31 results on '"Bassell, Gary J."'
Search Results
2. Efficient generation of a self-organizing neuromuscular junction model from human pluripotent stem cells
3. Muscleblind-like proteins use modular domains to localize RNAs by riding kinesins and docking to membranes
4. Correction to: Isoform-selective phosphoinositide 3-kinase inhibition ameliorates a broad range of fragile X syndrome-associated deficits in a mouse model
5. Metabolic effects of the schizophrenia-associated 3q29 deletion
6. Remembering Stephen T. Warren, a pillar of neurogenetics (1953–2021)
7. A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies
8. FMRP attenuates activity dependent modifications in the mitochondrial proteome
9. Cortical neurons derived from human pluripotent stem cells lacking FMRP display altered spontaneous firing patterns
10. A native function for RAN translation and CGG repeats in regulating fragile X protein synthesis
11. CRISPR-mediated gene correction links the ATP7A M1311V mutations with amyotrophic lateral sclerosis pathogenesis in one individual
12. Biased modulators of NMDA receptors control channel opening and ion selectivity
13. Behavioral changes and growth deficits in a CRISPR engineered mouse model of the schizophrenia-associated 3q29 deletion
14. Isoform-selective phosphoinositide 3-kinase inhibition ameliorates a broad range of fragile X syndrome-associated deficits in a mouse model
15. ZBP1 phosphorylation at serine 181 regulates its dendritic transport and the development of dendritic trees of hippocampal neurons
16. Trehalose upregulates progranulin expression in human and mouse models of GRN haploinsufficiency: a novel therapeutic lead to treat frontotemporal dementia
17. Increased expression of the PI3K catalytic subunit p110δ underlies elevated S6 phosphorylation and protein synthesis in an individual with autism from a multiplex family
18. Dysregulation and restoration of translational homeostasis in fragile X syndrome
19. Therapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and Back
20. Genetic and acute CPEB1 depletion ameliorate fragile X pathophysiology
21. Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis
22. Excess Protein Synthesis in FXS Patient Lymphoblastoid Cells Can Be Rescued with a p110β-Selective Inhibitor
23. Fragile balance: RNA editing tunes the synapse
24. Regulation of chemotropic guidance of nerve growth cones by microRNA
25. Automated 4D analysis of dendritic spine morphology: applications to stimulus-induced spine remodeling and pharmacological rescue in a disease model
26. Therapeutic Strategies in Fragile X Syndrome: Dysregulated mGluR Signaling and Beyond
27. High-efficiency transfection of cultured primary motor neurons to study protein localization, trafficking, and function
28. Single molecule–sensitive probes for imaging RNA in live cells
29. Reducing glutamate signaling pays off in fragile X
30. An essential role for β-actin mRNA localization and translation in Ca2+-dependent growth cone guidance
31. Spatial regulation of β-actin translation by Src-dependent phosphorylation of ZBP1
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