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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 9, 2008
[Deficient mRNA expression of specific protein 3 gene in peripheral blood mononuclear cells from patients with multiple sclerosis]Ai-yu Lin, Qi-dong Yang, Shen-xing Murong
ACS Applied Materials & Interfaces|February 25, 2020
Organic Thin-Film Red-Light Photodiodes with Tunable Spectral Response Via Selective Exciton ActivationShen Xing, Xiao Wang, Erjuan Guo, et al.
Neurology|August 12, 2004
FSHD in Chinese population: characteristics of translocation and genotype-phenotype correlationZhi-Ying Wu, Zhi-Qiang Wang, Shen-Xing Murong, et al.
Archives of Neurology|May 21, 2003
Molecular diagnosis and prophylactic therapy for presymptomatic Chinese patients with Wilson diseaseZhi-Ying Wu, Min-Ting Lin, Shen-Xing Murong, et al.
ACS Applied Materials & Interfaces|January 18, 2018
Three-Phase Morphology Evolution in Sequentially Solution-Processed Polymer Photodetector: Toward Low Dark Current and High PhotodetectivityHanyu Wang, Shen Xing, Yifan Zheng, et al.
Zhonghua Yi Xue Za Zhi|June 19, 2003
[Genotype-phenotype correlation of patients with wilson disease in Chinese population]Zhi-ying Wu, Ning Wang, Min-ting Lin, et al.
Chinese Medical Journal|June 27, 2015
New Insights into Genotype-phenotype Correlations in Chinese Facioscapulohumeral Muscular Dystrophy: A Retrospective Analysis of 178 PatientsFeng Lin, Zhi-Qiang Wang, Min-Ting Lin, et al.
Materials Horizons|October 27, 2021
Narrowband organic photodetectors - towards miniaturized, spectroscopic sensingYazhong Wang, Jonas Kublitski, Shen Xing, et al.
Zhonghua Yi Xue Za Zhi|July 1, 2009
[Characteristics of gene structure in facioscapulohumeral muscular dystrophy-related 4q35 subtelomere and genotype-phenotype correlation in Chinese Han population]Zhi-qiang Wang, Zhi-ying Wu, Ning Wang, et al.
Journal of Molecular Medicine (Berlin, Germany)|February 25, 2011
Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>AZhi-Qiang Wang, Xue-Jiao Chen, Shen-Xing Murong, et al.
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