Gillingwater TH - Search Results

1

Vascular Defects and Spinal Cord Hypoxia in Spinal Muscular Atrophy.

Somers E, Lees RD, Hoban K, Sleigh JN, Zhou H, Muntoni F, Talbot K, Gillingwater TH, Parson SH. Somers E, et al. Among authors: gillingwater th. Ann Neurol. 2016 Feb;79(2):217-30. doi: 10.1002/ana.24549. Epub 2016 Jan 13. Ann Neurol. 2016. PMID: 26506088

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

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.

4

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.

5

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: gillingwater th. 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.

6

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: gillingwater th. 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

7

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: gillingwater th. 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.

8

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. Among authors: gillingwater th. 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.

9

Using mouse cranial muscles to investigate neuromuscular pathology in vivo.

Murray LM, Gillingwater TH, Parson SH. Murray LM, et al. Among authors: gillingwater th. 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

10

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: gillingwater th. 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.

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