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Circulating hematopoietic stem cell count is a valuable predictor of prematurity complications in preterm newborns.Neural stem/progenitor cells circulating in peripheral blood of patients with neovascular form of AMD: a novel view on pathophysiology.Lack of association between CAG repeat polymorphism in the androgen receptor gene and the outcome of rheumatoid arthritis treatment with leflunomide.IL17A and IL17F gene polymorphisms in patients with rheumatoid arthritisEvidence for proangiogenic cellular and humoral systemic response in patients with acute onset of spinal cord injury.Effect of interleukin 6 -174G>C gene polymorphism on opioid requirements after total hip replacement.P2X and P2Y receptors—role in the pathophysiology of the nervous system.Purinergic signaling and the functioning of the nervous system cells.IL-1 and TNF-α regulation of aryl hydrocarbon receptor (AhR) expression in HSY human salivary cells.TNF-α concentrations in pre-operative synovial fluid for predicting early post-operative function and pain after fast-track total knee arthroplasty.Conjugated linoleic acid regulates phosphorylation of PPARγ by modulation of ERK 1/2 and p38 signaling in human macrophages/fatty acid-laden macrophages.An optimization of protocol for mixed chimerism induction in mice model.Effect of conjugated linoleic acids on the activity and mRNA expression of 5- and 15-lipoxygenases in human macrophages.Is plasma soluble CD36 associated with cardiovascular risk factors in early onset coronary artery disease patients?Adiponectin and leptin gene polymorphisms in patients with post-transplant diabetes mellitus.STAT4 gene polymorphism in patients after renal allograft transplantationAssociation of plasma pentosidine concentrations with renal function in kidney graft recipients.Plasma concentrations of TNF-alpha and its soluble receptors sTNFR1 and sTNFR2 in patients with coronary artery disease.Lack of association of polymorphisms 239+34A/C in the SOD1 gene and 47C/T in the SOD2 gene with delayed graft function and acute and chronic rejection of kidney allografts.A sensitive and specific HPLC method for the determination of total pentosidine concentration in plasma.Polymorphisms of superoxide dismutase, glutathione peroxidase and catalase genes in patients with post-transplant diabetes mellitus.Increased circulating endothelial progenitor cells in patients with haemorrhagic and ischaemic stroke: the role of endothelin-1.Inhibition of erythrocyte phosphoribosyltransferases (APRT and HPRT) by Pb2+: a potential mechanism of lead toxicity.Circulating adhesion molecules and purine nucleotides during kidney allograft reperfusion.The effect of exon (19C>A) dihydroorotate dehydrogenase gene polymorphism on rheumatoid arthritis treatment with leflunomide.Characterisation of rat and human tissue alkaline phosphatase isoforms by high-performance liquid chromatography and agarose gel electrophoresis.An optimization of hematopoietic stem and progenitor cell isolation for scientific and clinical purposes by the application of a new parameter determining the hematopoietic graft efficacy.Simple dietary interventions reduce the risk factors of atherosclerosis in renal graft recipients.Comparison of rat and human alkaline phosphatase isoenzymes and isoforms using HPLC and electrophoresis.Effect of trimetazidine on xanthine oxidoreductase expression in rat kidney with ischemia--reperfusion injury.Conjugated linoleic acid increases intracellular ROS synthesis and oxygenation of arachidonic acid in macrophages.Hypoxanthine as a graft ischemia marker stimulates catalase activity in the renal vein during reperfusion in humans.Elevated plasma levels of C3a complement compound in the exudative form of age-related macular degeneration.HNF1B, TSPAN8 and NOTCH2 gene polymorphisms in women with gestational diabetes.COX2 and NOS3 gene polymorphisms in women with gestational diabetes.Hematopoietically expressed homeobox (HHEX) gene polymorphism (rs5015480) is associated with increased risk of gestational diabetes mellitus.GCK, GCKR, FADS1, DGKB/TMEM195 and CDKAL1 Gene Polymorphisms in Women with Gestational Diabetes.CDC123/CAMK1D gene rs12779790 polymorphism and rs10811661 polymorphism upstream of the CDKN2A/2B gene in women with gestational diabetes.Common Missense Variant of SCN9A Gene Is Associated with Pain Intensity in Patients with Chronic Pain from Disc Herniation.Effects of common functional MMP12 gene polymorphisms on PD in a Polish population.
P50
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P50
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onderzoeker
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V Dziedziejko
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Violetta Dziedziejko
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Violetta Dziedziejko
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V Dziedziejko
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Violetta Dziedziejko
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V Dziedziejko
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V Dziedziejko
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Violetta Dziedziejko
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Violetta Dziedziejko
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