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Two novel mutations in the gene for copper zinc superoxide dismutase in UK families with amyotrophic lateral sclerosis.
Enayat ZE,
Orrell RW,
Claus A,
Ludolph A,
Bachus R,
Brockmüller J,
Ray-Chaudhuri K,
Radunovic A,
Shaw C,
Wilkinson J, et al.
Institute of Psychiatry, London, UK.
PMID: 8528216 [PubMed - indexed for MEDLINE]
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Cited by 5 PubMed Central articles
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Protein aggregation and protein instability govern familial amyotrophic lateral sclerosis patient survival.
Wang Q, Johnson JL, Agar NY, Agar JN.
PLoS Biol. 2008 Jul 29; 6(7):e170.
[PLoS Biol. 2008]
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Activation of the Nrf2-ARE pathway in muscle and spinal cord during ALS-like pathology in mice expressing mutant SOD1.
Kraft AD, Resch JM, Johnson DA, Johnson JA.
Exp Neurol. 2007 Sep; 207(1):107-17. Epub 2007 Jun 12.
[Exp Neurol. 2007]
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Subunit asymmetry in the three-dimensional structure of a human CuZnSOD mutant found in familial amyotrophic lateral sclerosis.
Hart PJ, Liu H, Pellegrini M, Nersissian AM, Gralla EB, Valentine JS, Eisenberg D.
Protein Sci. 1998 Mar; 7(3):545-55.
[Protein Sci. 1998]
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