Başlık için Fen Edebiyat Fakültesi listeleme

Functional characterisation of the type 1 von Willebrand disease candidate VWF gene variants: p. M771I, p. L881R and p. P1413L

Berber, Ergül; Özbil, Mehmet; Brown, Christine; Başlar, Zafer; Çağlayan, S. Hande; Lillicrap, David (SIMTI Servizi, 2017)

Background. Abnormalities in the biosynthetic pathway or increased clearance of plasma von Willebrand factor (VWF) are likely to contribute to decreased plasma VWF levels in inherited type 1 von Willebrand disease (VWD). ...

Functional characterization of c.4876instgc and c2555a > g VWF gene variants identified Type 2 VWD patient population in Turkey

Berber, Ergül; Taşkan, E.; Forghieri, G.; Çolakoğlu, S.; Baltacı, O.; Koç, B.; Oymak, Y. (Wiley, 2016)

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Functional Characterization of the Type 1 VWD Candidate VWF Gene Variants: P.M771I, p.L881R, p.P1413L, and p.Q1475X

Berber, Ergül; Brown, Christine; İncekara, Kutluhan; Baslar, Zafer; Çağlayan, Hande; Lillicrap, David (AMER SOC HEMATOLOGY, 2012)

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The future of humanity and the islamic civilization

Özakpınar, Yılmaz (The Istanbul Chamber of Commerce, 2013)

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Fuzûlî’nin Şiirdeki ‘Ben’liği

Aydın Yağcıoğlu, Songül (2015)

Fuzûlî, kendi 'ben'liğine şiirlerinde özellikle değinen, bu itibarla 'ben' zamirini çok kullanan bir divan şairidir. Fuzûlî'nin bu hususiyeti üzerinde yeterince durulmadığından yapılan bu çalışma ile Fuzûlî'nin şiirlerinde ...

Gender(ed) Subjectivity and Legitimacy in “Translation”: The Case of the Old Turkish Civil Code of 1926

Bulut, Senem Öner (Yakup YILMAZ, 2018)

Bu makalenin amacı, 1907 tarihli İsviçre Medeni Kanunu’nun çevrilmesi yoluyla yapılan ve 76 yıl yürürlükte kalmış olan 1926 tarihli Eski Türk Medeni Kanunu’nun “nesebi sahih çocuklar” ile ilgili maddelerinin çevirisini ...

Gene therapy in haemophilia: literature review and regional perspectives for Turkey

Kavakli, Kaan; Antmen, Bulent; Okan, Vahap; Sahin, Fahri; Aytac, Selin; Balkan, Can; Berber, Ergul; Kaya, Zuhre; Kupesiz, Alphan; Zulfikar, Bulent (SAGE Publications Ltd, 2022)

Haemophilia is an X-linked lifelong congenital bleeding disorder that is caused by insufficient levels of factor VIII (FVIII; haemophilia A) or factor IX (FIX; haemophilia B) and characterized by spontaneous and trauma-related ...

Genel bilim metodu yaklaşımıyla bir kültür ve medeniyet teorisi

Özakpınar, Yılmaz (İstanbul Medeniyet Üniversitesi, 2014)

Kültür ve medeniyet oluşturma, canlı türleri arasında insana özgü bir olgudur. Bu olgu, başka hiçbir canlı türünde bulunmayan sembol yaratma ve sembollerle zihin işlemi yapma kapasitesinin ürünüdür. İnsan, algıladıklarına ...

General and mental health outcomes and healthcare utilization in refugees

Kilic, Cengiz; Abohalaka, Reshed; Ulug, Ozlem Seyda; Magruder, Kathy (TAYLOR & FRANCIS LTD, 2023)

Erişilememiştir. DOI numaras yoktur.

Genes and molecular mechanisms involved in the epileptogenesis of idiopathic absence epilepsies

Yalçın Çapan, Özlem (Elsevier, 2012)

Idiopathic absence epilepsies (IAE), that have high prevalence particularly among children and adolescents, are complex disorders mainly caused by genetic factors. Childhood absence epilepsy and juvenile absence epilepsy ...

Gerçeğin kuramına giriş

Özcan, Ceylin (Bağlam Yayıncılık, 2012)

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A Grammar of Chagatay

Berbercan, Mehmet Turgut (2011)

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Habit reversal training and educational group treatments for children with tourette syndrome: A preliminary randomised controlled trial

Yates, Rachel; Edwards, Katie; King, John; Luzon, Olga; Evangeli, Michael; Stark, Daniel; McFarlane, Fiona; Heyman, Isobel; İnce, Başak; Kodric, Jana; Murphy, Tara (Elsevier, 2016)

Quality of life of children with Tourette Syndrome (TS) is impacted greatly by its symptoms and their social consequences. Habit Reversal Training (HRT) is effective but has not, until now, been empirically evaluated in ...