M. Vanišová

Mitochondrial organization and structure are compromised in fibroblasts from patients with Huntington’s disease

J. Roth, J. Klempír, J. Zeman, 2022, Ultrastructural pathology.

Mitochondrial Dysfunction in a High Intraocular Pressure-Induced Retinal Ischemia Minipig Model

G. Petrovski, J. Čížková, J. Motlík, 2022, Biomolecules.

Homozygous missense mutation in UQCRC2 associated with severe encephalomyopathy, mitochondrial complex III assembly defect and activation of mitochondrial protein quality control.

M. Tesařová, J. Zeman, Václav Martínek, 2021, Biochimica et biophysica acta. Molecular basis of disease.

Stable COX17 Downregulation Leads to Alterations in Mitochondrial Ultrastructure, Decreased Copper Content and Impaired Cytochrome c Oxidase Biogenesis in HEK293 Cells.

J. Zeman, H. Hansíková, L. Stiburek, 2019, Folia biologica.

Knock-Out of ACBD3 Leads to Dispersed Golgi Structure, but Unaffected Mitochondrial Functions in HEK293 and HeLa Cells

O. Kuda, M. Tesařová, J. Křížová, 2021, International journal of molecular sciences.

Metabolic adaptation of human skin fibroblasts to ER stress caused by glycosylation defect in PMM2-CDG.

N. Himmelreich, T. Honzík, H. Hansíková, 2023, Molecular genetics and metabolism.