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

PubMed ID

9030614

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9030614%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

title

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

1 reference

PubMed ID

9030614

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9030614%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

main subject

dendritic spine origin

1 reference

Gene Ontology release 2020-05-02

Y Feng

1

1 reference

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

15 May 2020

C A Gutekunst

2

1 reference

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

15 May 2020

D E Eberhart

3

1 reference

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

15 May 2020

H Yi

4

1 reference

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

15 May 2020

S T Warren

5

1 reference

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

15 May 2020

S M Hersch

6

1 reference

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

15 May 2020

language of work or name

English

0 references

publication date

1 March 1997

1 reference

PubMed ID

9030614

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9030614%20AND%20SRC:MED&resulttype=core&format=json

1 November 2019

published in

Journal of Neuroscience

1 reference

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

15 May 2020

volume

17

1 reference

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

15 May 2020

issue

5

1 reference

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

15 May 2020

page(s)

1539-1547

1 reference

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

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

15 May 2020

cites work

1 reference

12 December 2020

Analysis of neocortex in three males with the fragile X syndrome

1 reference

12 December 2020

Alterations in polyribosomes associated with dendritic spines during the reinnervation of the dentate gyrus of the adult rat.

1 reference

12 December 2020

Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test.

1 reference

12 December 2020

Tissue-specific expression of a FMR1/beta-galactosidase fusion gene in transgenic mice.

1 reference

12 December 2020

Antiribosomal S10 antibodies in humans and MRL/lpr mice with systemic lupus erythematosus

1 reference

12 December 2020

Quantitative comparison of FMR1 gene expression in normal and premutation alleles

1 reference

12 December 2020

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

1 reference

12 December 2020

Transport of BC1 RNA in hypothalamo-neurohypophyseal axons

1 reference

12 December 2020

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

1 reference

12 December 2020

FMR1 protein: conserved RNP family domains and selective RNA binding

1 reference

12 December 2020

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

1 reference

12 December 2020

Triplet repeat expansion mutations: the example of fragile X syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Metabotropic glutamate receptors trigger postsynaptic protein synthesis

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Selective localization of messenger RNA for cytoskeletal protein MAP2 in dendrites

1 reference

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.

1 reference

12 December 2020

DNA methylation represses FMR-1 transcription in fragile X syndrome

1 reference

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

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

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

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Conserved structures and diversity of functions of RNA-binding proteins

1 reference

12 December 2020

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

1 reference

12 December 2020

Dendritic location of neural BC1 RNA

1 reference

12 December 2020

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

1 reference

12 December 2020

Two new cases of FMR1 deletion associated with mental impairment.

1 reference

12 December 2020

Translational suppression by trinucleotide repeat expansion at FMR1.

1 reference

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

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

1 reference

12 December 2020

Occurrence and sequence complexity of polyadenylated RNA in squid axoplasm

1 reference

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.

1 reference

12 December 2020

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

1 reference

12 December 2020

The fragile X mental retardation protein is associated with ribosomes

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Dendrites as compartments for macromolecular synthesis.

1 reference

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

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

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

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

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Adult fragile X syndrome. Clinico-neuropathologic findings.

1 reference

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