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Article

MeCP2 function in the basolateral amygdala in Rett syndrome.

The Journal of neuroscience : the official journal of the Society for Neuroscience - 12 Aug 2009

Wu Synphen H, Camarena Vladimir

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 19675227
DOI: 10.1523/JNEUROSCI.2540-09.2009
PMCID: PMC4658513

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MeCP2 function in the basolateral amygdala in Rett syndrome.PMID 19675227Read ↗

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MeCP2-mediated transcription repression in the basolateral amygdala may underlie heightened anxiety in a mouse model of Rett syndrome.Semantic proximity Read ↗

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Loss of MeCP2 in cholinergic neurons causes part of RTT-like phenotypes via α7 receptor in hippocampus.Semantic proximity Read ↗

Rett Syndrome: Crossing the Threshold to Clinical Translation.Semantic proximity Read ↗

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Defining dysfunction due to loss of MECP2 in Rett Patient BrainSemantic proximity Read ↗

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Loss of the MeCP2 gene in parvalbumin interneurons leads to an inhibitory deficit in the amygdala and affects its functional connectivitySemantic proximity Read ↗

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