Search Results - "Kırac, D"
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Il-6 and UGT1A1 variations may related to furosemide resistance in heart failure patients
Published in IUBMB life (01-10-2023)“…Furosemide is a diuretic and is used for the treatment of patients with heart failure (HF). It has been found that in some HF patients, the drug does not treat…”
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Effects of PAX9 and MSX1 gene variants to hypodontia, tooth size and the type of congenitally missing teeth
Published in Cellular and molecular biology (Noisy-le-Grand, France) (30-11-2016)“…ooth agenesis, affecting up to 20% of human population, is one of the most common congenital disorder. The most frequent form of tooth agenesis is known as…”
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3
HMGCR and ApoE mutations may cause different responses to lipid lowering statin therapy
Published in Cellular and Molecular Biology (31-10-2017)“…Coronary artery disease (CAD) and its complications are the major causes of death in the world. Although statins have been used to lower lipid levels in CAD…”
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4
Effects of ACE polymorphisms and other risk factors on the severity of coronary artery disease
Published in Genetics and molecular research (19-12-2013)“…Coronary artery disease (CAD) is a multifactorial disease influenced by genetic and environmental factors. Major risk factors of CAD are hypertension,…”
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Effects of genetic factors to stent thrombosis due to clopidogrel resistance after coronary stent placement
Published in Cellular and molecular biology (Noisy-le-Grand, France) (19-01-2016)“…Stent thrombosis (ST) is considered as a multifactorial problem which is mostly occurs due to clopidogrel resistance. It may be due to some CYP450 enzyme…”
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6
Detection of Y chromosome microdeletions and mitochondrial DNA mutations in male infertility patients
Published in Genetics and molecular research (01-01-2012)“…Infertility affects about 10-15% of all couples attempting pregnancy with infertility attributed to the male partner in approximately half of the cases…”
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Predictors of atopic dermatitis phenotypes and severity: roles of serum immunoglobulins and filaggrin gene mutation R501X
Published in Allergologia et immunopathologia (01-03-2013)“…Atopic dermatitis (AD), the most common chronic relapsing skin condition of infancy and childhood, is a complex multifactorial disease, which arises from the…”
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Multifactor dimensionality reduction analysis of MTHFR, PAI-1, ACE, PON1, and eNOS gene polymorphisms in patients with early onset coronary artery disease
Published in European journal of cardiovascular prevention and rehabilitation (01-12-2011)“…Background: Association studies in the Turkish population have investigated the single locus effects of different gene polymorphisms on coronary artery disease…”
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Detection of mitochondrial DNA mutations in nonmuscle invasive bladder cancer
Published in Genetic testing and molecular biomarkers (01-07-2012)“…Mitochondrial DNA (mtDNA) mutations have been recently described in various tumors; however, data focusing on bladder cancer are scarce. To understand the…”
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