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http://purl.uniprot.org/citations/10551448http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/10551448http://www.w3.org/2000/01/rdf-schema#comment"Motor neuron disease is a general term applied to a broad class of neurodegenerative diseases that are characterized by fatally progressive muscular weakness, atrophy, and paralysis attributable to loss of motor neurons. At present, there is no cure for most motor neuron diseases, including amyotrophic lateral sclerosis (ALS), the most common human motor neuron disease--the cause of which remains largely unknown. Animal models of motor neuron disease (MND) have significantly contributed to the remarkable recent progress in understanding the cause, genetic factors, and pathologic mechanisms proposed for this class of human neurodegenerative disorders. Largely driven by ALS research, animal models of MND have proven their usefulness in elucidating potential causes and specific pathogenic mechanisms, and have helped to advance promising new treatments from "benchside to bedside." This review summarizes important features of selected established animal models of MND: genetically engineered mice and inherited or spontaneously occurring MND in the murine, canine, and equine species."xsd:string
http://purl.uniprot.org/citations/10551448http://purl.uniprot.org/core/author"Tolwani R.J."xsd:string
http://purl.uniprot.org/citations/10551448http://purl.uniprot.org/core/author"Green S.L."xsd:string
http://purl.uniprot.org/citations/10551448http://purl.uniprot.org/core/date"1999"xsd:gYear
http://purl.uniprot.org/citations/10551448http://purl.uniprot.org/core/name"Lab Anim Sci"xsd:string
http://purl.uniprot.org/citations/10551448http://purl.uniprot.org/core/pages"480-487"xsd:string
http://purl.uniprot.org/citations/10551448http://purl.uniprot.org/core/title"Animal models for motor neuron disease."xsd:string
http://purl.uniprot.org/citations/10551448http://purl.uniprot.org/core/volume"49"xsd:string
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