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Overexpression of Shox2 Leads to Congenital Dysplasia of the Temporomandibular Joint in Mice

Our previous study reported that inactivation of Shox2 led to dysplasia and ankylosis of the temporomandibular joint (TMJ), and that replacing Shox2 with human Shox partially rescued the phenotype with a prematurely worn out articular disc. However, the mechanisms of Shox2 activity in TMJ developmen...

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Detaylı Bibliyografya
Asıl Yazarlar: Li, Xihai, Liang, Wenna, Ye, Hongzhi, Weng, Xiaping, Liu, Fayuan, Liu, Xianxiang
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: MDPI 2014
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4159784/
https://ncbi.nlm.nih.gov/pubmed/25062348
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms150813135
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