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Article

Insertional Mutation of the Collagen Genes Col4a3 and Col4a4 in a Mouse Model of Alport Syndrome

1 Oct 1999

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 10534397
DOI: 10.1006/geno.1999.5943

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Insertional Mutation of the Collagen Genes Col4a3 and Col4a4 in a Mouse Model of Alport SyndromePMID 10534397Read ↗

Alport syndrome: abnormalities of type IV collagen genes and proteins.Semantic proximity Read ↗

Mutations in type IV collagen genes and Alport phenotypes.Semantic proximity Read ↗

Alport syndrome: clinical and genetic correlation in a type-IV collagen disease.Semantic proximity Read ↗

Identification of COL4A5 defects in Alport's syndrome by immunohistochemistry of skinSemantic proximity Read ↗

COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome11See Editorial by Monnens, p. 799Semantic proximity Read ↗

Characterization of the Ocular Phenotype in a Col4a3 Knockout Mouse Model of Alport Syndrome.Semantic proximity Read ↗

[An absence of the collagen type IV alpha5 chain in Alport Syndrome].Semantic proximity Read ↗

A Comparative Presentation of Mouse Models That Recapitulate Most Features of Alport Syndrome.Semantic proximity Read ↗

Genotype-Based Molecular Mechanisms in Alport Syndrome.Semantic proximity Read ↗

A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers.Semantic proximity Read ↗

Molecular genetics of basement membranes: the paradigm of Alport syndrome.Semantic proximity Read ↗

Alport's Syndrome, Goodpasture's Syndrome, and Type IV CollagenSemantic proximity Read ↗

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