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Association between reduced levels of MEFV messenger RNA in peripheral blood leukocytes and acute inflammationMitochondrial DNA profiling via genomic analysis in mesial temporal lobe epilepsy patients with hippocampal sclerosisGenome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet diseaseGenome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.Relationship between oral anaerobic bacteria and otitis media with effusionAlix protein is substrate of Ozz-E3 ligase and modulates actin remodeling in skeletal muscle.Genomic analysis reveals the biotechnological and industrial potential of levan producing halophilic extremophile, Halomonas smyrnensis AAD6TWater as Source of Francisella tularensis Infection in Humans, Turkey.A Homozygous Nonsense Thyroid Peroxidase Mutation (R540X) Consistently Causes Congenital Hypothyroidism in Two Siblings Born to a Consanguineous Family.Application of canonical correlation analysis for identifying viral integration preferences.Topical Single-dose Vascular Endothelial Growth Factor has No Effect on Soft Tissue Healing.MEFV gene variations in patients with systemic lupus erythematosus.MEFV gene variations in patients with systemic lupus erythematosus.The association of TNFRSF1A gene and MEFV gene mutations with adult onset Still's disease.Association of the MEFV gene variations with inflammatory bowel disease in Turkey.Association of familial Mediterranean fever-related MEFV variations with ankylosing spondylitis.A novel TNFRSF1 gene mutation in a Turkish family: a report of three cases.No association of the TLR2 gene Arg753Gln polymorphism with rheumatic heart disease and Behçet's disease.Can Helicobacter pylori be eradicated with high-dose proton pump inhibitor in extensive metabolizers with the CYP2C19 genotypic polymorphism?Effect of cytochrome P450 2C19 polymorphisms on the Helicobacter pylori eradication rate following two-week triple therapy with pantoprazole or rabeprazole.Recombinant plasmid-based quantitative Real-Time PCR analysis of Salmonella enterica serotypes and its application to milk samples.Draft genome sequence of Halomonas smyrnensis AAD6TAnalysis of potential antiviral resistance mutation profiles within the HBV reverse transcriptase in untreated chronic hepatitis B patients using an ultra-deep pyrosequencing method.Role of the line probe assay INNO-LiPA HBV DR and ultradeep pyrosequencing in detecting resistance mutations to nucleoside/nucleotide analogues in viral samples isolated from chronic hepatitis B patients.A large patient study confirming that facioscapulohumeral muscular dystrophy (FSHD) disease expression is almost exclusively associated with an FSHD locus located on a 4qA-defined 4qter subtelomere.Effects of curcumin on proinflammatory cytokines and tissue injury in the early and late phases of experimental acute pancreatitis.Evaluation of coronary microvascular function and nitric oxide synthase intron 4a/b polymorphism in patients with coronary slow flow.VEGF-A and FGF gene therapy accelerate healing of ischemic colonic anastomoses (experimental study).A genome-wide analysis of lentivector integration sites using targeted sequence capture and next generation sequencing technology.Levetiracetam decreases the seizure activity and blood-brain barrier permeability in pentylenetetrazole-kindled rats with cortical dysplasia.PW02-011 - Favorable response to anakinra in aisle patients.Morphological and functional changes of blood-brain barrier in kindled rats with cortical dysplasia.Metagenomic analysis of the microbial community in kefir grains.Designing of a novel dextransucrase efficient in acceptor reactions.ExonSuite: algorithmically optimizing alternative gene splicing for the PUF proteins.In vitro chromosomal radiosensitivity in common variable immune deficiency.A novel ATP8 gene mutation in an infant with tetralogy of Fallot.TT polymorphism in rs2165241 and rs1048661 region in lysyl oxidase like-1 gene may have a role in stress urinary incontinence physiopathology.A novel partial sequence alignment tool for finding large deletions.
P50
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P50
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hulumtues
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հետազոտող
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Duran Ustek
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Duran Ustek
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Duran Ustek
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Duran Ustek
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Duran Ustek
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P1053
C-3484-2009
P106
P1153
6507861517
P21
P2456
P31
P3829
P496
0000-0002-0060-2859