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Items: 1 to 20 of 163


S-nitrosothiol depletion in amyotrophic lateral sclerosis.

Schonhoff CM, Matsuoka M, Tummala H, Johnson MA, Estev├ęz AG, Wu R, Kamaid A, Ricart KC, Hashimoto Y, Gaston B, Macdonald TL, Xu Z, Mannick JB.

Proc Natl Acad Sci U S A. 2006 Feb 14;103(7):2404-9. Epub 2006 Feb 6.


S-nitrosylated protein disulfide isomerase contributes to mutant SOD1 aggregates in amyotrophic lateral sclerosis.

Chen X, Zhang X, Li C, Guan T, Shang H, Cui L, Li XM, Kong J.

J Neurochem. 2013 Jan;124(1):45-58. doi: 10.1111/jnc.12046. Epub 2012 Nov 1.


Complete dissociation of motor neuron death from motor dysfunction by Bax deletion in a mouse model of ALS.

Gould TW, Buss RR, Vinsant S, Prevette D, Sun W, Knudson CM, Milligan CE, Oppenheim RW.

J Neurosci. 2006 Aug 23;26(34):8774-86.


Cytochrome c association with the inner mitochondrial membrane is impaired in the CNS of G93A-SOD1 mice.

Kirkinezos IG, Bacman SR, Hernandez D, Oca-Cossio J, Arias LJ, Perez-Pinzon MA, Bradley WG, Moraes CT.

J Neurosci. 2005 Jan 5;25(1):164-72.


Metallothionein proteins expression, copper and zinc concentrations, and lipid peroxidation level in a rodent model for amyotrophic lateral sclerosis.

Tokuda E, Ono S, Ishige K, Naganuma A, Ito Y, Suzuki T.

Toxicology. 2007 Jan 5;229(1-2):33-41. Epub 2006 Sep 29.


Genetically decreased spinal cord copper concentration prolongs life in a transgenic mouse model of amyotrophic lateral sclerosis.

Kiaei M, Bush AI, Morrison BM, Morrison JH, Cherny RA, Volitakis I, Beal MF, Gordon JW.

J Neurosci. 2004 Sep 8;24(36):7945-50.


Dysregulation of intracellular copper trafficking pathway in a mouse model of mutant copper/zinc superoxide dismutase-linked familial amyotrophic lateral sclerosis.

Tokuda E, Okawa E, Ono S.

J Neurochem. 2009 Oct;111(1):181-91. doi: 10.1111/j.1471-4159.2009.06310.x. Epub 2009 Jul 27.


Proteomic analysis of 4-hydroxy-2-nonenal-modified proteins in G93A-SOD1 transgenic mice--a model of familial amyotrophic lateral sclerosis.

Perluigi M, Fai Poon H, Hensley K, Pierce WM, Klein JB, Calabrese V, De Marco C, Butterfield DA.

Free Radic Biol Med. 2005 Apr 1;38(7):960-8.


Superoxide dismutase 1 mutants related to amyotrophic lateral sclerosis induce endoplasmic stress in neuro2a cells.

Oh YK, Shin KS, Yuan J, Kang SJ.

J Neurochem. 2008 Feb;104(4):993-1005. doi: 10.1111/j.1471-4159.2007.05053.x.


Over-expression of Hsp27 does not influence disease in the mutant SOD1(G93A) mouse model of amyotrophic lateral sclerosis.

Krishnan J, Vannuvel K, Andries M, Waelkens E, Robberecht W, Van Den Bosch L.

J Neurochem. 2008 Sep;106(5):2170-83. doi: 10.1111/j.1471-4159.2008.05545.x. Epub 2008 Jul 4.


Overexpression of Abeta is associated with acceleration of onset of motor impairment and superoxide dismutase 1 aggregation in an amyotrophic lateral sclerosis mouse model.

Li QX, Mok SS, Laughton KM, McLean CA, Volitakis I, Cherny RA, Cheung NS, White AR, Masters CL.

Aging Cell. 2006 Apr;5(2):153-65.


Informatics-assisted protein profiling in a transgenic mouse model of amyotrophic lateral sclerosis.

Lukas TJ, Luo WW, Mao H, Cole N, Siddique T.

Mol Cell Proteomics. 2006 Jul;5(7):1233-44. Epub 2006 Mar 29.


Increased reactive oxygen species in familial amyotrophic lateral sclerosis with mutations in SOD1.

Said Ahmed M, Hung WY, Zu JS, Hockberger P, Siddique T.

J Neurol Sci. 2000 Jun 15;176(2):88-94.


Ammonium tetrathiomolybdate delays onset, prolongs survival, and slows progression of disease in a mouse model for amyotrophic lateral sclerosis.

Tokuda E, Ono S, Ishige K, Watanabe S, Okawa E, Ito Y, Suzuki T.

Exp Neurol. 2008 Sep;213(1):122-8. doi: 10.1016/j.expneurol.2008.05.011. Epub 2008 May 23.


Chromogranin-mediated secretion of mutant superoxide dismutase proteins linked to amyotrophic lateral sclerosis.

Urushitani M, Sik A, Sakurai T, Nukina N, Takahashi R, Julien JP.

Nat Neurosci. 2006 Jan;9(1):108-18. Epub 2005 Dec 20.


Mutant SOD1-induced neuronal toxicity is mediated by increased mitochondrial superoxide levels.

Zimmerman MC, Oberley LW, Flanagan SW.

J Neurochem. 2007 Aug;102(3):609-18. Epub 2007 Mar 23.


Progressive decrease in the level of YAPdeltaCs, prosurvival isoforms of YAP, in the spinal cord of transgenic mouse carrying a mutant SOD1 gene.

Morimoto N, Nagai M, Miyazaki K, Kurata T, Takehisa Y, Ikeda Y, Kamiya T, Okazawa H, Abe K.

J Neurosci Res. 2009 Mar;87(4):928-36. doi: 10.1002/jnr.21902.


Copper-binding-site-null SOD1 causes ALS in transgenic mice: aggregates of non-native SOD1 delineate a common feature.

Wang J, Slunt H, Gonzales V, Fromholt D, Coonfield M, Copeland NG, Jenkins NA, Borchelt DR.

Hum Mol Genet. 2003 Nov 1;12(21):2753-64. Epub 2003 Sep 9.


Induction of the unfolded protein response in familial amyotrophic lateral sclerosis and association of protein-disulfide isomerase with superoxide dismutase 1.

Atkin JD, Farg MA, Turner BJ, Tomas D, Lysaght JA, Nunan J, Rembach A, Nagley P, Beart PM, Cheema SS, Horne MK.

J Biol Chem. 2006 Oct 6;281(40):30152-65. Epub 2006 Jul 17.


Accelerated s-nitrosothiol breakdown by amyotrophic lateral sclerosis mutant copper,zinc-superoxide dismutase.

Johnson MA, Macdonald TL, Mannick JB, Conaway MR, Gaston B.

J Biol Chem. 2001 Oct 26;276(43):39872-8. Epub 2001 Aug 22.

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