Barrie JA - Search Results

1

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

2

Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia.

Edgar JM, McLaughlin M, Yool D, Zhang SC, Fowler JH, Montague P, Barrie JA, McCulloch MC, Duncan ID, Garbern J, Nave KA, Griffiths IR. Edgar JM, et al. Among authors: barrie ja. J Cell Biol. 2004 Jul 5;166(1):121-31. doi: 10.1083/jcb.200312012. Epub 2004 Jun 28. J Cell Biol. 2004. PMID: 15226307 Free PMC article.

3

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

4

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

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

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

7

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

8

Late-onset neurodegeneration in mice with increased dosage of the proteolipid protein gene.

Anderson TJ, Schneider A, Barrie JA, Klugmann M, McCulloch MC, Kirkham D, Kyriakides E, Nave KA, Griffiths IR. Anderson TJ, et al. Among authors: barrie ja. J Comp Neurol. 1998 May 18;394(4):506-19. doi: 10.1002/(sici)1096-9861(19980518)394:4<506::aid-cne8>3.0.co;2-5. J Comp Neurol. 1998. PMID: 9590558

9

Myelin proteolipid proteins promote the interaction of oligodendrocytes and axons.

Yool DA, Klugmann M, McLaughlin M, Vouyiouklis DA, Dimou L, Barrie JA, McCulloch MC, Nave KA, Griffiths IR. Yool DA, et al. Among authors: barrie ja. J Neurosci Res. 2001 Jan 15;63(2):151-64. doi: 10.1002/1097-4547(20010115)63:2<151::AID-JNR1007>3.0.CO;2-Y. J Neurosci Res. 2001. PMID: 11169625

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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