Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ş. Neslihan Şenel"'
Autor:
Virag Vas, Tamás Kovács, Szandra Körmendi, Andrea Bródy, Gyöngyi Kudlik, Bálint Szeder, Diána Mező, Dóra Kállai, Kitti Koprivanacz, Balázs L. Merő, Metta Dülk, József Tóvári, Péter Vajdovich, Ş. Neslihan Şenel, Ilknur Özcan, Zsuzsanna Helyes, Csaba Dobó-Nagy, László Buday
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Abstract The main driver of osteoporosis is an imbalance between bone resorption and formation. The pathogenesis of osteoporosis has also been connected to genetic alterations in key osteogenic factors and dysfunction of bone marrow mesenchymal stem/
Externí odkaz:
https://doaj.org/article/96550bcba65a4bb08c3d5a75f608f18c
Autor:
Bálint Szeder, Balázs Merő, Metta Dülk, Péter Vajdovich, József Tóvári, Andrea Brody, Ş. Neslihan Şenel, Szandra Körmendi, Virág Vas, Csaba Dobó-Nagy, Dóra Kállai, László Buday, Gyöngyi Kudlik, Tamás Kovács, İlknur Özcan, Zsuzsanna Helyes, Diána Mező, Kitti Koprivanacz
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
The main driver of osteoporosis is an imbalance between bone resorption and formation. The pathogenesis of osteoporosis has also been connected to genetic alterations in key osteogenic factors and dysfunction of bone marrow mesenchymal stem/stromal c
Publikováno v:
Dentomaxillofacial Radiology. 45:20150119
Frank–ter Haar syndrome is a genetic disease that is transmitted by autosomal recessive pattern with characteristic features such as megalocornea or glaucoma, a prominent coccyx, heart defects, developmental delays, brachycephaly, a wide anterior f