About: Evidence that fragile X mental retardation protein is a negative regulator of translation

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rdf:type	Item
description	artículu científicu espublizáu en 2001 (ast) vědecký článek publikovaný v roce 2001 (cs) 2001 թուականի Փետրուարին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована в лютому 2001 (uk) 2001 թվականի փետրվարին հրատարակված գիտական հոդված (hy) vedecký článok (publikovaný 2001/02/15) (sk) wetenschappelijk artikel (gepubliceerd op 2001/02/15) (nl) مقالة علمية (نشرت في 15-2-2001) (ar) im Februar 2001 veröffentlichter wissenschaftlicher Artikel (de) scientific journal article (en)
publication date	wds:Q28117211-4C9781F2-FA02-4F26-8F60-DB5CC335AC7C
publication date	2001-02-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28117211-B1625BF1-2CBB-4CD7-9B87-F709626B6D7C
language of work or name	English
author name string	wds:Q28117211-09FB65A8-A8A6-4709-8A6C-47F41DEF98D6 wds:Q28117211-44D30F25-5514-4277-8064-AD34F01315DE wds:Q28117211-A41D194A-2749-46BD-8D1A-E206F401A755 wds:Q28117211-BE2EDDF2-1379-4C26-AE41-1118F0523963
OpenCitations bibliographic resource ID	wds:Q28117211-726686F8-2D73-4B38-B3F5-154DED888829
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/579376
author name string	B Laggerbauer A Ostareck-Lederer D Ostareck E M Keidel
OpenCitations bibliographic resource ID	579376
rdfs:label	Evidence that fragile X mental retardation protein is a negative regulator of translation (en) Evidence that fragile X mental retardation protein is a negative regulator of translation (nl) Evidence that fragile X mental retardation protein is a negative regulator of translation (ast)
skos:prefLabel	Evidence that fragile X mental retardation protein is a negative regulator of translation (en) Evidence that fragile X mental retardation protein is a negative regulator of translation (nl) Evidence that fragile X mental retardation protein is a negative regulator of translation (ast)
name	Evidence that fragile X mental retardation protein is a negative regulator of translation (en) Evidence that fragile X mental retardation protein is a negative regulator of translation (nl) Evidence that fragile X mental retardation protein is a negative regulator of translation (ast)
author	wds:Q28117211-84C0AB75-4B71-417E-A577-88C154C65126
author	Utz Fischer
title	wds:Q28117211-795F0B2B-9A84-4541-B415-E1CA96842468
title	Evidence that fragile X mental retardation protein is a negative regulator of translation (en)
page(s)	wds:Q28117211-BE51A05E-6928-47E8-9C8F-686D880DE95F
page(s)	329-338
instance of	wds:Q28117211-8E7EA2E2-5D3C-4472-9EF5-B8EC4A592E6C
instance of	scholarly article
main subject	wds:Q28117211-AEF05055-6A61-4B3F-92B1-A3BC391639B5 wds:Q28117211-D4067DFE-5ED3-4EE7-B920-85A48C85BB39
main subject	wd:Q905435 identical protein binding
PubMed ID	wds:Q28117211-1F73A690-FA20-4D48-88FD-2E0FD2A8461B
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11157796
PubMed ID	11157796
published in	wds:Q28117211-7DF48B0C-AA86-4154-95FE-F995F155DF24
published in	Human Molecular Genetics
issue	wds:Q28117211-2E722F58-22CD-481B-81AB-EB4B192E5D52
volume	wds:Q28117211-2DDA152F-FB9B-447D-A768-B809A05D655F
issue	4
volume	10
DOI	wds:Q28117211-DFC36E5C-A5F5-4D01-BCF7-55F5CBCB76D8
DOI	http://dx.doi.org/10.1093/HMG/10.4.329
DOI	10.1093/HMG/10.4.329
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28117211
is cites work of	Altered synaptic plasticity in a mouse model of fragile X mental retardation Dendritic spines elongate after stimulation of group 1 metabotropic glutamate receptors in cultured hippocampal neurons The fragile X mental retardation protein and group I metabotropic glutamate receptors regulate levels of mRNA granules in brain Differential translation and fragile X syndrome Local protein synthesis and spine morphogenesis: Fragile X syndrome and beyond. Postadolescent changes in regional cerebral protein synthesis: an in vivo study in the FMR1 null mouse. A phenotypic and molecular characterization of the fmr1-tm1Cgr fragile X mouse. The fragile X mental retardation protein has nucleic acid chaperone properties Is fragile X mental retardation protein involved in activity-induced plasticity of dendritic spines? Loss of the fragile X mental retardation protein decouples metabotropic glutamate receptor dependent priming of long-term potentiation from protein synthesis Characterisation of Fmrp in zebrafish: evolutionary dynamics of the fmr1 gene. Analysis of the Fragile X mental retardation protein isoforms 1, 2 and 3 interactions with the G-quadruplex forming semaphorin 3F mRNA. Biophysical characterization of G-quadruplex forming FMR1 mRNA and of its interactions with different fragile X mental retardation protein isoforms MicroRNAs in gene regulation: when the smallest governs it all Fragile X mental retardation protein controls trailer hitch expression and cleavage furrow formation in Drosophila embryos The Drosophila fragile X-related gene regulates axoneme differentiation during spermatogenesis. Isolation of mouse neuritic mRNAs Fragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2P Cytoplasmic RNA-binding proteins and the control of complex brain function A 3' untranslated region variant in FMR1 eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuR Elevated glycogen synthase kinase-3 activity in Fragile X mice: key metabolic regulator with evidence for treatment potential. Lithium reverses increased rates of cerebral protein synthesis in a mouse model of fragile X syndrome The fragile X mental retardation protein in circadian rhythmicity and memory consolidation Casein kinase II phosphorylates the fragile X mental retardation protein and modulates its biological properties The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development. Genetics of human prefrontal function FMRP phosphorylation reveals an immediate-early signaling pathway triggered by group I mGluR and mediated by PP2A. Molecular and comparative genetics of mental retardation A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway The structure of the N-terminal domain of the fragile X mental retardation protein: a platform for protein-protein interaction NXF5, a novel member of the nuclear RNA export factor family, is lost in a male patient with a syndromic form of mental retardation Matrix metalloproteinases and minocycline: therapeutic avenues for fragile X syndrome Metabotropic glutamate receptor activation regulates fragile x mental retardation protein and FMR1 mRNA localization differentially in dendrites and at synapses The fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95 The Role of MicroRNAs in Human Diseases Evidence for the association of the human regulatory protein Ki-1/57 with the translational machinery. The fragile X gene and its function FMRP mediates mGluR5-dependent translation of amyloid precursor protein RNA cargoes associating with FMRP reveal deficits in cellular functioning in Fmr1 null mice.

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