Congenital disorders of glycosylation type I leads to altered processing of N-linked glycans, as well as underglycosylation

Biochemical Journal

Volumn 359, Issue 2, 2001, Pages 249-254

  Mills, P ^a   Mills, K ^a   Clayton, P ^a   Johnson, A ^a   Whitehouse, D ^a   Winchester, B ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

1 antitrypsin; Branching; Fucosylation; Glycoproteins; Transferrin

Indexed keywords

CONTROL SYSTEMS;

GLYCOSYLATION;

PATIENT TREATMENT;

ALPHA 1 ANTITRYPSIN; GLYCAN; TRANSFERRIN;

ARTICLE; CLINICAL ARTICLE; CONGENITAL DISORDERS OF GLYCOSYLATION; CONTROLLED STUDY; FUCOSYLATION; GENETIC DISORDER; GLYCOSYLATION; HUMAN; PLASMA; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; PROTEIN PROCESSING; PROTEIN PURIFICATION; PROTEIN SECRETION;

ALPHA 1-ANTITRYPSIN; AMIDOHYDROLASES; CARBOHYDRATE METABOLISM, INBORN ERRORS; CARBOHYDRATE SEQUENCE; CASE-CONTROL STUDIES; ELECTROPHORESIS, GEL, TWO-DIMENSIONAL; FUCOSE; GLYCOSYLATION; HUMANS; MOLECULAR SEQUENCE DATA; PEPTIDE-N4-(N-ACETYL-BETA-GLUCOSAMINYL) ASPARAGINE AMIDASE; POLYSACCHARIDES; PROTEIN PROCESSING, POST-TRANSLATIONAL; SPECTROMETRY, MASS, MATRIX-ASSISTED LASER DESORPTION-IONIZATION; TRANSFERRIN;

EID: 0035887188     PISSN: 02646021     EISSN: None     Source Type: Journal    
DOI: 10.1042/0264-6021:3590249     Document Type: Article

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