MeCP2 modulates gene expression pathways in astrocytes

BACKGROUND: Mutations in MECP2 encoding methyl-CpG-binding protein 2 (MeCP2) cause the X-linked neurodevelopmental disorder Rett syndrome. Rett syndrome patients exhibit neurological symptoms that include irregular breathing, impaired mobility, stereotypic hand movements, and loss of speech. MeCP2 p...

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Bibliografiset tiedot
Päätekijät: Yasui, Dag H, Xu, Huichun, Dunaway, Keith W, LaSalle, Janine M, Jin, Lee-Way, Maezawa, Izumi
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2013
Aiheet:
Research
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3561260/
https://ncbi.nlm.nih.gov/pubmed/23351786
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2040-2392-4-3
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