(Q35655203)

9 August 2017

title

Differentiation of multipotent neural stem cells derived from Rett syndrome patients is biased toward the astrocytic lineage (English)

1 reference

9 August 2017

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Manabu Ohyama

9

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Hideyuki Okano

13

object named as

Hideyuki Okano

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9 August 2017

10

Kinichi Nakashima

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9 August 2017

2

Wado Akamatsu

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9 August 2017

1

Tomoko Andoh-Noda

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9 August 2017

7

Yohei Okada

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9 August 2017

Kunio Miyake

3

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9 August 2017

Takuya Matsumoto

4

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9 August 2017

Ryo Yamaguchi

5

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9 August 2017

Tsukasa Sanosaka

6

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9 August 2017

Tetsuro Kobayashi

8

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9 August 2017

Hiroshi Kurosawa

11

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9 August 2017

Takeo Kubota

12

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9 August 2017

publication date

27 May 2015

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9 August 2017

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9 August 2017

volume

8

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9 August 2017

page(s)

31

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Creative Commons Attribution 4.0 International

9 August 2017

copyright license

start time

27 May 2015

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Mutant astrocytes differentiated from Rett syndrome patients-specific iPSCs have adverse effects on wild-type neurons

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12 July 2018

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Comparison of Genomic and Epigenomic Expression in Monozygotic Twins Discordant for Rett Syndrome

12 July 2018

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From pathophysiology to novel antidepressant drugs: glial contributions to the pathology and treatment of mood disorders

12 July 2018

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Antidepressants act directly on astrocytes: evidences and functional consequences.

12 July 2018

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Alterations of gene expression and glutamate clearance in astrocytes derived from an MeCP2-null mouse model of Rett syndrome

12 July 2018

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X-chromosome inactivation in rett syndrome human induced pluripotent stem cells

12 July 2018

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Isogenic pairs of wild type and mutant induced pluripotent stem cell (iPSC) lines from Rett syndrome patients as in vitro disease model

12 July 2018

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The protocadherins, PCDHB1 and PCDH7, are regulated by MeCP2 in neuronal cells and brain tissues: implication for pathogenesis of Rett syndrome

12 July 2018

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Neuronal maturation defect in induced pluripotent stem cells from patients with Rett syndrome

12 July 2018

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Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation

12 July 2018

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Generation of human melanocytes from induced pluripotent stem cells

12 July 2018

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L1 retrotransposition in neurons is modulated by MeCP2.

12 July 2018

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A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells

12 July 2018

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Female human iPSCs retain an inactive X chromosome

12 July 2018

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

12 July 2018

1 reference

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

12 July 2018

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Isolation of human iPS cells using EOS lentiviral vectors to select for pluripotency

12 July 2018

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

12 July 2018

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

12 July 2018

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Rett syndrome and the impact of MeCP2 associated transcriptional mechanisms on neurotransmission

12 July 2018

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Epigenetic regulation of neural cell differentiation plasticity in the adult mammalian brain

12 July 2018

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

12 July 2018

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The organization of histone H3 modifications as revealed by a panel of specific monoclonal antibodies

12 July 2018

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Induction of pluripotent stem cells from adult human fibroblasts by defined factors

12 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

The story of Rett syndrome: from clinic to neurobiology

12 July 2018

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Methyl-CpG binding proteins are involved in restricting differentiation plasticity in neurons

12 July 2018

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A transcriptional repressor MeCP2 causing Rett syndrome is expressed in embryonic non-neuronal cells and controls their growth

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

X chromosome inactivation patterns in brain in Rett syndrome: implications for the disease phenotype.

12 July 2018

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Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

Developmental stage dependent regulation of DNA methylation and chromatin modification in a immature astrocyte specific gene promoter.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

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

12 July 2018

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Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

TM4: a free, open-source system for microarray data management and analysis

12 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

MBD2 is a transcriptional repressor belonging to the MeCP1 histone deacetylase complex

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCR.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

Cluster analysis and display of genome-wide expression patterns

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

MeCP2 regulates GFAP expression within the developing brain

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

Clonal neural stem cells from human embryonic stem cell colonies.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

MeCP2 Rett mutations affect large scale chromatin organization.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

Neural development of methyl-CpG-binding protein 2 null embryonic stem cells: A system for studying Rett syndrome

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

Neuronal differentiation of neural precursor cells is promoted by the methyl-CpG-binding protein MeCP2.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4446051

Integrative analysis of the cancer transcriptome

25 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FS13041-015-0121-2

Neuropathology of Rett syndrome

21 January 2018

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12 December 2020

The role of stereotypies in overselectivity process in Rett syndrome

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12 December 2020

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

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12 December 2020

The incidence of Rett syndrome in France

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12 December 2020

10.1186/S13041-015-0121-2

Identifiers

DOI

1 reference

Dimensions Publication ID

9 August 2017

0 references

1 reference

9 August 2017

1 reference