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Items: 1 to 20 of 193

1.

Interaction between familial amyotrophic lateral sclerosis (ALS)-linked SOD1 mutants and the dynein complex.

Zhang F, Ström AL, Fukada K, Lee S, Hayward LJ, Zhu H.

J Biol Chem. 2007 Jun 1;282(22):16691-9. Epub 2007 Apr 2.

2.

Mitochondria in motor nerve terminals: function in health and in mutant superoxide dismutase 1 mouse models of familial ALS.

Barrett EF, Barrett JN, David G.

J Bioenerg Biomembr. 2011 Dec;43(6):581-6. doi: 10.1007/s10863-011-9392-1. Review.

3.
4.

Mitochondrial dysfunction in familial amyotrophic lateral sclerosis.

Faes L, Callewaert G.

J Bioenerg Biomembr. 2011 Dec;43(6):587-92. doi: 10.1007/s10863-011-9393-0. Review.

PMID:
22072073
5.

Retrograde axonal transport and motor neuron disease.

Ström AL, Gal J, Shi P, Kasarskis EJ, Hayward LJ, Zhu H.

J Neurochem. 2008 Jul;106(2):495-505. doi: 10.1111/j.1471-4159.2008.05393.x. Epub 2008 Apr 1. Review.

6.

Transgenics, toxicity and therapeutics in rodent models of mutant SOD1-mediated familial ALS.

Turner BJ, Talbot K.

Prog Neurobiol. 2008 May;85(1):94-134. doi: 10.1016/j.pneurobio.2008.01.001. Epub 2008 Jan 16. Review.

PMID:
18282652
7.

New consensus research on neuropathological aspects of familial amyotrophic lateral sclerosis with superoxide dismutase 1 (SOD1) gene mutations: inclusions containing SOD1 in neurons and astrocytes.

Kato S, Takikawa M, Nakashima K, Hirano A, Cleveland DW, Kusaka H, Shibata N, Kato M, Nakano I, Ohama E.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2000 Jun;1(3):163-84. Review.

PMID:
11464950
8.

Current hypotheses for the underlying biology of amyotrophic lateral sclerosis.

Rothstein JD.

Ann Neurol. 2009 Jan;65 Suppl 1:S3-9. doi: 10.1002/ana.21543. Review.

PMID:
19191304
9.

Lessons from models of SOD1-linked familial ALS.

Bendotti C, Carrì MT.

Trends Mol Med. 2004 Aug;10(8):393-400. Review.

PMID:
15310460
10.

Mutant SOD1 instability: implications for toxicity in amyotrophic lateral sclerosis.

Tiwari A, Hayward LJ.

Neurodegener Dis. 2005;2(3-4):115-27. Review.

PMID:
16909016
11.

Immature copper-zinc superoxide dismutase and familial amyotrophic lateral sclerosis.

Seetharaman SV, Prudencio M, Karch C, Holloway SP, Borchelt DR, Hart PJ.

Exp Biol Med (Maywood). 2009 Oct;234(10):1140-54. doi: 10.3181/0903-MR-104. Epub 2009 Jul 13. Review.

13.

Aggregation of copper-zinc superoxide dismutase in familial and sporadic ALS.

Chattopadhyay M, Valentine JS.

Antioxid Redox Signal. 2009 Jul;11(7):1603-14. doi: 10.1089/ARS.2009.2536. Review.

14.

Rodent Models of Amyotrophic Lateral Sclerosis.

Philips T, Rothstein JD.

Curr Protoc Pharmacol. 2015 Jun 1;69:5.67.1-21. doi: 10.1002/0471141755.ph0567s69. Review.

15.

Role of mitochondria in mutant SOD1 linked amyotrophic lateral sclerosis.

Tan W, Pasinelli P, Trotti D.

Biochim Biophys Acta. 2014 Aug;1842(8):1295-301. doi: 10.1016/j.bbadis.2014.02.009. Epub 2014 Feb 22. Review.

16.

[Implications of successful immunotherapy in ALS model mice].

Urushitani M.

Brain Nerve. 2008 Jun;60(6):643-51. Review. Japanese.

PMID:
18567360
17.

Superoxide dismutase-1 mutation-related neurotoxicity in familial amyotrophic lateral sclerosis.

Shibata N, Hirano A, Yamamoto T, Kato Y, Kobayashi M.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2000 Jun;1(3):143-61. Review.

PMID:
11464949
18.

Mechanism and treatment of motoneuron degeneration in ALS: what have SOD1 mutants told us?

Xu Z.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2000 Sep;1(4):225-34. Review.

PMID:
11465016
19.
20.

SOD1 aggregation and ALS: role of metallation states and disulfide status.

Sheng Y, Chattopadhyay M, Whitelegge J, Valentine JS.

Curr Top Med Chem. 2012;12(22):2560-72. Review.

PMID:
23339308

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