The fragile X mental retardation protein has nucleic acid chaperone properties. - Test2 - elhamkhani - TriplyDB

The fragile X mental retardation protein has nucleic acid chaperone properties.

The fragile X mental retardation protein has nucleic acid chaperone properties.

http://www.wikidata.org/entity/Q38342235

about

Interactions of the G quartet forming semaphorin 3F RNA with the RGG box domain of the fragile X protein family The pathophysiology of fragile X (and what it teaches us about synapses)The FMRP regulon: from targets to disease convergence RNA chaperoning and intrinsic disorder in the core proteins of Flaviviridae The HIV-1 transcriptional activator Tat has potent nucleic acid chaperoning activities in vitro Kissing complex RNAs mediate interaction between the Fragile-X mental retardation protein KH2 domain and brain polyribosomes.Dicer-derived microRNAs are utilized by the fragile X mental retardation protein for assembly on target RNAs A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability Translational regulation of the human achaete-scute homologue-1 by fragile X mental retardation protein From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome Strategies for RNA folding and assembly Fragile X related protein 1 isoforms differentially modulate the affinity of fragile X mental retardation protein for G-quartet RNA structure Argonaute2 suppresses Drosophila fragile X expression preventing neurogenesis and oogenesis defects.MicroRNAs as a molecular basis for mental retardation, Alzheimer's and prion diseases.Characterization of RNA binding and chaperoning activities of HIV-1 Vif protein. Importance of the C-terminal unstructured tail.Increasing our understanding of human cognition through the study of Fragile X Syndrome.Similarities and differences in the nucleic acid chaperone activity of HIV-2 and HIV-1 nucleocapsid proteins in vitro Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum Disorders Human FMRP contains an integral tandem Agenet (Tudor) and KH motif in the amino terminal domain.BC1-FMRP interaction is modulated by 2'-O-methylation: RNA-binding activity of the tudor domain and translational regulation at synapses Ty1 retrovirus-like element Gag contains overlapping restriction factor and nucleic acid chaperone functions.On BC1 RNA and the fragile X mental retardation protein.Translational control at the synapse: role of RNA regulators.Fragile X mental retardation protein interactions with the microtubule associated protein 1B RNA Human pathologies associated with defective RNA transport and localization in the nervous system.Cells lacking the fragile X mental retardation protein (FMRP) have normal RISC activity but exhibit altered stress granule assembly.Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles Reciprocal signaling between translational control pathways and synaptic proteins in autism spectrum disorders.Analysis of nucleic acid chaperoning by the prion protein and its inhibition by oligonucleotides.A structural perspective of RNA recognition by intrinsically disordered proteins.Hypothesis: a role for fragile X mental retardation protein in mediating and relieving microRNA-guided translational repression?Recombinant bacterial expression and purification of human fragile X mental retardation protein isoform 1.RNA chaperone activity and RNA-binding properties of the E. coli protein StpA.Conformational-dependent and independent RNA binding to the fragile x mental retardation protein.Proteins with RNA chaperone activity: a world of diverse proteins with a common task-impediment of RNA misfolding.Reply to Bagni: On BC1 RNA and the fragile X mental retardation protein.Alterations in the Sp1 binding and Fmr-1 gene expression in the cortex of the brain during maturation and aging of mouse.Fragile X mental retardation protein (FMRP) binds specifically to the brain cytoplasmic RNAs BC1/BC200 via a novel RNA-binding motif.

P2860

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P2860

The fragile X mental retardation protein has nucleic acid chaperone properties.

http://www.wikidata.org/entity/Q38342235

description

2004 nî lūn-bûn

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2004年の論文

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年学术文章

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2004年學術文章

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2004年學術文章

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2004年學術文章

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name

The fragile X mental retardation protein has nucleic acid chaperone properties.

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type

label

The fragile X mental retardation protein has nucleic acid chaperone properties.

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prefLabel

The fragile X mental retardation protein has nucleic acid chaperone properties.

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P1433

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P1433

Nucleic Acids Research

P1476

The fragile X mental retardation protein has nucleic acid chaperone properties.

@en

P2093

Caroline Gabus

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

Edouard W Khandjian

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

Jean-Luc Darlix

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

Rachid Mazroui

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

Sandra Tremblay

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

P2860

A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P

82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localization

NUFIP1 (nuclear FMRP interacting protein 1) is a nucleocytoplasmic shuttling protein associated with active synaptoneurosomes

Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation

FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association

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

The fragile X mental retardation protein binds and regulates a novel class of mRNAs containing U rich target sequences

New insights into fragile X syndrome: from molecules to neurobehaviors

A decade of molecular studies of fragile X syndrome

The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses

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2129-2137

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scholarly article

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10.1093/NAR/GKH535

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P433

7

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32

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2004-04-19T00:00:00Z

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8606905

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15096575

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P921

molecular chaperones

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407820

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