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Items: 39

1.

Role of the mitochondrial ATP synthase central stalk subunits γ and δ in the activity and assembly of the mammalian enzyme.

Pecina P, Nůsková H, Karbanová V, Kaplanová V, Mráček T, Houštěk J.

Biochim Biophys Acta Bioenerg. 2018 May;1859(5):374-381. doi: 10.1016/j.bbabio.2018.02.007. Epub 2018 Feb 27.

2.

Pleiotropic Effects of Biguanides on Mitochondrial Reactive Oxygen Species Production.

Pecinova A, Drahota Z, Kovalcikova J, Kovarova N, Pecina P, Alan L, Zima M, Houstek J, Mracek T.

Oxid Med Cell Longev. 2017;2017:7038603. doi: 10.1155/2017/7038603. Epub 2017 Aug 9.

3.

COX7AR is a Stress-inducible Mitochondrial COX Subunit that Promotes Breast Cancer Malignancy.

Zhang K, Wang G, Zhang X, Hüttemann PP, Qiu Y, Liu J, Mitchell A, Lee I, Zhang C, Lee JS, Pecina P, Wu G, Yang ZQ, Hüttemann M, Grossman LI.

Sci Rep. 2016 Aug 23;6:31742. doi: 10.1038/srep31742.

4.

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.

Hartmannová 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.

Hum Mol Genet. 2016 Sep 15;25(18):4062-4079. doi: 10.1093/hmg/ddw245. Epub 2016 Jul 27.

PMID:
27466185
5.

Data on cytochrome c oxidase assembly in mice and human fibroblasts or tissues induced by SURF1 defect.

Kovářová N, Pecina P, Nůsková H, Vrbacký M, Zeviani M, Mráček T, Viscomi C, Houštěk J.

Data Brief. 2016 Mar 26;7:1004-9. doi: 10.1016/j.dib.2016.03.065. eCollection 2016 Jun.

6.

Tissue- and species-specific differences in cytochrome c oxidase assembly induced by SURF1 defects.

Kovářová N, Pecina P, Nůsková H, Vrbacký M, Zeviani M, Mráček T, Viscomi C, Houštěk J.

Biochim Biophys Acta. 2016 Apr;1862(4):705-715. doi: 10.1016/j.bbadis.2016.01.007. Epub 2016 Jan 13.

7.

Noninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometry.

Pecina P, Houšťková H, Mráček T, Pecinová A, Nůsková H, Tesařová M, Hansíková H, Janota J, Zeman J, Houštěk J.

BBA Clin. 2014 Oct 1;2:62-71. doi: 10.1016/j.bbacli.2014.09.003. eCollection 2014 Dec.

8.

Mitochondrial ATP synthasome: Expression and structural interaction of its components.

Nůsková H, Mráček T, Mikulová T, Vrbacký M, Kovářová N, Kovalčíková J, Pecina P, Houštěk J.

Biochem Biophys Res Commun. 2015 Aug 28;464(3):787-93. doi: 10.1016/j.bbrc.2015.07.034. Epub 2015 Jul 10.

PMID:
26168732
9.

Domain adaptation of statistical machine translation with domain-focused web crawling.

Pecina P, Toral A, Papavassiliou V, Prokopidis P, Tamchyna A, Way A, van Genabith J.

Lang Resour Eval. 2015;49(1):147-193.

10.

Adaptation of machine translation for multilingual information retrieval in the medical domain.

Pecina P, Dušek O, Goeuriot L, Hajič J, Hlaváčová J, Jones GJ, Kelly L, Leveling J, Mareček D, Novák M, Popel M, Rosa R, Tamchyna A, Urešová Z.

Artif Intell Med. 2014 Jul;61(3):165-85. doi: 10.1016/j.artmed.2014.01.004. Epub 2014 Feb 5.

PMID:
24680188
11.

Nuclear genetic defects of mitochondrial ATP synthase.

Hejzlarová K, Mráček T, Vrbacký M, Kaplanová V, Karbanová V, Nůsková H, Pecina P, Houštěk J.

Physiol Res. 2014;63 Suppl 1:S57-71. Review.

12.

Cytochrome C is tyrosine 97 phosphorylated by neuroprotective insulin treatment.

Sanderson TH, Mahapatra G, Pecina P, Ji Q, Yu K, Sinkler C, Varughese A, Kumar R, Bukowski MJ, Tousignant RN, Salomon AR, Lee I, Hüttemann M.

PLoS One. 2013 Nov 5;8(11):e78627. doi: 10.1371/journal.pone.0078627. eCollection 2013.

13.

High molecular weight forms of mammalian respiratory chain complex II.

Kovářová N, Mráček T, Nůsková H, Holzerová E, Vrbacký M, Pecina P, Hejzlarová K, Kľučková K, Rohlena J, Neuzil J, Houštěk J.

PLoS One. 2013 Aug 13;8(8):e71869. doi: 10.1371/journal.pone.0071869. eCollection 2013.

14.

