(Q40889402)

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High-Throughput Screening Using iPSC-Derived Neuronal Progenitors to Identify Compounds Counteracting Epigenetic Gene Silencing in Fragile X Syndrome.

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26024946%20AND%20SRC:MED&resulttype=core&format=json

16 February 2020

High-Throughput Screening Using iPSC-Derived Neuronal Progenitors to Identify Compounds Counteracting Epigenetic Gene Silencing in Fragile X Syndrome (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26024946%20AND%20SRC:MED&resulttype=core&format=json

16 February 2020

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fragile X syndrome

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based on heuristic

inferred from title

12

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16 February 2020

Ansgar Schuffenhauer

2

object named as

Ansgar Schuffenhauer

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26024946%20AND%20SRC:MED&resulttype=core&format=json

16 February 2020

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Markus Kaufmann

1

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16 February 2020

Isabelle Fruh

3

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Europe PubMed Central

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16 February 2020

Jessica Klein

4

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16 February 2020

Anke Thiemeyer

5

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16 February 2020

Pierre Rigo

6

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16 February 2020

Baltazar Gomez-Mancilla

7

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Europe PubMed Central

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16 February 2020

Valerie Heidinger-Millot

8

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16 February 2020

Tewis Bouwmeester

9

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16 February 2020

Ulrich Schopfer

10

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Europe PubMed Central

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16 February 2020

Matthias Mueller

11

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16 February 2020

Amanda Cobos-Correa

13

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16 February 2020

publication date

29 May 2015

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16 February 2020

Journal of Biomolecular Screening

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16 February 2020

20

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16 February 2020

9

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Europe PubMed Central

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16 February 2020

1101-1111

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26024946%20AND%20SRC:MED&resulttype=core&format=json

16 February 2020

Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics.

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Fragile X mental retardation protein and synaptic plasticity

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Normal phenotype in two brothers with a full FMR1 mutation.

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056.

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Social behavior in Fmr1 knockout mice carrying a human FMR1 transgene

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Instability of a (CGG)98 repeat in the Fmr1 promoter.

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Disease modeling and drug screening for neurological diseases using human induced pluripotent stem cells

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Opportunities and challenges of pluripotent stem cell neurodegenerative disease models

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Differential modeling of fragile X syndrome by human embryonic stem cells and induced pluripotent stem cells

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Molecular analysis of FMR1 reactivation in fragile-X induced pluripotent stem cells and their neuronal derivatives.

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Translating molecular advances in fragile X syndrome into therapy: a review

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Signaling defects in iPSC-derived fragile X premutation neurons

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Promoter-bound trinucleotide repeat mRNA drives epigenetic silencing in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Generation of human-induced pluripotent stem cells

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Transneuronal propagation of mutant huntingtin contributes to non-cell autonomous pathology in neurons

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene.

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Cell-surface marker signatures for the isolation of neural stem cells, glia and neurons derived from human pluripotent stem cells

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Epigenetic drugs as pleiotropic agents in cancer treatment: biomolecular aspects and clinical applications.

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

Therapeutic application of histone deacetylase inhibitors for central nervous system disorders

1 reference

https://api.crossref.org/works/10.1177%2F1087057115588287

21 January 2018

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10.1177/1087057115588287

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30 July 2022

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https://api.fatcat.wiki/v0/release/seuhuwmoi5g3pa2icr7qsajnay

30 July 2022

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PubMed publication ID

1 reference

https://api.fatcat.wiki/v0/release/seuhuwmoi5g3pa2icr7qsajnay

30 July 2022

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