Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Merve Alaylıoğlu"'
Autor:
Spyridon N. Karras, Erdinç Dursun, Merve Alaylıoğlu, Duygu Gezen-Ak, Stefan Pilz, Cedric Annweiler, Fatme Al Anouti
Publikováno v:
Nutrients, Vol 14, Iss 18, p 3799 (2022)
Background: Vitamin D-binding protein (VDBP) is a vital regulator of optimal vitamin D homeostasis and bioavailability. Apart from its well-documented role as a key component in vitamin D dynamic transfer and circulation, it has a myriad of immunoreg
Externí odkaz:
https://doaj.org/article/7d0f6b77a32b46048e9c141576a52423
Autor:
Nuri Aydın, Bedri Karaismailoğlu, Merve Alaylıoğlu, Duygu Gezen-Ak, Büşra Şengül, Esin Candaş, Selma Yılmazer, Erdinç Dursun
Publikováno v:
Journal of Orthopaedic Surgery, Vol 29 (2021)
Purpose: This study aimed to investigate how fibroblastic and chondrocytic properties of human meniscal fibrochondrocytes are affected in culture conditions according to the type of meniscal pathology and localization, and to provide basic informatio
Externí odkaz:
https://doaj.org/article/06525b12787544ebb2ff633f512ce199
Autor:
Mustafa Sait Gönen, Merve Alaylıoğlu, Emre Durcan, Yusuf Özdemir, Serdar Şahin, Dildar Konukoğlu, Okan Kadir Nohut, Seval Ürkmez, Berna Küçükece, İlker İnanç Balkan, H. Volkan Kara, Şermin Börekçi, Hande Özkaya, Zekayi Kutlubay, Yalım Dikmen, Yılmaz Keskindemirci, Spyridon N. Karras, Cedric Annweiler, Duygu Gezen-Ak, Erdinç Dursun
Publikováno v:
Nutrients, Vol 13, Iss 11, p 4047 (2021)
Background: We aimed to establish an acute treatment protocol to increase serum vitamin D, evaluate the effectiveness of vitamin D3 supplementation, and reveal the potential mechanisms in COVID-19. Methods: We retrospectively analyzed the data of 867
Externí odkaz:
https://doaj.org/article/fb5f9c30585348a2ad4b4e547856908e
Autor:
Spyridon N. Karras, Erdinç Dursun, Merve Alaylıoğlu, Duygu Gezen-Ak, Cedric Annweiler, Fatme Al Anouti, Hana M. A. Fakhoury, Alkiviadis Bais, Dimitrios Kiortsis
Publikováno v:
Nutrients, Vol 13, Iss 9, p 3082 (2021)
Recent results indicate that dysregulation of vitamin D-binding protein (VDBP) could be involved in the development of hypovitaminosis D, and it comprises a risk factor for adverse fetal, maternal and neonatal outcomes. Until recently, there was a pa
Externí odkaz:
https://doaj.org/article/b7d34789cb4742ff8960f74a22f7dfbd
Autor:
Spyridon N. Karras, Erdinç Dursun, Merve Alaylıoğlu, Duygu Gezen-Ak, Cedric Annweiler, Dimitrios Skoutas, Dimosthenis Evangelidis, Dimitrios Kiortsis
Publikováno v:
Nutrients, Vol 13, Iss 2, p 443 (2021)
Vitamin D receptor (VDR) polymorphisms have been associated with a plethora of adverse pregnancy and offspring outcomes. The aim of this study was to evaluate the combined effect of maternal and neonatal VDR polymorphisms (ApaI, TaqI, BsmI, FokI, Tru
Externí odkaz:
https://doaj.org/article/0cac8fb9e18b48a98a151a327db33664
Autor:
Spyridon N. Karras, Duygu Gezen-Ak, Erdinç Dursun, Merve Alaylıoğlu, Büşra Şengül, Ulaş Yavuz
Publikováno v:
In Vitro Cellular & Developmental Biology - Animal. 57:704-714
Vitamin D is a secosteroid hormone mediating its functions via vitamin D receptor (VDR) and an endoplasmic reticulum chaperone, protein disulfide isomerase A3 (PDIA3). From a physiological perspective, there is also a well-established association of
Autor:
Duygu Gezen-Ak, Merve Alaylıoğlu, Zuhal Yurttaş, Tugay Çamoğlu, Büşra Şengül, Cihan İşler, Ümit Yaşar Kına, Ebru Keskin, İrem Lütfiye Atasoy, Ali Metin Kafardar, Mustafa Uzan, Cedric Annweiler, Erdinç Dursun
Publikováno v:
The Journal of Nutritional Biochemistry. 116:109322
Autor:
Yesim Parman, Duygu Gezen-Ak, Arman Çakar, Hacer Durmus, Hasan Demirci, Erdinç Dursun, Merve Alaylıoğlu
Publikováno v:
Acta Neurologica Scandinavica. 144:640-646
Objectives Hereditary amyloidogenic transthyretin (ATTRv) amyloidosis is an autosomal dominant disorder caused by mutations of the transthyretin (TTR) gene. The mutant ATTRv protein causes a systemic accumulation of amyloid fibrils in various organs.
Autor:
Murat Emre, Fatih Tepgec, Hasmet Hanagasi, Gamze Guven, Bedia Samanci, Zeynep Tufekcioglu, John Hardy, Rita Guerreiro, Merve Alaylıoğlu, Özlem Gelişin, Hakan Gurvit, Başar Bilgiç
Publikováno v:
European Journal of Neurology. 28:2603-2613
BACKGROUND AND PURPOSE: Nasu-Hakola disease (NHD) is a rare, autosomal recessive disorder characterized by skeletal and neurological symptoms. Behavioral symptoms with cognitive impairment may mimic the behavioral variant of frontotemporal dementia (
Autor:
Beyhan, Tuysuz, Dilek, Uludag Alkaya, Filiz, Geyik, Merve, Alaylıoğlu, Busra, Kasap, Sebuh, Kurugoğlu, Yunus Emre, Akman, Mehmet, Vural, Kaya, Bilguvar
Publikováno v:
Journal of medical genetics.
Osteogenesis imperfecta (OI) is a heterogeneous group of inherited disorders characterised by susceptibility to fractures, primarily due to defects in type 1 collagen. The aim of this study is to present a novel OI phenotype and its causative candida