about
The -930A>G polymorphism of the CYBA gene is associated with premature coronary artery disease. A case-control study and gene-risk factors interactionsCYP7A1 gene polymorphism located in the 5' upstream region modifies the risk of coronary artery disease.The rs2516839 Polymorphism of the USF1 Gene May Modulate Serum Triglyceride Levels in Response to Cigarette Smoking.The rs10757278 polymorphism of the 9p21.3 locus is associated with premature coronary artery disease in Polish patients.The CYBA Gene (⁎)49A>G Polymorphism (rs7195830) Is Associated with Hypertension in Patients with Coronary Artery Disease.CYP3A5*3 and C3435T MDR1 polymorphisms in prognostication of drug-resistant epilepsy in children and adolescentsMethylenetetrahydrofolate reductase gene A1298C polymorphism in pediatric stroke--case-control and family-based study.Fibrinogen alpha and beta gene polymorphisms in pediatric stroke--case-control and family based study.The C242T polymorphism of the gene encoding cytochrome b-245 alpha is not associated with paediatric ischaemic stroke: family-based and case-control study.Carrier-state of D allele in ACE gene insertion/deletion polymorphism is associated with coronary artery disease, in contrast to the C677-->T transition in the MTHFR gene.The risk of coronary artery disease associated with cigarette smoking and hypercholesterolemia is additionally increased by the presence of the AT1R gene 1166C allele.The M235T polymorphism of the AGT gene modifies the risk of coronary artery disease associated with the presence of hypercholesterolemia.Modification of the coronary artery disease risk associated with the presence of traditional risk factors by insertion/deletion polymorphism of the ACE gene.[Vascular NAD(P)H oxidases--role in the pathogenesis of atherosclerosis].Relationship between rs854560 PON1 Gene Polymorphism and Tobacco Smoking with Coronary Artery Disease.Five-year prevalence of recurrent shoulder dislocation in the entire Polish population.APOE gene epsilon polymorphism does not determine predisposition to ischemic stroke in children.Polymorphisms of genes encoding coagulation factors II, V, VII, and XIII in relation to pediatric ischemic stroke: family-based and case-control study.The rs10757278 Polymorphism of the 9p21.3 Locus in Children with Arterial Ischemic Stroke: A Family-Based and Case-Control Study.Combined "pro-atherosclerotic" variants of the ACE and APOE genes increase the risk of the coronary artery disease associated with the presence of cigarette smoking.The D allele of angiotensin I-converting enzyme gene insertion/deletion polymorphism is associated with the severity of atherosclerosis.Analysis of selected promoter polymorphisms and haplotypes of the CYBA gene encoding the p22phox, subunit of NADPH oxidases, in patients with coronary artery diseaseRelationship between CETP gene polymorphisms with coronary artery disease in Polish population.The 242T variant of the CYBA gene polymorphism increases the risk of coronary artery disease associated with cigarette smoking and hypercholesterolemiaContemporaneous carrier-state of two or three "proatherosclerotic" variants of APOE, ICAM1, PPARA and PAI-1 genes differentiate CAD patients from healthy individualsThe CYBA gene A640G polymorphism influences predispositions to coronary artery disease through interactions with cigarette smoking and hypercholesterolemiaUpstream Stimulating Factor 1 (USF-1) Gene Polymorphisms and the Risk, Symptoms, and Outcome of Pediatric Ischemic StrokeMale gender and age range 20-29 years are the most important non-modifiable risk factors for recurrence after primary post-traumatic shoulder dislocation[The p22phox protein and the CYBA gene. Their function and associations with atherosclerosis-related diseases]
P50
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P50
description
researcher ORCID ID = 0000-0001-5737-3674
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wetenschapper
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name
Pawel Niemiec
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Pawel Niemiec
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Pawel Niemiec
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Pawel Niemiec
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type
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Pawel Niemiec
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Pawel Niemiec
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Pawel Niemiec
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Pawel Niemiec
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prefLabel
Pawel Niemiec
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Pawel Niemiec
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Pawel Niemiec
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Pawel Niemiec
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P31
P496
0000-0001-5737-3674