Genetic Background of Idiopathic Pulmonary Fibrosis in the Czech Republic

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F27661989%3A_____%2F18%3AN0000019" target="_blank" >RIV/27661989:_____/18:N0000019 - isvavai.cz</a>
Result on the web
<a href="https://www.atsjournals.org/doi/abs/10.1164/ajrccm-conference.2018.197.1_MeetingAbstracts.A5746" target="_blank" >https://www.atsjournals.org/doi/abs/10.1164/ajrccm-conference.2018.197.1_MeetingAbstracts.A5746</a>
DOI - Digital Object Identifier
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Result language
angličtina
Original language name
Genetic Background of Idiopathic Pulmonary Fibrosis in the Czech Republic
Original language description
Idiopathic pulmonary fibrosis (IPF) is a disease characterized by progressive fibroproliferative healing in individuals of older age and with evidence of genetic predisposition. Genetic variants connected with IPF which have been described to date concern mainly the genes coding surfactant proteins, mucin, senescence related genes, telomerases and also cytokines. We aimed to investigate a panel of single nucleotide polymorphisms (SNPs) of these genes, namely MUC5B, DSP, DNASE1L3, ACE, TOLLIP, IL8, ATM, CYP2C9, TP53, CYP2C19, IL4, TREH_DDX6, FAM13A, FASTKD3, CDKN1A, IVD, MTR, SPPL2C, MDGA2, BHMT, PON1, C2, OBFC1, IL1RN, ATP11A, PRMT8, TLR3, ATG5, TGF-B1, IL12A-AS1, DPP9, SFTPC, and whole coding sequence of TERT and TERC genes.
Czech name
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Czech description
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Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical
American Journal of Respiratory and Critical Care Medicine
ISSN
1073-449X
e-ISSN
1535-4970
Volume of the periodical
197
Issue of the periodical within the volume
A5746
Country of publishing house
US - UNITED STATES
Number of pages
1
Pages from-to
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UT code for WoS article
000449980302199
EID of the result in the Scopus database
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