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Journal Abstract Search
514 related items for PubMed ID: 24023695
1. Molecular chaperone mediated late-stage neuroprotection in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis. Novoselov SS, Mustill WJ, Gray AL, Dick JR, Kanuga N, Kalmar B, Greensmith L, Cheetham ME. PLoS One; 2013; 8(8):e73944. PubMed ID: 24023695 [Abstract] [Full Text] [Related]
2. 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. PubMed ID: 18624915 [Abstract] [Full Text] [Related]
3. Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues. Watanabe M, Dykes-Hoberg M, Culotta VC, Price DL, Wong PC, Rothstein JD. Neurobiol Dis; 2001 Dec; 8(6):933-41. PubMed ID: 11741389 [Abstract] [Full Text] [Related]
4. Differential effects of mutant SOD1 on protein structure of skeletal muscle and spinal cord of familial amyotrophic lateral sclerosis: role of chaperone network. Wei R, Bhattacharya A, Hamilton RT, Jernigan AL, Chaudhuri AR. Biochem Biophys Res Commun; 2013 Aug 16; 438(1):218-23. PubMed ID: 23886956 [Abstract] [Full Text] [Related]
5. 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 16; 5(2):153-65. PubMed ID: 16626394 [Abstract] [Full Text] [Related]
6. Knocking down metabotropic glutamate receptor 1 improves survival and disease progression in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis. Milanese M, Giribaldi F, Melone M, Bonifacino T, Musante I, Carminati E, Rossi PI, Vergani L, Voci A, Conti F, Puliti A, Bonanno G. Neurobiol Dis; 2014 Apr 16; 64():48-59. PubMed ID: 24361555 [Abstract] [Full Text] [Related]
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 01; 19(17):3440-56. PubMed ID: 20570967 [Abstract] [Full Text] [Related]
15. In vivo quantification of spinal and bulbar motor neuron degeneration in the G93A-SOD1 transgenic mouse model of ALS by T2 relaxation time and apparent diffusion coefficient. Niessen HG, Angenstein F, Sander K, Kunz WS, Teuchert M, Ludolph AC, Heinze HJ, Scheich H, Vielhaber S. Exp Neurol; 2006 Oct 01; 201(2):293-300. PubMed ID: 16740261 [Abstract] [Full Text] [Related]
17. Overexpression of metallothionein-I, a copper-regulating protein, attenuates intracellular copper dyshomeostasis and extends lifespan in a mouse model of amyotrophic lateral sclerosis caused by mutant superoxide dismutase-1. Tokuda E, Okawa E, Watanabe S, Ono S. Hum Mol Genet; 2014 Mar 01; 23(5):1271-85. PubMed ID: 24163136 [Abstract] [Full Text] [Related]
20. Calcium dysregulation, mitochondrial pathology and protein aggregation in a culture model of amyotrophic lateral sclerosis: mechanistic relationship and differential sensitivity to intervention. Tradewell ML, Cooper LA, Minotti S, Durham HD. Neurobiol Dis; 2011 Jun 01; 42(3):265-75. PubMed ID: 21296666 [Abstract] [Full Text] [Related] Page: [Next] [New Search]