Zobrazeno 1 - 10
of 79
pro vyhledávání: '"Abdullah Tuli"'
Autor:
Ebru Dündar Yenilmez, Abdullah Tuli
Publikováno v:
Balkan Medical Journal, Vol 40, Iss 3, Pp 279-286 (2023)
Background: Hemoglobinopathies are the most common inherited diseases in humans resulting from impaired globin chain synthesis of hemoglobin. The progression of thalassemia rates is prevented with prenatal screening methods. Aims: To evaluate the he
Externí odkaz:
https://doaj.org/article/86eac92afc2a451390253bddab57ae26
Publikováno v:
Cukurova Medical Journal, Vol 46, Iss 1, Pp 208-215 (2021)
Amaç: Bu çalışmanın amacı, maternal kandaki “cell-free” fetal DNA'dan paternal mutasyon tayini için nanopolimer bazlı genosensör ile yeni bir prosedür geliştirmektir. Gereç ve Yöntem: Kuvars-kristal mikrobalans (QCM) ve biyosensör t
Externí odkaz:
https://doaj.org/article/87e201d11e39460f80ab65e50ae1bd45
Publikováno v:
Cukurova Medical Journal, Vol 44, Iss 3, Pp 882-890 (2019)
Amaç: Bu çalışmada osteoporozu olan β-talasemi hastalarında zoledronik asit tedavisinin etkinliği incelenmiştir.Gereç ve Yöntem: Çalışmaya 33 β-talasemili hasta ile kontrol grubu olarak yaş ve cinsiyetleri uyumlu 25 sağlıklı gönül
Externí odkaz:
https://doaj.org/article/3e46e013b3954bc6be5bf1fe90ff2ebd
Autor:
Guluzar Ozbolat, Abdullah Tuli
Publikováno v:
The Ukrainian Biochemical Journal, Vol 90, Iss 4, Pp 115-120 (2018)
β-Tthalassemia is common genetic disorders in Turkey that characterized by the reduced synthesis (β+) or absence (βo) of the β-globin chains in the HbA molecule. In this study, we aimed to determine the effect of the mutation type of the β-globi
Externí odkaz:
https://doaj.org/article/f9cbadcf2d0e446982c0163f77dfac4e
Autor:
Gulfidan Coskun, Leman Sencar, Abdullah Tuli, Dilek Saker, Mustafa Muhlis Alparslan, Sait Polat
Publikováno v:
International Journal of Endocrinology, Vol 2019 (2019)
Proliferation and differentiation of adult Leydig cells are mainly completed in puberty. In many studies, apart from normal postnatal development process, it is widely indicated that, through administrating EDS, Leydig cell population is eliminated a
Externí odkaz:
https://doaj.org/article/d071381dd35f42f89be759c56116223b
Publikováno v:
PLoS ONE, Vol 13, Iss 6, p e0197855 (2018)
Prenatal detection of the fetal RHD status can be useful in the management of RhD incompatibility to identify fetuses at risk of hemolytic disease. Hemolytic disease causes morbidity and mortality of the fetus in the neonatal period. The routine use
Externí odkaz:
https://doaj.org/article/f32e8bac19a7404daf982b3fa5452d7f
Publikováno v:
Cukurova Medical Journal, Vol 38, Iss 4, Pp 559-566 (2013)
Amaç: Koroner arter hastalığında (KAH) Lipoprotein (Lp) (a), homosistein (Hcy), yüksek duyarlıklı C-reaktif protein (hs-CRP) ve fibrinojen gibi majör ve diğer risk faktörlerinin tanısal değerini araştırmak amaçlanmıştır. Metotlar:
Externí odkaz:
https://doaj.org/article/ac6baf8a949544edaaaca0a66a009517
Autor:
Safiye TAGA, Hulya LEVENTERLER, Abdullah TULİ, İbrahim Ferhat ÜRÜNSAK, İbrahim Atilla ARIDOĞAN, Nesrin ERCELEN, Suna SOLMAZ, Mehmet Turan ÇETİN, Nurten DİKMEN
Publikováno v:
Cukurova Medical Journal, Vol 38, Iss 4, Pp 723-733 (2013)
Amaç: Y kromozomuna bağlı infertilite Y-bağlı kalıtım gösterir. Y kromozomunun uzun kolunda, spermatogenezden sorumlu ""Azospermik Faktör"" olarak anılan, AZFa, AZFb ve AZFc şeklinde üç farklı bölge tanımlanmıştır. Bu bölgelerin d
Externí odkaz:
https://doaj.org/article/fddc9689f8c04733874e44d8b1a96633
Autor:
Safiye Taga, Hulya Leventerler, Abdullah Tuli, Ibrahim Ferhat Urunsak, Ibrahim Atilla Aridogan, Nesrin Ercelen, Suna Solmaz, Mehmet Turan Cetin, Nurten Dikmen
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 38, Iss 4, Pp 723-733 (2013)
Purpose:Y Chromosome infertility is inherited in a Y-linked manner. Three different regions have been mapped on the long arm of the Y chromosome, named Azoospermic Factor (AZFa, AZFb and AZFc) are involved in the control of spermatogenesis. M
Externí odkaz:
https://doaj.org/article/991a36ba42bd4e6794dc355d71a9580c
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 38, Iss 4, Pp 559-566 (2013)
Backround: To evaluate the diagnostic value of major and other risk factors as lipoprotein (Lp) (a), homocysteine (Hcy), high sensitive C-reactive protein (hs-CRP) and fibrinogen in CAD patients. Methods: A total of 223 subjects (118 patients and 105
Externí odkaz:
https://doaj.org/article/695cb64414184bb18a55bd47aa85a8bb