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Turkey genomics 2012-2013

Master Author
Abstracts
********************************************Titles******************************************* Association of MEFV gene mutations with rheumatoid factor levels in patients with rheumatoid arthritis.
The association between Interleukin (IL)-4 gene intron 3 VNTR polymorphism and alopecia areata (AA) in Turkish population.
High Association of IL-4 Gene Intron 3 VNTR Polymorphism with Diabetic Peripheral Neuropathy.
Association between interleukin 4 gene intron 3 VNTR polymorphism and recurrent aphthous stomatitis in a cohort of Turkish patients.
Association of interleukin (IL)-4 gene intron 3 VNTR polymorphism with multiple sclerosis in Turkish population.
IL-4 and MTHFR gene polymorphism in rheumatoid arthritis and their effects.
Association of MTHFR gene C677T mutation with recurrent aphthous stomatitis and number of oral ulcers.
Association between MEFV gene mutations and recurrent aphthous stomatitis in a cohort of Turkish patients.
Association of MTHFR gene C677T mutation with diabetic peripheral neuropathy and diabetic retinopathy.
Association of IL-4 gene VNTR variant with deep venous thrombosis in Behcet's disease and its effect on ocular involvement.
Association of missense mutations of Mediterranean fever (MEFV) gene with multiple sclerosis in Turkish population.
MTHFR gene C677T mutation and ACE gene I/D polymorphism in Turkish patients with osteoarthritis.
DD genotype of ACE gene I/D polymorphism is associated with Behcet disease in a Turkish population.
Association between fibromyalgia syndrome and polymorphism of the IL-4 gene in a Turkish population.
Significance of MEFV gene R202Q polymorphism in Turkish familial Mediterranean fever patients.
Association between sequence variations of the Mediterranean fever gene and fibromyalgia syndrome in a cohort of Turkish patients.
Association of angiotensin converting enzyme (ACE) gene I/D polymorphism and rheumatoid arthritis.
Common Mediterranean fever (MEFV) gene mutations associated with ankylosing spondylitis in Turkish population.
Significant association between insertion/deletion polymorphism of the angiotensin-convertig enzyme gene and ankylosing spondylitis.
Association between the methylene tetrahydrofolate reductase gene C677T mutation and colchicine unresponsiveness in Behcet's disease.
*****************************************Affiliations***************************************** Gaziosmanpasa University, Faculty of Medicine, Department of Physical Medicine and Rehabilitation, Tokat, Turkey. ainanir@gmail.com Gaziosmanpasa University, Faculty of Medicine, Department of Dermatovenerology, Tokat, Turkey. Electronic address: goknurkalkan@yahoo.com.
Department of Medical Biology, Faculty of Medicine, Gaziosmanpasa University, 60100 Tokat, Turkey. yigit.serbulent@gmail.com Department of Medical Biology, Faculty of Medicine, Gaziosmanpasa University, Tokat, Turkey.
Department of Medical Biology, Faculty of Medicine, Gaziosmapasa University, Tokat, Turkey. serbulent.yigit@gmail.com Department of Physical Medicine and Rehabilitation, Faculty of Medicine, Gaziosmanpasa University, Tokat, Turkey. ainanir@gmail.com Department of Physical Therapy and Rehabilitation, Faculty of Medicine, Gaziosmanpasa University, Tokat, 60100, Turkey. Electronic address: inanira@gmail.com.
Department of Physical Therapy and Rehabilitation, Faculty of Medicine, Gaziosmanpasa University, Tokat, Turkey. inanira@gmail.com Faculty of Medicine, Department of Dermatology, Gaziosmanpasa University, 60100, Tokat, Turkey.
Department of Dermatovenerology, Faculty of Medicine, Gaziosmanpasa University, Tokat, Turkey.
Faculty of Medicine, Department of Medical Biology, Ondokuz Mayis University, Samsun, Turkey.
Ondokuz Mayis University, Faculty of Medicine, Department of Medical Biology, Samsun, Turkey. nevinbalci@hotmail.com Gaziosmanpasa University, Faculty of Medicine, Department of Medical Biology, Tokat, Turkey.
