Serum N-glycan and O-glycan analysis by mass spectrometry for diagnosis of congenital disorders of glycosylation

Analytical Biochemistry

Volumn 442, Issue 2, 2013, Pages 178-185

  Xia, Baoyun ^a   Zhang, Wenyue ^a   Li, Xueli ^a   Jiang, Rong ^a   Harper, Tisa ^a   Liu, Renpeng ^a   Cummings, Richard D ^a   He, Miao ^a  

^a EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Congenital disorders of glycosylation; LC MS MS; MALDI TOF MS; N glycan; O glycan; Permethylation

Indexed keywords

DIAGNOSIS; MASS SPECTROMETRY; POLYSACCHARIDES;

CONGENITAL DISORDERS; LC-MS/MS; MALDI-TOF/MS; N-GLYCAN; PERMETHYLATION;

GLYCOSYLATION;

GLYCAN; MEMBRANE PROTEIN; N GLYCAN; O GLYCAN; PHOSPHOGLUCOMUTASE; PROTEIN SLC35A2; UNCLASSIFIED DRUG; GLYCOPROTEIN; POLYSACCHARIDE;

ACCURACY; ARTICLE; CLINICAL ARTICLE; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 1; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 2; CONTROLLED STUDY; ENDOPLASMIC RETICULUM; GLYCOSYLATION; GOLGI COMPLEX; HUMAN; MASS SPECTROMETRY; MATRIX ASSISTED LASER DESORPTION IONIZATION TIME OF FLIGHT MASS SPECTROMETRY; METHYLATION; PRIORITY JOURNAL; PROTEIN GLYCOSYLATION; PROTEIN TRANSPORT; BLOOD; BLOOD ANALYSIS; CARBOHYDRATE ANALYSIS; CHEMISTRY; CONGENITAL DISORDERS OF GLYCOSYLATION; MOLECULAR GENETICS; PROCEDURES;

BLOOD CHEMICAL ANALYSIS; CARBOHYDRATE SEQUENCE; CONGENITAL DISORDERS OF GLYCOSYLATION; GLYCOPROTEINS; HUMANS; MASS SPECTROMETRY; METHYLATION; MOLECULAR SEQUENCE DATA; POLYSACCHARIDES;

EID: 84884498276     PISSN: 00032697     EISSN: 10960309     Source Type: Journal    
DOI: 10.1016/j.ab.2013.07.037     Document Type: Article

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