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FMRP binding to a ranked subset of long genes is revealed by coupled CLIP and TRAP in specific neuronal cell types
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inferredcites →https://doi.org/10.1002/(sici)1097-4547(19980101)51:1<41::aid-jnr4>3.0.co;2-lopenalex-snapshot
Overexpression of fragile X gene (FMR-1) transcripts increases cAMP production in neural cells.
inferredcites →https://doi.org/10.1002/ajmg.1320450120openalex-snapshot
Demonstration of abnormal cyclic AMP production in platelets from patients with fragile X syndrome
inferredcites →https://doi.org/10.1002/ajmg.a.36034openalex-snapshot
Duplication of the Xq27.3–q28 region, including the FMR1 gene, in an X‐linked hypogonadism, gynecomastia, intellectual disability, short stature, and obesity syndrome
inferredcites →https://doi.org/10.1002/ajmg.b.30765openalex-snapshot
Early‐phase ERK activation as a biomarker for metabolic status in fragile X syndrome
inferredcites →https://doi.org/10.1002/ana.21243openalex-snapshot
Neuroanatomy of fragile X syndrome is associated with aberrant behavior and the fragile X mental retardation protein (FMRP)
inferredcites →https://doi.org/10.1002/ana.410310105openalex-snapshot
Cyclic AMP metabolism in fragile X syndrome
inferredcites →https://doi.org/10.1002/bies.20298openalex-snapshot
The InsP3 receptor: its role in neuronal physiology and neurodegeneration
inferredcites →https://doi.org/10.1002/cne.24100openalex-snapshot
Cellular distribution of the fragile X mental retardation protein in the mouse brain
inferredcites →https://doi.org/10.1002/dneu.22574openalex-snapshot
New frontiers in RNA transport and local translation in neurons
inferredcites →https://doi.org/10.1002/j.1460-2075.1995.tb00220.xopenalex-snapshot
The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2.
inferredcites →https://doi.org/10.1002/mrdd.20004openalex-snapshot
The neuroanatomy and neuroendocrinology of fragile X syndrome
inferredcites →https://doi.org/10.1002/mus.21467openalex-snapshot
Enhanced homosynaptic LTD in cerebellar Purkinje cells of the dystrophic MDX mouse
inferredcites →https://doi.org/10.1007/978-1-4939-0512-6_2openalex-snapshot
Analysis of Next-Generation Sequencing Data Using Galaxy
inferredcites →https://doi.org/10.1007/978-1-4939-7213-5_5openalex-snapshot
Axon-TRAP-RiboTag: Affinity Purification of Translated mRNAs from Neuronal Axons in Mouse In Vivo
inferredcites →https://doi.org/10.1007/bf00582832openalex-snapshot
Review: The fragile X syndrome: Isolation of the FMR-1 gene and characterization of the fragile X mutation
inferredcites →https://doi.org/10.1007/bf02172283openalex-snapshot
Abnormal classical eye-blink conditioning in autism
inferredcites →https://doi.org/10.1007/bf02265272openalex-snapshot
Expression and regulation of the dystrophin Purkinje promoter in human skeletal muscle, heart, and brain
inferredcites →https://doi.org/10.1007/s00221-009-1965-4openalex-snapshot
Synaptic plasticity in the adult visual cortex is regulated by the metabotropic glutamate receptor, mGLUR5
inferredcites →https://doi.org/10.1007/s00441-006-0244-yopenalex-snapshot
Molecular organization of the presynaptic active zone
inferredcites →https://doi.org/10.1007/s10048-012-0340-yopenalex-snapshot
Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive function
inferredcites →https://doi.org/10.1007/s10571-017-0510-4openalex-snapshot
BDNF: A Key Factor with Multipotent Impact on Brain Signaling and Synaptic Plasticity
inferredcites →https://doi.org/10.1007/s12311-011-0342-6openalex-snapshot
Estradiol Promotes Purkinje Dendritic Growth, Spinogenesis, and Synaptogenesis During Neonatal Life by Inducing the Expression of BDNF
inferredcites →https://doi.org/10.1016/0022-2836(88)90482-2openalex-snapshot
Selection of DNA binding sites by regulatory proteins
inferredcites →https://doi.org/10.1016/0092-8674(91)90125-iopenalex-snapshot
Absence of expression of the FMR-1 gene in fragile X syndrome
