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Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease

Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4071383

Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease

About this item

Full title

Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease

Publisher

United States: American Society for Clinical Investigation

Journal title

The Journal of clinical investigation, 2014-07, Vol.124 (7), p.2947-2962

Language

English

Formats

Publication information

Publisher

United States: American Society for Clinical Investigation

More information

Scope and Contents

Contents

Microvillus inclusion disease (MVID) is a severe form of congenital diarrhea that arises from inactivating mutations in the gene encoding myosin Vb (MYO5B). We have examined the association of mutations in MYO5B and disruption of microvillar assembly and polarity in enterocytes. Stable MYO5B knockdown (MYO5B-KD) in CaCo2-BBE cells elicited loss of...

Alternative Titles

Full title

Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4071383

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4071383

Other Identifiers

ISSN

0021-9738

E-ISSN

1558-8238

DOI

10.1172/JCI71651

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