Difference between revisions of "Tauchmannova Katerina"
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{{Person | {{Person | ||
|lastname= | |lastname=Tauchmannová | ||
|firstname= | |firstname=Kateřina | ||
|institution=Academy of Sciences | |title=PhD | ||
|institution=[[File:Katerina Tauchmannova.jpg|right|180px|Tauchmannova Katerina]] Czech Academy of Sciences, | |||
Laboratory of Bioenergetics, | |||
Institute of Physiology | Institute of Physiology, CZ | ||
|address=Videnska | |address=Videnska 1083 | ||
|area code= | |area code=142 20 | ||
|city=Prague | |city=Prague | ||
|country=Czech Republic | |country=Czech Republic | ||
|mailaddress=katerina.hejzlarova@biomed.cas.cz | |mailaddress=katerina.hejzlarova@biomed.cas.cz | ||
}} | }} | ||
{{Labelingperson}} | == Participated at== | ||
::::* [[IOC54|IOC54 Schroecken AT]] (formerly Hejzlarová K) | |||
{{Labelingperson | |||
|field of research=Basic | |||
}} | |||
Latest revision as of 11:07, 8 September 2022
| Name | Tauchmannová Kateřina, PhD |
|---|---|
| Institution |  Laboratory of Bioenergetics, Institute of Physiology, CZ |
| Address | Videnska 1083, 142 20 |
| City | Prague |
| State/Province | |
| Country | Czech Republic |
| katerina.hejzlarova@biomed.cas.cz | |
| 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. |