inferredcites →https://doi.org/10.1016/0092-8674(93)90420-uopenalex-snapshot
The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein
inferredcites →https://doi.org/10.1016/0092-8674(94)90205-4openalex-snapshot
Deficient cerebellar long-term depression and impaired motor learning in mGluR1 mutant mice
inferredcites →https://doi.org/10.1016/0092-8674(94)90569-xopenalex-snapshot
Fmr1 knockout mice: A model to study fragile X mental retardation
inferredcites →https://doi.org/10.1016/0968-0004(88)90085-0openalex-snapshot
Selection of DNA binding sites by regulatory proteins
inferredcites →https://doi.org/10.1016/b978-0-444-63356-9.00001-7openalex-snapshot
Long-Term Depression as a Model of Cerebellar Plasticity
inferredcites →https://doi.org/10.1016/bs.vh.2016.10.004openalex-snapshot
BDNF and Hippocampal Synaptic Plasticity
inferredcites →https://doi.org/10.1016/j.ajhg.2008.06.003openalex-snapshot
Fragile X-Related Proteins Regulate Mammalian Circadian Behavioral Rhythms
inferredcites →https://doi.org/10.1016/j.ajhg.2013.09.013openalex-snapshot
The Roles of FMRP-Regulated Genes in Autism Spectrum Disorder: Single- and Multiple-Hit Genetic Etiologies
inferredcites →https://doi.org/10.1016/j.biopsych.2012.09.017openalex-snapshot
Lifting the Mood on Treating Fragile X
inferredcites →https://doi.org/10.1016/j.brainres.2014.10.019openalex-snapshot
Regulation of hippocampal synaptic plasticity by BDNF
inferredcites →https://doi.org/10.1016/j.ceca.2005.01.014openalex-snapshot
Determinants of postsynaptic Ca2+ signaling in Purkinje neurons
inferredcites →https://doi.org/10.1016/j.cell.2004.10.004openalex-snapshot
Ankyrin-Based Subcellular Gradient of Neurofascin, an Immunoglobulin Family Protein, Directs GABAergic Innervation at Purkinje Axon Initial Segment
inferredcites →https://doi.org/10.1016/j.cell.2008.10.028openalex-snapshot
A Translational Profiling Approach for the Molecular Characterization of CNS Cell Types
inferredcites →https://doi.org/10.1016/j.cell.2008.10.029openalex-snapshot
Application of a Translational Profiling Approach for the Comparative Analysis of CNS Cell Types
inferredcites →https://doi.org/10.1016/j.cell.2008.10.031openalex-snapshot
Unlocking CNS Cell Type Heterogeneity
inferredcites →https://doi.org/10.1016/j.cell.2011.06.013openalex-snapshot
FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism
inferredcites →https://doi.org/10.1016/j.cell.2011.10.002openalex-snapshot
Ribosome Profiling of Mouse Embryonic Stem Cells Reveals the Complexity and Dynamics of Mammalian Proteomes
inferredcites →https://doi.org/10.1016/j.cell.2013.10.031openalex-snapshot
Integrative Functional Genomic Analyses Implicate Specific Molecular Pathways and Circuits in Autism
inferredcites →https://doi.org/10.1016/j.cell.2014.03.040openalex-snapshot
A Chromatin-Dependent Role of the Fragile X Mental Retardation Protein FMRP in the DNA Damage Response
inferredcites →https://doi.org/10.1016/j.cell.2015.12.039openalex-snapshot
Long Neural Genes Harbor Recurrent DNA Break Clusters in Neural Stem/Progenitor Cells
inferredcites →https://doi.org/10.1016/j.cell.2016.08.071openalex-snapshot
Mutations in Human Accelerated Regions Disrupt Cognition and Social Behavior
inferredcites →https://doi.org/10.1016/j.cell.2018.05.021openalex-snapshot
Phenotypic Convergence: Distinct Transcription Factors Regulate Common Terminal Features
inferredcites →https://doi.org/10.1016/j.celrep.2014.02.005openalex-snapshot
HITS-CLIP and Integrative Modeling Define the Rbfox Splicing-Regulatory Network Linked to Brain Development and Autism
inferredcites →https://doi.org/10.1016/j.conb.2009.03.003openalex-snapshot
Assembling the presynaptic active zone
inferredcites →https://doi.org/10.1016/j.conb.2009.03.011openalex-snapshot
Protein translation in synaptic plasticity: mGluR-LTD, Fragile X
inferredcites →https://doi.org/10.1016/j.conb.2018.02.025openalex-snapshot
Molecular control of local translation in axon development and maintenance
