Fragile X mental retardation protein (FMRP) binds specifically to the brain cytoplasmic RNAs BC1/BC200 via a novel RNA-binding motif. - Test2 - elhamkhani - TriplyDB

Fragile X mental retardation protein (FMRP) binds specifically to the brain cytoplasmic RNAs BC1/BC200 via a novel RNA-binding motif.

Fragile X mental retardation protein (FMRP) binds specifically to the brain cytoplasmic RNAs BC1/BC200 via a novel RNA-binding motif.

http://www.wikidata.org/entity/Q48813739

about

Long noncoding RNA in genome regulation: prospects and mechanisms Regulatory long non-coding RNAs and neuronal disorders Dendritic BC1 RNA in translational control mechanisms RNA Secondary Structure Modulates FMRP's Bi-Functional Role in the MicroRNA Pathway The sweet side of RNA regulation: glyceraldehyde-3-phosphate dehydrogenase as a noncanonical RNA-binding protein The FMRP regulon: from targets to disease convergence Therapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and Back The amino-terminal structure of human fragile X mental retardation protein obtained using precipitant-immobilized imprinted polymers A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability In vitro and in cellulo evidences for association of the survival of motor neuron complex with the fragile X mental retardation protein Fragile X mental retardation protein FMRP binds mRNAs in the nucleus Alu RNP and Alu RNA regulate translation initiation in vitro Arc/Arg3.1 mRNA expression reveals a subcellular trace of prior sound exposure in adult primary auditory cortex.Fragile X mental retardation protein is required for programmed cell death and clearance of developmentally-transient peptidergic neurons.SINE RNA induces severe developmental defects in Arabidopsis thaliana and interacts with HYL1 (DRB1), a key member of the DCL1 complex.Specificity factors in cytoplasmic polyadenylation RNA exodus to Israel: RNA controlling function in the far reaches of the neuron. Workshop on RNA control on neuronal function.Increasing our understanding of human cognition through the study of Fragile X Syndrome.Genetic controls balancing excitatory and inhibitory synaptogenesis in neurodevelopmental disorder models.Poly(A) RNA-binding proteins and polyadenosine RNA: new members and novel functions.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.Substitution of critical isoleucines in the KH domains of Drosophila fragile X protein results in partial loss-of-function phenotypes.BC1-FMRP interaction is modulated by 2'-O-methylation: RNA-binding activity of the tudor domain and translational regulation at synapses MicroRNAs and other non-coding RNAs as targets for anticancer drug development.Comprehensive Identification of mRNA-Binding Proteins of Leishmania donovani by Interactome Capture.On BC1 RNA and the fragile X mental retardation protein.Translational control at the synapse: role of RNA regulators.Long noncoding RNAs in psychiatric disorders.Noncoding RNAs and RNA editing in brain development, functional diversification, and neurological disease.Human pathologies associated with defective RNA transport and localization in the nervous system.A study of the ultrastructure of fragile-X-related proteins Temporal requirements of the fragile x mental retardation protein in modulating circadian clock circuit synaptic architecture.The fragile X mental retardation protein in circadian rhythmicity and memory consolidation.The state of synapses in fragile X syndrome.Spatially restricting gene expression by local translation at synapses Role of a redox-based methylation switch in mRNA life cycle (pre- and post-transcriptional maturation) and protein turnover: implications in neurological disorders.Long non-coding RNAs in neurodevelopmental disorders.Discovery of protein-RNA networks.RNA-binding proteins as molecular links between cancer and neurodegeneration.

P2860

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P2860

Fragile X mental retardation protein (FMRP) binds specifically to the brain cytoplasmic RNAs BC1/BC200 via a novel RNA-binding motif.

http://www.wikidata.org/entity/Q48813739

description

2005 nî lūn-bûn

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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2005年學術文章

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name

Fragile X mental retardation p ...... via a novel RNA-binding motif.

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Fragile X mental retardation protein

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type

label

Fragile X mental retardation p ...... via a novel RNA-binding motif.

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Fragile X mental retardation protein

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prefLabel

Fragile X mental retardation p ...... via a novel RNA-binding motif.

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Fragile X mental retardation protein

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P1433

Journal of Biological Chemistry

P1476

Fragile X mental retardation p ...... via a novel RNA-binding motif.

@en

P2093

Eva Kühn-Hölsken

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

Henning Urlaub

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

Ilaria Napoli

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

Tilmann Achsel

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P2860

Functional interaction of a novel 15.5kD [U4/U6.U5] tri-snRNP protein with the 5' stem-loop of U4 snRNA

Facilitation of dendritic mRNA transport by CPEB

Crystal structures of transcription factor NusG in light of its nucleic acid- and protein-binding activities

Kissing complex RNAs mediate interaction between the Fragile-X mental retardation protein KH2 domain and brain polyribosomes.

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

The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein

Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations

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

Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway

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33403-33410

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scholarly article

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10.1074/JBC.M504286200

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39

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P478

280

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Annalisa Pastore

Salvatore Adinolfi

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2005-07-08T00:00:00Z

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16006558

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