Sökresultat med upphovsmän

1

Functional Characterization and Neuronal Modeling of the Effects of Childhood Absence Epilepsy Variants ofCACNA1H, a T-Type Calcium Channel av Iuliia Vitko, Yucai Chen, Juan Manuel Arias, Yen Shen, Xiru Wu, Edward Perez‐Reyes

Publicerad 2005

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ATP1A3 Mutations and Genotype-Phenotype Correlation of Alternating Hemiplegia of Childhood in Chinese Patients av Cheng Yang, Hua Gao, Jie Zhang, Xiaojing Xu, Xiaoyan Liu, Xiru Wu, Liping Wei, Yuehua Zhang

Publicerad 2014

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SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures av Jiaping Wang, Hua Gao, Xinhua Bao, Qingping Zhang, Jiarui Li, Liping Wei, Xiru Wu, Yan Chen, Shujie Yu

Publicerad 2017

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Phenotype–Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy av Dandan Tan, Haipo Yang, Yun Yuan, Carsten G. Bönnemann, Xingzhi Chang, Shuang Wang, Yuchen Wu, Xiru Wu, Hui Xiong

Publicerad 2015

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SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus av Huihui Sun, Yuehua Zhang, Jianmin Liang, Xiaoyan Liu, Xiuwei Ma, Husheng Wu, Keming Xu, Jiong Qin, Yu Qi, Xiru Wu

Publicerad 2008

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<scp>SCN</scp>8A mutations in Chinese children with early onset epilepsy and intellectual disability av Weijing Kong, Yujia Zhang, Yang Gao, Xiaoyan Liu, Kai Gao, Han Xie, Jingmin Wang, Ye Wu, Yuehua Zhang, Xiru Wu, Yuwu Jiang

Publicerad 2015

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Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental Disabilities av Yujia Zhang, Weijing Kong, Yang Gao, Xiaoyan Liu, Kai Gao, Han Xie, Ye Wu, Yuehua Zhang, Jingmin Wang, Feng Gao, Xiru Wu, Yuwu Jiang

Publicerad 2015

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Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort av Xiaoxu Yang, Aijie Liu, Xiaojing Xu, Xiaoling Yang, Qi Zeng, Adam Yongxin Ye, Zhe Yu, Sheng Wang, August Yue Huang, Xiru Wu, Qixi Wu, Liping Wei, Yuehua Zhang

Publicerad 2017

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Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “ de novo ” SCN1A Mutations in Children with Dravet Syndrome av Xiaojing Xu, Xiaoxu Yang, Qixi Wu, Aijie Liu, Xiaoling Yang, Adam Yongxin Ye, August Yue Huang, Jiarui Li, Meng Wang, Zhe Yu, Sheng Wang, Zhichao Zhang, Xiru Wu, Liping Wei, Yuehua Zhang

Publicerad 2015

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Association between genetic variation of CACNA1H and childhood absence epilepsy av Yucai Chen, Jianjun Lu, Hong Pan, Yuehua Zhang, Husheng Wu, Keming Xu, Xiaoyan Liu, Yuwu Jiang, Xinhua Bao, Zhijian Yao, Keyue Ding, Wilson H.Y. Lo, Boqin Qiang, Piu Chan, Yan Shen, Xiru Wu

Publicerad 2003

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Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation av Ye Wu, Taoyun Ji, Jingmin Wang, Jing Xiao, Huifang Wang, Jie Li, Zhijie Gao, Yanling Yang, Bin Cai, Liwen Wang, Zhongshu Zhou, Lili Tian, Xiaozhu Wang, Nan Zhong, Jiong Qin, Xiru Wu, Yuwu Jiang

Publicerad 2010

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Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals av August Yue Huang, Xiaojing Xu, Adam Yongxin Ye, Qixi Wu, Linlin Yan, Boxun Zhao, Xiaoxu Yang, Yao He, Sheng Wang, Zheng Zhang, Bowen Gu, Hanqing Zhao, Meng Wang, Hua Gao, Ge Gao, Zhichao Zhang, Xiaoling Yang, Xiru Wu, Yuehua Zhang, Liping Wei

Publicerad 2014

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Functional Characterization and Neuronal Modeling of the Effects of Childhood Absence Epilepsy Variants of<i>CACNA1H</i>, a T-Type Calcium Channel av Iuliia Vitko, Yucai Chen, Juan Manuel Arias, Yen Shen, Xiru Wu, Edward Perez‐Reyes

ATP1A3 Mutations and Genotype-Phenotype Correlation of Alternating Hemiplegia of Childhood in Chinese Patients av Cheng Yang, Hua Gao, Jie Zhang, Xiaojing Xu, Xiaoyan Liu, Xiru Wu, Liping Wei, Yuehua Zhang

SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures av Jiaping Wang, Hua Gao, Xinhua Bao, Qingping Zhang, Jiarui Li, Liping Wei, Xiru Wu, Yan Chen, Shujie Yu

Phenotype–Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy av Dandan Tan, Haipo Yang, Yun Yuan, Carsten G. Bönnemann, Xingzhi Chang, Shuang Wang, Yuchen Wu, Xiru Wu, Hui Xiong

SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus av Huihui Sun, Yuehua Zhang, Jianmin Liang, Xiaoyan Liu, Xiuwei Ma, Husheng Wu, Keming Xu, Jiong Qin, Yu Qi, Xiru Wu

<i><scp>SCN</scp>8A</i> mutations in Chinese children with early onset epilepsy and intellectual disability av Weijing Kong, Yujia Zhang, Yang Gao, Xiaoyan Liu, Kai Gao, Han Xie, Jingmin Wang, Ye Wu, Yuehua Zhang, Xiru Wu, Yuwu Jiang

Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental Disabilities av Yujia Zhang, Weijing Kong, Yang Gao, Xiaoyan Liu, Kai Gao, Han Xie, Ye Wu, Yuehua Zhang, Jingmin Wang, Feng Gao, Xiru Wu, Yuwu Jiang

Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort av Xiaoxu Yang, Aijie Liu, Xiaojing Xu, Xiaoling Yang, Qi Zeng, Adam Yongxin Ye, Zhe Yu, Sheng Wang, August Yue Huang, Xiru Wu, Qixi Wu, Liping Wei, Yuehua Zhang

Association between genetic variation of <i>CACNA1H</i> and childhood absence epilepsy av Yucai Chen, Jianjun Lu, Hong Pan, Yuehua Zhang, Husheng Wu, Keming Xu, Xiaoyan Liu, Yuwu Jiang, Xinhua Bao, Zhijian Yao, Keyue Ding, Wilson H.Y. Lo, Boqin Qiang, Piu Chan, Yan Shen, Xiru Wu

Sökresultat - Xiru Wu

Functional Characterization and Neuronal Modeling of the Effects of Childhood Absence Epilepsy Variants of<i>CACNA1H</i>, a T-Type Calcium Channel av Iuliia Vitko, Yucai Chen, Juan Manuel Arias, Yen Shen, Xiru Wu, Edward Perez‐Reyes

ATP1A3 Mutations and Genotype-Phenotype Correlation of Alternating Hemiplegia of Childhood in Chinese Patients av Cheng Yang, Hua Gao, Jie Zhang, Xiaojing Xu, Xiaoyan Liu, Xiru Wu, Liping Wei, Yuehua Zhang

SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures av Jiaping Wang, Hua Gao, Xinhua Bao, Qingping Zhang, Jiarui Li, Liping Wei, Xiru Wu, Yan Chen, Shujie Yu

Phenotype–Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy av Dandan Tan, Haipo Yang, Yun Yuan, Carsten G. Bönnemann, Xingzhi Chang, Shuang Wang, Yuchen Wu, Xiru Wu, Hui Xiong

SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus av Huihui Sun, Yuehua Zhang, Jianmin Liang, Xiaoyan Liu, Xiuwei Ma, Husheng Wu, Keming Xu, Jiong Qin, Yu Qi, Xiru Wu

<i><scp>SCN</scp>8A</i> mutations in Chinese children with early onset epilepsy and intellectual disability av Weijing Kong, Yujia Zhang, Yang Gao, Xiaoyan Liu, Kai Gao, Han Xie, Jingmin Wang, Ye Wu, Yuehua Zhang, Xiru Wu, Yuwu Jiang

Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental Disabilities av Yujia Zhang, Weijing Kong, Yang Gao, Xiaoyan Liu, Kai Gao, Han Xie, Ye Wu, Yuehua Zhang, Jingmin Wang, Feng Gao, Xiru Wu, Yuwu Jiang

Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort av Xiaoxu Yang, Aijie Liu, Xiaojing Xu, Xiaoling Yang, Qi Zeng, Adam Yongxin Ye, Zhe Yu, Sheng Wang, August Yue Huang, Xiru Wu, Qixi Wu, Liping Wei, Yuehua Zhang

Association between genetic variation of <i>CACNA1H</i> and childhood absence epilepsy av Yucai Chen, Jianjun Lu, Hong Pan, Yuehua Zhang, Husheng Wu, Keming Xu, Xiaoyan Liu, Yuwu Jiang, Xinhua Bao, Zhijian Yao, Keyue Ding, Wilson H.Y. Lo, Boqin Qiang, Piu Chan, Yan Shen, Xiru Wu

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