278 results on '"Bassell, Gary J."'
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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. Rab11 regulates autophagy at dendritic spines in an mTOR- and NMDA-dependent manner
24. Crosstalk of Local Translation and Mitochondria: Powering Plasticity in Axons and Dendrites
25. Aberrant RNA translation in fragile X syndrome: From FMRP mechanisms to emerging therapeutic strategies
26. Familiarity with a Vocal Category Biases the Compartmental Expression of 'Arc/Arg3.1' in Core Auditory Cortex
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. Cross-species analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion
30. The Conserved, Disease-Associated RNA Binding Protein dNab2 Interacts with the Fragile X Protein Ortholog in Drosophila 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. Muscleblind-like proteins use modular domains to localize RNAs by riding kinesins and docking to membranes
35. A role for the survival of motor neuron protein in mRNP assembly and transport
36. Antisense, but not sense, repeat expanded RNAs activate PKR/eIF2α-dependent ISR in C9ORF72 FTD/ALS
37. Author response: Antisense, but not sense, repeat expanded RNAs activate PKR/eIF2α-dependent ISR in C9ORF72 FTD/ALS
38. Therapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and Back
39. Increased Expression of the PI3K Enhancer PIKE Mediates Deficits in Synaptic Plasticity and Behavior in Fragile X Syndrome
40. A 3′ untranslated region variant in FMR1 eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuR
41. Cross-species transcriptomic analysis identifies mitochondrial dysregulation as a functional consequence of the schizophrenia-associated 3q29 deletion
42. Altered Behavioral Responses Show GABA Sensitivity in Muscleblind-Like 2-Deficient Mice: Implications for CNS Symptoms in Myotonic Dystrophy
43. The RNA-binding protein, ZC3H14, is required for proper poly(A) tail length control, expression of synaptic proteins, and brain function in mice
44. Muscleblind-like proteins use modular domains to localize RNAs by riding kinesins and docking to membranes
45. Antisense, but not sense, repeat expanded RNAs activate PKR/eIF2α-dependent integrated stress response in C9orf72 FTD/ALS
46. Mechanisms Driving the Emergence of Neuronal Hyperexcitability in Fragile X Syndrome
47. ALS-linked KIF5A ΔExon27 mutant causes neuronal toxicity through gain of function
48. Diversity on location
49. Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis
50. Hexanucleotide Repeat Expansions in c9FTD/ALS and SCA36 Confer Selective Patterns of Neurodegeneration In Vivo
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