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Impaired activity-dependent FMRP translation and enhanced mGluR-dependent LTD in Fragile X premutation mice

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/jama.291.4.460openalex-snapshot

Penetrance of the Fragile X–Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population

inferredcites →https://doi.org/10.1002/(sici)1096-8628(19990402)83:4<286::aid-ajmg10>3.0.co;2-hopenalex-snapshot

Genotype, molecular phenotype, and cognitive phenotype: Correlations in fragile X syndrome

inferredcites →https://doi.org/10.1002/1096-8628(20000918)94:3<232::aid-ajmg9>3.0.co;2-hopenalex-snapshot

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels ofFMR1 messenger RNA

inferredcites →https://doi.org/10.1002/1096-8628(200023)97:3<195::aid-ajmg1037>3.0.co;2-ropenalex-snapshot

Transcription of the FMR1 gene in individuals with fragile X syndrome

inferredcites →https://doi.org/10.1002/ajmg.a.20214openalex-snapshot

Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis

inferredcites →https://doi.org/10.1002/ajmg.a.32848openalex-snapshot

Autism spectrum disorder in fragile X syndrome: A longitudinal evaluation

inferredcites →https://doi.org/10.1002/ajmg.b.30241openalex-snapshot

Abnormal elevation ofFMR1mRNA is associated with psychological symptoms in individuals with the fragile X premutation

inferredcites →https://doi.org/10.1002/ajmg.b.30685openalex-snapshot

Impact of the Fragile X mental retardation 1 (FMR1) gene premutation on neuropsychiatric functioning in adult males without fragile X‐associated Tremor/Ataxia syndrome: A controlled study

inferredcites →https://doi.org/10.1002/ajmg.b.32065openalex-snapshot

Prevalence of CGG expansions of the FMR1 gene in a US population‐based sample

inferredcites →https://doi.org/10.1002/hipo.22043openalex-snapshot

CGG trinucleotide repeat length modulates neural plasticity and spatiotemporal processing in a mouse model of the fragile X premutation

inferredcites →https://doi.org/10.1002/humu.22177openalex-snapshot

Somatic Expansion in Mouse and Human Carriers of Fragile X Premutation Alleles

inferredcites →https://doi.org/10.1002/jnr.10453openalex-snapshot

Fragile X mental retardation protein in plasticity and disease

inferredcites →https://doi.org/10.1002/mds.21493openalex-snapshot

Fragile X‐associated tremor/ataxia syndrome: Clinical features, genetics, and testing guidelines

inferredcites →https://doi.org/10.1002/mrdd.20006openalex-snapshot

Phenotypic variation and FMRP levels in fragile X

inferredcites →https://doi.org/10.1007/978-3-642-21649-7_17openalex-snapshot

Fragile X Syndrome and Targeted Treatment Trials

inferredcites →https://doi.org/10.1007/s10519-005-2792-4openalex-snapshot

Examination of the Effect of the Polymorphic CGG Repeat in the FMR1 Gene on Cognitive Performance

inferredcites →https://doi.org/10.1007/s10519-008-9214-3openalex-snapshot

Investigation of Phenotypes Associated with Mood and Anxiety Among Male and Female Fragile X Premutation Carriers

inferredcites →https://doi.org/10.1007/s10803-006-0205-zopenalex-snapshot

Autism Spectrum Phenotype in Males and Females with Fragile X Full Mutation and Premutation

inferredcites →https://doi.org/10.1007/s11033-006-9032-8openalex-snapshot

Fragile x mental retardation (Fmr-1) gene expression is down regulated in brain of mice during aging

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(91)90397-hopenalex-snapshot

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

inferredcites →https://doi.org/10.1016/0092-8674(91)90514-yopenalex-snapshot

Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndrome

inferredcites →https://doi.org/10.1016/0092-8674(94)90232-1openalex-snapshot

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

inferredcites →https://doi.org/10.1016/j.bandc.2004.08.020openalex-snapshot

The emerging fragile X premutation phenotype: Evidence from the domain of social cognition

inferredcites →https://doi.org/10.1016/j.bandc.2012.02.005openalex-snapshot

Selective spatial processing deficits in an at-risk subgroup of the fragile X premutation

inferredcites →https://doi.org/10.1016/j.biopsych.2011.05.033openalex-snapshot

Decreased Fragile X Mental Retardation Protein Expression Underlies Amygdala Dysfunction in Carriers of the Fragile X Premutation

inferredcites →https://doi.org/10.1016/j.brainres.2012.02.057openalex-snapshot

RNA-mediated neurodegeneration in fragile X-associated tremor/ataxia syndrome

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.gene.2007.02.026openalex-snapshot

Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model

inferredcites →https://doi.org/10.1016/j.jmb.2011.01.006openalex-snapshot

Initiation of Translation of the FMR1 mRNA Occurs Predominantly through 5′-End-Dependent Ribosomal Scanning

inferredcites →https://doi.org/10.1016/j.jns.2006.05.016openalex-snapshot

Impairment in the cognitive functioning of men with fragile X-associated tremor/ataxia syndrome (FXTAS)

inferredcites →https://doi.org/10.1016/j.jocn.2006.01.015openalex-snapshot

Tremor/ataxia syndrome and fragile X premutation: Diagnostic caveats

inferredcites →https://doi.org/10.1016/j.nbd.2011.01.008openalex-snapshot

A mouse model of the fragile X premutation: Effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis

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.2006.08.034openalex-snapshot

Arc/Arg3.1 Mediates Homeostatic Synaptic Scaling of AMPA Receptors

inferredcites →https://doi.org/10.1016/j.neuron.2008.05.014openalex-snapshot

Rapid Translation of Arc/Arg3.1 Selectively Mediates mGluR-Dependent LTD through Persistent Increases in AMPAR Endocytosis Rate

inferredcites →https://doi.org/10.1016/j.neuron.2008.05.023openalex-snapshot

Elongation Factor 2 and Fragile X Mental Retardation Protein Control the Dynamic Translation of Arc/Arg3.1 Essential for mGluR-LTD

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.2010.11.034openalex-snapshot

Local Presynaptic Activity Gates Homeostatic Changes in Presynaptic Function Driven by Dendritic BDNF Synthesis

inferredcites →https://doi.org/10.1016/j.pneurobio.2011.10.006openalex-snapshot

Neurodegeneration the RNA way

inferredcites →https://doi.org/10.1016/j.tins.2004.04.009openalex-snapshot

The mGluR theory of fragile X mental retardation

inferredcites →https://doi.org/10.1016/j.yapd.2009.08.008openalex-snapshot

Fragile X: A Family of Disorders

inferredcites →https://doi.org/10.1016/s0169-328x(02)00657-5openalex-snapshot

Whisker stimulation-dependent translation of FMRP in the barrel cortex requires activation of type I metabotropic glutamate receptors

inferredcites →https://doi.org/10.1016/s1474-4422(06)70676-7openalex-snapshot

Fragile-X syndrome and fragile X-associated tremor/ataxia syndrome: two faces of FMR1

inferredcites →https://doi.org/10.1017/s1355838202020642openalex-snapshot

Reduced FMR1 mRNA translation efficiency in Fragile X patients with premutations

inferredcites →https://doi.org/10.1037/0894-4105.17.4.646openalex-snapshot

Effect of the Fragile X Status Categories and the Fragile X Mental Retardation Protein Levels on Executive Functioning in Males and Females With Fragile X.

inferredcites →https://doi.org/10.1037/a0017616openalex-snapshot

Progressive spatial processing deficits in a mouse model of the fragile X premutation.

inferredcites →https://doi.org/10.1038/72915openalex-snapshot

NMDA receptor-mediated control of protein synthesis at developing synapses

inferredcites →https://doi.org/10.1038/893openalex-snapshot

Non-invasive sexing of preimplantation stage mammalian embryos

inferredcites →https://doi.org/10.1038/nature08161openalex-snapshot

Evidence of Xist RNA-independent initiation of mouse imprinted X-chromosome inactivation

inferredcites →https://doi.org/10.1073/pnas.0707484104openalex-snapshot

Fragile X mental retardation protein deficiency leads to excessive mGluR5-dependent internalization of AMPA receptors

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.2336265100openalex-snapshot

The fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95

inferredcites →https://doi.org/10.1073/pnas.94.10.5395openalex-snapshot

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

inferredcites →https://doi.org/10.1074/jbc.c800055200openalex-snapshot

S6K1 Phosphorylates and Regulates Fragile X Mental Retardation Protein (FMRP) with the Neuronal Protein Synthesis-dependent Mammalian Target of Rapamycin (mTOR) Signaling Cascade

inferredcites →https://doi.org/10.1086/302720openalex-snapshot

Elevated Levels of FMR1 mRNA in Carrier Males: A New Mechanism of Involvement in the Fragile-X Syndrome

inferredcites →https://doi.org/10.1093/brain/awh683openalex-snapshot

Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS)

inferredcites →https://doi.org/10.1093/brain/awl338openalex-snapshot

Amygdala dysfunction in men with the fragile X premutation

inferredcites →https://doi.org/10.1093/hmg/10.4.329openalex-snapshot

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

inferredcites →https://doi.org/10.1093/hmg/ddp479openalex-snapshot

Murine hippocampal neurons expressing Fmr1 gene premutations show early developmental deficits and late degeneration

inferredcites →https://doi.org/10.1093/hmg/ddq432openalex-snapshot

Premutation CGG-repeat expansion of the Fmr1 gene impairs mouse neocortical development

inferredcites →https://doi.org/10.1093/hmg/dds118openalex-snapshot

Clustered burst firing in FMR1 premutation hippocampal neurons: amelioration with allopregnanolone

inferredcites →https://doi.org/10.1093/hmg/dds207openalex-snapshot

Signaling defects in iPSC-derived fragile X premutation neurons

inferredcites →https://doi.org/10.1093/humrep/deh635openalex-snapshot

Association of FMR1 repeat size with ovarian dysfunction

inferredcites →https://doi.org/10.1093/nar/29.11.2276openalex-snapshot

The fragile X mental retardation protein inhibits translation via interacting with mRNA

inferredcites →https://doi.org/10.1097/00004703-200112000-00008openalex-snapshot

The Behavioral Phenotype in Fragile X: Symptoms of Autism in Very Young Children with Fragile X Syndrome, Idiopathic Autism, and Other Developmental Disorders

inferredcites →https://doi.org/10.1097/00004703-200212000-00004openalex-snapshot

Effect of the Deficits of Fragile X Mental Retardation Protein on Cognitive Status of Fragile X Males and Females Assessed by Robust Pedigree Analysis

inferredcites →https://doi.org/10.1097/00004703-200604002-00012openalex-snapshot

Autism Spectrum Disorders and Attention-Deficit/Hyperactivity Disorder in Boys with the Fragile X Premutation

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.252.5009.1097openalex-snapshot

Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome

inferredcites →https://doi.org/10.1126/science.288.5469.1254openalex-snapshot

Role for Rapid Dendritic Protein Synthesis in Hippocampal mGluR-Dependent Long-Term Depression

inferredcites →https://doi.org/10.1126/science.7732383openalex-snapshot

Translational Suppression by Trinucleotide Repeat Expansion at FMR1

inferredcites →https://doi.org/10.1126/scitranslmed.3001708openalex-snapshot

Epigenetic Modification of the FMR1 Gene in Fragile X Syndrome Is Associated with Differential Response to the mGluR5 Antagonist AFQ056

inferredcites →https://doi.org/10.1136/jmg.2003.012518openalex-snapshot

Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome

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/10.1152/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/10.1152/jn.1998.80.2.989openalex-snapshot

Requirement of Protein Synthesis for Group I mGluR-Mediated Induction of Epileptiform Discharges

inferredcites →https://doi.org/10.1261/rna.280807openalex-snapshot

ElevatedFMR1mRNA in premutation carriers is due to increased transcription

inferredcites →https://doi.org/10.1371/journal.pgen.1001240openalex-snapshot

Histone Deacetylases Suppress CGG Repeat–Induced Neurodegeneration Via Transcriptional Silencing in Models of Fragile X Tremor Ataxia Syndrome

inferredcites →https://doi.org/10.1523/jneurosci.0093-05.2005openalex-snapshot

Postadolescent Changes in Regional Cerebral Protein Synthesis: AnIn VivoStudy in theFmr1Null Mouse

inferredcites →https://doi.org/10.1523/jneurosci.0099-04.2004openalex-snapshot

Metabotropic Glutamate Receptor Activation Regulates Fragile X Mental Retardation Protein and Fmr1 mRNA Localization Differentially in Dendrites and at Synapses

inferredcites →https://doi.org/10.1523/jneurosci.05-08-02240.1985openalex-snapshot

