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Yayın Arama

Toplam 26712 kayıt

Determination of effects of tumour necrosis factor-alpha and interleukin-6 promoter polymorphisms on chronic kidney disease in Turkish patients
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2015 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
5th International Congress of Molecular Medicine

Pharmacogenetic analysis of CYP genes VKORC1 UGT1A1 and MDR1 at West Anatolia Region
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human Genetics Conference 2016

Associations of fractalkine receptor CX3CR1 and CCR5 gene variants with hypertension diabetes and atherosclerosis in chronic renal failure patients undergoing hemodialysis
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human Genetics Conference 2016

UGT1A1 GENE MUTATIONS MAY CAUSE MYCOPHENOLATE MOFETIL INDUCED LEUCOPENIA AFTER RENALTRANSPLANTATION A CASE REPORT
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
Gevher Nesibe Tıp Günleri 2016 & Tıbbi Genetik ve Klinik Uygulamaları Kongresi

Alterations in the telomere length distribution of cell free DNA in human cancer
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Biotchnology Congress

Assessment of BMP 6 polymorphism and relationship with disease activity in Ankylosing Spondylitis patients
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
EUROPEAN BİOTECHNOLOGY CONFERENCE

Assessment of BMP 6 polymorphism and relationship with disease activity in Ankylosing Spondylitis patients 05 07 May 2016 Riga LATVIA Journal of Biotechnology 231 S23
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Biotchnology Congress

The thrombophilic gene polymorphisms and recurrent pregnancy loss dilemma From Minsk Belarus and Canakkale Sivas Turkish populations 05 07 May 2016 Riga LATVIA Journal of Biotechnology 231 S20
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Biotchnology Congress

The crucial role of Factor VLeiden mutation in cardiovascular complications in psoriasis
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Academy of Dermatology and Venereology Congress

GENETIC SCREENING FOR CFTR AND AZF REGION OF Y CHROMOSOME MICRODELETIONS IN IDIOPATHIC CASES OF AZOOSPERMIA AND OLIGOZOOSPERMIA A MOLECULAR AND CYTOGENETIC APPROACHE
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
Medical Genetics and Clinical Applications (with International Participation)

Clinical characteristics and cytogenetic abnormalities of chromosome 22q11 2 syndrome Results from thirteen patients with variable phenotypes
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Biotchnology Congress

Familial X chromosome translocation Xq triplication and SHOX gene deletion with short stature Conflicting results of QF PCR analysis for Xq segmental triplication
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human Genetics Conference 2016

AN İNFERTILE CASE OF 47 XYY SYNDROME WITHOUT AUTISTIC SPECTRUM COST EFFECTIVE WELL DEFINE OF EXTRA Y CHROMOSOME BY GTG C BANDINGS QF PCR AND FISH ANALYSE
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
Erciyes Medical Genetics, Abstracts 2016 Medical Genetics and Clinical Applications (with International Participation)

THE MOLECULAR ETHIOLOGICAL PARAMETERS IN PRELINGUAL SENSORINEURAL HEARING LOSS
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
Erciyes Medical Genetics, Abstracts, OP21, s16. Medical Genetics and Clinical Applications (with International Participation)

Fenotipik olarak normal fakat habitüel abortus öyküsü olan bayanda nadir rastlanılan dengeli non resiprokal 5p 14p translokasyonu Dengeli transloke olguların doğru tanısında kromozom analizinin önemi ve MicroArray CGH yöntemine üstünlüğü
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
XII. Ulusal Tıbbi Genetik Kongresi

The possible role of chromosome 9q11 1 1 2 duplication resultingwith infertility and recurrent pregnancy loss
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
ESHG 2016

Mental ve motor geriliği olan dismorfik olguda heterozigot 1p36 delesyonu Sitogenetik moleküler sitogenetik ArrayCGH FISH ve MLPA tekniklerinin heterozigot delesyon saptama etkinliklerinin karşılaştırılması
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
XII. Ulusal Tıbbi Genetik Kongrresi. Official Journal of Turkish Society of medical Genetics

The possible association of some thrombophilic gene polymorphisms with deep vein thrombosis and pulmonary thromboembolism
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2016 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
XII. Ulusal Tıbbi Genetik Kongrresi. Official Journal of Turkish Society of medical Genetics

KRAS BRAF Oncogene Mutations and Tissue Spesific promoterHypermethylation of Tumor Supressor HIC 1 P16 DAPK1 SFRP2 andMGMT Genes in Colorectal Cancer Patients
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2015 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human Genetics Conference

MEFV gene mutation frequency in Sivas population mutation types large families and phenotype genotype correlation X Ulusal Tıbbi Biyoloji ve Genetik Kongresi
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2007 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
MEFV gene mutation frequency in Sivas population: mutation types, large families and phenotype-genotype correlation” X. Ulusal Tıbbi Biyoloji ve Genetik Kongresi