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Modeling psychiatric disorders: from genomic findings to cellular phenotypes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F16%3A00088907" target="_blank" >RIV/00216224:14110/16:00088907 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1038/mp.2016.89" target="_blank" >http://dx.doi.org/10.1038/mp.2016.89</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1038/mp.2016.89" target="_blank" >10.1038/mp.2016.89</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Modeling psychiatric disorders: from genomic findings to cellular phenotypes

  • Original language description

    Major programs in psychiatric genetics have identified 4150 risk loci for psychiatric disorders. These loci converge on a small number of functional pathways, which span conventional diagnostic criteria, suggesting a partly common biology underlying schizophrenia, autism and other psychiatric disorders. Nevertheless, the cellular phenotypes that capture the fundamental features of psychiatric disorders have not yet been determined. Recent advances in genetics and stem cell biology offer new prospects for cell-based modeling of psychiatric disorders. The advent of cell reprogramming and induced pluripotent stem cells (iPSC) provides an opportunity to translate genetic findings into patient-specific in vitro models. iPSC technology is less than a decade old but holds great promise for bridging the gaps between patients, genetics and biology. Despite many obvious advantages, iPSC studies still present multiple challenges.

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/NV15-31063A" target="_blank" >NV15-31063A: Cellular-signature profiling: leading to tailored treatment for Schizophrenic patients</a><br>

  • Continuities

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

Others

  • Publication year

    2016

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Molecular Psychiatry

  • ISSN

    1359-4184

  • e-ISSN

  • Volume of the periodical

    21

  • Issue of the periodical within the volume

    9

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    13

  • Pages from-to

    1167-1179

  • UT code for WoS article

    000382328900003

  • EID of the result in the Scopus database