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Results: 1 to 20 of 109

1.

Misfolded SOD1 forms high-density molecular complexes with synaptic molecules in mutant SOD1-linked familial amyotrophic lateral sclerosis cases.

Araki T, Nagano S, Tateno M, Kaido M, Ogata K, Arima K.

J Neurol Sci. 2012 Mar 15;314(1-2):92-6. doi: 10.1016/j.jns.2011.10.017. Epub 2011 Nov 14.

PMID:
22088212
[PubMed - indexed for MEDLINE]
2.

Oxidized/misfolded superoxide dismutase-1: the cause of all amyotrophic lateral sclerosis?

Kabashi E, Valdmanis PN, Dion P, Rouleau GA.

Ann Neurol. 2007 Dec;62(6):553-9. Review.

PMID:
18074357
[PubMed - indexed for MEDLINE]
3.

Instability of mutant Cu/Zn superoxide dismutase (Ala4Thr) associated with familial amyotrophic lateral sclerosis.

Nakano R, Inuzuka T, Kikugawa K, Takahashi H, Sakimura K, Fujii J, Taniguchi N, Tsuji S.

Neurosci Lett. 1996 Jun 21;211(2):129-31.

PMID:
8830861
[PubMed - indexed for MEDLINE]
4.
5.

Lack of evidence of monomer/misfolded superoxide dismutase-1 in sporadic amyotrophic lateral sclerosis.

Liu HN, Sanelli T, Horne P, Pioro EP, Strong MJ, Rogaeva E, Bilbao J, Zinman L, Robertson J.

Ann Neurol. 2009 Jul;66(1):75-80. doi: 10.1002/ana.21704.

PMID:
19670443
[PubMed - indexed for MEDLINE]
6.

Superoxide dismutase activity, oxidative damage, and mitochondrial energy metabolism in familial and sporadic amyotrophic lateral sclerosis.

Bowling AC, Schulz JB, Brown RH Jr, Beal MF.

J Neurochem. 1993 Dec;61(6):2322-5.

PMID:
8245985
[PubMed - indexed for MEDLINE]
7.

Superoxide dismutase 1 encoding mutations linked to ALS adopts a spectrum of misfolded states.

Prudencio M, Borchelt DR.

Mol Neurodegener. 2011 Nov 17;6:77. doi: 10.1186/1750-1326-6-77.

PMID:
22094223
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Misfolded superoxide dismutase-1 in CSF from amyotrophic lateral sclerosis patients.

Zetterström P, Andersen PM, Brännström T, Marklund SL.

J Neurochem. 2011 Apr;117(1):91-9. doi: 10.1111/j.1471-4159.2011.07177.x. Epub 2011 Feb 9.

PMID:
21226712
[PubMed - indexed for MEDLINE]
9.

Copper chaperone for superoxide dismutase co-aggregates with superoxide dismutase 1 (SOD1) in neuronal Lewy body-like hyaline inclusions: an immunohistochemical study on familial amyotrophic lateral sclerosis with SOD1 gene mutation.

Kato S, Sumi-Akamaru H, Fujimura H, Sakoda S, Kato M, Hirano A, Takikawa M, Ohama E.

Acta Neuropathol. 2001 Sep;102(3):233-8.

PMID:
11585247
[PubMed - indexed for MEDLINE]
10.

Amyotrophic lateral sclerosis is a non-amyloid disease in which extensive misfolding of SOD1 is unique to the familial form.

Kerman A, Liu HN, Croul S, Bilbao J, Rogaeva E, Zinman L, Robertson J, Chakrabartty A.

Acta Neuropathol. 2010 Mar;119(3):335-44. doi: 10.1007/s00401-010-0646-5. Epub 2010 Jan 29.

PMID:
20111867
[PubMed - indexed for MEDLINE]
11.

Wild-type and mutant SOD1 share an aberrant conformation and a common pathogenic pathway in ALS.

Bosco DA, Morfini G, Karabacak NM, Song Y, Gros-Louis F, Pasinelli P, Goolsby H, Fontaine BA, Lemay N, McKenna-Yasek D, Frosch MP, Agar JN, Julien JP, Brady ST, Brown RH Jr.

Nat Neurosci. 2010 Nov;13(11):1396-403. doi: 10.1038/nn.2660. Epub 2010 Oct 17.

PMID:
20953194
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

The small heat shock protein B8 (HspB8) promotes autophagic removal of misfolded proteins involved in amyotrophic lateral sclerosis (ALS).

Crippa V, Sau D, Rusmini P, Boncoraglio A, Onesto E, Bolzoni E, Galbiati M, Fontana E, Marino M, Carra S, Bendotti C, De Biasi S, Poletti A.

Hum Mol Genet. 2010 Sep 1;19(17):3440-56. doi: 10.1093/hmg/ddq257. Epub 2010 Jun 22.

PMID:
20570967
[PubMed - indexed for MEDLINE]
Free Article
13.

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.

Eur J Neurosci. 2001 Dec;14(12):2032-6.

PMID:
11860498
[PubMed - indexed for MEDLINE]
15.

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

Turner BJ, Lopes EC, Cheema SS.

J Cell Biochem. 2004 Apr 1;91(5):1074-84.

PMID:
15034941
[PubMed - indexed for MEDLINE]
16.

Mutant SOD1 impairs axonal transport of choline acetyltransferase and acetylcholine release by sequestering KAP3.

Tateno M, Kato S, Sakurai T, Nukina N, Takahashi R, Araki T.

Hum Mol Genet. 2009 Mar 1;18(5):942-55. doi: 10.1093/hmg/ddn422. Epub 2008 Dec 16.

PMID:
19088126
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

A novel SOD1 mutation in amyotrophic lateral sclerosis with a distinct clinical phenotype.

Hu J, Chen K, Ni B, Li L, Chen G, Shi S.

Amyotroph Lateral Scler. 2012 Jan;13(1):149-54. doi: 10.3109/17482968.2011.621437. Epub 2011 Dec 20.

PMID:
22185396
[PubMed - indexed for MEDLINE]
18.

Expression of N19S-SOD1, an SOD1 mutant found in sporadic amyotrophic lateral sclerosis patients, induces low-grade motoneuronal toxicity.

Obata Y, Niikura T, Kanekura K, Hashimoto Y, Kawasumi M, Kita Y, Aiso S, Matsuoka M, Nishimoto I.

J Neurosci Res. 2005 Sep 1;81(5):720-9.

PMID:
16035108
[PubMed - indexed for MEDLINE]
19.

A novel mutation in Cu/Zn superoxide dismutase gene in Japanese familial amyotrophic lateral sclerosis.

Nakano R, Sato S, Inuzuka T, Sakimura K, Mishina M, Takahashi H, Ikuta F, Honma Y, Fujii J, Taniguchi N, et al.

Biochem Biophys Res Commun. 1994 Apr 29;200(2):695-703.

PMID:
8179602
[PubMed - indexed for MEDLINE]
20.

A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis.

Rosen DR, Bowling AC, Patterson D, Usdin TB, Sapp P, Mezey E, McKenna-Yasek D, O'Regan J, Rahmani Z, Ferrante RJ, et al.

Hum Mol Genet. 1994 Jun;3(6):981-7.

PMID:
7951249
[PubMed - indexed for MEDLINE]

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