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Mitochondrial translation is the primary determinant of secondary mitochondrial complex I deficiencies
- 1.0598238 - FGÚ 2025 RIV US eng J - Journal Article
Čunátová, Kristýna - Vrbacký, Marek - Puertas-Frias, Guillermo - Alán, Lukáš - Vanišová, M. - Saucedo-Rodríguez, María José - Houštěk, Josef - Fernández-Vizarra, E. - Neužil, Jiří - Pecinová, Alena - Pecina, Petr - Mráček, Tomáš
Mitochondrial translation is the primary determinant of secondary mitochondrial complex I deficiencies.
iScience. Roč. 27, č. 8 (2024), č. článku 110560. E-ISSN 2589-0042
R&D Projects: GA MŠMT(CZ) EF18_046/0016045; GA ČR(CZ) GA21-18993S; GA ČR(CZ) GA22-21082S; GA MŠMT(CZ) LX22NPO5104; GA MZd(CZ) NU22-01-00499
Research Infrastructure: Czech-BioImaging III - 90250
Institutional support: RVO:67985823 ; RVO:86652036 ; RVO:68378050
Keywords : oxidative phosphorylation system (OXPHOS) * ATP synthase * biogenesis * mitochondria
OECD category: Endocrinology and metabolism (including diabetes, hormones); Endocrinology and metabolism (including diabetes, hormones) (BTO-N)
Impact factor: 4.6, year: 2023 ; AIS: 1.5, rok: 2023
Method of publishing: Open access
Result website:
https://doi.org/10.1016/j.isci.2024.110560DOI: https://doi.org/10.1016/j.isci.2024.110560
Permanent Link: https://hdl.handle.net/11104/0355965File Download Size Commentary Version Access 24_0076_0598238.pdf 8 7.1 MB Publisher’s postprint open-access
Number of the records: 1