Zobrazeno 1 - 10
of 67
pro vyhledávání: '"Ximing, Shao"'
Autor:
Binghua Cheng, Yanyan Li, Ya-Bin Ji, Wenli Shi, Meiqing Li, Jiwei Zheng, Li Ding, Ke Liu, Lijing Fang, Ye Xu, Hongchang Li, Ximing Shao
Publikováno v:
ACS Omega, Vol 9, Iss 7, Pp 7502-7510 (2024)
Externí odkaz:
https://doaj.org/article/493702b042ce4225ae8561f1fc3392d7
Autor:
Ximing Shao, Krieger-Redwood, Katya, Meichao Zhang, Hoffman, Paul, Lanzoni, Lucilla, Leech, Robert, Smallwood, Jonathan, Jefferies, Elizabeth
Publikováno v:
Journal of Neuroscience; 5/15/2024, Vol. 44 Issue 20, p1-18, 18p
Autor:
Jiwei Zheng, Wanyi He, Jing Li, Xuejia Feng, Yanyan Li, Binghua Cheng, Yimin Zhou, Meiqing Li, Ke Liu, Ximing Shao, Jianchao Zhang, Hongchang Li, Liang Chen, Lijing Fang
Publikováno v:
Journal of the American Chemical Society. 144:21831-21836
As effective ways to regulate protein levels, targeted protein degradation technologies have attracted great attention in recent years. Here, we established a novel integrin-facilitated lysosomal degradation (IFLD) strategy to degrade extracellular a
Autor:
Haishan Zhang, Ximing Shao, Yin Peng, Yanning Teng, Konda Mani Saravanan, Huiling Zhang, Hongchang Li, Yanjie Wei
Publikováno v:
PLoS Computational Biology, Vol 15, Iss 12, p e1007351 (2019)
Identification of induced pluripotent stem (iPS) progenitor cells, the iPS forming cells in early stage of reprogramming, could provide valuable information for studying the origin and underlying mechanism of iPS cells. However, it is very difficult
Externí odkaz:
https://doaj.org/article/82dcaa32c6a14e979f24cd2db4a2f804
Autor:
Chunlei Wu, Yanyan Li, Zhehong Cheng, Pengxin Wang, Zhilong Ma, Ke Liu, Yulian Cheng, Yimin Zhou, Xian Lin, Ximing Shao, Yong Yang, Hongchang Li, Lijing Fang
Publikováno v:
Chinese Chemical Letters. 33:4339-4344
Autor:
Hongchang Li, Wu Su, Rui Wang, Huashun Li, Xiaoqi Liu, Chunlei Wu, Lijiao Ao, Zhihao Ding, Yuanyan Tan, Wei Wang, Ximing Shao, Juntao Chen, Jianchao Zhang, Zhengyin Pan, Haiyan Sun, Lijing Fang, Ke Liu
Hela cells or A549 cells stably expressing histone H2B-RFP were incubated with 10 μM of different PIPs for 24 h. Cells were then subjected to live-imaging using confocal microscopy. Scale bar, 10 μm.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::766a128153244511e9a4c75d74467c14
https://doi.org/10.1158/1535-7163.22504989.v1
https://doi.org/10.1158/1535-7163.22504989.v1
Autor:
Hongchang Li, Wu Su, Rui Wang, Huashun Li, Xiaoqi Liu, Chunlei Wu, Lijiao Ao, Zhihao Ding, Yuanyan Tan, Wei Wang, Ximing Shao, Juntao Chen, Jianchao Zhang, Zhengyin Pan, Haiyan Sun, Lijing Fang, Ke Liu
(a) Hela cells or (b) A549 cells stably expressing histone H2B-RFP were incubated with 10 μM of PIP3. At different time points, cells were harvested, stained, and imaged. Scale bar, 50 μm. (c) Nuclear localization of PIP3 in A549 cells. Scale bar,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4166127333aa2a480da5d08962df46e1
https://doi.org/10.1158/1535-7163.22504992.v1
https://doi.org/10.1158/1535-7163.22504992.v1
Autor:
Hongchang Li, Wu Su, Rui Wang, Huashun Li, Xiaoqi Liu, Chunlei Wu, Lijiao Ao, Zhihao Ding, Yuanyan Tan, Wei Wang, Ximing Shao, Juntao Chen, Jianchao Zhang, Zhengyin Pan, Haiyan Sun, Lijing Fang, Ke Liu
Live imaging of mitotic progression in PIP3 treated hTERT-RPE1 cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::121a9c05b24cec33975cd4f35c4e4d71
https://doi.org/10.1158/1535-7163.22504956.v1
https://doi.org/10.1158/1535-7163.22504956.v1
Autor:
Hongchang Li, Wu Su, Rui Wang, Huashun Li, Xiaoqi Liu, Chunlei Wu, Lijiao Ao, Zhihao Ding, Yuanyan Tan, Wei Wang, Ximing Shao, Juntao Chen, Jianchao Zhang, Zhengyin Pan, Haiyan Sun, Lijing Fang, Ke Liu
(a and b) Plk1 mRNA levels (a) and Plk1 protein levels (b) in various cell lines. (c-e) Pearson correlation co-efficiency was calculated between Plk1 mRNA level, Plk1 protein expression level, and PIP3 sensitivity (represented by IC50 value).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87cde1875e2e2f8eae2ca5a43f7c239e
https://doi.org/10.1158/1535-7163.22504983.v1
https://doi.org/10.1158/1535-7163.22504983.v1
Autor:
Hongchang Li, Wu Su, Rui Wang, Huashun Li, Xiaoqi Liu, Chunlei Wu, Lijiao Ao, Zhihao Ding, Yuanyan Tan, Wei Wang, Ximing Shao, Juntao Chen, Jianchao Zhang, Zhengyin Pan, Haiyan Sun, Lijing Fang, Ke Liu
(a and b) A549 cells were treated with different concentrations of PIP2 or PIP3. After 72 h of treatment, cells were incubated with 10 ng/ml TNF-α for additional 12 h, and then harvested for IL6 (a) and IL8 (b) qRT-PCR analysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98bcf9885ac5092ba74a2a2424370335
https://doi.org/10.1158/1535-7163.22504998
https://doi.org/10.1158/1535-7163.22504998