Animal Models for Coffin-Lowry Syndrome: RSK2 and Nervous System Dysfunction-Reference-Cited by-同舟云学术

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Animal Models for Coffin-Lowry Syndrome: RSK2 and Nervous System Dysfunction

Published:2018-05-23 Issue: Volume:12 Page:
ISSN:1662-5153
Container-title:Frontiers in Behavioral Neuroscience
language:
Short-container-title:Front. Behav. Neurosci.

Author:

Fischer Matthias,Raabe Thomas

Funder

Deutsche Forschungsgemeinschaft

Interdisziplinäres Zentrum für Klinische Forschung, Universitätsklinikum Würzburg

Publisher

Frontiers Media SA

Subject

Behavioral Neuroscience,Cognitive Neuroscience,Neuropsychology and Physiological Psychology

Reference52 articles.

1. Ribosomal s6 kinase cooperates with casein kinase 2 to modulate the Drosophila circadian molecular oscillator;Akten;J. Neurosci.,2009

2. The Coffin-Lowry syndrome-associated protein RSK2 regulates neurite outgrowth through phosphorylation of phospholipase D1 (PLD1) and synthesis of phosphatidic acid;Ammar;J. Neurosci.,2013

3. Adult hippocampal neurogenesis and cognitive flexibility—linking memory and mood;Anacker;Nat. Rev. Neurosci.,2017

4. From learning to memory: what flies can tell us about intellectual disability treatment;Androschuk;Front. Psychiatry,2015

5. Loss of the Coffin-Lowry syndrome-associated gene RSK2 alters ERK activity, synaptic function and axonal transport in Drosophila motoneurons;Beck;Dis. Model. Mech.,2015

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