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Han-Xiang Deng

Showing results (21-30 of 49) with videos related to

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Neuromolecular Medicine|August 31, 2019
Incidence and Clinical Features of TRPV4-Linked Axonal Neuropathies in a USA Cohort of Charcot-Marie-Tooth Disease Type 2Sheng Deng, Shawna M E Feely, Yong Shi, et al.
Elife|May 3, 2017
Nuclear export of misfolded SOD1 mediated by a normally buried NES-like sequence reduces proteotoxicity in the nucleusYongwang Zhong, Jiou Wang, Mark J Henderson, et al.
Journal of Lipid Research|October 9, 2009
Marked accumulation of 27-hydroxycholesterol in SPG5 patients with hereditary spastic paresisRebecca Schüle, Teepu Siddique, Han-Xiang Deng, et al.
Human Molecular Genetics|September 15, 2007
Distal axonopathy in an alsin-deficient mouse modelHan-Xiang Deng, Hong Zhai, Ronggen Fu, et al.
Plos One|May 26, 2016
Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger CamptodactylyHao Deng, Sheng Deng, Hongbo Xu, et al.
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|July 29, 2003
[Exclusive gene mapping on retinitis pigmentosa with markers on chromosomes 3 in a Chinese kindred]Zheng Liu, Hao Deng, Xing-hua Xi, et al.
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|December 2, 2005
[Splicing site mutation of D19S418 in PRPF-31 gene and its phenotypic characters with autosomal dominant retinitis pigmentosa]Xing-hua Xi, Duo Zheng, Kun Xia, et al.
Acta Neuropathologica|February 5, 2013
Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloidEileen H Bigio, Jane Y Wu, Han-Xiang Deng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 5, 2003
[Spastin gene mutation in Chinese patients with hereditary spastic paraplegia]Guo-hua Zhao, Bei-sha Tang, Wei Luo, et al.
Acta Neuropathologica|April 3, 2010
TDP-43 pathology in primary progressive aphasia and frontotemporal dementia with pathologic Alzheimer diseaseEileen H Bigio, Manjari Mishra, Kimmo J Hatanpaa, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
Neuromolecular Medicine|August 31, 2019
Incidence and Clinical Features of TRPV4-Linked Axonal Neuropathies in a USA Cohort of Charcot-Marie-Tooth Disease Type 2Sheng Deng, Shawna M E Feely, Yong Shi, et al.
Elife|May 3, 2017
Nuclear export of misfolded SOD1 mediated by a normally buried NES-like sequence reduces proteotoxicity in the nucleusYongwang Zhong, Jiou Wang, Mark J Henderson, et al.
Journal of Lipid Research|October 9, 2009
Marked accumulation of 27-hydroxycholesterol in SPG5 patients with hereditary spastic paresisRebecca Schüle, Teepu Siddique, Han-Xiang Deng, et al.
Human Molecular Genetics|September 15, 2007
Distal axonopathy in an alsin-deficient mouse modelHan-Xiang Deng, Hong Zhai, Ronggen Fu, et al.
Plos One|May 26, 2016
Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger CamptodactylyHao Deng, Sheng Deng, Hongbo Xu, et al.
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|July 29, 2003
[Exclusive gene mapping on retinitis pigmentosa with markers on chromosomes 3 in a Chinese kindred]Zheng Liu, Hao Deng, Xing-hua Xi, et al.
[Zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology|December 2, 2005
[Splicing site mutation of D19S418 in PRPF-31 gene and its phenotypic characters with autosomal dominant retinitis pigmentosa]Xing-hua Xi, Duo Zheng, Kun Xia, et al.
Acta Neuropathologica|February 5, 2013
Inclusions in frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP) and amyotrophic lateral sclerosis (ALS), but not FTLD with FUS proteinopathy (FTLD-FUS), have properties of amyloidEileen H Bigio, Jane Y Wu, Han-Xiang Deng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 5, 2003
[Spastin gene mutation in Chinese patients with hereditary spastic paraplegia]Guo-hua Zhao, Bei-sha Tang, Wei Luo, et al.
Acta Neuropathologica|April 3, 2010
TDP-43 pathology in primary progressive aphasia and frontotemporal dementia with pathologic Alzheimer diseaseEileen H Bigio, Manjari Mishra, Kimmo J Hatanpaa, et al.
Pageof 5