Yayınlar & Eserler

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Serum sirtuin 1 protein as a potential biomarker for type 2 diabetes: Increased expression of sirtuin 1 and the correlation with microRNAs.

Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences, cilt.24, ss.56, 2019 (SCI İndekslerine Giren Dergi) identifier identifier identifier

New Autoinflammatory Phenotype Associated with Homozygous AGBL3 Variant

ARTHRITIS & RHEUMATOLOGY, cilt.69, 2017 (SCI İndekslerine Giren Dergi) identifier

MEFV gene p.Met694Val variation is not associated with subacute thyroiditis in Turkish patients

INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE, cilt.9, ss.14758-14761, 2016 (SCI İndekslerine Giren Dergi) Creative Commons License identifier identifier

Association between non-coding polymorphisms of HOPX gene and syncope in hypertrophic cardiomyopathy.

Anadolu kardiyoloji dergisi : AKD = the Anatolian journal of cardiology, cilt.14, ss.617-24, 2014 (SCI Expanded İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

Metagenomic analysis of the microbial community in kefir grains

FOOD MICROBIOLOGY, cilt.41, ss.42-51, 2014 (SCI İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

Association between endothelial nitric oxide synthase intron 4a/b polymorphism and aortic dissection.

Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir, cilt.42, ss.55-60, 2014 (SCI Expanded İndekslerine Giren Dergi) identifier identifier

The association of TNFRSF1A gene and MEFV gene mutations with adult onset Still's disease

RHEUMATOLOGY INTERNATIONAL, cilt.33, ss.1675-1680, 2013 (SCI İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

Draft Genome Sequence of Halomonas smyrnensis AAD6(T)

JOURNAL OF BACTERIOLOGY, cilt.194, ss.5690-5691, 2012 (SCI İndekslerine Giren Dergi) identifier identifier

SET oncogene is upregulated in pediatric acute lymphoblastic leukemia.

Tumori, cilt.98, ss.252-6, 2012 (SCI Expanded İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

HYPOXIA INDUCES ERYTHROPOIETIN RECEPTOR EXPRESSION ON K562 CELL LINE

BIOTECHNOLOGY & BIOTECHNOLOGICAL EQUIPMENT, cilt.25, ss.2508-2512, 2011 (SCI İndekslerine Giren Dergi) identifier identifier

VEGF-A and FGF gene therapy accelerate healing of ischemic colonic anastomoses (experimental study)

INTERNATIONAL JOURNAL OF SURGERY, cilt.9, ss.467-471, 2011 (SCI İndekslerine Giren Dergi) identifier identifier identifier

The variations of BOP gene in hypertrophic cardiomyopathy.

Anadolu kardiyoloji dergisi : AKD = the Anatolian journal of cardiology, cilt.10, ss.303-9, 2010 (SCI Expanded İndekslerine Giren Dergi) identifier identifier identifier

3'-UTR HAPLOTYPES IN FMF PATIENTS

IUBMB LIFE, cilt.61, ss.307, 2009 (SCI İndekslerine Giren Dergi) identifier

The presence of erythropoietin receptor in parathyroid cells

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, cilt.30, 2007 (SCI İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

Prothrombotic gene mutations and Crohn's disease; is there any association?

HEPATO-GASTROENTEROLOGY, cilt.52, ss.1467-1469, 2005 (SCI İndekslerine Giren Dergi) Creative Commons License identifier identifier identifier

Prothrombin 20210A allele may not be an independent risk factor for myocardial infarction

Turkish Journal of Medical Sciences, cilt.35, ss.163-167, 2005 (SCI Expanded İndekslerine Giren Dergi) identifier identifier

Clinical characteristics and genetic screening of an extended family with MEN2A

JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, cilt.25, ss.603-608, 2002 (SCI İndekslerine Giren Dergi) identifier identifier identifier

Diğer Dergilerde Yayınlanan Makaleler

RE-EVALUATION OF LPS CONCENTRATIONS ON THE 293T HUMAN RENAL CELL LINE

Journal of Health Sciences of Kocaeli University, cilt.2, ss.20-22, 2016 (Hakemli Üniversite Dergisi)

