Developmental Defects of Caenorhabditis elegans Lacking Branched-chain α-Ketoacid Dehydrogenase Are Mainly Caused by Monomethyl Branched-chain Fatty Acid Deficiency
Journal Article
Overview
publication date
- February 5, 2016
has subject area
- 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide)
- Animal Diseases - Disease Models, Animal
- Animals
- Brain Diseases - Maple Syrup Urine Disease
- Caenorhabditis elegans
- Caenorhabditis elegans Proteins
- Cells - Neurons
- Fatty Acids
- Genetic Diseases, Inborn - Maple Syrup Urine Disease
- Genetic Diseases, Inborn - Maple Syrup Urine Disease
- Humans
- Metabolic Diseases - Maple Syrup Urine Disease
- Metabolic Diseases - Maple Syrup Urine Disease
- Metabolic Diseases - Maple Syrup Urine Disease
- Models, Animal - Disease Models, Animal
- Models, Biological - Disease Models, Animal
- Nervous System - Neurons
has restriction
- hybrid
Date in CU Experts
- December 24, 2015 4:47 AM
Full Author List
- Jia F; Cui M; Than MT; Han M
author count
- 4
citation count
- 20
published in
- Journal of Biological Chemistry Journal
Other Profiles
Electronic International Standard Serial Number (EISSN)
- 1083-351X
Digital Object Identifier (DOI)
Additional Document Info
start page
- 2967
end page
- 2973
volume
- 291
issue
- 6