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Shengxin Xu

tongji university

18H指数
48论文数
1.5K被引数
收录论文 20
发表时间
CLCN2 chloride channel mutations in familial hyperaldosteronism type II
err2018-02-05
err177
errOAAI
errScholl, Ute I.; Stoelting, Gabriel; Schewe, Julia; Thiel, Anne; Tan, Hua; Nelson-Williams, Carol; Vichot, Alfred A.; Jin, Sheng Chih; Loring, Erin; Untiet, Verena; Yoo, Taekyeong; Choi, Jungmin; Xu, Shengxin; Wu, Aihua; Kirchner, Marieluise; Mertins, Philipp; Rump, Lars C.; Onder, Ali Mirza; Gamble, Cory; McKenney, Daniel; Lash, Robert W.; Jones, Deborah P.; Chune, Gary; Gagliardi, Priscila; Choi, Murim; Gordon, Richard; Stowasser, Michael; Fahlke, Christoph; Lifton, Richard P.
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Towards robust and efficient device-free localization using UWB sensor network
err2017-10-01
err11
errOAAI
errWang, Zhenghuan; Liu, Heng; Xu, Shengxin; Gao, Fei; Bu, Xiangyuan; An, Jianping
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Bayesian Device-Free Localization and Tracking in a Binary RF Sensor Network
errSENSORS
IF3.5
err2017-04-27
err14
errOAAI
errWang, Zhenghuan; Liu, Heng; Xu, Shengxin; Bu, Xiangyuan; An, Jianping
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A Diffraction Measurement Model and Particle Filter Tracking Method for RSS-Based DFL
err2015-11-01
err60
PREAI
errWang, Zhenghuan; Liu, Heng; Xu, Shengxin; Bu, Xiangyuan; An, Jianping
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Seated Saline Suppression Testing For The Diagnosis Of Primary Aldosteronism: A Preliminary Study
err2014-08-01
err105
errOAAI
errAhmed, Ashraf H.; Cowley, Diane; Wolley, Martin; Gordon, Richard D.; Xu, Shengxin; Taylor, Paul J.; Stowasser, Michael
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Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome)
err2014-02-03
err44
errOAAI
errGlover, Mark; Ware, James S.; Henry, Amanda; Wolley, Martin; Walsh, Roddy; Wain, Louise V.; Xu, Shengxin; Van't Hoff, William G.; Tobin, Martin D.; Hall, Ian P.; Cook, Stuart; Gordon, Richard D.; Stowasser, Michael; O'Shaughnessy, Kevin M.
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Somatic Mutations Affecting the Selectivity Filter of KCNJ5 Are Frequent in 2 Large Unselected Collections of Adrenal Aldosteronomas
err2012-03-01
err138
errOAAI
errAzizan, Elena A. B.; Murthy, Meena; Stowasser, Michael; Gordon, Richard; Kowalski, Bartosz; Xu, Shengxin; Brown, Morris J.; O'Shaughnessy, Kevin M.
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Novel splice-site and frameshift ATP2A2 mutations in Chinese patients with Darier disease
err2012-02-14
err3
PREAI
errShi, H. J.; Li, M.; Zhang, G. L.; Xu, S. X.; Shao, M. H.; Gu, Y.; Du, X. F.; Mu, H. J.; Xie, P.
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A single nucleotide polymorphism of MHC region is associated with subphenotypes of Psoriasis in Chinese population
err2010-07-01
err6
PREAI
errZheng, Hou-Feng; Zhang, Chi; Sun, Liang-Dan; Ni, Cheng; Zuo, Xian-Bo; Zhang, Zheng; Lu, Wen-Sheng; Xu, Sheng-Xin; Han, Jian-Wen; Cheng, Hui; Zhu, Kun-Ju; Cheng, Yi-Lin; Yang, Sen; Zhang, Feng-Yu; Zhang, Xue-Jun
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Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC白癜风的全基因组关联研究确定了6q27和MHC的易感基因位点
err2010-06-06
err177
PREAI
errQuan, Cheng; Ren, Yun-Qing; Xiang, Lei-Hong; Sun, Liang-Dan; Xu, Ai-E; Gao, Xing-Hua; Chen, Hong-Duo; Pu, Xiong-Ming; Wu, Ri-Na; Liang, Chao-Zhao; Li, Jia-Bin; Gao, Tian-Wen; Zhang, Jian-Zhong; Wang, Xiu-Li; Wang, Jun; Yang, Rong-Ya; Liang, Ling; Yu, Jian-Bin; Zuo, Xian-Bo; Zhang, Sheng-Quan; Zhang, Shu-Mei; Chen, Gang; Zheng, Xiao-Dong; Li, Pan; Zhu, Jun; Li, Yong-Wei; Wei, Xiao-Dong; Hong, Wei-Song; Ye, Ying; Zhang, Yong; Wu, Wei-Su; Cheng, Hui; Dong, Pu-Ling; Hu, Da-Yan; Li, Yang; Li, Min; Zhang, Xin; Tang, Hua-Yang; Tang, Xian-Fa; Xu, Sheng-Xin; He, Su-Min; Lv, Yong-Mei; Shen, Min; Jiang, Hong-Quan; Wang, Ying; Li, Kai; Kang, Xiao-Jing; Liu, Yu-Qin; Sun, Li; Liu, Zhi-Fang; Xie, Shao-Qiong; Zhu, Cheng-Yao; Xu, Qiang; Gao, Jin-Ping; Hu, Wen-Long; Ni, Cheng; Pan, Ting-Meng; Li, Yun; Yao, Sha; He, Cai-Feng; Liu, Yang-Sheng; Yu, Ze-Ying; Yin, Xian-Yong; Zhang, Feng-Yu; Yang, Sen; Zhou, Youwen; Zhang, Xue-Jun
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Compound Astragalus and Salvia miltiorrhiza extract inhibits cell invasion by modulating transforming growth factor-β/Smad in HepG2 cell
err2010-01-28
err70
PREAI
errLiu, Xin; Yang, Yan; Zhang, Xiaoxiang; Xu, Shengxin; He, Shufang; Huang, Weijuan; Roberts, Michael S.
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A novel U2HR non-synonymous mutation in a Chinese patient with Marie Unna Hereditary Hypotrichosis
err2009-08-01
err9
PREAI
errCai, Li-Qiong; Wang, Pei-Guang; Gao, Min; Lu, Wen-Sheng; Xu, Sheng-Xin; Fang, Qiao-Yun; Zhou, Wen-Ming; Lin, Da; Du, Wen-Hui; Zhang, Shu-Mei; Yang, Sen; Zhang, Xue-Jun
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Genetic Variation of Promoter Sequence Modulates XBP1 Expression and Genetic Risk for Vitiligo
err2009-06-19
err75
errOAAI
errRen, Yunqing; Yang, Sen; Xu, Shengxin; Gao, Min; Huang, Wei; Gao, Tianwen; Fang, Qiaoyun; Quan, Cheng; Zhang, Chi; Sun, Liangdan; Liang, Yanhua; Han, Jianwen; Wang, Zhimin; Zhang, Fengyu; Zhou, Youwen; Liu, Jianjun; Zhang, Xuejun
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Follow-up analysis of 180 Chinese Han families: identification of a novel locus for psoriasis at 2p22.3-11.2
err2008-01-30
err9
PREAI
errSun, L. D.; Yang, S.; Liu, J. J.; Ren, Y. Q.; Fan, X.; Xu, S. X.; Zhou, L.; Yang, C. J.; Xiao, F. L.; Gao, M.; Cui, Y.; Du, W. H.; Huang, W.; Zhang, X. J.
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HLA haplotypic association with different phenotype of alopecia areata in Chinese Hans
err2007-03-01
err3
PREAI
errXiao, Feng-Li; Yang, Sen; Lin, Guo-Shu; Gao, Min; Cui, Yong; Yin, Xian-Yong; Wang, Pei-Guang; Xu, Shengxin; Zhang, Xue-Jun
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