Gaziosmanpasa University, Faculty of Medicine, Department of Medical Biology, Tokat, Turkey. Electronic address: nevinbalci@hotmail.com.
Gaziosmanpasa University, Faculty of Medicine, Department of Medical Biology, Tokat, Turkey. Electronic address: yigit.serbulent@gmail.com.
Gaziosmanpasa University, Faculty of Medicine, Department of Medical Biology, Tokat, Turkey. yigit.serbulent@gmail.com Gaziosmanpasa University, Faculy of Medicine, Department of Medical Biology, Tokat, Turkey. serbulent.yigit@gmail.com Gaziosmanpasa University, School of Medicine, Department of Dermatology, Tokat, Turkey. Electronic address: goknurkalkan@yahoo.com.
Faculty of Medicine, Department of Emergency Medicine, Gaziosmanpasa University, 60100, Tokat, Turkey, drnursahbs@hotmail.com.
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* A novel TNFRSF1 gene mutation in a Turkish family: a report of three cases.
Characterization of H3K9me3- and H4K20me3-associated circulating nucleosomal DNA by high-throughput sequencing in colorectal cancer.
The relationship between coronary artery ectasia and eNOS intron 4a/b gene polymorphisms.
Whole mitochondrial DNA variations in hippocampal surgical specimens and blood samples with high-throughput sequencing: A case of mesial temporal lobe epilepsy with hippocampal sclerosis.
Investigation of Arg399Gln and Arg194Trp polymorphisms of the XRCC1 (x-ray cross-complementing group 1) gene and its correlation to sister chromatid exchange frequency in patients with chronic lymphocytic leukemia.
A novel partial sequence alignment tool for finding large deletions.
A genome-wide analysis of lentivector integration sites using targeted sequence capture and next generation sequencing technology.
Whole mitochondrial genome analysis of a family with NARP/MILS caused by m.8993T>C mutation in the MT-ATP6 gene.
Draft genome sequence of Halomonas smyrnensis AAD6T.
*****************************************Affiliations***************************************** Scientific and Technological Research Council of Turkey (TUBITAK), 41470 Kocaeli, Turkey.
Medical Faculty, Deparment of Pediatrics, Division of Child Neurology, Kocaeli University, Kocaeli, Turkey. bulentkara@excite.com Division of Rheumatology, Department of Internal Medicine, Faculty of Medicine, Kocaeli University, Umuttepe, 42000 Kocaeli, Turkey. fulcosan@gmail.com Department of Internal Medicine, Division of Medical Genetics, Istanbul University, Istanbul Medical Faculty, Istanbul, Turkey.
Department of Genetics, Istanbul University, Institute for Experimental Medicine, Istanbul 34093, Turkey. dustek@istanbul.edu.tr Department of Genetics, Institute for Experimental Medicine, Istanbul University, Istanbul, Turkey.
Department of Cardiology, Siyami Ersek Cardiovascular and Thoracic Surgery Centre, Istanbul, Turkey.
Department of Bioengineering, Marmara University, Istanbul, Turkey.
Department of Basic Oncology, Istanbul University Oncology Institute, Capa, 34390, Istanbul, Turkey. ugurd@istanbul.edu.tr *****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Possible Roles of the Xenobiotic Transporter P-glycoproteins Encoded by the MDR1 3435 C>T Gene Polymorphism in Differentiated Thyroid Cancers.
Association Between ABCB1 (MDR1) Gene Polymorphism and Unresponsiveness Combined Therapy in Chronic Hepatitis C virus.
Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations.
Alterations in promoter methylation status of tumor suppressor HIC1, SFRP2, and DAPK1 genes in prostate carcinomas.
Increased T-allele frequency of 677 C>T polymorphism in the methylenetetrahydrofolate reductase gene in differentiated thyroid carcinoma.
The prevalence of VKORC1 1639 G>A and CYP2C9*2*3 genotypes in patients that requiring anticoagulant therapy in Turkish population.
*****************************************Affiliations***************************************** Department of Urology, Faculty of Medicine, Cumhuriyet University, Sivas, Turkey.
Department of Pharmacology, Faculty of Medicine, Canakkale Onsekiz Mart University, Canakkale, 17100, Turkey. csilan@yahoo.com Department of Nuclear Medicine, Faculty of Medicine, Canakkale Onsekiz Mart University, Canakkale, Turkey E-mail : semozdemir@yahoo.com.
