| scholarly article | Q13442814 |
| P2093 | author name string | Leonard K Kaczmarek | |
| Daniel B Polley | |||
| Jack Kronengold | |||
| Maile R Brown | |||
| John G Strumbos | |||
| P2860 | cites work | FMR1 Protein: Conserved RNP Family Domains and Selective RNA Binding | Q24311412 |
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| Properties and expression of Kv3 channels in cerebellar Purkinje cells | Q48430589 | ||
| Envelope coding in the lateral superior olive. III. Comparison with afferent pathways | Q48531193 | ||
| The potassium channel subunit KV3.1b is localized to somatic and axonal membranes of specific populations of CNS neurons | Q49049978 | ||
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| Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: a preliminary report. | Q51985541 | ||
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| Expression of the mRNAs for the Kv3.1 potassium channel gene in the adult and developing rat brain | Q28583610 | ||
| The fragile X mental retardation protein inhibits translation via interacting with mRNA | Q28588486 | ||
| Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function | Q29616372 | ||
| Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome | Q29616495 | ||
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| Kv3 channels: voltage-gated K+ channels designed for high-frequency repetitive firing | Q34086958 | ||
| Fast delayed rectifier potassium current is required for circadian neural activity | Q34595087 | ||
| Activation of Kv3.1 channels in neuronal spine-like structures may induce local potassium ion depletion | Q35895029 | ||
| Regulation of the timing of MNTB neurons by short-term and long-term modulation of potassium channels | Q36218700 | ||
| On BC1 RNA and the fragile X mental retardation protein. | Q36393017 | ||
| Fragile X-related proteins regulate mammalian circadian behavioral rhythms | Q36744675 | ||
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| The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development. | Q37589711 | ||
| Kv3.4 subunits enhance the repolarizing efficiency of Kv3.1 channels in fast-spiking neurons | Q39750760 | ||
| Distinct roles of Kv1 and Kv3 potassium channels at the calyx of Held presynaptic terminal. | Q39750979 | ||
| Fragile X mental retardation protein is associated with translating polyribosomes in neuronal cells. | Q40524276 | ||
| Differential subcellular localization of the two alternatively spliced isoforms of the Kv3.1 potassium channel subunit in brain. | Q40721414 | ||
| Contribution of the Kv3.1 potassium channel to high-frequency firing in mouse auditory neurones | Q41034714 | ||
| Encoding of timing in the brain stem auditory nuclei of vertebrates | Q41656227 | ||
| Fragile X mice develop sensory hyperreactivity to auditory stimuli | Q43574481 | ||
| Modulation of the kv3.1b potassium channel isoform adjusts the fidelity of the firing pattern of auditory neurons. | Q44323425 | ||
| The medial nucleus of the trapezoid body: comparative physiology. | Q45374692 | ||
| Systematic variation of potassium current amplitudes across the tonotopic axis of the rat medial nucleus of the trapezoid body | Q46635126 | ||
| Acoustic environment determines phosphorylation state of the Kv3.1 potassium channel in auditory neurons | Q46681614 | ||
| Fine-tuning an auditory synapse for speed and fidelity: developmental changes in presynaptic waveform, EPSC kinetics, and synaptic plasticity. | Q46689899 | ||
| Synaptic mitochondria are more susceptible to Ca2+overload than nonsynaptic mitochondria | Q46975941 | ||
| Distribution of HCN1 and HCN2 in rat auditory brainstem nuclei | Q47221332 | ||
| High-frequency firing helps replenish the readily releasable pool of synaptic vesicles | Q47741527 | ||
| Heterologous expression of the Kv3.1 potassium channel eliminates spike broadening and the induction of a depolarizing afterpotential in the peptidergic bag cell neurons. | Q47907181 | ||
| When, where, and how much? Expression of the Kv3.1 potassium channel in high-frequency firing neurons | Q47907391 | ||
| Loss of Kv3.1 tonotopicity and alterations in cAMP response element-binding protein signaling in central auditory neurons of hearing impaired mice. | Q48033911 | ||
| Epilepsy and EEG findings in males with fragile X syndrome. | Q48135370 | ||
