<didl:DIDL xsi:schemaLocation="urn:mpeg:mpeg21:2002:02-DIDL-NS 
			 http://standards.iso.org/ittf/PubliclyAvailableStandards/MPEG-21_schema_files/did/didmodel.xsd" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:didl="urn:mpeg:mpeg21:2002:02-DIDL-NS"><didl:Item><didl:Descriptior><didl:Statement mimeType="application/xml; charset=utf-8"><dii:Identifier xsi:schemaLocation="urn:mpeg:mpeg21:2002:01-DII-NS
		 	http://standards.iso.org/ittf/PubliclyAvailableStandards/MPEG-21_schema_files/dii/dii.xsd" xmlns:dii="urn:mpeg:mpeg21:2002:01-DII-NS" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">http://eprints.utas.edu.au/7123/</dii:Identifier></didl:Statement></didl:Descriptior><didl:Descriptior><didl:Statement mimeType="application/xml; charset=utf-8"><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/">
        <dc:title>Excitotoxicity mediated by non-NMDA receptors causes&#13;
distal axonopathy in long-term cultured spinal motor&#13;
neurons</dc:title>
        <dc:creator>King, AE</dc:creator>
        <dc:creator>Dickson, TC</dc:creator>
        <dc:creator>Blizzard, CA</dc:creator>
        <dc:creator>Foster, SS</dc:creator>
        <dc:creator>Chung, RS</dc:creator>
        <dc:creator>West, AK</dc:creator>
        <dc:creator>Chuah, MI</dc:creator>
        <dc:creator>Vickers, JC</dc:creator>
        <dc:description>Excitotoxicity has been implicated as a potential cause of neuronal degeneration in amyotrophic lateral sclerosis (ALS). It has not&#13;
been clear how excitotoxic injury leads to the hallmark pathological changes of ALS, such as the abnormal accumulation of&#13;
filamentous proteins in axons. We have investigated the effects of overactivation of excitatory receptors in rodent neurons maintained&#13;
in long-term culture. Excitotoxicity, mediated principally via non-N-methyl-d-aspartate (NMDA) receptors, caused axonal swelling and&#13;
accumulation of cytoskeletal proteins in the distal segments of the axons of cultured spinal, but not cortical, neurons. Axonopathy only&#13;
occurred in spinal neurons maintained for 3 weeks in vitro, indicating that susceptibility to axonal pathology may be related to relative&#13;
maturity of the neuron. Excitotoxic axonopathy was associated with the aberrant colocalization of phosphorylated and&#13;
dephosphorylated neurofilament proteins, indicating that disruption to the regulation of phosphorylation of neurofilaments may&#13;
lead to their abnormal accumulation. These data provide a strong link between excitotoxicity and the selective pattern of axonopathy&#13;
of lower motor neurons that underlies neuronal dysfunction in ALS.</dc:description>
        <dc:date>2007</dc:date>
        <dc:type>Article</dc:type>
        <dc:type>PeerReviewed</dc:type>
        <dc:format>application/pdf</dc:format>
        <dc:identifier>http://eprints.utas.edu.au/7123/1/King_Euro_J_Neurosci.pdf</dc:identifier>
        <dc:relation>http://dx.doi.org/10.1111/j.1460-9568.2007.05845.x</dc:relation>
        <dc:identifier>King, AE and Dickson, TC and Blizzard, CA and Foster, SS and Chung, RS and West, AK and Chuah, MI and Vickers, JC (2007) Excitotoxicity mediated by non-NMDA receptors causes distal axonopathy in long-term cultured spinal motor neurons. European Journal of Neuroscience, 26 (8). pp. 2151-2159. ISSN 0953-816X</dc:identifier>
        <dc:relation>http://eprints.utas.edu.au/7123/</dc:relation></oai_dc:dc></didl:Statement></didl:Descriptior><didl:Component><didl:Descriptior><didl:Statement mimeType="application/xml; charset=utf-8"><dii:Identifier xsi:schemaLocation="urn:mpeg:mpeg21:2002:01-DII-NS
		 	    http://standards.iso.org/ittf/PubliclyAvailableStandards/MPEG-21_schema_files/dii/dii.xsd" xmlns:dii="urn:mpeg:mpeg21:2002:01-DII-NS" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">http://eprints.utas.edu.au/7123/1/</dii:Identifier></didl:Statement></didl:Descriptior><didl:Resource ref="http://eprints.utas.edu.au/7123/1/King_Euro_J_Neurosci.pdf"></didl:Resource></didl:Component></didl:Item></didl:DIDL>