Concepedia

Juha M. Kerätär

JM

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Publications

4

Citations

190

H-Index

4

Active since

2016

Affiliations

University of Oulu(Current)

Juha M. Kerätär is an author at University of Oulu specializing in life sciences, mitochondrial metabolism, and molecular biology.

Publications per year

2016–2017

4

Publications

4

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 · 104 citations · Full text

, , +16

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 · 31 citations · Full text

, , +15

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 · 31 citations

, , +16

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

, , +17

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