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A correlation between the genotype and clinical course in hemophilia B patients

Koç, B.; Çolakoğlu, S.; Berber, Ergül; Zülfikar, B. (Wiley, 2018-02)

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Neuroprotective strategies against calpain-mediated neurodegeneration

Yildiz-Unal, Aysegul; Korulu, Şirin; Karabay, Arzu (DOVE MEDICAL PRESS LTD, 2015)

Calpains are calcium-dependent proteolytic enzymes that have deleterious effects on neurons upon their pathological over-activation. According to the results of numerous studies to date, there is no doubt that abnormal ...

Organisational design of non-governmental organisations related to hemophilia: An example from Turkey

Büyükpınarbaşılı, Yusuf; Berber, Ergül; Zülfikar, Haluk; Bezgal, Fikret; Kılıçaslan, Şule; Balı, Fatma; Balmumucu, İsmail H.; Zülfikar, Bülent (Wiley, 2014)

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p53: Transcription factor - regulatory partner for p60-katanin

Korulu Koç, Şirin (2013)

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Lack of association of plasma factor XI with bleeding and report of two novel factor VII mutations

Keskin, E. Yılmaz; Ayhan, E.; Çolakoğlu, S.; Fettah, A.; Keskin, M.; Berber, Ergül (Pergamon-Elsevier Science, 2016)

7th International Eurasian Hematology Congress

Regional hemophilia project in Turkey

Zülfikar, Bülent; Büyükpunarbasulu, Yusuf; Kuluçoğlu, Önder; Ak, Gülsüm; Koç, Başak; Berber, Ergül; Özdemir, Nihal; Ovalu, Fahri; Türkmen, Cüneyt; Zülfikar, Haluk (Wiley, 2016)

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A Review of Functional Characterization of Single Amino Acid Change Mutations in HNF Transcription Factors in MODY Pathogenesis

Çubuk, Hasan; Yalçın Çapan, Özlem (Springer, 2021)

Mutations in HNF transcription factor genes cause the most common subtypes of maturity-onset of diabetes of youth (MODY), a monogenic form of diabetes mellitus. Mutations in the HNF1-alpha, HNF4-alpha, and HNF1-beta genes ...

Molecular dynamic simulation analysis of p.Gln852Arg VWF gene variation

Berber, Ergül; Baltacu, Oğuzhan Fatih (Wiley, 2016)

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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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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 ...