Browsing by Author "Yildiz, Fazilet"
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Combined point mutations in codon 12 and 13 of KRAS oncogene in prostate carcinomas
Silan, Fatma; Gultekin, Yener; Atik, Sinem; Kilinc, Davran; Alan, Cabir; Yildiz, Fazilet; Uludag, Ahmet; Ozdemir, Ozturk (SPRINGER, 2012)Prostate cancer is a common malignancy that develops by structural mutation(s) and/or other genetic alterations in specific genes.The G to T transversions in codon 12 and C to T transitions in codon 13 of KRAS proto-oncogene ... -
Epigenetic Inactivation of Tumor Suppressor SFRP2 and Point Mutation in KRAS Proto-Oncogene in Fistula - Associated Mucinous Type Anal Adenocarcinoma: Report of Two Cases
Sen, Metin; Ozdemir, Oztuerk; Turan, Mustafa; Arici, Sema; Yildiz, Fazilet; Koksal, Binnur; Goze, Fahrettin (JAPAN SOC INTERNAL MEDICINE, 2010)The secreted frizzled-related proteins (SFRPs) genes are unmethylated in normal colorectal mucosa tissue but abberant methylation profiles can be detected in colorectal cancer (CRC), adenomas, and in aberrant crypt foci. ... -
Phenylthiocarbamide taste perception as a possible genetic association marker for nutritional habits and obesity tendency of people
Dastan, Sevgi Durna; Degerli, Naci; Dastan, Taner; Yildiz, Fazilet; Yildir, Yavuz; Durna, Yusuf Muhammed; Atessahin, Dilek; Karan, Tunay (UNIV KARACHI, 2015)Ability to taste Phenylthiocarbamide (PTC) a bitter molecule, is usually used to know the heritable characteristic in both genetic and physiological studies. So far, no research has yet attested whether PTC blindness ... -
Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers
Ozdemir, Ozturk; Sezgin, Ilhan; Kurtulgan, Hande Kucuk; Candan, Ferhan; Koksal, Binnur; Sumer, Haldun; Icagasioglu, Dilara; Uslu, Atilla; Yildiz, Fazilet; Arslan, Sulhattin; Cetinkaya, Selma; Citli, Senol; Oztemur, Zekeriya; Kayatas, Mansur (SPRINGER, 2011)The Familial Mediterranean Fever (FMF) shows an autosomal recessive pattern of inheritance and affects certain ethnic groups. Disease is caused by mutations in MEFV gene and more than 180 mutations have been defined in ...