(Q34193020)

English

MeCP2 mutation results in compartment-specific reductions in dendritic branching and spine density in layer 5 motor cortical neurons of YFP-H mice

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

MeCP2 mutation results in compartment-specific reductions in dendritic branching and spine density in layer 5 motor cortical neurons of YFP-H mice (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

author name string

David P Stuss

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Jamie D Boyd

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

David B Levin

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Kerry R Delaney

4

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

language of work or name

0 references

publication date

7 March 2012

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

e31896

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

copyright license

Creative Commons Attribution 4.0 International

7 March 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3296699/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

The short-time structural plasticity of dendritic spines is altered in a model of Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Transgenic miR132 alters neuronal spine density and impairs novel object recognition memory

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Multiple events lead to dendritic spine loss in triple transgenic Alzheimer's disease mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Genome-wide analysis reveals methyl-CpG-binding protein 2-dependent regulation of microRNAs in a mouse model of Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Downstream targets of methyl CpG binding protein 2 and their abnormal expression in the frontal cortex of the human Rett syndrome brain.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Delta-catenin is required for the maintenance of neural structure and function in mature cortex in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Novel subtype-specific genes identify distinct subpopulations of callosal projection neurons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

MeCP2 deficiency disrupts axonal guidance, fasciculation, and targeting by altering Semaphorin 3F function.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Local-Circuit Phenotypes of Layer 5 Neurons in Motor-Frontal Cortex of YFP-H Mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Two-photon imaging during prolonged middle cerebral artery occlusion in mice reveals recovery of dendritic structure after reperfusion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Mecp2-null mice provide new neuronal targets for Rett syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Selective cerebral volume reduction in Rett syndrome: a multiple-approach MR imaging study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

The story of Rett syndrome: from clinic to neurobiology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

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=3296699

5 July 2018

Imaging large-scale neural activity with cellular resolution in awake, mobile mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 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=3296699

5 July 2018

Neuronal subtype specification in the cerebral cortex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Intrinsic disorder and autonomous domain function in the multifunctional nuclear protein, MeCP2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 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=3296699

5 July 2018

Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Towards the classification of subpopulations of layer V pyramidal projection neurons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 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=3296699

5 July 2018

Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Molecular taxonomy of major neuronal classes in the adult mouse forebrain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Opinion: an integrated approach to classifying neuronal phenotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Transient and persistent dendritic spines in the neocortex in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

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=3296699

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

The major form of MeCP2 has a novel N-terminus generated by alternative splicing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Developmental expression of methyl-CpG binding protein 2 is dynamically regulated in the rodent brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Clinical manifestations and stages of Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Rett syndrome neuropathology review 2000.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Imaging neuronal subsets in transgenic mice expressing multiple spectral variants of GFP

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Stochastic, stage-specific mechanisms account for the variegation of a human globin transgene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Overexpression of growth-associated proteins in the neurons of adult transgenic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Morphological study of neocortical areas in Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Selective dendritic alterations in the cortex of Rett syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Enhancers increase the probability but not the level of gene expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

The transient corticospinal projection from the occipital cortex during the postnatal development of the rat.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Occipital cortical neurons with transient pyramidal tract axons extend and maintain collaterals to subcortical but not intracortical targets

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

Rett syndrome: qualitative and quantitative differentiation from autism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

The development of the corticotectal pathway in the albino rat: transient projections from the visual and motor cortices.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

5 July 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Comparative study of brain morphology in Mecp2 mutant mouse models of Rett syndrome

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Evidence for both neuronal cell autonomous and nonautonomous effects of methyl-CpG-binding protein 2 in the cerebral cortex of female mice with Mecp2 mutation.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Transgenic mice expressing a fluorescent in vivo label in a distinct subpopulation of neocortical layer 5 pyramidal cells.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Quantitative morphologic classification of layer 5 neurons from mouse primary visual cortex

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Layer V neurons in mouse cortex projecting to different targets have distinct physiological properties

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Rapid reversible changes in dendritic spine structure in vivo gated by the degree of ischemia.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Fine mapping of the spatial relationship between acute ischemia and dendritic structure indicates selective vulnerability of layer V neuron dendritic tufts within single neurons in vivo.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Long-term dendritic spine stability in the adult cortex

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Region-specific spike-frequency acceleration in layer 5 pyramidal neurons mediated by Kv1 subunits

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Quantitative and qualitative analysis of Wallerian degeneration using restricted axonal labelling in YFP-H mice

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3"-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Expression of the methyl-CpG-binding protein MeCP2 in rat brain. An ontogenetic study

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Expression of MeCP2 in olfactory receptor neurons is developmentally regulated and occurs before synaptogenesis

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3296699

28 October 2018

Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype–phenotype associations in Rett syndrome

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0031896

21 January 2018

Microscopic Observations of the Brain in Rett Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22412847

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22412847

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22412847

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0031896

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

2012PLoSO...731896S

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34193020&oldid=1977223674"