Department of Nuclear Medicine, Canakkale Onsekiz Mart University, Canakkale, Turkey. semozdemir@yahoo.com Department of Medical Genetics, Faculty of Medicine, Canakkale Onsekiz Mart University, Canakkale, Turkey. ozdemir615@yahoo.com Department of Gastroenterology, Faculty of Medicine, Cumhuriyet University, Sivas, Turkey.
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Physical mapping integrated with syntenic analysis to characterize the gene space of the long arm of wheat chromosome 1A.
Genomics Approaches for Crop Improvement against Abiotic Stress.
Unique and Conserved MicroRNAs in Wheat Chromosome 5D Revealed by Next-Generation Sequencing.
Functional features of a single chromosome arm in wheat (1AL) determined from its structure.
Subgenomic analysis of microRNAs in polyploid wheat.
Sorting the wheat from the chaff: identifying miRNAs in genomic survey sequences of Triticum aestivum chromosome 1AL.
*****************************************Affiliations***************************************** Sabanci University, Biological Sciences and Bioengineering Program, 34956 Tuzla, Istanbul, Turkey.
Faculty of Engineering and Natural Sciences, Sabanci University, Tuzla, Istanbul, Turkey.
Faculty of Engineering and Natural Sciences, Sabanci University, Orhanli, Tuzla, Istanbul, Turkey.
Faculty of Engineering and Natural Sciences, Sabanci University, Orhanli, Tuzla, 34956 Istanbul, Turkey.
Faculty of Engineering and Natural Sciences, Sabanci University, Orhanli, Istanbul, Turkey.
Biological Sciences and Bioengineering Program, Sabanci University, Tuzla, Istanbul, Turkey.
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Genome-wide identification of alternate bearing-associated microRNAs (miRNAs) in olive (Olea europaea L.).
Transcriptome-wide identification of R2R3-MYB transcription factors in barley with their boron responsive expression analysis.
Isolation and expression analysis of cDNAs that are associated with alternate bearing in Olea europaea L. cv. Ayvalik.
Nutrition metabolism plays an important role in the alternate bearing of the olive tree (Olea europaea L.).
Genome-wide identification of miRNAs responsive to drought in peach (Prunus persica) by high-throughput deep sequencing.
*****************************************Affiliations***************************************** Fen Edebiyat Fakultesi, Biyoloji Bolumu, Balikesir Universitesi, Balikesir, Turkey. dundar@balikesir.edu.tr Faculty of Science, Department of Biology, Cankiri Karatekin University, Cankiri, Turkey.
Faculty of Science, Department of Biology, Cankiri Karatekin University, 18100, Cankiri, Turkey.
Department of Biology, Faculty of Arts and Science, Fatih University, Buyukcekmece, Istanbul, Turkey. htombuloglu@fatih.edu.tr Cankiri Karatekin University, Faculty of Science, Department of Biology, Cankiri, Turkey ; Istanbul University, Faculty of Science, Department of Biology, Istanbul, Turkey.
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Genome-wide transcriptional reorganization associated with senescence-to-immortality switch during human hepatocellular carcinogenesis.
Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis.
Prohemostatic and antithrombin activities of Ankaferd hemostat are linked to fibrinogen gamma chain and prothrombin by functional proteomic analyses.
Intron F G79A polymorphism of the protein Z gene in Turkish Behcet patients.
Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis based proteomic analysis in hereditary elliptocytosis and spherocytosis.
*****************************************Affiliations***************************************** Proteomics Department, Central Laboratory of Ankara University Biotechnology Institute, Ankara, Turkey. ozel@medicine.ankara.edu.tr Department of Ophthalmology, Gaziosmanpasa University, Tokat, Turkey. helindeniz@hotmail.com BilGen Genetics and Biotechnology Center, Department of Molecular Biology and Genetics, Bilkent University, Ankara, Turkey.
Ankara University Biotechnology Institute, Ankara, Turkey. ozel@medicine.ankara.edu.tr Ankara University Biotechnology Institute, Ankara, Turkey.