inferredcites →https://doi.org/10.1016/j.conb.2019.02.008openalex-snapshot
Local translation in neuronal processes
inferredcites →https://doi.org/10.1016/j.copbio.2019.03.001openalex-snapshot
Beyond bulk: a review of single cell transcriptomics methodologies and applications
inferredcites →https://doi.org/10.1016/j.gdata.2016.12.005openalex-snapshot
Topoisomerase I inhibition leads to length-dependent gene expression changes in human primary astrocytes
inferredcites →https://doi.org/10.1016/j.mcn.2006.02.001openalex-snapshot
Local functions for FMRP in axon growth cone motility and activity-dependent regulation of filopodia and spine synapses
inferredcites →https://doi.org/10.1016/j.molcel.2014.01.011openalex-snapshot
Arginine Methylation Facilitates the Recruitment of TOP3B to Chromatin to Prevent R Loop Accumulation
inferredcites →https://doi.org/10.1016/j.molcel.2014.03.023openalex-snapshot
Fragile X Mental Retardation Protein Regulates Translation by Binding Directly to the Ribosome
inferredcites →https://doi.org/10.1016/j.molmed.2017.04.006openalex-snapshot
Single-Cell RNA Sequencing: Unraveling the Brain One Cell at a Time
inferredcites →https://doi.org/10.1016/j.nbd.2005.08.019openalex-snapshot
The generation of a conditional Fmr1 knock out mouse model to study Fmrp function in vivo
inferredcites →https://doi.org/10.1016/j.neubiorev.2015.01.023openalex-snapshot
A possible role of dystrophin in neuronal excitability: A review of the current literature
inferredcites →https://doi.org/10.1016/j.neuron.2005.07.005openalex-snapshot
Deletion of FMR1 in Purkinje Cells Enhances Parallel Fiber LTD, Enlarges Spines, and Attenuates Cerebellar Eyelid Conditioning in Fragile X Syndrome
inferredcites →https://doi.org/10.1016/j.neuron.2006.07.005openalex-snapshot
Dynamic Translational and Proteasomal Regulation of Fragile X Mental Retardation Protein Controls mGluR-Dependent Long-Term Depression
inferredcites →https://doi.org/10.1016/j.neuron.2007.12.001openalex-snapshot
Correction of Fragile X Syndrome in Mice
inferredcites →https://doi.org/10.1016/j.neuron.2008.10.004openalex-snapshot
Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
inferredcites →https://doi.org/10.1016/j.neuron.2008.10.055openalex-snapshot
Translational Control of Long-Lasting Synaptic Plasticity and Memory
inferredcites →https://doi.org/10.1016/j.neuron.2010.01.016openalex-snapshot
Group 1 mGluR-Dependent Synaptic Long-Term Depression: Mechanisms and Implications for Circuitry and Disease
inferredcites →https://doi.org/10.1016/j.neuron.2010.01.024openalex-snapshot
Critical Period Plasticity Is Disrupted in the Barrel Cortex of Fmr1 Knockout Mice
inferredcites →https://doi.org/10.1016/j.neuron.2010.11.010openalex-snapshot
Mechanism of ER Stress-Induced Brain Damage by IP3 Receptor
inferredcites →https://doi.org/10.1016/j.neuron.2012.01.034openalex-snapshot
Lovastatin Corrects Excess Protein Synthesis and Prevents Epileptogenesis in a Mouse Model of Fragile X Syndrome
inferredcites →https://doi.org/10.1016/j.neuron.2012.03.009openalex-snapshot
Chronic Pharmacological mGlu5 Inhibition Corrects Fragile X in Adult Mice
inferredcites →https://doi.org/10.1016/j.neuron.2012.04.009openalex-snapshot
De Novo Gene Disruptions in Children on the Autistic Spectrum
inferredcites →https://doi.org/10.1016/j.neuron.2012.06.012openalex-snapshot
The Presynaptic Active Zone
inferredcites →https://doi.org/10.1016/j.neuron.2014.07.016openalex-snapshot
The Cerebellum, Sensitive Periods, and Autism
inferredcites →https://doi.org/10.1016/j.neuron.2014.11.016openalex-snapshot
Fmr1 KO and Fenobam Treatment Differentially Impact Distinct Synapse Populations of Mouse Neocortex
inferredcites →https://doi.org/10.1016/j.neuron.2015.03.059openalex-snapshot
Gene Length Matters in Neurons
inferredcites →https://doi.org/10.1016/j.neuron.2017.08.024openalex-snapshot
cTag-PAPERCLIP Reveals Alternative Polyadenylation Promotes Cell-Type Specific Protein Diversity and Shifts Araf Isoforms with Microglia Activation
