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cycloheximide and Carbohydrate Metabolism, Inborn Error

cycloheximide has been researched along with Carbohydrate Metabolism, Inborn Error in 2 studies

Research

Studies (2)

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

Authors

Authors	Studies
Denecke, J; Kemming, D; Koch, HG; Kranz, C; Marquardt, T	1
Ikeda, Y; Keese, SM; Tanaka, K	1

Other Studies

2 other study(ies) available for cycloheximide and Carbohydrate Metabolism, Inborn Error

Article	Year
An activated 5' cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id). Human mutation, 2004, Volume: 23, Issue:5 Topics: Amino Acid Sequence; Base Sequence; Carbohydrate Metabolism, Inborn Errors; Codon, Nonsense; Codon, Terminator; Cycloheximide; DNA Mutational Analysis; Exons; Glycosylation; Humans; Mannosyltransferases; Molecular Sequence Data; RNA Precursors; RNA Splice Sites; RNA Splicing; RNA Stability; RNA, Messenger; Sequence Deletion	2004
Biosynthesis of electron transfer flavoprotein in a cell-free system and in cultured human fibroblasts. Defect in the alpha subunit synthesis is a primary lesion in glutaric aciduria type II. The Journal of clinical investigation, 1986, Volume: 78, Issue:4 Topics: Adipates; Animals; Carbohydrate Metabolism, Inborn Errors; Cell-Free System; Cycloheximide; Electron-Transferring Flavoproteins; Electrophoresis, Polyacrylamide Gel; Fibroblasts; Flavoproteins; Glutarates; Malonates; Molecular Weight; Protein Processing, Post-Translational; Rabbits; Rhodamines	1986

Article

Year

An activated 5' cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id).

Human mutation, 2004, Volume: 23, Issue:5

Topics: Amino Acid Sequence; Base Sequence; Carbohydrate Metabolism, Inborn Errors; Codon, Nonsense; Codon, Terminator; Cycloheximide; DNA Mutational Analysis; Exons; Glycosylation; Humans; Mannosyltransferases; Molecular Sequence Data; RNA Precursors; RNA Splice Sites; RNA Splicing; RNA Stability; RNA, Messenger; Sequence Deletion

2004

Biosynthesis of electron transfer flavoprotein in a cell-free system and in cultured human fibroblasts. Defect in the alpha subunit synthesis is a primary lesion in glutaric aciduria type II.

The Journal of clinical investigation, 1986, Volume: 78, Issue:4

Topics: Adipates; Animals; Carbohydrate Metabolism, Inborn Errors; Cell-Free System; Cycloheximide; Electron-Transferring Flavoproteins; Electrophoresis, Polyacrylamide Gel; Fibroblasts; Flavoproteins; Glutarates; Malonates; Molecular Weight; Protein Processing, Post-Translational; Rabbits; Rhodamines

1986