Juha M. Kerätär

MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder

Gali Heimer, Juha M. Kerätär, Lisa G. Riley et al. · The American Journal of Human Genetics · 2016 · 101 citations · Full text

Mitochondrial Myopathy, Neurodegenerative Diseases, Mendelian Disorder +10

Genetic modifications of Mecr reveal a role for mitochondrial 2-enoyl-CoA/ACP reductase in placental development in mice

R. Nair, Juha M. Kerätär, Kaija J. Autio et al. · Human Molecular Genetics · 2017 · 30 citations · Full text

Mitophagy, Genetics, Molecular Genetics +18

A conserved mammalian mitochondrial isoform of acetyl-CoA carboxylase ACC1 provides the malonyl-CoA essential for mitochondrial biogenesis in tandem with ACSF3

Geoffray Monteuuis, Fumi Suomi, Juha M. Kerätär et al. · Biochemical Journal · 2017 · 30 citations

Mitophagy, Mitochondrial Biogenesis, Mitochondrial Function +15

Non-electron transfer chain mitochondrial defects differently regulate HIF-1α degradation and transcription

Antonina Shvetsova, Daniela Mennerich, Juha M. Kerätär et al. · Redox Biology · 2017 · 24 citations · Full text