scholarly article | Q13442814 |
P50 | author | Michael W. Hess | Q77125208 |
Natalia Schiefermeier | Q79279057 | ||
Hannes Ebner | Q79810273 | ||
Andreas Janecke | Q42884028 | ||
??? | Q40826377 | ||
P2093 | author name string | Thomas Müller | |
Olivier Goulet | |||
Heinz Zoller | |||
Kristian Pfaller | |||
Gerd Utermann | |||
Thomas Berger | |||
Hannes Ponstingl | |||
Silvia Lechner | |||
Frank M Ruemmele | |||
Christopher J Taylor | |||
Peter Heinz-Erian | |||
Henrik Köhler | |||
Henning Lenhartz | |||
Barbara Schlenck | |||
Barbara Röllinghoff | |||
Joachim Partsch | |||
Roderick J Houwen | |||
P2860 | cites work | Microvillus inclusion disease: a genetic defect affecting apical membrane protein traffic in intestinal epithelium | Q73511577 |
Microvillous inclusion disease (microvillous atrophy) | Q21203045 | ||
Rab11a and myosin Vb are required for bile canalicular formation in WIF-B9 cells | Q24536054 | ||
Rab8, a small GTPase involved in vesicular traffic between the TGN and the basolateral plasma membrane | Q24673790 | ||
Novel myosin heavy chain encoded by murine dilute coat colour locus | Q28590446 | ||
Myosin Vb interacts with Rab8a on a tubular network containing EHD1 and EHD3. | Q30479902 | ||
Autophagocytosis of the apical membrane in microvillus inclusion disease | Q31109538 | ||
Dietary inulin affects the expression of intestinal enterocyte iron transporters, receptors and storage protein and alters the microbiota in the pig intestine | Q34687504 | ||
A role for tumour necrosis factor alpha in human small bowel iron transport | Q42953190 | ||
The Rab8 GTPase regulates apical protein localization in intestinal cells | Q47068868 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | microvillus inclusion disease | Q4293116 |
P304 | page(s) | 1163-1165 | |
P577 | publication date | 2008-08-24 | |
P1433 | published in | Nature Genetics | Q976454 |
P1476 | title | MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity | |
P478 | volume | 40 |
Q34930137 | A case of Protracted Diarrhea in a Newborn: a Diagnostic Challenge |
Q33573318 | A central role for vesicle trafficking in epithelial neoplasia: intracellular highways to carcinogenesis |
Q24316145 | A flippase-independent function of ATP8B1, the protein affected in familial intrahepatic cholestasis type 1, is required for apical protein expression and microvillus formation in polarized epithelial cells |
Q41017862 | A genetic framework controlling the differentiation of intestinal stem cells during regeneration in Drosophila. |
Q91370790 | A molecular mechanism underlying genotype-specific intrahepatic cholestasis resulting from MYO5B mutations |
Q39550889 | A novel QTL underlying early-onset, low-frequency hearing loss in BXD recombinant inbred strains. |
Q34278445 | A novel familial mutation in the PCSK1 gene that alters the oxyanion hole residue of proprotein convertase 1/3 and impairs its enzymatic activity. |
Q90147077 | A2ML1 and otitis media: novel variants, differential expression, and relevant pathways |
Q46789322 | Abnormal Rab11-Rab8-vesicles cluster in enterocytes of patients with microvillus inclusion disease |
Q57098797 | Abnormal Small Intestinal Epithelial Microvilli in Patients With Crohn's Disease |
Q36155098 | An inducible mouse model for microvillus inclusion disease reveals a role for myosin Vb in apical and basolateral trafficking |
Q38135356 | An overview and online registry of microvillus inclusion disease patients and their MYO5B mutations. |
Q46194285 | Apical Membrane Alterations in Non-intestinal Organs in Microvillus Inclusion Disease. |
Q37634760 | Apical trafficking in epithelial cells: signals, clusters and motors |
Q36266151 | Cargo-selective apical exocytosis in epithelial cells is conducted by Myo5B, Slp4a, Vamp7, and Syntaxin 3. |
Q57636949 | Case of syndromic tufting enteropathy harbors SPINT2 mutation seen in congenital sodium diarrhea |
Q35780286 | Cdc42 and Rab8a are critical for intestinal stem cell division, survival, and differentiation in mice |
Q37423093 | Cdc42 coordinates proliferation, polarity, migration, and differentiation of small intestinal epithelial cells in mice |
