Detalhe da pesquisa
1.
Genetic modifications of Mecr reveal a role for mitochondrial 2-enoyl-CoA/ACP reductase in placental development in mice.
Hum Mol Genet
; 26(11): 2104-2117, 2017 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28369354
2.
MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder.
Am J Hum Genet
; 99(6): 1229-1244, 2016 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27817865
3.
A conserved mammalian mitochondrial isoform of acetyl-CoA carboxylase ACC1 provides the malonyl-CoA essential for mitochondrial biogenesis in tandem with ACSF3.
Biochem J
; 474(22): 3783-3797, 2017 11 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28986507
4.
Mitochondrial fatty acid synthesis, fatty acids and mitochondrial physiology.
Biochim Biophys Acta Mol Cell Biol Lipids
; 1862(1): 39-48, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27553474
5.
Non-electron transfer chain mitochondrial defects differently regulate HIF-1α degradation and transcription.
Redox Biol
; 12: 1052-1061, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28531964