inferredcites →https://doi.org/10.1016/j.neuron.2018.08.004openalex-snapshot
Presynaptic Biogenesis Requires Axonal Transport of Lysosome-Related Vesicles
inferredcites →https://doi.org/10.1016/j.neuron.2018.12.006openalex-snapshot
Developmental Heterogeneity of Microglia and Brain Myeloid Cells Revealed by Deep Single-Cell RNA Sequencing
inferredcites →https://doi.org/10.1016/j.neuron.2018.12.019openalex-snapshot
Differential NOVA2-Mediated Splicing in Excitatory and Inhibitory Neurons Regulates Cortical Development and Cerebellar Function
inferredcites →https://doi.org/10.1016/j.neuron.2019.06.022openalex-snapshot
How mRNA Localization and Protein Synthesis Sites Influence Dendritic Protein Distribution and Dynamics
inferredcites →https://doi.org/10.1016/j.neuropharm.2013.05.018openalex-snapshot
BDNF in fragile X syndrome
inferredcites →https://doi.org/10.1016/j.neuroscience.2010.08.012openalex-snapshot
Membrane estrogen receptors activate the metabotropic glutamate receptors mGluR5 and mGluR3 to bidirectionally regulate CREB phosphorylation in female rat striatal neurons
inferredcites →https://doi.org/10.1016/j.neuroscience.2013.06.007openalex-snapshot
Children with autism spectrum disorders show abnormal conditioned response timing on delay, but not trace, eyeblink conditioning
inferredcites →https://doi.org/10.1016/j.tins.2005.07.003openalex-snapshot
Activity-dependent modulation of the BDNF receptor TrkB: mechanisms and implications
inferredcites →https://doi.org/10.1016/j.tins.2006.02.001openalex-snapshot
The fragile X–cerebellum connection
inferredcites →https://doi.org/10.1016/j.tins.2010.01.005openalex-snapshot
Spatially restricting gene expression by local translation at synapses
inferredcites →https://doi.org/10.1016/j.yfrne.2014.08.001openalex-snapshot
Molecular signature of rapid estrogen regulation of synaptic connectivity and cognition
inferredcites →https://doi.org/10.1016/j.yhbeh.2015.05.001openalex-snapshot
Molecular mechanisms underlying the memory-enhancing effects of estradiol
inferredcites →https://doi.org/10.1016/j.yhbeh.2015.05.024openalex-snapshot
Hippocampal learning, memory, and neurogenesis: Effects of sex and estrogens across the lifespan in adults
inferredcites →https://doi.org/10.1016/j.ymeth.2005.07.018openalex-snapshot
CLIP: A method for identifying protein–RNA interaction sites in living cells
inferredcites →https://doi.org/10.1016/s0021-9258(19)84994-3openalex-snapshot
Facilitated Target Location in Biological Systems
inferredcites →https://doi.org/10.1016/s0092-8674(02)00617-7openalex-snapshot
Integrating mRNA Processing with Transcription
inferredcites →https://doi.org/10.1016/s0166-2236(99)01510-6openalex-snapshot
The neurobiology of Duchenne muscular dystrophy: learning lessons from muscle?
inferredcites →https://doi.org/10.1016/s0896-6273(00)00099-4openalex-snapshot
Local Calcium Release in Dendritic Spines Required for Long-Term Synaptic Depression
inferredcites →https://doi.org/10.1016/s0896-6273(00)80079-3openalex-snapshot
Strong Activation of Parallel Fibers Produces Localized Calcium Transients and a Form of LTD That Spreads to Distant Synapses
inferredcites →https://doi.org/10.1016/s0896-6273(00)80180-4openalex-snapshot
A Protein Synthesis–Dependent Late Phase of Cerebellar Long-Term Depression
inferredcites →https://doi.org/10.1016/s0959-4388(00)00154-9openalex-snapshot
Mechanisms of cerebellar learning suggested by eyelid conditioning
inferredcites →https://doi.org/10.1016/s1097-2765(00)80012-xopenalex-snapshot
FMRP Associates with Polyribosomes as an mRNP, and the I304N Mutation of Severe Fragile X Syndrome Abolishes This Association
inferredcites →https://doi.org/10.1021/bi034909gopenalex-snapshot
The N-Terminus of the Fragile X Mental Retardation Protein Contains a Novel Domain Involved in Dimerization and RNA Binding
inferredcites →https://doi.org/10.1038/348725a0openalex-snapshot
Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons
inferredcites →https://doi.org/10.1038/ejhg.2009.159openalex-snapshot
Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition
inferredcites →https://doi.org/10.1038/ejhg.2012.78openalex-snapshot
De novo microduplication of the FMR1 gene in a patient with developmental delay, epilepsy and hyperactivity
inferredcites →https://doi.org/10.1038/ejhg.2013.311openalex-snapshot
Fragile X syndrome due to a missense mutation
inferredcites →https://doi.org/10.1038/nature02033openalex-snapshot
A gene expression atlas of the central nervous system based on bacterial artificial chromosomes
inferredcites →https://doi.org/10.1038/nature07488openalex-snapshot
HITS-CLIP yields genome-wide insights into brain alternative RNA processing
inferredcites →https://doi.org/10.1038/nature10726openalex-snapshot
Topoisomerase inhibitors unsilence the dormant allele of Ube3a in neurons
inferredcites →https://doi.org/10.1038/nature11011openalex-snapshot
Patterns and rates of exonic de novo mutations in autism spectrum disorders
inferredcites →https://doi.org/10.1038/nature11310openalex-snapshot
Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice
inferredcites →https://doi.org/10.1038/nature11737openalex-snapshot
FMRP targets distinct mRNA sequence elements to regulate protein expression
inferredcites →https://doi.org/10.1038/nature12504openalex-snapshot
Topoisomerases facilitate transcription of long genes linked to autism
inferredcites →https://doi.org/10.1038/nature12975openalex-snapshot
A polygenic burden of rare disruptive mutations in schizophrenia
inferredcites →https://doi.org/10.1038/nature13169openalex-snapshot
Scalable control of mounting and attack by Esr1+ neurons in the ventromedial hypothalamus
inferredcites →https://doi.org/10.1038/nature13772openalex-snapshot
Synaptic, transcriptional and chromatin genes disrupted in autism
inferredcites →https://doi.org/10.1038/nature14319openalex-snapshot
Disruption of DNA-methylation-dependent long gene repression in Rett syndrome
inferredcites →https://doi.org/10.1038/nbt.3343openalex-snapshot
Affinity regression predicts the recognition code of nucleic acid–binding proteins
inferredcites →https://doi.org/10.1038/ncb2132openalex-snapshot
Myosin-Va transports the endoplasmic reticulum into the dendritic spines of Purkinje neurons
inferredcites →https://doi.org/10.1038/ncomms13316openalex-snapshot
De novo genic mutations among a Chinese autism spectrum disorder cohort
inferredcites →https://doi.org/10.1038/ncomms6586openalex-snapshot
Cerebellar plasticity and motor learning deficits in a copy-number variation mouse model of autism
inferredcites →https://doi.org/10.1038/ng0193-31openalex-snapshot
A point mutation in the FMR-1 gene associated with fragile X mental retardation
inferredcites →https://doi.org/10.1038/ng0196-91openalex-snapshot
The fragile X mental retardation protein is associated with ribosomes
inferredcites →https://doi.org/10.1038/nn.3479openalex-snapshot
Top3β is an RNA topoisomerase that works with fragile X syndrome protein to promote synapse formation
inferredcites →https://doi.org/10.1038/nn.3484openalex-snapshot
Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders
inferredcites →https://doi.org/10.1038/nn.4589openalex-snapshot
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
inferredcites →https://doi.org/10.1038/nn1618openalex-snapshot
Molecular taxonomy of major neuronal classes in the adult mouse forebrain
inferredcites →https://doi.org/10.1038/npp.2017.177openalex-snapshot
Effect of the mGluR5-NAM Basimglurant on Behavior in Adolescents and Adults with Fragile X Syndrome in a Randomized, Double-Blind, Placebo-Controlled Trial: FragXis Phase 2 Results
inferredcites →https://doi.org/10.1038/nrd.2017.221openalex-snapshot
Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome
inferredcites →https://doi.org/10.1038/nrm2774openalex-snapshot
Kinesin superfamily motor proteins and intracellular transport
inferredcites →https://doi.org/10.1038/nrn.2016.101openalex-snapshot
Topoisomerases and the regulation of neural function