15 Yıllık Huntington Hastalığı Genetik Test Sonuçları ve Literatürdeki HH Test Kılavuzları

Deneysel Tıp Araştırma Enstitüsü Dergisi, cilt.4, ss.10-16, 2016 (Hakemli Üniversite Dergisi)

15 Yıllık Huntington Hastalığının Genetik Test Sonuçları ve Literatürdeki HH Test Klavuzları

deneysel tıp araştırma enstitüsü dergisi, cilt.5, ss.10-16, 2015 (Hakemli Üniversite Dergisi)

Yeni Nesil Dizileme Teknolojisi Ile Transkriptom Analizi

Deneysel Tıp Dergisi, cilt.5, ss.51-59, 2015 (Hakemli Üniversite Dergisi)

Transcriptom Analysis Using Next Generation Sequencing

Deneysel Tıp Araştırma Enstitüsü Dergisi, cilt.4, ss.51-59, 2015 (Hakemli Üniversite Dergisi)

Association between endothelial nitric oxide synthase intron 4a b polymorphism and aortic dissection.

Archives of the Turkish Society of Cardiology, cilt.42, ss.55-60, 2014 (Diğer Kurumların Hakemli Dergileri)

Association between endothelial nitric oxide synthase intron 4a/b polymorphism and aortic dissection.

Türk Kardiyoloji Derneği Arşivi, cilt.42, ss.55-60, 2014 (Diğer Kurumların Hakemli Dergileri)

The identification of the integration sites of the plasmids that have been used to transduce cell lines

Deneysel Tıp Araştırma Enstitüsü Dergisi, cilt.2, ss.11-15, 2012 (Hakemli Üniversite Dergisi)

Hücre hatlarını oluşturmakta kullanılan plasmidlerin genomik lokasyonları

Deneysel Tıp Araştırma Enstitüsü Dergisi, cilt.2, ss.11-15, 2012 (Hakemli Üniversite Dergisi)

Hücre hatlarını olusturmakta kulllanılan plazmidlerin integrasyon bölgelerinin tanımlanması

Deneysel Tıp Arastırma Enstitüsü Dergisi, 2(3), 11-15, cilt.23, ss.11-15, 2012 (Hakemli Üniversite Dergisi)

Yeni Nesil DNA Dizileme

Deneysel Tıp Araştırma Enstitüsü Dergisi, cilt.1, ss.11-18, 2011 (Hakemli Üniversite Dergisi)

Yeni Nesil DNA Dizileme New Generation DNA Sequencing.

Deneysel Tıp Arastırma Enstitüsü Dergisi, cilt.1, ss.1-4, 2011 (Hakemli Üniversite Dergisi)

Hakemli Kongre / Sempozyum Bildiri Kitaplarında Yer Alan Yayınlar

A MEFV Gene 3’UTR Region Alu-Repeats May Have an Effecton The Gene Expression

6th International Congress on FMF and SAID,. Autoinflamation 2010, Hollanda, ss.1

An Insertion Mutation in the MDFIC (MyoD Family Inhibitor Domain Containing) Gene Defines a Novel Autoinflammatory Syndrome Associated with Lymphedema

75th Annual Scientific Meeting of the American-College-of-Rheumatology/46th Annual Scientific Meeting of the Association-of-Rheumatology-Health-Professionals, Amerika Birleşik Devletleri, ss.60

Effect of Doxorubicin on Expression of RNA m6A Methylation Enzymes in Leukemia Cell Lines

1.International Multidisciplinary Cancer Research Congres, Diyarbakır, Türkiye, 19 - 22 September 2019, ss.127

Investigation of DHRS2 Gene Effects on Breast Cancer Cell Line

1.International Multidisciplinary Cancer Research Congress, Diyarbakır, Türkiye, 18 - 22 September 2019, ss.63

Investigation of TMD-ERAP1 Candidate Gene Expressions Obtained from Multiple Myeloma Transcriptome Data by RT-PCR

1.International Multidisciplinary Cancer Research Congress, Diyarbakır, Türkiye, 18 - 22 Eylül 2019, ss.96

The Oral Microbiome of Dental Plaque in Dental Carries

2.International Symposium Prevent from Carries, İstanbul, Türkiye, 26 - 27 April 2019, ss.100-1

