Mitochondrial translation is the primary determinant of secondary mitochondrial complex I deficiencies-Reference-Cited by-同舟云学术

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Mitochondrial translation is the primary determinant of secondary mitochondrial complex I deficiencies

Published:2024-08 Issue:8 Volume:27 Page:110560
ISSN:2589-0042
Container-title:iScience
language:en
Short-container-title:iScience

Author:

Čunátová Kristýna,Vrbacký Marek,Puertas-Frias Guillermo,Alán Lukáš,Vanišová Marie,Saucedo-Rodríguez María José,Houštěk Josef,Fernández-Vizarra Erika,Neužil Jiří,Pecinová Alena,Pecina Petr,Mráček Tomáš^ORCID

Funder

Ministry of Education Youth and Sports of the Czech Republic

European Regional Development Fund

Charles University

Grantová Agentura, Univerzita Karlova

Agentura Pro Zdravotnický Výzkum České Republiky

Czech Science Foundation

Czech Academy of Sciences

Publisher

Elsevier BV

Reference87 articles.

1. Assembly of mammalian oxidative phosphorylation complexes I–V and supercomplexes;Signes;Essays Biochem.,2018

2. Mitochondrial transcription and translation: overview;D’Souza;Essays Biochem.,2018

3. Making proteins in the powerhouse;Hällberg;Cell Metabol.,2014

4. Organization and expression of the mammalian mitochondrial genome;Rackham;Nat. Rev. Genet.,2022

5. Mechanisms and regulation of protein synthesis in mitochondria;Kummer;Nat. Rev. Mol. Cell Biol.,2021

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