Biochemical characterization of a filtered synaptoneurosome preparation from guinea pig cerebral cortex: cyclic adenosine 3':5'-monophosphate- generating systems, receptors, and enzymes

inferredcites →https://doi.org/10.1523/jneurosci.0937-07.2007openalex-snapshot

Dysregulated Metabotropic Glutamate Receptor-Dependent Translation of AMPA Receptor and Postsynaptic Density-95 mRNAs at Synapses in a Mouse Model of Fragile X Syndrome

inferredcites →https://doi.org/10.1523/jneurosci.2969-07.2007openalex-snapshot

FMRP Phosphorylation Reveals an Immediate-Early Signaling Pathway Triggered by Group I mGluR and Mediated by PP2A

inferredcites →https://doi.org/10.1523/jneurosci.4650-11.2012openalex-snapshot

Evidence for a Fragile X Mental Retardation Protein-Mediated Translational Switch in Metabotropic Glutamate Receptor-Triggered Arc Translation and Long-Term Depression

inferredcites →https://doi.org/10.1523/jneurosci.4717-06.2007openalex-snapshot

PresynapticFmr1Genotype Influences the Degree of Synaptic Connectivity in a Mosaic Mouse Model of Fragile X Syndrome

inferredcites →https://doi.org/10.1523/jneurosci.5057-11.2012openalex-snapshot

Dephosphorylation-Induced Ubiquitination and Degradation of FMRP in Dendrites: A Role in Immediate Early mGluR-Stimulated Translation

inferredcites →https://doi.org/10.1542/peds.97.1.122openalex-snapshot

Learning-disabled Males With a Fragile X CGG Expansion in the Upper Premutation Size Range

inferredcites →https://doi.org/10.2310/jim.0b013e3181af59d6openalex-snapshot

Mouse Models of Fragile X-Associated Tremor Ataxia

inferredcites →https://doi.org/10.2353/jmoldx.2008.070073openalex-snapshot

A Rapid Polymerase Chain Reaction-Based Screening Method for Identification of All Expanded Alleles of the Fragile X (FMR1) Gene in Newborn and High-Risk Populations

inferredcites →https://doi.org/10.4088/jcp.08m04476openalex-snapshot

A Review of Fragile X Premutation Disorders

inferredcites →https://doi.org/10.4088/jcp.08r04476openalex-snapshot

A Review of Fragile X Premutation Disorders

inferredcites →https://doi.org/10.4161/rna.4.2.5039openalex-snapshot

Secondary Structure and Dynamics of the r(CGG) Repeat in the mRNA of the Fragile X Mental Retardation 1(FMR1)Gene

inferredcites →https://doi.org/10.7916/d80c4th0openalex-snapshot

Current Gaps in Understanding the Molecular Basis of FXTAS

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4767644openalex-extracted

The RNA-Binding Protein FMRP Induced by Mycoplasma Pneumoniae CARDS Toxin Regulates Multiciliogenesis and Inflammation

inferred← citeshttps://doi.org/10.1007/978-3-032-18296-8_18openalex-snapshot

Rodent Models of Recessive Cerebellar Ataxias and Spontaneous Cerebellar Mutants

inferred← citeshttps://doi.org/10.1007/978-3-319-33898-9_6openalex-snapshot

The Molecular Biology of Premutation Expanded Alleles

inferred← citeshttps://doi.org/10.1007/s00401-013-1138-1openalex-snapshot

Fragile X-associated tremor/ataxia syndrome (FXTAS): pathology and mechanisms

inferred← citeshttps://doi.org/10.1007/s12035-023-03562-xopenalex-snapshot

Utilities of Isolated Nerve Terminals in Ex Vivo Analyses of Protein Translation in (Patho)physiological Brain States: Focus on Alzheimer’s Disease

inferred← citeshttps://doi.org/10.1007/s12311-016-0797-6openalex-snapshot

Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) Motor Dysfunction Modeled in Mice

inferred← citeshttps://doi.org/10.1007/s13311-014-0292-zopenalex-snapshot

Repeat-Associated Non-AUG Translation and Its Impact in Neurodegenerative Disease

inferred← citeshttps://doi.org/10.1016/b978-0-12-398270-4.00008-2openalex-snapshot

Fragile X-Associated Disorders

inferred← citeshttps://doi.org/10.1016/b978-0-12-405195-9.00039-1openalex-snapshot

