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Last modified: 15/04/2002 by
Publications
Samsam M, Mi W, Wessig C, Zielasek, J, Toyka KV, Coleman MP and Martini R. The WldS
mutation delays robust axonal loss in a genetic model for myelin-related
axonopathy. J.
Neurosci. 2003 Apr 1; 23(7): 2833-9.
Conforti L, Dell'Agnello C, Calvaresi N, Tortarolo M, Giorgini A, Coleman MP,
Bendotti C. Kif1Bbeta isoform is enriched in motor neurons but does not change
in a mouse model of amyotrophic lateral sclerosis. J
Neurosci Res 2003 Mar 1; 71 (5): 732-9.
Mi W, Glass JD, Coleman MP. Stable inheritance of an 85-kb triplication in
C57BL/WldS mice. Mutat. Res. In press.
Gillingwater TH, Thomson D, Mack TG, Soffin EM, Mattison RJ, Coleman MP,
Ribchester RR. Age-dependent synapse withdrawal at axotomised
neuromuscular junctions in Wld(s) mutant and Ube4b/Nmnat transgenic mice. J
Physiol 2002 Sep 15;543(Pt 3):739-55.
Coleman MP, Perry VH. Axon pathology in neurological disease: a
neglected therapeutic target. Trends
Neurosci 2002 Oct;25(10):532-7.
Mack TGA, Reiner M, Beirowski B, Mi W, Emanuelli M, Wagner
D, Thomson D, Gillingwater T, Court F, Conforti L,
Fernando FS, Tarlton A, Andressen
C, Addicks K, Magni G, Ribchester RR, Perry VH, Coleman MP:
Wallerian degeneration of injured axons and synapses is delayed by a
Ube4b/Nmnat chimeric gene
Nat
Neurosci 2001 Dec
4(12):1199-1206.
Mi W, Conforti L, Coleman MP: A genotyping method to detect a
unique neuroprotective factor for axons (WldS)
J.
Neurosci. Meth. 2002
Jan 30; 113(2): 215-8.
Fernando FS, Conforti L, Tosi S, Smith AD,
Coleman MP: Human homologue of a gene mutated in the slow Wallerian degeneration
(C57BL/WldS) mouse.
Gene
2002 Feb 6;284(1-2):23-9.
Conforti, L., Tarlton, A., Mack, T.G.A.,
Mi, W., Buckmaster, E.A.,Wagner, D., Perry, V.H., and Coleman, M.P. (2000). A chimeric protein and overexpression of Rbp7 in the slow wallerian degeneration (WldS)
mouse. Proc. Natl. Acad.
Sci. 97: 11377-11382. PDF
Conforti,
L., Buckmaster, E.A., Tarlton, A., Brown, M.C., Lyon, M.F., Perry,V.H., and
Coleman, M.P. (1999) The major brain isoform of Kif1b lacks the putative
mitochondria-binding domain.
Mammalian Genome 10- 617-622.
Coleman
, M.P., Conforti, L., Buckmaster, E.A., Tarlton, A., Ewing, R.M., Brown, M.C.,
Lyon, M.F., and Perry, V.H. (1998) An 85kb tandem triplication in the slow
Wallerian degeneration (Wlds) mouse.
Proc. Natl. Acad.
Sci. 95- 9985-9990.
PDF
Coleman, M.P., Buckmaster, E.A., Ogunkolade, B.W.,
Tarlton, A., Lyon, M.F., Brown, M.C. and Perry, V.H. (1996). High resolution
mapping of the genes Kcnb3 and Ly63 on distal mouse chromosome 4.
Mammalian
Genome 7- 552-553.