Q37435101 | Chapter 3: acquisition of membrane polarity in epithelial tube formation patterns, signaling pathways, molecular mechanisms, and disease. |
Q35944782 | Clathrin and AP-1 regulate apical polarity and lumen formation during C. elegans tubulogenesis |
Q50129254 | Clinical features and MYO5B mutations of a family affected by microvillus inclusion disease |
Q35100466 | Coding and noncoding expression patterns associated with rare obesity-related disorders: Prader-Willi and Alström syndromes. |
Q53215506 | Common structural features characterize interstitial intrachromosomal Xp and 18q triplications. |
Q53095799 | Congenital Fatal Diarrhea in Newborns. |
Q83226421 | Crumbs organizes the transport machinery by regulating apical levels of PI(4,5)P in |
Q39058928 | Defects in myosin VB are associated with a spectrum of previously undiagnosed low γ-glutamyltransferase cholestasis |
Q36447456 | Diagnosis of microvillous inclusion disease: a case report and literature review with significance for oman |
Q38696809 | Disrupted apical exocytosis of cargo vesicles causes enteropathy in FHL5 patients with Munc18-2 mutations. |
Q38735421 | Disruption of Rab8a and Rab11a causes formation of basolateral microvilli in neonatal enteropathy. |
Q61135840 | Dissecting myosin-5B mechanosensitivity and calcium regulation at the single molecule level |
Q58565354 | Dynamic Formation of Microvillus Inclusions During Enterocyte Differentiation in -Deficient Intestinal Organoids |
Q89951757 | Editing Myosin VB Gene to Create Porcine Model of Microvillus Inclusion Disease, With Microvillus-lined Inclusions and Alterations in Sodium Transporters |
Q38780999 | Endocytosis in enterocytes |
Q85640640 | Enteropathies of infancy and childhood |
Q34219041 | Exome sequencing finds a novel PCSK1 mutation in a child with generalized malabsorptive diarrhea and diabetes insipidus |
Q85964803 | Extraintestinal manifestations in an infant with microvillus inclusion disease: complications or features of the disease? |
Q24323378 | Functional characterization of mutations in the myosin Vb gene associated with microvillus inclusion disease |
Q37213744 | Functions of class V myosins in neurons |
Q28077353 | Generation of intestinal surface: an absorbing tale |
Q48858412 | Genetic variation in the lymphotoxin-α (LTA)/tumour necrosis factor-α (TNFα) locus as a risk factor for idiopathic achalasia |
Q34244330 | Genome-wide analysis of Pax8 binding provides new insights into thyroid functions |
Q42008380 | Identification of intestinal ion transport defects in microvillus inclusion disease |
Q39434310 | Inactivation of MYO5B promotes invasion and motility in gastric cancer cells |
Q52723533 | Intestinal epithelial cell polarity defects in disease: lessons from microvillus inclusion disease. |
Q47695282 | Kinetic signatures of myosin-5B, the motor involved in microvillus inclusion disease |
Q89311714 | Lipid malabsorption from altered hormonal signaling changes early gut microbial responses |
Q36724921 | Loss of MYO5B in mice recapitulates Microvillus Inclusion Disease and reveals an apical trafficking pathway distinct to neonatal duodenum |
Q47661261 | Loss of Myosin Vb in colorectal cancer is a strong prognostic factor for disease recurrence |
Q90339196 | Loss of myosin Vb promotes apical bulk endocytosis in neonatal enterocytes |
Q50076522 | Loss-of-Function Mutations in UNC45A Cause a Syndrome Associating Cholestasis, Diarrhea, Impaired Hearing, and Bone Fragility. |
Q34617207 | Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model. |
Q39283295 | MYO5B and bile salt export pump contribute to cholestatic liver disorder in microvillous inclusion disease |
Q39185993 | MYO5B is epigenetically silenced and associated with MET signaling in human gastric cancer |
Q39482657 | MYO5B mutations cause cholestasis with normal serum gamma-glutamyl transferase activity in children without microvillous inclusion disease |
Q47269140 | MYO5B, STX3 and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update |
Q39141488 | Membrane Transport across Polarized Epithelia |
Q38199403 | Microfluidic approaches for epithelial cell layer culture and characterisation |
