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Human cardiac progenitor analysis in dystrophin cardiomyopathy after cardiac transplantation

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F18%3A00100947" target="_blank" >RIV/00216224:14110/18:00100947 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1093/cvr/cvy060.101" target="_blank" >http://dx.doi.org/10.1093/cvr/cvy060.101</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1093/cvr/cvy060.101" target="_blank" >10.1093/cvr/cvy060.101</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Human cardiac progenitor analysis in dystrophin cardiomyopathy after cardiac transplantation

  • Original language description

    We report for the first time human dystrophy (Becker type, BMD) cardiac progenitor analysis. Following rare cardiac transplantation in case of a symptomatic BMD samples were obtained and compared to healthy control samples. Heart failure is a frequent cause of death in muscle dystrophy patients. We hypothesized lower repair capacity of myocardium, possibly due to decreased percentage of reparative c-kit+ cells and their impaired migration capacity.

  • Czech name

  • Czech description

Classification

  • Type

    O - Miscellaneous

  • CEP classification

  • OECD FORD branch

    30201 - Cardiac and Cardiovascular systems

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů