Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Shi Wu Li"'
Autor:
Zhi-Hui Yang, Xin Cai, Zhong-Li Ding, Wei Li, Chu-Yi Zhang, Jin-Hua Huo, Yue Zhang, Lu Wang, Lin-Ming Zhang, Shi-Wu Li, Ming Li, Chen Zhang, Hong Chang, Xiao Xiao
Publikováno v:
BMC Medicine, Vol 21, Iss 1, Pp 1-14 (2023)
Abstract Background Schizophrenia and bipolar disorder (BD) are believed to share clinical symptoms, genetic risk, etiological factors, and pathogenic mechanisms. We previously reported that single nucleotide polymorphisms spanning chromosome 3p21.1
Externí odkaz:
https://doaj.org/article/87ea1fa31ead4449991435132ff5af5a
Autor:
Mei-Yu Yin, Lei Guo, Li-Juan Zhao, Chen Zhang, Wei-Peng Liu, Chu-Yi Zhang, Jin-Hua Huo, Lu Wang, Shi-Wu Li, Chang-Bo Zheng, Xiao Xiao, Ming Li, Chuang Wang, Hong Chang
Publikováno v:
BMC Medicine, Vol 21, Iss 1, Pp 1-17 (2023)
Abstract Background Genome-wide association studies (GWAS) have reported single-nucleotide polymorphisms (SNPs) in the VRK serine/threonine kinase 2 gene (VRK2) showing genome-wide significant associations with major depression, but the regulation ef
Externí odkaz:
https://doaj.org/article/8f382a613f084c21b5aafce6fd25e3a7
Publikováno v:
Jichu yixue yu linchuang, Vol 41, Iss 7, Pp 1052-1055 (2021)
This review reported lipid mediators associated with inflammatory responses in adipose tissue, pro-inflammatory mediators: eicosane compounds derived from cyclooxy-genase (e.g. prostaglandins); Pro-resolving mediators: lipoxins produced by omega-6 po
Externí odkaz:
https://doaj.org/article/d622b4bcf8ff439b8b6a54fbe6811087
Publikováno v:
Organic Letters; 8/2/2024, Vol. 26 Issue 30, p6309-6313, 5p
Publikováno v:
Cogent Engineering, Vol 6, Iss 1 (2019)
In order to improve the recognition accuracy of parking space change, a new fusion model is proposed. The image-aware hash technique and image structure similarity algorithm are combined to construct a new parking space state combination discriminati
Externí odkaz:
https://doaj.org/article/ad5ccf0b0b4b437385e8857baa7847db
Publikováno v:
The Journal of Organic Chemistry. 87:5497-5509
Asymmetric catalytic vinylogous Michael addition of 2-methyl-3,5-dinitrobenzoates to unsaturated ketones catalyzed by chiral rhodium catalysts has been established. This strategy allowed the synthesis of a variety of optically pure compounds containi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6466bf4ff93a9847849c3a50abfa1dd
https://doi.org/10.1021/acs.joc.1c02757
https://doi.org/10.1021/acs.joc.1c02757
Publikováno v:
Organic Letters. 24:2585-2589
The first highly enantioselective asymmetric decarboxylative addition of β-keto acids with 3-alkenyl-oxindoles bearing an all-carbon quaternary stereocenter have been developed. The relevant products were acquired in 49-98% yields with 88-98% enanti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2a6f37fcc22435db52bb4fe9531d7c2
https://doi.org/10.1021/acs.orglett.2c00411
https://doi.org/10.1021/acs.orglett.2c00411
Publikováno v:
Organic Chemistry Frontiers. 9:3446-3451
Direct catalytic asymmetric vinylogous Michael addition to construct an acyclic all-carbon quaternary center with novel 3-alkenyl-oxindoles.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74e98f8a5eae207959430545bfdc0f64
https://doi.org/10.1039/d2qo00223j
https://doi.org/10.1039/d2qo00223j
Publikováno v:
Lecture Notes in Electrical Engineering ISBN: 9789811956140
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd382cf8ff29488692abaf2c9b9e670f
https://doi.org/10.1007/978-981-19-5615-7_9
https://doi.org/10.1007/978-981-19-5615-7_9
Autor:
Yan, Zhang, Chu-Yi, Zhang, Shi-Wu, Li, Jing, Yuan, Li, Xu, Yu-Jun, Wei, Fang, Zhou, Jun-Yang, Wang, Jin-Hua, Huo, Lu, Wang, Li-Mei, Feng, Chuan-Yuan, Kang, Jian-Zhong, Yang
Publikováno v:
Asian journal of psychiatry. 77
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a46f30c00a153fdb73a864fec74609ac
https://pubmed.ncbi.nlm.nih.gov/36181755
https://pubmed.ncbi.nlm.nih.gov/36181755