Unraveling molecular, cellular and cognitive defects in the mouse model for mental retardation caused by Rsk2 gene mutation

Unraveling molecular, cellular and cognitive defects in the mouse model for mental retardation caused by Rsk2 gene mutation

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Le syndrome de Coffin-Lowry (CLS), une déficience intellectuelle liée à l'X, est causée par des mutations du gène RPS6KA3 codant pour la kinase RSK2 régulée par les facteurs de croissance.Pour comprendre les conséquences du déficit en RSK2 dans l'hippocampe nous avons effectué une comparai...

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Bibliographic Details
Main Author:	Mehmood, Tahir
Other Authors:	Strasbourg
Language:	en
Published:	2012
Subjects:	Syndrome de Coffin-Lowry RSK2 Gria2 Récepteur glutamate AMPA ERK CREB PC12 Sp1 Coffin-Lowry Syndrome Glutamate receptor 572.8 572.6
Online Access:	http://www.theses.fr/2012STRAJ112/document

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