(Q33756455)

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MeCP2 functions largely cell-autonomously, but also non-cell-autonomously, in neuronal maturation and dendritic arborization of cortical pyramidal neurons

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Europe PubMed Central

PubMed publication ID

29 July 2017

MeCP2 functions largely cell-autonomously, but also non-cell-autonomously, in neuronal maturation and dendritic arborization of cortical pyramidal neurons (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

author name string

Noriyuki Kishi

1

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Europe PubMed Central

PubMed publication ID

29 July 2017

Jeffrey D Macklis

2

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Europe PubMed Central

PubMed publication ID

29 July 2017

language of work or name

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publication date

16 December 2009

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Europe PubMed Central

PubMed publication ID

29 July 2017

Experimental Neurology

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Europe PubMed Central

PubMed publication ID

29 July 2017

222

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Europe PubMed Central

PubMed publication ID

29 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

51-58

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

SOX6 controls dorsal progenitor identity and interneuron diversity during neocortical development

1 reference

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21 June 2018

Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions

1 reference

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Lmo4 and Clim1 progressively delineate cortical projection neuron subtypes during development

1 reference

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21 June 2018

MeCP2-mediated transcription repression in the basolateral amygdala may underlie heightened anxiety in a mouse model of Rett syndrome

1 reference

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21 June 2018

Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology

1 reference

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21 June 2018

Bhlhb5 regulates the postmitotic acquisition of area identities in layers II-V of the developing neocortex.

1 reference

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21 June 2018

Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2846301

21 June 2018

MeCP2, a key contributor to neurological disease, activates and represses transcription

1 reference

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21 June 2018

Molecular development of corticospinal motor neuron circuitry

1 reference

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Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure.

1 reference

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Pyramidal neurons: dendritic structure and synaptic integration

1 reference

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21 June 2018

Satb2 is a postmitotic determinant for upper-layer neuron specification in the neocortex

1 reference

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21 June 2018

Satb2 regulates callosal projection neuron identity in the developing cerebral cortex

1 reference

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21 June 2018

SOX5 controls the sequential generation of distinct corticofugal neuron subtypes

1 reference

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Ube3a mRNA and protein expression are not decreased in Mecp2R168X mutant mice

1 reference

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MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2846301

21 June 2018

Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neurons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2846301

21 June 2018

Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2846301

21 June 2018

Mechanisms of disease: neurogenetics of MeCP2 deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2846301

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Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2846301

21 June 2018

MeCP2 dysfunction in Rett syndrome and related disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2846301

21 June 2018

Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2846301

21 June 2018

Zfp312 is required for subcortical axonal projections and dendritic morphology of deep-layer pyramidal neurons of the cerebral cortex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2846301

21 June 2018

Dissecting MECP2 function in the central nervous system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2846301

21 June 2018

Fezl is required for the birth and specification of corticospinal motor neurons

1 reference

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21 June 2018

Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome

1 reference

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Neuronal subtype-specific genes that control corticospinal motor neuron development in vivo

1 reference

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Neurogenesis of corticospinal motor neurons extending spinal projections in adult mice

1 reference

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2846301

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X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.

1 reference

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Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

1 reference

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1 reference

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1 reference

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Signaling mechanisms underlying dendrite formation

1 reference

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Corepressor-dependent silencing of chromosomal regions encoding neuronal genes

1 reference

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21 June 2018

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

1 reference

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Specific neurotrophic factors support the survival of cortical projection neurons at distinct stages of development.

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Rett syndrome: clinical characteristics and recent genetic advances

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1 reference

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1 reference

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1 reference

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Selective dendritic alterations in the cortex of Rett syndrome

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MeCP2-dependent transcriptional repression regulates excitatory neurotransmission

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2846301

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

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Pervasive neuroanatomic abnormalities of the brain in three cases of Rett's syndrome

1 reference

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12 December 2020

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10.1016/J.EXPNEUROL.2009.12.007

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

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