Biological roles of oligosaccharides: all of the theories are correct
about
N-glycan alterations are associated with drug resistance in human hepatocellular carcinomaThe human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene familyThree proteins involved in Caenorhabditis elegans vulval invagination are similar to components of a glycosylation pathwayMPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type IfCongenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferaseSynthesis of disialyl Lewis a (Le(a)) structure in colon cancer cell lines by a sialyltransferase, ST6GalNAc VI, responsible for the synthesis of alpha-series gangliosidesIn vitro mannose trimming property of human ER α-1,2 mannosidase IO-fucosylation is required for ADAMTS13 secretionUniversal phosphatase-coupled glycosyltransferase assayThe X-ray crystal structures of human alpha-phosphomannomutase 1 reveal the structural basis of congenital disorder of glycosylation type 1aExpression cloning of a cDNA for human ceramide glucosyltransferase that catalyzes the first glycosylation step of glycosphingolipid synthesisDifferences between the catalytic properties of recombinant human PC2 and endogenous rat PC2A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylationAnalysis of site-specific glycosylation of renal and hepatic γ-glutamyl transpeptidase from normal human tissueCyclic nucleotide-gated channel subunit glycosylation regulates matrix metalloproteinase-dependent changes in channel gatingPost-translational modification of the myxoma-virus anti-inflammatory serpin SERP-1 by a virally encoded sialyltransferaseCloning, expression and gene organization of a human Neu5Ac alpha 2-3Gal beta 1-3GalNAc alpha 2,6-sialyltransferase: hST6GalNAcIVIdentification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL.N-glycosylation is required for full enzymic activity of the murine galactosylceramide sulphotransferaseHuman meprin beta: O-linked glycans in the intervening region of the type I membrane protein protect the C-terminal region from proteolytic cleavage and diminish its secretionMutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndromeLarge-scale sequencing of the CD33-related Siglec gene cluster in five mammalian species reveals rapid evolution by multiple mechanismsExpression cloning of a CMP-NeuAc:NeuAc alpha 2-3Gal beta 1-4Glc beta 1-1'Cer alpha 2,8-sialyltransferase (GD3 synthase) from human melanoma cellsA novel carbohydrate-deficient glycoprotein syndrome characterized by a deficiency in glucosylation of the dolichol-linked oligosaccharideDeficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type IeGingipain-dependent interactions with the host are important for survival of Porphyromonas gingivalisN-acetylgalactosaminyl transferase-3 is a potential new marker for non-small cell lung cancersMolecular cloning of a human cDNA encoding beta-1,4-galactosyltransferase with 37% identity to mammalian UDP-Gal:GlcNAc beta-1,4-galactosyltransferaseMammalian cytidine 5'-monophosphate N-acetylneuraminic acid synthetase: a nuclear protein with evolutionarily conserved structural motifsDifferent glycosylation of cadherins from human bladder non-malignant and cancer cell linesModulation of Cell Sialoglycophenotype: A Stylish Mechanism Adopted by Trypanosoma cruzi to Ensure Its Persistence in the Infected HostMass Spectrometry-Based N-Glycomics of Colorectal CancerDiatom-Specific Oligosaccharide and Polysaccharide Structures Help to Unravel Biosynthetic Capabilities in DiatomsLactobacillus adhesion to mucusNeurological aspects of human glycosylation disordersThe role of carbohydrates in infection strategies of enteric pathogensClick chemistry in peptide-based drug designCrossroads between Bacterial and Mammalian GlycosyltransferasesRecent advances in sialic acid-focused glycomicsSialic acids in the brain: gangliosides and polysialic acid in nervous system development, stability, disease, and regeneration
P2860
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P2860
Biological roles of oligosaccharides: all of the theories are correct
description
1993 nî lūn-bûn
@nan
1993 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Biological roles of oligosaccharides: all of the theories are correct
@ast
Biological roles of oligosaccharides: all of the theories are correct
@en
type
label
Biological roles of oligosaccharides: all of the theories are correct
@ast
Biological roles of oligosaccharides: all of the theories are correct
@en
prefLabel
Biological roles of oligosaccharides: all of the theories are correct
@ast
Biological roles of oligosaccharides: all of the theories are correct
@en
P3181
P356
P1433
P1476
Biological roles of oligosaccharides: all of the theories are correct
@en
P2093
P304
P3181
P356
10.1093/GLYCOB/3.2.97
P407
P577
1993-04-01T00:00:00Z