Mouse Models of the Fragile X Tremor/Ataxia Syndrome (FXTAS) and the Fragile X Premutation

inferred← citeshttps://doi.org/10.1016/b978-0-12-408139-0.00006-7openalex-snapshot

Unpacking Memory Processes

inferred← citeshttps://doi.org/10.1016/b978-0-12-410529-4.00017-6openalex-snapshot

Fragile X-Associated Disorders

inferred← citeshttps://doi.org/10.1016/b978-0-12-800109-7.00020-0openalex-snapshot

Fragile X Syndrome

inferred← citeshttps://doi.org/10.1016/b978-0-444-63233-3.00025-7openalex-snapshot

Fragile X syndrome and fragile X-associated tremor ataxia syndrome

inferred← citeshttps://doi.org/10.1016/j.bbr.2014.03.013openalex-snapshot

Impaired sensorimotor gating in Fmr1 knock out and Fragile X premutation model mice

inferred← citeshttps://doi.org/10.1016/j.isci.2026.115066openalex-snapshot

Stimulation of the medial septum diagonal band of broca rescues learning and memory deficits in Fmr1 KO mice

inferred← citeshttps://doi.org/10.1016/j.nbd.2013.06.013openalex-snapshot

Phosphorylation of FMRP and alterations of FMRP complex underlie enhanced mLTD in adult rats triggered by early life seizures

inferred← citeshttps://doi.org/10.1016/j.neulet.2014.11.035openalex-snapshot

Effects of clonidine and methylphenidate on motor activity in Fmr1 knockout mice

inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2013.11.009openalex-snapshot

Reduced excitatory amino acid transporter 1 and metabotropic glutamate receptor 5 expression in the cerebellum of fragile X mental retardation gene 1 premutation carriers with fragile X-associated tremor/ataxia syndrome

inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2016.10.017openalex-snapshot

Cerebellar volume mediates the relationship between FMR1 mRNA levels and voluntary step initiation in males with the premutation

inferred← citeshttps://doi.org/10.1016/j.neuron.2013.02.022openalex-snapshot

The Unstable Repeats—Three Evolving Faces of Neurological Disease

inferred← citeshttps://doi.org/10.1016/j.neuropharm.2018.09.035openalex-snapshot

Regulation of hippocampal long term depression by Neuroligin 1

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2025.12.033openalex-snapshot

Early postsynaptic potentiation in hippocampal somatostatin interneurons is mTORC1-dependent and disrupted in Fmr1 mice

inferred← citeshttps://doi.org/10.1016/j.nlm.2014.01.011openalex-snapshot

Reduced activity-dependent protein levels in a mouse model of the fragile X premutation

inferred← citeshttps://doi.org/10.1016/j.pneurobio.2024.102685openalex-snapshot

Cerebellar impairments in genetic models of autism spectrum disorders: A neurobiological perspective

inferred← citeshttps://doi.org/10.1038/nrdp.2017.65openalex-snapshot

Fragile X syndrome

inferred← citeshttps://doi.org/10.1038/s41593-020-0590-1openalex-snapshot

A native function for RAN translation and CGG repeats in regulating fragile X protein synthesis

inferred← citeshttps://doi.org/10.1038/s41598-018-34978-4openalex-snapshot

Mavoglurant in Fragile X Syndrome: Results of two open-label, extension trials in adults and adolescents

inferred← citeshttps://doi.org/10.1042/bsr20180118openalex-snapshot

Neonatal maternal deprivation impairs localized de novo activity-induced protein translation at the synapse in the rat hippocampus

inferred← citeshttps://doi.org/10.1073/pnas.1514260112openalex-snapshot

A 3′ untranslated region variant in FMR1 eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuR

inferred← citeshttps://doi.org/10.1074/jbc.m112.441055openalex-snapshot

Enhanced Asynchronous Ca2+ Oscillations Associated with Impaired Glutamate Transport in Cortical Astrocytes Expressing Fmr1 Gene Premutation Expansion

inferred← citeshttps://doi.org/10.1074/jbc.m113.515056openalex-snapshot

F-box Only Protein 2 (Fbxo2) Regulates Amyloid Precursor Protein Levels and Processing

inferred← citeshttps://doi.org/10.1093/brain/awaf203openalex-snapshot

Modelling fragile X-associated neuropsychiatric disorders in young inducible 90CGG premutation mice

