593 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. A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies
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. The M1311V variant of ATP7A is associated with impaired trafficking and copper homeostasis in models of motor neuron disease
11. TBK1 interacts with tau and enhances neurodegeneration in tauopathy
12. ALS‐linked KIF5A ΔExon27 mutant causes neuronal toxicity through gain‐of‐function
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. FMRP attenuates activity dependent modifications in the mitochondrial proteome
20. Caregiver Perspectives on a Childʼs Diagnosis of 3q29 Deletion: “We Canʼt Just Wish This Thing Away”
21. Rab11 regulates autophagy at dendritic spines in an mTOR- and NMDA-dependent manner
22. Crosstalk of Local Translation and Mitochondria: Powering Plasticity in Axons and Dendrites
23. Aberrant RNA translation in fragile X syndrome: From FMRP mechanisms to emerging therapeutic strategies
24. Correction to: Isoform-selective phosphoinositide 3-kinase inhibition ameliorates a broad range of fragile X syndrome-associated deficits in a mouse model
25. Familiarity with a Vocal Category Biases the Compartmental Expression of 'Arc/Arg3.1' in Core Auditory Cortex
26. Biased modulators of NMDA receptors control channel opening and ion selectivity
27. Where to start? Activity-dependent alternative translation initiation generates multifunctional proteoforms in the brain.
28. Remembering Stephen T. Warren, a pillar of neurogenetics (1953–2021)
29. The Conserved, Disease-Associated RNA Binding Protein dNab2 Interacts with the Fragile X Protein Ortholog in Drosophila Neurons
30. A Predominantly Nuclear Protein Affecting Cytoplasmic Localization of β-Actin mRNA in Fibroblasts and Neurons
31. CRISPR-mediated gene correction links the ATP7A M1311V mutations with amyotrophic lateral sclerosis pathogenesis in one individual
32. Cortical neurons derived from human pluripotent stem cells lacking FMRP display altered spontaneous firing patterns
33. Isoform-selective phosphoinositide 3-kinase inhibition ameliorates a broad range of fragile X syndrome-associated deficits in a mouse model
34. Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion
35. Muscleblind-like proteins use modular domains to localize RNAs by riding kinesins and docking to membranes
36. A role for the survival of motor neuron protein in mRNP assembly and transport
37. Antisense, but not sense, repeat expanded RNAs activate PKR/eIF2α-dependent ISR in C9ORF72 FTD/ALS
38. Author response: Antisense, but not sense, repeat expanded RNAs activate PKR/eIF2α-dependent ISR in C9ORF72 FTD/ALS
39. Therapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and Back
40. Increased Expression of the PI3K Enhancer PIKE Mediates Deficits in Synaptic Plasticity and Behavior in Fragile X Syndrome
41. A 3′ untranslated region variant in FMR1 eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuR
42. Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion
43. Spinal Muscular Atrophy and a Model for Survival of Motor Neuron Protein Function in Axonal Ribonucleoprotein Complexes
44. Altered Behavioral Responses Show GABA Sensitivity in Muscleblind-Like 2-Deficient Mice: Implications for CNS Symptoms in Myotonic Dystrophy
45. Neuronal RNA Localization and the Cytoskeleton
46. The RNA-binding protein, ZC3H14, is required for proper poly(A) tail length control, expression of synaptic proteins, and brain function in mice
47. The Fragile X Syndrome: From Molecular Genetics to Neurobiology
48. Bidirectional Control of mRNA Translation and Synaptic Plasticity by the Cytoplasmic Polyadenylation Complex
49. Spinal muscular atrophy: The role of SMN in axonal mRNA regulation
50. Muscleblind-like proteins use modular domains to localize RNAs by riding kinesins and docking to membranes
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