Q53060624 | Microvilli as markers of disordered apical-membrane trafficking and assembly: bowel and liver. |
Q49546561 | Microvillus Inclusion Disease Variant in an Infant with Intractable Diarrhea |
Q34550390 | Microvillus inclusion disease associated with necrotizing enterocolitis in a premature infant |
Q39076973 | Microvillus inclusion disease: loss of Myosin vb disrupts intracellular traffic and cell polarity. |
Q37825691 | Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea |
Q58555958 | Modeling Microvillus Inclusion Formation In Vitro |
Q38104258 | Molecular motors and apical CFTR traffic in epithelia |
Q50529787 | Multilabel immunofluorescence and antigen reprobing on formalin-fixed paraffin-embedded sections: novel applications for precision pathology diagnosis. |
Q35710172 | Mutations in Plasmalemma Vesicle Associated Protein Result in Sieving Protein-Losing Enteropathy Characterized by Hypoproteinemia, Hypoalbuminemia, and Hypertriglyceridemia |
Q24324212 | Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea |
Q35195413 | Mutations in TTC37 cause trichohepatoenteric syndrome (phenotypic diarrhea of infancy) |
Q24301355 | Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization |
Q35880786 | Myo5b knockout mice as a model of microvillus inclusion disease. |
Q34519300 | Myosin 5b loss of function leads to defects in polarized signaling: implication for microvillus inclusion disease pathogenesis and treatment |
Q36094961 | Myosin Ia is required for CFTR brush border membrane trafficking and ion transport in the mouse small intestine |
Q41551108 | Myosin Va plays essential roles in maintaining normal mitosis, enhancing tumor cell motility and viability |
Q63681854 | Myosin Vb is required for correct trafficking of N‐cadherin and cardiac chamber ballooning |
Q27313515 | Myosin Vb mediated plasma membrane homeostasis regulates peridermal cell size and maintains tissue homeostasis in the zebrafish epidermis |
Q36743873 | Myosin Vb mediates Cu+ export in polarized hepatocytes |
Q30581661 | Myosin Vb uncoupling from RAB8A and RAB11A elicits microvillus inclusion disease |
Q38088529 | Myosin motors at neuronal synapses: drivers of membrane transport and actin dynamics. |
Q27940249 | Myosin-V is activated by binding secretory cargo and released in coordination with Rab/exocyst function |
Q30513859 | Myosin-X functions in polarized epithelial cells |
Q26749344 | Myosins as fundamental components during tumorigenesis: diverse and indispensable |
Q51377017 | Myosins: Domain Organisation, Motor Properties, Physiological Roles and Cellular Functions. |
Q42364743 | New Mouse Models for Microvillus Inclusion Disease (MVID): Where Do the Inclusions Come From and Are They Cause or Consequence? |
Q39440937 | Newcomers in paediatric GI pathology: childhood enteropathies including very early onset monogenic IBD. |
Q35193732 | Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children. |
Q26771646 | Organoid Models of Human Gastrointestinal Development and Disease |
Q43745780 | Persistent defective membrane trafficking in epithelial cells of patients with familial hemophagocytic lymphohistiocytosis type 5 due to STXBP2/MUNC18-2 mutations |
Q50436014 | Phospholipase Cδ3 is a novel binding partner of myosin VI and functions as anchoring of myosin VI on plasma membrane |
Q92677838 | Physiology of Electrolyte Transport in the Gut: Implications for Disease |
Q41774355 | Plasmalemma Vesicle Associated Protein Truncation Causes Lethal Protein-Losing Enteropathy in Humans |
Q38720389 | Plasticity of the brush border - the yin and yang of intestinal homeostasis |
Q30513401 | Plus-end directed myosins accelerate actin filament sliding by single-headed myosin VI. |
Q37052115 | Polarized protein transport and lumen formation during epithelial tissue morphogenesis |
Q40112268 | Protein losing enteropathy: comprehensive review of the mechanistic association with clinical and subclinical disease states |
Q41785586 | Purification, crystallization and preliminary crystallographic analysis of the globular domain of the human type V myosin Myo5a |
