Gillingwater TH - 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: gillingwater th. 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

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. Among authors: gillingwater th. J Neurosci Res. 2004 Apr 1;76(1):64-75. doi: 10.1002/jnr.20016. J Neurosci Res. 2004. PMID: 15048930

3

Progressive abnormalities in skeletal muscle and neuromuscular junctions of transgenic mice expressing the Huntington's disease mutation.

Ribchester RR, Thomson D, Wood NI, Hinks T, Gillingwater TH, Wishart TM, Court FA, Morton AJ. Ribchester RR, et al. Among authors: gillingwater th. Eur J Neurosci. 2004 Dec;20(11):3092-114. doi: 10.1111/j.1460-9568.2004.03783.x. Eur J Neurosci. 2004. PMID: 15579164

4

The neuroprotective WldS gene regulates expression of PTTG1 and erythroid differentiation regulator 1-like gene in mice and human cells.

Gillingwater TH, Wishart TM, Chen PE, Haley JE, Robertson K, MacDonald SH, Middleton S, Wawrowski K, Shipston MJ, Melmed S, Wyllie DJ, Skehel PA, Coleman MP, Ribchester RR. Gillingwater TH, et al. Hum Mol Genet. 2006 Feb 15;15(4):625-35. doi: 10.1093/hmg/ddi478. Epub 2006 Jan 10. Hum Mol Genet. 2006. PMID: 16403805

5

Delayed synaptic degeneration in the CNS of Wlds mice after cortical lesion.

Gillingwater TH, Ingham CA, Parry KE, Wright AK, Haley JE, Wishart TM, Arbuthnott GW, Ribchester RR. Gillingwater TH, et al. Brain. 2006 Jun;129(Pt 6):1546-56. doi: 10.1093/brain/awl101. Brain. 2006. PMID: 16738060

6

Synaptic vulnerability in neurodegenerative disease.

Wishart TM, Parson SH, Gillingwater TH. Wishart TM, et al. Among authors: gillingwater th. 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.

7

Differential proteomics analysis of synaptic proteins identifies potential cellular targets and protein mediators of synaptic neuroprotection conferred by the slow Wallerian degeneration (Wlds) gene.

Wishart TM, Paterson JM, Short DM, Meredith S, Robertson KA, Sutherland C, Cousin MA, Dutia MB, Gillingwater TH. Wishart TM, et al. Among authors: gillingwater th. Mol Cell Proteomics. 2007 Aug;6(8):1318-30. doi: 10.1074/mcp.M600457-MCP200. Epub 2007 Apr 29. Mol Cell Proteomics. 2007. PMID: 17470424 Free PMC article.

8

Design of a novel quantitative PCR (QPCR)-based protocol for genotyping mice carrying the neuroprotective Wallerian degeneration slow (Wlds) gene.

Wishart TM, Macdonald SH, Chen PE, Shipston MJ, Coleman MP, Gillingwater TH, Ribchester RR. Wishart TM, et al. Among authors: gillingwater th. Mol Neurodegener. 2007 Oct 30;2:21. doi: 10.1186/1750-1326-2-21. Mol Neurodegener. 2007. PMID: 17971231 Free PMC article.

9

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. Among authors: gillingwater th. 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.

10

VAPB interacts with and modulates the activity of ATF6.

Gkogkas C, Middleton S, Kremer AM, Wardrope C, Hannah M, Gillingwater TH, Skehel P. Gkogkas C, et al. Among authors: gillingwater th. Hum Mol Genet. 2008 Jun 1;17(11):1517-26. doi: 10.1093/hmg/ddn040. Epub 2008 Feb 8. Hum Mol Genet. 2008. PMID: 18263603 Free article.

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