Effects of etanercept on cell proliferation in Huvec cell lines

13.Balkan Congress of Human Genetics, Edirne, Türkiye, 17 - 20 April 2019, ss.111

New Autoinflammatory Phenotype Associated with Homozygous AGBL3 Variant

2017 ACR/ARHP Annual Meeting, San Diago, Amerika Birleşik Devletleri, 3 - 08 November 2017, cilt.69, ss.169

Mefv Geni P.Met694val Mutasyonu Subakut Tiroidit Patogeneziyle İlişkili Değildir

38. TÜRKİYE ENDOKRİNOLOJİ VE METABOLİZMA HASTALIKLARI KONGRESİ, Antalya, Türkiye, 11 - 15 May 2016, ss.231

A15924G mt-tRNAT Gene Mutation is not the Primary Cause of Mitochondrial Myopathies

64th American Society of Human Genetics Annual Meeting in San Diego, California, Amerika Birleşik Devletleri, 18 - 22 October 2014, ss.68

MITOCHONDRIAL DNA PROFILING VIA GENOMIC ANALYSIS IN MESIAL TEMPORAL LOBE EPILEPSY PATIENTS WITH HIPPOCAMPAL SCLEROSIS

11th European Congress on Epileptology, Stockholm, İsveç, 29 Haziran - 03 Temmuz 2014, cilt.55, ss.215-216 identifier

LEF1 controls expression of HEP27, which is a posttanslational regulator of p53

XIII.National congress of medical biology and genetics, Aydın, Türkiye, 27 - 31 October 2013, ss.360-361

XBP1 Splicing and reduced xbp1 expression in behcet s Disease.

15th International Conference on Behçet's Disease,, Yokohama, Japonya, 3 - 13 Temmuz 2012, ss.1-2

Behçet Hastalığı Patogenezinde Endoplazmik Retikulum Stresinin Rolü

12. Ulusal Romatoloji Kongresi, Antalya, Türkiye, 16 October - 20 November 2011, cilt.3, ss.34

An Insertion Mutation in the MDFIC (MyoD Family Inhibitor Domain Containing) Gene Defines a Novel Autoinflammatory Syndrome Associated with Lymphedema

75th Annual Scientific Meeting of the American-College-of-Rheumatology/46th Annual Scientific Meeting of the Association-of-Rheumatology-Health-Professionals, Illinois, Amerika Birleşik Devletleri, 4 - 09 Kasım 2011, cilt.63 identifier

Characterization of H3K9me3- and H4K20me3-associated nucleosomal DNA by high-throughput sequencing in colorectal cancer

7th International Conference on Circulating Nucleic Acids in Plasma and Serum, İspanya, 1 - 04 October 2011, ss.19

Whole Mitochondrial DNA Sequencing in Mesial Temporal Lobe Epilepsy Patients with Mesial Temporal Sclerosis

Annual Meeting, "NEUROLOGY", Honolulu, Amerika Birleşik Devletleri, 9 - 16 April 2011, cilt.76, no.9, ss.653

PRECORE/CORE PROMOTER MUTATIONS BY ULTRA-DEEP PYROSEQUENCING IN GENOTYPE D CHRONIC HEPATITIS B NAIVE PATIENTS

45th Annual Meeting of the European-Association-for-the-Study-of-the-Liver, Viyana, Avusturya, 14 April 2010 - 18 April 2014, ss.238

The MEFV gene 3 '-UTR alu repeat Polymorphisms in patients with familial Mediterranean

72nd Annual Scientific Meeting of the American-College-of-Rheumatology/43rd Annual Scientific Meeting of the Association-of-Rheumatology-Health-Professionals, San-Francisco, Kostarika, 24 - 29 Ekim 2008, cilt.58 identifier

P Selectin Glycoprotein Ligand I Gene VNTR Polymorphism and Risk of Thrombosis in Behcet’s Disease

13th. International Conference and 5th. Patient's Convention with Behcet's Disease, Piza, İtalya, 1 - 02 August 2008, cilt.26, no.4, ss.25-26

Cytokine gene polymorphism in patients with graft-versus-host disease after HLA-matched bone marrow transplantion

43th ASC Congree, Washington, Amerika Birleşik Devletleri, 16 - 17 Kasım 2001, cilt.98, no.11, ss.361