Neurobiology of disease - JoVE Visualize

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Neurobiology of Disease|April 13, 2001

Prion protein affects Ca2+-activated K+ currents in cerebellar purkinje cellsJ W Herms, T Tings, S Dunker, et al.

Neurobiology of Disease|April 13, 2001

Seasonal affective disorder and serotonin-related polymorphismsC Johansson, C Smedh, T Partonen, et al.

Neurobiology of Disease|December 15, 2000

PMP22 carrying the trembler or trembler-J mutation is intracellularly retained in myelinating Schwann cellsJ Colby, R Nicholson, K M Dickson, et al.

Neurobiology of Disease|December 15, 2000

Apoptosis in the central nervous system of cerebral adrenoleukodystrophy patientsV Feigenbaum, A Gélot, P Casanova, et al.

Neurobiology of Disease|December 15, 2000

p53 is abnormally elevated and active in the CNS of patients with amyotrophic lateral sclerosisL J Martin

Neurobiology of Disease|December 15, 2000

Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SOD1D Jaarsma, E D Haasdijk, J A Grashorn, et al.

Neurobiology of Disease|December 15, 2000

Cellular expression of alpha7 nicotinic acetylcholine receptor protein in the temporal cortex in Alzheimer's and Parkinson's disease--a stereological approachC Banerjee, J R Nyengaard, A Wevers, et al.

Neurobiology of Disease|August 9, 2001

Retrovirus-mediated gene transfer and galactocerebrosidase uptake into twitcher glial cells results in appropriate localization and phenotype correctionA Luddi, M Volterrani, M Strazza, et al.

Neurobiology of Disease|August 9, 2001

Impaired neuronal plasticity in transgenic mice expressing human apolipoprotein E4 compared to E3 in a model of entorhinal cortex lesionF White, J A Nicoll, A D Roses, et al.

Neurobiology of Disease|July 20, 2002

Fibrillar inclusions and motor neuron degeneration in transgenic mice expressing superoxide dismutase 1 with a disrupted copper-binding siteJiou Wang, Guilian Xu, Victoria Gonzales, et al.

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Showing results (511-520 of 6,669) with videos related to

Sort By:

Pageof 667

Neurobiology of Disease|April 13, 2001

Prion protein affects Ca2+-activated K+ currents in cerebellar purkinje cellsJ W Herms, T Tings, S Dunker, et al.

Neurobiology of Disease|April 13, 2001

Seasonal affective disorder and serotonin-related polymorphismsC Johansson, C Smedh, T Partonen, et al.

Neurobiology of Disease|December 15, 2000

PMP22 carrying the trembler or trembler-J mutation is intracellularly retained in myelinating Schwann cellsJ Colby, R Nicholson, K M Dickson, et al.

Neurobiology of Disease|December 15, 2000

Apoptosis in the central nervous system of cerebral adrenoleukodystrophy patientsV Feigenbaum, A Gélot, P Casanova, et al.

Neurobiology of Disease|December 15, 2000

p53 is abnormally elevated and active in the CNS of patients with amyotrophic lateral sclerosisL J Martin

Neurobiology of Disease|December 15, 2000

Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SOD1D Jaarsma, E D Haasdijk, J A Grashorn, et al.

Neurobiology of Disease|December 15, 2000

Cellular expression of alpha7 nicotinic acetylcholine receptor protein in the temporal cortex in Alzheimer's and Parkinson's disease--a stereological approachC Banerjee, J R Nyengaard, A Wevers, et al.

Neurobiology of Disease|August 9, 2001

Retrovirus-mediated gene transfer and galactocerebrosidase uptake into twitcher glial cells results in appropriate localization and phenotype correctionA Luddi, M Volterrani, M Strazza, et al.

Neurobiology of Disease|August 9, 2001

Impaired neuronal plasticity in transgenic mice expressing human apolipoprotein E4 compared to E3 in a model of entorhinal cortex lesionF White, J A Nicoll, A D Roses, et al.

Neurobiology of Disease|July 20, 2002

Fibrillar inclusions and motor neuron degeneration in transgenic mice expressing superoxide dismutase 1 with a disrupted copper-binding siteJiou Wang, Guilian Xu, Victoria Gonzales, et al.

Pageof 667