Fragile X mental retardation protein FMRP binds mRNAs in the nucleus - Test2 - elhamkhani - TriplyDB

Fragile X mental retardation protein FMRP binds mRNAs in the nucleus

Fragile X mental retardation protein FMRP binds mRNAs in the nucleus

http://www.wikidata.org/entity/Q28119156

about

On the aggregation properties of FMRP--a link with the FXTAS syndrome?RNA Secondary Structure Modulates FMRP's Bi-Functional Role in the MicroRNA Pathway The pathophysiology of fragile X (and what it teaches us about synapses)The unstable repeats--three evolving faces of neurological disease Therapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and Back Structural Studies of the Tandem Tudor Domains of Fragile X Mental Retardation Related Proteins FXR1 and FXR2 Fragile X mental retardation protein: A paradigm for translational control by RNA-binding proteins Subcellular fractionation and localization studies reveal a direct interaction of the fragile X mental retardation protein (FMRP) with nucleolin Nuclear Fragile X Mental Retardation Protein is localized to Cajal bodies Fragile X mental retardation protein stimulates ribonucleoprotein assembly of influenza A virus A chromatin-dependent role of the fragile X mental retardation protein FMRP in the DNA damage response MOV10 and FMRP regulate AGO2 association with microRNA recognition elements Positive feedback regulation of Akt-FMRP pathway protects neurons from cell death Identification and characterisation of Simiate, a novel protein linked to the fragile X syndrome Potential therapeutic interventions for fragile X syndrome Fragile X syndrome: an update on developing treatment modalities.Increasing our understanding of human cognition through the study of Fragile X Syndrome.FMRP: a new chapter with chromatin A new regulatory function of the region proximal to the RGG box in the fragile X mental retardation protein A novel fragile X syndrome mutation reveals a conserved role for the carboxy-terminus in FMRP localization and function.Arginine methylation of RNA-binding proteins regulates cell function and differentiation New X-chromosomal interactors of dFMRP regulate axonal and synaptic morphology of brain neurons in Drosophila melanogaster Zfrp8 forms a complex with fragile-X mental retardation protein and regulates its localization and function.FMR1: a gene with three faces.The fragile X mental retardation protein in circadian rhythmicity and memory consolidation.Ultrastructural analysis of the functional domains in FMRP using primary hippocampal mouse neurons.The fate of the messenger is pre-determined: a new model for regulation of gene expression Murine leukemia virus uses NXF1 for nuclear export of spliced and unspliced viral transcripts.The Atypical Dual Specificity Phosphatase hYVH1 Associates with Multiple Ribonucleoprotein Particles.Molecular modulators of the circadian clock: lessons from flies and mice.Fragile X premutation in women: recognizing the health challenges beyond primary ovarian insufficiency.MicroRNA-mediated mRNA translation activation in quiescent cells and oocytes involves recruitment of a nuclear microRNP.The Conserved, Disease-Associated RNA Binding Protein dNab2 Interacts with the Fragile X Protein Ortholog in Drosophila Neurons.Recombinant bacterial expression and purification of human fragile X mental retardation protein isoform 1.Reversal of disease-related pathologies in the fragile X mouse model by selective activation of GABAB receptors with arbaclofen.Genome wide assessment of mRNA in astrocyte protrusions by direct RNA sequencing reveals mRNA localization for the intermediate filament protein nestin.Fragile X mental retardation protein recognizes a G quadruplex structure within the survival motor neuron domain containing 1 mRNA 5'-UTR.Splice form-dependent regulation of axonal arbor complexity by FMRP.Analysis of the Fragile X mental retardation protein isoforms 1, 2 and 3 interactions with the G-quadruplex forming semaphorin 3F mRNA.The Illinois Biology and Politics summer institute.

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P2860

Fragile X mental retardation protein FMRP binds mRNAs in the nucleus

http://www.wikidata.org/entity/Q28119156

description

2009 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հունվարին հրատարակված գիտական հոդված

@hy

artículu científicu espublizáu en 2009

@ast

im Januar 2009 veröffentlichter wissenschaftlicher Artikel

@de

scientific journal article

@en

vedecký článok (publikovaný 2009/01/01)

@sk

vědecký článek publikovaný v roce 2009

@cs

wetenschappelijk artikel (gepubliceerd op 2009/01/01)

@nl

наукова стаття, опублікована в січні 2009

@uk

مقالة علمية (نشرت عام 2009)

@ar

name

Fragile X mental retardation protein FMRP binds mRNAs in the nucleus

@ast

Fragile X mental retardation protein FMRP binds mRNAs in the nucleus

@en

Fragile X mental retardation protein FMRP binds mRNAs in the nucleus

@nl

type

label

Fragile X mental retardation protein FMRP binds mRNAs in the nucleus

@ast

Fragile X mental retardation protein FMRP binds mRNAs in the nucleus

@en

Fragile X mental retardation protein FMRP binds mRNAs in the nucleus

@nl

prefLabel

Fragile X mental retardation protein FMRP binds mRNAs in the nucleus

@ast

Fragile X mental retardation protein FMRP binds mRNAs in the nucleus

@en

Fragile X mental retardation protein FMRP binds mRNAs in the nucleus

@nl

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P1433

Molecular and Cellular Biology

P1476

Fragile X mental retardation protein FMRP binds mRNAs in the nucleus

@en

P2093

Michel Bellini

http://www.w3.org/2001/XMLSchema#string

Miri Kim

http://www.w3.org/2001/XMLSchema#string

Stephanie Ceman

http://www.w3.org/2001/XMLSchema#string

P2860

Pre-mRNA splicing imprints mRNA in the nucleus with a novel RNA-binding protein that persists in the cytoplasm

FBXO11/PRMT9, a new protein arginine methyltransferase, symmetrically dimethylates arginine residues

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

FMR1 protein: conserved RNP family domains and selective RNA binding

TAP binds to the constitutive transport element (CTE) through a novel RNA-binding motif that is sufficient to promote CTE-dependent RNA export from the nucleus

Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex

The spliceosome deposits multiple proteins 20-24 nucleotides upstream of mRNA exon-exon junctions

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

Identification and characterization of the mouse nuclear export factor (Nxf) family members

Exportin 1 (Crm1p) is an essential nuclear export factor.

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214–228

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scholarly article

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579374

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P356

10.1128/MCB.01377-08

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P407

P433

1

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P478

29

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2009-01-01T00:00:00Z

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P698

18936162

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P921

FMRP translational regulator 1

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2612477

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