Gary J. Bassell, Ph.D.

Cell Biology Emory University School of Medicine, Atlanta, GA, United States 
mRNA transport, local protein synthesis
"Gary Bassell"
Mean distance: 15.81 (cluster 11)
Cross-listing: Chemistry Tree

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Edokpolor KS, Banerjee A, McEachin ZT, et al. (2022) Altered behavioral responses show GABA sensitivity in Muscleblind-like 2 deficient mice: Implications for CNS symptoms in myotonic dystrophy. Eneuro
Pant DC, Parameswaran J, Rao L, et al. (2022) ALS-linked KIF5A ΔExon27 mutant causes neuronal toxicity through gain-of-function. Embo Reports. e54234
Gross C, Banerjee A, Tiwari D, et al. (2022) Correction to: Isoform-selective phosphoinositide 3-kinase inhibition ameliorates a broad range of fragile X syndrome-associated deficits in a mouse model. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
Bülow P, Segal M, Bassell GJ. (2022) Mechanisms Driving the Emergence of Neuronal Hyperexcitability in Fragile X Syndrome. International Journal of Molecular Sciences. 23
Pollak RM, Purcell RH, Rutkowski TP, et al. (2022) Metabolic effects of the schizophrenia-associated 3q29 deletion. Translational Psychiatry. 12: 66
Yoon YJ, Bassell GJ. (2022) Diversity on location. Elife. 11
Kang Y, Zhou Y, Li Y, et al. (2021) A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies. Nature Neuroscience
Glassford MR, Purcell RH, Pass S, et al. (2021) Caregiver Perspectives on a Child's Diagnosis of 3q29 Deletion: "We Can't Just Wish This Thing Away". Journal of Developmental and Behavioral Pediatrics : Jdbp
Sefik E, Purcell RH, et al. (2021) Convergent and distributed effects of the 3q29 deletion on the human neural transcriptome. Translational Psychiatry. 11: 357
Raj N, McEachin ZT, Harousseau W, et al. (2021) Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis. Cell Reports. 35: 108991
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