(Q48835247)

16 February 2018

title

Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice (English)

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16 February 2018

author name string

Tetsuya Fukuda

1

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16 February 2018

Masayuki Itoh

2

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16 February 2018

Tomio Ichikawa

3

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16 February 2018

Kazuo Washiyama

4

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16 February 2018

Yu-ichi Goto

5

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16 February 2018

publication date

1 June 2005

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16 February 2018

Journal of Neuropathology & Experimental Neurology

published in

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16 February 2018

volume

64

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16 February 2018

issue

6

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16 February 2018

page(s)

537-544

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16 February 2018

Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

cites work

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https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin

21 January 2018

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Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

21 January 2018

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Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

The expression of methyl CpG binding factor MeCP2 correlates with cellular differentiation in the developing rat brain and in cultured cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

MECP2 is highly mutated in X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

MECP2 mutation in male patients with non-specific X-linked mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

MECP2 mutation in non-fatal, non-progressive encephalopathy in a male

21 January 2018

1 reference

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Neuropathology of Rett syndrome

21 January 2018

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https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

Neuropathology of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

The transcriptional repressor Mecp2 regulates terminal neuronal differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

Morphological study of neocortical areas in Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

The methyl-CpG binding protein MeCP2 is essential for embryonic development in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

Methyl-CpG-binding protein 2 is localized in the postsynaptic compartment: an immunochemical study of subcellular fractions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

Postnatal development and migration of cholecystokinin-immunoreactive interneurons in rat hippocampus

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

Neurotrophic factors in the pathogenesis of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

BDNF overexpression increases dendrite complexity in hippocampal dentate gyrus

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

Dendritic anomalies in disorders associated with mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

Neuropathological findings in autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

Rett syndrome: A disorder affecting early brain growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

Neuroanatomy of Rett syndrome: a volumetric imaging study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossa

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

Decreased dendritic branching in frontal, motor and limbic cortex in Rett syndrome compared with trisomy 21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.537

21 January 2018

Identifiers

DOI

10.1093/JNEN/64.6.537

1 reference

16 February 2018

1 reference

16 February 2018