inferredcites →https://doi.org/10.1038/nsmb.1666openalex-snapshot
Rates of in situ transcription and splicing in large human genes
inferredcites →https://doi.org/10.1038/nsmb.1838openalex-snapshot
iCLIP reveals the function of hnRNP particles in splicing at individual nucleotide resolution
inferredcites →https://doi.org/10.1038/nsmb1280openalex-snapshot
In vivo dynamics of RNA polymerase II transcription
inferredcites →https://doi.org/10.1038/s41467-018-07101-4openalex-snapshot
Topoisomerase 3β interacts with RNAi machinery to promote heterochromatin formation and transcriptional silencing in Drosophila
inferredcites →https://doi.org/10.1038/s41583-019-0152-2openalex-snapshot
Emerging connections between cerebellar development, behaviour and complex brain disorders
inferredcites →https://doi.org/10.1038/s41594-019-0263-5openalex-snapshot
Local translation in neurons: visualization and function
inferredcites →https://doi.org/10.1038/s41598-017-00250-4openalex-snapshot
Length-dependent gene misexpression is associated with Alzheimer’s disease progression
inferredcites →https://doi.org/10.1038/s41598-017-12981-5openalex-snapshot
Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy
inferredcites →https://doi.org/10.1038/tp.2015.123openalex-snapshot
Shared functional defect in IP3R-mediated calcium signaling in diverse monogenic autism syndromes
inferredcites →https://doi.org/10.1042/bj20030110openalex-snapshot
Carbonic anhydrase-related protein is a novel binding protein for inositol 1,4,5-trisphosphate receptor type 1
inferredcites →https://doi.org/10.1046/j.0953-816x.2001.01570.xopenalex-snapshot
Deficient long‐term synaptic depression in the rostral cerebellum correlated with impaired motor learning in phospholipase C β4 mutant mice
inferredcites →https://doi.org/10.1046/j.1460-9568.2002.02407.xopenalex-snapshot
mGluR1 in cerebellar Purkinje cells is required for normal association of temporally contiguous stimuli in classical conditioning
inferredcites →https://doi.org/10.1073/pnas.0405398101openalex-snapshot
Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles
inferredcites →https://doi.org/10.1073/pnas.0504684102openalex-snapshot
Hzf protein regulates dendritic localization and BDNF-induced translation of type 1 inositol 1,4,5-trisphosphate receptor mRNA
inferredcites →https://doi.org/10.1073/pnas.0509723103openalex-snapshot
A base-excision DNA-repair protein finds intrahelical lesion bases by fast sliding in contact with DNA
inferredcites →https://doi.org/10.1073/pnas.0707054104openalex-snapshot
Essential role of Epac2/Rap1 signaling in regulation of insulin granule dynamics by cAMP
inferredcites →https://doi.org/10.1073/pnas.0907143106openalex-snapshot
Cell-type-specific isolation of ribosome-associated mRNA from complex tissues
inferredcites →https://doi.org/10.1073/pnas.1002262107openalex-snapshot
Characterization and reversal of synaptic defects in the amygdala in a mouse model of fragile X syndrome
inferredcites →https://doi.org/10.1073/pnas.1012496107openalex-snapshot
Dendritic spine instability and insensitivity to modulation by sensory experience in a mouse model of fragile X syndrome
inferredcites →https://doi.org/10.1073/pnas.1013855108openalex-snapshot
Cognitive dysfunction and prefrontal synaptic abnormalities in a mouse model of fragile X syndrome
inferredcites →https://doi.org/10.1073/pnas.122205699openalex-snapshot
Altered synaptic plasticity in a mouse model of fragile X mental retardation
inferredcites →https://doi.org/10.1073/pnas.1307747110openalex-snapshot
Reactivation of stalled polyribosomes in synaptic plasticity
inferredcites →https://doi.org/10.1073/pnas.1413204111openalex-snapshot
Topoisomerase 1 inhibition reversibly impairs synaptic function
inferredcites →https://doi.org/10.1073/pnas.1817562115openalex-snapshot
“Fragile” equilibrium between translation and transcription
inferredcites →https://doi.org/10.1073/pnas.83.6.1608openalex-snapshot
On the specificity of DNA-protein interactions.
