279 results on '"Bassell, Gary J."'
Search Results
2. Isoform balance of the long noncoding RNA NEAT1 is regulated by the RNA-binding protein QKI, governs the glioma transcriptome, and impacts cell migration
3. Efficient generation of a self-organizing neuromuscular junction model from human pluripotent stem cells
4. FMRP phosphorylation and interactions with Cdh1 regulate association with dendritic RNA granules and MEF2-triggered synapse elimination
5. Development of single-molecule ubiquitination mediated fluorescence complementation to visualize protein ubiquitination dynamics in dendrites
6. Metabolic effects of the schizophrenia-associated 3q29 deletion
7. ALS‐linked KIF5A ΔExon27 mutant causes neuronal toxicity through gain‐of‐function
8. The PI3-Kinase p110β Isoform Controls Severity of Cocaine-Induced Sequelae and Alters the Striatal Transcriptome
9. Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care
10. A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies
11. The M1311V variant of ATP7A is associated with impaired trafficking and copper homeostasis in models of motor neuron disease
12. TBK1 interacts with tau and enhances neurodegeneration in tauopathy
13. Divergent FUS phosphorylation in primate and mouse cells following double-strand DNA damage
14. RNA-mediated toxicity in C9orf72 ALS and FTD
15. Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36
16. Cdh1-APC Regulates Protein Synthesis and Stress Granules in Neurons through an FMRP-Dependent Mechanism
17. Behavioral changes and growth deficits in a CRISPR engineered mouse model of the schizophrenia-associated 3q29 deletion
18. A native function for RAN translation and CGG repeats in regulating fragile X protein synthesis
19. Biased modulators of NMDA receptors control channel opening and ion selectivity
20. FMRP attenuates activity dependent modifications in the mitochondrial proteome
21. Caregiver Perspectives on a Childʼs Diagnosis of 3q29 Deletion: “We Canʼt Just Wish This Thing Away”
22. Correction to: Isoform-selective phosphoinositide 3-kinase inhibition ameliorates a broad range of fragile X syndrome-associated deficits in a mouse model
23. Crosstalk of Local Translation and Mitochondria: Powering Plasticity in Axons and Dendrites
24. Aberrant RNA translation in fragile X syndrome: From FMRP mechanisms to emerging therapeutic strategies
25. Familiarity with a Vocal Category Biases the Compartmental Expression of 'Arc/Arg3.1' in Core Auditory Cortex
26. Where to start? Activity-dependent alternative translation initiation generates multifunctional proteoforms in the brain.
27. Remembering Stephen T. Warren, a pillar of neurogenetics (1953–2021)
28. The Conserved, Disease-Associated RNA Binding Protein dNab2 Interacts with the Fragile X Protein Ortholog in Drosophila Neurons
29. A Predominantly Nuclear Protein Affecting Cytoplasmic Localization of β-Actin mRNA in Fibroblasts and Neurons
30. CRISPR-mediated gene correction links the ATP7A M1311V mutations with amyotrophic lateral sclerosis pathogenesis in one individual
31. Cortical neurons derived from human pluripotent stem cells lacking FMRP display altered spontaneous firing patterns
32. Isoform-selective phosphoinositide 3-kinase inhibition ameliorates a broad range of fragile X syndrome-associated deficits in a mouse model
33. A role for the survival of motor neuron protein in mRNP assembly and transport
34. Therapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and Back
35. Increased Expression of the PI3K Enhancer PIKE Mediates Deficits in Synaptic Plasticity and Behavior in Fragile X Syndrome
36. A 3′ untranslated region variant in FMR1 eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuR
37. The RNA-binding protein, ZC3H14, is required for proper poly(A) tail length control, expression of synaptic proteins, and brain function in mice
38. Muscleblind-like proteins use modular domains to localize RNAs by riding kinesins and docking to membranes.
39. The Fragile X Syndrome: From Molecular Genetics to Neurobiology
40. Bidirectional Control of mRNA Translation and Synaptic Plasticity by the Cytoplasmic Polyadenylation Complex
41. Spinal muscular atrophy: The role of SMN in axonal mRNA regulation
42. Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humans
43. Plastin 3 Is a Protective Modifier of Autosomal Recessive Spinal Muscular Atrophy
44. Reversible Inhibition of PSD-95 mRNA Translation by miR-125a, FMRP Phosphorylation, and mGluR Signaling
45. Making and breaking synapses through local mRNA regulation
46. Fragile X Mental Retardation Protein Deficiency Leads to Excessive mGluR5-Dependent Internalization of AMPA Receptors
47. Extracellular Stimuli Specifically Regulate Localized Levels of Individual Neuronal mRNAs
48. Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis
49. Single mRNAs Visualized by Ultrastructural in situ Hybridization Are Principally Localized at Actin Filament Intersections in Fibroblasts
50. Localization of HIV RNA in Mitochondria of Infected Cells: Potential Role in Cytopathogenicity
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