Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Cengiz Yakıcıer"'
Autor:
Ahmet Dursun, Hatice Gul Durakbasi-Dursun, Ayse Gul Zamani, Zerrin Gülin Gulbahar, Recep Dursun, Cengiz Yakicier
Publikováno v:
Mediators of Inflammation, Vol 2006 (2006)
Objectives. Behçet's disease (BD) is a systemic vasculitis with recurrent oral and genital ulcers and uveitis. MEFV gene, which is the main factor in familial Mediterranean fever (FMF), is also reported to be a susceptibility gene for BD. The pyrin
Externí odkaz:
https://doaj.org/article/1a521141283e46a497f3d74f81612f03
Autor:
Erman Aytaç, Leyla Özer, Bilgi Baca, Emre Balık, Yersu Kapran, Orhun Cığ Taşkın, Başak Oyan Uluç, Mehmet Ufuk Abacıoğlu, Murat Gönenç, Yasemin Bölükbaşı, Barbaros E. Çil, Bülent Baran, Cem Aygün, Mehmet Erdem Yıldız, Kemal Ünal, Burçak Erkol, Tunç Yaltı, Uğur Özbek, Tan Attila, Nurdan Tözün, Bengi Gürses, Sibel Erdamar, Özlem Er, Nuran Beşe, Orhan Bilge, Güralp Onur Ceyhan, Nil Molinas Mandel, Uğur Selek, Cengiz Yakıcıer, Hülya Kayserili Karabey, Murat Saruç, Volkan Özben, Eren Esen, Emre Özoran, Erkan Vardareli, Levent Güner, İsmail Hamzaoğlu, Dursun Buğra, Tayfun Karahasanoğlu, The İstanbul Group
Publikováno v:
The Turkish Journal of Gastroenterology, Vol 33, Iss 8, Pp 627-663 (2022)
Externí odkaz:
https://doaj.org/article/3a4dc67bbb9c4476af188695c8366dbe
Autor:
Hilal Keskin Karakoyun, Şirin K. Yüksel, Ilayda Amanoglu, Lara Naserikhojasteh, Ahmet Yeşilyurt, Cengiz Yakıcıer, Emel Timuçin, Cemaliye B. Akyerli
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Identifying pathogenic missense variants in hereditary cancer is critical to the efforts of patient surveillance and risk-reduction strategies. For this purpose, many different gene panels consisting of different number and/or set of genes are availa
Externí odkaz:
https://doaj.org/article/9609d396b686479bb092e4939c09e502
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 39, Iss 1, Pp 63-65
Externí odkaz:
https://doaj.org/article/f688f767512542039f5a13de06076724
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S29- (2021)
Objective: Pediatric glial tumors comprise wide range pathologies which may mimic histomorphological features of each other's but generally have very diverse disease course. WHO Classification of Tumors of Central Nervous System (2016 and 2021) point
Externí odkaz:
https://doaj.org/article/881ea9405b304f34a4816eb35c809fde
Autor:
M. Cengiz Yakıcıer, O. Uğur Sezerman, Kaya Bilguvar, Ayça Erşen Danyeli, Cemaliye B Akyerli, M. Necmettin Pamir, Özge Can, Yavuz Oktay, Ege Ülgen, Koray Özduman
Publikováno v:
Journal of Neurosurgery. 132:1435-1446
OBJECTIVEProcesses that cause or contribute to cancer, such as aging, exposure to carcinogens, or DNA damage repair deficiency (DDRd), create predictable and traceable nucleotide alterations in one’s genetic code (termed “mutational signatures”
Publikováno v:
Turkish Journal of Biochemistry. 45:451-453
Objective Despite the recent advances in diagnosis and treatment of hepatocellular carcinoma (HCC), it is still a major health problem. Therefore, understanding the molecular mechanism is very important. Our aim is to investigate the molecular basis
Autor:
Ülgen, Ege, Can, Özge, Bilguvar, Kaya, Cemaliye Akyerli Boylu, Şirin Kılıçturgay Yüksel, Danyeli, Ayça Erşen, O. Uğur Sezerman, M. Cengiz Yakıcıer, M. Necmettin Pamir, Özduman, Koray
Additional file 2. Supplementary figures and tables.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fab3bc65bcc4e4d08b00329eb259361
Autor:
Şirin Yüksel, Umut Gerlevik, Ayça Erşen Danyeli, Sıla Karacan, Cemaliye B Akyerli, Koray Özduman, O. Uğur Sezerman, Özge Can, M. Necmettin Pamir, M. Cengiz Yakıcıer, Tarik Tihan, Kaya Bilguvar, Yavuz Oktay, Ege Ülgen
Publikováno v:
Biomedicines, Vol 8, Iss 574, p 574 (2020)
Biomedicines
Volume 8
Issue 12
Biomedicines
Volume 8
Issue 12
Little is known about the mutational processes that shape the genetic landscape of gliomas. Numerous mutational processes leave marks on the genome in the form of mutations, copy number alterations, rearrangements or their combinations. To explore gl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c476df8dbbefd2e95524b3bc7546a12c
https://avesis.deu.edu.tr/publication/details/94160af9-8c10-4728-a828-32b493600f2b/oai
https://avesis.deu.edu.tr/publication/details/94160af9-8c10-4728-a828-32b493600f2b/oai
Autor:
Kaya Bilguvar, Ege Ülgen, Koray Özduman, Cemaliye Akyerli Boylu, M. Cengiz Yakıcıer, Ayça Erşen Danyeli, O. Uğur Sezerman, M. Necmettin Pamir, Özge Can, Şirin Yüksel
Publikováno v:
BMC Medical Genomics
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-14 (2021)
BMC Medical Genomics, Vol 14, Iss 1, Pp 1-14 (2021)
Background In the clinical setting, workflows for analyzing individual genomics data should be both comprehensive and convenient for clinical interpretation. In an effort for comprehensiveness and practicality, we attempted to create a clinical indiv