Cortical Layer Inversion and Deregulation of Reelin Signaling in the Absence of SOCS6 and SOCS7

Mutations of the reelin gene cause severe defects in cerebral cortex development and profound intellectual impairment. While many aspects of the reelin signaling pathway have been identified, the molecular and ultimate cellular consequences of reelin signaling remain unknown. Specifically, it is unc...

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Bibliographic Details
Published inCerebral cortex (New York, N.Y. 1991) Vol. 27; no. 1; pp. 576 - 588
Main Authors Lawrenson, Isobel D, Krebs, Danielle L, Linossi, Edmond M, Zhang, Jian-Guo, McLennan, Tamara J, Collin, Caitlin, McRae, Helen M, Kolesnik, Tatiana B, Koh, Katrina, Britto, Joanne M, Kueh, Andrew J, Sheikh, Bilal N, El-Saafin, Farrah, Nicola, Nicos A, Tan, Seong-Seng, Babon, Jeffrey J, Nicholson, Sandra E, Alexander, Warren S, Thomas, Tim, Voss, Anne K
Format Journal Article
LanguageEnglish
Published United States 01.01.2017
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