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JingMin Wang

Showing results (111-120 of 175) with videos related to

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Epilepsia|March 19, 2015
SCN8A mutations in Chinese children with early onset epilepsy and intellectual disabilityWeijing Kong, Yujia Zhang, Yang Gao, et al.
Journal of Human Genetics|January 23, 2009
Identification of novel EIF2B mutations in Chinese patients with vanishing white matter diseaseYe Wu, Yanxia Pan, Li Du, et al.
Brain & Development|December 11, 2014
Identification and functional study of novel PLP1 mutations in Chinese patients with Pelizaeus-Merzbacher diseaseHan Xie, Hongchun Feng, Jinhua Ji, et al.
Journal of Human Genetics|February 11, 2011
Functional analysis of recently identified mutations in eukaryotic translation initiation factor 2Bɛ (eIF2Bɛ) identified in Chinese patients with vanishing white matter diseaseXuerong Leng, Ye Wu, Xuemin Wang, et al.
Plos One|March 15, 2012
Functional studies of MLC1 mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cystsHan Xie, Jingmin Wang, Ajit Singh Dhaunchak, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 5, 2024
Focal cortical dysplasia II caused by brain somatic mutation of IRS-1 is associated with ERK signaling pathway activationXiao Li, Tianshuang Wang, Nana Liu, et al.
The Science of the Total Environment|January 19, 2016
Removal mechanisms and plant species selection by bioaccumulative factors in surface flow constructed wetlands (CWs): In the case of triclosanCongcong Zhao, HuiJun Xie, Jingtao Xu, et al.
Epilepsia|August 14, 2023
De novo CLPTM1 variants with reduced GABA<sub>A</sub> R current response in patients with epilepsyNana Liu, Jinliang Li, Kai Gao, et al.
Plos One|November 7, 2015
Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental DisabilitiesYujia Zhang, Weijing Kong, Yang Gao, et al.
Acta Epileptologica|April 11, 2025
SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathyWenwei Liu, Kai Gao, Xilong Du, et al.
Pageof 18

Showing results (111-120 of 175) with videos related to

Sort By:
Pageof 18
Epilepsia|March 19, 2015
SCN8A mutations in Chinese children with early onset epilepsy and intellectual disabilityWeijing Kong, Yujia Zhang, Yang Gao, et al.
Journal of Human Genetics|January 23, 2009
Identification of novel EIF2B mutations in Chinese patients with vanishing white matter diseaseYe Wu, Yanxia Pan, Li Du, et al.
Brain & Development|December 11, 2014
Identification and functional study of novel PLP1 mutations in Chinese patients with Pelizaeus-Merzbacher diseaseHan Xie, Hongchun Feng, Jinhua Ji, et al.
Journal of Human Genetics|February 11, 2011
Functional analysis of recently identified mutations in eukaryotic translation initiation factor 2Bɛ (eIF2Bɛ) identified in Chinese patients with vanishing white matter diseaseXuerong Leng, Ye Wu, Xuemin Wang, et al.
Plos One|March 15, 2012
Functional studies of MLC1 mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cystsHan Xie, Jingmin Wang, Ajit Singh Dhaunchak, et al.
Cerebral Cortex (New York, N.Y. : 1991)|June 5, 2024
Focal cortical dysplasia II caused by brain somatic mutation of IRS-1 is associated with ERK signaling pathway activationXiao Li, Tianshuang Wang, Nana Liu, et al.
The Science of the Total Environment|January 19, 2016
Removal mechanisms and plant species selection by bioaccumulative factors in surface flow constructed wetlands (CWs): In the case of triclosanCongcong Zhao, HuiJun Xie, Jingtao Xu, et al.
Epilepsia|August 14, 2023
De novo CLPTM1 variants with reduced GABA<sub>A</sub> R current response in patients with epilepsyNana Liu, Jinliang Li, Kai Gao, et al.
Plos One|November 7, 2015
Gene Mutation Analysis in 253 Chinese Children with Unexplained Epilepsy and Intellectual/Developmental DisabilitiesYujia Zhang, Weijing Kong, Yang Gao, et al.
Acta Epileptologica|April 11, 2025
SPOUT1 variants associated with autosomal-recessive developmental and epileptic encephalopathyWenwei Liu, Kai Gao, Xilong Du, et al.
Pageof 18