Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ruobin Zhang"'
Autor:
Dali Zhang, Junlan Huang, Xianding Sun, Hangang Chen, Shuo Huang, Jing Yang, Xiaolan Du, Qiaoyan Tan, Fengtao Luo, Ruobin Zhang, Siru Zhou, Wanling Jiang, Zhenhong Ni, Zuqiang Wang, Min Jin, Meng Xu, Fangfang Li, Liang Chen, Mi Liu, Nan Su, Xiaoqing Luo, Liangjun Yin, Ying Zhu, Jerry Q. Feng, Di Chen, Huabing Qi, Lin Chen, Yangli Xie
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-16 (2021)
Different types of mesenchymal progenitors participate in ectopic bone formation. Here, the authors show Col2+ lineage cells adopt a lymphatic endothelium cell fate, which regulates local inflammatory microenvironment after trauma, thus influencing h
Externí odkaz:
https://doaj.org/article/98970981f1554eb68ed709ba30420a0f
Autor:
Xianding Sun, Yang Zhou, Ruobin Zhang, Zuqiang Wang, Meng Xu, Dali Zhang, Junlan Huang, Fengtao Luo, Fangfang Li, Zhenhong Ni, Siru Zhou, Hangang Chen, Shuai Chen, Liang Chen, Xiaolan Du, Bo Chen, Haiyang Huang, Peng Liu, Liangjun Yin, Juhui Qiu, Di Chen, Chuxia Deng, Yangli Xie, Lingfei Luo, Lin Chen
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-17 (2020)
Congenital scoliosis is a complex genetic disorder characterized by vertebral malformation. Here, the authors demonstrate that loss of dstyk leads to scoliosis in zebrafish due to dysregulated biogenesis of notochord vacuoles and that DSTYK is requir
Externí odkaz:
https://doaj.org/article/ed0a4b1f8cee4de29d66e4c76ba8d534
Autor:
Dali Zhang, Chu-Xia Deng, Meng Xu, Liangjun Yin, Peng Liu, Hangang Chen, Juhui Qiu, Yangli Xie, Fengtao Luo, Xiaolan Du, Lin Chen, Ruobin Zhang, Zhenhong Ni, Liang Chen, Xianding Sun, Zuqiang Wang, Di Chen, Fangfang Li, Shuai Chen, Junlan Huang, Bo Chen, Siru Zhou, Yang Zhou, Haiyang Huang, Lingfei Luo
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-17 (2020)
Nature Communications
Nature Communications
Congenital scoliosis (CS) is a complex genetic disorder characterized by vertebral malformations. The precise etiology of CS is not fully defined. Here, we identify that mutation in dual serine/threonine and tyrosine protein kinase (dstyk) lead to CS
Autor:
Shuo Huang, Ying Zhu, Fangfang Li, Min Jin, Nan Su, Fengtao Luo, Xiaoqing Luo, Meng Xu, Dali Zhang, Zhenhong Ni, Mi Liu, Huabing Qi, Zuqiang Wang, Yangli Xie, Qiaoyan Tan, Di Chen, Xianding Sun, Xiaolan Du, Liang Chen, Wanling Jiang, Ruobin Zhang, Siru Zhou, Junlan Huang, Lin Chen, Jerry Q. Feng, Jing Yang, Liangjun Yin, Hangang Chen
Publikováno v:
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-16 (2021)
Nature Communications, Vol 12, Iss 1, Pp 1-16 (2021)
Acquired heterotopic ossification (HO) is the extraskeletal bone formation after trauma. Various mesenchymal progenitors are reported to participate in ectopic bone formation. Here we induce acquired HO in mice by Achilles tenotomy and observe that c