inferredcites →https://doi.org/10.1074/jbc.m210146200openalex-snapshot
Piccolo, a Ca2+ Sensor in Pancreatic β-Cells
inferredcites →https://doi.org/10.1074/jbc.m602044200openalex-snapshot
Characterization of the δ2 Glutamate Receptor-binding Protein Delphilin
inferredcites →https://doi.org/10.1093/bioinformatics/btp101openalex-snapshot
ClueGO: a Cytoscape plug-in to decipher functionally grouped gene ontology and pathway annotation networks
inferredcites →https://doi.org/10.1093/brain/awf012openalex-snapshot
Brain function in Duchenne muscular dystrophy
inferredcites →https://doi.org/10.1093/hmg/1.6.397openalex-snapshot
DNA methylation represses FMR-1 transcription in fragile X syndrome
inferredcites →https://doi.org/10.1093/hmg/5.6.809openalex-snapshot
FMRP is associated to the ribosomes via RNA
inferredcites →https://doi.org/10.1093/hmg/6.8.1315openalex-snapshot
Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis
inferredcites →https://doi.org/10.1093/hmg/9.8.1145openalex-snapshot
(Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features
inferredcites →https://doi.org/10.1093/hmg/ddg350openalex-snapshot
Phosphorylation influences the translation state of FMRP-associated polyribosomes
inferredcites →https://doi.org/10.1093/hmg/ddn219openalex-snapshot
Tdrd3 is a novel stress granule-associated protein interacting with the Fragile-X syndrome protein FMRP
inferredcites →https://doi.org/10.1093/hmg/ddu272openalex-snapshot
Analysis of FMRP mRNA target datasets reveals highly associated mRNAs mediated by G-quadruplex structures formed via clustered WGGA sequences
inferredcites →https://doi.org/10.1093/hmg/ddv299openalex-snapshot
Conserved hippocampal cellular pathophysiology but distinct behavioural deficits in a new rat model of FXS
inferredcites →https://doi.org/10.1093/nar/gkw1293openalex-snapshot
Topoisomerase 3β is the major topoisomerase for mRNAs and linked to neurodevelopment and mental dysfunction
inferredcites →https://doi.org/10.1093/nar/gkw593openalex-snapshot
Identification of consensus binding sites clarifies FMRP binding determinants
inferredcites →https://doi.org/10.1093/nar/gni149openalex-snapshot
Isolation of mRNA from specific tissues of Drosophila by mRNA tagging
inferredcites →https://doi.org/10.1098/rstb.2008.2270openalex-snapshot
Type-1 metabotropic glutamate receptor in cerebellar Purkinje cells: a key molecule responsible for long-term depression, endocannabinoid signalling and synapse elimination
inferredcites →https://doi.org/10.1101/cshperspect.a032243openalex-snapshot
The Future of Cross-Linking and Immunoprecipitation (CLIP)
inferredcites →https://doi.org/10.1101/cshperspect.a032912openalex-snapshot
Translational Control in the Brain in Health and Disease
inferredcites →https://doi.org/10.1101/gad.604610openalex-snapshot
SMG6 interacts with the exon junction complex via two conserved EJC-binding motifs (EBMs) required for nonsense-mediated mRNA decay
inferredcites →https://doi.org/10.1101/lm.049965.119openalex-snapshot
Polysomes identified by live imaging of nascent peptides are stalled in hippocampal and cortical neurites
inferredcites →https://doi.org/10.1101/pdb.top097931openalex-snapshot
Mapping of In Vivo RNA-Binding Sites by Ultraviolet (UV)-Cross-Linking Immunoprecipitation (CLIP)
inferredcites →https://doi.org/10.1104/pp.107.115246openalex-snapshot
Global Characterization of Cell-Specific Gene Expression through Fluorescence-Activated Sorting of Nuclei
inferredcites →https://doi.org/10.1111/j.1471-4159.2012.07722.xopenalex-snapshot
Activation of the extracellular signal‐regulated kinase pathway contributes to the behavioral deficit of fragile x‐syndrome
inferredcites →https://doi.org/10.1111/j.1601-183x.2005.00128.xopenalex-snapshot
Localization of FMRP‐associated mRNA granules and requirement of microtubules for activity‐dependent trafficking in hippocampal neurons
inferredcites →https://doi.org/10.1111/j.1601-183x.2008.00417.xopenalex-snapshot
Savings and extinction of conditioned eyeblink responses in fragile X syndrome
inferredcites →https://doi.org/10.1111/j.1742-4658.2008.06411.xopenalex-snapshot
Structure and function of KH domains
inferredcites →https://doi.org/10.1113/jp274885openalex-snapshot
The presynaptic scaffolding protein Piccolo organizes the readily releasable pool at the calyx of Held
inferredcites →https://doi.org/10.1126/science.1090095openalex-snapshot
CLIP Identifies Nova-Regulated RNA Networks in the Brain
inferredcites →https://doi.org/10.1126/science.1224159openalex-snapshot
Shared Synaptic Pathophysiology in Syndromic and Nonsyndromic Rodent Models of Autism
inferredcites →https://doi.org/10.1126/science.1589758openalex-snapshot
Triplet Repeat Mutations in Human Disease
inferredcites →https://doi.org/10.1126/science.1675488openalex-snapshot
Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n
inferredcites →https://doi.org/10.1126/science.aac7368openalex-snapshot
