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Bioresource Technology|April 20, 2013
The evolution of Anammox performance and granular sludge characteristics under the stress of phenolGuang-Feng Yang, Xia-Li Guo, Shen-Xing Chen, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|January 7, 2022
Photomultiplication-Type Organic Photodetectors for Near-Infrared Sensing with High and Bias-Independent Specific DetectivityShen Xing, Jonas Kublitski, Christian Hänisch, et al.
Nature Communications|July 16, 2021
Enhancing sub-bandgap external quantum efficiency by photomultiplication for narrowband organic near-infrared photodetectorsJonas Kublitski, Axel Fischer, Shen Xing, et al.
Journal of Child Neurology|September 12, 2013
Variations of IGHMBP2 gene was not the major cause of Han Chinese patients with non-5q-spinal muscular atrophiesXiang Lin, Qi-Jie Zhang, Jin He, et al.
Zhonghua Yi Xue Za Zhi|July 31, 2003
[Mechanism of translocation between chromosomes 4q and 10q in facioscapulohumeral muscular dystrophy]Ning Wang, Zhi-ying Wu, Chao-dong Wang, et al.
World Journal of Emergency Medicine|September 13, 2014
Therapeutic effect of recombinant tissue plasminogen activator on acute cerebral infarction at different timesMing Liu, Hai-Rong Wang, Jia-Fu Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 10, 2004
[The quantitative analysis of protein particles of erythrocyte membrane from Duchenne muscular dystrophy patients and the gene carriers]Zhi-lin Hong, Shen-xing Murong, Xiu-rong Zhong, et al.
Archives of Neurology|February 14, 2007
Molecular analysis and prenatal prediction of spinal muscular atrophy in Chinese patients by the combination of restriction fragment length polymorphism analysis, denaturing high-performance liquid chromatography, and linkage analysisWan-Jin Chen, Zhi-Ying Wu, Min-Ting Lin, et al.
BMC Medical Genetics|June 2, 2009
Rapid diagnosis of spinal muscular atrophy using high-resolution melting analysisWan Jin Chen, Wan Juan Dong, Xiao Zhen Lin, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|December 6, 2008
A novel mutation in the senataxin gene identified in a Chinese patient with sporadic amyotrophic lateral sclerosisZhen-hua Zhao, Wen-Zu Chen, Zhi-ying Wu, et al.
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