Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein - Wikidata - wikimedia - TriplyDB

Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein

Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein

http://www.wikidata.org/entity/Q33605779

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Kep1 interacts genetically with dredd/caspase-8, and kep1 mutants alter the balance of dredd isoforms The Presynaptic Microtubule Cytoskeleton in Physiological and Pathological Conditions: Lessons from Drosophila Fragile X Syndrome and Hereditary Spastic Paraplegias Modeling congenital disease and inborn errors of development in Drosophila melanogaster Learning and behavioral deficits associated with the absence of the fragile X mental retardation protein: what a fly and mouse model can teach us.From Learning to Memory: What Flies Can Tell Us about Intellectual Disability Treatment Regulatory BC1 RNA and the fragile X mental retardation protein: convergent functionality in brain Elevated levels of the vesicular monoamine transporter and a novel repetitive behavior in the Drosophila model of fragile X syndrome Motility screen identifies Drosophila IGF-II mRNA-binding protein--zipcode-binding protein acting in oogenesis and synaptogenesis Characterization of fragile X mental retardation protein recruitment and dynamics in Drosophila stress granules The RNA-binding proteins FMR1, rasputin and caprin act together with the UBA protein lingerer to restrict tissue growth in Drosophila melanogaster Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells Fragile X mental retardation protein: A paradigm for translational control by RNA-binding proteins Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures The fragile X gene and its function Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway RNA and microRNAs in fragile X mental retardation The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif.Nuclear translocation controlled by alternatively spliced isoforms inactivates the QUAKING apoptotic inducer Rasputin functions as a positive regulator of orb in Drosophila oogenesis Expression of fragile X mental retardation protein within the vocal control system of developing and adult male zebra finches The fragile X mental retardation 1 gene (FMR1): historical perspective, phenotypes, mechanism, pathology, and epidemiology Progress toward therapeutic potential for AFQ056 in Fragile X syndrome.From FMRP function to potential therapies for fragile X syndrome.Fragile X mental retardation protein controls trailer hitch expression and cleavage furrow formation in Drosophila embryos Testing candidate genes for attention-deficit/hyperactivity disorder in fruit flies using a high throughput assay for complex behavior Transport of Drosophila fragile X mental retardation protein-containing ribonucleoprotein granules by kinesin-1 and cytoplasmic dynein.Novel RNA-binding properties of the MTG chromatin regulatory proteins.The zinc finger protein Zn72D and DEAD box helicase Belle interact and control maleless mRNA and protein levels Argonaute2 suppresses Drosophila fragile X expression preventing neurogenesis and oogenesis defects.Genome analysis: RNA recognition motif (RRM) and K homology (KH) domain RNA-binding proteins from the flowering plant Arabidopsis thaliana.Fragile X mental retardation protein regulates translation by binding directly to the ribosome The fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95.Four decades of leading-edge research in the reproductive and developmental sciences: the Infant Primate Research Laboratory at the University of Washington National Primate Research Center.dFmr1 Plays Roles in Small RNA Pathways of Drosophila melanogaster.Disruption of the MAP1B-related protein FUTSCH leads to changes in the neuronal cytoskeleton, axonal transport defects, and progressive neurodegeneration in Drosophila Lithium: a promising treatment for fragile X syndrome.Age-dependent cognitive impairment in a Drosophila fragile X model and its pharmacological rescue Short- and long-term memory are modulated by multiple isoforms of the fragile X mental retardation protein Fragile X protein controls neural stem cell proliferation in the Drosophila brain.A feed-forward mechanism involving Drosophila fragile X mental retardation protein triggers a replication stress-induced DNA damage response

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P2860

Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein

http://www.wikidata.org/entity/Q33605779

description

2000 nî lūn-bûn

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2000 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

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2000 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2000年の論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年論文

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2000年论文

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Characterization of dFMR1, a D ...... e X mental retardation protein

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Characterization of dFMR1, a D ...... e X mental retardation protein

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Characterization of dFMR1, a D ...... e X mental retardation protein

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Characterization of dFMR1, a D ...... e X mental retardation protein

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Characterization of dFMR1, a D ...... e X mental retardation protein

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Characterization of dFMR1, a D ...... e X mental retardation protein

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MCB.20.22.8536-8547.2000

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Molecular and Cellular Biology

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Characterization of dFMR1, a D ...... e X mental retardation protein

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Dockendorff TC

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Dreyfuss G

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Jongens TA

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Wan L

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P2860

Primary structure and binding activity of the hnRNP U protein: binding RNA through RGG box

The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2

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

FXR1, an autosomal homolog of the fragile X mental retardation gene

Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis

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

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

Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

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

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10.1128/MCB.20.22.8536-8547.2000

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12278645

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11046149

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Drosophila melanogaster

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102159

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