hnRNP C promotes APP translation by competing with FMRP for APP mRNA recruitment to P bodies - Wikidata - wikimedia - TriplyDB

hnRNP C promotes APP translation by competing with FMRP for APP mRNA recruitment to P bodies

hnRNP C promotes APP translation by competing with FMRP for APP mRNA recruitment to P bodies

http://www.wikidata.org/entity/Q34013644

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Competitive regulation of nucleolin expression by HuR and miR-494 The hnRNP family: insights into their role in health and disease RNA Secondary Structure Modulates FMRP's Bi-Functional Role in the MicroRNA Pathway Alzheimer-related decrease in CYFIP2 links amyloid production to tau hyperphosphorylation and memory loss.Nucleocytoplasmic shuttling of Ssd1 defines the destiny of its bound mRNAs PAK in Alzheimer disease, Huntington disease and X-linked mental retardation Hormone response element binding proteins: novel regulators of vitamin D and estrogen signaling Novel RNA- and FMRP-binding protein TRF2-S regulates axonal mRNA transport and presynaptic plasticity Overexpression of hnRNPC2 induces multinucleation by repression of Aurora B in hepatocellular carcinoma cells Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics RNA-Binding Protein AUF1 Promotes Myogenesis by Regulating MEF2C Expression Levels HuD regulates coding and noncoding RNA to induce APP→Aβ processing.Activation of TRPML1 clears intraneuronal Aβ in preclinical models of HIV infection.miR-503 represses CUG-binding protein 1 translation by recruiting CUGBP1 mRNA to processing bodies.HnRNP C, YB-1 and hnRNP L coordinately enhance skipping of human MUSK exon 10 to generate a Wnt-insensitive MuSK isoform.RNA-binding protein HuR promotes growth of small intestinal mucosa by activating the Wnt signaling pathway.Fragile X mental retardation protein expression in Alzheimer's disease Post-transcriptional regulation of amyloid precursor protein by microRNAs and RNA binding proteins.Modulation of amyloid precursor protein expression reduces β-amyloid deposition in a mouse model.Impact of acamprosate on plasma amyloid-β precursor protein in youth: a pilot analysis in fragile X syndrome-associated and idiopathic autism spectrum disorder suggests a pharmacodynamic protein marker.miR-27 regulates mitochondrial networks by directly targeting the mitochondrial fission factor.Fragile X mental retardation protein: from autism to neurodegenerative disease.Coding region: the neglected post-transcriptional code.Regulation of cyclin-dependent kinase 4 translation through CUG-binding protein 1 and microRNA-222 by polyamines Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum Disorders Glycogen synthase kinase-3: a promising therapeutic target for fragile x syndrome High-Throughput Screening to Identify Compounds That Increase Fragile X Mental Retardation Protein Expression in Neural Stem Cells Differentiated From Fragile X Syndrome Patient-Derived Induced Pluripotent Stem Cells.Amyloid Precursor Protein Translation Is Regulated by a 3'UTR Guanine Quadruplex Heterogeneous Nuclear Ribonucleoprotein C Proteins Interact with the Human Papillomavirus Type 16 (HPV16) Early 3'-Untranslated Region and Alleviate Suppression of HPV16 Late L1 mRNA Splicing.Neurodegeneration-associated TDP-43 interacts with fragile X mental retardation protein (FMRP)/Staufen (STAU1) and regulates SIRT1 expression in neuronal cells.The regulation of AβPP expression by RNA-binding proteins FMRP Associates with Cytoplasmic Granules at the Onset of Meiosis in the Human Oocyte.RNA imaging in living cells - methods and applications.Heterogeneous nuclear ribonucleoprotein C1/C2 controls the metastatic potential of glioblastoma by regulating PDCD4.Genome-wide approaches to dissect the roles of RNA binding proteins in translational control: implications for neurological diseases Heterogeneous nuclear ribonucleoprotein A1 post-transcriptionally regulates Drp1 expression in neuroblastoma cells The essential polysome-associated RNA-binding protein RBP42 targets mRNAs involved in Trypanosoma brucei energy metabolism.MS2-TRAP (MS2-tagged RNA affinity purification): tagging RNA to identify associated miRNAs.The tRNA methyltransferase NSun2 stabilizes p16INK⁴ mRNA by methylating the 3'-untranslated region of p16 LincRNA-p21 suppresses target mRNA translation

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P2860

hnRNP C promotes APP translation by competing with FMRP for APP mRNA recruitment to P bodies

http://www.wikidata.org/entity/Q34013644

description

2010 nî lūn-bûn

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2010 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2010 թվականի մայիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年學術文章

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name

hnRNP C promotes APP translati ...... P mRNA recruitment to P bodies

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hnRNP C promotes APP translati ...... P mRNA recruitment to P bodies

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hnRNP C promotes APP translati ...... P mRNA recruitment to P bodies

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Nature Structural & Molecular Biology

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hnRNP C promotes APP translati ...... P mRNA recruitment to P bodies

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Eun Kyung Lee

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Hyeon Ho Kim

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

Jennifer L Martindale

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Marc Gleichmann

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Mohamed R Mughal

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

Paul F Worley

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

Sarah S Subaran

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

Subramanya Srikantan

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

Xiaoling Yang

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

Yuki Kuwano

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

P2860

Translation repression in human cells by microRNA-induced gene silencing requires RCK/p54

Phosphorylation of HuR by Chk2 regulates SIRT1 expression

A 57-nucleotide upstream early polyadenylation element in human papillomavirus type 16 interacts with hFip1, CstF-64, hnRNP C1/C2, and polypyrimidine tract binding protein.

The human LSm1-7 proteins colocalize with the mRNA-degrading enzymes Dcp1/2 and Xrnl in distinct cytoplasmic foci.

Human Dcp2: a catalytically active mRNA decapping enzyme located in specific cytoplasmic structures

Cytoplasmic foci are sites of mRNA decay in human cells

The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics

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

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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scholarly article

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10.1038/NSMB.1815

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6

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17

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Kotb Abdelmohsen

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2010-05-16T00:00:00Z

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44602494

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