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A dataset of 26 candidate gene and pro-inflammatory cytokine variants for association studies in idiopathic pulmonary fibrosis: frequency distribution in normal Czech population

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F15%3A33156197" target="_blank" >RIV/61989592:15110/15:33156197 - isvavai.cz</a>

  • Result on the web

    <a href="http://journal.frontiersin.org/article/10.3389/fimmu.2015.00476/full" target="_blank" >http://journal.frontiersin.org/article/10.3389/fimmu.2015.00476/full</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3389/fimmu.2015.00476" target="_blank" >10.3389/fimmu.2015.00476</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A dataset of 26 candidate gene and pro-inflammatory cytokine variants for association studies in idiopathic pulmonary fibrosis: frequency distribution in normal Czech population

  • Original language description

    Idiopathic pulmonary fibrosis (IPF) is a specific form of chronic, progressive fibrosing interstitial pneumonia with poor diagnosis and a median survival of 2-3 years from initial diagnosis. The cellular inflammation drives the fibrotic response in lungand plays a major role in IPF pathogenesis. Inflammatory cells (majorly, type 2 alveolar epithelial cells) release TGF-?, the key mediator of pulmonary fibrosis, that regulates several profibrotic cytokines/chemokines, their receptors, receptor subunits,and growth factors inducing process of epithelial-mesenchymal transition (EMT). Among the pro-inflammatory and profibrotic cytokines involved in IPF pathogenesis, interleukin (IL)-1, IL-1?, IL-4, IL-5, IL-6R?, angiogenic IL-8/CXCL-8, IL-13, its receptorIL-13 R?2, and IL-33 have been implicated in accelerated inflammation and irreversible damage to lung architecture with loss of alveolar-capillary barrier basal membrane leading to persistent fibrosis. Genes encoding these factors exhibi

  • 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

    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)<br>S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2015

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Frontiers in Immunology

  • ISSN

    1664-3224

  • e-ISSN

  • Volume of the periodical

    6

  • Issue of the periodical within the volume

    September

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    7

  • Pages from-to

    1-7

  • UT code for WoS article

    000361912300001

  • EID of the result in the Scopus database