Molecular analyses of neurogenic defects in a human pluripotent stem cell model of fragile X syndrome (Q46696575)

4 July 2018

title

Molecular analyses of neurogenic defects in a human pluripotent stem cell model of fragile X syndrome (English)

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4 July 2018

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10

Jeanne F Loring

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4 July 2018

author name string

Michael J Boland

1

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4 July 2018

Kristopher L Nazor

2

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4 July 2018

Ha T Tran

3

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4 July 2018

Attila Szücs

4

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4 July 2018

Candace L Lynch

5

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4 July 2018

Ryder Paredes

6

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4 July 2018

Flora Tassone

7

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4 July 2018

Pietro Paolo Sanna

8

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4 July 2018

Randi J Hagerman

9

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4 July 2018

language of work or name

English

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publication date

1 March 2017

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4 July 2018

published in

Brain

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4 July 2018

volume

140

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4 July 2018

issue

3

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4 July 2018

page(s)

582-598

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4 July 2018

describes a project that uses

ImageJ

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC5837342/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

limma

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22 June 2022

https://europepmc.org/article/PMC/5837342

based on heuristic

inferred from PubMed Central ID database lookup

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Molecular mechanisms regulating the defects in fragile X syndrome neurons derived from human pluripotent stem cells

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10 July 2018

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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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10 July 2018

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10 July 2018

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Fragile X Mental Retardation Protein is Involved in Protein Synthesis-Dependent Collapse of Growth Cones Induced by Semaphorin-3A.

10 July 2018

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10 July 2018

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10 July 2018

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10 July 2018

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10 July 2018

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10 July 2018

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10 July 2018

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10 July 2018

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10 July 2018

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Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome

10 July 2018

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Dendritic spine structural anomalies in fragile-X mental retardation syndrome

10 July 2018

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Silencing of TGF-beta signalling by the pseudoreceptor BAMBI.

10 July 2018

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10 July 2018

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Functional Deficiencies in Fragile X Neurons Derived from Human Embryonic Stem Cells

10 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5837342

Neural differentiation of Fragile X human Embryonic Stem Cells reveals abnormal patterns of development despite successful neurogenesis.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5837342

FMRP Regulates the Transition from Radial Glial Cells to Intermediate Progenitor Cells during Neocortical Development

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5837342

Aberrant differentiation of glutamatergic cells in neocortex of mouse model for fragile X syndrome

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5837342

New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder-Robinson X-linked recessive mental retardation syndrome.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5837342

RNA cargoes associating with FMRP reveal deficits in cellular functioning in Fmr1 null mice

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5837342

Interference with DNA methyltransferase activity and genome methylation during F9 teratocarcinoma stem cell differentiation induced by polyamine depletion.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5837342

Mosaicism in fragile X affected males.

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5837342

15 August 2018

Identifiers

DOI

10.1093/BRAIN/AWW357

1 reference

4 July 2018

PMC publication ID

5837342

1 reference

4 July 2018

PubMed publication ID

28137726

1 reference

4 July 2018