Multiple repressive mechanisms in the hippocampus during memory formation
inferredcites →https://doi.org/10.1126/science.aam8999openalex-snapshot
Single-cell profiling of the developing mouse brain and spinal cord with split-pool barcoding
inferredcites →https://doi.org/10.1126/science.aas9963openalex-snapshot
Fragile X mental retardation 1 gene enhances the translation of large autism-related proteins
inferredcites →https://doi.org/10.1126/science.aau3644openalex-snapshot
Local protein synthesis is a ubiquitous feature of neuronal pre- and postsynaptic compartments
inferredcites →https://doi.org/10.1126/scitranslmed.aao0498openalex-snapshot
Sustained correction of associative learning deficits after brief, early treatment in a rat model of Fragile X Syndrome
inferredcites →https://doi.org/10.1128/mcb.16.7.3825openalex-snapshot
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
inferredcites →https://doi.org/10.1128/mcb.20.22.8536-8547.2000openalex-snapshot
Characterization of dFMR1, a Drosophila melanogaster Homolog of the Fragile X Mental Retardation Protein
inferredcites →https://doi.org/10.1146/annurev-neuro-060909-153138openalex-snapshot
The Pathophysiology of Fragile X (and What It Teaches Us about Synapses)
inferredcites →https://doi.org/10.1146/annurev-pathol-011811-132457openalex-snapshot
Molecular Mechanisms of Fragile X Syndrome: A Twenty-Year Perspective
inferredcites →https://doi.org/10.1146/annurev.biophys.34.040204.144521openalex-snapshot
From “Simple” DNA-Protein Interactions to the Macromolecular Machines of Gene Expression
inferredcites →https://doi.org/10.1146/annurev.genom.8.080706.092249openalex-snapshot
The Pathophysiology of Fragile X Syndrome
inferredcites →https://doi.org/10.1152/jn.01316.2005openalex-snapshot
Metabotropic Receptor-Dependent Long-Term Depression Persists in the Absence of Protein Synthesis in the Mouse Model of Fragile X Syndrome
inferredcites →https://doi.org/10.1159/000123040openalex-snapshot
Systems Biology Perspectives on Cerebellar Long-Term Depression
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What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/ajmg.a.63523openalex-snapshot
Fragile X syndrome in the largest world clustering. I. Genetic epidemiology and founder effect outline
inferred← citeshttps://doi.org/10.1007/978-3-031-15070-8_81openalex-snapshot
Cerebellar Pathology in Autism
inferred← citeshttps://doi.org/10.1007/978-3-031-15070-8_82openalex-snapshot
Cerebellar Pathology in Schizophrenia, Bipolar Disorder, and Major Depression
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2021.06.025openalex-snapshot
Mechanisms regulating input-output function and plasticity of neurons in the absence of FMRP
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.02.076openalex-snapshot
FMRP Control of Ribosome Translocation Promotes Chromatin Modifications and Alternative Splicing of Neuronal Genes Linked to Autism
inferred← citeshttps://doi.org/10.1016/j.ejmg.2020.104041openalex-snapshot
Excess of RALGAPB de novo variants in neurodevelopmental disorders
inferred← citeshttps://doi.org/10.1016/j.neuron.2020.10.002openalex-snapshot
Parallel Social Information Processing Circuits Are Differentially Impacted in Autism
inferred← citeshttps://doi.org/10.1038/s41583-021-00432-0openalex-snapshot
The molecular biology of FMRP: new insights into fragile X syndrome
inferred← citeshttps://doi.org/10.1073/pnas.2009161117openalex-snapshot
FMRP links optimal codons to mRNA stability in neurons
inferred← citeshttps://doi.org/10.1101/2024.08.13.607210openalex-snapshot
Opto-CLIP reveals dynamic FMRP regulation of mRNAs upon CA1 neuronal activation
inferred← citeshttps://doi.org/10.1101/801449openalex-snapshot
FMRP Links Optimal Codons to mRNA stability in Neurons
inferred← citeshttps://doi.org/10.1146/annurev-neuro-100119-024851openalex-snapshot
The Genetic Control of Stoichiometry Underlying Autism
inferred← citeshttps://doi.org/10.1186/s13229-020-00384-9openalex-snapshot
Ribosome profiling in mouse hippocampus: plasticity-induced regulation and bidirectional control by TSC2 and FMRP
inferred← citeshttps://doi.org/10.3389/fmolb.2021.699613openalex-snapshot
FMRP-Driven Neuropathology in Autistic Spectrum Disorder and Alzheimer's disease: A Losing Game
inferred← citeshttps://doi.org/10.70675/4a7c9911z5df2z4b98zaf99z156d40ddf6f7openalex-snapshot
Spatial control of nucleoporin condensation by Fragile X-related proteins
inferred← citeshttps://doi.org/10.7554/elife.46919openalex-snapshot
FMRP has a cell-type-specific role in CA1 pyramidal neurons to regulate autism-related transcripts and circadian memory
inferred← citeshttps://doi.org/10.7554/elife.71892openalex-snapshot
FMRP regulates mRNAs encoding distinct functions in the cell body and dendrites of CA1 pyramidal neurons
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