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Determination of the effects of alcohol dehydrogenase (ADH) 1B and ADH1C polymorphisms on alcohol dependence in Turkey.
Gene polymorphism of complement factor H in a Turkish patient with membranoproliferative glomerulonephritis type II.
Novel mutations and diverse clinical phenotypes in recombinase-activating gene 1 deficiency.
SPP1 gene polymorphisms associated with nephrolithiasis in Turkish pediatric patients.
[Familial Mediterranean fever with pulmonary manifestations alone; early diagnosis with genetic analysis].
*****************************************Affiliations***************************************** Ege University School of Medicine, Department of Forensic Medicine, Izmir, Turkey. ekin.aktas@ege.edu.tr Department of Pediatrics, Faculty of Medicine, Ege University, 35100 Bornova, Izmir, Turkey.
Department of Pediatric Nephrology, Ege University Faculty of Medicine, Bornova, Izmir, Turkey. betulsozeri@yahoo.com Department of Pediatric Nephrology, Celal Bayar University, Manisa, Turkey.
Department of Chest Diseases, Faculty of Medicine, Sifa University, Izmir, Turkey. fidanyildiz@yahoo.com *****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Protective effect of paraoxonase 1 gene variant L55M in retinal vein occlusion.
Association of MMP2-1306C/T and TIMP2G-418C polymorphisms in retinal vein occlusion.
Predictive value of the vitamin K epoxide reductase complex subunit 1 G-1639A and C1173T single nucleotide polymorphisms in retinal vein occlusion.
Manganese-superoxide dismutase and glutathione peroxidase 1 polymorphisms in recurrent tonsillitis and tonsillar hypertrophy.
*****************************************Affiliations***************************************** Gaziosmanpasa University Faculty of Medicine, Department of Ophthalmology, Tokat, Turkey. huseyin.ortak@hotmail.com Gaziosmanpasa University Faculty of Medicine, Department of Ophthalmology, Tokat, Turkey. Electronic address: huseyin.ortak@hotmail.com.
Department of Otorhinolaryngology, Gaziosmanpasa University, School of Medicine, Tokat, Turkey. gurbuzler@yahoo.com Department of Ophthalmology, Gaziosmanpasa University, Faculty of Medicine, Tokat, Turkey. huseyin.ortak@hotmail.com *****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Determination of protective role of selenium against aflatoxin B1-induced DNA damage.
Determination of the genotoxic effects of Convolvulus arvensis extracts on corn (Zea mays L.) seeds.
Molecular determination of genotoxic effects of cobalt and nickel on maize (Zea mays L.) by RAPD and protein analyses.
Determination of genetic diversity of Vitis vinifera cv. Kabarcik populations from the Coruh Valley using SSR markers.
*****************************************Affiliations***************************************** Department of Biology, Ataturk University, Erzurum, Turkey.
Faculty of Science, Department of Biology, Ataturk University, 25240 Erzurum, Turkey.
Department of Biology, Ataturk University, Turkey.
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Role of rho-kinase gene polymorphisms and protein expressions in colorectal cancer development.
Endothelial NOS gene Glu298Asp polymorphism in preterm neonates with respiratory Distress syndrome.
Association between Rho-kinase (ROCK2) gene polymorphisms and Behcet's disease.
Mutational screening of the SOCS3 gene promoter in metastatic colorectal cancer patients.
*****************************************Affiliations***************************************** Faculty of Medicine, Division of Neonatology, Department of Pediatrics, University of Gaziantep, Gaziantep, Turkey.
Department of Pathology, Faculty of Medicine, University of Gaziantep, Gaziantep, Turkey. isari@gantep.edu.tr Department of Medical Pharmacology, University of Gaziantep, Gaziantep, Turkey.
Department of Medical Biology, Gaziantep University, Gaziantep, Turkey. mehriigci@gantep.edu.tr *****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Genotyping of beta-globin gene mutations in single lymphocytes: a preliminary study for preimplantation genetic diagnosis of monogenic disorders.
A novel KIF11 mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous family.
Mannose-binding lectin gene codon 54 polymorphism susceptible to brucellosis in Turkish children.
Analysis of the beta-glucocerebrosidase gene in Turkish Gaucher disease patients: mutation profile and description of a novel mutant allele.
