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Modeling neurodevelopmental disorders using human neurons
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scholarly article
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PubMed
title
Modeling neurodevelopmental disorders using human neurons
(English)
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stated in
PubMed
main subject
neurodevelopmental disorder
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based on heuristic
inferred from title
author
Alysson Muotri
series ordinal
3
object named as
Alysson Renato Muotri
1 reference
stated in
Crossref
author name string
Thanathom Chailangkarn
series ordinal
1
1 reference
stated in
Crossref
Allan Acab
series ordinal
2
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stated in
Crossref
language of work or name
English
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stated in
PubMed
publication date
October 2012
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stated in
PubMed
published in
Current Opinion in Neurobiology
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stated in
PubMed
volume
22
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stated in
PubMed
issue
5
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stated in
PubMed
page(s)
785-90
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PubMed
cites work
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Direct conversion of fibroblasts to functional neurons by defined factors
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PubMed Central
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Initial sequencing and analysis of the human genome
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PubMed Central
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Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
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Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors
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Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism
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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
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Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation
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L1 retrotransposition in human neural progenitor cells
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Somatic mosaicism in neuronal precursor cells mediated by L1 retrotransposition
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Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome
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Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome
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28 September 2017
Induced pluripotent stem cells (iPSCs) and neurological disease modeling: progress and promises
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28 September 2017
Neuronal maturation defect in induced pluripotent stem cells from patients with Rett syndrome
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PubMed Central
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28 September 2017
Generation of isogenic pluripotent stem cells differing exclusively at two early onset Parkinson point mutations
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PubMed Central
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28 September 2017
iPS cells to model CDKL5-related disorders.
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PubMed Central
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28 September 2017
Targeted gene correction of laminopathy-associated LMNA mutations in patient-specific iPSCs
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Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation
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Integration-free induced pluripotent stem cells derived from schizophrenia patients with a DISC1 mutation
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PubMed Central
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L1 retrotransposition in neurons is modulated by MeCP2.
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PubMed Central
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28 September 2017
Induced pluripotent stem cells can be used to model the genomic imprinting disorder Prader-Willi syndrome
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PubMed Central
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28 September 2017
Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes
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28 September 2017
Differential modeling of fragile X syndrome by human embryonic stem cells and induced pluripotent stem cells
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PubMed Central
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28 September 2017
Clinical and genetic aspects of Angelman syndrome
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PubMed Central
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28 September 2017
Pluripotent stem cells in neurodegenerative and neurodevelopmental diseases.
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587787
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28 September 2017
Transcriptional signature and memory retention of human-induced pluripotent stem cells
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587787
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28 September 2017
Modeling epilepsy with pluripotent human cells
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PubMed Central
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28 September 2017
Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure.
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587787
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28 September 2017
Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587787
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28 September 2017
The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587787
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28 September 2017
FMR1 and the fragile X syndrome: human genome epidemiology review
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587787
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28 September 2017
Autism in Angelman syndrome: a population-based study
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PubMed Central
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28 September 2017
A typological model of schizophrenia based on age at onset, sex and familial morbidity
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587787
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31 May 2018
A rare association of long QT syndrome and syndactyly: Timothy syndrome (LQT 8).
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PubMed Central
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28 November 2018
Identification of a novel CDKL5 exon and pathogenic mutations in patients with severe mental retardation, early-onset seizures and Rett-like features.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587787
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28 November 2018
Early onset seizures and Rett-like features associated with mutations in CDKL5.
1 reference
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3587787
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28 November 2018
The de facto US mental and addictive disorders service system. Epidemiologic catchment area prospective 1-year prevalence rates of disorders and services.
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PubMed Central
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retrieved
28 November 2018
Prader-Willi syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22717528
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Neuropathology of Rett syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/22717528
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/J.CONB.2012.04.004
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2026411
Fatcat ID
release_tjgibc5lqvgkrgdpdk37aj7gye
0 references
OpenCitations bibliographic resource ID
2026411
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2026411
PMCID
3587787
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2026411
PubMed ID
22717528
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2026411
ResearchGate publication ID
227708873
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