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anthranilamide and Carbohydrate Metabolism, Inborn Error

anthranilamide has been researched along with Carbohydrate Metabolism, Inborn Error in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aebi, M; Berger, EG; Frank, CG; Grubenmann, CE; Hennet, T; Hülsmeier, AJ; Matthijs, G; Mayatepek, E; Schollen, E1

Other Studies

1 other study(ies) available for anthranilamide and Carbohydrate Metabolism, Inborn Error

ArticleYear
Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik.
    Human molecular genetics, 2004, Mar-01, Volume: 13, Issue:5

    Topics: Amino Acid Sequence; Carbohydrate Metabolism, Inborn Errors; Chromatography, High Pressure Liquid; DNA Primers; Fluorescence; Genetic Complementation Test; Glucosyltransferases; Glycosylation; Humans; Mannose; Mannosyltransferases; Molecular Sequence Data; Mutation; Oligosaccharides; ortho-Aminobenzoates; Plasmids; Reverse Transcriptase Polymerase Chain Reaction; Saccharomyces cerevisiae; Sequence Alignment; Sequence Analysis, DNA

2004