Complex changes in the liver mitochondrial proteome of short chain acyl-CoA dehydrogenase deficient mice-Reference-Cited by-同舟云学术

Complex changes in the liver mitochondrial proteome of short chain acyl-CoA dehydrogenase deficient mice

Published:2014-05 Issue:1 Volume:112 Page:30-39
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Wang Wei,Mohsen Al-Walid,Uechi Guy,Schreiber Emanuel,Balasubramani Manimalha,Day Billy,Michael Barmada M.,Vockley Jerry^ORCID

Funder

NIH

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference33 articles.

1. Mechanistic studies with general acyl-CoA dehydrogenase and butyryl-CoA dehydrogenase: evidence for the transfer of the b-hydrogen to the flavin N(5)-position as a hydride;Ghisla;Biochemistry,1984

2. Molecular cloning and nucleotide sequence of cDNAs encoding the precursors of rat long chain acyl-CoA, short chain acyl-CoA, and isovaleryl CoA dehydrogenases: sequence homology of four enzymes of the acyl-CoA dehydrogenase family;Matsubara;J. Biol. Chem.,1989

3. Acyl-CoA dehydrogenases and acyl-CoA oxidases. Structural basis for mechanistic similarities and differences;Kim;Eur. J. Biochem.,2004

4. Structural organization of the human short-chain acyl-CoA dehydrogenase gene;Corydon;Mamm. Genome,1997

5. Cloning and characterization of the mouse short-chain acyl-CoA dehydrogenase gene;Kelly;Mamm. Genome,1996

Cited by 11 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Biochemical Markers for the Diagnosis of Mitochondrial Fatty Acid Oxidation Diseases;Journal of Clinical Medicine;2021-10-22

2. Evidence that Oxidative Disbalance and Mitochondrial Dysfunction are Involved in the Pathophysiology of Fatty Acid Oxidation Disorders;Cellular and Molecular Neurobiology;2020-09-02

3. Exploring the contribution of mitochondrial dynamics to multiple acyl-CoA dehydrogenase deficiency-related phenotype;Archives of Physiology and Biochemistry;2019-06-19

4. SucStruct: Prediction of succinylated lysine residues by using structural properties of amino acids;Analytical Biochemistry;2017-06

5. Short-chain acyl-CoA dehydrogenase deficiency: from gene to cell pathology and possible disease mechanisms;Journal of Inherited Metabolic Disease;2017-05-17