Intestinal mucins from cystic fibrosis mice show increased fucosylation due to an induced Fucalpha1-2 glycosyltransferase.
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A refined palate: bacterial consumption of host glycans in the gutSerum amyloid A is a retinol binding protein that transports retinol during bacterial infectionBicarbonate and functional CFTR channel are required for proper mucin secretion and link cystic fibrosis with its mucus phenotype.Histo-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severityIntestinal goblet cells and mucins in health and disease: recent insights and progress.Fucose: biosynthesis and biological function in mammals.Gastrointestinal mucins of Fut2-null mice lack terminal fucosylation without affecting colonization by Candida albicans.Rapid fucosylation of intestinal epithelium sustains host-commensal symbiosis in sickness.LacZ expression in Fut2-LacZ reporter mice reveals estrogen-regulated endocervical glandular expression during estrous cycle, hormone replacement, and pregnancy.Studies of mucus in mouse stomach, small intestine, and colon. III. Gastrointestinal Muc5ac and Muc2 mucin O-glycan patterns reveal a regiospecific distribution.Ion mobility mass spectrometry analysis of isomeric disaccharide precursor, product and cluster ions.Bacteroides in the infant gut consume milk oligosaccharides via mucus-utilization pathwaysIntestinal fucose as a mediator of host-microbe symbiosis.Normalization of Host Intestinal Mucus Layers Requires Long-Term Microbial ColonizationDetailed O-glycomics of the Muc2 mucin from colon of wild-type, core 1- and core 3-transferase-deficient mice highlights differences compared with human MUC2.Carbohydrate structure characterization by tandem ion mobility mass spectrometry (IMMS)2.Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulator-dependent bicarbonate secretion.Loss of NHE3 alters gut microbiota composition and influences Bacteroides thetaiotaomicron growth.Cervical mucins carry alpha(1,2)fucosylated glycans that partly protect from experimental vaginal candidiasis.γδ T-cell-deficient mice show alterations in mucin expression, glycosylation, and goblet cells but maintain an intact mucus layer.Salmonella enterica serotype Typhimurium Std fimbriae bind terminal alpha(1,2)fucose residues in the cecal mucosa.Activation of CFTR by ASBT-mediated bile salt absorption.Motility allows S. Typhimurium to benefit from the mucosal defence.Increased levels of mucins in the cystic fibrosis mouse small intestine, and modulator effects of the Muc1 mucin expression.Mucins and their O-Glycans from human bronchial epithelial cell cultures.Intestinal Muc2 mucin O-glycosylation is affected by microbiota and regulated by differential expression of glycosyltranferases.Absence of CFTR is associated with pleiotropic effects on mucins in mouse gallbladder epithelial cells.
P2860
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P2860
Intestinal mucins from cystic fibrosis mice show increased fucosylation due to an induced Fucalpha1-2 glycosyltransferase.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
2002年论文
@zh
2002年论文
@zh-cn
name
Intestinal mucins from cystic ...... calpha1-2 glycosyltransferase.
@en
Intestinal mucins from cystic ...... calpha1-2 glycosyltransferase.
@nl
type
label
Intestinal mucins from cystic ...... calpha1-2 glycosyltransferase.
@en
Intestinal mucins from cystic ...... calpha1-2 glycosyltransferase.
@nl
prefLabel
Intestinal mucins from cystic ...... calpha1-2 glycosyltransferase.
@en
Intestinal mucins from cystic ...... calpha1-2 glycosyltransferase.
@nl
P2093
P2860
P356
P1433
P1476
Intestinal mucins from cystic ...... calpha1-2 glycosyltransferase.
@en
P2093
Gunnar C Hansson
John B Lowe
Karin A Axelsson
Kristina A Thomsson
Marina Hinojosa-Kurtzberg
Sandra J Gendler
Steven E Domino
P2860
P304
P356
10.1042/BJ20020371
P407
P577
2002-11-01T00:00:00Z