| Slack and Slick K(Na) channels regulate the accuracy of timing of auditory neurons | Q48250784 | ||
| Subcellular localization of the voltage-dependent potassium channel Kv3.1b in postnatal and adult rat medial nucleus of the trapezoid body. | Q48317618 | ||
| Principal cells of the rat medial nucleus of the trapezoid body: an intracellular in vivo study of their physiology and morphology. | Q48381661 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 31 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 10263-10271 | |
| P577 | publication date | 2010-08-01 | |
| P1433 | published in | Journal of Neuroscience | Q1709864 |
| P1476 | title | Fragile X mental retardation protein is required for rapid experience-dependent regulation of the potassium channel Kv3.1b | |
| P478 | volume | 30 |
| Q30841903 | A resting EEG study of neocortical hyperexcitability and altered functional connectivity in fragile X syndrome |
| Q95930009 | ATP synthase c-subunit ring as the channel of mitochondrial permeability transition: Regulator of metabolism in development and degeneration |
| Q48244382 | Abnormal presynaptic short-term plasticity and information processing in a mouse model of fragile X syndrome |
| Q35514214 | Altered neocortical rhythmic activity states in Fmr1 KO mice are due to enhanced mGluR5 signaling and involve changes in excitatory circuitry |
| Q30442883 | Auditory processing in fragile x syndrome |
| Q34785622 | Bidirectional control of BK channel open probability by CAMKII and PKC in medial vestibular nucleus neurons |
| Q30460772 | Bidirectional regulation of dendritic voltage-gated potassium channels by the fragile X mental retardation protein |
| Q92920694 | Cataloguing and Selection of mRNAs Localized to Dendrites in Neurons and Regulated by RNA-Binding Proteins in RNA Granules |
| Q42054553 | Cell-Type Specific Channelopathies in the Prefrontal Cortex of the fmr1-/y Mouse Model of Fragile X Syndrome. |
| Q90910835 | Cellular and synaptic phenotypes lead to disrupted information processing in Fmr1-KO mouse layer 4 barrel cortex |
| Q41428079 | Cellular distribution of the fragile X mental retardation protein in the mouse brain |
| Q27022703 | Channelopathies and dendritic dysfunction in fragile X syndrome |
| Q92739252 | Characterization of Auditory and Binaural Spatial Hearing in a Fragile X Syndrome Mouse Model |
| Q30411291 | Degraded speech sound processing in a rat model of fragile X syndrome |
| Q30418164 | Deletion of Fmr1 alters function and synaptic inputs in the auditory brainstem. |
| Q48209105 | Disrupted-in-schizophrenia 1 regulates transport of ITPR1 mRNA for synaptic plasticity |
| Q92213850 | Disruption of GpI mGluR-Dependent Cav2.3 Translation in a Mouse Model of Fragile X Syndrome |
| Q95656749 | Dynamics of the Fragile X Mental Retardation Protein Correlates with Cellular and Synaptic Properties in Primary Auditory Neurons following Afferent Deprivation |
| Q26782616 | Dysregulation and restoration of translational homeostasis in fragile X syndrome |
| Q47678007 | Enhanced Excitatory Connectivity and Disturbed Sound Processing in the Auditory Brainstem of Fragile X Mice. |
| Q30536899 | FMRP regulates neurotransmitter release and synaptic information transmission by modulating action potential duration via BK channels |
| Q30432990 | Failed stabilization for long-term potentiation in the auditory cortex of FMR1 knockout mice |
| Q47626153 | Fragile X Mental Retardation Protein Restricts Small Dye Iontophoresis Entry into Central Neurons. |
| Q38097197 | Fragile X mental retardation protein and synaptic plasticity |
| Q48915976 | Fragile X mental retardation protein controls ion channel expression and activity |
| Q34952541 | Fragile X mental retardation protein regulates protein expression and mRNA translation of the potassium channel Kv4.2. |
| Q30448604 | Fragile X syndrome: mechanistic insights and therapeutic avenues regarding the role of potassium channels. |
| Q30410502 | From FMRP function to potential therapies for fragile X syndrome |
| Q50561718 | Genetic upregulation of BK channel activity normalizes multiple synaptic and circuit defects in a mouse model of fragile X syndrome. |
| Q30469392 | Gradients and modulation of K(+) channels optimize temporal accuracy in networks of auditory neurons |
