Results 11 to 20 of about 4,157 (190)
Background Cytochrome P450 4F2 (CYP4F2) enzyme is a member of the CYP4 family responsible for the metabolism of fatty acids, therapeutic drugs, and signaling molecules such as arachidonic acid, tocopherols, and vitamin K.
Mahvash Farajzadeh-Dehkordi +3 more
doaj +3 more sources
NFLUENCE OF CYP4F2*3 ON RESPONSE TO CLOPIDOGREL IN PATIENTS WITH ACUTE CORONARY SYNDROME
Background. Carriership of CYP4F2*3 (rs2108622, Val433Met) allelic variant can affect antiplatelet effect of clopidogrel, thus changing efficacy and safety of its standard dose.Aim.
K. B. Mirzaev +7 more
doaj +5 more sources
Genetic variants in CYP4F2 were significantly correlated with susceptibility to ischemic stroke [PDF]
Background Ischemic stroke (IS) is a serious cardiovascular disease and is associated with several single nucleotide polymorphisms (SNPs). However, the role of Cytochrome P450 family 4 subfamily F member 2 (CYP4F2) gene in IS remains unknown.
Yuan Wu +6 more
doaj +3 more sources
EFFECT OF HIGH SALT ON RENAL NKCC2 IN CYP4F2 transgenic mice
Cytochrome P450 4F2 (CYP4F2) catalyzes the ω-hydroxylation of arachidonic acid (AA) to 20-HETE. We previously generated a CYP4F2 transgenic (TG) mouse model, and demonstrated that overexpressed CYP4F2 elevates 20-HETE production and blood pressure in the
Yanyan Zhao, Jingjing Wu, Guangrei Lai
doaj +2 more sources
Effect of CYP4F2 Polymorphisms on Ticagrelor Pharmacokinetics in Healthy Chinese Volunteers [PDF]
Background: Ticagrelor belongs to a new class of P2Y12 receptor inhibitor that has been widely used for antiplatelet therapy. This study aimed to explore the effect of single nucleotide polymorphisms (SNPs) in metabolic enzymes, transporters, and other ...
Shanshan Nie +12 more
doaj +4 more sources
Pharmacogenomic Calling From Whole-Exome Sequencing in the Taiwanese Population-A Real-World Experience. [PDF]
This study evaluated pharmacogenomic (PGx) calling from whole‐exome sequencing (WES) in 3562 Taiwanese individuals. Fourteen pharmacogenes were reliably identified, with each person carrying an average of ~2.4 actionable phenotypes. The high actionable frequencies of G6PD deficiency and HLA‐B*58:01 highlight ethnic differences and support WES as a ...
Lin HH +9 more
europepmc +2 more sources
PharmVar GeneFocus: CYP4F2. [PDF]
The Pharmacogene Variation Consortium (PharmVar) serves as a global repository providing star (*) allele nomenclature for the polymorphic human CYP4F2 gene. CYP4F2 genetic variation impacts the metabolism of vitamin K, which is associated with warfarin dose requirements, and the metabolism of drugs, such as imatinib or fingolimod, and certain ...
Zubiaur P +13 more
europepmc +5 more sources
CYP4F2 and VKORC1 Polymorphisms Amplify the Risk of Carotid Plaque Formation [PDF]
Introduction: Atherosclerosis represents the process by which fibrous plaques are formed in the arterial wall, increasing its rigidity with a subsequent decrease in blood flow which can lead to several cardiovascular events. Seeing as vitamin K antagonists are involved in the pathogenesis of atherosclerosis, we decided to investigate whether ...
Stefan Cristian Vesa +9 more
openaire +3 more sources
Empirical Drug Dosage Validates Pharmacogenomic Associations in All of Us. [PDF]
ABSTRACT The All of Us research program, a national longitudinal study conducted by the US National Institutes of Health, provides robust medical history, drug dosage and genomic data from a diverse population. All of Us offers an opportunity to discover novel correlations between drug dosage and genetic variation.
Matthias J, Falaguera MJ, Altman RB.
europepmc +2 more sources
The aim. To evaluate the efficacy and safety of warfarin (WF) therapy in patients with atrial fibrillation (AF) using pharmacogenetic dosing method at an anticoagulant monitoring office according to the results of a one-year prospective follow-up ...
M. Yu. Kolesnyk, Ya. M. Mykhailovskyi
doaj +1 more source

