Tauchmannova Katerina: Difference between revisions
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{{Person | {{Person | ||
|lastname= | |lastname=Tauchmannová | ||
|firstname= | |firstname=Kateřina | ||
|institution=Academy of Sciences of the Czech Republic | |institution=Academy of Sciences of the Czech Republic | ||
Revision as of 16:00, 5 September 2022
Name | Tauchmannová Kateřina, |
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Institution | Academy of Sciences of the Czech Republic
Dept of Bioenergetics Institute of Physiology |
Address | Videnska, 1083142 20 |
City | Prague |
State/Province | |
Country | Czech Republic |
[email protected] | |
Weblink | |
O2k-Network Lab | CZ Prague Houstek J |
Labels:
Publications
Published | Reference | |
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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 | |
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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. |