Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Qing-xia Zhang"'
Publikováno v:
Guoji Yanke Zazhi, Vol 18, Iss 12, Pp 2213-2216 (2018)
AIM: To probe into the related influencing factors of serum lipoprotein associated phospholipase A2(Lp-PLA2)level in patients with diabetic retinopathy. METHODS: Totally 174 cases of patients with type 2 diabetes mellitus and who treated in Departmen
Externí odkaz:
https://doaj.org/article/61f0ba8fd26a4b9bba25e92ca82a911e
Autor:
Qing-Xia Zhang, Jie Li, Qin Zhang, Yi Li, Cong-Han Lei, Bai-Xue Shang, Xiao-Shuang Guan, Qing Zhang
Publikováno v:
Chinese Medical Journal, Vol 131, Iss 14, Pp 1750-1752 (2018)
Externí odkaz:
https://doaj.org/article/ef8f93fee3fc4ac8be14f6c6bcbb01fe
Publikováno v:
PLoS ONE, Vol 10, Iss 10, p e0140372 (2015)
Malignant clonal cells purification can greatly benefit basic and clinical studies in myelodysplastic syndrome (MDS). In this study, we investigated the potential of using type 1 insulin-like growth factor receptor (IGF-IR) as a marker for purificati
Externí odkaz:
https://doaj.org/article/61ce5c10b728411492fdaf5a12939e34
Autor:
Qing Xia Zhang, Zheng Wen Xiong, Shen Yu Li, Yue Yin, Cheng Lin Xing, De Yu Wen, Jian Xu, Qin Liu
Publikováno v:
Frontiers in Microbiology, Vol 13 (2022)
The rhizosphere microbe Pseudomonas protegens FD6 possesses beneficial traits such as the production of antibiotics like pyoluteorin (Plt) and 2,4-diacetylphloroglucinol (2,4-DAPG). The alternative RpoS (σ38 factor), as a master regulator, activates
Externí odkaz:
https://doaj.org/article/0f6fd72fc13a4401875776af8e3f04b5
Autor:
Hua lin Huang, Qing xia Zhang, Fei Huang, Xiao yan Long, Zhi Song, Bo Xiao, Guo liang Li, Cai yu Ma, Ding Liu
TMEM151A, located at 11q13.2 and encoding transmembrane protein 151A, was recently reported as causative for autosomal dominant paroxysmal kinesigenic dyskinesia (PKD). Here, through comprehensive analysis of sporadic and familial cases, we expand th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e1d1adee356aaff78a92e394f52516d
https://doi.org/10.21203/rs.3.rs-2390835/v1
https://doi.org/10.21203/rs.3.rs-2390835/v1
Publikováno v:
Organic letters. 24(43)
Pd-catalyzed intermolecular asymmetric allylic dearomatization of substituted β-naphthol derivatives with Boc-protected Morita-Baylis-Hillman (MBH) adducts was developed. The reaction occurs smoothly in 1,4-dioxane at room temperature in the presenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e72763029e52554487be5b6607e7a43
https://pubmed.ncbi.nlm.nih.gov/36264244
https://pubmed.ncbi.nlm.nih.gov/36264244
Autor:
Ding Liu, Pei-Hao Lin, Hui-Lu Li, Jie Yang, Yong You, Xiao Yang, Li-Hong Jiang, Cai-Yu Ma, Lu-Fen Xu, Qing-Xia Zhang, Sha Liao, Han Chen, Jia-Jia Yue, Yu-Ying Lu, Chun Lian, Yin Liu, Zhan-Hang Wang, Jin-Long Ye, Wei Qiu, Ya-Qing Shu
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry; Aug2023, Vol. 94 Issue 8, p605-613, 9p
Publikováno v:
Angewandte Chemie. 133:17749-17755
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::392fc6479fe4f8aa3edd4774fa44bbb9
https://doi.org/10.1002/ange.202104788
https://doi.org/10.1002/ange.202104788
Publikováno v:
Angewandte Chemie. 132:4580-4586
The enantioselective ketimine-ene reaction is one of the most challenging stereocontrolled reaction types in organic synthesis. In this work, catalytic enantioselective ketimine-ene reactions of 2-aryl-3H-indol-3-ones with α-methylstyrenes were achi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03364c321ddb335f3d9b57671bf0f418
https://doi.org/10.1002/ange.201915226
https://doi.org/10.1002/ange.201915226
Publikováno v:
Chemical Communications. 56:261-264
Herein, we disclosed an efficient protocol for the construction of chiral 3-allyl-3-hydroxyoxindoles via the enantioselective allylation reaction of isatins and allylboronates catalyzed by a simple binary acid Bi(OAc)3/CPA system under mild condition
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbb9d394fe58862008bb7c7757f152ba
https://doi.org/10.1039/c9cc07944k
https://doi.org/10.1039/c9cc07944k