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Decreased hepatotoxic bile acid composition and altered synthesis in progressive human nonalcoholic fatty liver disease

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F13%3A00393133" target="_blank" >RIV/60077344:_____/13:00393133 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.taap.2013.01.022" target="_blank" >http://dx.doi.org/10.1016/j.taap.2013.01.022</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.taap.2013.01.022" target="_blank" >10.1016/j.taap.2013.01.022</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Decreased hepatotoxic bile acid composition and altered synthesis in progressive human nonalcoholic fatty liver disease

  • Original language description

    Nonalcoholic fatty liver disease (NAFLD) is a prevalent form of chronic liver disease characterized by the pathophysiological progression from simple steatosis to nonalcoholic steatohepatitis (NASH). The hypothesis of this study is that the classical? (neutral) and alternative? (acidic) BA synthesis pathways are altered together with hepatic BA composition during progression of human NAFLD. This study employed the use of transcriptomic andmetabolomic assays to study the hepatic toxicologic BA profile inprogressive human NAFLD. Individual human liver samples diagnosed as normal, steatosis, and NASH were utilized in the assays. The transcriptomic analysis of 70 BA genes revealed an enrichment of downregulated BA metabolism and transcription factor/receptor genes in livers diagnosed as NASH. Increased mRNA expression of BAAT and CYP7B1was observed in contrast to decreased CYP8B1 expression in NASH samples. The BA metabolomic profile of NASH livers exhibited an increase in taurine togethe

  • 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

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

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

    Toxicology and Applied Pharmacology

  • ISSN

    0041-008X

  • e-ISSN

  • Volume of the periodical

    268

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    9

  • Pages from-to

    132-140

  • UT code for WoS article

    000316978700005

  • EID of the result in the Scopus database