Page last updated: 2024-08-18

isomethyleugenol and Congenital Disorders of Glycosylation

isomethyleugenol has been researched along with Congenital Disorders of Glycosylation in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Cummings, RD; Harper, T; He, M; Jiang, R; Li, X; Liu, R; Xia, B; Zhang, W	1
Conradt, HS; Hoffmann, A; Jaeken, J; Nimtz, M; Pohl, S; Rüdiger, A	1

Other Studies

2 other study(ies) available for isomethyleugenol and Congenital Disorders of Glycosylation

Article	Year
Serum N-glycan and O-glycan analysis by mass spectrometry for diagnosis of congenital disorders of glycosylation. Analytical biochemistry, 2013, Nov-15, Volume: 442, Issue:2 Topics: Blood Chemical Analysis; Carbohydrate Sequence; Congenital Disorders of Glycosylation; Glycoproteins; Humans; Mass Spectrometry; Methylation; Molecular Sequence Data; Polysaccharides	2013
Hypoglycosylation of a brain glycoprotein (beta-trace protein) in CDG syndromes due to phosphomannomutase deficiency and N-acetylglucosaminyl-transferase II deficiency. Glycobiology, 1997, Volume: 7, Issue:8 Topics: Adult; Beta-Globulins; Blotting, Western; Brain; Carbohydrate Conformation; Carbohydrate Sequence; Congenital Disorders of Glycosylation; Electrophoresis, Polyacrylamide Gel; Glycosylation; Humans; Intramolecular Oxidoreductases; Lipocalins; Mass Spectrometry; Methylation; Molecular Sequence Data; N-Acetylglucosaminyltransferases; Oligosaccharides; Phosphotransferases (Phosphomutases)	1997

Article

Year

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

Analytical biochemistry, 2013, Nov-15, Volume: 442, Issue:2

Topics: Blood Chemical Analysis; Carbohydrate Sequence; Congenital Disorders of Glycosylation; Glycoproteins; Humans; Mass Spectrometry; Methylation; Molecular Sequence Data; Polysaccharides

2013

Hypoglycosylation of a brain glycoprotein (beta-trace protein) in CDG syndromes due to phosphomannomutase deficiency and N-acetylglucosaminyl-transferase II deficiency.

Glycobiology, 1997, Volume: 7, Issue:8

Topics: Adult; Beta-Globulins; Blotting, Western; Brain; Carbohydrate Conformation; Carbohydrate Sequence; Congenital Disorders of Glycosylation; Electrophoresis, Polyacrylamide Gel; Glycosylation; Humans; Intramolecular Oxidoreductases; Lipocalins; Mass Spectrometry; Methylation; Molecular Sequence Data; N-Acetylglucosaminyltransferases; Oligosaccharides; Phosphotransferases (Phosphomutases)

1997