Zobrazeno 1 - 10
of 42
pro vyhledávání: '"ÇİM, ABDULLAH"'
Autor:
Coşkun, Salih a, ⁎, Şimşek, Şeref b, Camkurt, Mehmet Akif c, Çim, Abdullah a, Çelik, Sercan Bulut d
Publikováno v:
In Gene 22 August 2016 588(2):109-114
Autor:
Canatan, Duran, Yılmaz, Özlem, Sönmez, Yonca, Çim, Abdullah, Baykara, Mehmet, Savaş, Murat, Coşkun, Hasan Şenol, Göksu, Sema Sezgin, Aktekin, Mehmet Rıfkı
Introduction: Prostate cancer (PCa) is a common type of cancer in western countries and prominent cause of mortality in men. The aim of the study was to evaluate miRNAs as biomarkers in PCa in healthy individuals and prostate cancer with patients, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9456::570e8a5c7005e1dde7a86da5ae7e87a3
https://doi.org/10.23750/abm.v93i3.11642
https://doi.org/10.23750/abm.v93i3.11642
Autor:
Coşkun, Salih a, ⁎, Ustyol, Lokman b, Bayram, Yasemin c, Selçuk Bektaş, M. d, Gulsen, Suleyman d, Çim, Abdullah a, Uluca, Unal e, Savaş, Didem f
Publikováno v:
In Gene 10 May 2015 562(1):128-131
Autor:
Canatan, Duran, Yılmaz, Özlem, Sönmez, Yonca, Çim, Abdullah, Coşkun, Hasan Şenol, Sezgin Göksu, Sema, Ucar, Selda, Aktekin, Mehmet Rıfkı
Publikováno v:
Acta Bio Medica : Atenei Parmensis
Breast cancer is one of the most common cancers among women and is the second leading cause of cancer-related deaths. Mammography is currently the gold standard diagnostic tool however it is not without limitations. Over the past decade, research has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::05ec5b9d31a33853e4870bdac5c04632
http://europepmc.org/articles/PMC8182592
http://europepmc.org/articles/PMC8182592
Publikováno v:
Dicle Medical Journal / Dicle Tip Dergisi. 2015, Vol. 42 Issue 4, p518-521. 4p.
Autor:
Çim, Abdullah1 drabdullahcim@yahoo.com, Coşkun, Salih1, Görükmez, Orhan2, Yüksel, Hatice3, Uluca, Ünal4, Di Pietro, Erminia5, Plourde, François5, Braverman, Nancy Elise5
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. Mar2015, Vol. 7 Issue 1, p69-72. 4p.
Noonan sendromu (NS); boy kısalığı, konjenital kalp defektleri, iskelet anomalileri ve yeleboyun ile karakterize genetik bir hastalıktır. Ayrıca kanama diyatezi, ekdodermal anomaliler, len-fatik displazi, inmemiş testis ve kognitif fonksiyonl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3346::606942296579abb61c0a650427043217
https://hdl.handle.net/11468/7875
https://hdl.handle.net/11468/7875
Autor:
Canatan, Duran1,2 durancanatan@gmail.com, Çim, Abdullah1, Delibaş, Serpil2, Altunsoy, Emel1, Ceylaner, Serdar3
Publikováno v:
Turkish Journal of Hematology. 2020, Vol. 37 Issue 2, p134-135. 2p.
Autor:
Şimşek, Şeref, Yıldırım, Veli, Çim, Abdullah, Kaya, Savaş, Şimşek, Şeref, Yıldırım, Veli, Çim, Abdullah, Kaya, Savaş
Publikováno v:
Journal of Child & Adolescent Psychopharmacology; Oct2016, Vol. 26 Issue 8, p721-726, 6p
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