Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Kirectepe Aydin A"'
Autor:
Gokce Celikyapi Erdem, Sule Erdemir, Irem Abaci, Asli K. Kirectepe Aydin, Elif Everest, Eda Tahir Turanli
Publikováno v:
Genetics and Molecular Biology, Vol 40, Iss 3, Pp 688-697 (2017)
Abstract The function of gene body DNA methylation in alternative splicing, and its relation to disease pathogenesis is not fully elucidated. The gene for familial Mediterranean fever (MEFV) encodes the pyrin protein and contains a 998 bp CpG island,
Externí odkaz:
https://doaj.org/article/9806ab04d25b4e79b525488b748e380b
Autor:
Parlar, Kerem, Tahir Turanli, Eda, Nuhoglu Kantarci, Eda, Hacioglu, Aysa, Kirectepe Aydin, Asli, Ayla, Ali Yagiz, Voyvoda, Umut, Ozdogan, Huri, Ugurlu, Serdal
Publikováno v:
Modern Rheumatology Case Reports; Jan2024, Vol. 8 Issue 1, p121-124, 3p
Publikováno v:
International Journal of Hydrogen Energy. 46:27941-27955
In this study, long term continuous bioH2 and volatile fatty acids (VFA) production potential in anaerobic membrane bioreactors (anMBR) from food waste by dark fermentation is investigated. Experiments of total 868 days are divided into 8 periods, ea
Publikováno v:
Stress. 24:348-352
A growing number of studies in humans have linked chronic stress, particularly during early life, to telomere shortening and increased oxidative stress. The effect of stress on telomerase activity, however, is understudied. Given the importance of te
Autor:
Murat Kasap, Emire Seyahi, Asli Kirectepe Aydin, Eda Tahir Turanli, Gurler Akpinar, Didar Ucar, Yesim Ozguler
Publikováno v:
Rheumatology International. 40:65-74
Behçet's syndrome (BS) is a systemic inflammatory disorder with unknown etiology. Investigation of proteome profiles of disease specific cells facilitates our understanding of the processes and related molecular pathways, especially in disorders lik
Publikováno v:
Türk Pediatri Arşivi. 52:113-121
Pediatric rheumatology includes autoinflammatory monogenic diseases, autoinflammatory multifactorial diseases with complex inheritance, and diseases with uncertain clinical diagnosis or undefined conditions, even though they show signs of autoinflamm
Autor:
Asli Kirectepe Aydin, Sule Erdemir, Eda Tahir Turanli, Elif Everest, Gokce Celikyapi Erdem, Irem Abaci
Publikováno v:
Genetics and Molecular Biology, Vol 40, Iss 3, Pp 688-697 (2017)
Genetics and Molecular Biology, Volume: 40, Issue: 3, Pages: 688-697, Published: 31 AUG 2017
Genetics and Molecular Biology v.40 n.3 2017
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
Genetics and Molecular Biology, Volume: 40, Issue: 3, Pages: 688-697, Published: 31 AUG 2017
Genetics and Molecular Biology v.40 n.3 2017
Genetics and Molecular Biology
Sociedade Brasileira de Genética (SBG)
instacron:SBG
The function of gene body DNA methylation in alternative splicing, and its relation to disease pathogenesis is not fully elucidated. The gene for familial Mediterranean fever (MEFV) encodes the pyrin protein and contains a 998 bp CpG island, covering
Autor:
Merve Özkilinç Önen, Ozan Ozkaya, Oguz Soylemezoglu, Kubra Ozturk, Sezgin Sahin, Nuray Aktay Ayaz, Ayse Balamir, Seyit Zor, Deniz Gezgin Yıldırım, Huri Ozdogan, Selçuk Yüksel, Asli Kirectepe Aydin, Abdurrahman Tufan, Eda Tahir Turanli, Serdal Ugurlu, Rukiye Eker Omeroglu, Emire Seyahi, Amra Adrovic, Kenan Barut, Selcuk Dasdemir, Mustafa Çakan, Ilker Karacan, Ozgur Kasapcopur, Betül Sözeri, Elif Everest
The second affiliation of the corresponding author Eda Tahir Turanlı was incorrectly published as İstanbul Medeniyet University instead of Istanbul Technical University.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50f269738c6412c107db8fb2b0de60c9
https://avesis.gazi.edu.tr/publication/details/73a0c837-8d23-4a35-880b-003aa90f6137/oai
https://avesis.gazi.edu.tr/publication/details/73a0c837-8d23-4a35-880b-003aa90f6137/oai
Autor:
Kirectepe Aydin, Asli, Özgüler, Yeşim, Uçar, Didar, Kasap, Murat, Akpınar, Gürler, Seyahi, Emire, Tahir Turanli, Eda
Publikováno v:
Rheumatology International; Jan2020, Vol. 40 Issue 1, p65-74, 10p, 2 Diagrams, 3 Charts
Publikováno v:
Pediatric Rheumatology Online Journal
Case A patient with juvenile onset recurrent febrile attacks associated with familial polyarteritis nodosa (PAN) and who carries CECR1 and MEFVgene mutations is described. The index case, a 23 year old male patient with recurrent attacks of fever and