Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Xingqiao Xie"'
Autor:
Xuanyan Jia, Leishu Lin, Siqi Guo, Lulu Zhou, Gaowei Jin, Jiayuan Dong, Jinman Xiao, Xingqiao Xie, Yiming Li, Sicong He, Zhiyi Wei, Cong Yu
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-18 (2024)
Abstract Microtubule organization in cells relies on targeting mechanisms. Cytoplasmic linker proteins (CLIPs) and CLIP-associated proteins (CLASPs) are key regulators of microtubule organization, yet the underlying mechanisms remain elusive. Here, w
Externí odkaz:
https://doaj.org/article/2fdf9539cfff4df9896d18446605dca5
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-12 (2020)
Leukocyte common antigen-related receptor protein tyrosine phosphatases (LAR-RPTPs) mediate guided axon growth and synapse formation and liprin-α proteins are their intracellular binding partners. Here the authors present the crystal structure of th
Externí odkaz:
https://doaj.org/article/b7627407bf5a414782b084a50ea87bfd
Autor:
Mingfu Liang, Gaowei Jin, Xingqiao Xie, Wenchao Zhang, Kaiyue Li, Fengfeng Niu, Cong Yu, Zhiyi Wei
Publikováno v:
Cell Reports, Vol 36, Iss 4, Pp 109476- (2021)
Externí odkaz:
https://doaj.org/article/ec1689a90a5d4e65ae60b681d2ede681
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Brain’s functions, such as memory and learning, rely on synapses that are highly specialized cellular junctions connecting neurons. Functional synapses orchestrate the assembly of ion channels, receptors, enzymes, and scaffold proteins in both pre-
Externí odkaz:
https://doaj.org/article/627860cdfcc745e8bfcfbe0b6e8f4d3e
Autor:
Faxiang Li, Xingqiao Xie, Yingli Wang, Jianping Liu, Xiaofang Cheng, Yujiao Guo, Yukang Gong, Shichen Hu, Lifeng Pan
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-12 (2016)
Mutations in optineurin that cause defects in the interaction with TBK1 are associated with neurodegenerative diseases. Here, the authors report the structure of this complex, and outline a general binding mode for these proteins.
Externí odkaz:
https://doaj.org/article/6f149eadfad341e89e90455b3ba5ac86
Publikováno v:
Journal of Biomaterials Applications. 37:1767-1775
Adipose-derived mesenchymal stem cell (Ad-MSC) with capacities of releasing trophic factors and chondrogenic differentiation was a promising candidate for tracheal reconstruction. Silk fibroin (SF)- hydroxyapatite (HA) scaffolds were fabricated by th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6111328b3ae93718398abf3ef84c9736
https://doi.org/10.1177/08853282231168730
https://doi.org/10.1177/08853282231168730
Autor:
Xiangyu Chen, Xumao Li, Xidong Cui, Xingqiao Xie, Chenshan Zhang, Xinsheng Lin, Guangbin Sun, Guangfei Li
Publikováno v:
Otolaryngology–Head and Neck Surgery. 168:1245-1248
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64fda1d96e8eef69d87fdadd94191196
https://doi.org/10.1002/ohn.192
https://doi.org/10.1002/ohn.192
Autor:
Cong Yu, Mingfu Liang, Gaowei Jin, Xingqiao Xie, Kaiyue Li, Wenchao Zhang, Fengfeng Niu, Zhiyi Wei
Publikováno v:
Cell Reports, Vol 36, Iss 4, Pp 109476-(2021)
Cell Reports, Vol 34, Iss 12, Pp 108901-(2021)
Cell Reports, Vol 34, Iss 12, Pp 108901-(2021)
Brain functions rely on synapses that are highly specialized cellular junctions connecting neurons. Synaptic scaffold proteins (e.g. liprin-α, ELKS, RIM and RIM-BP) orchestrate ion channels, receptors and enzymes at presynaptic terminals to form act
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::498a81bacd428a5b49413eaca677626d
http://www.sciencedirect.com/science/article/pii/S2211124721009037
http://www.sciencedirect.com/science/article/pii/S2211124721009037
Publikováno v:
Journal of Biological Chemistry. 294:5827-5839
Focal adhesions (FAs) are specialized sites where intracellular cytoskeleton elements connect to the extracellular matrix and thereby control cell motility. FA assembly depends on various scaffold proteins, including the G protein–coupled receptor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2de11b5e83353cc5d17df56c7601f9d
https://doi.org/10.1074/jbc.ra118.006915
https://doi.org/10.1074/jbc.ra118.006915
Autor:
Chan Zhao, Chen Guo, Wenfei Pan, Ying Sun, Yuqun Xu, Cong Yu, Xingqiao Xie, Zhiyi Wei, Yanyan Ding
Publikováno v:
The Journal of Biological Chemistry
Nephrotic syndrome (NS) is a common kidney disorder caused by dysfunction of the glomerular filtration barrier. Some genetic mutations identified in NS patients cause amino acid substitutions of kidney ankyrin repeat-containing (KANK) proteins, which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba1c330d62edfb55cf9670150864b3e9
https://doi.org/10.1016/j.jbc.2021.100958
https://doi.org/10.1016/j.jbc.2021.100958