Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Osteoklast"'
Autor:
Gefel, Eugen
Für die Behandlung von Knochendefekten kritischer Größe gibt es heute eine Reihe von Therapiemöglichkeiten. Neuartige Ansätze mit Magnesiumphosphat- (MPC) und Calciummagnesiumphosphatzementen (CMPC) haben sich als echte Alternativen zu den etabl
Increased osteoclastogenesis contributes to bone loss in the Costello syndrome Hras G12V mouse model
Autor:
Sayantan Nandi, Saravanakkumar Chennappan, Yannik Andrasch, Miray Fidan, Melanie Engler, Mubashir Ahmad, Jan P. Tuckermann, Martin Zenker, Ion Cristian Cirstea
Publikováno v:
Frontiers in Cell and Developmental Biology. 10
RAS GTPases are ubiquitous GDP/GTP-binding proteins that function as molecular switches in cellular signalling and control numerous signalling pathways and biological processes. Pathogenic mutations in RAS genes severely affect cellular homeostasis,
Autor:
Renz, Nikolai Maximilian
Untersuchung und Phänotypisierung der Knochen von Mäusen, die mit einem Osteoklasten-spezifischen C5aR1 Knockout versehen wurden. Hierbei wurden biomechanische, radiologische und histologische Parameter für die Bewertung herangezogen.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5402b876c6fab420ae19687bbcbd80aa
Autor:
Jumaboyeva Nilufar Soyibjon Qizi, Jumaboyev Abdulla Tolibjon O'g'li, Jumaboyeva Yulduz Soyibjon Qizi, Yangiyeva Qurbonoy
Odam tanasining 1,5 - 1,7 qismi suyaklardan iborat bo‘lib, suyaklar yig‘indisiga skelet deyiladi. Skelet degan suzi grekcha ―skeleton‖ so‘zidan kelib chiqib, ―kuritilgan‖ degan ma‘noni anglatadi. Bunday ma‘noni kiritilishiga sabab,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1236f2a8c9437bbf085471013067674c
Die atrophe Pseudarthrose ist eine Komplikation der Frakturheilung. Mithilfe eines murinen Femurdefektmodells untersuchten wir die dynamische Entwicklung dieser Problematik über einen Zeitraum von insgesamt zehn Wochen. Die Ergebnisse wurden auf his
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04ebd2b95f22befd2001616dcde85068
Autor:
Oguz Kul, Şule Yurdagül Özsoy
Publikováno v:
Volume: 3, Issue: 1 71-78
Veterinary Journal of Mehmet Akif Ersoy University
Mehmet Akif Ersoy Üniversitesi Veteriner Fakültesi Dergisi, Vol 3, Iss 1, Pp 71-78 (2018)
Veterinary Journal of Mehmet Akif Ersoy University
Mehmet Akif Ersoy Üniversitesi Veteriner Fakültesi Dergisi, Vol 3, Iss 1, Pp 71-78 (2018)
Bu vaka raporunda 10 yaşlı, dişi, Setter ırkı, bir köpekte uterusta nadir gözlenen osteoklast-benzeri dev hücreli tümör bildirilmiştir. Makroskobik olarak 27x24x11 cm ölçülen tümöral kitle serviks tabanında yer alıyordu. Histopatolo
Autor:
Elson, Ari, Stein, Merle, Rabie, Grace, Barnea-Zohar, Maayan, Winograd-Katz, Sabina, Reuven, Nina, Shalev, Moran, Sekeres, Juraj, Kanaan, Moien, Tuckermann, Jan, Geiger, Benjamin
Publikováno v:
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Bone homeostasis is a complex, multi-step process, which is based primarily on a tightly orchestrated interplay between bone formation and bone resorption that is executed by osteoblasts and osteoclasts (OCLs), respectively. The essential physiologic
Autor:
Jelínková, Ivana
Introduction: Extracellular DNA (ecDNA) is a common component of blood plasma. Increased levels of ecDNA in plasma can be found in some autoimmune diseases like systemic lupus erythematosus (SLE), rheumatoid arthritis or celiac disease which are asso
Externí odkaz:
http://www.nusl.cz/ntk/nusl-436130
Autor:
Jelínková, Ivana
Introduction: Extracellular DNA (ecDNA) is a common component of blood plasma. Increased levels of ecDNA in plasma can be found in some autoimmune diseases like systemic lupus erythematosus (SLE), rheumatoid arthritis or celiac disease which are asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2186::7c3b11d620c196951159db013433cbdc
http://www.nusl.cz/ntk/nusl-436130
http://www.nusl.cz/ntk/nusl-436130
Autor:
Wagner, Alessa, Alan, Betül, Yilmaz, Dilay, Ahmad, Mubashir, Liu, Peng, Tangudu, Naveen Kumar, Tuckermann, Jan P, Vujic Spasic, Maja
Publikováno v:
JBMR Plus, Vol 3, Iss 9, Pp n/a-n/a (2019)
JBMR Plus
JBMR Plus
One of the most prevalent genetic iron overload disorders in Caucasians is caused by mutations in the HFE gene. Both HFE patients and Hfe‐mouse models develop a progressive accumulation of iron in the parenchymal cells of various tissues, eventuall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5213a0f83058b88e31c80b6129a787d8