相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Rab11a regulates syntaxin 3 localization and microvillus assembly in enterocytes
Byron C. Knowles et al.
JOURNAL OF CELL SCIENCE (2015)
Animal model of Sar1b deficiency presents lipid absorption deficits similar to Anderson disease
Daniel S. Levic et al.
JOURNAL OF MOLECULAR MEDICINE-JMM (2015)
Correlated light and electron microscopy: ultrastructure lights up!
Pascal de Boer et al.
NATURE METHODS (2015)
Mechanisms of apical-basal axis orientation and epithelial lumen positioning
Arend W. Overeem et al.
TRENDS IN CELL BIOLOGY (2015)
Myo5b knockout mice as a model of microvillus inclusion disease
Fernando Carton-Garcia et al.
SCIENTIFIC REPORTS (2015)
Myosin 5b loss of function leads to defects in polarized signaling: implication for microvillus inclusion disease pathogenesis and treatment
Dmitri Kravtsov et al.
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY (2014)
Intravital correlated microscopy reveals differential macrophage and microglial dynamics during resolution of neuroinflammation
Tjakko J. van Ham et al.
DISEASE MODELS & MECHANISMS (2014)
Loss of Syntaxin 3 Causes Variant Microvillus Inclusion Disease
Caroline L. Wiegerinck et al.
GASTROENTEROLOGY (2014)
Could a Swimming Creature Inform Us on Intestinal Diseases? Lessons from Zebrafish
Ye Yang et al.
INFLAMMATORY BOWEL DISEASES (2014)
Shaping the intestinal brush border
Scott W. Crawley et al.
JOURNAL OF CELL BIOLOGY (2014)
Myosin Vb and Rab11a regulate phosphorylation of ezrin in enterocytes
Herschel S. Dhekne et al.
JOURNAL OF CELL SCIENCE (2014)
TTC7A mutations disrupt intestinal epithelial apicobasal polarity
Amelie E. Bigorgne et al.
JOURNAL OF CLINICAL INVESTIGATION (2014)
Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease
Byron C. Knowles et al.
JOURNAL OF CLINICAL INVESTIGATION (2014)
Targeted gene panel sequencing in children with very early onset inflammatory bowel disease-evaluation and prospective analysis
Jochen Kammermeier et al.
JOURNAL OF MEDICAL GENETICS (2014)
Crumbs3 Is Essential for Proper Epithelial Development and Viability
Eileen L. Whiteman et al.
MOLECULAR AND CELLULAR BIOLOGY (2014)
An in vivo model of human small intestine using pluripotent stem cells
Carey L. Watson et al.
NATURE MEDICINE (2014)
Functional Analysis of a Missense Mutation in the Serine Protease Inhibitor SPINT2 Associated with Congenital Sodium Diarrhea
Nicolas Faller et al.
PLOS ONE (2014)
Myosin Vb Mediated Plasma Membrane Homeostasis Regulates Peridermal Cell Size and Maintains Tissue Homeostasis in the Zebrafish Epidermis
Sonal et al.
PLOS GENETICS (2014)
Cdc42 Coordinates Proliferation, Polarity, Migration, and Differentiation of Small Intestinal Epithelial Cells in Mice
Jaime Melendez et al.
GASTROENTEROLOGY (2013)
Absence of cell-surface EpCAM in congenital tufting enteropathy
Ulrike Schnell et al.
HUMAN MOLECULAR GENETICS (2013)
An Overview and Online Registry of Microvillus Inclusion Disease Patients and their MYO5B Mutations
K. Joeri van der Velde et al.
HUMAN MUTATION (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)
SKIV2L Mutations Cause Syndromic Diarrhea, or Trichohepatoenteric Syndrome
Alexandre Fabre et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
Enterocyte Microvillus-Derived Vesicles Detoxify Bacterial Products and Regulate Epithelial-Microbial Interactions
David A. Shifrin et al.
CURRENT BIOLOGY (2012)
Cdc42 and Rab8a are critical for intestinal stem cell division, survival, and differentiation in mice
Ryotaro Sakamori et al.
JOURNAL OF CLINICAL INVESTIGATION (2012)
DGAT1 mutation is linked to a congenital diarrheal disorder
Joel T. Haas et al.
JOURNAL OF CLINICAL INVESTIGATION (2012)
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)
Caenorhabditis elegans screen reveals role of PAR-5 in RAB-11-recycling endosome positioning and apicobasal cell polarity
Julia Franziska Winter et al.
NATURE CELL BIOLOGY (2012)
Functional engraftment of colon epithelium expanded in vitro from a single adult Lgr5+ stem cell
Shiro Yui et al.
NATURE MEDICINE (2012)
Familial Diarrhea Syndrome Caused by an Activating GUCY2C Mutation
Torunn Fiskerstrand et al.
NEW ENGLAND JOURNAL OF MEDICINE (2012)
mTrop1/Epcam Knockout Mice Develop Congenital Tufting Enteropathy through Dysregulation of Intestinal E-cadherin/β-catenin
Emanuela Guerra et al.
PLOS ONE (2012)
Expression of Sar1b Enhances Chylomicron Assembly and Key Components of the Coat Protein Complex II System Driving Vesicle Budding
Emile Levy et al.
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2011)
Update on SLC26A3 Mutations in Congenital Chloride Diarrhea
Satu Wedenoja et al.