inferred← citeshttps://doi.org/10.1093/hmg/ddx148openalex-snapshot

Calcium dysregulation and Cdk5-ATM pathway involved in a mouse model of fragile X-associated tremor/ataxia syndrome

inferred← citeshttps://doi.org/10.1097/cm9.0000000000003474openalex-snapshot

FMRP, an RNA-binding protein induced by the Mycoplasma pneumonia CARDS toxin, regulates multiciliogenesis and inflammation

inferred← citeshttps://doi.org/10.1111/jcpp.12374openalex-snapshot

Annual Research Review: Rare genotypes and childhood psychopathology – uncovering diverse developmental mechanisms of ADHD risk

inferred← citeshttps://doi.org/10.1111/nyas.12693openalex-snapshot

Fragile X–associated tremor/ataxia syndrome

inferred← citeshttps://doi.org/10.11144/javeriana.umed61-4.fmrpopenalex-snapshot

FMRP y las neuroliginas: la influencia de la actividad sensorial en las dinámicas del neurodesarrollo

inferred← citeshttps://doi.org/10.1155/2016/9353929openalex-snapshot

Synaptic Plasticity, a Prominent Contributor to the Anxiety in Fragile X Syndrome

inferred← citeshttps://doi.org/10.1155/2018/8423420openalex-snapshot

Impaired GABA Neural Circuits Are Critical for Fragile X Syndrome

inferred← citeshttps://doi.org/10.11606/d.41.2018.tde-15052018-092019openalex-snapshot

Transtornos do espectro autista em pacientes com a pré-mutação do gene FMR1

inferred← citeshttps://doi.org/10.1186/1866-1955-6-25openalex-snapshot

Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndrome

inferred← citeshttps://doi.org/10.1186/s40478-020-01002-8openalex-snapshot

The carboxyl termini of RAN translated GGGGCC nucleotide repeat expansions modulate toxicity in models of ALS/FTD

inferred← citeshttps://doi.org/10.1371/journal.pone.0096956openalex-snapshot

FMRP S499 Is Phosphorylated Independent of mTORC1-S6K1 Activity

inferred← citeshttps://doi.org/10.1523/eneuro.0091-18.2018openalex-snapshot

BC RNA Mislocalization in the Fragile X Premutation

inferred← citeshttps://doi.org/10.1523/jneurosci.0807-25.2025openalex-snapshot

Activity Deprivation Modulates the Shank3/Homer1/mGluR5 Signaling Pathway to Enable Synaptic Upscaling

inferred← citeshttps://doi.org/10.1523/jneurosci.1978-24.2025openalex-snapshot

Hippocampal Place Cell Sequences Are Impaired in a Rat Model of Fragile X Syndrome

inferred← citeshttps://doi.org/10.1523/jneurosci.3013-14.2015openalex-snapshot

Loss of F-box Only Protein 2 (Fbxo2) Disrupts Levels and Localization of Select NMDA Receptor Subunits, and Promotes Aberrant Synaptic Connectivity

inferred← citeshttps://doi.org/10.2147/ndt.s174083openalex-snapshot

Developmental lead (Pb)-induced deficits in hippocampal protein translation at the synapses are ameliorated by ascorbate supplementation

inferred← citeshttps://doi.org/10.3389/fgene.2014.00360openalex-snapshot

Fragile X mental retardation protein expression in Alzheimer’s disease

inferred← citeshttps://doi.org/10.3389/fgene.2023.1113086openalex-snapshot

Rare diseases of epigenetic origin: Challenges and opportunities

inferred← citeshttps://doi.org/10.3389/fnmol.2018.00282openalex-snapshot

Targeted Reactivation of FMR1 Transcription in Fragile X Syndrome Embryonic Stem Cells

inferred← citeshttps://doi.org/10.3390/genes7100077openalex-snapshot

Modeling Fragile X Syndrome Using Human Pluripotent Stem Cells

inferred← citeshttps://doi.org/10.4137/jen.s25524openalex-snapshot

Single-Nucleotide Mutations in FMR1 Reveal Novel Functions and Regulatory Mechanisms of the Fragile X Syndrome Protein FMRP

inferred← citeshttps://doi.org/10.4172/2168-9296.1000e124openalex-snapshot

Translational Dysregulation in Autism

inferred← citeshttps://doi.org/10.70675/b8e86263z5926z4a83zbaf6z0f61bf2d15f9openalex-snapshot

Pathophysiological consequences of a Fragile X missense mutation

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