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Yayın Arama

Toplam 26712 kayıt

Epigenetik alterations and oncogenes mutations in urinary bladder carcinoma
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
7th European Cytogenetics Conference

The crucial role of MDR1 ABCB1 gene polymorphism in abdominal aortic aneurysm A preliminary results of a pilot study
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
7th European Cytogenetics Conference

Tumoral tissue specific promoter hypermethylation of tumor supressor genes SFRp2 p16 DAPK1 HIC and MGMT in a case with non small cell carcinoma A case report
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
7th European Cytogenetics Conference

CRUCIAL ROLE OF PARENTAL MTHFR GENE POLYMORPHISM INVOLVED IN HOMOCYSTEINE METABOLISM IN DOWN SYNDROME
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
IUBMB LIFE

ETERMINATION OF DISTRIBUTION OF COMMON MEFV GENE MUTATIONS IN HEALTHY INDIVIDUALS WHO HAD BEEN EXPOSED TO APPENDECTOMY IN CHILDHOOD AGE
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
IUBMB LIFE

ANGIOTENSIN CONVERTING ENZYME ACE GENE POLYMORPHISM AND BUERGER S DISEASE
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
IUBMB LIFE

Increased T allele frequency in MTHFR C677T gene in thyroid carcinme
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
8th European Cytogenetic Conference

The endemic RTL80V I and RTM204V I YMDD mutation profiles in a case of chronic hepatitis B
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
8th European Cytogenetic Conference

Epigenetic silencing of the tumor supressor HIC1 and SFRP2 genes in prostate carcinomas
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Cytogenetic Conference

Increased T allele frequency in multidrug transporter ABCB1 MDR1 gene in FMF patients of colchicine unresponsiveness
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human Genetics Conference

Recurrent Pregnancy Loss and Its Relation to Combined Parental Thrombophilic Gene Mutations
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human Genetics Conference

Combine effect of Factor V Leiden MTHFR and Angiotensin converting enzyme insertion deletion gene mutations in hypertensive adult individuals a population based study from Sivas and Canakkale TURKEY
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human Genetics Conference

GJB2 35delG and Mitochondrial A1555G mutations and etiology of deafness at the Gelibolu School for the Deaf in Turkey
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human Genetics Conference

Genome based transcriptome profile of some etiological parameters in breast cancer
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
Abstracts of the 2011 MASCC\ISOO Symposium

The prevalence of VKORC1 1639 G A and CYP2C9 2 3 genotypes in patients that requiring anticoagulant therapy in Turkish population
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human GeneticsConference

Strong association between ABCB1 gene MDR1 3435 C T polymorphism and multiple drug nonresponder patients of chronic hepatitis C
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human Genetics Conference

The possible role of the xenobiotic transporter P glycoproteinpolymorphism that encoded by the MDR1 3435 C T gene in the susceptibility of differentiated thyroid cancer
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human Genetics Conference

Evaluation of CYP2C9 CYP2C19 and CYP2D6 gene polymorphisms in thyroid cancer
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human Genetics Conference

What about the relatives who have MTHFR C677T polymorphism
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0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human GeneticsConference

KRAS mutation genotypes and prometer methylation of tumor suppressor genes in cancer tissue and peripheral blood in colorectal cancer patients
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2012 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Human GeneticsConference