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Toplam 27839 kayıt

Anti HLA Antikorlarının Multipar Gebelerden Alınan SerumlardaTespiti

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2006 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
The Eurasian Journal of Medicine

Effect of Colchicine on Th1 and Th17 Cytokines, Cytokine Receptors, and Chemokine Gene Expression Profiles in Behçet’xxs Disease

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2019 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Trends Journal of Sciences Research

VDR gene FokI polymorphism as a poor prognostic factor for papillary thyroid cancer/title

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2018 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Tumor Biology

Association of MICA Alleles and Human Leukocyte Antigen B in Turkish Patients Diagnosed With Behçet’xxs Disease

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2018 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Archives of Rheumatology

Comparison of non-invasive tests with invasive tests in the diagnosis of celiac disease

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2019 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
JOURNAL OF CLINICAL LABORATORY ANALYSIS

Melanocortin 3 receptor gene polymorphism is associated with polycystic ovary syndrome in Turkish population

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2019 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Gynecological Endocrinology

Association of vitamin D receptor gene FokI and TaqI polymorphisms and risk of RDS

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2019 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
The Journal of Maternal-Fetal Neonatal Medicine

Role of p97 Valosin containing protein VCP and Jab1 CSN5 in testicular ischaemia reperfusion injury

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2016 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Journal of Molecular Histology

HLA B27 Subtype Distribution Among Patients with Ankylosing Spondylitis in Eastern Turkey

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2012 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Genetic Testing and Molecular Biomarkers

Evaluation of HLA-B51 Subtypes in Behçet’s Patients with Uveitis

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2017 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Kafkas Tıp Bilimleri Dergisi

Association between alopecia areata and HLA Class I and II in Turkey

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2005 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
J.Dermatol.

Association between factor V Leiden mutation and coronary artery disease in the northeast region of Turkey

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2007 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
BLOOD COAGULATION FIBRINOLYSIS

Combined genetic mutations have remarkable effect on deep venous thrombosis and or pulmonary embolism occurence

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2014 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Gene

BEHÇET HASTALARINDA IFNgamag, IFNgama R,CRP, ISP70 mRNA EKSPRESYONSEViYESiNiN BELiRLENMESi

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2017 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
V.DOD DERMOTOLOJI GÜNDEMİ

Multigen Panel ile saptanan Varyantların Kalıtsal Kanserler ile İlişkisi

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2019 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
13.Uluslararası katılımlı Tıbbi Genetik Kongresi

FTO gene variants are associated with polyciystic ovary sydrome in women in Turkey

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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
ENDO 2016

Importance of Rare Compound Heterozygous c.12580t C Variant in the USH2A Gene

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2018 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
13. Ulusal Tıbbi Genetik Kongresi

Hear-‘n-SEQ: an international collaboration todiscover unknown genetic etiologies of hearingloss in kids

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2018 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
41st Annual MidWinter Meeting

Tıpta Bir Veri Madenciliği Uygulaması Türk Popülasyonunda Organ Nakilleri için CPRA Hesaplama

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2015 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
XVII. AKADEMİK BİLİŞİM KONFERANSI

Gluten Sensıtıf Enteropatı (Çölyak Hastalığı) Tanısında Non-Invazıv Tanı Testlerı İle İnvazıv Tanı Testlerının Karşılaştırılması

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2015 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
3. Ulusal Klinik Mikrobiyoloji Kongresi