All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”
OC08017

The mitochondrial genome and oxidative phosphorylation system in metabolic syndrome

Public support

  • Provider

    Ministry of Education, Youth and Sports

  • Programme

    COST

  • Call for proposals

    COST 6 (SMSM2008OC3)

  • Main participants

  • Contest type

    VS - Public tender

  • Contract ID

    1146/2010-32

Alternative language

  • Project name in Czech

    Mitochondriální genom a oxidačně fosforylační systém u metabolického syndromu

  • Annotation in Czech

    Cílem projektu je přispět k poznání úlohy mitochondrií a mitochondriálního genomu v patogenezi a fenotypických projevech metabolického syndromu.

Scientific branches

  • R&D category

    ZV - Basic research

  • CEP classification - main branch

    FB - Endocrinology, diabetology, metabolism, nutrition

  • CEP - secondary branch

    ED - Physiology

  • CEP - another secondary branch

    CE - Biochemistry

  • OECD FORD - equivalent branches <br>(according to the <a href="http://www.vyzkum.cz/storage/att/E6EF7938F0E854BAE520AC119FB22E8D/Prevodnik_oboru_Frascati.pdf">converter</a>)

    10608 - Biochemistry and molecular biology<br>10609 - Biochemical research methods<br>30105 - Physiology (including cytology)<br>30202 - Endocrinology and metabolism (including diabetes, hormones)

Completed project evaluation

  • Provider evaluation

    V - Vynikající výsledky projektu (s mezinárodním významem atd.)

  • Project results evaluation

    Conplastic strains with different haplotypes of mitochondrial mtDNA have been derived from SHR rats. Studies on mitochondrial oxidative phosphorylation system and metabolic phenotypes revealed that inherited changes in mtDNA without changes in nuclear genome may predispose to metabolic syndrome in a tissue specific manner. Analysis of CD36/FAT permease showed its extramitochondrial location.

Solution timeline

  • Realization period - beginning

    Jan 1, 2008

  • Realization period - end

    May 31, 2011

  • Project status

    U - Finished project

  • Latest support payment

    Feb 22, 2011

Data delivery to CEP

  • Confidentiality

    C - Předmět řešení projektu podléhá obchodnímu tajemství (§ 504 Občanského zákoníku), ale název projektu, cíle projektu a u ukončeného nebo zastaveného projektu zhodnocení výsledku řešení projektu (údaje P03, P04, P15, P19, P29, PN8) dodané do CEP, jsou upraveny tak, aby byly zveřejnitelné.

  • Data delivery code

    CEP12-MSM-OC-U/01:1

  • Data delivery date

    Jul 12, 2012

Finance

  • Total approved costs

    1,706 thou. CZK

  • Public financial support

    1,706 thou. CZK

  • Other public sources

    0 thou. CZK

  • Non public and foreign sources

    0 thou. CZK