M E Gurney - JoVE Visualize

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Proceedings of the National Academy of Sciences of the United States of America|May 28, 1996

The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the diseaseZ Mourelatos, N K Gonatas, A Stieber, et al.

The European Journal of Neuroscience|July 1, 1997

The copper chelator d-penicillamine delays onset of disease and extends survival in a transgenic mouse model of familial amyotrophic lateral sclerosisA F Hottinger, E G Fine, M E Gurney, et al.

Age|April 23, 2013

Mutant Cu,Zn superoxide dismutase in motor neuron diseaseM E Gurney, R Liu, J S Althaus, et al.

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.

Laboratory Investigation; a Journal of Technical Methods and Pathology|April 1, 1997

Oxidative stress, mutant SOD1, and neurofilament pathology in transgenic mouse models of human motor neuron diseaseP H Tu, M E Gurney, J P Julien, et al.

Journal of Neuroscience Research|July 22, 1998

Relationship of oxygen radical-induced lipid peroxidative damage to disease onset and progression in a transgenic model of familial ALSE D Hall, P K Andrus, J A Oostveen, et al.

Journal of Neuropathology and Experimental Neurology|June 18, 1998

Intracellular calcium parallels motoneuron degeneration in SOD-1 mutant miceL Siklós, J I Engelhardt, M E Alexianu, et al.

Proceedings of the National Academy of Sciences of the United States of America|April 2, 1996

Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesionsP H Tu, P Raju, K A Robinson, et al.

The Journal of Biological Chemistry|May 20, 2000

Tau phosphorylation at serine 396 and serine 404 by human recombinant tau protein kinase II inhibits tau's ability to promote microtubule assemblyD B Evans, K B Rank, K Bhattacharya, et al.

Annals of Neurology|January 5, 2002

Disease mechanisms revealed by transcription profiling in SOD1-G93A transgenic mouse spinal cordM K Olsen, S L Roberds, B R Ellerbrock, et al.

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Showing results (41-50 of 64) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|May 28, 1996

The Golgi apparatus of spinal cord motor neurons in transgenic mice expressing mutant Cu,Zn superoxide dismutase becomes fragmented in early, preclinical stages of the diseaseZ Mourelatos, N K Gonatas, A Stieber, et al.

The European Journal of Neuroscience|July 1, 1997

The copper chelator d-penicillamine delays onset of disease and extends survival in a transgenic mouse model of familial amyotrophic lateral sclerosisA F Hottinger, E G Fine, M E Gurney, et al.

Age|April 23, 2013

Mutant Cu,Zn superoxide dismutase in motor neuron diseaseM E Gurney, R Liu, J S Althaus, et al.

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.

Laboratory Investigation; a Journal of Technical Methods and Pathology|April 1, 1997

Oxidative stress, mutant SOD1, and neurofilament pathology in transgenic mouse models of human motor neuron diseaseP H Tu, M E Gurney, J P Julien, et al.

Journal of Neuroscience Research|July 22, 1998

Relationship of oxygen radical-induced lipid peroxidative damage to disease onset and progression in a transgenic model of familial ALSE D Hall, P K Andrus, J A Oostveen, et al.

Journal of Neuropathology and Experimental Neurology|June 18, 1998

Intracellular calcium parallels motoneuron degeneration in SOD-1 mutant miceL Siklós, J I Engelhardt, M E Alexianu, et al.

Proceedings of the National Academy of Sciences of the United States of America|April 2, 1996

Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesionsP H Tu, P Raju, K A Robinson, et al.

The Journal of Biological Chemistry|May 20, 2000

Tau phosphorylation at serine 396 and serine 404 by human recombinant tau protein kinase II inhibits tau's ability to promote microtubule assemblyD B Evans, K B Rank, K Bhattacharya, et al.

Annals of Neurology|January 5, 2002

Disease mechanisms revealed by transcription profiling in SOD1-G93A transgenic mouse spinal cordM K Olsen, S L Roberds, B R Ellerbrock, et al.

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