Inhibitor of neurite outgrowth in humans
Rabinder Prinjha,
Stephen E. Moore,
Mary Vinson,
Sian Blake,
Rachel Morrow,
Gary Christie,
David Michalovich,
David L. Simmons and
Frank S. Walsh ()
Additional contact information
Rabinder Prinjha: Department of Neuroscience Research
Stephen E. Moore: Department of Neuroscience Research
Mary Vinson: Department of Neuroscience Research
Sian Blake: Department of Neuroscience Research
Rachel Morrow: Department of Neuroscience Research
Gary Christie: Department of Neuroscience Research
David Michalovich: Departments of Neuroscience Research and Bioinformatics
David L. Simmons: Department of Neuroscience Research
Frank S. Walsh: Department of Neuroscience Research
Nature, 2000, vol. 403, issue 6768, 383-384
Abstract:
Abstract Axons are generally believed to be incapable of regeneration in the adult central nervous system1,2. Inhibition results from physical barriers imposed by glial scars, a lack of neurotrophic factors, and growth-inhibitory molecules associated with myelin3,4,5, the insulating axon sheath. These molecules include proteoglycans6, myelin-associated glycoprotein3,5 and, in bovine brain, two proteins called Nogo7,8,9. We have used this bovine sequence to identify the human Nogo gene and have isolated complementary DNA clones encoding three different Nogo isoforms that are potent inhibitors of neurite outgrowth and which may help block the regeneration of the central nervous system in adults.
Date: 2000
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Persistent link: https://EconPapers.repec.org/RePEc:nat:nature:v:403:y:2000:i:6768:d:10.1038_35000287
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DOI: 10.1038/35000287
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