Cargando…
The protocadherins, PCDHB1 and PCDH7, are regulated by MeCP2 in neuronal cells and brain tissues: implication for pathogenesis of Rett syndrome
BACKGROUND: Rett syndrome is a neurodevelopmental and autistic disease caused by mutations of Methyl-CpG-binding protein 2 (MECP2) gene. MeCP2 protein is mainly expressed in neurons and binds to methylated gene promoters to suppress their expression, indicating that Rett syndrome is caused by the de...
Autores principales: | Miyake, Kunio, Hirasawa, Takae, Soutome, Masaki, Itoh, Masayuki, Goto, Yu-ichi, Endoh, Kazushi, Takahashi, Kenichiro, Kudo, Shinichi, Nakagawa, Takayuki, Yokoi, Sana, Taira, Takahiro, Inazawa, Johji, Kubota, Takeo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3160964/ https://www.ncbi.nlm.nih.gov/pubmed/21824415 http://dx.doi.org/10.1186/1471-2202-12-81 |
Ejemplares similares
-
Adjuvant Treatment for Protocadherin 19 (PCDH19) Syndrome
por: Moncayo, Juan A, et al.
Publicado: (2022) -
Comparison of Genomic and Epigenomic Expression in Monozygotic Twins Discordant for Rett Syndrome
por: Kunio, Miyake, et al.
Publicado: (2013) -
Biallelic mutation of Protocadherin-21 (PCDH21) causes retinal degeneration in humans
por: Henderson, Robert H., et al.
Publicado: (2010) -
Epigenetic understanding of gene-environment interactions in psychiatric disorders: a new concept of clinical genetics
por: Kubota, Takeo, et al.
Publicado: (2012) -
Epigenetic Mechanisms and Therapeutic Perspectives for Neurodevelopmental Disorders
por: Kubota, Takeo, et al.
Publicado: (2012)