Q36997840 | RAB and RHO GTPases regulate intestinal crypt cell homeostasis and enterocyte function. |
Q34582966 | Rab GTPase-Myo5B complexes control membrane recycling and epithelial polarization. |
Q41665284 | Rab11a is required for apical protein localisation in the intestine. |
Q37808351 | Rab25 as a tumour suppressor in colon carcinogenesis |
Q36680569 | Rab25 regulates integrin expression in polarized colonic epithelial cells |
Q37919430 | Rab8 GTPase as a regulator of cell shape |
Q41884848 | Rab8a and Rab8b are essential for several apical transport pathways but insufficient for ciliogenesis |
Q39104860 | Rabs set the stage for polarity |
Q91869822 | Recent advances in understanding and managing malabsorption: focus on microvillus inclusion disease |
Q37865415 | Recent progress in congenital diarrheal disorders |
Q85236652 | Recycling endosomes |
Q37787522 | Recycling endosomes in apical plasma membrane domain formation and epithelial cell polarity |
Q28119064 | Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea |
Q58545180 | Regulation of actin-based apical structures on epithelial cells |
Q24338831 | Requirement of myosin Vb.Rab11a.Rab11-FIP2 complex in cholesterol-regulated translocation of NPC1L1 to the cell surface |
Q39164306 | Role of Polarity Proteins in the Generation and Organization of Apical Surface Protrusions |
Q54638679 | Severe hypernatremic dehydration and metabolic acidosis due to neonatal intestinal microvillus inclusion disease. |
Q34566715 | Shaping the intestinal brush border |
Q27680148 | Structural Insights into Functional Overlapping and Differentiation among Myosin V Motors |
Q27680896 | Structural Insights into the Globular Tails of the Human Type V Myosins Myo5a, Myo5b, and Myo5c |
Q36090717 | Structural and functional hepatocyte polarity and liver disease |
Q27678783 | Structural basis of cargo recognitions for class V myosins |
Q49491930 | The Endosomal Protein Endotubin Is Required for Enterocyte Differentiation |
Q33761526 | The Na+/H+ exchanger NHE6 in the endosomal recycling system is involved in the development of apical bile canalicular surface domains in HepG2 cells |
Q97418340 | The actin nucleator Cobl organises the terminal web of enterocytes |
Q27026016 | The bigger the better: determining nephron size in kidney |
Q90604736 | The challenge of personalized cell biology: The example of microvillus inclusion disease |
Q42484529 | The localisation of the apical Par/Cdc42 polarity module is specifically affected in microvillus inclusion disease. |
Q27011868 | The myosin superfamily at a glance. |
Q30485266 | The recycling and transcytotic pathways for IgG transport by FcRn are distinct and display an inherent polarity |
Q26770040 | The role of enterocyte defects in the pathogenesis of congenital diarrheal disorders |
Q36096812 | The zebrafish goosepimples/myosin Vb mutant exhibits cellular attributes of human microvillus inclusion disease. |
Q41838926 | Towards understanding microvillus inclusion disease. |
Q45940827 | Toxic peptides in Frazer's fraction interact with the actin cytoskeleton and affect the targeting and function of intestinal proteins. |
Q47144215 | Trafficking Ion Transporters to the Apical Membrane of Polarized Intestinal Enterocytes. |
Q90624307 | Two cases of microvillous inclusion disease caused by novel mutations in MYO5B gene |
Q37747364 | Ultrastructural aspects of enterocyte defects in infancy and childhood. |
Q96689322 | Unequal effects of MYO5B mutations in liver and intestine determine the clinical presentation of low-GGT cholestasis |
Q58572571 | Unusual feature of neonatal hypernatremic dehydration due to microvillus inclusion disease: a case report |
Q38127174 | Update on small intestinal stem cells |
Q33867868 | Using linkage information to weight a genome-wide association of bipolar disorder |
Q39200385 | Vesicular sorting controls the polarity of expanding membranes in the C. elegans intestine |
Q34238805 | Walking to work: roles for class V myosins as cargo transporters |
Q89030144 | Weibel-Palade Body Localized Syntaxin-3 Modulates Von Willebrand Factor Secretion From Endothelial Cells |
Search more.