*****************************************Affiliations***************************************** Division of Pediatric Infectious Diseases, Dr. Behcet Uz Child Diseases and Pediatric Surgery Training and Research Hospital, Izmir, Turkey.
Department of Medical Genetics, Ege University, Faculty of Medicine, Bornova, Izmir, Turkey. burak.durmaz@ege.edu.tr Department of Medical Genetics, Ege University Faculty of Medicine, Bornova-Izmir, Turkey. karacaemin@gmail.com Department of Medical Genetics, Dr. Behcet Uz Children's Hospital, Izmir, Turkey. filizhazan@hotmail.com *****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Exceptional complex chromosomal rearrangement and microdeletions at the 4q22.3q23 and 14q31.1q31.3 regions in a patient with azoospermia.
A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement.
Mixed gonadal dysgenesis in a patient with de novo tas(Y;19)(p11.3;q13.4) and 45,X mosaicism.
A patient with Down syndrome with a de novo derivative chromosome 21.
*****************************************Affiliations***************************************** Department of Medical Biology and Genetics, Faculty of Medicine, Akdeniz University, Antalya, Turkey.
Department of Medical Biology, Faculty of Medicine, Akdeniz University, Antalya, Turkey.
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* A novel missense mutation of the paired box 3 gene in a Turkish family with Waardenburg syndrome type 1.
Disruption of HDX gene in premature ovarian failure.
Relationship between antimetabolite toxicity and pharmacogenetics in Turkish cancer patients.
Hypochondroplasia in a child with 1620C>G (Asn540Lys) mutation in FGFR3.
*****************************************Affiliations***************************************** Ondokuz Mayis University, Faculty of Medicine , Department of Medical Biology, Samsun , Turkey.
Dr. Behcet Uz Children Disease and Surgery Training and Research Hospital, Department of Pediatric Endocrinology, Izmir, Turkey. drkorkmazanil@hotmail.com Dept of Medical Oncology, School of Medicine, Ankara University, Ankara, Turkey. mutludogan1@yahoo.com Department of Medical Genetics, Dr. Behcet Uz Children's Hospital, Izmir, Turkey. filizhazan@hotmail.com *****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Mutations in RIPK4 cause the autosomal-recessive form of popliteal pterygium syndrome.
A large duplication involving the IHH locus mimics acrocallosal syndrome.
A novel c.1255G>T (p.D419Y) mutation in SH3BP2 gene causes cherubism in a Turkish family.
*****************************************Affiliations***************************************** Department of Medical Genetics, Istanbul Medical Faculty, Istanbul University, Istanbul, Turkey.
Department of Medical Biology, Karadeniz Technical University Faculty of Medicine, Trabzon, Turkey. ersankalay@hotmail.com *****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* -765 G-->C and -1195 A-->G promoter variants of the cyclooxygenase-2 gene decrease the risk for preeclampsia.
Association of the CC chemokine receptor 5 (CCR5) polymorphisms with preeclampsia in Turkish women.
Association of polymorphisms in MCP-1, CCR2, and CCR5 genes with the risk and clinicopathological characteristics of prostate cancer.
*****************************************Affiliations***************************************** Department of Biochemistry, Istanbul University, Istanbul, Turkey. figur@istanbul.edu.tr Department of Biochemistry, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey. figur@istanbul.edu.tr Department of Biochemistry, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* A novel COL4A3 mutation causes autosomal-recessive Alport syndrome in a large Turkish family.
ATP6V1B1 mutations in distal renal tubular acidosis and sensorineural hearing loss: clinical and genetic spectrum of five families.
Autosomal recessive nonsyndromic deafness genes: a review.
*****************************************Affiliations***************************************** Division of Genetics, Department of Pediatrics, Ankara University School of Medicine, Dikimevi, Ankara, Turkey.
Department of Medical Genetics, Erciyes University School of Medicine, Kayseri, Turkey.
Department of Medical Genetics, Erciyes University School of Medicine , Kayseri , Turkey .
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* HLA class-II allele frequencies in Turkish breast cancer patients.
Diversity of killer cell immunoglobulin-like receptor genes in Southern Turkey.
