Yazar "Akkiprik, Mustafa" için Fen Edebiyat Fakültesi Koleksiyonu listeleme
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Association of ACP1 genotypes and clinical parameters in patients with metabolic syndrome
Akkiprik, Mustafa; Özdemir Sertoğlu, Filiz; Çaglayan, Sinan; Aral, Cenk; Özışık, Gökhan; Atabey, Zebra; Özer, Sıdıka Ayşe (Tubitak Scientific & Technical Research Council Turkey, 2011)Aim: Acid phosphatase locus 1 (ACP1) encodes a polymorphic enzyme and has potential implications for the development of metabolic syndrome (MS) by altering insulin sensitivity. The aim of this study was to determine whether ... -
Impact of glucocorticoid receptor gene (NR3C1) polymorphisms in Turkish patients with metabolic syndrome
Kaya, Zeki; Çaglayan, S.; Akkiprik, Mustafa; Aral, Cenk; Özışık, Gökhan; Özata, M.; Özer, A. (Springer, 2016)Background The metabolic syndrome (MetS) is characterized by a cluster of metabolic factors, including insulin resistance and type-2 diabetes, abdominal obesity, dyslipidemia, hypertension and microalbuminuria. Impaired ... -
Investigation of relationship of the mitochondrial DNA 16189 T > C polymorphism with metabolic syndrome and its associated clinical parameters in Turkish patients
Aral, Cenk; Akkiprik, Mustafa; Çaglayan, Sinan; Atabey, Zehra; Özışık, Gökhan; Bekiroglu, Nuray; Özer, Ayşe (Hellenic Endocrine Soc, 2011)OBJECTIVE: Mitochondrial DNA (mtDNA) polymorphisms have been implicated in the pathophysiology of human diseases. Among them, a T>C nucleotide transition on the 16189 nucleotide position of mtDNA has been studied in several ... -
Mitochondrial DNA common deletion is not associated with thyroid, breast and colorectal tumors in Turkish patients
Aral, Cenk; Akkiprik, Mustafa; Kaya, Handan; Ataizi-Celikel, Çiğdem; Çaglayan, Sinan; Özışık, Gökhan; Özer, Ayşe (Soc Brasil Genetica, 2010)Recently, efforts have been focused on mitochondrial DNA changes and their relation to human cancers. Among them, a 4977 bp deletion of mitochondrial DNA, named common deletion, has been investigated in several types of ...