The FMRP regulon: from targets to disease convergence (Q27014002)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24167470%20AND%20SRC:MED&resulttype=core&format=json

3 June 2020

author name string

Esperanza Fernández

series ordinal

1

2 references

Crossref

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3 June 2020

Nicholas Rajan

series ordinal

2

2 references

Crossref

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24167470%20AND%20SRC:MED&resulttype=core&format=json

3 June 2020

language of work or name

1 reference

24 October 2013

1 reference

Frontiers in Neuroscience

published in

2 references

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3 June 2020

volume

7

2 references

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3 June 2020

page(s)

191

2 references

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FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism

3 June 2020

cites work

1 reference

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Structure and control of the actin regulatory WAVE complex

21 March 2017

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The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP

21 March 2017

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

21 March 2017

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Interactions of the G quartet forming semaphorin 3F RNA with the RGG box domain of the fragile X protein family

21 March 2017

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21 March 2017

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The structure of the N-terminal domain of the fragile X mental retardation protein: a platform for protein-protein interaction

21 March 2017

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Stress granules and processing bodies are dynamically linked sites of mRNP remodeling

21 March 2017

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82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localization

21 March 2017

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Altered synaptic plasticity in a mouse model of fragile X mental retardation

21 March 2017

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A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P

21 March 2017

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Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P

21 March 2017

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Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them

21 March 2017

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Downregulation of tonic GABAergic inhibition in a mouse model of fragile X syndrome

21 March 2017

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A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability

21 March 2017

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The nuclear microspherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons

21 March 2017

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In vitro and in cellulo evidences for association of the survival of motor neuron complex with the fragile X mental retardation protein

21 March 2017

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

21 March 2017

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The fragile X mental retardation protein binds and regulates a novel class of mRNAs containing U rich target sequences

21 March 2017

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FMRP targets distinct mRNA sequence elements to regulate protein expression

21 March 2017

1 reference

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The G-quartet containing FMRP binding site in FMR1 mRNA is a potent exonic splicing enhancer

21 March 2017

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The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses

21 March 2017

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Mechanism of regulation of WAVE1-induced actin nucleation by Rac1 and Nck

21 March 2017

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Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders

21 March 2017

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Patterns and rates of exonic de novo mutations in autism spectrum disorders

21 March 2017

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Confirmed rare copy number variants implicate novel genes in schizophrenia

21 March 2017

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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia

21 March 2017

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Dysregulated metabotropic glutamate receptor-dependent translation of AMPA receptor and postsynaptic density-95 mRNAs at synapses in a mouse model of fragile X syndrome

21 March 2017

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Dynamic translational and proteasomal regulation of fragile X mental retardation protein controls mGluR-dependent long-term depression

21 March 2017

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Localization of FMRP-associated mRNA granules and requirement of microtubules for activity-dependent trafficking in hippocampal neurons

21 March 2017

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Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway

21 March 2017

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FMR1 transcript isoforms: association with polyribosomes; regional and developmental expression in mouse brain

21 March 2017

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Regulation of synaptic structure and function by FMRP-associated microRNAs miR-125b and miR-132

21 March 2017

1 reference

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CYFIP1 coordinates mRNA translation and cytoskeleton remodeling to ensure proper dendritic spine formation

21 March 2017

1 reference

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Association of mouse Dlg4 (PSD-95) gene deletion and human DLG4 gene variation with phenotypes relevant to autism spectrum disorders and Williams' syndrome

21 March 2017

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Fragile X mental retardation protein deficiency leads to excessive mGluR5-dependent internalization of AMPA receptors

21 March 2017

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The fragile X mental retardation protein-RNP granules show an mGluR-dependent localization in the post-synaptic spines

21 March 2017

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Metabotropic glutamate receptor activation regulates fragile x mental retardation protein and FMR1 mRNA localization differentially in dendrites and at synapses

21 March 2017

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Molecular phenotype of Fragile X syndrome: FMRP, FXRPs, and protein targets

