Search Results - "Cim, Abdullah"
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Association of polymorphisms in the vitamin D receptor gene and serum 25-hydroxyvitamin D levels in children with autism spectrum disorder
Published in Gene (22-08-2016)“…Vitamin D is implicated in several aspects of human physiology, and polymorphisms in the vitamin D receptor gene (VDR) are associated with a variety of…”
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2
Serum IL-4 and IL-10 Levels Correlate with the Symptoms of the Drug-Naive Adolescents with First Episode, Early Onset Schizophrenia
Published in Journal of child and adolescent psychopharmacology (01-10-2016)“…In this study, it was aimed to understand the underlying possible immunopathogenesis of first episode, early onset schizophrenia (EOS) through profiling the T…”
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3
Serum Cytokine Profiles of Children with Obsessive-Compulsive Disorder Shows the Evidence of Autoimmunity
Published in The international journal of neuropsychopharmacology (01-08-2016)“…Background: Previous reports have described an association between autoimmunity and primary obsessive compulsive disorder. This study aimed to investigate any…”
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4
Importance of DNA Sequencing for Abnormal Hemoglobins Detected by HPLC Screening
Published in Turkish journal of haematology (01-01-2020)“…Hemoglobinopathies are the most common health problem in Turkey. A hemoglobinopathy prevention program has been implemented by the Ministry of Health in Turkey…”
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The spectrum of MEFV gene mutations and genotypes in Van province, the eastern region of Turkey, and report of a novel mutation (R361T)
Published in Gene (10-05-2015)“…Familial Mediterranean fever (FMF) is the most common hereditary inflammatory periodic disease, characterized by recurrent episodes of fever and abdominal…”
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Elevated levels of tissue plasminogen activator and E-selectin in male children with autism spectrum disorder
Published in Autism research (01-12-2016)“…Although the etiopathology of autism spectrum disorder (ASD) is not clear, immune dysfunction has been proposed as a mechanism for the pathophysiology of ASD…”
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Use of MicroRNAs as biomarkers in the early diagnosis of prostate cancer
Published in Acta bio-medica de l'Ateneo Parmense (01-07-2022)Get full text
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Association of Polymorphisms within the Serotonin Receptor Genes 5-HTR1A, 5-HTR1B, 5-HTR2A and 5-HTR2C and Migraine Susceptibility in a Turkish Population
Published in Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology (31-08-2016)“…Migraine, a highly prevelant headache disorder, is regarded as a polygenic multifactorial disease. Serotonin (5-HT) and their respective receptors have been…”
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Contribution of polymorphisms in ESR1, ESR2, FSHR, CYP19A1, SHBG and NRIP1 genes to migraine susceptibility in Turkish population
Published in Journal of genetics (01-03-2016)“…Migraine, a highly prevalent headache disorder, is regarded as a polygenic multifactorial disease. Single-nucleotide polymorphisms (SNPs) in the genes that…”
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10
Association between sequence variations of the Mediterranean fever gene and the risk of migraine: a case-control study
Published in Neuropsychiatric disease and treatment (01-01-2016)“…Migraine pathogenesis involves a complex interaction between hormones, neurotransmitters, and inflammatory pathways, which also influence the migraine…”
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Factors influencing insulin usage among type 2 diabetes mellitus patients: A study in Turkish primary care
Published in The European journal of general practice (01-10-2016)“…Background: DM (diabetes mellitus) patients with poorly regulated blood glucose levels are at risk of increased morbidity and mortality. There are different…”
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12
Rhizomelic Chondrodysplasia Punctata Type 1 Caused by a Novel Mutation in the PEX7 Gene
Published in Journal of clinical research in pediatric endocrinology (01-03-2015)“…Peroxisomes are involved in various metabolic reactions. Rhizomelic chondrodysplasia punctata (RCDP) type 1 is one of the peroxisomal biogenesis disorders…”
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13
In vivo studies on non-viral transdifferentiation of liver cells towards pancreatic β cells
Published in Journal of endocrinology (01-09-2012)“…Transdifferentiation in vivo is an attractive option for autologous replacement of pancreatic β cells in patients with type 1 diabetes. It has been achieved by…”
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14
Pompe disease: A case report
Published in Dicle tıp dergisi (01-12-2015)“…Pompe disease is inherited in an autosomal recessive manner, and is usually observed in the children of asymptomatic carriers. Pompe disease, known as Glycogen…”
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Effect of lisinopril on rat liver tissues in L-NAME induced hypertension model
Published in Molecular and cellular biochemistry (01-02-2007)“…N G-Nitro-l-arginine methyl ester hydrochloride (L-NAME) is a non-specific nitric oxide (NO) inhibitor and it has been used to eliminate the role of NO in many…”
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Increased Caspase-3 Immunoreactivity of Erythrocytes in STZ Diabetic Rats
Published in Experimental diabetes research (01-01-2012)“…Eryptosis is a term to define apoptosis of erythrocytes. Oxidative stress and hyperglycemia, both of which exist in the diabetic intravascular environment, can…”
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Circulating microRNAs as Potential Non-invasive Biomarkers for Breast Cancer Detection
Published in Acta bio-medica de l'Ateneo Parmense (01-01-2021)“…Breast cancer is one of the most common cancers among women and is the second leading cause of cancer-related deaths. Mammography is currently the gold…”
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Pompe disease: A case report/Pompe hastaligi: Olgu sunumu
Published in Dicle tıp dergisi (01-12-2015)Get full text
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19
A duplication mutation in KCNQ1 gene in Romano-Ward syndrome
Published in Medical Genetics (2015)“…Romano-Ward syndrome (RWS, Long QT syndrome 1) is a rare familial congenital cardiac disorder characterized by a prolonged QT interval on electrocardiograph…”
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