about
Molecular 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 IIA novel disorder caused by defective biosynthesis of N-linked oligosaccharides due to glucosidase I deficiency.Carbohydrate-deficient glycoprotein syndrome: not an N-linked oligosaccharide processing defect, but an abnormality in lipid-linked oligosaccharide biosynthesis?Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide searchComplex asparagine-linked oligosaccharides are required for morphogenic events during post-implantation development.Golgi glycosylation and human inherited diseases.Processing of N-linked oligosaccharide depends on its location in the anion exchanger, AE1, membrane glycoprotein.Two glycoprotein populations of band 3 dimers are present in human erythrocytes.Clinical aspects of glycoprotein biosynthesis.Protein N-glycosylation: molecular genetics and functional significance.Congenital dyserythropoietic anemia type II with a positive sucrose hemolysis test.Successful management of concurrent congenital dyserythropoietic anaemia and autoimmune haemolytic anaemia with splenectomy.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on September 1990
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
HEMPAS disease: genetic defect of glycosylation.
@en
HEMPAS disease: genetic defect of glycosylation.
@nl
type
label
HEMPAS disease: genetic defect of glycosylation.
@en
HEMPAS disease: genetic defect of glycosylation.
@nl
prefLabel
HEMPAS disease: genetic defect of glycosylation.
@en
HEMPAS disease: genetic defect of glycosylation.
@nl
P356
P1433
P1476
HEMPAS disease: genetic defect of glycosylation.
@en
P2093
P356
10.1093/GLYCOB/1.1.9
P577
1990-09-01T00:00:00Z