A Model for Neural Development and Treatment of Rett Syndrome Using Human Induced Pluripotent Stem Cells (Q29619964)

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21074045

30 April 2017

A Model for Neural Development and Treatment of Rett Syndrome Using Human Induced Pluripotent Stem Cells (English)

1 reference

Crossref

https://api.crossref.org/works/10.1016/J.CELL.2010.10.016

induced pluripotent stem cell

25 August 2024

main subject

Rett syndrome

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nervous system development

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cell line

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Human Induced Pluripotent Stem Cells

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1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21074045

25 August 2024

2

Cassiano Carromeu

1 reference

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25 August 2024

5

Gene W. Yeo

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21074045

25 August 2024

author name string

Marchetto MC

1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21074045

30 April 2017

Maria C. N. Marchetto

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21074045

25 August 2024

Allan Acab

3

1 reference

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25 August 2024

Diana Yu

4

1 reference

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25 August 2024

Yangling Mu

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21074045

25 August 2024

Gong Chen

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21074045

25 August 2024

Fred H. Gage

8

1 reference

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25 August 2024

Alysson R. Muotri

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21074045

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21074045

25 August 2024

language of work or name

1 reference

30 April 2017

publication date

12 November 2010

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21074045

full work available at URL

30 April 2017

http://www.cell.com/article/S0092867410011864/pdf

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21074045

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21074045/?tool=EBI

25 August 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21074045

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21074045/pdf/?tool=EBI

25 August 2024

file format

Portable Document Format

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21074045

https://europepmc.org/articles/PMC3003590

25 August 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21074045

https://europepmc.org/articles/PMC3003590?pdf=render

25 August 2024

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21074045

https://doi.org/10.1016/j.cell.2010.10.016

25 August 2024

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21074045

https://api.elsevier.com/content/article/PII:S0092867410011864?httpAccept=text/xml

25 August 2024

1 reference

Crossref

https://api.crossref.org/works/10.1016/J.CELL.2010.10.016

https://api.elsevier.com/content/article/PII:S0092867410011864?httpAccept=text/plain

25 August 2024

1 reference

Crossref

https://api.crossref.org/works/10.1016/J.CELL.2010.10.016

25 August 2024

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21074045

30 April 2017

volume

143

1 reference

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30 April 2017

issue

4

1 reference

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30 April 2017

page(s)

527-39

1 reference

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describes a project that uses

30 April 2017

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1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3003590/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

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

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

30 April 2017

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30 April 2017

1 reference

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Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons

30 April 2017

1 reference

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

30 April 2017

1 reference

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Directly reprogrammed fibroblasts show global epigenetic remodeling and widespread tissue contribution

30 April 2017

1 reference

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

30 April 2017

1 reference

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

30 April 2017

1 reference

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Induced pluripotent stem cell lines derived from human somatic cells

30 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

30 April 2017

1 reference

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Reversal of neurological defects in a mouse model of Rett syndrome

30 April 2017

1 reference

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

30 April 2017

1 reference

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Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors

30 April 2017

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Genetic heterogeneity between the three components of the autism spectrum: a twin study

30 April 2017

1 reference

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Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

30 April 2017

1 reference

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

30 April 2017

1 reference

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Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

30 April 2017

1 reference

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Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations

30 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Identification of a vesicular glutamate transporter that defines a glutamatergic phenotype in neurons

30 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

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

30 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Embryonic stem cell lines derived from human blastocysts

30 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Broader autism phenotype: evidence from a family history study of multiple-incidence autism families

30 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Interaction between the C terminus of NMDA receptor subunits and multiple members of the PSD-95 family of membrane-associated guanylate kinases

30 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

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30 April 2017

1 reference

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Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome

3 June 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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Early postnatal behavioral changes in the Mecp2-308 truncation mouse model of Rett syndrome.

3 June 2018

1 reference

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3 June 2018

1 reference

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3 June 2018

1 reference

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

3 June 2018

1 reference

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Development of novel aminoglycoside (NB54) with reduced toxicity and enhanced suppression of disease-causing premature stop mutations

3 June 2018

1 reference

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

3 June 2018

1 reference

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

3 June 2018

1 reference

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Modeling epilepsy with pluripotent human cells

3 June 2018

1 reference

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PTC124 targets genetic disorders caused by nonsense mutations

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Prevalence of autism spectrum disorders--autism and developmental disabilities monitoring network, six sites, United States, 2000.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Translational readthrough induction of pathogenic nonsense mutations

3 June 2018

1 reference

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Chromatin remodeling in dosage compensation

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Gene trap as a tool for genome annotation and analysis of X chromosome inactivation in human embryonic stem cells

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Orchestrating neuronal differentiation: patterns of Ca2+ spikes specify transmitter choice

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Head growth in Rett syndrome

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

The hands, and the mind, pre- and post-regression, in Rett syndrome

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Remodelling of the respiratory network in a mouse model of Rett syndrome depends on brain-derived neurotrophic factor regulated slow calcium buffering.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Evidence for abnormal early development in a mouse model of Rett syndrome.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

CACNA1H mutations in autism spectrum disorders.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

An altered neonatal behavioral phenotype in Mecp2 mutant mice.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Evidence of brain overgrowth in the first year of life in autism

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Study of MECP2 gene in Rett syndrome variants and autistic girls.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Establishment of histone h3 methylation on the inactive X chromosome requires transient recruitment of Eed-Enx1 polycomb group complexes

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Regression in individuals with Rett syndrome

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

An MRI study of brain size in autism

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3003590

Mutation spectrum in patients with Rett syndrome in the German population: Evidence of hot spot regions

26 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/21074045

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome

1 reference

24 May 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/J.CELL.2010.10.016

Development of functional human embryonic stem cell-derived neurons in mouse brain

1 reference

24 May 2022

https://opencitations.net/index/coci/api/v1/references/10.1016/J.CELL.2010.10.016

Identifiers

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21074045

30 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21074045

2 references

30 April 2017

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21074045

2 references

30 April 2017