Wishart TM - Search Results

1

Retinoid-independent motor neurogenesis from human embryonic stem cells reveals a medial columnar ground state.

Patani R, Hollins AJ, Wishart TM, Puddifoot CA, Alvarez S, de Lera AR, Wyllie DJ, Compston DA, Pedersen RA, Gillingwater TH, Hardingham GE, Allen ND, Chandran S. Patani R, et al. Among authors: wishart tm. Nat Commun. 2011;2:214. doi: 10.1038/ncomms1216. Nat Commun. 2011. PMID: 21364553 Free PMC article.

2

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: wishart tm. 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

3

Synaptic vulnerability in neurodegenerative disease.

Wishart TM, Parson SH, Gillingwater TH. Wishart TM, et al. 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

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. Mol Neurodegener. 2007 Oct 30;2:21. doi: 10.1186/1750-1326-2-21. Mol Neurodegener. 2007. PMID: 17971231 Free PMC article.

5

VCP binding influences intracellular distribution of the slow Wallerian degeneration protein, Wld(S).

Wilbrey AL, Haley JE, Wishart TM, Conforti L, Morreale G, Beirowski B, Babetto E, Adalbert R, Gillingwater TH, Smith T, Wyllie DJ, Ribchester RR, Coleman MP. Wilbrey AL, et al. Among authors: wishart tm. Mol Cell Neurosci. 2008 Jul;38(3):325-40. doi: 10.1016/j.mcn.2008.03.004. Epub 2008 Mar 25. Mol Cell Neurosci. 2008. PMID: 18468455

6

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. 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.

7

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: wishart tm. 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.

8

Protein product of CLN6 gene responsible for variant late-onset infantile neuronal ceroid lipofuscinosis interacts with CRMP-2.

Benedict JW, Getty AL, Wishart TM, Gillingwater TH, Pearce DA. Benedict JW, et al. Among authors: wishart tm. J Neurosci Res. 2009 Jul;87(9):2157-66. doi: 10.1002/jnr.22032. J Neurosci Res. 2009. PMID: 19235893 Free PMC article.

9

Expression of the neuroprotective slow Wallerian degeneration (WldS) gene in non-neuronal tissues.

Wishart TM, Brownstein DG, Thomson D, Tabakova AM, Boothe KM, Tsao JW, Gillingwater TH. Wishart TM, et al. BMC Neurosci. 2009 Dec 16;10:148. doi: 10.1186/1471-2202-10-148. BMC Neurosci. 2009. PMID: 20015399 Free PMC article.

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. 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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