Fragile X syndrome: mechanistic insights and therapeutic avenues regarding the role of potassium channels. (Q30448604)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22483378%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

title

Fragile X syndrome: mechanistic insights and therapeutic avenues regarding the role of potassium channels (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22483378%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

1 reference

2

1 reference

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28 January 2020

author name string

Hye Young Lee

series ordinal

1

1 reference

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28 January 2020

publication date

5 April 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22483378%20AND%20SRC:MED&resulttype=core&format=json

Current Opinion in Neurobiology

28 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22483378%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

volume

22

1 reference

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28 January 2020

issue

5

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28 January 2020

page(s)

887-894

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Bidirectional regulation of dendritic voltage-gated potassium channels by the fragile X mental retardation protein

28 January 2020

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A direct role for FMRP in activity-dependent dendritic mRNA transport links filopodial-spine morphogenesis to fragile X syndrome.

20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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20 June 2018

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Evidence that fragile X mental retardation protein is a negative regulator of translation

20 June 2018

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20 June 2018

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Contribution of the Kv3.1 potassium channel to high-frequency firing in mouse auditory neurones

20 June 2018

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Inward rectifier potassium channels

20 June 2018

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Characterization and localization of the FMR-1 gene product associated with fragile X syndrome

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A point mutation in the FMR-1 gene associated with fragile X mental retardation

20 June 2018

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The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

20 June 2018

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20 June 2018

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Speech disturbances (cluttering) in mildly impaired males with the Martin-Bell/fragile X syndrome.

20 June 2018

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Absence of expression of the FMR-1 gene in fragile X syndrome

20 June 2018

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Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

20 June 2018

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Analysis of neocortex in three males with the fragile X syndrome

20 June 2018

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

20 June 2018

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Hypersensitivity to mGluR5 and ERK1/2 leads to excessive protein synthesis in the hippocampus of a mouse model of fragile X syndrome

20 June 2018

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Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males.

26 November 2018

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Fragile X mental retardation protein is required for chemically-induced long-term potentiation of the hippocampus in adult mice.

26 November 2018

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Phosphorylation of FMRP inhibits association with Dicer

26 November 2018

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Synaptic ionotropic glutamate receptors and plasticity are developmentally altered in the CA1 field of Fmr1 knockout mice

26 November 2018

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26 November 2018

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Compartmentalized dendritic plasticity and input feature storage in neurons

26 November 2018

1 reference

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Regulation of Kv4.2 channels by glutamate in cultured hippocampal neurons

26 November 2018

1 reference

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Reducing glutamate signaling pays off in fragile X.

26 November 2018

1 reference

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FMRP phosphorylation reveals an immediate-early signaling pathway triggered by group I mGluR and mediated by PP2A.

26 November 2018

1 reference

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Brain-derived neurotrophic factor rescues synaptic plasticity in a mouse model of fragile X syndrome

26 November 2018

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Slack and Slick K(Na) channels regulate the accuracy of timing of auditory neurons.

26 November 2018

1 reference

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Deletion of Kv4.2 gene eliminates dendritic A-type K+ current and enhances induction of long-term potentiation in hippocampal CA1 pyramidal neurons.

26 November 2018

1 reference

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Metabotropic receptor-dependent long-term depression persists in the absence of protein synthesis in the mouse model of fragile X syndrome

26 November 2018

1 reference

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Prolonged epileptiform discharges induced by altered group I metabotropic glutamate receptor-mediated synaptic responses in hippocampal slices of a fragile X mouse model.

26 November 2018

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Suppression of two major Fragile X Syndrome mouse model phenotypes by the mGluR5 antagonist MPEP.

26 November 2018

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Postadolescent changes in regional cerebral protein synthesis: an in vivo study in the FMR1 null mouse.

26 November 2018

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Phosphorylation influences the translation state of FMRP-associated polyribosomes

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3393774

RNA cargoes associating with FMRP reveal deficits in cellular functioning in Fmr1 null 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=3393774

Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: a preliminary report.

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3393774

Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X 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=3393774

Analysis of the fragile-X chromosome: localization and detection of the fragile site in high resolution preparations

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22483378

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: a case report and review of the literature

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22483378

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.CONB.2012.03.010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22483378%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22483378%20AND%20SRC:MED&resulttype=core&format=json

28 January 2020

PubMed publication ID

22483378

1 reference