Similar articles for PMID: 16814528

Year	Number of Results
1990	1
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1996	13
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2024	0

1

Structure, folding, and misfolding of Cu,Zn superoxide dismutase in amyotrophic lateral sclerosis.

Rakhit R, Chakrabartty A. Rakhit R, et al. Biochim Biophys Acta. 2006 Nov-Dec;1762(11-12):1025-37. doi: 10.1016/j.bbadis.2006.05.004. Epub 2006 May 22. Biochim Biophys Acta. 2006. PMID: 16814528 Free article. Review.

2

Unveiling the unfolding pathway of FALS associated G37R SOD1 mutant: a computational study.

Milardi D, Pappalardo M, Grasso DM, La Rosa C. Milardi D, et al. Mol Biosyst. 2010 Jun;6(6):1032-9. doi: 10.1039/b918662j. Epub 2010 Feb 23. Mol Biosyst. 2010. PMID: 20485746

3

Wild-type Cu/Zn superoxide dismutase (SOD1) does not facilitate, but impedes the formation of protein aggregates of amyotrophic lateral sclerosis causing mutant SOD1.

Witan H, Gorlovoy P, Kaya AM, Koziollek-Drechsler I, Neumann H, Behl C, Clement AM. Witan H, et al. Neurobiol Dis. 2009 Nov;36(2):331-42. doi: 10.1016/j.nbd.2009.07.024. Epub 2009 Aug 4. Neurobiol Dis. 2009. PMID: 19660548

4

Heterodimer formation of wild-type and amyotrophic lateral sclerosis-causing mutant Cu/Zn-superoxide dismutase induces toxicity independent of protein aggregation.

Witan H, Kern A, Koziollek-Drechsler I, Wade R, Behl C, Clement AM. Witan H, et al. Hum Mol Genet. 2008 May 15;17(10):1373-85. doi: 10.1093/hmg/ddn025. Epub 2008 Jan 22. Hum Mol Genet. 2008. PMID: 18211954

5

Copper-zinc superoxide dismutase and amyotrophic lateral sclerosis.

Valentine JS, Doucette PA, Zittin Potter S. Valentine JS, et al. Annu Rev Biochem. 2005;74:563-93. doi: 10.1146/annurev.biochem.72.121801.161647. Annu Rev Biochem. 2005. PMID: 15952898 Review.

6

Folding of Cu, Zn superoxide dismutase and familial amyotrophic lateral sclerosis.

Khare SD, Ding F, Dokholyan NV. Khare SD, et al. J Mol Biol. 2003 Nov 28;334(3):515-25. doi: 10.1016/j.jmb.2003.09.069. J Mol Biol. 2003. PMID: 14623191

7

Human Cu/Zn superoxide dismutase (SOD1) overexpression in mice causes mitochondrial vacuolization, axonal degeneration, and premature motoneuron death and accelerates motoneuron disease in mice expressing a familial amyotrophic lateral sclerosis mutant SOD1.

Jaarsma D, Haasdijk ED, Grashorn JA, Hawkins R, van Duijn W, Verspaget HW, London J, Holstege JC. Jaarsma D, et al. Neurobiol Dis. 2000 Dec;7(6 Pt B):623-43. doi: 10.1006/nbdi.2000.0299. Neurobiol Dis. 2000. PMID: 11114261

8

Stabilization of mutant Cu/Zn superoxide dismutase (SOD1) protein by coexpressed wild SOD1 protein accelerates the disease progression in familial amyotrophic lateral sclerosis mice.

Fukada K, Nagano S, Satoh M, Tohyama C, Nakanishi T, Shimizu A, Yanagihara T, Sakoda S. Fukada K, et al. Eur J Neurosci. 2001 Dec;14(12):2032-6. doi: 10.1046/j.0953-816x.2001.01828.x. Eur J Neurosci. 2001. PMID: 11860498

9

Inducible superoxide dismutase 1 aggregation in transgenic amyotrophic lateral sclerosis mouse fibroblasts.

Turner BJ, Lopes EC, Cheema SS. Turner BJ, et al. J Cell Biochem. 2004 Apr 1;91(5):1074-84. doi: 10.1002/jcb.10782. J Cell Biochem. 2004. PMID: 15034941

10

Increased affinity for copper mediated by cysteine 111 in forms of mutant superoxide dismutase 1 linked to amyotrophic lateral sclerosis.

Watanabe S, Nagano S, Duce J, Kiaei M, Li QX, Tucker SM, Tiwari A, Brown RH Jr, Beal MF, Hayward LJ, Culotta VC, Yoshihara S, Sakoda S, Bush AI. Watanabe S, et al. Free Radic Biol Med. 2007 May 15;42(10):1534-42. doi: 10.1016/j.freeradbiomed.2007.02.004. Epub 2007 Feb 15. Free Radic Biol Med. 2007. PMID: 17448900

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