Fisher EMC - Search Results

1

Author Correction: TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A.

Brown AL, Wilkins OG, Keuss MJ, Hill SE, Zanovello M, Lee WC, Bampton A, Lee FCY, Masino L, Qi YA, Bryce-Smith S, Gatt A, Hallegger M, Fagegaltier D, Phatnani H; NYGC ALS Consortium; Newcombe J, Gustavsson EK, Seddighi S, Reyes JF, Coon SL, Ramos D, Schiavo G, Fisher EMC, Raj T, Secrier M, Lashley T, Ule J, Buratti E, Humphrey J, Ward ME, Fratta P. Brown AL, et al. Among authors: fisher emc. Nature. 2024 Jul;631(8020):E7. doi: 10.1038/s41586-024-07577-9. Nature. 2024. PMID: 38890465 Free PMC article. No abstract available.

2

A mutation in dynein rescues axonal transport defects and extends the life span of ALS mice.

Kieran D, Hafezparast M, Bohnert S, Dick JR, Martin J, Schiavo G, Fisher EM, Greensmith L. Kieran D, et al. J Cell Biol. 2005 May 23;169(4):561-7. doi: 10.1083/jcb.200501085. J Cell Biol. 2005. PMID: 15911875 Free PMC article.

3

Modification of superoxide dismutase 1 (SOD1) properties by a GFP tag--implications for research into amyotrophic lateral sclerosis (ALS).

Stevens JC, Chia R, Hendriks WT, Bros-Facer V, van Minnen J, Martin JE, Jackson GS, Greensmith L, Schiavo G, Fisher EM. Stevens JC, et al. PLoS One. 2010 Mar 8;5(3):e9541. doi: 10.1371/journal.pone.0009541. PLoS One. 2010. PMID: 20221404 Free PMC article.

4

SOD1 and TDP-43 animal models of amyotrophic lateral sclerosis: recent advances in understanding disease toward the development of clinical treatments.

Joyce PI, Fratta P, Fisher EM, Acevedo-Arozena A. Joyce PI, et al. Mamm Genome. 2011 Aug;22(7-8):420-48. doi: 10.1007/s00335-011-9339-1. Epub 2011 Jun 26. Mamm Genome. 2011. PMID: 21706386 Review.

5

FUS is not dysregulated by the spinal bulbar muscular atrophy androgen receptor polyglutamine repeat expansion.

Fratta P, Malik B, Gray A, La Spada AR, Hanna MG, Fisher EM, Greensmith L. Fratta P, et al. Neurobiol Aging. 2013 May;34(5):1516.e17-9. doi: 10.1016/j.neurobiolaging.2012.09.008. Epub 2012 Oct 9. Neurobiol Aging. 2013. PMID: 23062703 Free article.

6

C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms RNA G-quadruplexes.

Fratta P, Mizielinska S, Nicoll AJ, Zloh M, Fisher EM, Parkinson G, Isaacs AM. Fratta P, et al. Sci Rep. 2012;2:1016. doi: 10.1038/srep01016. Epub 2012 Dec 21. Sci Rep. 2012. PMID: 23264878 Free PMC article.

7

Is SOD1 loss of function involved in amyotrophic lateral sclerosis?

Saccon RA, Bunton-Stasyshyn RK, Fisher EM, Fratta P. Saccon RA, et al. Brain. 2013 Aug;136(Pt 8):2342-58. doi: 10.1093/brain/awt097. Epub 2013 May 17. Brain. 2013. PMID: 23687121 Free PMC article. Review.

8

An unusual presentation for SOD1-ALS: isolated facial diplegia.

Fratta P, Hanna MG, Fisher EM, Sidle K. Fratta P, et al. Muscle Nerve. 2013 Dec;48(6):994-5. doi: 10.1002/mus.23958. Muscle Nerve. 2013. PMID: 23873540 Free article. No abstract available.

9

Cytoplasmic dynein heavy chain: the servant of many masters.

Schiavo G, Greensmith L, Hafezparast M, Fisher EM. Schiavo G, et al. Trends Neurosci. 2013 Nov;36(11):641-51. doi: 10.1016/j.tins.2013.08.001. Epub 2013 Sep 10. Trends Neurosci. 2013. PMID: 24035135 Free PMC article. Review.

10

Profilin1 E117G is a moderate risk factor for amyotrophic lateral sclerosis.

Fratta P, Charnock J, Collins T, Devoy A, Howard R, Malaspina A, Orrell R, Sidle K, Clarke J, Shoai M, Lu CH, Hardy J, Plagnol V, Fisher EM. Fratta P, et al. J Neurol Neurosurg Psychiatry. 2014 May;85(5):506-8. doi: 10.1136/jnnp-2013-306761. Epub 2013 Dec 5. J Neurol Neurosurg Psychiatry. 2014. PMID: 24309268 Free PMC article.

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