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Article

WT1 mutations associated with incomplete Denys-Drash syndrome define a domain predicted to behave in a dominant-negative fashion.

Genomics - 1 Jun 1994

Bardeesy N, Zabel B, Schmitt K, Pelletier J

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 7959750
DOI: 10.1006/geno.1994.1333

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

WT1 mutations associated with incomplete Denys-Drash syndrome define a domain predicted to behave in a dominant-negative fashion.PMID 7959750Read ↗

Clinical features and an atypical WT1 mutant site in a child with incomplete Denys-Drash syndrome.Semantic proximity Read ↗

Denys-Drash syndrome: Relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1Semantic proximity Read ↗

Atypical presentation of Denys-Drash syndrome in a female with a novel Wt1 gene mutation.Semantic proximity Read ↗

Clinical Aspects of WT1 and the Kidney.Semantic proximity Read ↗

Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children.Semantic proximity Read ↗

A necropsy case of Denys-Drash syndrome with a WT1 mutation in exon 7.Semantic proximity Read ↗

Two N-terminal self-association domains are required for the dominant negative transcriptional activity of WT1 Denys-Drash mutant proteins.Semantic proximity Read ↗

Wilms' Tumor Suppressor Gene WT1Semantic proximity Read ↗

A familial WT1 mutation associated with incomplete Denys-Drash syndrome.Semantic proximity Read ↗

A WT1 exon 1 mutation in a child diagnosed with Denys-Drash syndrome.Semantic proximity Read ↗

New insights into the function of the Wilms tumor suppressor geneWT1in podocytesSemantic proximity Read ↗

Mice lacking the 68-amino-acid, mammal-specific N-terminal extension of WT1 develop normally and are fertile.Semantic proximity Read ↗

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