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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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Detalhes bibliográficos
Publicado no:J Biol Chem
Main Authors: Wasser, Catherine R., Herz, Joachim
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Biochemistry and Molecular Biology 2017
Assuntos:
Acesso em linha: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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