Murray LM - Search Results

1

Reversible molecular pathology of skeletal muscle in spinal muscular atrophy.

Mutsaers CA, Wishart TM, Lamont DJ, Riessland M, Schreml J, Comley LH, Murray LM, Parson SH, Lochmüller H, Wirth B, Talbot K, Gillingwater TH. Mutsaers CA, et al. Among authors: murray lm. Hum Mol Genet. 2011 Nov 15;20(22):4334-44. doi: 10.1093/hmg/ddr360. Epub 2011 Aug 12. Hum Mol Genet. 2011. PMID: 21840928

2

Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy.

Murray LM, Comley LH, Thomson D, Parkinson N, Talbot K, Gillingwater TH. Murray LM, et al. Hum Mol Genet. 2008 Apr 1;17(7):949-62. doi: 10.1093/hmg/ddm367. Epub 2007 Dec 8. Hum Mol Genet. 2008. PMID: 18065780 Free article.

3

Loss of translation elongation factor (eEF1A2) expression in vivo differentiates between Wallerian degeneration and dying-back neuronal pathology.

Murray LM, Thomson D, Conklin A, Wishart TM, Gillingwater TH. Murray LM, et al. J Anat. 2008 Dec;213(6):633-45. doi: 10.1111/j.1469-7580.2008.01007.x. J Anat. 2008. PMID: 19094180 Free PMC article.

4

Transcriptional regulation of the AP-1 and Nrf2 target gene sulfiredoxin.

Soriano FX, Baxter P, Murray LM, Sporn MB, Gillingwater TH, Hardingham GE. Soriano FX, et al. Among authors: murray lm. Mol Cells. 2009 Mar 31;27(3):279-82. doi: 10.1007/s10059-009-0050-y. Epub 2009 Mar 19. Mol Cells. 2009. PMID: 19326073 Free PMC article. Review.

5

Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy.

Murray LM, Lee S, Bäumer D, Parson SH, Talbot K, Gillingwater TH. Murray LM, et al. Hum Mol Genet. 2010 Feb 1;19(3):420-33. doi: 10.1093/hmg/ddp506. Epub 2009 Nov 2. Hum Mol Genet. 2010. PMID: 19884170

6

Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy.

Bäumer D, Lee S, Nicholson G, Davies JL, Parkinson NJ, Murray LM, Gillingwater TH, Ansorge O, Davies KE, Talbot K. Bäumer D, et al. Among authors: murray lm. PLoS Genet. 2009 Dec;5(12):e1000773. doi: 10.1371/journal.pgen.1000773. Epub 2009 Dec 18. PLoS Genet. 2009. PMID: 20019802 Free PMC article.

7

Review: neuromuscular synaptic vulnerability in motor neurone disease: amyotrophic lateral sclerosis and spinal muscular atrophy.

Murray LM, Talbot K, Gillingwater TH. Murray LM, et al. Neuropathol Appl Neurobiol. 2010 Apr;36(2):133-56. doi: 10.1111/j.1365-2990.2010.01061.x. Epub 2010 Feb 19. Neuropathol Appl Neurobiol. 2010. PMID: 20202121 Review.

8

Using mouse cranial muscles to investigate neuromuscular pathology in vivo.

Murray LM, Gillingwater TH, Parson SH. Murray LM, et al. Neuromuscul Disord. 2010 Nov;20(11):740-3. doi: 10.1016/j.nmd.2010.06.013. Epub 2010 Jul 15. Neuromuscul Disord. 2010. PMID: 20637618

9

SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy.

Wishart TM, Huang JP, Murray LM, Lamont DJ, Mutsaers CA, Ross J, Geldsetzer P, Ansorge O, Talbot K, Parson SH, Gillingwater TH. Wishart TM, et al. Among authors: murray lm. Hum Mol Genet. 2010 Nov 1;19(21):4216-28. doi: 10.1093/hmg/ddq340. Epub 2010 Aug 12. Hum Mol Genet. 2010. PMID: 20705736 Free PMC article.

10

The response of neuromuscular junctions to injury is developmentally regulated.

Murray LM, Comley LH, Gillingwater TH, Parson SH. Murray LM, et al. FASEB J. 2011 Apr;25(4):1306-13. doi: 10.1096/fj.10-171934. Epub 2011 Jan 12. FASEB J. 2011. PMID: 21228222

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