Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Xuezhi Ouyang"'
Publikováno v:
Catalysts, Vol 12, Iss 9, p 966 (2022)
The transition metal-based catalysts have excellent electrochemical oxygen evolution reaction catalytic activity in alkaline electrolytes, attracting a significant number of researchers’ attention. Herein, we used two-step hydrothermal and solvothe
Externí odkaz:
https://doaj.org/article/957940185f2c4d3ab6f8f66ea8ee5154
Autor:
Xuezhi Ouyang1,2, Xiaoqian Ma2, Shuli Wang2, Gang Li2, Jianguo He1, Qiuyun Liu1,2 lsbrc12@zsu.edu.cn
Publikováno v:
Journal of Rapid Methods & Automation in Microbiology. Sep2006, Vol. 14 Issue 3, p283-290. 8p. 1 Diagram, 2 Charts.
Autor:
Shaun Z.S. Mok, Chee-Hoe Ng, Marc Fivaz, Valina L. Dawson, Xuezhi Ouyang, Ted M. Dawson, Fengwei Yu, Eng-King Tan, Kah-Leong Lim, Cherlyn Koh
Publikováno v:
The Journal of Neuroscience. 29:11257-11262
Mutations in theleucine-rich repeat kinase 2(LRRK2) gene are currently recognized as the most common genetic cause of parkinsonism. Among the large number of LRRK2 mutations identified to date, the G2019S variant is the most common. In Asia, however,
Publikováno v:
Journal of Rapid Methods and Automation in Microbiology. 14:389-394
A method for the rapid recovery of DNA from agarose gel slices for polymerase chain reaction (PCR) applications was described. DNA bands were excised from agarose gel and diluted with distilled water. One-minute microwave treatment at full power was
Publikováno v:
Journal of Rapid Methods and Automation in Microbiology. 14:283-290
Autor:
Chee-Hoe Ng, Xiao-Dong Zhang, Cherlyn Koh, Kah-Leong Lim, Jongkyeong Chung, Eng-King Tan, Xuezhi Ouyang, Fengwei Yu, Sharon Philomena O'Neill, Melissa S. H. Guan
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience. 32(41)
Mutations in parkin and LRRK2 together account for the majority of familial Parkinson's disease (PD) cases. Interestingly, recent evidence implicates the involvement of parkin and LRRK2 in mitochondrial homeostasis. Supporting this, we show here by m
Autor:
Kah-Leong Lim, Ruifeng Lu, Cheng Wang, Michelle W L Ho, Fengwei Yu, Xuezhi Ouyang, William Chia
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience. 27(32)
Mutations in the parkin gene are a predominant cause of familial parkinsonism. Although initially described as a recessive disorder, emerging evidence suggest that single parkin mutations alone may confer increased susceptibility to Parkinson's disea
Publikováno v:
BMC Microbiology; 2010, Vol. 10, Special section p1-11, 11p, 1 Chart, 5 Graphs
Autor:
Chee-Hoe Ng, Mok, Shaun Z. S., Koh, Cherlyn, Xuezhi Ouyang, Fivaz, Marc L., Eng-King Tan, Dawson, Valina L., Dawson, Ted M., Fengwei Yu, Kah-Leong Lim
Publikováno v:
Journal of Neuroscience; 9/9/2009, Vol. 29 Issue 36, p11257-11262, 6p, 4 Graphs
Autor:
Cheng Wang, Ruifeng Lu, Xuezhi Ouyang, Ho, Michelle W. L., Chia, William, Fengwei Yu, Lim, Kah-Leong
Publikováno v:
Journal of Neuroscience; 8/8/2007, Vol. 27 Issue 32, p8563-8570, 8p, 5 Diagrams, 3 Graphs