| P50 | author | Nancy M. Bonini | Q47503546 |
| | Michael R Akins | Q59683218 |
| P2093 | author name string | Robert Kalb | |
| | Fen-Biao Gao | |
| | Sandra Almeida | |
| | Alondra Schweizer Burguete | |
| P2860 | cites work | Identification of STAT5A and STAT5B target genes in human T cells | Q21132341 |
| | Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS | Q24297462 |
| | Multiple autism-linked genes mediate synapse elimination via proteasomal degradation of a synaptic scaffold PSD-95 | Q24306675 |
| | FMR1 Protein: Conserved RNP Family Domains and Selective RNA Binding | Q24311412 |
| | A novel role of CPEB3 in regulating EGFR gene transcription via association with Stat5b in neurons | Q24338958 |
| | RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention | Q24562489 |
| | Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS | Q24608159 |
| | FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism | Q24631425 |
| | Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS | Q24633692 |
| | A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD | Q24634583 |
| | A direct role for FMRP in activity-dependent dendritic mRNA transport links filopodial-spine morphogenesis to fragile X syndrome. | Q24644826 |
| | The unstable repeats--three evolving faces of neurological disease | Q27025923 |
| | Genome-wide screen for modifiers of ataxin-3 neurodegeneration in Drosophila | Q27314808 |
| | A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability | Q28116039 |
| | Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy | Q28257074 |
| | gurken and the I factor retrotransposon RNAs share common localization signals and machinery | Q28259364 |
| | A small predicted stem-loop structure mediates oocyte localization of Drosophila K10 mRNA | Q28274596 |
| | RNA toxicity is a component of ataxin-3 degeneration in Drosophila | Q28278448 |
| | Dysregulated metabotropic glutamate receptor-dependent translation of AMPA receptor and postsynaptic density-95 mRNAs at synapses in a mouse model of fragile X syndrome | Q28302665 |
| | CPEB3 and CPEB4 in neurons: analysis of RNA-binding specificity and translational control of AMPA receptor GluR2 mRNA | Q28507871 |
| | The FXG: a presynaptic fragile X granule expressed in a subset of developing brain circuits | Q28588310 |
| | The fragile X mental retardation protein-RNP granules show an mGluR-dependent localization in the post-synaptic spines | Q28588500 |
| | Trinucleotide Repeat Disorders | Q29038716 |
| | Localization of ASH1 mRNA particles in living yeast | Q29614818 |
| | Automatic and quantitative measurement of protein-protein colocalization in live cells. | Q29616276 |
| | The C9orf72 repeat expansion disrupts nucleocytoplasmic transport. | Q29871482 |
| | G-quadruplex RNA structure as a signal for neurite mRNA targeting | Q30502060 |
| | Modeling key pathological features of frontotemporal dementia with C9ORF72 repeat expansion in iPSC-derived human neurons | Q30543660 |
| | Tiling of the Drosophila epidermis by multidendritic sensory neurons. | Q45960946 |
| | Control of dendritic development by theDrosophila fragile X-relatedgene involves the small GTPase Rac1 | Q46237451 |
| | Different levels of the homeodomain protein cut regulate distinct dendrite branching patterns of Drosophila multidendritic neurons | Q46682237 |
| | Spatial control of branching within dendritic arbors by dynein-dependent transport of Rab5-endosomes | Q47070282 |
| | Protecting motor neurons from toxic insult by antagonism of adenosine A2a and Trk receptors. | Q48427578 |
| | A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study | Q48791547 |
| | Staufen protein associates with the 3'UTR of bicoid mRNA to form particles that move in a microtubule-dependent manner | Q49075903 |
| | Spatiotemporal expression of PSD-95 in Fmr1 knockout mice brain | Q51828032 |
| | m-TAG: a PCR-based genomic integration method to visualize the localization of specific endogenous mRNAs in vivo in yeast. | Q54469369 |
| | A census of human RNA-binding proteins | Q58283908 |
| | CUG repeats present in myotonin kinase RNA form metastable "slippery" hairpins | Q73919886 |
| | Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations | Q30573122 |
| | C9orf72 nucleotide repeat structures initiate molecular cascades of disease. | Q33715387 |
| | The fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95 | Q33717210 |
| | Recognition of the bcd mRNA localization signal in Drosophila embryos and ovaries | Q33823726 |
| | Drosophila Orb2 targets genes involved in neuronal growth, synapse formation, and protein turnover | Q33978069 |
| | The C9orf72 GGGGCC repeat is translated into aggregating dipeptide-repeat proteins in FTLD/ALS. | Q34326849 |
| | Expanded GGGGCC repeat RNA associated with amyotrophic lateral sclerosis and frontotemporal dementia causes neurodegeneration | Q34336948 |
| | The positional, structural, and sequence requirements of the Drosophila TLS RNA localization element | Q34366453 |
| | The central dogma decentralized: new perspectives on RNA function and local translation in neurons | Q34381996 |
| | Nuclear accumulation of mRNAs underlies G4C2-repeat-induced translational repression in a cellular model of C9orf72 ALS. | Q34467825 |
| | Non-ATG-initiated translation directed by microsatellite expansions | Q34471662 |
| | GGGGCC repeat expansion in C9orf72 compromises nucleocytoplasmic transport | Q34491033 |
| | RNA structure of trinucleotide repeats associated with human neurological diseases | Q34542108 |
| | mRNA localization: gene expression in the spatial dimension | Q34951203 |
| | Poly-dipeptides encoded by the C9orf72 repeats bind nucleoli, impede RNA biogenesis, and kill cells | Q35695216 |
| | Pur alpha binds to rCGG repeats and modulates repeat-mediated neurodegeneration in a Drosophila model of fragile X tremor/ataxia syndrome. | Q36014935 |
| | Differential Toxicity of Nuclear RNA Foci versus Dipeptide Repeat Proteins in a Drosophila Model of C9ORF72 FTD/ALS. | Q36108576 |
| | Fragile X mental retardation protein interactions with a G quadruplex structure in the 3'-untranslated region of NR2B mRNA | Q36275855 |
| | Neuronal RNA granules: movers and makers | Q36597037 |
| | Modulation of dendritic AMPA receptor mRNA trafficking by RNA splicing and editing. | Q36668729 |
| | The disease-associated r(GGGGCC)n repeat from the C9orf72 gene forms tract length-dependent uni- and multimolecular RNA G-quadruplex structures | Q36742244 |
| | RNA localization signals: deciphering the message with bioinformatics | Q36798894 |
| | A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats | Q36801066 |
| | C9orf72 repeat expansions cause neurodegeneration in Drosophila through arginine-rich proteins | Q37094833 |
| | RNA-mediated toxicity in neurodegenerative disease | Q37216891 |
| | Genetic modifiers of dFMR1 encode RNA granule components in Drosophila | Q37310268 |
| | Cellular toxicity of expanded RNA repeats: focus on RNA foci | Q37897768 |
| | Cytoplasmic RNA-binding proteins and the control of complex brain function | Q38020814 |
| | PolyQ disease: misfiring of a developmental cell death program? | Q38066311 |
| | TDP-43 pathology in polyglutamine diseases: with reference to amyotrphic lateral sclerosis | Q38124396 |
| | Combating neurodegenerative disease with chemical probes and model systems | Q38261089 |
| | C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms RNA G-quadruplexes | Q42424866 |
| | Modifiers of C9orf72 dipeptide repeat toxicity connect nucleocytoplasmic transport defects to FTD/ALS. | Q42925023 |
| | RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTAS. | Q42975231 |
| | Egalitarian is a selective RNA-binding protein linking mRNA localization signals to the dynein motor | Q43102909 |
| | Molecular architecture of CAG repeats in human disease related transcripts | Q45293998 |
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | microsatellite | Q265193 |
| P304 | page(s) | e08881 | |
| P577 | publication date | 2015-12-09 | |
| P1433 | published in | eLife | Q2000008 |
| P1476 | title | GGGGCC microsatellite RNA is neuritically localized, induces branching defects, and perturbs transport granule function | |
| P478 | volume | 4 | |