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Ahmet Arman
Ahmet Arman
Verified email at marmara.edu.tr
Title
Cited by
Cited by
Year
Interleukin 1 activates STAT3/nuclear factor-κB cross-talk via a unique TRAF6-and p65-dependent mechanism
Y Yoshida, A Kumar, Y Koyama, H Peng, A Arman, JA Boch, PE Auron
Journal of Biological Chemistry 279 (3), 1768-1776, 2004
1682004
Interleukin-1 receptor antagonist (IL-1RN) and interleukin-1B gene polymorphisms in Turkish patients with rheumatoid arthritis
A Arman, B Yilmaz, A Coker, N Inanc, H Direskeneli
Clin Exp Rheumatol 24 (6), 643-8, 2006
532006
Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features
A Arman, A Bereket, A Coker, PÖŞ Kiper, T Güran, B Özkan, Z Atay, ...
Orphanet journal of rare diseases 9, 1-8, 2014
502014
Assessment of Interleukin‐1 Gene Cluster Polymorphisms in Lone Atrial Fibrillation: New Insight into the Role of Inflammation in Atrial Fibrillation
B Gungor, A Ekmekci, A Arman, KS Ozcan, E Ucer, AT Alper, N Calik, ...
Pacing and Clinical Electrophysiology 36 (10), 1220-1227, 2013
442013
Interleukin-1 receptor antagonist gene VNTR polymorphism is associated with coronary artery disease
A Arman, O Soylu, A Yildirim, A Furman, N Ercelen, H Aydogan, A Coker, ...
Arquivos brasileiros de cardiologia 91, 293-298, 2008
442008
Lack of association between IL-6 gene polymorphisms and rheumatoid arthritis in Turkish population
A Arman, A Coker, O Sarioz, N Inanc, H Direskeneli
Rheumatology international 32, 2199-2201, 2012
332012
Multiple sclerosis: association with the interleukin-1 gene family polymorphisms in the Turkish population
N Isik, A Arman, IA Canturk, AC Gurkan, F Candan, S Aktan, N Erzaim, ...
International Journal of Neuroscience 123 (10), 711-718, 2013
252013
Association between sporadic Parkinson disease and interleukin-1β-511 gene polymorphisms in the Turkish population
A Arman, N Isık, A Coker, F Candan, KS Becit, EO List
European cytokine network 21 (2), 116-121, 2010
232010
Interleukin-1B (-511) gene polymorphism is associated with acute coronary syndrome in the Turkish population
O Soylu, A Yildirim, A Coker, T Tezel, EO List, A Arman
European cytokine network 19 (1), 42-48, 2008
212008
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
M Dundar, U Fahrioglu, SH Yildiz, B Bakir-Gungor, SG Temel, H Akin, ...
Functional & integrative genomics 22 (3), 291-315, 2022
162022
Whole-exome sequencing reveals new potential genes and variants in patients with premature ovarian insufficiency
A Turkyilmaz, C Alavanda, EA Ates, BB Geckinli, H Polat, M Gokcu, ...
Journal of Assisted Reproduction and Genetics 39 (3), 695-710, 2022
152022
Secondary findings in 622 Turkish clinical exome sequencing data
E Arslan Ateş, A Türkyilmaz, Ö Yıldırım, C Alavanda, H Polat, Ş Demir, ...
Journal of Human Genetics 66 (11), 1113-1119, 2021
112021
Association between IL7R promoter polymorphisms and multiple sclerosis in turkish population
H Simsek, H Geckin, NP Sensoz, EO List, A Arman
Journal of Molecular Neuroscience 67, 38-47, 2019
102019
Novel growth hormone-releasing hormone receptor gene mutations in Turkish children with isolated growth hormone deficiency
A Arman, BN Dündar, E Çetinkaya, N Erzaim, A Büyükgebiz
Journal of Clinical Research in Pediatric Endocrinology 6 (4), 202, 2014
102014
Novel growth hormone receptor gene mutation in a patient with Laron syndrome
A Arman, B Yüksel, A Coker, O Sarioz, F Temiz, AK Topaloglu
Walter de Gruyter GmbH & Co. KG 23 (4), 407-414, 2010
102010
Novel splice site mutation in the growth hormone receptor gene in Turkish patients with Laron-type dwarfism
A Arman, A Ozon, PS Isguven, A Coker, I Peker, N Yordam
Journal of Pediatric Endocrinology and Metabolism 21 (1), 47-58, 2008
102008
Interleukin 1 (IL-1) induces the activation of Stat3
A Arman, PE Auron
Tissue Engineering, Stem Cells, and Gene Therapies, 297-307, 2003
102003
Array-based comparative genomic hybridization analysis in children with developmental delay/intellectual disability
A Türkyılmaz, BB Geckinli, E Tekin, EA Ates, O Yarali, AH Cebi, A Arman
Balkan Journal of Medical Genetics 24 (2), 15-24, 2022
72022
Meckel-Gruber syndrome: clinical and molecular genetic profiles in two fetuses and review of the current literature
A Turkyilmaz, BB Geckinli, C Alavanda, E Arslan Ates, EE Buyukbayrak, ...
Genetic testing and molecular biomarkers 25 (6), 445-451, 2021
72021
Characterization of GH-1 mutations in children with isolated growth hormone deficiency in the Turkish population
A Coker, E Cetinkaya, B Dundar, Z Siklar, A Buyukgebiz, A Arman
Journal of Pediatric Endocrinology and Metabolism 22 (10), 937-946, 2009
72009
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Articles 1–20