Cargando…
Dysfunction of Collagen Synthesis and Secretion in Chondrocytes Induced by Wisp3 Mutation
Wisp3 gene mutation was shown to cause spondyloepiphyseal dysplasia tarda with progressive arthropathy (SRDT-PA), but the underlying mechanism is not clear. To clarify this mechanism, we constructed the wild and mutated Wisp3 expression vectors and transfected into human chondrocytes lines C-20/A4;...
Autores principales: | Wang, Min, Man, Xiao-Fei, Liu, Ya-Qing, Liao, Er-Yuan, Shen, Zhi-Feng, Luo, Xiang-Hang, Guo, Li-Juan, Wu, Xian-Ping, Zhou, Hou-De |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614060/ https://www.ncbi.nlm.nih.gov/pubmed/23573089 http://dx.doi.org/10.1155/2013/679763 |
Ejemplares similares
-
CCN4/WISP1 Promotes Migration of Human Primary Osteoarthritic
Chondrocytes
por: Timmermans, Ritchie G.M., et al.
Publicado: (2022) -
Repairing a critical cranial defect using WISP1-pretreated
chondrocyte scaffolds
por: Carmon, Idan, et al.
Publicado: (2023) -
WISP3 mutation associated with pseudorheumatoid dysplasia
por: Sailani, M. Reza, et al.
Publicado: (2018) -
PERK-mediated translational control is required for collagen secretion in chondrocytes
por: Hisanaga, Satoshi, et al.
Publicado: (2018) -
Astrophysics Ethereal wisps
Publicado: (2009)