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Increased susceptibility of HIF-1 alpha heterozygous-null mice to cardiovascular malformations associated with maternal diabetes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F13%3A10188753" target="_blank" >RIV/00216208:11110/13:10188753 - isvavai.cz</a>

  • Alternative codes found

    RIV/86652036:_____/13:00395068 RIV/67985823:_____/13:00395068

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.yjmcc.2013.04.015" target="_blank" >http://dx.doi.org/10.1016/j.yjmcc.2013.04.015</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.yjmcc.2013.04.015" target="_blank" >10.1016/j.yjmcc.2013.04.015</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Increased susceptibility of HIF-1 alpha heterozygous-null mice to cardiovascular malformations associated with maternal diabetes

  • Original language description

    Cardiovascular malformations are the most common manifestation of diabetic embryopathy. The molecular mechanisms underlying the teratogenic effect of maternal diabetes have not been fully elucidated. Using genome-wide expression profiling, we previouslydemonstrated that exposure to maternal diabetes resulted in dysregulation of the hypoxia-inducible factor 1 (HIF-1) pathway in the developing embryo. We thus considered a possible link between HIF-1-regulated pathways and the development of congenital malformations. HIF-1 alpha heterozygous-null (Hif1a(+/-)) and wild type (Wt) littermate embryos were exposed to the intrauterine environment of a diabetic mother to analyze the frequency and morphology of congenital defects, and assess gene expression changes in Wt and Hif1a(+/-) embryos. We observed a decreased number of embryos per litter and an increased incidence of heart malformations, including atrioventricular septal defects and reduced myocardial mass, in diabetes-exposed Hif1a(+/-

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FA - Cardiovascular diseases including cardio-surgery

  • OECD FORD branch

Result continuities

  • Project

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

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2013

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Molecular and Cellular Cardiology

  • ISSN

    0022-2828

  • e-ISSN

  • Volume of the periodical

    60

  • Issue of the periodical within the volume

    JUL

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    13

  • Pages from-to

    129-141

  • UT code for WoS article

    000320429100017

  • EID of the result in the Scopus database