Search Results - "McCulloch, M.C."
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Genetic background determines phenotypic severity of the Plp rumpshaker mutation
Published in Journal of neuroscience research (01-04-2003)“…The rumpshaker mutation of the proteolipid protein (Plp) gene causes dysmyelination in man and mouse. We show that the phenotype in the mouse depends…”
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Late-onset neurodegeneration in mice with increased dosage of the proteolipid protein gene
Published in Journal of comparative neurology (1911) (18-05-1998)“…Mutations of the proteolipid protein (Plp) gene cause a generalized central nervous system (CNS) myelin deficit in Pelizaeus‐Merzbacher disease of man and…”
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Myelin proteolipid proteins promote the interaction of oligodendrocytes and axons
Published in Journal of neuroscience research (15-01-2001)“…Although proteolipid protein (PLP) and its DM20 isoform are the major membrane proteins of CNS myelin, their absence causes surprisingly few developmental…”
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Phenotypic analysis of mice deficient in the major myelin protein MOBP, and evidence for a novel Mobp isoform
Published in Glia (01-09-2002)“…Myelin‐associated oligodendrocytic basic protein (MOBP) is a recently identified major component of central nervous system (CNS) myelin. We previously reported…”
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Survival of, and Competition between, Oligodendrocytes Expressing Different Alleles of the Plp Gene
Published in The Journal of cell biology (19-08-2002)“…Mutations in the X-linked Plp gene lead to dysmyelinating phenotypes and oligodendrocyte cell death. Here, we exploit the X inactivation phenomenon to show…”
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Nerve fibres in spinal cord impact injuries. Part 1. Changes in the myelin sheath during the initial 5 weeks
Published in Journal of the neurological sciences (1983)“…The spinal cords of cats were subjected to an impact injury using a "weight dropping" technique and sequential changes in the sheaths of non-degenerate…”
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