about
Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes.GTP cyclohydrolase I gene polymorphisms are associated with endothelial dysfunction and oxidative stress in patients with type 2 diabetes mellitus.Comprehensive detection and identification of bacterial DNA in the blood of patients with sepsis and healthy volunteers using next-generation sequencing method - the observation of DNAemia.Elevated urinary excretion of immunoglobulins in nonproteinuric patients with type 1 diabetes.Association of urinary inflammatory markers and renal decline in microalbuminuric type 1 diabeticsInfluence of rs1080985 single nucleotide polymorphism of the CYP2D6 gene on response to treatment with donepezil in patients with alzheimer's disease.Exogenous Angiotensin I Metabolism in Aorta Isolated from Streptozotocin Treated Diabetic Rats.Qualitative Parameters of the Colonic Flora in Patients with HNF1A-MODY Are Different from Those Observed in Type 2 Diabetes Mellitus.Vascular transcriptome profiling identifies Sphingosine kinase 1 as a modulator of angiotensin II-induced vascular dysfunction.The effect of the plasma n-3/n-6 polyunsaturated fatty acid ratio on the dietary LDL phenotype transformation - insights from the LIPGENE study.n-3 Fatty acids regulate the inflammatory-state related genes in the lung epithelial cells exposed to polycyclic aromatic hydrocarbons.Resolvin D1 down-regulates CYP1A1 and PTGS2 gene in the HUVEC cells treated with benzo(a)pyrene.Docosahexaenoic acid regulates gene expression in HUVEC cells treated with polycyclic aromatic hydrocarbons.Lipoprotein profile, plasma ischemia modified albumin and LDL density change in the course of postprandial lipemia. Insights from the LIPGENE study.Alanine variant of the Pro12Ala polymorphism of the PPARgamma gene might be associated with decreased risk of diabetic retinopathy in type 2 diabetes.Variants of the adiponectin gene and type 2 diabetes in a Polish population.The relationship between myocardial fibrosis and myocardial microRNAs in dilated cardiomyopathy: A link between mir-133a and cardiovascular events.Paraoxonase 2 gene C311S polymorphism is associated with a risk of large vessel disease stroke in a Polish population.The presence of IL-8 +781 T/C polymorphism is associated with the parameters of severe Clostridium difficile infection.Altered fibrin-clot properties are associated with retinopathy in type 2 diabetes mellitus.A1/A2 polymorphism of GpIIIa gene and a risk of aneurysmal subarachnoid haemorrhage.Characteristics of the gut microbiota in adult patients with type 1 and 2 diabetes based on the analysis of a fragment of 16S rRNA gene using next-generation sequencing.Relations between circulating microRNAs (miR-21, miR-26, miR-29, miR-30 and miR-133a), extracellular matrix fibrosis and serum markers of fibrosis in dilated cardiomyopathy.Interleukin-1 gene -511 CT polymorphism and the risk of Alzheimer's disease in a Polish population.Paraoxonase gene polymorphism and the risk for Alzheimer's disease in the polish population.Paraoxonase 1 gene polymorphisms do not influence the response to treatment in Alzheimer's disease.Lack of association between VEGF gene polymorphisms and plasma VEGF levels and sporadic AL.In vitro maturation of monocyte-derived dendritic cells results in two populations of cells with different surface marker expression, independently of applied concentration of interleukin-4Comparative iTRAQ analysis of protein abundance in the human sinoatrial node and working cardiomyocytesNegative pressure wound therapy in the treatment of diabetic foot ulcers may be mediated through differential gene expressionA family with the Arg103Pro mutation in the NEUROD1 gene detected by next-generation sequencing – Clinical characteristics of mutation carriersAssociation of plasma miR-223 and platelet reactivity in patients with coronary artery disease on dual antiplatelet therapy: A preliminary reportDenser plasma clot formation and impaired fibrinolysis in paroxysmal and persistent atrial fibrillation while on sinus rhythm: Association with thrombin generation, endothelial injury and platelet activationGenetic testing for monogenic diabetes using targeted next-generation sequencing in patients with maturity-onset diabetes of the youngThe rs2200733 variant on chromosome 4q25 is a risk factor for cardioembolic stroke related to atrial fibrillation in Polish patientsFibrin clot properties in acute ischemic stroke: relation to neurological deficitThe –A162G polymorphism of the PON1 gene and the risk of sporadic amyotrophic lateral sclerosisA-G-4G haplotype ofPAI-1gene polymorphisms −844 G/A,HindIIIG/C, and −675 4G/5G is associated with increased risk of ischemic stroke caused by small vessel diseaseErratum to: Variants of the adiponectin gene and type 2 diabetes in a Polish populationPlasma Asymmetric Dimethylarginine (ADMA) Is Associated With Retinopathy in Type 2 Diabetes
P50
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P50
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onderzoeker
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researcher ORCID ID = 0000-0002-9322-5545
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name
Pawel Wolkow
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Pawel Wolkow
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Pawel Wolkow
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Pawel Wolkow
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type
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Pawel Wolkow
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Pawel Wolkow
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Pawel Wolkow
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Pawel Wolkow
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Pawel Wolkow
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Pawel Wolkow
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Pawel Wolkow
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Pawel Wolkow
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P214
P106
P21
P214
P31
P496
0000-0002-9322-5545
P7859
viaf-266063004