Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase II
about
Molecular cloning and expression of GDP-D-mannose-4,6-dehydratase, a key enzyme for fucose metabolism defective in Lec13 cellsMolecular cloning and expression of cDNAs encoding human alpha-mannosidase II and a previously unrecognized alpha-mannosidase IIx isozymeIsolation, characterization, and expression of cDNAs encoding murine alpha-mannosidase II, a Golgi enzyme that controls conversion of high mannose to complex N-glycansMolecular cloning and expression of cDNA encoding the rat UDP-N-acetylglucosamine:alpha-6-D-mannoside beta-1,2-N-acetylglucosaminyltransferase IIMice lacking N-acetylglucosaminyltransferase I activity die at mid-gestation, revealing an essential role for complex or hybrid N-linked carbohydratesMutations in four glycosyl hydrolases reveal a highly coordinated pathway for rhodopsin biosynthesis and N-glycan trimming in Drosophila melanogaster.Screening for "prelysosomal disorders": carbohydrate-deficient glycoprotein syndromes.Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship.Congenital disorders of glycosylation: glycosylation defects in man and biological models for their study.Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide searchThe COPII pathway and hematologic diseaseChanges in architecture of the Golgi complex and other subcellular organelles during myogenesis.Naturally occurring anti-band 3 antibodies in clearance of senescent and oxidatively stressed human red blood cells.A human embryonic kidney 293T cell line mutated at the Golgi alpha-mannosidase II locus.Processing of N-linked oligosaccharide depends on its location in the anion exchanger, AE1, membrane glycoprotein.Disruption of alpha-mannosidase processing induces non-canonical hybrid-type glycosylation.Incompletely processed N-glycans of serum glycoproteins in congenital dyserythropoietic anaemia type II (HEMPAS).Protein N-glycosylation: molecular genetics and functional significance.Identification of distinct nanoparticles and subsets of extracellular vesicles by asymmetric flow field-flow fractionation.
P2860
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P2860
Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase II
description
1990 nî lūn-bûn
@nan
1990 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
Incomplete synthesis of N-glyc ...... encoding alpha-mannosidase II
@ast
Incomplete synthesis of N-glyc ...... encoding alpha-mannosidase II
@en
type
label
Incomplete synthesis of N-glyc ...... encoding alpha-mannosidase II
@ast
Incomplete synthesis of N-glyc ...... encoding alpha-mannosidase II
@en
prefLabel
Incomplete synthesis of N-glyc ...... encoding alpha-mannosidase II
@ast
Incomplete synthesis of N-glyc ...... encoding alpha-mannosidase II
@en
P2093
P2860
P356
P1476
Incomplete synthesis of N-glyc ...... encoding alpha-mannosidase II
@en
P2093
P2860
P304
P356
10.1073/PNAS.87.19.7443
P407
P577
1990-10-01T00:00:00Z