Related references
Note: Only part of the references are listed.Pathogenic STX3 variants affecting the retinal and intestinal transcripts cause an early-onset severe retinal dystrophy in microvillus inclusion disease subjects
Andreas R. Janecke et al.
HUMAN GENETICS (2021)
Pathogenic Variants in the Myosin Chaperone UNC-45B Cause Progressive Myopathy with Eccentric Cores
Sandra Donkervoort et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2020)
UNC-45A is preferentially expressed in epithelial cells and binds to and co-localizes with interphase MTs
Juri Habicht et al.
CANCER BIOLOGY & THERAPY (2019)
Loss of MYO5B expression deregulates late endosome size which hinders mitotic spindle orientation
Changsen Leng et al.
PLOS BIOLOGY (2019)
UNC-45A Is a Novel Microtubule-Associated Protein and Regulator of Paclitaxel Sensitivity in Ovarian Cancer Cells
Ashley Mooneyham et al.
MOLECULAR CANCER RESEARCH (2019)
Loss-of-Function Mutations in UNC45A Cause a Syndrome Associating Cholestasis, Diarrhea, Impaired Hearing, and Bone Fragility
Clothilde Esteve et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2018)
MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update
Herschel S. Dhekne et al.
HUMAN MUTATION (2018)
Loss of MYO5B Leads to Reductions in Na+ Absorption With Maintenance of CFTR-Dependent Cl- Secretion in Enterocytes
Amy C. Engevik et al.
GASTROENTEROLOGY (2018)
Dynamic Formation of Microvillus Inclusions During Enterocyte Differentiation in Munc18-2-Deficient Intestinal Organoids
Mohammed H. Mosa et al.
CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY (2018)
MYO5B Mutations Cause Cholestasis With Normal Serum Gamma-Glutamyl Transferase Activity in Children Without Microvillous Inclusion Disease
Emmanuel Gonzales et al.
HEPATOLOGY (2017)
Defects in Myosin VB Are Associated With a Spectrum of Previously Undiagnosed Low γ-Glutamyltransferase Cholestasis
Yi-Ling Qiu et al.
HEPATOLOGY (2017)
UNC-45a promotes myosin folding and stress fiber assembly
Jaakko I. Lehtimaki et al.
JOURNAL OF CELL BIOLOGY (2017)
Disrupted apical exocytosis of cargo vesicles causes enteropathy in FHL5 patients with Munc18-2 mutations
Georg F. Vogel et al.
JCI INSIGHT (2017)
Identification of intestinal ion transport defects in microvillus inclusion disease
Dmitri V. Kravtsov et al.
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY (2016)
The zebrafish goosepimples/myosin Vb mutant exhibits cellular attributes of human microvillus inclusion disease
Jaydeep Sidhaye et al.
MECHANISMS OF DEVELOPMENT (2016)
Cargo-selective apical exocytosis in epithelial cells is conducted by Myo5B, Slp4a, Vamp7, and Syntaxin 3
Georg F. Vogel et al.
JOURNAL OF CELL BIOLOGY (2015)
Loss of Syntaxin 3 Causes Variant Microvillus Inclusion Disease
Caroline L. Wiegerinck et al.
GASTROENTEROLOGY (2014)
Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease
Byron C. Knowles et al.
JOURNAL OF CLINICAL INVESTIGATION (2014)
Microvillous Atrophy: Atypical Presentations
Ariane Perry et al.
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION (2014)
The Myosin Chaperone UNC-45 Is Organized in Tandem Modules to Support Myofilament Formation in C. elegans
Linn Gazda et al.
CELL (2013)
Persistent defective membrane trafficking in epithelial cells of patients with familial hemophagocytic lymphohistiocytosis type 5 due to STXBP2/MUNC18-2 mutations
Polina Stepensky et al.
PEDIATRIC BLOOD & CANCER (2013)
Microvillus Inclusion Disease: Loss of Myosin Vb Disrupts Intracellular Traffic and Cell Polarity
Cornelia E. Thoeni et al.
TRAFFIC (2013)
MYO5B Mutations in Patients With Microvillus Inclusion Disease Presenting With Transient Renal Fanconi Syndrome
Magdalena R. Golachowska et al.
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION (2012)
Functional Characterization of Mutations in the Myosin Vb Gene Associated With Microvillus Inclusion Disease
Agata M. Szperl et al.
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION (2011)
Motor Number Controls Cargo Switching at Actin-Microtubule Intersections In Vitro
Harry W. Schroeder et al.
CURRENT BIOLOGY (2010)
Loss-of-Function of MYO5B is the Main Cause of Microvillus Inclusion Disease: 15 Novel Mutations and a CaCo-2 RNAi Cell Model
Frank M. Ruemmele et al.
HUMAN MUTATION (2010)
Unc45 activates hsp90-dependent folding of the myosin motor domain
Li Liu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity
Thomas Mueller et al.
NATURE GENETICS (2008)
Myosin II regulatory light chain is required for trafficking of bile salt export protein to the apical membrane in Madin-Darby canine kidney cells
W Chan et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Maternal UNC-45 is involved in cytokinesis and colocalizes with non-muscle myosin in the early Caenorhabditis elegans embryo
T Kachur et al.
JOURNAL OF CELL SCIENCE (2004)
She4p/Dim1p interacts with the motor domain of unconventional Myosins in the budding yeast, Saccharomyces cerevisiae
H Toi et al.
MOLECULAR BIOLOGY OF THE CELL (2003)
The UCS family of myosin chaperones
AH Hutagalung et al.
JOURNAL OF CELL SCIENCE (2002)
Role of the myosin assembly protein UNC-45 as a molecular chaperone for myosin
JM Barral et al.
SCIENCE (2002)
Myosin Vb is associated with plasma membrane recycling systems
LA Lapierre et al.
MOLECULAR BIOLOGY OF THE CELL (2001)