Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Yinglong, Gao"'
Publikováno v:
iScience, Vol 26, Iss 7, Pp 107198- (2023)
Summary: Nutrients are vital to cellular activities, yet it is largely unknown how individual cells respond to nutrient deprivation. Live imaging results show that unlike the removal of amino acids or glutamine that immediately halts cell cycle progr
Externí odkaz:
https://doaj.org/article/767268070b5547fe9f281f07483b3a4b
Autor:
Lingling Li, Mingyuan Zhang, Tianhua Zhang, Yinglong Gao, Jun Ni, Yanliang Zhou, Jianxin Lin, Xiuyun Wang, Lilong Jiang
Publikováno v:
Catalysis Science & Technology. 13:2134-2141
The low-temperature N2-to-NH3 conversion of Ru/BN catalysts could be improved via dopant of Ce species. A strong Ruδ+–Ce3+ electronic interaction induced by a CeOy overlayer resulted in an excellent performance for NH3 synthesis over RuCex/BN.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b07c5a89bace142a4bd8031032e8bd8
https://doi.org/10.1039/d2cy02041f
https://doi.org/10.1039/d2cy02041f
Autor:
Jing Zheng, Zhengbiao Ying, Zhaoyang Cai, Dongmei Sun, Zheyun He, Yinglong Gao, Ting Zhang, Yi Zhu, Ye Chen, Min-Xin Guan
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0128691 (2015)
Mutations in Gap Junction Beta 2 (GJB2) have been reported to be a major cause of non-syndromic hearing loss in many populations worldwide. The spectrums and frequencies of GJB2 variants vary substantially among different ethnic groups, and the genot
Externí odkaz:
https://doaj.org/article/f89b69ba003d4be895dcb78c4bdd9506
Autor:
Tao Yang, Huimin Wu, Shiquan Wang, Qinwen Zhou, Jianwen Liu, Ying Zheng, Wei Song, Yinglong Gao, Chen Zeng, Chuanqi Feng
Publikováno v:
ACS Applied Energy Materials. 2:6952-6959
Currently extensive attention on reuse and recovery of spent lithium ion batteries has been paid by researchers, especially for power applications in electric vehicles and hybrid electric vehicles,...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::336beef17595e15ee1218cbddcf72728
https://doi.org/10.1021/acsaem.9b01647
https://doi.org/10.1021/acsaem.9b01647
Autor:
Zaiping Guo, Wenjia Xu, Ruonan Yin, Yinglong Gao, Qinwen Zhou, Jianwen Liu, Shiquan Wang, Lei You, Wei Song
Publikováno v:
Journal of Power Sources. 419:192-202
Currently extensive attentions on application of LiFePO4 batteries in electric vehicles are attracted to the researchers. Owing to the high cost of raw materials and burdensome preparation process, the re-synthesis of LiFePO4 from spent batteries bec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d89c705fcdbba01f8394d90c7f9e4906
https://doi.org/10.1016/j.jpowsour.2019.02.065
https://doi.org/10.1016/j.jpowsour.2019.02.065
Autor:
Xiaoling Liu, Min-Xin Guan, Yinglong Gao, Juanjuan Zhang, Qi‑Ping Wei, Ling Zhu, Zidong Jia, Xiaoyang Liang, Yanchun Ji, Pingping Jiang, Lihua Qiao
Publikováno v:
Molecular Medicine Reports. 16:8997-9004
Mitochondrial (mt)DNA mutations have been revealed to be associated with Leber's hereditary optic neuropathy (LHON). The present study conducted clinical, genetic and molecular evaluations of two Han Chinese families. A total of 4 (3 men and 1 female
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a02d4766814f4e2877a5245c4ba4b73a
https://doi.org/10.3892/mmr.2017.7734
https://doi.org/10.3892/mmr.2017.7734
Autor:
Xiaohui Bai, Maerhaba Aishanjiang, Feilong Meng, Yinglong Gao, Yanchun Ji, Jing Zheng, Min-Xin Guan, Haibo Wang, Yong Fu, Yun Xiao
Publikováno v:
Mitochondrion. 52
Mutations in the mitochondrial tRNAs have been reported to be the important cause of hearing loss. However, only a few cases have been identified thus far and the prevalence of mitochondrial tRNA mutations in hearing-impaired patients remain unclear.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1e2fb785220d3e4b7cf1916018d0629
https://pubmed.ncbi.nlm.nih.gov/32169613
https://pubmed.ncbi.nlm.nih.gov/32169613
Autor:
Tao Zhu, Yinglong Gao, Yinsheng Wei, Min-Xin Guan, Juanjuan Zhang, Yi Tong, Jun Qin Mo, Xiaohui Cang, Min Liang, Xiaofen Jin, Minglian Zhang, Ying Wang, Feilong Meng, Yuanyuan Lu, Pingping Jiang, Yanchun Ji, Xiaoling Liu, Qiang Li, Peifang Jiang, Jialing Yu, Taosheng Huang
Publikováno v:
Human molecular genetics. 28(9)
Mitochondrial DNA (mtDNA) mutations have been associated with Leber’s hereditary optic neuropathy (LHON) and their pathophysiology remains poorly understood. In this study, we investigated the pathophysiology of a LHON susceptibility allele (m.3394
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce586cfcec2fc2ef6e1ac3b48adeba2f
https://pubmed.ncbi.nlm.nih.gov/30597069
https://pubmed.ncbi.nlm.nih.gov/30597069
Autor:
Yinglong Gao, Zhaoyang Cai, Hui Wang, Ye Chen, Xiaowen Tang, Li Liu, Juan Yao, Min-Xin Guan, Jing Zheng, Binjiao Zheng, Zhengbiao Ying, Yi Zhu, Yu Dai
Publikováno v:
Protein & Cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f63d8765bfaad0d85c132518f24a49af
https://doi.org/10.1007/s13238-015-0203-z
https://doi.org/10.1007/s13238-015-0203-z
Autor:
Min-Xin Guan, Zhengbiao Ying, Hui Wang, Xiaowen Tang, Jing Zheng, Juan Yao, Han Yu, Ya-ling Yang, Ye Chen, Zhaoyang Cai, Yinglong Gao, Zheyun He
Publikováno v:
Mitochondrion. 23:17-24
Mutations in the mitochondrial DNA have been associated with hearing loss. However, the prevalence and spectrum of mitochondrial tRNA mutations in hearing-impaired subjects are poorly understood. In this report, we have investigated the prevalence an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5530ae8c31cca64e7c619b35198f05f9
https://doi.org/10.1016/j.mito.2015.05.001
https://doi.org/10.1016/j.mito.2015.05.001