Cytochrome c oxidase subunit 4 isoform 2-knockout mice show reduced enzyme activity, airway hyporeactivity, and lung pathology.

Hüttemann M, Lee I, Gao X, Pecina P, Pecinova A, Liu J, Aras S, Sommer N, Sanderson TH, Tost M, Neff F, Aguilar-Pimentel JA, Becker L, Naton B, Rathkolb B, Rozman J, Favor J, Hans W, Prehn C, Puk O, Schrewe A, Sun M, Höfler H, Adamski J, Bekeredjian R, Graw J, Adler T, Busch DH, Klingenspor M, Klopstock T, Ollert M, Wolf E, Fuchs H, Gailus-Durner V, Hrabě de Angelis M, Weissmann N, Doan JW, Bassett DJ, Grossman LI.

FASEB J. 2012 Sep;26(9):3916-30. doi: 10.1096/fj.11-203273. Epub 2012 Jun 22.

15.

Adaptation of respiratory chain biogenesis to cytochrome c oxidase deficiency caused by SURF1 gene mutations.

Kovářová N, Cížková Vrbacká A, Pecina P, Stránecký V, Pronicka E, Kmoch S, Houštěk J.

Biochim Biophys Acta. 2012 Jul;1822(7):1114-24. doi: 10.1016/j.bbadis.2012.03.007. Epub 2012 Mar 20.

16.

Mice deleted for heart-type cytochrome c oxidase subunit 7a1 develop dilated cardiomyopathy.

Hüttemann M, Klewer S, Lee I, Pecinova A, Pecina P, Liu J, Lee M, Doan JW, Larson D, Slack E, Maghsoodi B, Erickson RP, Grossman LI.

Mitochondrion. 2012 Mar;12(2):294-304. doi: 10.1016/j.mito.2011.11.002. Epub 2011 Nov 20.

17.

Evaluation of basic mitochondrial functions using rat tissue homogenates.

Pecinová A, Drahota Z, Nůsková H, Pecina P, Houštěk J.

Mitochondrion. 2011 Sep;11(5):722-8. doi: 10.1016/j.mito.2011.05.006. Epub 2011 Jun 2.

PMID:
21664301
18.

The multiple functions of cytochrome c and their regulation in life and death decisions of the mammalian cell: From respiration to apoptosis.

Hüttemann M, Pecina P, Rainbolt M, Sanderson TH, Kagan VE, Samavati L, Doan JW, Lee I.

Mitochondrion. 2011 May;11(3):369-81. doi: 10.1016/j.mito.2011.01.010. Epub 2011 Feb 4. Review.

19.

Phosphomimetic substitution of cytochrome C tyrosine 48 decreases respiration and binding to cardiolipin and abolishes ability to trigger downstream caspase activation.

Pecina P, Borisenko GG, Belikova NA, Tyurina YY, Pecinova A, Lee I, Samhan-Arias AK, Przyklenk K, Kagan VE, Hüttemann M.

Biochemistry. 2010 Aug 10;49(31):6705-14. doi: 10.1021/bi100486s.

PMID:
20586425
20.

A suggested role for mitochondria in Noonan syndrome.

Lee I, Pecinova A, Pecina P, Neel BG, Araki T, Kucherlapati R, Roberts AE, Hüttemann M.

Biochim Biophys Acta. 2010 Feb;1802(2):275-83. doi: 10.1016/j.bbadis.2009.10.005. Epub 2009 Oct 14.

21.

Isolation of regulatory-competent, phosphorylated cytochrome C oxidase.

Lee I, Salomon AR, Yu K, Samavati L, Pecina P, Pecinova A, Hüttemann M.

Methods Enzymol. 2009;457:193-210. doi: 10.1016/S0076-6879(09)05011-3.

PMID:
19426869
22.

Regulation of oxidative phosphorylation, the mitochondrial membrane potential, and their role in human disease.

Hüttemann M, Lee I, Pecinova A, Pecina P, Przyklenk K, Doan JW.

J Bioenerg Biomembr. 2008 Oct;40(5):445-56. doi: 10.1007/s10863-008-9169-3. Epub 2008 Oct 9. Review.

PMID:
18843528
23.

HIF and reactive oxygen species regulate oxidative phosphorylation in cancer.

Hervouet E, Cízková A, Demont J, Vojtísková A, Pecina P, Franssen-van Hal NL, Keijer J, Simonnet H, Ivánek R, Kmoch S, Godinot C, Houstek J.

Carcinogenesis. 2008 Aug;29(8):1528-37. doi: 10.1093/carcin/bgn125. Epub 2008 May 29.

PMID:
18515279
24.

Direct linkage of mitochondrial genome variation to risk factors for type 2 diabetes in conplastic strains.

Pravenec M, Hyakukoku M, Houstek J, Zidek V, Landa V, Mlejnek P, Miksik I, Dudová-Mothejzikova K, Pecina P, Vrbacky M, Drahota Z, Vojtiskova A, Mracek T, Kazdova L, Oliyarnyk O, Wang J, Ho C, Qi N, Sugimoto K, Kurtz T.

