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Volumn 12, Issue 8, 2002, Pages 473-483
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Processing of N-linked carbohydrate chains in a patient with glucosidase I deficiency (CDG type IIb)
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Author keywords
CDG type II; Genomic DNA; Glucosidase I deficiency; Glycoprotein processing; Sialotransferrin
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Indexed keywords
ARGININE;
ASPARAGINE LINKED OLIGOSACCHARIDE;
CARBOHYDRATE;
CYTOSINE;
GLUCOSE;
GLUCOSIDASE;
GLUCOSIDASE 1;
GLYCOPROTEIN;
LEUCINE;
MANNOSE;
MANNOSIDASE;
MESSENGER RNA;
MUTANT PROTEIN;
PHENYLALANINE;
POLYPEPTIDE;
THREONINE;
THYMINE;
TRANSFERASE;
TRANSFERRIN;
TRITIUM;
UNCLASSIFIED DRUG;
ALPHA GLUCOSIDASE;
GLUCOSIDASE I;
POLYSACCHARIDE;
ALLELE;
AMINO ACID SUBSTITUTION;
ARTICLE;
BINDING AFFINITY;
CARBOHYDRATE ANALYSIS;
CELL STRAIN COS1;
CONGENITAL DISORDER OF GLYCOSYLATION;
CONTROLLED STUDY;
DISEASE SEVERITY;
ENZYME ACTIVE SITE;
ENZYME ACTIVITY;
ENZYME DEFICIENCY;
ENZYME KINETICS;
ENZYME SPECIFICITY;
EXON;
FIBROBLAST CULTURE;
GENE MUTATION;
GENE OVEREXPRESSION;
GENETIC CODE;
GLYCOSIDASE 1 DEFICIENCY;
HETEROZYGOSITY;
HUMAN;
HUMAN CELL;
INTRON;
NUCLEIC ACID BASE SUBSTITUTION;
PRECURSOR;
PRIORITY JOURNAL;
PROTEIN BINDING;
PROTEIN FOLDING;
STRUCTURE ANALYSIS;
WILD TYPE;
ANIMAL;
CELL CULTURE;
CHEMISTRY;
COMPARATIVE STUDY;
CONFORMATION;
DISORDERS OF CARBOHYDRATE METABOLISM;
ENZYMOLOGY;
FEMALE;
FIBROBLAST;
GENETICS;
GLYCOSYLATION;
HETEROZYGOTE;
MALE;
METABOLISM;
MISSENSE MUTATION;
NEWBORN;
PEDIGREE;
POINT MUTATION;
PROTEIN PROCESSING;
URINE;
TRIXIS;
ALPHA-GLUCOSIDASES;
AMINO ACID SUBSTITUTION;
ANIMALS;
CARBOHYDRATE CONFORMATION;
CARBOHYDRATE METABOLISM, INBORN ERRORS;
CARBOHYDRATE SEQUENCE;
CELLS, CULTURED;
COS CELLS;
FEMALE;
FIBROBLASTS;
GLYCOSYLATION;
HETEROZYGOTE;
HUMANS;
INFANT, NEWBORN;
MALE;
MANNOSIDASES;
MUTATION, MISSENSE;
PEDIGREE;
POINT MUTATION;
POLYSACCHARIDES;
PROTEIN PROCESSING, POST-TRANSLATIONAL;
RNA, MESSENGER;
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EID: 0036668097
PISSN: 09596658
EISSN: None
Source Type: Journal
DOI: 10.1093/glycob/cwf050 Document Type: Article |
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Times cited : (41)
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References (33)
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