Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes (Q28303541)

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1 November 2019

title

Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes (English)

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1 November 2019

main subject

dendritic spine origin

1 reference

Gene Ontology release 2020-05-02

Y Feng

1

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15 May 2020

C A Gutekunst

2

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15 May 2020

D E Eberhart

3

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15 May 2020

H Yi

4

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15 May 2020

S T Warren

5

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15 May 2020

S M Hersch

6

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15 May 2020

language of work or name

English

0 references

publication date

1 March 1997

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1 November 2019

published in

Journal of Neuroscience

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15 May 2020

volume

17

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15 May 2020

issue

5

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15 May 2020

page(s)

1539-1547

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FXR1, an autosomal homolog of the fragile X mental retardation gene

15 May 2020

cites work

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Quantitative comparison of FMR1 gene expression in normal and premutation alleles

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12 December 2020

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

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Transport of BC1 RNA in hypothalamo-neurohypophyseal axons

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

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12 December 2020

FMR1 Protein: Conserved RNP Family Domains and Selective RNA Binding

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Synapsin I (protein I), a nerve terminal-specific phosphoprotein. III. Its association with synaptic vesicles studied in a highly purified synaptic vesicle preparation

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Triplet Repeat Expansion Mutations: The Example of Fragile X Syndrome

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12 December 2020

mRNA coding for oxytocin is present in axons of the hypothalamo-neurohypophysial tract

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12 December 2020

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

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12 December 2020

Metabotropic glutamate receptors trigger postsynaptic protein synthesis

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12 December 2020

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

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12 December 2020

In situ hybridization histochemistry of Ca2+/calmodulin-dependent protein kinase in developing rat brain

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12 December 2020

On the nature and differential distribution of mRNAs in hippocampal neurites: implications for neuronal functioning

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12 December 2020

Localization and active transport of mRNA in axons of sympathetic neurons in culture

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12 December 2020

Investigation of the subcellular distribution of the bcl-2 oncoprotein: residence in the nuclear envelope, endoplasmic reticulum, and outer mitochondrial membranes

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12 December 2020

Long-term potentiation induced changes in protein synthesis of hippocampal subfields of freely moving rats: time-course

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12 December 2020

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

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12 December 2020

Selective localization of messenger RNA for cytoskeletal protein MAP2 in dendrites

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12 December 2020

Aggregation of vasopressin mRNA in a subset of axonal swellings of the median eminence and posterior pituitary: light and electron microscopic evidence.

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12 December 2020

DNA methylation represses FMR-1 transcription in fragile X syndrome

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12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9030614

12 December 2020

Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9030614

12 December 2020

The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals

1 reference

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12 December 2020

Protein-synthetic machinery beneath postsynaptic sites on CNS neurons: association between polyribosomes and other organelles at the synaptic site.

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12 December 2020

The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2

1 reference

https://pubmed.ncbi.nlm.nih.gov/9030614

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9030614

12 December 2020

The nontransmembrane tyrosine phosphatase PTP-1B localizes to the endoplasmic reticulum via its 35 amino acid C-terminal sequence

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12 December 2020

RNA in the axonal domain: a new dimension in neuronal functioning?

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12 December 2020

Conserved structures and diversity of functions of RNA-binding proteins

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12 December 2020

Protein-synthetic machinery at postsynaptic sites during synaptogenesis: a quantitative study of the association between polyribosomes and developing synapses

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12 December 2020

Dendritic location of neural BC1 RNA

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12 December 2020

Fmr1 knockout mice: a model to study fragile X mental retardation. The Dutch-Belgian Fragile X Consortium

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12 December 2020

Two new cases of FMR1 deletion associated with mental impairment.

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12 December 2020

Translational suppression by trinucleotide repeat expansion at FMR1.

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12 December 2020

A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome

1 reference

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12 December 2020

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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12 December 2020

Occurrence and sequence complexity of polyadenylated RNA in squid axoplasm

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12 December 2020

Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

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12 December 2020

Changes in protein synthesis accompanying long-term potentiation in the dentate gyrus in vivo.

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12 December 2020

The fragile X mental retardation protein is associated with ribosomes

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12 December 2020

Antibodies to bovine liver branched-chain 2-oxo acid dehydrogenase cross-react with this enzyme complex from other tissues and species

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12 December 2020

Three-dimensional analysis of dendritic spines. II. Spine apparatus and other cytoplasmic components

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12 December 2020

Dendrites as compartments for macromolecular synthesis.

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12 December 2020

Differential subcellular mRNA targeting: deletion of a single nucleotide prevents the transport to axons but not to dendrites of rat hypothalamic magnocellular neurons

1 reference

https://pubmed.ncbi.nlm.nih.gov/9030614

12 December 2020

The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/9030614

12 December 2020

Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/9030614

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9030614

12 December 2020

Highly conserved 3' UTR and expression pattern of FXR1 points to a divergent gene regulation of FXR1 and FMR1

1 reference

https://pubmed.ncbi.nlm.nih.gov/9030614

12 December 2020

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://pubmed.ncbi.nlm.nih.gov/9030614

12 December 2020

Inhibition of in vivo and in vitro transcription by monoclonal antibodies prepared against wheat germ RNA polymerase II that react with the heptapeptide repeat of eukaryotic RNA polymerase II.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9030614

12 December 2020

High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9030614

12 December 2020

Preferential localization of polyribosomes under the base of dendritic spines in granule cells of the dentate gyrus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/9030614

12 December 2020

Adult fragile X syndrome. Clinico-neuropathologic findings

1 reference

https://pubmed.ncbi.nlm.nih.gov/9030614

12 December 2020

10.1523/JNEUROSCI.17-05-01539.1997

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6573369&resulttype=core&format=json

OpenCitations bibliographic resource ID

15 May 2020

4040220

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6573369&resulttype=core&format=json

15 May 2020

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4040220