Kaplanova V

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Name Kaplanova V,
Institution Department of Bioenergetics

Institute of Physiology AS CR v.v.i.

Address ,
City Prague
State/Province
Country Czech Republic
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O2k-Network Lab


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Publications

 PublishedReference
Hartmannova 2016 Hum Mol Genet2016Hartmannová H, Piherová L, Tauchmannová K, Kidd K, Acott PD, Crocker JF, Oussedik Y, Mallet M, Hodaňová K, Stránecký V, Přistoupilová A, Barešová V, Jedličková I, Živná M, Sovová J, Hůlková H, Robins V, Vrbacký M, Pecina P, Kaplanová V, Houštěk J, Mráček T, Thibeault Y, Bleyer AJ, Kmoch S (2016) Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6. Hum Mol Genet 25:4062-79.
Hejzlarova 2015 Biochem J2015Hejzlarová K, Kaplanová V, Nůsková H, Kovářová N, Ješina P, Drahota Z, Mráček T, Seneca S, Houštěk J (2015) Alteration of structure and function of ATP synthase and cytochrome c oxidase by lack of Fo-a and Cox3 subunits caused by mitochondrial DNA 9205delTA mutation. Biochem J 466:601-11.
Havlickova 2010 Biochim Biophys Acta2010Havlíčková V, Kaplanová V, Nůsková H, Drahota Z, Houštěk J (2010) Knockdown of F1 epsilon subunit decreases mitochondrial content of ATP synthase 2 and leads to accumulation of subunit c. Biochim Biophys Acta 1797:1124-9.
Jesina 2004 Biochem J2004Jesina P, Tesarova M, Fornuskova D, Vojtiskova A, Pecina P, Kaplanova V, Hansikova H, Zeman J, Houstek J (2004) Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206. Biochem J 383:561-71.

Abstracts

 PublishedReference
Mracek 2017 MiP20172017
Mracek Tomas
Knockout of DAPIT, an accessory subunit of mitochondrial ATP synthase, causes right ventricular hypertrophy and pulmonary hypertension.
Alan 2017 MiP20172017
Alan Lukas
Role of MLQ protein in the structure and function of mammalian F1FO ATP-synthase.
Cunatova 2017 MiP20172017
Cunatova Kristyna
COX4-1/4-2 knock-out causes total cytochrome c oxidase deficiency and partial impairment of mitochondrial proteosynthesis.
Kaplanova 2015 Abstract MiP20152015Functional ablation of Tmem70 alters biogenesis of ATP synthase and leads to embryonal lethality in mice.
Houstek 2014 Abstract MiP20142014Alteration of structure and function of ATP synthase and cytochrome c oxidase by lack of Fo-a and Cox3 subunits caused by mitochondrial DNA 9205delTA mutation.