| Year |
Citation |
Score |
| 2006 |
Montague P, McCallion AS, Davies RW, Griffiths IR. Myelin-associated oligodendrocytic basic protein: a family of abundant CNS myelin proteins in search of a function. Developmental Neuroscience. 28: 479-87. PMID 17028425 DOI: 10.1159/000095110 |
0.689 |
|
| 2005 |
Montague P, McCallion AS, Barrie JE, Edgar JM, McLaughlin M, Davies RW, Griffiths IR. Characterization of the murine splice variant Mobp155: developmental CNS expression pattern and subcellular localization of epitope-tagged protein. Glia. 50: 80-5. PMID 15625715 DOI: 10.1002/Glia.20155 |
0.675 |
|
| 2002 |
Yool D, Montague P, McLaughlin M, McCulloch MC, Edgar JM, Nave KA, Davies RW, Griffiths IR, McCallion AS. Phenotypic analysis of mice deficient in the major myelin protein MOBP, and evidence for a novel Mobp isoform. Glia. 39: 256-67. PMID 12203392 DOI: 10.1002/glia.10103 |
0.675 |
|
| 2001 |
Craig NJ, Durán Alonso MB, Hawker KL, Shiels P, Glencorse TA, Campbell JM, Bennett NK, Canham M, Donald D, Gardiner M, Gilmore DP, MacDonald RJ, Maitland K, McCallion AS, Russell D, ... ... Davies RW, et al. A candidate gene for human neurodegenerative disorders: a rat PKC gamma mutation causes a Parkinsonian syndrome. Nature Neuroscience. 4: 1061-2. PMID 11600890 DOI: 10.1038/Nn740 |
0.612 |
|
| 1999 |
McCallion AS, Stewart GJ, Montague P, Griffiths IR, Davies RW. Splicing pattern, transcript start distribution, and DNA sequence of the mouse gene (Mobp) encoding myelin-associated oligodendrocytic basic protein. Molecular and Cellular Neurosciences. 13: 229-36. PMID 10328883 DOI: 10.1006/mcne.1999.0745 |
0.651 |
|
| 1999 |
Montague P, Kirkham D, McCallion AS, Davies RW, Kennedy PG, Klugmann M, Nave K, Griffiths IR. Reduced levels of a specific myelin-associated oligodendrocytic basic protein isoform in shiverer myelin. Developmental Neuroscience. 21: 36-42. PMID 10077700 DOI: 10.1159/000017364 |
0.682 |
|
| 1998 |
Montague P, Barrie JA, Thomson CE, Kirkham D, McCallion AS, Davies RW, Kennedy PG, Griffths IR. Cytoskeletal and nuclear localization of myelin oligodendrocytic basic protein isoforms. The European Journal of Neuroscience. 10: 1321-8. PMID 9749786 |
0.674 |
|
| 1997 |
Duran Alonso MB, Shiels P, McCallion AS, Bennett NK, Payne AP, Szpirer J, Szpirer C, Brodie MJ, Davies RW, Sutcliffe RG, Alonso MB. The cystatin S gene maps to rat chromosome 3, to which D1mgh18 is re-assigned from chromosome 1. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 946-7. PMID 9383294 DOI: 10.1007/S003359900645 |
0.583 |
|
| 1997 |
Montague P, Dickinson PJ, McCallion AS, Stewart GJ, Savioz A, Davies RW, Kennedy PG, Griffiths IR. Developmental expression of the murine Mobp gene. Journal of Neuroscience Research. 49: 133-43. PMID 9272636 DOI: 10.1002/(Sici)1097-4547(19970715)49:2<133::Aid-Jnr2>3.0.Co;2-A |
0.693 |
|
| 1996 |
McCallion AS, Guénet JL, Montague P, Griffiths IR, Savioz A, Davies RW. The mouse gene (Mobp) encoding myelin-associated oligodendrocytic basic protein maps to distal chromosome 9. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 847-9. PMID 8875894 DOI: 10.1007/s003359900248 |
0.656 |
|
| 1995 |
Savioz A, Davies RW. Discovering genes with localised expression in the mouse brain: cDNAs specific to the substantia nigra. Gene. 154: 225-30. PMID 7890168 DOI: 10.1016/0378-1119(94)00864-O |
0.357 |
|
| 1994 |
Davies RW, Gallagher EJ, Savioz A. Reverse genetics of the mouse central nervous system: targeted genetic analysis of neuropeptide function and reverse genetic screens for genes involved in human neurodegenerative disease. Progress in Neurobiology. 42: 319-31. PMID 8008831 DOI: 10.1016/0301-0082(94)90072-8 |
0.372 |
|
| 1994 |
Davies RW, Roberts AB, Morris AJ, Griffith GW, Jerecìć J, Ghandi S, Kaiser K, Savioz A. Enhanced access to rare brain cDNAs by prescreening libraries: 207 new mouse brain ESTs. Genomics. 24: 456-63. PMID 7713496 DOI: 10.1006/Geno.1994.1653 |
0.335 |
|
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