Cargando…
A mutation in SLC20A2 (c.C1849T) promotes proliferation while inhibiting hypertrophic differentiation in ATDC5 chondrocytes
AIMS: This study aimed to investigate the effect of solute carrier family 20 member 2 (SLC20A2) gene mutation (identified from a hereditary multiple exostoses family) on chondrocyte proliferation and differentiation. METHODS: ATDC5 chondrocytes were cultured in insulin-transferrin-selenium medium to...
Autores principales: | Li, YiQiang, Lin, XueMei, Zhu, MingWei, Xun, FuXing, Li, JingChun, Yuan, Zhe, Liu, YanHan, Xu, HongWen |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The British Editorial Society of Bone & Joint Surgery
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7649514/ https://www.ncbi.nlm.nih.gov/pubmed/33135420 http://dx.doi.org/10.1302/2046-3758.911.BJR-2020-0112.R1 |
Ejemplares similares
-
Whole-exome sequencing identifies a novel mutation of SLC20A2 (c.C1849T) as a possible cause of hereditary multiple exostoses in a Chinese family
por: Li, Yiqiang, et al.
Publicado: (2020) -
GDF11 inhibits abnormal adipogenesis of condylar chondrocytes in temporomandibular joint osteoarthritis
por: Wang, Helin, et al.
Publicado: (2022) -
Decreased Peli1 expression attenuates osteoarthritis by protecting chondrocytes and inhibiting M1-polarization of macrophages
por: Mo, Haokun, et al.
Publicado: (2023) -
Clinical evaluation after matrix-associated autologous chondrocyte transplantation: a comparison of four different graft types
por: Binder, Harald, et al.
Publicado: (2021) -
Upregulated ribosome pathway plays a key role in HDAC4, improving the survival rate and biofunction of chondrocytes
por: Guo, Li, et al.
Publicado: (2023)