The Story of Rett Syndrome: From Clinic to Neurobiology
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference133 articles.
1. Cell-specific expression of wild-type MeCP2 in mouse models of Rett syndrome yields insight about pathogenesis;Alvarez-Saavedra;Hum. Mol. Genet.,2007
2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999
3. NTNG1 mutations are a rare cause of Rett syndrome;Archer;Am. J. Med. Genet. A.,2006
4. Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome patients;Archer;J. Med. Genet.,2006
5. Real-time quantitative PCR as a routine method for screening large rearrangements in Rett syndrome: Report of one case of MECP2 deletion and one case of MECP2 duplication;Ariani;Hum. Mutat.,2004
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1. POMC-specific knockdown of MeCP2 leads to adverse phenotypes in mice chronically exposed to high fat diet;Behavioural Brain Research;2024-03
2. RIPK1 activation in Mecp2-deficient microglia promotes inflammation and glutamate release in RTT;Proceedings of the National Academy of Sciences;2024-01-30
3. Neural precursor cells rescue symptoms of Rett syndrome by activation of the Interferon γ pathway;2024-01-08
4. Umbelliprenin via increase in the MECP2 and attenuation of oxidative stress mitigates the autistic-like behaviors in mouse model of maternal separation stress;Frontiers in Pharmacology;2024-01-08
5. TRPC4 deletion elicits behavioral defects in sociability by dysregulating expression of microRNA-138-2;iScience;2024-01
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