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Han-Xiang Deng

Showing results (11-20 of 49) with videos related to

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Human Molecular Genetics|January 25, 2017
The Parkinson's disease-linked protein TMEM230 is required for Rab8a-mediated secretory vesicle trafficking and retromer traffickingMyung Jong Kim, Han-Xiang Deng, Yvette C Wong, et al.
Biomed Research International|June 17, 2015
Human Genetic DiseasesHao Deng, Peter Riederer, Han-Xiang Deng, et al.
Human Molecular Genetics|February 24, 2009
Wild-type SOD1 overexpression accelerates disease onset of a G85R SOD1 mouseLijun Wang, Han-Xiang Deng, Gabriella Grisotti, et al.
Elife|May 3, 2017
A novel ALS-associated variant in <i>UBQLN4</i> regulates motor axon morphogenesisBrittany M Edens, Jianhua Yan, Nimrod Miller, et al.
The Journal of Biological Chemistry|November 6, 2009
Hyperactive intracellular calcium signaling associated with localized mitochondrial defects in skeletal muscle of an animal model of amyotrophic lateral sclerosisJingsong Zhou, Jianxun Yi, Ronggen Fu, et al.
Human Molecular Genetics|April 4, 2017
Sirt3 protects dopaminergic neurons from mitochondrial oxidative stressHan Shi, Han-Xiang Deng, David Gius, et al.
Neurobiology of Disease|December 7, 2007
Restricted expression of mutant SOD1 in spinal motor neurons and interneurons induces motor neuron pathologyLijun Wang, Kamal Sharma, Han-Xiang Deng, et al.
Acta Neuropathologica|October 19, 2013
Alzheimer disease and amyotrophic lateral sclerosis: an etiopathogenic connectionXiaochuan Wang, Julie Blanchard, Inge Grundke-Iqbal, et al.
Iscience|March 4, 2021
Early death of ALS-linked CHCHD10-R15L transgenic mice with central nervous system, skeletal muscle, and cardiac pathologyÉanna B Ryan, Jianhua Yan, Nimrod Miller, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|September 18, 2003
A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset, incomplete penetrance and a sensory neuropathyKourosh Rezania, Jianhua Yan, Lisa Dellefave, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Human Molecular Genetics|January 25, 2017
The Parkinson's disease-linked protein TMEM230 is required for Rab8a-mediated secretory vesicle trafficking and retromer traffickingMyung Jong Kim, Han-Xiang Deng, Yvette C Wong, et al.
Biomed Research International|June 17, 2015
Human Genetic DiseasesHao Deng, Peter Riederer, Han-Xiang Deng, et al.
Human Molecular Genetics|February 24, 2009
Wild-type SOD1 overexpression accelerates disease onset of a G85R SOD1 mouseLijun Wang, Han-Xiang Deng, Gabriella Grisotti, et al.
Elife|May 3, 2017
A novel ALS-associated variant in <i>UBQLN4</i> regulates motor axon morphogenesisBrittany M Edens, Jianhua Yan, Nimrod Miller, et al.
The Journal of Biological Chemistry|November 6, 2009
Hyperactive intracellular calcium signaling associated with localized mitochondrial defects in skeletal muscle of an animal model of amyotrophic lateral sclerosisJingsong Zhou, Jianxun Yi, Ronggen Fu, et al.
Human Molecular Genetics|April 4, 2017
Sirt3 protects dopaminergic neurons from mitochondrial oxidative stressHan Shi, Han-Xiang Deng, David Gius, et al.
Neurobiology of Disease|December 7, 2007
Restricted expression of mutant SOD1 in spinal motor neurons and interneurons induces motor neuron pathologyLijun Wang, Kamal Sharma, Han-Xiang Deng, et al.
Acta Neuropathologica|October 19, 2013
Alzheimer disease and amyotrophic lateral sclerosis: an etiopathogenic connectionXiaochuan Wang, Julie Blanchard, Inge Grundke-Iqbal, et al.
Iscience|March 4, 2021
Early death of ALS-linked CHCHD10-R15L transgenic mice with central nervous system, skeletal muscle, and cardiac pathologyÉanna B Ryan, Jianhua Yan, Nimrod Miller, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|September 18, 2003
A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset, incomplete penetrance and a sensory neuropathyKourosh Rezania, Jianhua Yan, Lisa Dellefave, et al.
Pageof 5