth factor II gene by the Wilms tumor suppressor WT1

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965264-9

Familial early-onset nephrotic syndrome: diffuse mesangial sclerosis. Clinico-pathological study of a kindred

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965264-9

Familial infantile nephrotic syndrome with ocular abnormalities

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965264-9

Diffuse mesangial sclerosis: a unique type of congenital and infantile nephrotic syndrome

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2965264-9

The Wilms' tumor gene product, WT1, represses transcription of the platelet-derived growth factor A-chain gene

7 January 2021

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12 December 2020

The nephropathy associated with male pseudohermaphroditism and Wilms' tumor (Drash syndrome): a distinctive glomerular lesion--report of 10 cases

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12 December 2020

[Mesangial sclerosis in the pathogenesis of the familial nephrotic syndrome]

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12 December 2020

Diffuse mesangial sclerosis--light, immunofluorescent and electronmicroscopy findings

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12 December 2020

[Association of early-onset nephrotic syndrome and microcephaly. Apropos of 4 cases in 2 families]

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12 December 2020

Diffuse mesangial sclerosis and ocular abnormalities in two siblings

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12 December 2020

Expression of WT1 protein in fetal kidneys and Wilms tumors

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12 December 2020

Loss of mitotic activity and the expression of vimentin in glomerular epithelial cells of developing human kidneys

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12 December 2020

10.1016/S0002-9440(10)65264-9

Identifiers

DOI

1 reference

10 August 2017

1 reference

10 August 2017

1 reference