Publications by authors named "Ajda Coker"

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Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features.
Ahmet Arman, Abdullah Bereket, Ajda Coker, Pelin Özlem Simşek Kiper, Tülay Güran

Orphanet J Rare Dis· April 2014

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Assessment of interleukin-1 gene cluster polymorphisms in lone atrial fibrillation: new insight into the role of inflammation in atrial fibrillation.
Baris Gungor, Ahmet Ekmekci, Ahmet Arman, Kazim S Ozcan, Ekrem Ucer, Ajda Coker

Pacing Clin Electrophysiol· October 2013

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Inhibition of ornithine decarboxylase alters the roscovitine-induced mitochondrial-mediated apoptosis in MCF-7 breast cancer cells.
Elif Damla Arisan, Pinar Obakan, Ajda Coker, Narcin Palavan-Unsal

Mol Med Rep· May 2012

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Polyamine depletion enhances the roscovitine-induced apoptosis through the activation of mitochondria in HCT116 colon carcinoma cells.
Elif Damla Arısan, Ajda Coker, Narçin Palavan-Ünsal

Amino Acids· February 2012

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Association between sporadic Parkinson disease and interleukin-1 beta -511 gene polymorphisms in the Turkish population.
Ahmet Arman, Nihal Isik, Ajda Coker, Fatma Candan, Kezban Serap Becit

Eur Cytokine Netw· June 2010

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Novel growth hormone receptor gene mutation in a patient with Laron syndrome.
Ahmet Arman, Bilgin Yüksel, Ajda Coker, Ozlem Sarioz, Fatih Temiz

J Pediatr Endocrinol Metab· April 2010

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Characterization of GH-1 mutations in children with isolated growth hormone deficiency in the Turkish population.
Ajda Coker, Ergun Cetinkaya, Bumin Dundar, Zeynep Siklar, Atilla Buyukgebiz

J Pediatr Endocrinol Metab· October 2009

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Interleukin-1 receptor antagonist gene VNTR polymorphism is associated with coronary artery disease.
Ahmet Arman, Ozer Soylu, Ahmet Yildirim, Andrzej Furman, Nesrin Ercelen, Ajda Coker

Arq Bras Cardiol· November 2008

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Interleukin-1B (-511) gene polymorphism is associated with acute coronary syndrome in the Turkish population.
Ozer Soylu, Aydin Yildirim, Ajda Coker, Tuna Tezel, Edward O List

Eur Cytokine Netw· March 2008

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Novel splice site mutation in the growth hormone receptor gene in Turkish patients with Laron-type dwarfism.
Ahmet Arman, Alev Ozon, Pinar S Isguven, Ajda Coker, Ismail Peker

J Pediatr Endocrinol Metab· January 2008

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