Epigenetic characterization of the FMR1 promoter in induced pluripotent stem cells from human fibroblasts carrying an unmethylated full mutation (Q34469474)

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English	Epigenetic characterization of the FMR1 promoter in induced pluripotent stem cells from human fibroblasts carrying an unmethylated full mutation	scientific article

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22 February 2020

Epigenetic characterization of the FMR1 promoter in induced pluripotent stem cells from human fibroblasts carrying an unmethylated full mutation (English)

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22 February 2020

Human Induced Pluripotent Stem Cells

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Steven A Kushner

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22 February 2020

Femke M de Vrij

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22 February 2020

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Celine E F de Esch

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22 February 2020

Mehrnaz Ghazvini

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22 February 2020

Friedemann Loos

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22 February 2020

Nune Schelling-Kazaryan

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22 February 2020

W Widagdo

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22 February 2020

Shashini T Munshi

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22 February 2020

Erik van der Wal

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22 February 2020

Hannie Douben

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22 February 2020

Nilhan Gunhanlar

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22 February 2020

W W M Pim Pijnappel

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22 February 2020

Niels Geijsen

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22 February 2020

Joost Gribnau

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22 February 2020

Rob Willemsen

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22 February 2020

publication date

11 September 2014

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22 February 2020

Stem Cell Reports

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22 February 2020

3

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22 February 2020

4

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22 February 2020

548-555

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22 February 2020

The DNA replication program is altered at the FMR1 locus in fragile X embryonic stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

6 July 2018

Epigenetic characterization of the FMR1 gene and aberrant neurodevelopment in human induced pluripotent stem cell models of fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

6 July 2018

Modelling schizophrenia using human induced pluripotent stem cells

1 reference

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6 July 2018

Lentiviral vector design and imaging approaches to visualize the early stages of cellular reprogramming.

1 reference

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6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

6 July 2018

Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

6 July 2018

Repeat instability: mechanisms of dynamic mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

6 July 2018

Differential epigenetic modifications in the FMR1 gene of the fragile X syndrome after reactivating pharmacological treatments.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

6 July 2018

Molecular dissection of the events leading to inactivation of the FMR1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

6 July 2018

Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile x syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

6 July 2018

In vitro reactivation of the FMR1 gene involved in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

6 July 2018

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

6 July 2018

DNA methylation represses FMR-1 transcription in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

6 July 2018

Derivation of novel human ground state naive pluripotent stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

27 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

27 October 2018

Induction of pluripotent stem cells from fibroblast cultures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

27 October 2018

Timing of the absence of FMR1 expression in full mutation chorionic villi.

1 reference

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27 October 2018

Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4223701

27 October 2018

Normal phenotype in two brothers with a full FMR1 mutation.

1 reference

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27 October 2018

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10.1016/J.STEMCR.2014.07.013

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22 February 2020

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22 February 2020

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22 February 2020

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