Haplotype variability in mitochondrial rRNA predisposes to metabolic syndrome.

Autor: Pecina P; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic., Čunátová K; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic., Kaplanová V; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic., Puertas-Frias G; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic., Šilhavý J; Laboratory of Genetics of Model Diseases, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic., Tauchmannová K; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic., Vrbacký M; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic., Čajka T; Laboratory of Translational Metabolism, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic., Gahura O; Institute of Parasitology, Biology Centre, Czech Academy of Sciences, České Budějovice, Czech Republic., Hlaváčková M; Laboratory of Developmental Cardiology, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic., Stránecký V; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, 1st Faculty of Medicine, Charles University, Prague, Czech Republic., Kmoch S; Research Unit for Rare Diseases, Department of Pediatrics and Adolescent Medicine, 1st Faculty of Medicine, Charles University, Prague, Czech Republic., Pravenec M; Laboratory of Genetics of Model Diseases, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic., Houštěk J; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic., Mráček T; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic. tomas.mracek@fgu.cas.cz., Pecinová A; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic. alena.pecinova@fgu.cas.cz.

Publikováno v: Communications biology [Commun Biol] 2024 Sep 11; Vol. 7 (1), pp. 1116. Date of Electronic Publication: 2024 Sep 11.

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

Autor: Čunátová K; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, 14200 Prague, Czech Republic.; Department of Biomedical Sciences, University of Padova, 35131 Padova, Italy.; Veneto Institute of Molecular Medicine, 35129 Padova, Italy., Vrbacký M; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, 14200 Prague, Czech Republic., Puertas-Frias G; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, 14200 Prague, Czech Republic.; Department of Genetics and Microbiology, Faculty of Science, Charles University, 12800 Prague, Czech Republic., Alán L; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, 14200 Prague, Czech Republic., Vanišová M; Laboratory for Study of Mitochondrial Disorders, First Faculty of Medicine, Charles University and General University Hospital, 12808 Prague, Czech Republic., Saucedo-Rodríguez MJ; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, 14200 Prague, Czech Republic.; Department of Cell Biology, Faculty of Science, Charles University, 12800 Prague, Czech Republic., Houštěk J; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, 14200 Prague, Czech Republic., Fernández-Vizarra E; Department of Biomedical Sciences, University of Padova, 35131 Padova, Italy.; Veneto Institute of Molecular Medicine, 35129 Padova, Italy., Neužil J; School of Pharmacy and Medical Science, Griffith University, Southport, Qld 4222, Australia.; Laboratory of Molecular Therapy, Institute of Biotechnology, Czech Academy of Sciences, 25250 Prague, Czech Republic.; Department of Pediatrics and Inherited Diseases, First Faculty of Medicine, Charles University, 12108 Prague, Czech Republic.; Department of Physiology, Faculty of Science, Charles University, 12800 Prague, Czech Republic., Pecinová A; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, 14200 Prague, Czech Republic., Pecina P; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, 14200 Prague, Czech Republic., Mráček T; Laboratory of Bioenergetics, Institute of Physiology, Czech Academy of Sciences, 14200 Prague, Czech Republic.

Publikováno v: IScience [iScience] 2024 Jul 19; Vol. 27 (8), pp. 110560. Date of Electronic Publication: 2024 Jul 19 (Print Publication: 2024).

Deficiency of mitochondrial ATP synthase of nuclear genetic origin

Autor: Sperl, W., Ješina, P., Zeman, J., Mayr, J.A., DeMeirleir, L., VanCoster, R., Pícková, A., Hansíková, H., Houšt’ková, H., Krejčík, Z., Koch, J., Smet, J., Muss, W., Holme, E., Houštěk, J.

Publikováno v: In Neuromuscular Disorders 2006 16(12):821-829

Flow-cytometric monitoring of mitochondrial depolarisation: from fluorescence intensities to millivolts

Autor: Plášek, J. ^⁎, Vojtíšková, A., Houštěk, J.

Publikováno v: In Journal of Photochemistry & Photobiology, B: Biology 2005 78(2):99-108

GUG is an efficient initiation codon to translate the human mitochondrial ATP6 gene

Autor: Dubot, A, Godinot, C, Dumur, V, Sablonnière, B, Stojkovic, T, Cuisset, J.M, Vojtiskova, A, Pecina, P, Jesina, P, Houstek, J

Publikováno v: In Biochemical and Biophysical Research Communications 2004 313(3):687-693