Glycine

superoxide dismutase 1, soluble ; Mus musculus







8 Article(s)
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Pub. Year
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1 27098371 Altered development in GABA co-release shapes glycinergic synaptic currents in cultured spinal slices of the SOD1(G93A) mouse model of amyotrophic lateral sclerosis. 2016 Jul 1 1
2 21414903 Glycine receptor channels in spinal motoneurons are abnormal in a transgenic mouse model of amyotrophic lateral sclerosis. 2011 Feb 23 1
3 17706944 Antioxidant strategies based on tomato-enriched food or pyruvate do not affect disease onset and survival in an animal model of amyotrophic lateral sclerosis. 2007 Sep 7 1
4 16309674 Molecular and synaptic changes in the hippocampus underlying superior spatial abilities in pre-symptomatic G93A+/+ mice overexpressing the human Cu/Zn superoxide dismutase (Gly93 --> ALA) mutation. 2006 Feb 1
5 16436205 Primary glia expressing the G93A-SOD1 mutation present a neuroinflammatory phenotype and provide a cellular system for studies of glial inflammation. 2006 Jan 25 1
6 15885796 Glutamate release induced by activation of glycine and GABA transporters in spinal cord is enhanced in a mouse model of amyotrophic lateral sclerosis. 2005 Oct 5
7 15033338 Excessive and precocious glutamate release in a mouse model of amyotrophic lateral sclerosis. 2004 May 4
8 12684256 Activation of a glycine transporter on spinal cord neurons causes enhanced glutamate release in a mouse model of amyotrophic lateral sclerosis. 2003 Mar 1