Genome Res. 2007 Sep;17(9):1319-26. Epub 2007 Aug 10. Erratum in: Genome Res. 2008 Oct;18(10):1680.

25.

Mitochondrial diseases and genetic defects of ATP synthase.

Houstek J, Pícková A, Vojtísková A, Mrácek T, Pecina P, Jesina P.

Biochim Biophys Acta. 2006 Sep-Oct;1757(9-10):1400-5. Epub 2006 Apr 19. Review.

26.

Inhibition of cytochrome c oxidase subunit 4 precursor processing by the hypoxia mimic cobalt chloride.

Hervouet E, Pecina P, Demont J, Vojtísková A, Simonnet H, Houstek J, Godinot C.

Biochem Biophys Res Commun. 2006 Jun 16;344(4):1086-93. Epub 2006 Apr 19.

PMID:
16643849
27.

Two components in pathogenic mechanism of mitochondrial ATPase deficiency: energy deprivation and ROS production.

Mrácek T, Pecina P, Vojtísková A, Kalous M, Sebesta O, Houstek J.

Exp Gerontol. 2006 Jul;41(7):683-7. Epub 2006 Apr 3.

PMID:
16581217
28.

Polyunsaturated fatty acids of marine origin upregulate mitochondrial biogenesis and induce beta-oxidation in white fat.

Flachs P, Horakova O, Brauner P, Rossmeisl M, Pecina P, Franssen-van Hal N, Ruzickova J, Sponarova J, Drahota Z, Vlcek C, Keijer J, Houstek J, Kopecky J.

Diabetologia. 2005 Nov;48(11):2365-75. Epub 2005 Oct 5.

PMID:
16205884
29.

Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1.

Stiburek L, Vesela K, Hansikova H, Pecina P, Tesarova M, Cerna L, Houstek J, Zeman J.

Biochem J. 2005 Dec 15;392(Pt 3):625-32.

30.

A new role for the von Hippel-Lindau tumor suppressor protein: stimulation of mitochondrial oxidative phosphorylation complex biogenesis.

Hervouet E, Demont J, Pecina P, Vojtísková A, Houstek J, Simonnet H, Godinot C.

Carcinogenesis. 2005 Mar;26(3):531-9. Epub 2004 Dec 16.

PMID:
15604095
31.

Decreased affinity for oxygen of cytochrome-c oxidase in Leigh syndrome caused by SURF1 mutations.

Pecina P, Gnaiger E, Zeman J, Pronicka E, Houstek J.

Am J Physiol Cell Physiol. 2004 Nov;287(5):C1384-8. Epub 2004 Jul 21.

32.

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.

Jesina P, Tesarová M, Fornůsková D, Vojtísková A, Pecina P, Kaplanová V, Hansíková H, Zeman J, Houstek J.

Biochem J. 2004 Nov 1;383(Pt. 3):561-71.

33.

Reduced respiratory control with ADP and changed pattern of respiratory chain enzymes as a result of selective deficiency of the mitochondrial ATP synthase.

Mayr JA, Paul J, Pecina P, Kurnik P, Förster H, Fötschl U, Sperl W, Houstek J.

Pediatr Res. 2004 Jun;55(6):988-94.

PMID:
15155867
34.

Genetic defects of cytochrome c oxidase assembly.

Pecina P, Houstková H, Hansíková H, Zeman J, Houstek J.

Physiol Res. 2004;53 Suppl 1:S213-23. Review.

35.

GUG is an efficient initiation codon to translate the human mitochondrial ATP6 gene.

Dubot A, Godinot C, Dumur V, Sablonnière B, Stojkovic T, Cuisset JM, Vojtiskova A, Pecina P, Jesina P, Houstek J.

Biochem Biophys Res Commun. 2004 Jan 16;313(3):687-93.

PMID:
14697245
36.

Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome.

Pecina P, Capková M, Chowdhury SK, Drahota Z, Dubot A, Vojtísková A, Hansíková H, Houst'ková H, Zeman J, Godinot C, Houstek J.

Biochim Biophys Acta. 2003 Sep 1;1639(1):53-63.

37.

Adult outpatients with depression: worse quality of life than in other chronic medical diseases in Argentina.

Bonicatto SC, Dew MA, Zaratiegui R, Lorenzo L, Pecina P.

Soc Sci Med. 2001 Mar;52(6):911-9.

PMID:
11234864
38.

Airborne polycyclic aromatic hydrocarbons in the city of Zagreb, Yugoslavia.

Bozicević Z, Cvitas T, Curić M, Klasinc L, Pećina P.

Sci Total Environ. 1987 Oct;66:127-36.

PMID:
2446385
39.

[Fundamental measurements on siemens 42-mev betatron in Brno (author's transl)].

Caha A, Kotas J, Spurný V, Krystof V, Ott O, Koukola V, Tauer Z, Pecina P.

Radiobiol Radiother (Berl). 1976;17(3):377-82. German. No abstract available.

PMID:
981543

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