Parson SH - Search Results

1

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: parson sh. 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.

2

Axotomy-dependent and -independent synapse elimination in organ cultures of Wld(s) mutant mouse skeletal muscle.

Parson SH, Ribchester RR, Davie N, Gandhi NP, Malik RQ, Gillingwater TH, Thomson D. Parson SH, et al. J Neurosci Res. 2004 Apr 1;76(1):64-75. doi: 10.1002/jnr.20016. J Neurosci Res. 2004. PMID: 15048930

3

Synaptic vulnerability in neurodegenerative disease.

Wishart TM, Parson SH, Gillingwater TH. Wishart TM, et al. Among authors: parson sh. J Neuropathol Exp Neurol. 2006 Aug;65(8):733-9. doi: 10.1097/01.jnen.0000228202.35163.c4. J Neuropathol Exp Neurol. 2006. PMID: 16896307 Review.

4

Rapid loss of motor nerve terminals following hypoxia-reperfusion injury occurs via mechanisms distinct from classic Wallerian degeneration.

Baxter B, Gillingwater TH, Parson SH. Baxter B, et al. Among authors: parson sh. J Anat. 2008 Jun;212(6):827-35. doi: 10.1111/j.1469-7580.2008.00909.x. J Anat. 2008. PMID: 18510509 Free PMC article.

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. Among authors: parson sh. 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

Using mouse cranial muscles to investigate neuromuscular pathology in vivo.

Murray LM, Gillingwater TH, Parson SH. Murray LM, et al. Among authors: parson sh. 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

7

The response of neuromuscular junctions to injury is developmentally regulated.

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

8

Induction of cell stress in neurons from transgenic mice expressing yellow fluorescent protein: implications for neurodegeneration research.

Comley LH, Wishart TM, Baxter B, Murray LM, Nimmo A, Thomson D, Parson SH, Gillingwater TH. Comley LH, et al. Among authors: parson sh. PLoS One. 2011 Mar 8;6(3):e17639. doi: 10.1371/journal.pone.0017639. PLoS One. 2011. PMID: 21408118 Free PMC article.

9

ApoE isoform-specific regulation of regeneration in the peripheral nervous system.

Comley LH, Fuller HR, Wishart TM, Mutsaers CA, Thomson D, Wright AK, Ribchester RR, Morris GE, Parson SH, Horsburgh K, Gillingwater TH. Comley LH, et al. Among authors: parson sh. Hum Mol Genet. 2011 Jun 15;20(12):2406-21. doi: 10.1093/hmg/ddr147. Epub 2011 Apr 8. Hum Mol Genet. 2011. PMID: 21478199 Free PMC article.

10

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: parson sh. 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

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