Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Xi-Yuan Li"'
Publikováno v:
Frontiers in Materials, Vol 11 (2024)
Oxygen evolution reaction (OER) is one of the most important components of various electrochemical systems such as water splitting, metal air batteries, and carbon dioxide reduction. However, the four-electron process of OER suffers from intrinsicall
Externí odkaz:
https://doaj.org/article/d6ccce3075f546f698e2956c79e2057a
Autor:
Shu‐Wei Chen, Meng‐Hua Li, Jian‐Liang Liu, Jing‐Tao Chen, Jia Wang, Hui Li, Xi‐Yuan Li, Ying Zhang, Ming Song, Jia‐Xuan Lu, Wen‐Kuan Chen
Publikováno v:
Laryngoscope Investigative Otolaryngology, Vol 8, Iss 3, Pp 686-692 (2023)
Abstract Objectives To analyze the treatment outcomes and prognostic factors of mucosal melanoma of the head and neck (MMHN) from a single institution. Methods From December 1989 to November 2018, 190 patients diagnosed with MMHN were included. Survi
Externí odkaz:
https://doaj.org/article/823c8b22cf7b4ffebc4463ecad74a217
Autor:
Zhao Chen, Dongmei Li, Xi-Yuan Li, Guanlin Xiao, Xiaoli Bi, Weitao Chen, Zhiqi Shi, Xiaohui Zeng, Dongmei Sun, Li-Zhong Cao
Publikováno v:
Phytomedicine Plus, Vol 1, Iss 3, Pp 100086- (2021)
Background: Yinlan capsule is a complex TCM formulation that is prescribed for the treatment and prevention of hyperlipidemia. Our previous study indicated that one of the key targets of Yinlan is the Pregnane X Receptor (PXR). Purpose: To verify tha
Externí odkaz:
https://doaj.org/article/fc4b7744a1e04c009c27d522073c8316
Autor:
kai-yi Shu, Wei Liu, Jiu-li Zhao, Zhi-yong Zhang, Xi-yuan Li, Ba-ga Shan, Lun-Kun Ma, Ying-xiang Liang
Publikováno v:
Journal of Craniofacial Surgery. 34:591-596
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46af9c91a8f8e8e57cd02f02ec571a6d
https://doi.org/10.1097/scs.0000000000008854
https://doi.org/10.1097/scs.0000000000008854
Autor:
Tian-Jiao Wei, Dong-Xing Guan, Xi-Yuan Li, Yi-Long Hao, H. Henry Teng, Ji-Feng Yang, Yao-Yang Xu, Gang Li
Publikováno v:
Journal of Soils and Sediments. 22:1069-1079
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a57ff87afadb63c573ce4778eea924c7
https://doi.org/10.1007/s11368-022-03168-1
https://doi.org/10.1007/s11368-022-03168-1
Autor:
Yi Liu, Mengqiu Li, Jinqing Song, Ying Jin, Hui Dong, Jiong Qin, Yuwu Jiang, Yaping Tian, Zhehui Chen, Yao Zhang, Xi-Yuan Li, Ming Shen, Chunyan Zhang, Yongxing Chen, Huifeng Zhang, Yanling Yang, Yupeng Liu, Haiyan Wei, Dongxiao Li, Lulu Kang, Hongwu Zhang, Hongxin Yao, Desheng Liang, Ruxuan He, Hong Zheng, Min Huang, Ruo Mo
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Cobalamin C deficiency (cblC) caused by the MMACHC mutations is the most common type of the disorders of intracellular cobalamin metabolism. While the c.609G > A mutation is most frequent in Chinese cblC patients, its correlation with phen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f76e1246235ff8d0503fa743b92317b
http://link.springer.com/article/10.1186/s13023-020-01485-7
http://link.springer.com/article/10.1186/s13023-020-01485-7
Autor:
Xi-Yuan Li, Lulu Kang, Jianlong Men, Min Huang, Jing Ren, Yi Liu, Jinqing Song, Yang Li, Ruxuan He, Yanling Yang, Rui Ma
Publikováno v:
Clinica Chimica Acta. 503:218-222
Very long-chain acyl-coenzyme A dehydrogenase deficiency (VLCAD deficiency), a rare autosomal recessive disorder, is characterized by hypoketotic hypoglycemia, cardiomyopathy, liver damage, and myopathy. VLCAD deficiency is caused by defects of ACADV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::774d082c5a0b57b67e6d9bf5fa75011e
https://doi.org/10.1016/j.cca.2019.11.034
https://doi.org/10.1016/j.cca.2019.11.034
Autor:
Ying Xin Liu, Xi Yuan Li
Publikováno v:
Procedia Computer Science. 166:150-153
The business platform service is an e-commerce model based on campus users. The system is aimed at teachers and students. The two sides of the transaction conduct various business activities online. It is a new business operation mode that is differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::829c2293f14f4b32dda158931140acd4
https://doi.org/10.1016/j.procs.2020.02.038
https://doi.org/10.1016/j.procs.2020.02.038
Autor:
Dong Han, Lihong Wang, Yilun Tao, Chenggang Huang, Xiaoze Li, Lili Yue, Xi-Yuan Li, Dandan Lu
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 509
Ethylmalonic encephalopathy (EE) is a rare and devastating neurodegenerative disease caused by mutations in the ETHE1 gene. It is characterized by early-onset encephalopathy, chronic diarrhea, petechiae, orthostatic acrocyanosis, and high levels of m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87f775e62eee34727aa3409e0aa1bcd5
https://pubmed.ncbi.nlm.nih.gov/32485156
https://pubmed.ncbi.nlm.nih.gov/32485156
Autor:
Leopoldo Duailibe Nogueira Santos, Annie Tran, Kevin J. McElwee, Katrina Woo, Jerry Shapiro, Eddy Hsi Chun Wang, Xi Yuan Li, Sandra S Y Kim
Publikováno v:
Web of Science
Repositório Institucional da UNITAU
Universidade de Taubaté (UNITAU)
instacron:UNITAU
Acta Dermato-Venereologica, Vol 98, Iss 8, Pp 776-782 (2018)
Repositório Institucional da UNITAU
Universidade de Taubaté (UNITAU)
instacron:UNITAU
Acta Dermato-Venereologica, Vol 98, Iss 8, Pp 776-782 (2018)
Made available in DSpace on 2019-09-12T16:57:00Z (GMT). No. of bitstreams: 0 Previous issue date: 2018 Canadian Institutes of Health Research (CIHR) Banting Postdoctoral Fellowship The development of androgenetic alopecia is associated with a risk of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47d51c154e7a3c3ec2bdf8c0664ef7f0
https://doi.org/10.2340/00015555-2964
https://doi.org/10.2340/00015555-2964