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Knock-Out of ACBD3 Leads to Dispersed Golgi Structure, but Unaffected Mitochondrial Functions in HEK293 and HeLa Cells.
Int J Mol Sci. 2021 Jul 6;22(14):7270. doi: 10.3390/ijms22147270.
Int J Mol Sci. 2021.
PMID: 34298889
Free PMC article.
Stable COX17 Downregulation Leads to Alterations in Mitochondrial Ultrastructure, Decreased Copper Content and Impaired Cytochrome c Oxidase Biogenesis in HEK293 Cells.
Vanišová M, Burská D, Křížová J, Daňhelovská T, Dosoudilová Ž, Zeman J, Stibůrek L, Hansíková H.
Vanišová M, et al.
Folia Biol (Praha). 2019;65(4):181-187.
Folia Biol (Praha). 2019.
PMID: 31903891
Free article.
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Homozygous missense mutation in UQCRC2 associated with severe encephalomyopathy, mitochondrial complex III assembly defect and activation of mitochondrial protein quality control.
Burska D, Stiburek L, Krizova J, Vanisova M, Martinek V, Sladkova J, Zamecnik J, Honzik T, Zeman J, Hansikova H, Tesarova M.
Burska D, et al. Among authors: vanisova m.
Biochim Biophys Acta Mol Basis Dis. 2021 Aug 1;1867(8):166147. doi: 10.1016/j.bbadis.2021.166147. Epub 2021 Apr 15.
Biochim Biophys Acta Mol Basis Dis. 2021.
PMID: 33865955
Free article.
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Mitochondrial organization and structure are compromised in fibroblasts from patients with Huntington's disease.
Vanisova M, Stufkova H, Kohoutova M, Rakosnikova T, Krizova J, Klempir J, Rysankova I, Roth J, Zeman J, Hansikova H.
Vanisova M, et al.
Ultrastruct Pathol. 2022 Sep 3;46(5):462-475. doi: 10.1080/01913123.2022.2100951. Epub 2022 Aug 10.
Ultrastruct Pathol. 2022.
PMID: 35946926
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Mitochondrial Dysfunction in a High Intraocular Pressure-Induced Retinal Ischemia Minipig Model.
Pasák M, Vanišová M, Tichotová L, Křížová J, Ardan T, Nemesh Y, Čížková J, Kolesnikova A, Nyshchuk R, Josifovska N, Lytvynchuk L, Kolko M, Motlík J, Petrovski G, Hansíková H.
Pasák M, et al. Among authors: vanisova m.
Biomolecules. 2022 Oct 21;12(10):1532. doi: 10.3390/biom12101532.
Biomolecules. 2022.
PMID: 36291741
Free PMC article.
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Metabolic adaptation of human skin fibroblasts to ER stress caused by glycosylation defect in PMM2-CDG.
Zdrazilova L, Rakosnikova T, Himmelreich N, Ondruskova N, Pasak M, Vanisova M, Volfova N, Honzik T, Thiel C, Hansikova H.
Zdrazilova L, et al. Among authors: vanisova m.
Mol Genet Metab. 2023 Aug;139(4):107629. doi: 10.1016/j.ymgme.2023.107629. Epub 2023 Jun 19.
Mol Genet Metab. 2023.
PMID: 37392701
Free article.
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