Mackenzie IR - Search Results

1

Progranulin deficiency decreases gross neural connectivity but enhances transmission at individual synapses.

Tapia L, Milnerwood A, Guo A, Mills F, Yoshida E, Vasuta C, Mackenzie IR, Raymond L, Cynader M, Jia W, Bamji SX. Tapia L, et al. Among authors: mackenzie ir. J Neurosci. 2011 Aug 3;31(31):11126-32. doi: 10.1523/JNEUROSCI.6244-10.2011. J Neurosci. 2011. PMID: 21813674 Free PMC article.

2

Critical role of integrin-linked kinase in granule cell precursor proliferation and cerebellar development.

Mills J, Niewmierzycka A, Oloumi A, Rico B, St-Arnaud R, Mackenzie IR, Mawji NM, Wilson J, Reichardt LF, Dedhar S. Mills J, et al. Among authors: mackenzie ir. J Neurosci. 2006 Jan 18;26(3):830-40. doi: 10.1523/JNEUROSCI.1852-05.2006. J Neurosci. 2006. PMID: 16421303 Free PMC article.

3

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.

Mackenzie IR, Baker M, Pickering-Brown S, Hsiung GY, Lindholm C, Dwosh E, Gass J, Cannon A, Rademakers R, Hutton M, Feldman HH. Mackenzie IR, et al. Brain. 2006 Nov;129(Pt 11):3081-90. doi: 10.1093/brain/awl271. Brain. 2006. PMID: 17071926

4

Progranulin expression in the developing and adult murine brain.

Petkau TL, Neal SJ, Orban PC, MacDonald JL, Hill AM, Lu G, Feldman HH, Mackenzie IR, Leavitt BR. Petkau TL, et al. Among authors: mackenzie ir. J Comp Neurol. 2010 Oct 1;518(19):3931-47. doi: 10.1002/cne.22430. J Comp Neurol. 2010. PMID: 20737593

5

rs5848 polymorphism and serum progranulin level.

Hsiung GY, Fok A, Feldman HH, Rademakers R, Mackenzie IR. Hsiung GY, et al. Among authors: mackenzie ir. J Neurol Sci. 2011 Jan 15;300(1-2):28-32. doi: 10.1016/j.jns.2010.10.009. Epub 2010 Nov 2. J Neurol Sci. 2011. PMID: 21047645 Free PMC article.

6

Synaptic dysfunction in progranulin-deficient mice.

Petkau TL, Neal SJ, Milnerwood A, Mew A, Hill AM, Orban P, Gregg J, Lu G, Feldman HH, Mackenzie IR, Raymond LA, Leavitt BR. Petkau TL, et al. Among authors: mackenzie ir. Neurobiol Dis. 2012 Feb;45(2):711-22. doi: 10.1016/j.nbd.2011.10.016. Epub 2011 Oct 25. Neurobiol Dis. 2012. PMID: 22062772

7

Early neuropsychological characteristics of progranulin mutation carriers.

Hallam BJ, Jacova C, Hsiung GY, Wittenberg D, Sengdy P, Bouchard-Kerr P, Slack P, Rademakers R, Baker M, Chow TW, Levine B, Feldman HH, Mackenzie IR. Hallam BJ, et al. Among authors: mackenzie ir. J Int Neuropsychol Soc. 2014 Aug;20(7):694-703. doi: 10.1017/S1355617714000551. Epub 2014 Jul 4. J Int Neuropsychol Soc. 2014. PMID: 24993774

8

Neuronal intranuclear inclusions distinguish familial FTD-MND type from sporadic cases.

Mackenzie IR, Feldman H. Mackenzie IR, et al. Dement Geriatr Cogn Disord. 2004;17(4):333-6. doi: 10.1159/000077166. Dement Geriatr Cogn Disord. 2004. PMID: 15178948

9

A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17.

Mackenzie IR, Baker M, West G, Woulfe J, Qadi N, Gass J, Cannon A, Adamson J, Feldman H, Lindholm C, Melquist S, Pettman R, Sadovnick AD, Dwosh E, Whiteheart SW, Hutton M, Pickering-Brown SM. Mackenzie IR, et al. Brain. 2006 Apr;129(Pt 4):853-67. doi: 10.1093/brain/awh724. Epub 2006 Jan 9. Brain. 2006. PMID: 16401619

10

The neuropathology and clinical phenotype of FTD with progranulin mutations.

Mackenzie IR. Mackenzie IR. Acta Neuropathol. 2007 Jul;114(1):49-54. doi: 10.1007/s00401-007-0223-8. Epub 2007 Apr 26. Acta Neuropathol. 2007. PMID: 17458552 Review.

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