HUMAN MUTATION (2011)
Microvillous Inclusion Disease: How to Improve the Prognosis of a Severe Congenital Enterocyte Disorder
Ugur Halac et al.
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION (2011)
Intractable Diarrhea With Tufting Enteropathy: A Favorable Outcome Is Possible
Julie Lemale et al.
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION (2011)
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)
Directed differentiation of human pluripotent stem cells into intestinal tissue in vitro
Jason R. Spence et al.
NATURE (2011)
Epithelial Barriers in Homeostasis and Disease
Amanda M. Marchiando et al.
ANNUAL REVIEW OF PATHOLOGY-MECHANISMS OF DISEASE (2010)
The Biogenesis of Chylomicrons
Charles M. Mansbach et al.
ANNUAL REVIEW OF PHYSIOLOGY (2010)
Mutations in TTC37 Cause Trichohepatoenteric Syndrome (Phenotypic Diarrhea of Infancy)
Jane Louise Hartley et al.
GASTROENTEROLOGY (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)
A molecular network for de novo generation of the apical surface and lumen
David M. Bryant et al.
NATURE CELL BIOLOGY (2010)
Membrane-anchored serine protease matriptase regulates epithelial barrier formation and permeability in the intestine
Marguerite S. Buzza et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Recycling endosomes in apical plasma membrane domain formation and epithelial cell polarity
Magdalena R. Golachowska et al.
TRENDS IN CELL BIOLOGY (2010)
Mutations in SPINT2 Cause a Syndromic Form of Congenital Sodium Diarrhea
Peter Heinz-Erian et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL-5) Is Caused by Mutations in Munc18-2 and Impaired Binding to Syntaxin 11
Udo zur Stadt et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Regulation of cell surface protease matriptase by HAI2 is essential for placental development, neural tube closure and embryonic survival in mice
Roman Szabo et al.
DEVELOPMENT (2009)
Apical Secretion in Epithelial Tubes of the Drosophila Embryo Is Directed by the Formin-Family Protein Diaphanous
R'ada Massarwa et al.
DEVELOPMENTAL CELL (2009)
Impaired Trafficking and Subcellular Localization of a Mutant Lactase Associated With Congenital Lactase Deficiency
Marc Behrendt et al.
GASTROENTEROLOGY (2009)
Apical trafficking in epithelial cells: signals, clusters and motors
Ora A. Weisz et al.
JOURNAL OF CELL SCIENCE (2009)
Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche
Toshiro Sato et al.
NATURE (2009)
The Epithelial Cell Adhesion Molecule EpCAM Is Required for Epithelial Morphogenesis and Integrity during Zebrafish Epiboly and Skin Development
Krasimir Slanchev et al.
PLOS GENETICS (2009)
Identification of EpCAM as the gene for congenital tufting enteropathy
Mamata Sivagnanam et al.
GASTROENTEROLOGY (2008)
MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity
Thomas Mueller et al.
NATURE GENETICS (2008)
Syndromic (phenotypic) diarrhea in early infancy
Olivier Goulet et al.
ORPHANET JOURNAL OF RARE DISEASES (2008)
The Rab8 GTPase regulates apical protein localization in intestinal cells
Takashi Sato et al.
NATURE (2007)
Intestinal epithelial dysplasia (tufting enteropathy)
Olivier Goulet et al.
ORPHANET JOURNAL OF RARE DISEASES (2007)
Mutations in the translated region of the lactase gene (LCT) underlie congenital lactase deficiency
M Kuokkanen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Rab11a and myosin Vb are required for bile canalicular formation in WIF-B9 cells
Y Wakabayashi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
STa and cGMP stimulate CFTR translocation to the surface of villus enterocytes in rat jejunum and is regulated by protein kinase G
F Golin-Bisello et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2005)
Ezrin is essential for epithelial organization and villus morphogenesis in the developing intestine
I Saotome et al.
DEVELOPMENTAL CELL (2004)
COPII-dependent export of cystic fibrosis transmembrane conductance regulator from the ER uses a di-acidic exit code
XD Wang et al.
JOURNAL OF CELL BIOLOGY (2004)
Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders
B Jones et al.
NATURE GENETICS (2003)
Congenital sucrase-isomaltase deficiency because of an accumulation of the mutant enzyme in the endoplasmic reticulum
V Ritz et al.
GASTROENTEROLOGY (2003)
DGAT1 is not essential for intestinal triacylglycerol absorption or chylomicron synthesis
KK Buhman et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Loss of the NHE2 Na+/H+ exchanger has no apparent effect on diarrheal state of NHE3-deficient mice
C Ledoussal et al.
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY (2001)
Microvillous inclusion disease: Report of a case with atypical features (vol 25, pg 275, 2001)
GW Mierau et al.
ULTRASTRUCTURAL PATHOLOGY (2001)
Munc18-2, a functional partner of syntaxin 3, controls apical membrane trafficking in epithelial cells
K Riento et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Periodic acid-Schiff staining abnormality in microvillous atrophy: Photometric and ultrastructural studies
AD Phillips et al.
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION (2000)
Microvillus inclusion disease: A genetic defect affecting apical membrane protein traffic in intestinal epithelium
NA Ameen et al.
TRAFFIC (2000)