Associated Papers
Beyond CYP2C19: inflammation and angiogenesis gene variants drive clopidogrel resistance in CAD patients.
Hajer F et al.
Inflammation Research : Official Journal of the European Histamine Research Society ... [et Al.], 2025
The KDR Gene rs2071559 and the VEGF Gene rs6921438 May Be Associated with Diabetic Nephropathy in Caucasians with Type 2 Diabetes Mellitus.
Nussdorfer P et al.
International Journal of Molecular Sciences, 2024
Association of single nucleotide variants in VEGFA and KDR with the risk and angiogenic features of diffuse large B-cell lymphoma.
Assis-Mendonça GR et al.
Leukemia & Lymphoma, 2023
Genetic polymorphisms in VEGFA and VEGFR2 genes associated with coronary heart disease susceptibility and severity.
Hajer F et al.
Molecular Biology Reports, 2023
Analysis of endothelial gene polymorphisms in Spanish patients with vascular dementia and Alzheimer´s disease.
Manso-Calderón R et al.
Scientific Reports, 2023
KDR polymorphism (1192G/A, 1719A/T) and modulation of ARV drug-induced hepatotoxicity.
Singh H et al.
Microbial Pathogenesis, 2021
Angiogenesis' related genetic variants alter clinical features and prognosis of diffuse large B-cell lymphoma patients.
Brito ABC et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine, 2021
A meta-analysis of the relationship between VEGFR2 polymorphisms and atherosclerotic cardiovascular diseases.
Wang L et al.
Clinical Cardiology, 2019
Associations of VEGFA and KDR single-nucleotide polymorphisms and increased risk and aggressiveness of high-grade gliomas.
Vasconcelos VCA et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine, 2019
The association of Q472H variant in the KDR gene with recurrent pregnancy loss in Southern Iran: A case-control study.
Keshavarz L et al.
International Journal of Reproductive Biomedicine, 2019
Maternal genetic polymorphisms and unexplained recurrent miscarriage: a systematic review and meta-analysis.
Shi X et al.
Clinical Genetics, 2017
KDR gene polymorphisms and idiopathic recurrent spontaneous abortion.
Honarvar N et al.
The Journal of Maternal-fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2016
Genetic Variations of Kinase Inserts Domain Receptor (KDR) Gene Are Associated with the Risk of Astrocytomas.
Gao Y et al.
Molecular Neurobiology, 2016
VEGFR2 Gene Polymorphism Correlates with Deep Venous Thrombosis Risk in Chinese Han Population.
Wang X et al.
Genetic Testing and Molecular Biomarkers, 2015
Association of kinase insert domain-containing receptor (KDR) gene polymorphism/ haplotypes with recurrent spontaneous abortion and genetic structure.
Shahsavari S et al.
International Journal of Reproductive Biomedicine, 2015
Minor association of kinase insert domain-containing receptor gene polymorphism (rs2071559) with myocardial infarction in Caucasians with type 2 diabetes mellitus: case-control cross-sectional study.
Kariž S et al.
Clinical Biochemistry, 2014
Association of VEGF and KDR single nucleotide polymorphisms with colorectal cancer susceptibility in Koreans.
Jang MJ et al.
Molecular Carcinogenesis, 2013
Association of kinase insert domain-containing receptor (KDR) gene polymorphisms with idiopathic recurrent spontaneous abortion in Korean women.
Rah H et al.
Fertility and Sterility, 2013
Association between kinase insert domain-containing receptor polymorphisms (-604T>C, 1192G>A, 1719A>T) and premature ovarian failure in Korean women.
Rah H et al.
Menopause (new York, N.y.), 2012
Association between kinase insert domain-containing receptor gene polymorphisms and silent brain infarction: a Korean study.
Han IB et al.
Journal of the Neurological Sciences, 2012
Potentially functional genetic variants in KDR gene as prognostic markers in patients with resected colorectal cancer.
Dong G et al.
Cancer Science, 2012
The role of VEGF and KDR polymorphisms in moyamoya disease and collateral revascularization.
Park YS et al.
Plos One, 2012
Influence of pharmacogenetic variability on the pharmacokinetics and toxicity of the aurora kinase inhibitor danusertib.
Steeghs N et al.
Investigational New Drugs, 2011
Association between kinase insert domain-containing receptor gene polymorphism and haplotypes and ischemic stroke.
Oh SH et al.
Journal of the Neurological Sciences, 2011
Pharmacogenetics of telatinib, a VEGFR-2 and VEGFR-3 tyrosine kinase inhibitor, used in patients with solid tumors.
Steeghs N et al.
Investigational New Drugs, 2011
Screening of the transcriptional regulatory regions of vascular endothelial growth factor receptor 2 (VEGFR2) in amyotrophic lateral sclerosis.
Brockington A et al.
Bmc Medical Genetics, 2007
Genes of Inflammation and Placental Function GWAS Associated with Idiopathic Recurrent Miscarriage in the Kazakh Population.
Murtazaliyeva A et al.
Journal of Human Reproductive Sciences, 0