| Q64289005 | Homeostatic Intrinsic Plasticity Is Functionally Altered in Fmr1 KO Cortical Neurons |
| Q48098924 | Identification and characterization of site-specific N-glycosylation in the potassium channel Kv3.1b. |
| Q91494891 | Identification of a molecular locus for normalizing dysregulated GABA release from interneurons in the Fragile X brain |
| Q47550815 | Imbalance of synaptic actin dynamics as a key to the Fragile X syndrome? |
| Q37564195 | Impaired activity-dependent neural circuit assembly and refinement in autism spectrum disorder genetic models |
| Q30440653 | Impaired critical period plasticity in primary auditory cortex of fragile X model mice |
| Q30406616 | In vivo synaptic transmission and morphology in mouse models of Tuberous sclerosis, Fragile X syndrome, Neurofibromatosis type 1, and Costello syndrome |
| Q34435526 | Increasing our understanding of human cognition through the study of Fragile X Syndrome |
| Q28115339 | Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures |
| Q38441936 | Integrated transcriptome analysis of human iPS cells derived from a fragile X syndrome patient during neuronal differentiation |
| Q97522071 | Intellectual Disability and Potassium Channelopathies: A Systematic Review |
| Q41468658 | Intense and specialized dendritic localization of the fragile X mental retardation protein in binaural brainstem neurons: a comparative study in the alligator, chicken, gerbil, and human |
| Q47681198 | Kv3 Channels: Enablers of Rapid Firing, Neurotransmitter Release, and Neuronal Endurance |
| Q30416917 | Linking neural activity and molecular oscillations in the SCN. |
| Q37381803 | Loss of functional A-type potassium channels in the dendrites of CA1 pyramidal neurons from a mouse model of fragile X syndrome |
| Q30357779 | Matrix metalloproteinase-9 deletion rescues auditory evoked potential habituation deficit in a mouse model of Fragile X Syndrome |
| Q89624618 | Mechanisms underlying auditory processing deficits in Fragile X syndrome |
| Q92765746 | Modulators of Kv3 Potassium Channels Rescue the Auditory Function of Fragile X Mice |
| Q38639448 | Multifarious Functions of the Fragile X Mental Retardation Protein |
| Q64950869 | Neuroligin 1, 2, and 3 Regulation at the Synapse: FMRP-Dependent Translation and Activity-Induced Proteolytic Cleavage. |
| Q38884036 | Neuron class-specific requirements for Fragile X Mental Retardation Protein in critical period development of calcium signaling in learning and memory circuitry |
| Q37127783 | Physiological modulators of Kv3.1 channels adjust firing patterns of auditory brain stem neurons |
| Q92308939 | Polysomnographic Findings in Fragile X Syndrome Children with EEG Abnormalities |
| Q30464105 | Potassium channel modulation and auditory processing |
| Q42290506 | Reduced Lateral Inhibition Impairs Olfactory Computations and Behaviors in a Drosophila Model of Fragile X Syndrome |
| Q58718525 | Sensory Processing Phenotypes in Fragile X Syndrome |
| Q90029168 | Subtle differences in synaptic transmission in medial nucleus of trapezoid body neurons between wild-type and Fmr1 knockout mice |
| Q27023257 | Targeted pharmacological treatment of autism spectrum disorders: fragile X and Rett syndromes |
| Q35680726 | Targeted treatments for fragile X syndrome |
| Q38775856 | The need for new approaches in CNS drug discovery: Why drugs have failed, and what can be done to improve outcomes |
| Q38098906 | The translation of translational control by FMRP: therapeutic targets for FXS. |
| Q27337360 | Therapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and Back |
| Q35614072 | Therapeutic strategies in fragile X syndrome: dysregulated mGluR signaling and beyond |
| Q47660831 | Tonotopic alterations in inhibitory input to the medial nucleus of the trapezoid body in a mouse model of Fragile X syndrome. |
| Q91062840 | Tsc1 represses parvalbumin expression and fast-spiking properties in somatostatin lineage cortical interneurons |
| Q58800979 | Unraveling the Pathways to Neuronal Homeostasis and Disease: Mechanistic Insights into the Role of RNA-Binding Proteins and Associated Factors |
| Q58617074 | Voltage-Independent SK Channel Dysfunction Causes Neuronal Hyperexcitability in the Hippocampus of KO mice |
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