(Q51751487)

English

WT1 gene mutations in three girls with nephrotic syndrome.

scientific article published in June 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17541636

WT1 gene mutations in three girls with nephrotic syndrome. (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17541636

author name string

Khalid Ismaili

1

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17541636

Véronique Verdure

2

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17541636

Katherina Vandenhoute

3

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17541636

Françoise Janssen

4

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17541636

Michelle Hall

5

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17541636

publication date

1 June 2007

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17541636

European Journal of Pediatrics

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17541636

167

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17541636

5

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17541636

579-581

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17541636

https://scigraph.springernature.com/pub.10.1007/s00431-007-0514-z

0 references

Diffuse mesangial sclerosis: a congenital glomerulopathy with nephrotic syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Denys-Drash syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical spectrum of Denys-Drash and Frasier syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic renal failure and XY gonadal dysgenesis: "Frasier" syndrome--a commentary on reported cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

WT1 and glomerular diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital nephrotic syndrome presenting with increased nuchal translucency in the first trimester

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alternative splicing and genomic structure of the Wilms tumor gene WT1

1 reference

https://pubmed.ncbi.nlm.nih.gov/17541636

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00431-007-0514-Z

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17541636

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 April 2018

http://europepmc.org/abstract/MED/17541636

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