我们总结了TBX6基因通过三个主要信号通路相互作用在脊柱发育中的关键作用
我们总结了TBX6基因通过三个主要信号通路相互作用在脊柱发育中的关键作用 Congenital vertebr […]
通过蛋白组学分析，我们揭示了先天性脊柱侧凸的潜在蛋白标记
This study is the first proteomic research to delineate the total and differential serum proteins in TBX6 haploinsufficiency-caused CS. The proteins discovered in this experiment may serve as potential biomarkers for CS, and lipid metabolism might play important roles in the pathogenesis of CS.
吴南博士受邀在加拿大Mount Sinai 医院发表演讲
Dr. Nan Wu was invited to present at the Mount Sinai Hospital, Toronto, Canada, where he introduced the genetic studies of bone and joint disease of PUMCH On October 24th, 2016.
TBX6基因罕见突变联合常见亚效等位基因导致先天性脊柱侧凸的遗传学模型
TBX6基因罕见突变联合常见亚效等位基因导致先天性脊柱侧凸的遗传学模型 Generally, the mole […]
TBX6复合遗传导致先天性脊柱侧凸被揭示
TBX6复合遗传导致先天性脊柱侧凸被揭示 A genomewide analysis of copy-numb […]
