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Fragile X mental retardation protein FMRP binds mRNAs in the nucleus
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scholarly article
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stated in
PubMed
PubMed ID
18936162
retrieved
4 January 2017
title
Fragile X mental retardation protein FMRP binds mRNAs in the nucleus
(English)
1 reference
stated in
PubMed
PubMed ID
18936162
retrieved
4 January 2017
main subject
FMRP translational regulator 1
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stated in
GOA release 2020-03-11
author
Stephanie Ceman
series ordinal
3
object named as
Stephanie Ceman
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stated in
PubMed
PubMed ID
18936162
retrieved
4 January 2017
author name string
Miri Kim
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1
1 reference
stated in
PubMed
PubMed ID
18936162
retrieved
4 January 2017
Michel Bellini
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
18936162
retrieved
4 January 2017
language of work or name
English
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publication date
1 January 2009
1 reference
stated in
PubMed
PubMed ID
18936162
retrieved
4 January 2017
published in
Molecular and Cellular Biology
1 reference
stated in
PubMed
PubMed ID
18936162
retrieved
4 January 2017
volume
29
1 reference
stated in
PubMed
PubMed ID
18936162
retrieved
4 January 2017
page(s)
214–228
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stated in
PubMed
PubMed ID
18936162
retrieved
4 January 2017
issue
1
1 reference
stated in
PubMed
PubMed ID
18936162
retrieved
4 January 2017
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Essential role for KH domains in RNA binding: impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome
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TAP binds to the constitutive transport element (CTE) through a novel RNA-binding motif that is sufficient to promote CTE-dependent RNA export from the nucleus
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Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex
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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
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Kissing complex RNAs mediate interaction between the Fragile-X mental retardation protein KH2 domain and brain polyribosomes
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FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association
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The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein
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The G-quartet containing FMRP binding site in FMR1 mRNA is a potent exonic splicing enhancer
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RNA and microRNAs in fragile X mental retardation
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The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif
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TAP, the human homolog of Mex67p, mediates CTE-dependent RNA export from the nucleus
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Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes
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Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
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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
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The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules
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The fragile X mental retardation protein interacts with a distinct mRNA nuclear export factor NXF2
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Metabotropic glutamate receptor activation regulates fragile x mental retardation protein and FMR1 mRNA localization differentially in dendrites and at synapses
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Transport of fragile X mental retardation protein via granules in neurites of PC12 cells
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REF, an evolutionary conserved family of hnRNP-like proteins, interacts with TAP/Mex67p and participates in mRNA nuclear export.
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Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains
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CRM1 is responsible for intracellular transport mediated by the nuclear export signal
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Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function
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Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome
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The exon-exon junction complex provides a binding platform for factors involved in mRNA export and nonsense-mediated mRNA decay
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Transport of proteins and RNAs in and out of the nucleus
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Evidence for a role of CRM1 in signal-mediated nuclear protein export
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Formation of a Tap/NXF1 homotypic complex is mediated through the amino-terminal domain of Tap and enhances interaction with nucleoporins
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Splicing-independent recruitment of spliceosomal small nuclear RNPs to nascent RNA polymerase II transcripts
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Fragile X mental retardation protein FMRP and the RNA export factor NXF2 associate with and destabilize Nxf1 mRNA in neuronal cells
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29 September 2017
AU-rich-element-mediated upregulation of translation by FXR1 and Argonaute 2.
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29 September 2017
The tripartite motif of nuclear factor 7 is required for its association with transcriptional units
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Fragile X mental retardation protein controls trailer hitch expression and cleavage furrow formation in Drosophila embryos
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29 September 2017
An intron with a constitutive transport element is retained in a Tap messenger RNA.
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Dynamic nuclear pore complexes: life on the edge.
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29 September 2017
The Wilms' tumor 1 (WT1) gene (+KTS isoform) functions with a CTE to enhance translation from an unspliced RNA with a retained intron
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Transcription, translation and fragile X syndrome
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29 September 2017
Identification and characterization of the methyl arginines in the fragile X mental retardation protein Fmrp
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29 September 2017
Mutations in tap uncouple RNA export activity from translocation through the nuclear pore complex
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29 September 2017
SRprises along a messenger's journey
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Tap and NXT promote translation of unspliced mRNA.
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29 September 2017
A novel family of nuclear transport receptors mediates the export of messenger RNA to the cytoplasm
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The nuclear connection in RNA transport and localization
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29 September 2017
Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression
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29 September 2017
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29 September 2017
Small bristles, the Drosophila ortholog of NXF-1, is essential for mRNA export throughout development
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29 September 2017
Nucleocytoplasmic transport enters the atomic age.
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29 September 2017
REF proteins mediate the export of spliced and unspliced mRNAs from the nucleus
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29 September 2017
A nuclear role for the Fragile X mental retardation protein
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29 September 2017
Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms
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29 September 2017
The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation
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PubMed Central
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29 September 2017
Fine structure of the human FMR1 gene
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PubMed Central
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29 September 2017
High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome
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29 September 2017
A major developmental transition in early xenopus embryos: I. characterization and timing of cellular changes at the midblastula stage
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29 September 2017
Dissection of a nuclear localization signal
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2 June 2018
Analysis of domains affecting intracellular localization of the FMRP protein.
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2 June 2018
The molecular basis of fragile X syndrome
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2 June 2018
A point mutation in the FMR-1 gene associated with fragile X mental retardation
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612477
retrieved
2 June 2018
Polarization of both major body axes in Drosophila by gurken-torpedo signalling.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612477
retrieved
2 June 2018
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612477
retrieved
2 June 2018
DNA methylation represses FMR-1 transcription in fragile X syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612477
retrieved
2 June 2018
Fragile X mental retardation protein (FMRP) binds specifically to the brain cytoplasmic RNAs BC1/BC200 via a novel RNA-binding motif.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612477
retrieved
27 November 2018
Two members of the Fxr gene family, Fmr1 and Fxr1, are differentially expressed in Xenopus tropicalis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612477
retrieved
27 November 2018
Characterisation of Fmrp in zebrafish: evolutionary dynamics of the fmr1 gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612477
retrieved
27 November 2018
The N-terminus of the fragile X mental retardation protein contains a novel domain involved in dimerization and RNA binding.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612477
retrieved
27 November 2018
SR splicing factors serve as adapter proteins for TAP-dependent mRNA export
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612477
retrieved
27 November 2018
RNA cargoes associating with FMRP reveal deficits in cellular functioning in Fmr1 null mice.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612477
retrieved
27 November 2018
Development and characterization of antibodies that immunoprecipitate the FMR1 protein.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612477
retrieved
27 November 2018
Binding and internalization of fluorescent opioid peptide conjugates in living cells
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612477
retrieved
27 November 2018
Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2612477
retrieved
27 November 2018
The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/18936162
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1128/MCB.01377-08
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
579374
OpenCitations bibliographic resource ID
579374
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
579374
PMCID
2612477
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
579374
PubMed ID
18936162
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
579374
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