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Journal Abstract Search
734 related items for PubMed ID: 12437574
1. Proteasomal inhibition by misfolded mutant superoxide dismutase 1 induces selective motor neuron death in familial amyotrophic lateral sclerosis. Urushitani M, Kurisu J, Tsukita K, Takahashi R. J Neurochem; 2002 Dec; 83(5):1030-42. PubMed ID: 12437574 [Abstract] [Full Text] [Related]
7. Functional alterations of the ubiquitin-proteasome system in motor neurons of a mouse model of familial amyotrophic lateral sclerosis. Cheroni C, Marino M, Tortarolo M, Veglianese P, De Biasi S, Fontana E, Zuccarello LV, Maynard CJ, Dantuma NP, Bendotti C. Hum Mol Genet; 2009 Jan 01; 18(1):82-96. PubMed ID: 18826962 [Abstract] [Full Text] [Related]
9. Co-chaperone CHIP associates with mutant Cu/Zn-superoxide dismutase proteins linked to familial amyotrophic lateral sclerosis and promotes their degradation by proteasomes. Choi JS, Cho S, Park SG, Park BC, Lee DH. Biochem Biophys Res Commun; 2004 Aug 27; 321(3):574-83. PubMed ID: 15358145 [Abstract] [Full Text] [Related]
20. Accumulation of human SOD1 and ubiquitinated deposits in the spinal cord of SOD1G93A mice during motor neuron disease progression correlates with a decrease of proteasome. Cheroni C, Peviani M, Cascio P, Debiasi S, Monti C, Bendotti C. Neurobiol Dis; 2005 Apr 03; 18(3):509-22. PubMed ID: 15755678 [Abstract] [Full Text] [Related] Page: [Next] [New Search]