Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Longsheng Zhan"'
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Abstract Background The collagen alpha‐1(X) chain gene (COL10A1) is a known causative gene for Schmid metaphyseal chondrodysplasia (SMCD). This study clinically examined a Chinese family (n = 42) for SMCD and inheritance pattern. Fifteen individual
Externí odkaz:
https://doaj.org/article/f3382b9a793d4a758843d73a1c83f42b
Autor:
Fu-Rong Xiu, Ruiqi Yang, Yingying Qi, Ke Zhou, Jiali Wang, Wenting Shao, Haipeng Zhou, Longsheng Zhan
Publikováno v:
Process Safety and Environmental Protection. 174:1056-1064
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a9aa40b7b04e10ed8028e557b2cc670
https://doi.org/10.1016/j.psep.2023.05.020
https://doi.org/10.1016/j.psep.2023.05.020
Autor:
Jiao Wu, Qingguo Feng, Yuchao Wang, Jinxian Wang, Xin Zhao, Longsheng Zhan, Mengjie Liu, Zhaoqing Jin, Zhiyan Chen, Yongpeng Lei
Publikováno v:
Chemical Communications. 59:2966-2969
The polar IO-700 could effectively adsorb LiPSs and inhibit their shuttle effect, so its use as a separator modifier for Li–S batteries provides a long cycle performance with a low rate of capacity decay of 0.0487% per cycle.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50922312c4318fc477392da0c8d10e46
https://doi.org/10.1039/d2cc06893a
https://doi.org/10.1039/d2cc06893a
Autor:
Mengjie Liu, Yuchao Wang, Tingting Yu, Longsheng Zhan, Xin Zhao, Cheng Lian, Yu Xiong, Xiang Xiong, Yongpeng Lei
Publikováno v:
Science Bulletin.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aedee720e9258c604752cb3ee09f1c77
https://doi.org/10.1016/j.scib.2023.05.016
https://doi.org/10.1016/j.scib.2023.05.016
Autor:
Liming Miao, Gang Xiao, Wanqi Chen, Guisheng Yang, Denghui Hong, Zhenshan Wang, Longsheng Zhang, Weipeng Huang
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Programmed cell death ligand-1 (PD-L1) is an ideal checkpoint for immunohistochemical detection. The method of obtaining PD-L1 expression through biopsy can impact the accurate assessment of PD-L1 expression due to the spatial and temporal h
Externí odkaz:
https://doaj.org/article/3dabe050a6064f3d8bccb7f2f3c55d5d
Autor:
Xin Zhao, Yuchao Wang, Longsheng Zhan, Mengjie Liu, Jiao Wu, Danni Deng, Jiabi Jiang, Xinran Zheng, Xiang Xiong, Yongpeng Lei
Publikováno v:
Chemical Communications. 58:12716-12719
In-doped SnO2 nanoparticles with enhanced electron transfer from Sn species to In were synthesized. The maximum FEC1 was 96.46% at −0.75 V and JC1 reached −20.12 mA cm−2 at −0.95 V.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1448ddcc47eecdec7bf492b2cced99c2
https://doi.org/10.1039/d2cc05042k
https://doi.org/10.1039/d2cc05042k
Autor:
Yuchao Wang, Zisheng Huang, Yongpeng Lei, Jiao Wu, Yu Bai, Xin Zhao, Mengjie Liu, Longsheng Zhan, Shuaihao Tang, Xiaobin Zhang, Fenghua Luo, Xiang Xiong
Publikováno v:
Chemical Communications. 58:3621-3624
The abundant defects in bismuth boosted the formate selectivity of electrocatalytic CO2 reduction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d1002bcfeb10340ab6d13cb91edd58a
https://doi.org/10.1039/d2cc00114d
https://doi.org/10.1039/d2cc00114d
Publikováno v:
Korean Journal of Anesthesiology, Vol 77, Iss 3, Pp 392-396 (2024)
Background Vocal cord polyps are commonly encountered in the otorhinolaryngology department. The risk of anesthesia is high in patients with large vocal cord polyps. Awake intubation with appropriate airway tools provides a favorable safety profile.
Externí odkaz:
https://doaj.org/article/b60edbd0b7d949d2a41e46c5f8ec2680
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 10, Pp n/a-n/a (2021)
Background The collagen alpha‐1(X) chain gene (COL10A1) is a known causative gene for Schmid metaphyseal chondrodysplasia (SMCD). This study clinically examined a Chinese family (n = 42) for SMCD and inheritance pattern. Fifteen individuals were di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35123cace3b7556792154006a2aa1ff9
https://doi.org/10.1002/mgg3.1758
https://doi.org/10.1002/mgg3.1758