Tauchmannova Katerina

Name	Tauchmannová Kateřina, PhD
Institution	Academy of Sciences of the Czech Republic, Laboratory of Bioenergetics, Institute of Physiology, CZ
Address	Videnska 1083, 142 20
City	Prague
State/Province
Country	Czech Republic
Email	[email protected]
Weblink
O2k-Network Lab	CZ Prague Houstek J

Participated at

• IOC54 Schroecken AT (formerly Hejzlarová K)

Labels: Field of research: Basic 

Publications

	Published	Reference
Markovic 2022 Biomedicines	2022	Marković A, Tauchmannová K, Šimáková M, Mlejnek P, Kaplanová V, Pecina P, Pecinová A, Papoušek F, Liška F, Šilhavý J, Mikešová J, Neckář J, Houštěk J, Pravenec M, Mráček T (2022) Genetic complementation of ATP synthase deficiency due to dysfunction of TMEM70 assembly factor in rat. https://doi.org/10.3390/biomedicines10020276
Hejzlarova 2015 Biochem J	2015	Hejzlarová 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.
Cizkova 2008 Nat Genet	2008	Cızkova A, Stranecky V, Mayr JA, Tesarova M, Havlıckova V, Paul J, Ivanek R, Kuss AW, Hansıkova H, Kaplanova W, Vrbacky M, Hartmannova H, Noskova L, Honzık T, Drahota Z, Magner M, Hejzlarova K, Sperl W, Zeman J, Houstek J, Kmoch S (2008) TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy. Nat Genet 40:1288-90.

Abstracts

	Published	Reference
Houstek 2014 Abstract MiP2014	2014	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.