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English
FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association
scientific journal article
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scholarly article
1 reference
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PubMed
PubMed ID
9659908
retrieved
3 January 2017
title
FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association
(English)
1 reference
stated in
PubMed
PubMed ID
9659908
retrieved
3 January 2017
main subject
FMRP translational regulator 1
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stated in
GOA release 2020-03-11
fragile X syndrome
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inferred from title
author name string
Y. Feng
series ordinal
1
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PubMed
PubMed ID
9659908
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3 January 2017
D. Absher
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2
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stated in
PubMed
PubMed ID
9659908
retrieved
3 January 2017
D. E. Eberhart
series ordinal
3
1 reference
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PubMed
PubMed ID
9659908
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3 January 2017
V. Brown
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4
1 reference
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PubMed
PubMed ID
9659908
retrieved
3 January 2017
H. E. Malter
series ordinal
5
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PubMed
PubMed ID
9659908
retrieved
3 January 2017
S. T. Warren
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6
1 reference
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PubMed
PubMed ID
9659908
retrieved
3 January 2017
language of work or name
English
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publication date
1 December 1997
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PubMed
PubMed ID
9659908
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3 January 2017
published in
Molecular Cell
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PubMed
PubMed ID
9659908
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3 January 2017
volume
1
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PubMed
PubMed ID
9659908
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3 January 2017
page(s)
109–118
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PubMed
PubMed ID
9659908
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3 January 2017
issue
1
1 reference
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PubMed
PubMed ID
9659908
retrieved
3 January 2017
cites work
FMR1 protein: conserved RNP family domains and selective RNA binding
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Antiribosomal S10 antibodies in humans and MRL/lpr mice with systemic lupus erythematosus
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
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Conserved structures and diversity of functions of RNA-binding proteins
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
The KH module has an αβ fold
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Reversal of creatine kinase translational repression by 3' untranslated sequences
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
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Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits
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Crossref
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https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
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The fragile X mental retardation protein is associated with poly(A)+ mRNA in actively translating polyribosomes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
A point mutation in the FMR-1 gene associated with fragile X mental retardation
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
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The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
hnRNP proteins and the biogenesis of mRNA
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
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Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Inducers of erythroleukemic differentiation cause messenger RNAs that lack poly(A)-binding protein to accumulate in translationally inactive, salt-labile 80 S ribosomal complexes.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Tissue-specific expression of a FMR1/beta-galactosidase fusion gene in transgenic mice.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Importance of polysomal mRNA-associated polypeptides for protein synthesis initiation in yeast.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of neocortex in three males with the fragile X syndrome
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The fragile X mental retardation protein is associated with ribosomes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterisation of two major cellular poly(rC)-binding human proteins, each containing three K-homologous (KH) domains
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Localized Bicaudal-C RNA encodes a protein containing a KH domain, the RNA binding motif of FMR1.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Three-dimensional structure and stability of the KH domain: molecular insights into the fragile X syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The translation machinery and 70 kd heat shock protein cooperate in protein synthesis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Growth-dependent translation of IGF-II mRNA by a rapamycin-sensitive pathway
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adult fragile X syndrome. Clinico-neuropathologic findings.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA methylation represses FMR-1 transcription in fragile X syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
FMRP is associated to the ribosomes via RNA.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Protein-rRNA binding features and their structural and functional implications in ribosomes as determined by cross-linking studies.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Advances in molecular analysis of fragile X syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1097-2765%2800%2980012-X
retrieved
7 January 2021
based on heuristic
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Identifiers
DOI
10.1016/S1097-2765(00)80012-X
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
579346
OpenCitations bibliographic resource ID
579346
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
579346
PubMed ID
9659908
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
579346
ResearchGate publication ID
13624772
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