Marek Vrbacký

Czech Academy of Sciences — Czech Republic

Biochemistry, Genetics and Molecular Biology · Life Sciences

25h-index1.7kcitations76works2.02yr avg
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Research Topics

Mitochondrial Function and Pathology(46), ATP Synthase and ATPases Research(29), Metabolism and Genetic Disorders(19), Adipose Tissue and Metabolism(13), RNA modifications and cancer(10)

Publications76 total

The cytochrome c oxidase subunit COX6B1 is required for redox-sensitive early assembly and late stabilization of complex IV
Journal of Biological Chemistry·2025Open Access
Sequestration of the polyunsaturated fatty acids protects the cells with oxidative phosphorylation deficiency from ferroptosis
2025Open Access
Mitochondrial metabolism and hypoxic signaling in differentiated human cardiomyocyte AC16 cell line
American Journal of Physiology-Cell Physiology·2025· 5 citedOpen Access
COX6B1 secures a redox-sensitive step in early cytochrome <i>c</i> oxidase assembly
2025Open Access
Haplotype variability in mitochondrial rRNA predisposes to metabolic syndrome
Communications Biology·2024· 6 citedOpen Access
MITOCHONDRIAL TRANSLATION IS THE PRIMARY DETERMINANT OF SECONDARY MITOCHONDRIAL COMPLEX I DEFICIENCIESv
RedoXplore.·2024Open Access
EFFECT OF SUCCINATE DEHYDROGENASE DEFICIENCY ON MITOCHONDRIAL FUNCTION
RedoXplore.·2024Open Access
Haplotype variability in mitochondrial rRNA predisposes to metabolic syndrome
Biochimica et Biophysica Acta (BBA) - Bioenergetics·2024
Ketogenic diet mitigates the pathogenic phenotype in TMEM70 deficient animal models
Biochimica et Biophysica Acta (BBA) - Bioenergetics·2024
The role of COX6B subunit in the assembly and function of cytochrome c oxidase
Biochimica et Biophysica Acta (BBA) - Bioenergetics·2024
Mitochondrial translation is the primary determinant of secondary mitochondrial complex I deficiencies
Biochimica et Biophysica Acta (BBA) - Bioenergetics·2024
Mitochondrial translation is the primary determinant of secondary mitochondrial complex I deficiencies
iScience·2024· 11 citedOpen Access
Haptoglobin is dispensable for haemoglobin uptake by Trypanosoma brucei
Frontiers in Immunology·2024Open Access
Mitochondrial <scp>HER</scp>2 stimulates respiration and promotes tumorigenicity
European Journal of Clinical Investigation·2024· 6 citedOpen Access
Spontaneous nonsense mutation in the tuftelin 1 gene is associated with abnormal hair appearance and amelioration of glucose and lipid metabolism in the rat
Physiological Genomics·2023· 1 citedOpen Access
Physiological variability in mitochondrial rRNA predisposes to metabolic syndrome
2023· 1 citedOpen Access
Adipose-Derived Stem Cells in Reinforced Collagen Gel: A Comparison between Two Approaches to Differentiation towards Smooth Muscle Cells
International Journal of Molecular Sciences·2023· 2 citedOpen Access
Impairment of adrenergically-regulated thermogenesis in brown fat of obesity-resistant mice is compensated by non-shivering thermogenesis in skeletal muscle
Molecular Metabolism·2023· 19 citedOpen Access
Hypolipidemic Effects of Beetroot Juice in SHR-CRP and HHTg Rat Models of Metabolic Syndrome: Analysis of Hepatic Proteome
Metabolites·2023· 5 citedOpen Access
Generation and characterization of human U-2 OS cell lines with the CRISPR/Cas9-edited protoporphyrinogen oxidase IX gene
Scientific Reports·2022· 1 citedOpen Access
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Frequent Co-authors

J Houštěk(36), Tomáš Mráček(29), Z Drahota(18), Petr Pecina(17), Hana Nůsková(13), Michal Pravenec(10), Alena Pecinová(10), Vilma Kaplanová(9), Kateřina Hejzlarová(8), Kristýna Čunátová(8), Jan Šilhavý(8), Ludmila Kazdová(7), Stanislav Kmoch(6), Václav Zı́dek(6), Petr Mlejnek(6), Kateřina Tauchmannová(6), Nikola Kovářová(6), Lukáš Alán(6), Vladimír Landa(5), Miroslava Šimáková(5)