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pubmed-article:15512862pubmed:abstractTextAmyotrophic lateral sclerosis (ALS) is a fatal paralytic neurodegenerative disorder. Experimental models of ALS such as the transgenic rodents expressing mutant superoxide dimutase-1 are playing a pivotal role in our understanding of ALS pathogenesis, and in our testing of new therapeutic interventions aimed at protecting against neurodegeneration. Apoptosis has emerged as a significant pathogenic factor in several neurodegenerative diseases, including ALS. Constructed of multiple interacting molecules, the apoptosis machinery offers a host of attractive targets for pharmacological and genetic interventions to be tested in experimental models of ALS. Information generated by these pre-clinical studies holds the promise to provide sound scientific basis for the development of effective neuroprotective therapies for ALS.lld:pubmed
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pubmed-article:15512862pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:15512862pubmed:articleTitleMolecular targets for neuroprotection.lld:pubmed
pubmed-article:15512862pubmed:affiliationDepartments of Neurology and Pathology, and the Center for Neurobiology and Behavior, Columbia University, New York, NY 10032, USA. SP30@columbia.edulld:pubmed
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