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Literature watch. FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.

Lymphatic research and biology - 1 Jan 2003

Pepper Michael S

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Share to Disease Models, Animal
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15624441
DOI: 10.1089/153968503768330274

Genes

FOXC2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

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Literature watch. FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.PMID 15624441Read ↗

FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndromeSemantic proximity Read ↗

Lymphoedema-distichiasis and FOXC2: unreported mutations, de novo mutation estimate, families without coding mutationsSemantic proximity Read ↗

Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndrome.Semantic proximity Read ↗

Novel FOXC2 Mutation and Distichiasis in a Patient With Lymphedema-Distichiasis Syndrome.Semantic proximity Read ↗

Truncating mutations in FOXC2 cause multiple lymphedema syndromes.Semantic proximity Read ↗

Lymphedema-distichiasis syndrome and FOXC2 gene mutation.Semantic proximity Read ↗

FOXC2 disease-mutations identified in lymphedema-distichiasis patients cause both loss and gain of protein function.Semantic proximity Read ↗

Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24.Semantic proximity Read ↗

Genetic landscape of FOXC2 mutations in lymphedema-distichiasis syndrome: Different mechanism of pathogenicity for mutations in different domains.Semantic proximity Read ↗

[Genetic variant analysis of a pedigree affected with lymphedema-distichiasis syndrome].Semantic proximity Read ↗

Ophtalmologic diagnosis of lymphedema-distichiasis syndrome through the FOXC2 mutation.Semantic proximity Read ↗

Analysis of lymphoedema-distichiasis families for FOXC2 mutations reveals small insertions and deletions throughout the gene.Semantic proximity Read ↗

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