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Targeted gene expression profiling predicts meningioma outcomes and radiotherapy responses.
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Sisodia, Sangram S.
One or more keywords matched the following items that are connected to
Sisodia, Sangram S.
Item Type
Name
Concept
Amyotrophic Lateral Sclerosis
Concept
Motor Neuron Disease
Academic Article
Transgenic models of neurodegenerative diseases.
Academic Article
Neurodegenerative diseases and model systems.
Academic Article
Neuronal degeneration in human diseases and animal models.
Academic Article
Motor neuron disease and model systems: aetiologies, mechanisms and therapies.
Academic Article
Mechanisms of selective motor neuron death in transgenic mouse models of motor neuron disease.
Academic Article
Inherited neurodegenerative diseases and transgenic models.
Academic Article
ALS-linked SOD1 mutant G85R mediates damage to astrocytes and promotes rapidly progressive disease with SOD1-containing inclusions.
Academic Article
Familial amyotrophic lateral sclerosis and Alzheimer's disease. Transgenic models.
Academic Article
Genetic neurodegenerative diseases: the human illness and transgenic models.
Academic Article
Amyotrophic lateral sclerosis and Alzheimer disease. Lessons from model systems.
Academic Article
The value of transgenic models for the study of neurodegenerative diseases.
Academic Article
Transgenic mouse models of Alzheimer's disease and amyotrophic lateral sclerosis.
Academic Article
Impairments in fast axonal transport and motor neuron deficits in transgenic mice expressing familial Alzheimer's disease-linked mutant presenilin 1.
Academic Article
An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria.
Academic Article
Mutations associated with amyotrophic lateral sclerosis convert superoxide dismutase from an antiapoptotic gene to a proapoptotic gene: studies in yeast and neural cells.
Academic Article
Superoxide dismutase 1 subunits with mutations linked to familial amyotrophic lateral sclerosis do not affect wild-type subunit function.
Academic Article
Superoxide dismutase 1 with mutations linked to familial amyotrophic lateral sclerosis possesses significant activity.
Search Criteria
Motor Neuron Disease