Functional analyses of MeCP2 mutations associated with Rett syndrome using transient expression systems.
about
Comparative study of methyl-CpG-binding domain proteinsRett syndrome and MeCP2: linking epigenetics and neuronal functionAnalysis of protein domains and Rett syndrome mutations indicate that multiple regions influence chromatin-binding dynamics of the chromatin-associated protein MECP2 in vivoDendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutationsBdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutationsPeople with MECP2 mutation-positive Rett disorder who converse.Preclinical research in Rett syndrome: setting the foundation for translational success.Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.MeCP2 dependent heterochromatin reorganization during neural differentiation of a novel Mecp2-deficient embryonic stem cell reporter line.Experimental models of Rett syndrome based on Mecp2 dysfunction.The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.Heterogeneity in residual function of MeCP2 carrying missense mutations in the methyl CpG binding domain.Clinical variability in Rett syndrome.MECP2 and beyond: phenotype-genotype correlations in Rett syndrome.Does genotype predict phenotype in Rett syndrome?Creb1-Mecp2-(m)CpG complex transactivates postnatal murine neuronal glucose transporter isoform 3 expressionRett syndrome: recent research progress.Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.Rett syndrome-causing mutations in human MeCP2 result in diverse structural changes that impact folding and DNA interactions.Functional conservation of MBD proteins: MeCP2 and Drosophila MBD proteins alter sleep.MeCP2 expression in human cerebral cortex and lymphoid cells: immunochemical characterization of a novel higher-molecular-weight form.RettBASE: Rett syndrome database update.
P2860
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P2860
Functional analyses of MeCP2 mutations associated with Rett syndrome using transient expression systems.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh-hant
name
Functional analyses of MeCP2 m ...... transient expression systems.
@en
Functional analyses of MeCP2 m ...... transient expression systems.
@nl
type
label
Functional analyses of MeCP2 m ...... transient expression systems.
@en
Functional analyses of MeCP2 m ...... transient expression systems.
@nl
prefLabel
Functional analyses of MeCP2 m ...... transient expression systems.
@en
Functional analyses of MeCP2 m ...... transient expression systems.
@nl
P2093
P1476
Functional analyses of MeCP2 m ...... transient expression systems.
@en
P2093
P304
P356
10.1016/S0387-7604(01)00345-X
P478
23 Suppl 1
P577
2001-12-01T00:00:00Z