Barrie JA - Search Results

1

PLP/DM20 expression and turnover in a transgenic mouse model of Pelizaeus-Merzbacher disease.

Karim SA, Barrie JA, McCulloch MC, Montague P, Edgar JM, Iden DL, Anderson TJ, Nave KA, Griffiths IR, McLaughlin M. Karim SA, et al. Among authors: barrie ja. Glia. 2010 Nov 1;58(14):1727-38. doi: 10.1002/glia.21043. Glia. 2010. PMID: 20629189

2

Processing of PLP in a model of Pelizaeus-Merzbacher disease/SPG2 due to the rumpshaker mutation.

McLaughlin M, Barrie JA, Karim S, Montague P, Edgar JM, Kirkham D, Thomson CE, Griffiths IR. McLaughlin M, et al. Among authors: barrie ja. Glia. 2006 May;53(7):715-22. doi: 10.1002/glia.20325. Glia. 2006. PMID: 16506223

3

PLP overexpression perturbs myelin protein composition and myelination in a mouse model of Pelizaeus-Merzbacher disease.

Karim SA, Barrie JA, McCulloch MC, Montague P, Edgar JM, Kirkham D, Anderson TJ, Nave KA, Griffiths IR, McLaughlin M. Karim SA, et al. Among authors: barrie ja. Glia. 2007 Mar;55(4):341-51. doi: 10.1002/glia.20465. Glia. 2007. PMID: 17133418

4

Early ultrastructural defects of axons and axon-glia junctions in mice lacking expression of Cnp1.

Edgar JM, McLaughlin M, Werner HB, McCulloch MC, Barrie JA, Brown A, Faichney AB, Snaidero N, Nave KA, Griffiths IR. Edgar JM, et al. Among authors: barrie ja. Glia. 2009 Dec;57(16):1815-24. doi: 10.1002/glia.20893. Glia. 2009. PMID: 19459211

5

Modulation of rumpshaker phenotype with wild-type PLP/DM20 suggests several pathogenic mechanisms.

Barrie JA, Montague P, Karim S, Kirkham D, Nave KA, Anderson TJ, Griffiths IR, McLaughlin M. Barrie JA, et al. J Neurosci Res. 2010 Aug 1;88(10):2135-45. doi: 10.1002/jnr.22379. J Neurosci Res. 2010. PMID: 20175203

6

High-resolution diffusion tensor imaging of fixed brain in a mouse model of Pelizaeus-Merzbacher disease: comparison with quantitative measures of white matter pathology.

Ruest T, Holmes WM, Barrie JA, Griffiths IR, Anderson TJ, Dewar D, Edgar JM. Ruest T, et al. Among authors: barrie ja. NMR Biomed. 2011 Dec;24(10):1369-79. doi: 10.1002/nbm.1700. Epub 2011 Mar 24. NMR Biomed. 2011. PMID: 22223367

7

Neural stem cells restore myelin in a demyelinating model of Pelizaeus-Merzbacher disease.

Gruenenfelder FI, McLaughlin M, Griffiths IR, Garbern J, Thomson G, Kuzman P, Barrie JA, McCulloch ML, Penderis J, Stassart R, Nave KA, Edgar JM. Gruenenfelder FI, et al. Among authors: barrie ja. Brain. 2020 May 1;143(5):1383-1399. doi: 10.1093/brain/awaa080. Brain. 2020. PMID: 32419025 Free PMC article.

8

Rumpshaker: an X-linked mutation causing hypomyelination: developmental differences in myelination and glial cells between the optic nerve and spinal cord.

Fanarraga ML, Griffiths IR, McCulloch MC, Barrie JA, Kennedy PG, Brophy PJ. Fanarraga ML, et al. Among authors: barrie ja. Glia. 1992;5(3):161-70. doi: 10.1002/glia.440050302. Glia. 1992. PMID: 1375190

9

Genetic background determines phenotypic severity of the Plp rumpshaker mutation.

Al-Saktawi K, McLaughlin M, Klugmann M, Schneider A, Barrie JA, McCulloch MC, Montague P, Kirkham D, Nave KA, Griffiths IR. Al-Saktawi K, et al. Among authors: barrie ja. J Neurosci Res. 2003 Apr 1;72(1):12-24. doi: 10.1002/jnr.10561. J Neurosci Res. 2003. PMID: 12645075

10

Age-related axonal and myelin changes in the rumpshaker mutation of the Plp gene.

Edgar JM, McLaughlin M, Barrie JA, McCulloch MC, Garbern J, Griffiths IR. Edgar JM, et al. Among authors: barrie ja. Acta Neuropathol. 2004 Apr;107(4):331-5. doi: 10.1007/s00401-003-0808-9. Epub 2004 Jan 24. Acta Neuropathol. 2004. PMID: 14745569

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