H X Deng|T Siddique - JoVE Visualize

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Human Molecular Genetics|January 1, 1996

Genetics of amyotrophic lateral sclerosisT Siddique, H X Deng

Annals of Neurology|April 1, 1997

Midbrain dopaminergic neuronal degeneration in a transgenic mouse model of familial amyotrophic lateral sclerosisV Kostic, M E Gurney, H X Deng, et al.

Biochemical and Biophysical Research Communications|September 28, 2000

Multiple transcripts of the human Cu,Zn superoxide dismutase geneM Hirano, W Y Hung, N Cole, et al.

Journal of Neuropathology and Experimental Neurology|April 1, 1996

Intense superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvementN Shibata, A Hirano, M Kobayashi, et al.

Neurology|January 30, 2009

Age and founder effect of SOD1 A4V mutation causing ALSM Saeed, Y Yang, H-X Deng, et al.

Annals of Neurology|March 1, 1996

Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiencyA Hentati, H X Deng, W Y Hung, et al.

Nature|March 4, 1993

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisD R Rosen, T Siddique, D Patterson, et al.

Neurogenetics|May 1, 1997

Exon 5 encoded domain is not required for the toxic function of mutant SOD1 but essential for the dismutase activity: identification and characterization of two new SOD1 mutations associated with familial amyotrophic lateral sclerosisJ S Zu, H X Deng, T P Lo, et al.

Human Molecular Genetics|September 1, 1996

Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31K Isozumi, R DeLong, J Kaplan, et al.

Clinical Neuroscience (New York, N.Y.)|January 1, 1995

Familial amyotrophic lateral sclerosisT Siddique, A Hentati

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Showing results (1-10 of 110) with videos related to

Sort By:

Pageof 11

Human Molecular Genetics|January 1, 1996

Genetics of amyotrophic lateral sclerosisT Siddique, H X Deng

Annals of Neurology|April 1, 1997

Midbrain dopaminergic neuronal degeneration in a transgenic mouse model of familial amyotrophic lateral sclerosisV Kostic, M E Gurney, H X Deng, et al.

Biochemical and Biophysical Research Communications|September 28, 2000

Multiple transcripts of the human Cu,Zn superoxide dismutase geneM Hirano, W Y Hung, N Cole, et al.

Journal of Neuropathology and Experimental Neurology|April 1, 1996

Intense superoxide dismutase-1 immunoreactivity in intracytoplasmic hyaline inclusions of familial amyotrophic lateral sclerosis with posterior column involvementN Shibata, A Hirano, M Kobayashi, et al.

Neurology|January 30, 2009

Age and founder effect of SOD1 A4V mutation causing ALSM Saeed, Y Yang, H-X Deng, et al.

Annals of Neurology|March 1, 1996

Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiencyA Hentati, H X Deng, W Y Hung, et al.

Nature|March 4, 1993

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisD R Rosen, T Siddique, D Patterson, et al.

Neurogenetics|May 1, 1997

Exon 5 encoded domain is not required for the toxic function of mutant SOD1 but essential for the dismutase activity: identification and characterization of two new SOD1 mutations associated with familial amyotrophic lateral sclerosisJ S Zu, H X Deng, T P Lo, et al.

Human Molecular Genetics|September 1, 1996

Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31K Isozumi, R DeLong, J Kaplan, et al.

Clinical Neuroscience (New York, N.Y.)|January 1, 1995

Familial amyotrophic lateral sclerosisT Siddique, A Hentati

Pageof 11