(Q62810883)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112732%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

title

WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele origin (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112732%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112732%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

author name string

E Friedman

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112732%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

M Anvret

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112732%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

publication date

1 February 1994

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112732%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112732%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

volume

93

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112732%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112732%20AND%20SRC:MED&resulttype=core&format=json

25 October 2019

page(s)

115-120

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8112732%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00210593

25 October 2019

exact match

0 references

cites work

PCR Amplification from Paraffin-Embedded Tissues: Effects of Fixative and Fixation Time

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12 December 2020

Parental origin of mutations of the retinoblastoma gene

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12 December 2020

Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome

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12 December 2020

Preferential loss of maternal alleles in sporadic Wilms' tumour.

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12 December 2020

Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT

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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

An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor

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12 December 2020

Recent advances in the polymerase chain reaction

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12 December 2020

The candidate Wilms' tumour gene is involved in genitourinary development

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12 December 2020

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

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12 December 2020

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

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12 December 2020

WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour.

1 reference

12 December 2020

Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene (TH).

1 reference

12 December 2020

A novel insertional mutation at the third zinc finger coding region of the WT1 gene in Denys-Drash syndrome

1 reference

12 December 2020

Inherited WT1 mutation in Denys-Drash syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

The genomic organization and expression of the WT1 gene

1 reference

12 December 2020

Distinct molecular origins for Denys-Drash and Frasier syndromes

1 reference

12 December 2020

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

1 reference

12 December 2020

Insulin-IGF2 region on chromosome 11p encodes a gene implicated in HLA-DR4-dependent diabetes susceptibility

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12 December 2020

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

1 reference

12 December 2020

Zinc finger point mutations within the WT1 gene in Wilms tumor patients

1 reference

12 December 2020

Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development

1 reference

12 December 2020

Alternative splicing and genomic structure of the Wilms tumor gene WT1

1 reference

12 December 2020

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

1 reference

12 December 2020