Development of a primary mouse intestinal epithelial cell monolayer culture system to evaluate factors that modulate IgA transcytosis
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Use of Cancer Stem Cells to Investigate the Pathogenesis of Colitis-associated CancerHuman Enteroids as a Model of Upper Small Intestinal Ion Transport Physiology and Pathophysiology.Cooperativity among secretory IgA, the polymeric immunoglobulin receptor, and the gut microbiota promotes host-microbial mutualismIntestinal Interleukin-17 Receptor Signaling Mediates Reciprocal Control of the Gut Microbiota and Autoimmune Inflammation.Determining microbial products and identifying molecular targets in the human microbiome.Development of an enhanced human gastrointestinal epithelial culture system to facilitate patient-based assays.Vertically transmitted faecal IgA levels determine extra-chromosomal phenotypic variation.Expression of human decay-accelerating factor on intestinal epithelium of transgenic mice does not facilitate infection by the enteral routeIncreased Expression of DUOX2 Is an Epithelial Response to Mucosal Dysbiosis Required for Immune Homeostasis in Mouse IntestineLong-term renewable human intestinal epithelial stem cells as monolayers: A potential for clinical use.Gastrointestinal Organoids: Understanding the Molecular Basis of the Host-Microbe Interface.A simple, cost-effective method for generating murine colonic 3D enteroids and 2D monolayers for studies of primary epithelial cell function.Intestinal M cells.A method for high purity intestinal epithelial cell culture from adult human and murine tissues for the investigation of innate immune function.Membrane Transport across Polarized Epithelia.The intestinal barrier: a fundamental role in health and disease.Reciprocal Inflammatory Signaling Between Intestinal Epithelial Cells and Adipocytes in the Absence of Immune Cells.Nonsteroidal Anti-Inflammatory Drug-Induced Leaky Gut Modeled Using Polarized Monolayers of Primary Human Intestinal Epithelial Cells.Self-renewing Monolayer of Primary Colonic or Rectal Epithelial Cells.Advancing Intestinal Organoid Technology Toward Regenerative Medicine.IL-17A-Induced PLET1 Expression Contributes to Tissue Repair and Colon Tumorigenesis.Development and characterization of 2-dimensional culture for buffalo intestinal cells.Using 3D Organoid Cultures to Model Intestinal Physiology and Colorectal Cancer.Prostaglandin E2 promotes intestinal repair through an adaptive cellular response of the epithelium.Development and Characterization of a Human and Mouse Intestinal Epithelial Cell Monolayer Platform.C1orf106 is a colitis risk gene that regulates stability of epithelial adherens junctions.Enteric Nervous System Regulation of Intestinal Stem Cell Differentiation and Epithelial Monolayer Function.Bioengineered Systems and Designer Matrices That Recapitulate the Intestinal Stem Cell Niche.Engineered Human Gastrointestinal Cultures to Study the Microbiome and Infectious Diseases.Mucosal Bioengineering: Gut in a Dish.Intestinal epithelial cell polarity defects in disease: lessons from microvillus inclusion disease.The Noncaloric Sweetener Rebaudioside A Stimulates Glucagon-Like Peptide 1 Release and Increases Enteroendocrine Cell Numbers in 2-Dimensional Mouse Organoids Derived from Different Locations of the Intestine.The Role of the Polymeric Immunoglobulin Receptor and Secretory Immunoglobulins during Mucosal Infection and Immunity.Enteroid Monolayers Reveal an Autonomous WNT and BMP Circuit Controlling Intestinal Epithelial Growth and Organization.P2Y6 Receptors Regulate CXCL10 Expression and Secretion in Mouse Intestinal Epithelial Cells.Integration of Sensors in Gastrointestinal Organoid Culture for Biological Analysis.Harnessing single-cell genomics to improve the physiological fidelity of organoid-derived cell types.Monoclonal Antibodies to Intracellular Stages of Cryptosporidium parvum Define Life Cycle Progression In Vitro.Generation of renewable mouse intestinal epithelial cell monolayers and organoids for functional analyses
P2860
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P2860
Development of a primary mouse intestinal epithelial cell monolayer culture system to evaluate factors that modulate IgA transcytosis
description
2013 nî lūn-bûn
@nan
2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Development of a primary mouse ...... that modulate IgA transcytosis
@ast
Development of a primary mouse ...... that modulate IgA transcytosis
@en
type
label
Development of a primary mouse ...... that modulate IgA transcytosis
@ast
Development of a primary mouse ...... that modulate IgA transcytosis
@en
prefLabel
Development of a primary mouse ...... that modulate IgA transcytosis
@ast
Development of a primary mouse ...... that modulate IgA transcytosis
@en
P2860
P356
P1433
P1476
Development of a primary mouse ...... that modulate IgA transcytosis
@en
P2093
T S Stappenbeck
P2860
P2888
P304
P356
10.1038/MI.2013.98
P577
2013-11-13T00:00:00Z
P5875
P6179
1013071066