Wood JD - Search Results

1

The cellular and molecular pathology of the motor system in hereditary spastic paraparesis due to mutation of the spastin gene.

Wharton SB, McDermott CJ, Grierson AJ, Wood JD, Gelsthorpe C, Ince PG, Shaw PJ. Wharton SB, et al. Among authors: wood jd. J Neuropathol Exp Neurol. 2003 Nov;62(11):1166-77. doi: 10.1093/jnen/62.11.1166. J Neuropathol Exp Neurol. 2003. PMID: 14656074

2

Protein aggregation in motor neurone disorders.

Wood JD, Beaujeux TP, Shaw PJ. Wood JD, et al. Neuropathol Appl Neurobiol. 2003 Dec;29(6):529-45. doi: 10.1046/j.0305-1846.2003.00518.x. Neuropathol Appl Neurobiol. 2003. PMID: 14636160 Review.

3

Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutation.

McDermott CJ, Grierson AJ, Wood JD, Bingley M, Wharton SB, Bushby KM, Shaw PJ. McDermott CJ, et al. Among authors: wood jd. Ann Neurol. 2003 Dec;54(6):748-59. doi: 10.1002/ana.10757. Ann Neurol. 2003. PMID: 14681884

4

Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients.

Kasher PR, De Vos KJ, Wharton SB, Manser C, Bennett EJ, Bingley M, Wood JD, Milner R, McDermott CJ, Miller CC, Shaw PJ, Grierson AJ. Kasher PR, et al. Among authors: wood jd. J Neurochem. 2009 Jul;110(1):34-44. doi: 10.1111/j.1471-4159.2009.06104.x. Epub 2009 Apr 22. J Neurochem. 2009. PMID: 19453301 Free article.

5

Motor neurone disease/amyotrophic lateral sclerosis associated with intermediate-length CAG repeat expansions in Ataxin-2 does not have 1C2-positive polyglutamine inclusions.

Highley JR, Lorente Pons A, Cooper-Knock J, Wharton SB, Ince PG, Shaw PJ, Wood J, Kirby J. Highley JR, et al. Neuropathol Appl Neurobiol. 2016 Jun;42(4):377-89. doi: 10.1111/nan.12254. Epub 2015 Jul 7. Neuropathol Appl Neurobiol. 2016. PMID: 26095883

6

The microtubule-severing protein Spastin is essential for axon outgrowth in the zebrafish embryo.

Wood JD, Landers JA, Bingley M, McDermott CJ, Thomas-McArthur V, Gleadall LJ, Shaw PJ, Cunliffe VT. Wood JD, et al. Hum Mol Genet. 2006 Sep 15;15(18):2763-71. doi: 10.1093/hmg/ddl212. Epub 2006 Aug 7. Hum Mol Genet. 2006. PMID: 16893913

7

Oligodendrocyte pathology exceeds axonal pathology in white matter in human amyotrophic lateral sclerosis.

Lorente Pons A, Higginbottom A, Cooper-Knock J, Alrafiah A, Alofi E, Kirby J, Shaw PJ, Wood JD, Highley JR. Lorente Pons A, et al. Among authors: wood jd. J Pathol. 2020 Jul;251(3):262-271. doi: 10.1002/path.5455. Epub 2020 Jun 8. J Pathol. 2020. PMID: 32391572 Free article.

8

Genetic and chemical modulation of spastin-dependent axon outgrowth in zebrafish embryos indicates a role for impaired microtubule dynamics in hereditary spastic paraplegia.

Butler R, Wood JD, Landers JA, Cunliffe VT. Butler R, et al. Among authors: wood jd. Dis Model Mech. 2010 Nov-Dec;3(11-12):743-51. doi: 10.1242/dmm.004002. Epub 2010 Sep 9. Dis Model Mech. 2010. PMID: 20829563 Free PMC article.

9

Widespread occurrence of intranuclear atrophin-1 accumulation in the central nervous system neurons of patients with dentatorubral-pallidoluysian atrophy.

Yamada M, Wood JD, Shimohata T, Hayashi S, Tsuji S, Ross CA, Takahashi H. Yamada M, et al. Among authors: wood jd. Ann Neurol. 2001 Jan;49(1):14-23. doi: 10.1002/1531-8249(200101)49:1<14::aid-ana5>3.0.co;2-x. Ann Neurol. 2001. PMID: 11198291

10

Disrupted-in-schizophrenia 1 and neuregulin 1 are required for the specification of oligodendrocytes and neurones in the zebrafish brain.

Wood JD, Bonath F, Kumar S, Ross CA, Cunliffe VT. Wood JD, et al. Hum Mol Genet. 2009 Feb 1;18(3):391-404. doi: 10.1093/hmg/ddn361. Epub 2008 Nov 7. Hum Mol Genet. 2009. PMID: 18996920

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