Altered MYO5B Function Underlies Microvillus Inclusion Disease: Opportunities for Intervention at a Cellular Level
Author:
Funder
National Institutes of Health
National Institute of Diabetes and Digestive and Kidney Diseases
Publisher
Elsevier BV
Subject
Gastroenterology,Hepatology
Reference120 articles.
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2. Microvillus inclusion disease: an inherited defect of brush-border assembly and differentiation;Cutz;N Engl J Med,1989
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3. The MYO1B and MYO5B motor proteins and the SNX27 sorting nexin regulate membrane mucin MUC17 trafficking in enterocytes;2023-03-07
4. Therapy Development for Microvillus Inclusion Disease using Patient-derived Enteroids;2023-01-29
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