21 March 2017

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

21 March 2017

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De Novo Gene Disruptions in Children on the Autistic Spectrum

7 April 2017

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism

7 April 2017

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Dendritic spine pathology in neuropsychiatric disorders

7 April 2017

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RNA recognition motifs: boring? Not quite

7 April 2017

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RNA regulons: coordination of post-transcriptional events

7 April 2017

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Understanding alternative splicing: towards a cellular code

7 April 2017

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Kinesin transports RNA: isolation and characterization of an RNA-transporting granule

7 April 2017

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The mGluR theory of fragile X mental retardation

7 April 2017

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Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function

7 April 2017

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

7 April 2017

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Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

7 April 2017

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Top3β is an RNA topoisomerase that works with fragile X syndrome protein to promote synapse formation

28 September 2017

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A proof-of-concept study: exon-level expression profiling and alternative splicing in autism using lymphoblastoid cell lines

28 September 2017

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RNA-binding proteins and translational regulation in axons and growth cones

28 September 2017

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The targeting and functions of miRNA-383 are mediated by FMRP during spermatogenesis.

28 September 2017

1 reference

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The translation of translational control by FMRP: therapeutic targets for FXS.

28 September 2017

1 reference

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

28 September 2017

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De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.

28 September 2017

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KIF1Bβ transports dendritically localized mRNPs in neurons and is recruited to synapses in an activity-dependent manner.

28 September 2017

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mRNA localization: an orchestration of assembly, traffic and synthesis

28 September 2017

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RNA binding protein/RNA element interactions and the control of translation

28 September 2017

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RNA-protein interactions in vivo: global gets specific

28 September 2017

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New perspectives on the biology of fragile X syndrome

28 September 2017

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Rare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese population

28 September 2017

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BC1-FMRP interaction is modulated by 2'-O-methylation: RNA-binding activity of the tudor domain and translational regulation at synapses

28 September 2017

1 reference

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Modulation of dADAR-dependent RNA editing by the Drosophila fragile X mental retardation protein.

28 September 2017

1 reference

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Fragile X syndrome: lifespan developmental implications for those without as well as with intellectual disability

28 September 2017

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Therapeutic strategies in fragile X syndrome: dysregulated mGluR signaling and beyond

28 September 2017

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Reversible inhibition of PSD-95 mRNA translation by miR-125a, FMRP phosphorylation, and mGluR signaling

28 September 2017

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dFMRP and Caprin, translational regulators of synaptic plasticity, control the cell cycle at the Drosophila mid-blastula transition

28 September 2017

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Protein homeostasis and synaptic plasticity

28 September 2017

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Altered mRNA transport, docking, and protein translation in neurons lacking fragile X mental retardation protein

28 September 2017

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Characterization and reversal of synaptic defects in the amygdala in a mouse model of fragile X syndrome

28 September 2017

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Abnormal mGlu 5 receptor/endocannabinoid coupling in mice lacking FMRP and BC1 RNA.

28 September 2017

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Arginines of the RGG box regulate FMRP association with polyribosomes and mRNA.

28 September 2017

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A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder

28 September 2017

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A mouse model of the human Fragile X syndrome I304N mutation

28 September 2017

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Fragile X mental retardation protein control of neuronal mRNA metabolism: Insights into mRNA stability

28 September 2017

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A review of fragile X premutation disorders: expanding the psychiatric perspective

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

The long journey of actin and actin-associated proteins from genes to polysomes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Making synaptic plasticity and memory last: mechanisms of translational regulation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Local protein synthesis, actin dynamics, and LTP consolidation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Tdrd3 is a novel stress granule-associated protein interacting with the Fragile-X syndrome protein FMRP.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Fragile X mental retardation protein interactions with the microtubule associated protein 1B RNA

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Structure and function of KH domains

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

The GABAA receptor: a novel target for treatment of fragile X?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Fragile X mental retardation protein FMRP and the RNA export factor NXF2 associate with and destabilize Nxf1 mRNA in neuronal cells

