Zobrazeno 1 - 10
of 104
pro vyhledávání: '"Kai‐Yue Zhang"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Background Oral prednisone has been recognized as the first-line therapy for the treatment of ocular myasthenia gravis (OMG). However, its long-term use is complicated by numerous adverse effects and is ineffective for some OMG patients in r
Externí odkaz:
https://doaj.org/article/2fd1fc784e5e436380e0258b9eef1ab9
Autor:
Kai‐Yue Zhang, Geng‐Jian Zhang, Hui‐Qian Duan, Qiu‐Xiang Li, Kun Huang, Li‐Qun Xu, Huan Yang, Yue‐Bei Luo
Publikováno v:
Clinical Case Reports, Vol 10, Iss 12, Pp n/a-n/a (2022)
Abstract Calsequestrin 1 (CASQ1) is the most crucial Ca2+ binding protein localized in the sarcoplasmic reticulum (SR) of skeletal muscle. With high capacity and low affinity for Ca2+, CASQ1 plays a significant role in maintaining a large amount of C
Externí odkaz:
https://doaj.org/article/4c66764f85fd49e3987badbc899c1f1b
Autor:
Kai-Yue Zhang, Chun-Nan Li, Nan-Xi Zhang, Xiao-Chen Gao, Jia-Ming Shen, Duan-Duan Cheng, Yue-Long Wang, Hui Zhang, Jing-Wei Lv, Jia-Ming Sun
Publikováno v:
Molecules, Vol 28, Iss 10, p 4064 (2023)
Testicular dysfunction (TDF) is characterized by testosterone deficiency and is caused by oxidative stress injury in Leydig cells. A natural fatty amide named N-benzylhexadecanamide (NBH), derived from cruciferous maca, has been shown to promote test
Externí odkaz:
https://doaj.org/article/4dcee319d4c1437b890b11f205aded7d
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Purpose: The aim of the present study was to evaluate the effects of dexmedetomidine compared with propofol in mechanically ventilated patients with sepsis.Methods: We searched PubMed, EMBASE, and Cochrane Library for randomized controlled trials com
Externí odkaz:
https://doaj.org/article/fd9174ab25fe418e9d11b0223fbfac2d
Autor:
Xiao-Chen Gao, Nan-Xi Zhang, Jia-Ming Shen, Jing-Wei Lv, Kai-Yue Zhang, Yao Sun, Hang Li, Yue-Long Wang, Duan-Duan Cheng, Meng-Ya Zhao, Hui Zhang, Chun-Nan Li, Jia-Ming Sun
Publikováno v:
Molecules, Vol 27, Iss 24, p 9061 (2022)
The neuroprotective properties of ginsenosides have been found to reverse the neurological damage caused by oxidation in many neurodegenerative diseases. However, the distribution of ginsenosides in different tissues of the main root, which was regar
Externí odkaz:
https://doaj.org/article/361bed22674e4069bc21853d24952f5b
Publikováno v:
BMC Microbiology, Vol 17, Iss 1, Pp 1-10 (2017)
Abstract Background Genomic islands (GIs) are genomic regions that reveal evidence of horizontal DNA transfer. They can code for many functions and may augment a bacterium’s adaptation to its host or environment. GIs have been identified in strain
Externí odkaz:
https://doaj.org/article/917c3db937574291bea8813799e90feb
Publikováno v:
Frontiers in Microbiology, Vol 10 (2019)
The in-depth study of viral genomes is of great help in many aspects, especially in the treatment of human diseases caused by viral infections. With the rapid accumulation of viral sequencing data, improved, or alternative gene-finding systems have b
Externí odkaz:
https://doaj.org/article/145e4b49b04c4e7d9a6962e2d8214e94
Autor:
Kai‐Yue Zhang, Geng‐Jian Zhang, Hui‐Qian Duan, Qiu‐Xiang Li, Kun Huang, Li‐Qun Xu, Huan Yang, Yue‐Bei Luo
Publikováno v:
Clinical Case Reports. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab0a27a1aff3ed356c3ee44409727dfb
https://doi.org/10.1002/ccr3.6689
https://doi.org/10.1002/ccr3.6689
Publikováno v:
Molecules, Vol 25, Iss 18, p 4095 (2020)
Based on the ligand H4Salen-8tBu (salen-4), a new dinuclear cobalt complex (salen-4)[Co(III)TFA]2 (salen-4 = 3,5-di-tert-butylsalicylaldehyde-3,3′-diaminobiphenylamine; TFA = trifluoroacetic acid) has been firstly synthesized and characterized. It
Externí odkaz:
https://doaj.org/article/123f926ec48e4b9e962295b22f1e8dcb
Expanding the clinicopathological‐genetic spectrum of GNE myopathy by a Chinese neuromuscular centre
Publikováno v:
Journal of Cellular and Molecular Medicine
GNE myopathy is a heterogeneous group of ultrarare neuromuscular disorders caused by mutations in the GNE gene. An estimated prevalence of 1~21/1,000,000 leads to a deficiency of data and a lack of availability of samples to conduct clinical research
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b3815ed2ff549dc0116a41642164685
https://doi.org/10.1111/jcmm.16978
https://doi.org/10.1111/jcmm.16978