Congenital disorders of glycosylation: genetic model systems lead the way.
about
MPDU1 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 mannosyltransferaseA deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylationSRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorderIdentification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL.Human RFT1 deficiency leads to a disorder of N-linked glycosylationNeurological aspects of human glycosylation disordersAlg14 recruits Alg13 to the cytoplasmic face of the endoplasmic reticulum to form a novel bipartite UDP-N-acetylglucosamine transferase required for the second step of N-linked glycosylation.Hetero-oligomeric interactions between early glycosyltransferases of the dolichol cycle.ALG9 mannosyltransferase is involved in two different steps of lipid-linked oligosaccharide biosynthesis.DHPLC analysis as a platform for molecular diagnosis of congenital disorders of glycosylation (CDG)Congenital disorders of glycosylation type I leads to altered processing of N-linked glycans, as well as underglycosylationRat kidney MAP17 induces cotransport of Na-mannose and Na-glucose in Xenopus laevis oocytes.Transposon mutagenesis of Trypanosoma brucei identifies glycosylation mutants resistant to concanavalin A.Proteomics and glycomics analyses of N-glycosylated structures involved in Toxoplasma gondii--host cell interactions.The compartmentalisation of phosphorylated free oligosaccharides in cells from a CDG Ig patient reveals a novel ER-to-cytosol translocation processMolecular analysis of phosphomannomutase (PMM) genes reveals a unique PMM duplication event in diverse Triticeae species and the main PMM isozymes in bread wheat tissues.The diversity of dolichol-linked precursors to Asn-linked glycans likely results from secondary loss of sets of glycosyltransferases.Comparative Analysis of Protein Glycosylation Pathways in Humans and the Fungal Pathogen Candida albicans.Differential analysis of N-glycoproteome between hepatocellular carcinoma and normal human liver tissues by combination of multiple protease digestion and solid phase based labeling.Update and perspectives on congenital disorders of glycosylation.The search for glycan function: fucosylation of the TGF-beta1 receptor is required for receptor activationSolid-phase extraction of N-linked glycopeptides.What can yeast tell us about N-linked glycosylation in the Golgi apparatus?An evolving view of the eukaryotic oligosaccharyltransferase.The normal phenotype of Pmm1-deficient mice suggests that Pmm1 is not essential for normal mouse development.Fibrotic response in fibroblasts from congenital disorders of glycosylation.Reduced expression of the oligosaccharyltransferase exacerbates protein hypoglycosylation in cells lacking the fully assembled oligosaccharide donor.More Than Just Oligomannose: An N-glycomic Comparison of Penicillium SpeciesDrosophila, the golden bug, emerges as a tool for human genetics.Research network: EUROGLYCANET: a European network focused on congenital disorders of glycosylation.The Campylobacter jejuni glycome.Congenital disorders of N-glycosylation including diseases associated with O- as well as N-glycosylation defects.Thematic review series: lipid posttranslational modifications. GPI anchoring of protein in yeast and mammalian cells, or: how we learned to stop worrying and love glycophospholipids.Demonstration of an oligosaccharide-diphosphodolichol diphosphatase activity whose subcellular localization is different than those of dolichyl-phosphate-dependent enzymes of the dolichol cycleA case of fatal Type I congenital disorders of glycosylation (CDG I) associated with low dehydrodolichol diphosphate synthase (DHDDS) activityN-linked glycosylation in bacteria: an unexpected application.The usefulness of hydrazine derivatives for mass spectrometric analysis of carbohydrates.Alg14 organizes the formation of a multiglycosyltransferase complex involved in initiation of lipid-linked oligosaccharide biosynthesis.Requirement of N-glycan on GPI-anchored proteins for efficient binding of aerolysin but not Clostridium septicum alpha-toxin.
P2860
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P2860
Congenital disorders of glycosylation: genetic model systems lead the way.
description
2001 nî lūn-bûn
@nan
2001 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի մարտին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
Congenital disorders of glycosylation: genetic model systems lead the way.
@ast
Congenital disorders of glycosylation: genetic model systems lead the way.
@en
Congenital disorders of glycosylation: genetic model systems lead the way.
@nl
type
label
Congenital disorders of glycosylation: genetic model systems lead the way.
@ast
Congenital disorders of glycosylation: genetic model systems lead the way.
@en
Congenital disorders of glycosylation: genetic model systems lead the way.
@nl
prefLabel
Congenital disorders of glycosylation: genetic model systems lead the way.
@ast
Congenital disorders of glycosylation: genetic model systems lead the way.
@en
Congenital disorders of glycosylation: genetic model systems lead the way.
@nl
P1476
Congenital disorders of glycosylation: genetic model systems lead the way.
@en
P304
P356
10.1016/S0962-8924(01)01925-0
P577
2001-03-01T00:00:00Z