On BC1 RNA and the fragile X mental retardation protein. - Wikidata - awgldk - TriplyDB

On BC1 RNA and the fragile X mental retardation protein.

On BC1 RNA and the fragile X mental retardation protein.

http://www.wikidata.org/entity/Q36393017

about

Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function Regulatory long non-coding RNAs and neuronal disorders The pathophysiology of fragile X (and what it teaches us about synapses)A novel function for fragile X mental retardation protein in translational activation The G-quartet containing FMRP binding site in FMR1 mRNA is a potent exonic splicing enhancer Dendritic mRNA targeting of Jacob and N-methyl-d-aspartate-induced nuclear translocation after calpain-mediated proteolysis Elongation factor 2 and fragile X mental retardation protein control the dynamic translation of Arc/Arg3.1 essential for mGluR-LTD Genomic organization of eukaryotic tRNAs The RNA-binding protein MARTA2 regulates dendritic targeting of MAP2 mRNAs in rat neurons Fragile X mental retardation protein is required for rapid experience-dependent regulation of the potassium channel Kv3.1b BC1 regulation of metabotropic glutamate receptor-mediated neuronal excitability.SINE RNA induces severe developmental defects in Arabidopsis thaliana and interacts with HYL1 (DRB1), a key member of the DCL1 complex.New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes.The function of activity-regulated genes in the nervous system.Functional characterization of the dendritically localized mRNA neuronatin in hippocampal neurons The pur protein family: genetic and structural features in development and disease.Increasing our understanding of human cognition through the study of Fragile X Syndrome.A presynaptic role for FMRP during protein synthesis-dependent long-term plasticity in Aplysia.The FMR1 gene and fragile X-associated tremor/ataxia syndrome.Human FMRP contains an integral tandem Agenet (Tudor) and KH motif in the amino terminal domain.The Aβ oligomer hypothesis for synapse failure and memory loss in Alzheimer's disease.A metabolomic and systems biology perspective on the brain of the fragile X syndrome mouse model Evidence for a fragile X mental retardation protein-mediated translational switch in metabotropic glutamate receptor-triggered Arc translation and long-term depression.Long non-coding RNAs: versatile master regulators of gene expression and crucial players in cancer.Translational control at the synapse: role of RNA regulators.Rapid translation of Arc/Arg3.1 selectively mediates mGluR-dependent LTD through persistent increases in AMPAR endocytosis rate.Cells lacking the fragile X mental retardation protein (FMRP) have normal RISC activity but exhibit altered stress granule assembly.BC1 RNA motifs required for dendritic transport in vivo.Translational control of long-lasting synaptic plasticity and memory.The state of synapses in fragile X syndrome.CYFIP family proteins between autism and intellectual disability: links with Fragile X syndrome.Spatially restricting gene expression by local translation at synapses Aβ oligomer-induced synapse degeneration in Alzheimer's disease.Dendritic protein synthesis in the normal and diseased brain.Fragile X mental retardation protein and synaptic plasticity Long non-coding RNAs in neurodevelopmental disorders.FMRP regulates miR196a-mediated repression of HOXB8 via interaction with the AGO2 MID domain.Fragile X mental retardation protein regulates the levels of scaffold proteins and glutamate receptors in postsynaptic densities Conformational-dependent and independent RNA binding to the fragile x mental retardation protein.Reply to Bagni: On BC1 RNA and the fragile X mental retardation protein.

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P2860

On BC1 RNA and the fragile X mental retardation protein.

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On BC1 RNA and the fragile X mental retardation protein.

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On BC1 RNA and the fragile X mental retardation protein.

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On BC1 RNA and the fragile X mental retardation protein.

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On BC1 RNA and the fragile X mental retardation protein.

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On BC1 RNA and the fragile X mental retardation protein.

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On BC1 RNA and the fragile X mental retardation protein.

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Proceedings of the National Academy of Sciences of the United States of America

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On BC1 RNA and the fragile X mental retardation protein.

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Barthélémy Tournier

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Edouard W Khandjian

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Henri Tiedge

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Janin Schütt

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Jürgen Brosius

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Natalia Dolzhanskaya

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Robert B Denman

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Stefan Kindler

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P2860

Characterization of Staufen 1 ribonucleoprotein complexes

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

Dendritic BC1 RNA in translational control mechanisms

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

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

CLIP: a method for identifying protein-RNA interaction sites in living cells

The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif.

Neuronal BC1 RNA structure: evolutionary conversion of a tRNA(Ala) domain into an extended stem-loop structure.

Fragile X related protein 1 isoforms differentially modulate the affinity of fragile X mental retardation protein for G-quartet RNA structure

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2

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105

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Anna Iacoangeli

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5665531

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