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Article

MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity

24 Aug 2008

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 18724368
DOI: 10.1038/ng.225

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Related research

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Click a neighbor to travelStep 1 · 12 closest

MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarityPMID 18724368Read ↗

Microvillus inclusion disease with novel MYO5B pathogenic variants.Semantic proximity Read ↗

Altered MYO5B Function Underlies Microvillus Inclusion Disease: Opportunities for Intervention at a Cellular LevelSemantic proximity Read ↗

Microvillus inclusion disease: loss of Myosin vb disrupts intracellular traffic and cell polarity.Semantic proximity Read ↗

An overview and online registry of microvillus inclusion disease patients and their MYO5B mutations.Semantic proximity Read ↗

Myo5b knockout mice as a model of microvillus inclusion diseaseSemantic proximity Read ↗

MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update.Semantic proximity Read ↗

Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease.Semantic proximity Read ↗

Towards understanding microvillus inclusion diseaseSemantic proximity Read ↗

Uncovering the Relationship Between Genes and Phenotypes Beyond the Gut in Microvillus Inclusion Disease.Semantic proximity Read ↗

An inducible mouse model for microvillus inclusion disease reveals a role for myosin Vb in apical and basolateral traffickingSemantic proximity Read ↗

Loss of MYO5B in Mice Recapitulates Microvillus Inclusion Disease and Reveals an Apical Trafficking Pathway Distinct to Neonatal DuodenumSemantic proximity Read ↗

Novel MYO5B mutation in microvillous inclusion disease of Syrian ancestry.Semantic proximity Read ↗

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