Evaluation of KIR genes in recurrent miscarriage.
*****************************************Affiliations***************************************** Faculty of Medicine, Department of Clinical Biochemistry, Cukurova University, Adana, Turkey. ozlem_goruroglu@yahoo.com Department of Clinical Biochemistry, Faculty of Medicine, Cukurova Universitesi, Tip Fakultesi, Tibbi Biyokimya AD, 01330 Adana, Turkey. ozlem_goruroglu@yahoo.com Birecik State Hospital, Sanliurfa, Turkey.
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Clonal analysis of the quasispecies of antiviral-resistant HBV genomes in patients with entecavir resistance during rescue treatment and successful treatment of entecavir resistance with tenofovir.
Potential proteomic biomarkers in assessing liver fibrosis using SELDI-TOF MS.
Molecular characterization of hepatitis A virus isolated from acute infections in Turkey.
*****************************************Affiliations***************************************** Ankara University, School of Medicine Institute of Hepatology, Ankara, Turkey. mithat.bozdayi@medicine.ankara.edu.tr Ankara University, Institute of Hepatology, Ankara, Turkey.
Ankara University, Institute of Hepatology, Ankara University, Cebeci Hospital, Dikimevi 06100. Ankara, Turkey Phone: + 90 312 362 05 66 * Fax: + 90 312 363 57 75 E-mail: bozdayi@medicine.ankara.edu.tr.
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Effect of lomeguatrib-temozolomide combination on MGMT promoter methylation and expression in primary glioblastoma tumor cells.
Variations in glutathione-S-transferase genes influence risk of chronic myeloid leukemia.
The effect of CYP1A1, GSTT1 and GSTM1 polymorphisms on the risk of lung cancer: a case-control study.
*****************************************Affiliations***************************************** Department of Thoracic Surgery, Kirikkale University, Kirikkale, Turkey.
Department of Medical Biology, School of Medicine, Ankara University, Ankara, Turkey. nurozten@uic.edu Department of Medical Biology, Ankara University School of Medicine, Ankara, Turkey. mtaspinartr@gmail.com *****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Is there any relationship between decreased AgNOR protein synthesis and human hair loss? Does higher NORs expression affect the developmental stages of Down syndrome infants? EEC syndrome with a de novo mutation (c.953g > a) on exon 7 of P63 gene: a case report.
*****************************************Affiliations***************************************** Duzce University Medical Faculty, Department of Pediatrics, Duzce, Turkey. okurmesut@yahoo.com Duzce University Medical Faculty, Department of Medical Genetics, Duzce, Turkey.
Department of Medical Genetics, Duzce University Medical School, Duzce, Turkey. receperoz@duzce.edu.tr *****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Radioprotection by two phenolic compounds: chlorogenic and quinic acid, on X-ray induced DNA damage in human blood lymphocytes in vitro.
Influence of naringin on cadmium-induced genomic damage in human lymphocytes in vitro.
Genotoxic and anti-genotoxic effects of vanillic acid against mitomycin C-induced genomic damage in human lymphocytes in vitro.
*****************************************Affiliations***************************************** Uludag University, Faculty of Arts and Sciences, Department of Biology, Cell Culture and Genetic Toxicology Laboratory, Bursa, Turkey. aydemirn@uludag.edu.tr Department of Biology, Uludag University Faculty of Science and Arts, Gorukle, Bursa, Turkey.
Department of Biology, Faculty of Science and Arts, Cell Culture and Genetic Toxicology Laboratory, Bursa, Turkey.
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Relationship between genomic damage and clinical features in dialysis patients.
Rheumatoid arthritis risk associates with DNA repair gene XRCC1 Arg399Gln polymorphism in Turkish patients.
DNA repair XRCC1 Arg399Gln polymorphism is associated with the risk of development of end-stage renal disease.
*****************************************Affiliations***************************************** Department of Medical Genetics, Istanbul University, Istanbul, Turkey. mgguven@istanbul.edu.tr Department of Medical Genetics, Cerrahpasa Medical School, Istanbul University, Selamicesme Goktepe sok. No:3/26 Kadikoy, Istanbul, Turkey. yosunkayafenerci@hotmail.com Department of Internal Medicine, Division of Nephrology, Istanbul University, Cerrahpasa Medical Faculty, Istanbul, Turkey.
