About: Role of rare variants in genetic predisposition to statin myopathy     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : http://linked.opendata.cz/ontology/domain/vavai/Projekt, within Data Space : linked.opendata.cz associated with source document(s)

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Description
  • The project objective is to determine the contribution of rare gene variants in SLCO1B1, SLCO1B3, and other known or unknown candidate genes to the mechanism of statin-induced myopathy. The presence of variants in approximately 70 patients with statin myopathy will be determined combination of genomic methods. The results will be validated by standard techniques of mutation analysis and evaluated using bioinformatics tools. (en)
  • Cílem projektu je zjistit příspěvek vzácných genových variant v SLCO1B1, SLCO1B3 a v dalších známých či dosud neznámých kandidátních genech k mechanismu vzniku statiny indukované myopatie. Přítomnost variant u cca 70 nemocných se statinovou myopatií bude zjišťována kombinací genomických metod. Výsledky budou validovány standardními technikami mutační analýzy a zhodnoceny pomocí bioinformatických nástrojů.
Title
  • Role of rare variants in genetic predisposition to statin myopathy (en)
  • Úloha vzácných variant v genetické predispozici ke statiny indukované myopatii
skos:notation
  • NT14025
http://linked.open...avai/cep/aktivita
http://linked.open...kovaStatniPodpora
http://linked.open...ep/celkoveNaklady
http://linked.open...datumDodatniDoRIV
http://linked.open...i/cep/druhSouteze
http://linked.open...ep/duvernostUdaju
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http://linked.open...ai/cep/hlavniObor
http://linked.open...vai/cep/kategorie
http://linked.open.../cep/klicovaSlova
  • statin; myopathy; SLCO1B1; SLCO1B3 (en)
http://linked.open...ep/partnetrHlavni
http://linked.open...inujicichPrijemcu
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http://linked.open...ep/ukonceniReseni
http://linked.open...ep/zahajeniReseni
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http://linked.open.../cep/klicoveSlovo
  • statin
  • SLCO1B1
  • myopathy
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