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Han-Xiang Deng

Showing results (41-50 of 49) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|April 26, 2006
Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondriaHan-Xiang Deng, Yong Shi, Yoshiaki Furukawa, et al.
Nature Genetics|December 29, 2009
Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4Han-Xiang Deng, Christopher J Klein, Jianhua Yan, et al.
Plos One|April 25, 2012
Iron accumulation in deep cortical layers accounts for MRI signal abnormalities in ALS: correlating 7 tesla MRI and pathologyJustin Y Kwan, Suh Young Jeong, Peter Van Gelderen, et al.
Archives of Neurology|November 16, 2011
SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosisFaisal Fecto, Jianhua Yan, S Pavan Vemula, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 24, 2014
Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2George H Gorrie, Faisal Fecto, Daniel Radzicki, et al.
Human Molecular Genetics|April 22, 2008
Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approachHan-Xiang Deng, Deng Han-Xiang, Hujun Jiang, et al.
Nature|August 23, 2011
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementiaHan-Xiang Deng, Wenjie Chen, Seong-Tshool Hong, et al.
Nature Genetics|June 9, 2016
Identification of TMEM230 mutations in familial Parkinson's diseaseHan-Xiang Deng, Yong Shi, Yi Yang, et al.
Acta Neuropathologica|May 22, 2010
FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degenerationHazel Urwin, Keith A Josephs, Jonathan D Rohrer, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Proceedings of the National Academy of Sciences of the United States of America|April 26, 2006
Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondriaHan-Xiang Deng, Yong Shi, Yoshiaki Furukawa, et al.
Nature Genetics|December 29, 2009
Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4Han-Xiang Deng, Christopher J Klein, Jianhua Yan, et al.
Plos One|April 25, 2012
Iron accumulation in deep cortical layers accounts for MRI signal abnormalities in ALS: correlating 7 tesla MRI and pathologyJustin Y Kwan, Suh Young Jeong, Peter Van Gelderen, et al.
Archives of Neurology|November 16, 2011
SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosisFaisal Fecto, Jianhua Yan, S Pavan Vemula, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 24, 2014
Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2George H Gorrie, Faisal Fecto, Daniel Radzicki, et al.
Human Molecular Genetics|April 22, 2008
Molecular dissection of ALS-associated toxicity of SOD1 in transgenic mice using an exon-fusion approachHan-Xiang Deng, Deng Han-Xiang, Hujun Jiang, et al.
Nature|August 23, 2011
Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementiaHan-Xiang Deng, Wenjie Chen, Seong-Tshool Hong, et al.
Nature Genetics|June 9, 2016
Identification of TMEM230 mutations in familial Parkinson's diseaseHan-Xiang Deng, Yong Shi, Yi Yang, et al.
Acta Neuropathologica|May 22, 2010
FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degenerationHazel Urwin, Keith A Josephs, Jonathan D Rohrer, et al.
Pageof 5