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* The determination of relationship between "excision repair cross-complementing group 1" (ERCC1) gene T19007C and C8092A single nucleotide polymorphisms and clinicopathological parameters in non-small cell lung cancer.
Expression of ERCC1 and its clinicopathological correlations in non-small cell lung cancer.
Investigation of microRNA expression changes in HepG2 cell line in presence of URG4/URGCP and in absence of URG4/URGCP suppressed by RNA interference.
*****************************************Affiliations***************************************** School of Medicine, Department of Genetics, Pamukkale University, Doktorlar Cad. Kat:3, Bayramyeri, Denizli, Turkey. emre_tepeli@yahoo.com Department of Medical Biology, School of Medicine, Pamukkale University, Kinikli Kampusu Morfoloji Binasi Kat:3 Kinikli, Denizli, Turkey. yavuzdodurga@gmail.com Department of Medical Biology, Pamukkale University, School of Medicine, Morfoloji Binasi Kat: 3, 20070, Kinikli, Denizli, Turkey. ekoc@yahoo.com *****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Recessive truncating NALCN mutation in infantile neuroaxonal dystrophy with facial dysmorphism.
A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood.
Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephaly.
*****************************************Affiliations***************************************** Department of Neurology, Istanbul Faculty of Medicine, Istanbul University, Istanbul 34390, Turkey.
Department of Molecular Biology and Genetics, Bogazici University, KP 301, Bebek, Istanbul 34342, Turkey; tolun@boun.edu.tr.
Department of Molecular Biology and Genetics, Bogazici University, KP 301, Bebek, 34342 Istanbul, Turkey.
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Effects of curcumin on global gene expression profiles in the highly invasive human breast carcinoma cell line MDA-MB 231: A gene network-based microarray analysis.
Evaluation of glutathione S-transferase P1 polymorphisms (Ile105Val and Ala114Val) in patients with small cell lung cancer.
A case of del(13)(q14.2)(q31.3) associated with hypothyroidism, hypertriglyceridemia, hypercholesterolemia and total ophthalmoplegia.
*****************************************Affiliations***************************************** Department of Pediatrics, Gulhane Military Medical Academy, Istanbul, Turkey. barismalbora@gmail.com Department of Medical Genetics and Clinical Research Unit, Faculty of Medicine, Kocaeli University, Kocaeli, Turkey ; Department of Genetics, Institute for Experimental Medicine (DETAE), Istanbul University, Istanbul, Turkey. vburcak@istanbul.edu.tr *****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Flavobacterium anatoliense sp. nov., isolated from fresh water, and emended description of Flavobacterium ceti.
Brevibacillus aydinogluensis sp. nov., a moderately thermophilic bacterium isolated from Karakoc hot spring.
Molecular analysis of the genus Anoxybacillus based on sequence similarity of the genes recN, flaA, and ftsY.
*****************************************Affiliations***************************************** Karadeniz Technical University, Faculty of Sciences, Department of Biology, 61080 Trabzon, Turkey.
Department of Biology, Faculty of Sciences, Karadeniz Technical University, Trabzon, Turkey.
*****************************************Coauthors***************************************** Master Author
Abstracts
********************************************Titles******************************************* Lack of genetic diversity in Crimean-Congo hemorrhagic fever viruses in Turkey: assessment of present and future patterns of disease.
Distribution of spoligotyping defined genotypic lineages among drug-resistant Mycobacterium tuberculosis complex clinical isolates in Ankara, Turkey.
Antimicrobial susceptibility and molecular subtyping of 55 Turkish Bacillus anthracis strains using 25-loci multiple-locus VNTR analysis.
*****************************************Affiliations***************************************** Faculty of Veterinary Medicine, Department of Microbiology, Kafkas University, Kars, Turkey. atakal61@hotmail.com Department of Medical Microbiology, Gulhane Military Medical Academy and School of Medicine, Ankara, Turkey. okisa@gata.edu.tr Department of Medical CBRN Defense, Gulhane Military Medical Academy, Ankara, Turkey. mortatatli@gata.edu.tr *****************************************Coauthors*****************************************

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