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The Effect of Single Dose Methylphenidate on Neurometabolites according to COMT Gene Val158Met Polymorphism in the Patient with Attention Deficit Hyperactivity Disorder: A Study Using Magnetic Resonance SpectroscopyCan Peripheral MicroRNA Expression Data Serve as Epigenomic (Upstream) Biomarkers of Alzheimer's Disease?FSHR single nucleotide polymorphism frequencies in proven fathers and infertile men in Southeast Turkey.Is catechol-o-methyltransferase gene polymorphism a risk factor in the development of premenstrual syndrome?A Study of the Impact of Death Receptor 4 (DR4) Gene Polymorphisms in Alzheimer's Disease.Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation.Association of SNAP-25 Gene Ddel and Mnll Polymorphisms with Adult Attention Deficit Hyperactivity DisorderAssociation among SNAP-25 gene DdeI and MnlI polymorphisms and hemodynamic changes during methylphenidate use: a functional near-infrared spectroscopy study.Microribonucleic acid dysregulations in children and adolescents with obsessive-compulsive disorder.MicroRNA Expression Analysis in Patients with Primary Myelofibrosis, Polycythemia vera and Essential Thrombocythemia.The impact of synapsin III gene on the neurometabolite level alterations after single-dose methylphenidate in attention-deficit hyperactivity disorder patients.Investigation of Dysregulation of Several MicroRNAs in Peripheral Blood of Schizophrenia PatientsAssociation of VAMP-2 and Syntaxin 1A Genes with Adult Attention Deficit Hyperactivity Disorder.SNP Variation in MicroRNA Biogenesis Pathway Genes as a New Innovation Strategy for Alzheimer Disease Diagnostics: A Study of 10 Candidate Genes in an Understudied Population From the Eastern Mediterranean.Folate metabolism gene polymorphisms and risk for down syndrome offspring in Turkish women.Association of microRNA biogenesis pathway gene variants and alcohol dependence risk.White matter alterations related to attention-deficit hyperactivity disorder and COMT val(158)met polymorphism: children with valine homozygote attention-deficit hyperactivity disorder have altered white matter connectivity in the right cingulum (ciBrain-Derived Neurotrophic Factor Gene Val66Met Polymorphism Is a Risk Factor for Attention-Deficit Hyperactivity Disorder in a Turkish Sample.Utilizing ethnic-specific differences in minor allele frequency to recategorize reported pathogenic deafness variants.Significance of serotonin transporter gene polymorphism in tinnitus.Significance of serotonin transporter gene polymorphism in migraine.Association of T102C polymorphism of the 5-HT2A receptor gene with psychiatric status in fibromyalgia syndrome.[Determination of the cytokine gene polymorphism and genetic susceptibility in tuberculosis patients].Frequency of the 17-bp variable number of tandem repeat polymorphism in Turkish schizophrenic patients.Lack of association between the C276T polymorphism of the neuronal nitric oxide synthase gene and migraine.T102C and -1438 G/A polymorphisms of the 5-HT2A receptor gene in Turkish patients with obsessive-compulsive disorder.Association of the -1438 G/A and 102 T/C polymorphism of the 5-Ht2A receptor gene with irritable bowel syndrome 5-Ht2A gene polymorphism in irritable bowel syndrome.The importance of IRS-1 Gly972Arg polymorphism in evaluating the response to metformin treatment in polycystic ovary syndrome.Relation of the Fas and FasL gene polymorphisms with susceptibility to and severity of rheumatoid arthritis.The association of olanzapine-induced weight gain with peroxisome proliferator-activated receptor-gamma2 Pro12Ala polymorphism in patients with schizophrenia.Association of serotonin transporter gene-linked polymorphic region and variable number of tandem repeat polymorphism of the serotonin transporter gene in lichen simplex chronicus patients with psychiatric status.Association of serotonin transporter gene polymorphism with obstructive sleep apnea syndrome.Lack of association between DRD3 gene polymorphism and response to clozapine in Turkish schizoprenia patients.Association of Gly972Arg variant of insulin receptor substrate-1 with metabolic features in women with polycystic ovary syndrome.Association of the -1438G/A polymorphism of the 5-HT2A receptor gene with obstructive sleep apnea syndrome.Association of insulin receptor substrate-1 G972R variant with baseline characteristics of the patients with gestational diabetes mellitus.PPAR-gamma2 Pro12Ala polymorphism is associated with weight gain in women with gestational diabetes mellitus.Association of (-1,607) 1G/2G polymorphism of matrix metalloproteinase-1 gene with knee osteoarthritis in the Turkish population (knee osteoarthritis and MMPs gene polymorphisms).Effects of 2.4 GHz radiofrequency radiation emitted from Wi-Fi equipment on microRNA expression in brain tissue.Long term and excessive use of 900 MHz radiofrequency radiation alter microRNA expression in brain.
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Mehmet Erdal
@ast
Mehmet Erdal
@en
Mehmet Erdal
@es
Mehmet Erdal
@nl
Mehmet Erdal
@sl
type
label
Mehmet Erdal
@ast
Mehmet Erdal
@en
Mehmet Erdal
@es
Mehmet Erdal
@nl
Mehmet Erdal
@sl
prefLabel
Mehmet Erdal
@ast
Mehmet Erdal
@en
Mehmet Erdal
@es
Mehmet Erdal
@nl
Mehmet Erdal
@sl
P1053
F-9241-2015
P106
P1153
7004645777
P21
P31
P3829
P496
0000-0002-6191-2930