Mice heterozygous for an osteogenesis imperfecta-linked MBTPS2 variant display a compromised subchondral osteocyte lacunocanalicular network associated with abnormal articular cartilage-Reference-Cited by-同舟云学术

Mice heterozygous for an osteogenesis imperfecta-linked MBTPS2 variant display a compromised subchondral osteocyte lacunocanalicular network associated with abnormal articular cartilage

Published:2023-12 Issue: Volume:177 Page:116927
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Danyukova Tatyana,Alimy Assil-Ramin,Velho Renata Voltolini,Yorgan Timur A.,Di Lorenzo Giorgia,von Kroge Simon,Tidow Henning,Wiegert J. Simon,Hermans-Borgmeyer Irm,Schinke Thorsten,Rolvien Tim,Pohl Sandra

Funder

Universitätsklinikum Hamburg-Eppendorf

Deutsche Forschungsgemeinschaft

Else Kröner-Fresenius-Stiftung

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference75 articles.

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2. DNA sequence analysis in 598 individuals with a clinical diagnosis of osteogenesis imperfecta: diagnostic yield and mutation spectrum;Bardai;Osteoporos. Int.,2016

3. Genetic causes and mechanisms of osteogenesis imperfecta;Lim;Bone,2017

4. Signaling pathways affected by mutations causing osteogenesis imperfecta;Etich;Cell. Signal.,2020

5. Osteogenesis imperfecta: mechanisms and signaling pathways connecting classical and rare OI types;Jovanovic;Endocr. Rev.,2022

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3. Alterations in compositional and cellular properties of the subchondral bone are linked to cartilage degeneration in hip osteoarthritis;Osteoarthritis and Cartilage;2024-05