Progressive Loss of Striatal Neurons Causes Motor Dysfunction in MND2 Mutant Mice and Is Not Prevented by Bcl-2
- 31 May 2002
- journal article
- Published by Elsevier in Experimental Neurology
- Vol. 175 (1), 87-97
- https://doi.org/10.1006/exnr.2002.7868
Abstract
No abstract availableKeywords
This publication has 31 references indexed in Scilit:
- Pathophysiology of idiopathic dystonia: findings from genetic animal modelsProgress in Neurobiology, 1998
- A susceptibility locus for Parkinson's disease maps to chromosome 2p13Nature Genetics, 1998
- Expression of nerve-regulated genes in muscles of mouse mutants affected by spinal muscular atrophies and muscular dystrophiesMuscle & Nerve, 1997
- Cytokines in inflammatory brain lesions: helpful and harmfulTrends in Neurosciences, 1996
- Overexpression of BCL-2 in transgenic mice protects neurons from naturally occurring cell death and experimental ischemiaNeuron, 1994
- mnd2: A New Mouse Model of Inherited Motor Neuron DiseaseGenomics, 1993
- Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation.The Journal of cell biology, 1992
- The dystonias.BMJ, 1990
- The functional anatomy of basal ganglia disordersTrends in Neurosciences, 1989
- Astrocyte Overgrowth in the Brain Stem and Spinal Cord of Mice Affected by Spinal Atrophy, WobblerDevelopmental Neuroscience, 1988