Increased oxidative damage to DNA in a transgenic mouse model of Huntington's disease
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Abstract
References (22)
Exon 1 of the HD Gene with an Expanded CAG Repeat Is Sufficient to Cause a Progressive Neurological Phenotype in Transgenic Mice
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8-Hydroxyguanine, an abundant form of oxidative DNA damage, causes G-T and A-C substitutions.
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Oxidative damage to mitochondrial DNA is increased in Alzheimer's disease
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Increased oxidative damage to DNA in ALS patients
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Oxidative damage to mitochondrial DNA in Huntington's disease parietal cortex
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Striatal oxidative damage parallels the expression of a neurological phenotype in mice transgenic for the mutation of Huntington’s disease
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Distribution of phosphate-activated glutaminase, succinic dehydrogenase, pyruvate dehydrogenase and γ-glutamyl transpeptidase in post-mortem brain from Huntington's disease and agonal cases
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No Evidence for Increased Oxidative Damage to Lipids, Proteins, or DNA in Huntington's Disease
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