Kabashi E - Search Results

1

Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo.

Kabashi E, Lin L, Tradewell ML, Dion PA, Bercier V, Bourgouin P, Rochefort D, Bel Hadj S, Durham HD, Vande Velde C, Rouleau GA, Drapeau P. Kabashi E, et al. Hum Mol Genet. 2010 Feb 15;19(4):671-83. doi: 10.1093/hmg/ddp534. Epub 2009 Dec 3. Hum Mol Genet. 2010. PMID: 19959528

2

Focal dysfunction of the proteasome: a pathogenic factor in a mouse model of amyotrophic lateral sclerosis.

Kabashi E, Agar JN, Taylor DM, Minotti S, Durham HD. Kabashi E, et al. J Neurochem. 2004 Jun;89(6):1325-35. doi: 10.1111/j.1471-4159.2004.02453.x. J Neurochem. 2004. PMID: 15189335 Free article.

3

Proteasome activity or expression is not altered by activation of the heat shock transcription factor Hsf1 in cultured fibroblasts or myoblasts.

Taylor DM, Kabashi E, Agar JN, Minotti S, Durham HD. Taylor DM, et al. Among authors: kabashi e. Cell Stress Chaperones. 2005 Autumn;10(3):230-41. doi: 10.1379/csc-119r.1. Cell Stress Chaperones. 2005. PMID: 16184768 Free PMC article.

4

Failure of protein quality control in amyotrophic lateral sclerosis.

Kabashi E, Durham HD. Kabashi E, et al. Biochim Biophys Acta. 2006 Nov-Dec;1762(11-12):1038-50. doi: 10.1016/j.bbadis.2006.06.006. Epub 2006 Jun 18. Biochim Biophys Acta. 2006. PMID: 16876390 Free article. Review.

5

Tryptophan 32 potentiates aggregation and cytotoxicity of a copper/zinc superoxide dismutase mutant associated with familial amyotrophic lateral sclerosis.

Taylor DM, Gibbs BF, Kabashi E, Minotti S, Durham HD, Agar JN. Taylor DM, et al. Among authors: kabashi e. J Biol Chem. 2007 Jun 1;282(22):16329-35. doi: 10.1074/jbc.M610119200. Epub 2007 Mar 27. J Biol Chem. 2007. PMID: 17389599 Free article.

6

ALS predisposition modifiers: knock NOX, who's there? SOD1 mice still are.

Valdmanis PN, Kabashi E, Dion PA, Rouleau GA. Valdmanis PN, et al. Among authors: kabashi e. Eur J Hum Genet. 2008 Feb;16(2):140-2. doi: 10.1038/sj.ejhg.5201961. Epub 2007 Nov 28. Eur J Hum Genet. 2008. PMID: 18043718 No abstract available.

7

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

Kabashi E, Valdmanis PN, Dion P, Rouleau GA. Kabashi E, et al. Ann Neurol. 2007 Dec;62(6):553-9. doi: 10.1002/ana.21319. Ann Neurol. 2007. PMID: 18074357 Review.

8

Proteasomes remain intact, but show early focal alteration in their composition in a mouse model of amyotrophic lateral sclerosis.

Kabashi E, Agar JN, Hong Y, Taylor DM, Minotti S, Figlewicz DA, Durham HD. Kabashi E, et al. J Neurochem. 2008 Jun 1;105(6):2353-66. doi: 10.1111/j.1471-4159.2008.05317.x. J Neurochem. 2008. PMID: 18315558 Free article.

9

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.

Kabashi E, Valdmanis PN, Dion P, Spiegelman D, McConkey BJ, Vande Velde C, Bouchard JP, Lacomblez L, Pochigaeva K, Salachas F, Pradat PF, Camu W, Meininger V, Dupre N, Rouleau GA. Kabashi E, et al. Nat Genet. 2008 May;40(5):572-4. doi: 10.1038/ng.132. Epub 2008 Mar 30. Nat Genet. 2008. PMID: 18372902

10

Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish.

Gros-Louis F, Kriz J, Kabashi E, McDearmid J, Millecamps S, Urushitani M, Lin L, Dion P, Zhu Q, Drapeau P, Julien JP, Rouleau GA. Gros-Louis F, et al. Among authors: kabashi e. Hum Mol Genet. 2008 Sep 1;17(17):2691-702. doi: 10.1093/hmg/ddn171. Epub 2008 Jun 16. Hum Mol Genet. 2008. PMID: 18558633

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