Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Zaisheng LIN"'
Autor:
Muqing Cao, Xiaoxiao Zou, Chaoyi Li, Zaisheng Lin, Ni Wang, Zhongju Zou, Youqiong Ye, Joachim Seemann, Beth Levine, Zaiming Tang, Qing Zhong
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-18 (2023)
Abstract Dysfunction of cell cycle control and defects of primary ciliogenesis are two features of many cancers. Whether these events are interconnected and the driving mechanism coordinating them remains elusive. Here, we identify an actin filament
Externí odkaz:
https://doaj.org/article/5a4e7b718e5d4006ac84d208fd7b4f6c
Autor:
Muqing Cao, Xiaoxiao Zou, Chaoyi Li, Zaisheng Lin, Ni Wang, Zhongju Zou, Youqiong Ye, Joachim Seemann, Beth Levine, Zaiming Tang, Qing Zhong
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/4b6f113d046c4d62bdde598209ce488f
Publikováno v:
环境与职业医学, Vol 39, Iss 11, Pp 1277-1283 (2022)
BackgroundPM2.5 pollution has become a widely concerned environmental health problem. Polycyclic aromatic hydrocarbons(PAHs) are the main harmful components of PM2.5, and their sources and carcinogenic risk deserve attention.ObjectiveTo analyze the s
Externí odkaz:
https://doaj.org/article/49ce4b83b48544bab206af3db8a0e32c
Autor:
Liang Wang, Xin Wen, Zhengmao Wang, Zaisheng Lin, Chunhong Li, Huilin Zhou, Huimin Yu, Yuhan Li, Yifei Cheng, Yuling Chen, Geer Lou, Junmin Pan, Muqing Cao
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-14 (2022)
Cilia project from cells to serve sensory functions, and ciliary disruption can result in multiple disorders known as ciliopathies. Here the authors show that the ciliopathy gene TCTN1 functions to regulate the ciliary transition zone and ectosome fo
Externí odkaz:
https://doaj.org/article/85d1b55cb67f4439a4edee58ba23ae86
Autor:
Minna Luo, Ruida He, Zaisheng Lin, Yue Shen, Guangyu Zhang, Zongfu Cao, Chao Lu, Dan Meng, Jing Zhang, Xu Ma, Muqing Cao
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Joubert syndrome (JBTS) and Meckel–Gruber syndrome (MKS) are rare recessive disorders caused by defects of cilia, and they share overlapping clinical features and allelic loci. Mutations of MKS1 contribute approximately 7% to all MKS cases and are
Externí odkaz:
https://doaj.org/article/25ff5ae307f843df99e0f832d1325b91
Autor:
Minna Luo, Li Cao, Zongfu Cao, Siyu Ma, Yue Shen, Di Yang, Chao Lu, Zaisheng Lin, Zhimin Liu, Yufei Yu, Ruikun Cai, Cuixia Chen, Huafang Gao, Xueyan Wang, Muqing Cao, Xu Ma
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 12, Pp n/a-n/a (2019)
Abstract Background Joubert syndrome (JS, OMIM: 213300) is a recessive developmental disorder characterized by cerebellar vermis hypoplasia and a distinctive mid‐hindbrain malformation called the “molar tooth sign” on axial magnetic resonance i
Externí odkaz:
https://doaj.org/article/9975034e43444eb393db7afdced195b9
Publikováno v:
Applied Sciences, Vol 10, Iss 10, p 3608 (2020)
We propose a compact 4He magnetometer realizing magnetic field measurement and laser-frequency stabilization simultaneously in a single 4He atomic cell. The frequency stabilization scheme is based on the asymmetric line shape of magnetic resonance wh
Externí odkaz:
https://doaj.org/article/78ae9e435c8c4cc4a09321cac2788030
Publikováno v:
Journal of Cellular Physiology. 237:2703-2712
Cilia assembly and centriole duplication are closely coordinated with cell cycle progression, and inhibition of cilia disassembly impedes cell cycle progression. The centrosomal protein trichoplein (TCHP) has been shown to promote cell cycle progress
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f41b7d0856753a6f315763526a200bac
https://doi.org/10.1002/jcp.30693
https://doi.org/10.1002/jcp.30693
Autor:
Muqing Cao, Dan Meng, Minjun Jin, Tian Zhu, Chao Lu, Yong Zhao, Xuan Zou, Huike Jiao, Gao Huafang, Chengtian Zhao, Zaisheng Lin, Yue Shen, Xueyan Wang, Li Cao, Min Huang, Hui Li, Cai Ruikun, Xu Ma, Minna Luo, Ruida He, Guanjun Luo, Cao Zongfu, Ruifang Sui, Shijing Wu
Publikováno v:
Genetics in Medicine. 23:1041-1049
Ciliopathies are a group of disorders caused by defects of the cilia. Joubert syndrome (JBTS) is a recessive and pleiotropic ciliopathy that causes cerebellar vermis hypoplasia and psychomotor delay. Although the intraflagellar transport (IFT) comple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::127ad44b0bfaf0e2964913f0402a42d6
https://doi.org/10.1038/s41436-021-01106-z
https://doi.org/10.1038/s41436-021-01106-z
Autor:
Liang Wang, Xin Wen, Zhengmao Wang, Zaisheng Lin, Chunhong Li, Huilin Zhou, Huimin Yu, Yuhan Li, Yifei Cheng, Geer Lou, Junmin Pan, Muqing Cao
The transition zone (TZ) of the cilium/flagellum serves as a diffusion barrier that controls the entry/exit of ciliary proteins. Mutations of the TZ proteins disrupt barrier function and lead to multiple human diseases. However, the systematic regula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29e853373512d5f1d0325b6fe9a06ff8
https://doi.org/10.21203/rs.3.rs-1142196/v1
https://doi.org/10.21203/rs.3.rs-1142196/v1
