Page last updated: 2024-08-24

5-methylcytosine and Lipid Metabolism, Inborn Error

5-methylcytosine has been researched along with Lipid Metabolism, Inborn Error in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Brown, WT; Dobkin, C; He, XY; Philipp, M; Yang, SY	1

Other Studies

1 other study(ies) available for 5-methylcytosine and Lipid Metabolism, Inborn Error

Article	Year
A 5-methylcytosine hotspot responsible for the prevalent HSD17B10 mutation. Gene, 2013, Feb-25, Volume: 515, Issue:2 Topics: 3-Hydroxyacyl CoA Dehydrogenases; 5-Methylcytosine; Acetyl-CoA C-Acetyltransferase; Base Sequence; DNA Methylation; Dyskinesias; Female; Genetic Association Studies; Humans; Hydrogen Bonding; Lipid Metabolism, Inborn Errors; Male; Mental Retardation, X-Linked; Meta-Analysis as Topic; Models, Molecular; Mutation, Missense; Point Mutation; Protein Structure, Quaternary; Protein Structure, Secondary; Protein Structure, Tertiary; Sequence Analysis, DNA	2013

Article

Year

A 5-methylcytosine hotspot responsible for the prevalent HSD17B10 mutation.

Gene, 2013, Feb-25, Volume: 515, Issue:2

Topics: 3-Hydroxyacyl CoA Dehydrogenases; 5-Methylcytosine; Acetyl-CoA C-Acetyltransferase; Base Sequence; DNA Methylation; Dyskinesias; Female; Genetic Association Studies; Humans; Hydrogen Bonding; Lipid Metabolism, Inborn Errors; Male; Mental Retardation, X-Linked; Meta-Analysis as Topic; Models, Molecular; Mutation, Missense; Point Mutation; Protein Structure, Quaternary; Protein Structure, Secondary; Protein Structure, Tertiary; Sequence Analysis, DNA

2013