Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tinglin Ren"'
Autor:
Mingze Yao, Lei Zhang, Xiaojuan Teng, Yu Lei, Xiaoyu Xing, Tinglin Ren, Yuanqing Pan, Liwen Zhang, Zhengfeng Li, Jingxia Lin, Yaowu Zheng, Li Xing, Jiajian Zhou, Changxin Wu
Publikováno v:
Computational and Structural Biotechnology Journal, Vol 23, Iss , Pp 700-710 (2024)
Introduction: The disconnected-interacting protein 2 homolog A (DIP2A), a member of disconnected-interacting 2 protein family, has been shown to be involved in human nervous system-related mental illness. This protein is highly expressed in the nervo
Externí odkaz:
https://doaj.org/article/4f2c9fa6cc2f40fc92dc8628c2ae5261
Autor:
Mingze Yao, Yuanqing Pan, Tinglin Ren, Caiting Yang, Yu Lei, Xiaoyu Xing, Lei Zhang, Xiaogang Cui, Yaowu Zheng, Li Xing, Changxin Wu
Publikováno v:
Stem Cell Research & Therapy, Vol 14, Iss 1, Pp 1-14 (2023)
Abstract Background Disco-interacting protein 2 homolog B is a member of the Dip2 family encoded by the Dip2b gene. Dip2b is widely expressed in neuro-related tissues and is essential in axonal outgrowth during embryogenesis. Methods Dip2b knockout m
Externí odkaz:
https://doaj.org/article/d141083135fa49a4ba5ab690c68354f3
Autor:
Mingze Yao, Pengfei Su, Zhengfeng Li, Xiaogang Cui, Qian Yang, Xiaoyu Xing, Yu Lei, Mengqiao Lian, Tinglin Ren, Xiedong Wang, Yaowu Zheng, Changxin Wu
Publikováno v:
Stem Cell Research, Vol 53, Iss , Pp 102236- (2021)
DIP2 protein contains three members: DIP2A, DIP2B and DIP2C, and are broadly expressed in the nervous system from Drosophila to human during embryonic development. Dip2c gene-associated mutations have been reported in tumors and neuronal diseases. Ho
Externí odkaz:
https://doaj.org/article/a1d989e1136d45a6b47656a1217edd8b
Autor:
Mingze Yao, Qian Yang, Mengqiao Lian, Pengfei Su, Xiaogang Cui, Tinglin Ren, Xiedong Wang, Changxin Wu, Yaowu Zheng
Publikováno v:
Stem Cell Research, Vol 45, Iss , Pp - (2020)
DIP2A mutation is associated with abnormal brain development and diseases including dyslexia, autism and Alzheimer's disease. However, the role and the involved mechanisms remain unknown. To study the biological function of DIP2A during mESCs neural
Externí odkaz:
https://doaj.org/article/e26a0efdba9f41dba3a0cf184cfd64fc
Autor:
Pengfei Su, Changxin Wu, Xiaogang Cui, Tinglin Ren, Yaowu Zheng, Mingze Yao, Xiedong Wang, Qian Yang, Mengqiao Lian
Publikováno v:
Stem Cell Research, Vol 45, Iss, Pp-(2020)
DIP2A mutation is associated with abnormal brain development and diseases including dyslexia, autism and Alzheimer's disease. However, the role and the involved mechanisms remain unknown. To study the biological function of DIP2A during mESCs neural
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19b4b09e047c96bf2f571532c644e4de
https://pubmed.ncbi.nlm.nih.gov/32361465
https://pubmed.ncbi.nlm.nih.gov/32361465
Autor:
Qian Yang, Changxin Wu, Yu Lei, Mingze Yao, Xiaoyu Xing, Tinglin Ren, Yaowu Zheng, Zhengfeng Li, Pengfei Su, Xiedong Wang, Xiaogang Cui, Mengqiao Lian
Publikováno v:
Stem Cell Research, Vol 53, Iss, Pp 102236-(2021)
DIP2 protein contains three members: DIP2A, DIP2B and DIP2C, and are broadly expressed in the nervous system from Drosophila to human during embryonic development. Dip2c gene-associated mutations have been reported in tumors and neuronal diseases. Ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93672c5c5d3262f4bf7f1427ac56a189
https://doi.org/10.1016/j.scr.2021.102236
https://doi.org/10.1016/j.scr.2021.102236