Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q28588486)
Watch
English
The fragile X mental retardation protein inhibits translation via interacting with mRNA
scientific journal article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
11376146
retrieved
31 January 2017
title
The fragile X mental retardation protein inhibits translation via interacting with mRNA
(English)
1 reference
stated in
PubMed
PubMed ID
11376146
retrieved
31 January 2017
main subject
Synaptic functional regulator FMR1
1 reference
stated in
GOA release 2020-03-11
author name string
Z. Li
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
11376146
retrieved
31 January 2017
Y. Zhang
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
11376146
retrieved
31 January 2017
L. Ku
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
11376146
retrieved
31 January 2017
K. D. Wilkinson
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
11376146
retrieved
31 January 2017
S. T. Warren
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
11376146
retrieved
31 January 2017
Y. Feng
series ordinal
6
1 reference
stated in
PubMed
PubMed ID
11376146
retrieved
31 January 2017
language of work or name
English
0 references
publication date
1 June 2001
1 reference
stated in
PubMed
PubMed ID
11376146
retrieved
31 January 2017
published in
Nucleic Acids Research
1 reference
stated in
PubMed
PubMed ID
11376146
retrieved
31 January 2017
volume
29
1 reference
stated in
PubMed
PubMed ID
11376146
retrieved
31 January 2017
page(s)
2276–2283
1 reference
stated in
PubMed
PubMed ID
11376146
retrieved
31 January 2017
issue
11
1 reference
stated in
PubMed
PubMed ID
11376146
retrieved
31 January 2017
cites work
Evidence that fragile X mental retardation protein is a negative regulator of translation
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=55699
retrieved
17 March 2017
Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex
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=55699
retrieved
17 March 2017
A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (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=55699
retrieved
17 March 2017
The STAR protein QKI-6 is a translational repressor
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=55699
retrieved
17 March 2017
FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association
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=55699
retrieved
17 March 2017
Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation 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=55699
retrieved
17 March 2017
Interaction of polyadenylate-binding protein with the eIF4G homologue PAIP enhances translation
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=55699
retrieved
17 March 2017
Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis
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=55699
retrieved
17 March 2017
Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes
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=55699
retrieved
17 March 2017
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
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=55699
retrieved
17 March 2017
FMR1 protein: conserved RNP family domains and selective 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=55699
retrieved
17 March 2017
The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding 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=55699
retrieved
17 March 2017
The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2
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=55699
retrieved
17 March 2017
Translational control in mammalian cells
2 references
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=55699
retrieved
17 March 2017
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=55699
retrieved
6 April 2017
Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains
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=55699
retrieved
17 March 2017
Understanding the molecular basis of 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=55699
retrieved
29 September 2017
The STAR protein, GLD-1, is a translational regulator of sexual identity in Caenorhabditis elegans
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=55699
retrieved
29 September 2017
RNA-Protein binding and post-transcriptional regulation of parathyroid hormone gene expression by calcium and phosphate
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=55699
retrieved
29 September 2017
mRNA silencing in erythroid differentiation: hnRNP K and hnRNP E1 regulate 15-lipoxygenase translation from the 3' end.
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=55699
retrieved
29 September 2017
Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms
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=55699
retrieved
29 September 2017
The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation
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=55699
retrieved
29 September 2017
Advances in molecular analysis of 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=55699
retrieved
29 September 2017
Quantitative comparison of FMR1 gene expression in normal and premutation alleles
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=55699
retrieved
29 September 2017
The human 18S ribosomal RNA gene: evolution and stability
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=55699
retrieved
29 September 2017
Molecular evolution of human and rabbit beta-globin mRNAs
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=55699
retrieved
29 September 2017
The molecular basis of 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=55699
retrieved
3 June 2018
FMRP is associated to the ribosomes via RNA.
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=55699
retrieved
3 June 2018
Translational regulation of myelin basic protein synthesis.
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=55699
retrieved
3 June 2018
(Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features
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=55699
retrieved
27 November 2018
The fragile X mental retardation protein is associated with poly(A)+ mRNA in actively translating polyribosomes
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=55699
retrieved
27 November 2018
Tissue specific expression of FMR-1 provides evidence for a functional role 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=55699
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=55699
retrieved
27 November 2018
The major core protein of messenger ribonucleoprotein particles (p50) promotes initiation of protein biosynthesis in vitro
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11376146
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell culture
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11376146
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
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/11376146
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The fragile X syndrome
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11376146
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1093/NAR/29.11.2276
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2297828
OpenCitations bibliographic resource ID
2297828
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2297828
PMCID
55699
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2297828
PubMed ID
11376146
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2297828
ResearchGate publication ID
276943279
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
