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Reelin: Neurodevelopmental Architect and Homeostatic Regulator of Excitatory Synapses
Over half a century ago, D. S. Falconer first reported a mouse with a reeling gate. Four decades later, the Reln gene was isolated and identified as the cause of the reeler phenotype. Initial studies found that loss of Reelin, a large, secreted glycoprotein encoded by the Reln gene, results in abnor...
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| Publié dans: | J Biol Chem |
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| Auteurs principaux: | , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
American Society for Biochemistry and Molecular Biology
2017
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5270476/ https://ncbi.nlm.nih.gov/pubmed/27994051 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.R116.766782 |
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