Gillingwater TH - Search Results

1

Pre-natal manifestation of systemic developmental abnormalities in spinal muscular atrophy.

Motyl AAL, Faller KME, Groen EJN, Kline RA, Eaton SL, Ledahawsky LM, Chaytow H, Lamont DJ, Wishart TM, Huang YT, Gillingwater TH. Motyl AAL, et al. Among authors: gillingwater th. Hum Mol Genet. 2020 Sep 29;29(16):2674-2683. doi: 10.1093/hmg/ddaa146. Hum Mol Genet. 2020. PMID: 32644120 Free PMC article.

2

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

3

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

4

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

5

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.

6

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.

7

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.

8

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.

9

Modified cell cycle status in a mouse model of altered neuronal vulnerability (slow Wallerian degeneration; Wlds).

Wishart TM, Pemberton HN, James SR, McCabe CJ, Gillingwater TH. Wishart TM, et al. Among authors: gillingwater th. Genome Biol. 2008;9(6):R101. doi: 10.1186/gb-2008-9-6-r101. Epub 2008 Jun 20. Genome Biol. 2008. PMID: 18570652 Free PMC article.

10

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. Among authors: gillingwater th. 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.

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