The role of TNFRSF11B in development of osteoarthritic cartilage

OBJECTIVES: OA is a complex genetic disease with different risk factors contributing to its development. One of the genes, TNFRSF11B, previously identified with gain-of-function mutation in a family with early-onset OA with chondrocalcinosis, is among the highest upregulated genes in lesioned OA car...

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Detalles Bibliográficos
Autores principales: Rodríguez Ruiz, Alejandro, Tuerlings, Margo, Das, Ankita, Coutinho de Almeida, Rodrigo, Suchiman, H Eka D, Nelissen, Rob G H H, Ramos, Yolande F M, Meulenbelt, Ingrid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Basic Science
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8824428/
https://www.ncbi.nlm.nih.gov/pubmed/33989379
http://dx.doi.org/10.1093/rheumatology/keab440

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8824428/
https://www.ncbi.nlm.nih.gov/pubmed/33989379
http://dx.doi.org/10.1093/rheumatology/keab440

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