Skehel PA - Search Results

1

Loss of cerebellar glutamate transporters EAAT4 and GLAST differentially affects the spontaneous firing pattern and survival of Purkinje cells.

Perkins EM, Clarkson YL, Suminaite D, Lyndon AR, Tanaka K, Rothstein JD, Skehel PA, Wyllie DJA, Jackson M. Perkins EM, et al. Among authors: skehel pa. Hum Mol Genet. 2018 Aug 1;27(15):2614-2627. doi: 10.1093/hmg/ddy169. Hum Mol Genet. 2018. PMID: 29741614 Free PMC article.

2

β-III spectrin underpins ankyrin R function in Purkinje cell dendritic trees: protein complex critical for sodium channel activity is impaired by SCA5-associated mutations.

Clarkson YL, Perkins EM, Cairncross CJ, Lyndon AR, Skehel PA, Jackson M. Clarkson YL, et al. Among authors: skehel pa. Hum Mol Genet. 2014 Jul 15;23(14):3875-82. doi: 10.1093/hmg/ddu103. Epub 2014 Mar 6. Hum Mol Genet. 2014. PMID: 24603075 Free PMC article.

3

Functional assessment of triheteromeric NMDA receptors containing a human variant associated with epilepsy.

Marwick KFM, Hansen KB, Skehel PA, Hardingham GE, Wyllie DJA. Marwick KFM, et al. Among authors: skehel pa. J Physiol. 2019 Mar;597(6):1691-1704. doi: 10.1113/JP277292. Epub 2019 Jan 30. J Physiol. 2019. PMID: 30604514 Free PMC article.

4

The human NMDA receptor GluN2A^N615K variant influences channel blocker potency.

Marwick KFM, Skehel PA, Hardingham GE, Wyllie DJA. Marwick KFM, et al. Among authors: skehel pa. Pharmacol Res Perspect. 2019 Jun 20;7(4):e00495. doi: 10.1002/prp2.495. eCollection 2019 Aug. Pharmacol Res Perspect. 2019. PMID: 31249692 Free PMC article.

5

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. Among authors: skehel pa. 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

6

Mitochondrial calcium uniporter Mcu controls excitotoxicity and is transcriptionally repressed by neuroprotective nuclear calcium signals.

Qiu J, Tan YW, Hagenston AM, Martel MA, Kneisel N, Skehel PA, Wyllie DJ, Bading H, Hardingham GE. Qiu J, et al. Among authors: skehel pa. Nat Commun. 2013;4:2034. doi: 10.1038/ncomms3034. Nat Commun. 2013. PMID: 23774321 Free PMC article.

7

GRIN2A-related disorders: genotype and functional consequence predict phenotype.

Strehlow V, Heyne HO, Vlaskamp DRM, Marwick KFM, Rudolf G, de Bellescize J, Biskup S, Brilstra EH, Brouwer OF, Callenbach PMC, Hentschel J, Hirsch E, Kind PC, Mignot C, Platzer K, Rump P, Skehel PA, Wyllie DJA, Hardingham GE, van Ravenswaaij-Arts CMA, Lesca G, Lemke JR; GRIN2A study group. Strehlow V, et al. Among authors: skehel pa. Brain. 2019 Jan 1;142(1):80-92. doi: 10.1093/brain/awy304. Brain. 2019. PMID: 30544257 Free PMC article.

8

Initial characterisation of adult human ovarian cell populations isolated by DDX4 expression and aldehyde dehydrogenase activity.

Clarkson YL, McLaughlin M, Waterfall M, Dunlop CE, Skehel PA, Anderson RA, Telfer EE. Clarkson YL, et al. Among authors: skehel pa. Sci Rep. 2018 May 3;8(1):6953. doi: 10.1038/s41598-018-25116-1. Sci Rep. 2018. PMID: 29725036 Free PMC article.

9

Functional assessment of the NMDA receptor variant GluN2A ^R586K.

Marwick KFM, Parker P, Skehel P, Hardingham G, Wyllie DJA. Marwick KFM, et al. Wellcome Open Res. 2017 Mar 17;2:20. doi: 10.12688/wellcomeopenres.10985.2. Wellcome Open Res. 2017. PMID: 28459106 Free PMC article.

10

Effect of a GRIN2A de novo mutation associated with epilepsy and intellectual disability on NMDA receptor currents and Mg(2+) block in cultured primary cortical neurons.

Marwick K, Skehel P, Hardingham G, Wyllie D. Marwick K, et al. Lancet. 2015 Feb 26;385 Suppl 1:S65. doi: 10.1016/S0140-6736(15)60380-4. Lancet. 2015. PMID: 26312887

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