An inducible mouse model for microvillus inclusion disease reveals a role for myosin Vb in apical and basolateral trafficking

Rab11a regulates syntaxin 3 localization and microvillus assembly in enterocytes

(2015) B. C. Knowles et al.   JOURNAL OF CELL SCIENCE

Myo5b knockout mice as a model of microvillus inclusion disease

(2015) Fernando Cartón-García et al.   Scientific Reports

Myosin 5b loss of function leads to defects in polarized signaling: implication for microvillus inclusion disease pathogenesis and treatment

(2014) Dmitri Kravtsov et al.   AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY

Loss of Syntaxin 3 Causes Variant Microvillus Inclusion Disease

(2014) Caroline L. Wiegerinck et al.   GASTROENTEROLOGY

Myosin Vb and Rab11a regulate phosphorylation of ezrin in enterocytes

(2014) H. S. Dhekne et al.   JOURNAL OF CELL SCIENCE

Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease

(2014) Byron C. Knowles et al.   JOURNAL OF CLINICAL INVESTIGATION

Adult Stem Cells in the Small Intestine Are Intrinsically Programmed with Their Location-Specific Function

(2014) Sabine Middendorp et al.   STEM CELLS

Rab11a is required for apical protein localisation in the intestine

(2014) T. Sobajima et al.   Biology Open

Cdc42 Coordinates Proliferation, Polarity, Migration, and Differentiation of Small Intestinal Epithelial Cells in Mice

(2013) Jaime Melendez et al.   GASTROENTEROLOGY

An Overview and Online Registry of Microvillus Inclusion Disease Patients and theirMYO5BMutations

(2013) K. Joeri van der Velde et al.   HUMAN MUTATION

A functional CFTR assay using primary cystic fibrosis intestinal organoids

(2013) Johanna F Dekkers et al.   NATURE MEDICINE

Microvillus Inclusion Disease: Loss of Myosin Vb Disrupts Intracellular Traffic and Cell Polarity

(2013) Cornelia E. Thoeni et al.   TRAFFIC

Cdc42 and Rab8a are critical for intestinal stem cell division, survival, and differentiation in mice

(2012) Ryotaro Sakamori et al.   JOURNAL OF CLINICAL INVESTIGATION

Functional Characterization of Mutations in the Myosin Vb Gene Associated With Microvillus Inclusion Disease

(2011) Agata M Szperl et al.   JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION

Functional ESCRT machinery is required for constitutive recycling of claudin-1 and maintenance of polarity in vertebrate epithelial cells

(2011) Joseph D. Dukes et al.   MOLECULAR BIOLOGY OF THE CELL

Rab GTPase-Myo5B complexes control membrane recycling and epithelial polarization

(2011) J. T. Roland et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model

(2010) Frank M. Ruemmele et al.   HUMAN MUTATION

The scaffolding protein EBP50 regulates microvillar assembly in a phosphorylation-dependent manner

(2010) Damien Garbett et al.   JOURNAL OF CELL BIOLOGY

Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche

(2009) Toshiro Sato et al.   NATURE

Navajo microvillous inclusion disease is due to a mutation inMYO5B

(2008) Robert P. Erickson et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity

(2008) Thomas Müller et al.   NATURE GENETICS