437 results on '"Bassell, Gary J."'
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2. Efficient generation of a self-organizing neuromuscular junction model from human pluripotent stem cells
3. FMRP phosphorylation and interactions with Cdh1 regulate association with dendritic RNA granules and MEF2-triggered synapse elimination
4. Development of single-molecule ubiquitination mediated fluorescence complementation to visualize protein ubiquitination dynamics in dendrites
5. Metabolic effects of the schizophrenia-associated 3q29 deletion
6. ALS‐linked KIF5A ΔExon27 mutant causes neuronal toxicity through gain‐of‐function
7. Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care
8. The M1311V variant of ATP7A is associated with impaired trafficking and copper homeostasis in models of motor neuron disease
9. TBK1 interacts with tau and enhances neurodegeneration in tauopathy
10. Divergent FUS phosphorylation in primate and mouse cells following double-strand DNA damage
11. RNA-mediated toxicity in C9orf72 ALS and FTD
12. Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36
13. Cdh1-APC Regulates Protein Synthesis and Stress Granules in Neurons through an FMRP-Dependent Mechanism
14. FMRP attenuates activity dependent modifications in the mitochondrial proteome
15. Correction to: Isoform-selective phosphoinositide 3-kinase inhibition ameliorates a broad range of fragile X syndrome-associated deficits in a mouse model
16. Rab11 regulates autophagy at dendritic spines in an mTOR- and NMDA-dependent manner
17. Crosstalk of Local Translation and Mitochondria: Powering Plasticity in Axons and Dendrites
18. Familiarity with a Vocal Category Biases the Compartmental Expression of 'Arc/Arg3.1' in Core Auditory Cortex
19. Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion
20. The Conserved, Disease-Associated RNA Binding Protein dNab2 Interacts with the Fragile X Protein Ortholog in Drosophila Neurons
21. A Predominantly Nuclear Protein Affecting Cytoplasmic Localization of β-Actin mRNA in Fibroblasts and Neurons
22. CRISPR-mediated gene correction links the ATP7A M1311V mutations with amyotrophic lateral sclerosis pathogenesis in one individual
23. Cortical neurons derived from human pluripotent stem cells lacking FMRP display altered spontaneous firing patterns
24. Isoform-selective phosphoinositide 3-kinase inhibition ameliorates a broad range of fragile X syndrome-associated deficits in a mouse model
25. Muscleblind-like proteins use modular domains to localize RNAs by riding kinesins and docking to membranes
26. Antisense, but not sense, repeat expanded RNAs activate PKR/eIF2α-dependent ISR in C9ORF72 FTD/ALS
27. Therapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and Back
28. Increased Expression of the PI3K Enhancer PIKE Mediates Deficits in Synaptic Plasticity and Behavior in Fragile X Syndrome
29. A 3′ untranslated region variant in FMR1 eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuR
30. Altered Behavioral Responses Show GABA Sensitivity in Muscleblind-Like 2-Deficient Mice: Implications for CNS Symptoms in Myotonic Dystrophy
31. The RNA-binding protein, ZC3H14, is required for proper poly(A) tail length control, expression of synaptic proteins, and brain function in mice
32. Bidirectional Control of mRNA Translation and Synaptic Plasticity by the Cytoplasmic Polyadenylation Complex
33. Mechanisms Driving the Emergence of Neuronal Hyperexcitability in Fragile X Syndrome
34. Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humans
35. Plastin 3 Is a Protective Modifier of Autosomal Recessive Spinal Muscular Atrophy
36. Reversible Inhibition of PSD-95 mRNA Translation by miR-125a, FMRP Phosphorylation, and mGluR Signaling
37. Making and breaking synapses through local mRNA regulation
38. Fragile X Mental Retardation Protein Deficiency Leads to Excessive mGluR5-Dependent Internalization of AMPA Receptors
39. Extracellular Stimuli Specifically Regulate Localized Levels of Individual Neuronal mRNAs
40. Diversity on location
41. Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis
42. Single mRNAs Visualized by Ultrastructural in situ Hybridization Are Principally Localized at Actin Filament Intersections in Fibroblasts
43. Localization of HIV RNA in Mitochondria of Infected Cells: Potential Role in Cytopathogenicity
44. Genetic and acute CPEB1 depletion ameliorate fragile X pathophysiology
45. Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
46. Excess Protein Synthesis in FXS Patient Lymphoblastoid Cells Can Be Rescued with a p110β-Selective Inhibitor
47. Limited availability of ZBP1 restricts axonal mRNA localization and nerve regeneration capacity
48. S6K1 Phosphorylates and Regulates Fragile X Mental Retardation Protein (FMRP) with the Neuronal Protein Synthesis-dependent Mammalian Target of Rapamycin (mTOR) Signaling Cascade
49. A Direct Role for FMRP in Activity-Dependent Dendritic mRNA Transport Links Filopodial-Spine Morphogenesis to Fragile X Syndrome
50. Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
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