Griffiths IR - Search Results

1

Phenotypic analysis of mice deficient in the major myelin protein MOBP, and evidence for a novel Mobp isoform.

Yool D, Montague P, McLaughlin M, McCulloch MC, Edgar JM, Nave KA, Davies RW, Griffiths IR, McCallion AS. Yool D, et al. Among authors: griffiths ir. Glia. 2002 Sep;39(3):256-67. doi: 10.1002/glia.10103. Glia. 2002. PMID: 12203392

2

Characterization of the murine splice variant Mobp155: developmental CNS expression pattern and subcellular localization of epitope-tagged protein.

Montague P, McCallion AS, Barrie JE, Edgar JM, McLaughlin M, Davies RW, Griffiths IR. Montague P, et al. Among authors: griffiths ir. Glia. 2005 Apr 1;50(1):80-5. doi: 10.1002/glia.20155. Glia. 2005. PMID: 15625715

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: griffiths ir. Glia. 2006 May;53(7):715-22. doi: 10.1002/glia.20325. Glia. 2006. PMID: 16506223

4

Myelin-associated oligodendrocytic basic protein: a family of abundant CNS myelin proteins in search of a function.

Montague P, McCallion AS, Davies RW, Griffiths IR. Montague P, et al. Among authors: griffiths ir. Dev Neurosci. 2006;28(6):479-87. doi: 10.1159/000095110. Dev Neurosci. 2006. PMID: 17028425 Review.

5

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: griffiths ir. Glia. 2007 Mar;55(4):341-51. doi: 10.1002/glia.20465. Glia. 2007. PMID: 17133418

6

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: griffiths ir. Glia. 2009 Dec;57(16):1815-24. doi: 10.1002/glia.20893. Glia. 2009. PMID: 19459211

7

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: griffiths ir. Glia. 2010 Nov 1;58(14):1727-38. doi: 10.1002/glia.21043. Glia. 2010. PMID: 20629189

8

Axonal swellings and degeneration in mice lacking the major proteolipid of myelin.

Griffiths I, Klugmann M, Anderson T, Yool D, Thomson C, Schwab MH, Schneider A, Zimmermann F, McCulloch M, Nadon N, Nave KA. Griffiths I, et al. Science. 1998 Jun 5;280(5369):1610-3. doi: 10.1126/science.280.5369.1610. Science. 1998. PMID: 9616125

9

The mouse gene (Mobp) encoding myelin-associated oligodendrocytic basic protein maps to distal chromosome 9.

McCallion AS, Guénet JL, Montague P, Griffiths IR, Savioz A, Davies RW. McCallion AS, et al. Among authors: griffiths ir. Mamm Genome. 1996 Nov;7(11):847-9. doi: 10.1007/s003359900248. Mamm Genome. 1996. PMID: 8875894 No abstract available.

10

Phenotypic severity of murine Plp mutants reflects in vivo and in vitro variations in transport of PLP isoproteins.

Thomson CE, Montague P, Jung M, Nave KA, Griffiths IR. Thomson CE, et al. Among authors: griffiths ir. Glia. 1997 Aug;20(4):322-32. doi: 10.1002/(sici)1098-1136(199708)20:4<322::aid-glia5>3.0.co;2-7. Glia. 1997. PMID: 9262236

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