FEBS Letters · 2002 · 81 citations · 22 references
Life SciencesMolecular BiologyNeuroscienceGene ExpressionMolecular NeurobiologyMolecular NeuroscienceAmyotrophic Lateral SclerosisMolecular Basis Of NeurodegenerationMolecular NeurogeneticsNeurodegenerative DiseasesNeurodegenerative DisordersNeuroinflammationAmyotrophic Lateral Sclerosis PathologyExpression Level VariationMicroarray AnalysisProteasome SystemSporadic Amyotrophic Lateral Sclerosis
To analyze the genes related to the pathophysiology of sporadic amyotrophic lateral sclerosis (SALS) we performed gene profiling of SALS spinal cords using molecular indexing combined with cDNA microarray. Eighty-four fragments were cloned in the first screening procedure with molecular indexing. Subsequent quantitative microarray screening revealed 11 genes which were differentially expressed in SALS. Real-time RT-PCR verified that the expression level of the following six genes was altered in SALS: dorfin, metallothionein-3, 30 kDa TATA-binding protein-associated factor, neugrin, ubiquitin-like protein 5 and macrophage-inhibiting factor-related protein-8. These results indicated that genes associated with the ubiquitin-proteasome system, oxidative toxicity, transcription, neuronal differentiation and inflammation might be involved in the pathogenesis of SALS.
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Epidemiology of mutations in superoxide dismutase in amyotrophic lateal sclerosis
Merit Cudkowicz, D. McKenna‐Yasek, Phillip Sapp et al. · Annals of Neurology · 1997 · 530 citations · Full text
Life Sciences, Genetics, Neurology +13
Tsuyoshi Yoshihara, Shinsuke Ishigaki, Masahiko Yamamoto et al. · Journal of Neurochemistry · 2001 · 270 citations