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

FMRP mediates mGluR5-dependent translation of amyloid precursor protein

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Fragile X mental retardation protein controls trailer hitch expression and cleavage furrow formation in Drosophila embryos

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Role of Pur alpha in targeting mRNA to sites of translation in hippocampal neuronal dendrites

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

RNA binding proteins and the regulation of neuronal synaptic plasticity.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype-phenotype correlations

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Regulation of actin dynamics by WASP and WAVE family proteins.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

The fragile X mental retardation protein has nucleic acid chaperone properties

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Compartmentalized synthesis and degradation of proteins in neurons.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

28 September 2017

(S)-3,5-DHPG: a review.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

p140Sra-1 (specifically Rac1-associated protein) is a novel specific target for Rac1 small GTPase.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Association of FMRP with ribosomal precursor particles in the nucleolus

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Fine structure of the human FMR1 gene

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Synaptic plasticity: LTP and LTD.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Reversal of disease-related pathologies in the fragile X mouse model by selective activation of GABAB receptors with arbaclofen.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

BDNF and TrkB in neuronal differentiation of Fmr1-knockout mouse.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Fragile X mental retardation protein levels are decreased in major psychiatric disorders

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

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

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Psychiatric disability in female carriers of the fragile X chromosome.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Contrast, motion, perceptual integration, and neurocognition in schizophrenia: the role of fragile-X related mechanisms.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Targeting the endocannabinoid system in the treatment of fragile X syndrome.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Molecular dynamics simulations show how the FMRP Ile304Asn mutation destabilizes the KH2 domain structure and affects its function

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Decreased fragile X mental retardation protein (FMRP) is associated with lower IQ and earlier illness onset in patients with schizophrenia.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

A numbers game underpins cytoplasmic mRNA transport.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

15q11.2 microdeletion - seven new patients with delayed development and/or behavioural problems.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Fragile X mice: reduced long-term potentiation and N-Methyl-D-Aspartate receptor-mediated neurotransmission in dentate gyrus

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

NMDA receptor hypofunction in the dentate gyrus and impaired context discrimination in adult Fmr1 knockout mice

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

FMR1/FXR1 and the miRNA pathway are required for eye and neural crest development.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Tissue and developmental regulation of fragile X mental retardation 1 exon 12 and 15 isoforms

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader-Willi critical region, possibly associated with behavioural disturbances

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Phosphorylation of FMRP inhibits association with Dicer

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

FMRP acts as a key messenger for dopamine modulation in the forebrain

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Abnormal striatal GABA transmission in the mouse model for the fragile X syndrome.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Expression profiling suggests underexpression of the GABA(A) receptor subunit delta in the fragile X knockout mouse model

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

NMDA receptor subunit NRI and postsynaptic protein PSD-95 in hippocampus and orbitofrontal cortex in schizophrenia and mood disorder

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Fragile X mental retardation protein (FMRP) binds specifically to the brain cytoplasmic RNAs BC1/BC200 via a novel RNA-binding motif

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Decreased GABA(A) receptor expression in the seizure-prone fragile X mouse.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Phosphorylation influences the translation state of FMRP-associated polyribosomes

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Rare variants in the promoter of the fragile X syndrome gene (FMR1)

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Clinical description of an adult male with psychosis who showed FMR1 gene methylation mosaicism

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Linkage analysis of the fragile X gene FMR-1 and schizophrenia: no evidence for linkage but report of a family with schizophrenia and an unstable triplet repeat.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

Screening for CGG trinucleotide repeat expansion in the fragile X mental retardation 1 gene in schizophrenic patients

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3807044

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

28 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/24167470

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3389/FNINS.2013.00191

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24167470%20AND%20SRC:MED&resulttype=core&format=json

3 June 2020

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24167470%20AND%20SRC:MED&resulttype=core&format=json

3 June 2020

PubMed publication ID

24167470

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24167470%20AND%20SRC:MED&resulttype=core&format=json