Activity-induced MeCP2 phosphorylation regulates retinogeniculate synapse refinement
Author:
Affiliation:
1. Department of Neurobiology, Harvard Medical School, Boston, MA 02115
2. Program in Neuroscience, Harvard Medical School, Boston, MA 02115
3. Department of Neurology, F.M. Kirby Neurobiology Center, Children’s Hospital, Boston, MA 02115
Abstract
Funder
HHS | NIH | National Institute of Neurological Disorders and Stroke
HHS | NIH | National Eye Institute
Department of Neurobiology, Harvard Medical School
Stuart H.Q. & Victoria Quan
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Link
https://pnas.org/doi/pdf/10.1073/pnas.2310344120
Reference60 articles.
1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
2. Purification, sequence, and cellular localization of a novel chromosomal protein that binds to Methylated DNA
3. The Story of Rett Syndrome: From Clinic to Neurobiology
4. MeCP2 Controls Excitatory Synaptic Strength by Regulating Glutamatergic Synapse Number
5. Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome
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