Breathing dysfunction in Rett syndrome: Understanding epigenetic regulation of the respiratory network
- 18 April 2008
- journal article
- review article
- Published by Elsevier in Respiratory Physiology & Neurobiology
- Vol. 164 (1-2) , 55-63
- https://doi.org/10.1016/j.resp.2008.04.005
Abstract
No abstract availableKeywords
This publication has 123 references indexed in Scilit:
- A partial loss of function allele of Methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndromeHuman Molecular Genetics, 2008
- Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genesProceedings of the National Academy of Sciences, 2007
- Autonomic cardiovascular control in methyl-CpG-binding protein 2 (Mecp2) deficient miceAutonomic Neuroscience, 2007
- MeCP2 Controls Excitatory Synaptic Strength by Regulating Glutamatergic Synapse NumberNeuron, 2007
- Developmental changes in brain-derived neurotrophic factor-mediated modulations of synaptic activities in the pontine Kölliker-Fuse nucleus of the ratThe Journal of Physiology, 2007
- Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neuronsNeurobiology of Disease, 2007
- Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2−/y knockout miceThe Journal of Physiology, 2007
- Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2Proceedings of the National Academy of Sciences, 2007
- Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndromeHuman Molecular Genetics, 2006
- Genomic DNA methylation: the mark and its mediatorsPublished by Elsevier ,2006