Number of the records: 1  

Mitochondrial diseases and genetic defects of ATP synthase

  1. 1.
    SYSNO ASEP0048102
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleMitochondrial diseases and genetic defects of ATP synthase
    TitleMitochondriální choroby a genetické defekty ATP syntázy
    Author(s) Houštěk, Josef (FGU-C) RID, ORCID
    Pícková, Andrea (FGU-C)
    Vojtíšková, Alena (FGU-C)
    Mráček, Tomáš (FGU-C) RID, ORCID
    Pecina, Petr (FGU-C) RID, ORCID
    Ješina, Pavel (FGU-C)
    Source TitleBiochimica Et Biophysica Acta-Bioenergetics. - : Elsevier - ISSN 0005-2728
    Roč. 1757, č. 9-10 (2006), s. 1400-1405
    Number of pages6 s.
    Languageeng - English
    CountryNL - Netherlands
    Keywordsmitochondrial diseases ; ATP synthase ; ROS
    Subject RIVEB - Genetics ; Molecular Biology
    R&D ProjectsNR7790 GA MZd - Ministry of Health (MZ)
    1M0520 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z50110509 - FGU-C (2005-2011)
    AnnotationDisorders of ATP synthase, the key enzyme of cellular energy provision, can be caused by qualitative changes in enzyme structure and function or by its diminished content. In both cases the ATP production is impaired, mitochondrií retain high values of membrane potential and as a result, mitochondrial ROS production is stimulated
    WorkplaceInstitute of Physiology
    ContactLucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400
    Year of Publishing2007
Number of the records: 1  

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