Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yingbao Zhu"'
Autor:
Guangxu Li, Yuanjiang Huang, Wenbo Han, Liyi Wei, Hongjing Huang, Yingbao Zhu, Qiao Xiao, Zujia Wang, Wen Huang, Ranhui Duan
Publikováno v:
Cell Death and Disease, Vol 15, Iss 7, Pp 1-13 (2024)
Abstract UFMylation is a highly conserved ubiquitin-like post-translational modification that catalyzes the covalent linkage of UFM1 to its target proteins. This modification plays a critical role in the maintenance of endoplasmic reticulum proteosta
Externí odkaz:
https://doaj.org/article/b21f9406ffeb47c3a48196e31193bb66
Publikováno v:
Polymers, Vol 15, Iss 19, p 3955 (2023)
Lithium–sulfur (Li-S) batteries are considered one of the most promising energy storage systems due to their high theoretical capacity, high theoretical capacity density, and low cost. However, challenges such as poor conductivity of sulfur (S) ele
Externí odkaz:
https://doaj.org/article/fe9b5fd06bac415e913a1312298b3492
Publikováno v:
Biosensors, Vol 12, Iss 10, p 876 (2022)
In recent years, many different biosensors are being used to monitor physical health. Electrospun nanofiber materials have the advantages of high specific surface area, large porosity and simple operation. These properties play a vital role in biosen
Externí odkaz:
https://doaj.org/article/a9bc332d87834f089b22364a870cf080
Autor:
Fei Gao, Wen Huang, Yanjun You, Jie Huang, Juan Zhao, Jin Xue, Huaixing Kang, Yingbao Zhu, Zhengmao Hu, Emily G. Allen, Peng Jin, Kun Xia, Ranhui Duan
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 6, Pp n/a-n/a (2020)
Abstract Background Fragile X syndrome (FXS) is the most common inherited form of intellectual disability caused by a CGG repeat expansion in the 5′ untranslated region of the FMR1 gene. When the number of repeats exceeds 200, the gene becomes hype
Externí odkaz:
https://doaj.org/article/4c49a3325c194a33b146a972c5a33cc8
Publikováno v:
FASEB journal : official publication of the Federation of American Societies for Experimental BiologyREFERENCES. 36(7)
NgBR is the Nogo-B receptor, encoded by NUS1 gene. As NgBR contains a C-terminal domain that is similar to cis-isoprenyltransferase (cis-IPTase), NgBR was speculated to stabilize nascent Niemann-Pick type C 2 (NPC2) to facilitate cholesterol transpor
Autor:
Wen Huang, Li Yu, Yingbao Zhu, Jin Xue, Beisha Tang, Ranhui Duan, Guangxu Li, Xuan Jiang, Jing Deng
Publikováno v:
The FASEB Journal. 34:1319-1330
Posttranslational modifications enhance the functional diversity of the proteome by modifying the substrates. The UFM1 cascade is a novel ubiquitin-like modification system. The mutations in UFM1, its E1 (UBA5) and E2 (UFC1), have been identified in
Autor:
Kun Xia, Yingbao Zhu, Zhengmao Hu, Juan Zhao, Jin Xue, Jie Huang, Fei Gao, Peng Jin, Yanjun You, Huaixing Kang, Wen Huang, Ranhui Duan, Emily G. Allen
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 6, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 6, Pp n/a-n/a (2020)
Background Fragile X syndrome (FXS) is the most common inherited form of intellectual disability caused by a CGG repeat expansion in the 5′ untranslated region of the FMR1 gene. When the number of repeats exceeds 200, the gene becomes hypermethylat
Publikováno v:
Chinese Journal of Integrative Medicine. 4:123-125
Objective: To observe the effect of purified Xuefu Capsule (PXC) on endothelin (ET) and nitric oxide synthetase (NOS) gene expression and proliferation of vascular smooth muscle cell (VSMC) in atherosclerotic rabbits.Methods: Molecular biological tec