Joseph J. LoTurco

University of Connecticut, Storrs, CT, United States 
"Joseph LoTurco"
Mean distance: 13.1 (cluster 11)
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Rendall AR, Perrino PA, LoTurco JJ, et al. (2017) Evaluation of visual motion perception ability in mice with knockout of the dyslexia candidate susceptibility gene Dcdc2. Genes, Brain, and Behavior
Fekete CD, Goz RU, Dinallo S, et al. (2016) In vivo transgenic expression of collybistin in neurons of the rat cerebral cortex. The Journal of Comparative Neurology
Centanni TM, Booker AB, Chen F, et al. (2016) Knockdown of Dyslexia-Gene Dcdc2 Interferes with Speech Sound Discrimination in Continuous Streams. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 4895-906
Chen F, Becker A, LoTurco J. (2016) Overview of Transgenic Glioblastoma and Oligoastrocytoma CNS Models and Their Utility in Drug Discovery. Current Protocols in Pharmacology / Editorial Board, S.J. Enna (Editor-in-Chief) ... [Et Al.]. 72: 14.37.1-12
Chen F, Rosiene J, Che A, et al. (2015) Tracking and transforming neocortical progenitors by CRISPR/Cas9 gene targeting and PiggyBac transposase lineage labeling. Development (Cambridge, England)
Che A, Truong DT, Fitch RH, et al. (2015) Mutation of the Dyslexia-Associated Gene Dcdc2 Enhances Glutamatergic Synaptic Transmission Between Layer 4 Neurons in Mouse Neocortex. Cerebral Cortex (New York, N.Y. : 1991)
Rendall AR, Tarkar A, Contreras-Mora HM, et al. (2015) Deficits in learning and memory in mice with a mutation of the candidate dyslexia susceptibility gene Dyx1c1. Brain and Language
Malyshev A, Goz R, LoTurco JJ, et al. (2015) Advantages and limitations of the use of optogenetic approach in studying fast-scale spike encoding. Plos One. 10: e0122286
Fekete CD, Chiou TT, Miralles CP, et al. (2015) In vivo clonal overexpression of neuroligin 3 and neuroligin 2 in neurons of the rat cerebral cortex: Differential effects on GABAergic synapses and neuronal migration. The Journal of Comparative Neurology. 523: 1359-78
Schueler M, Braun DA, Chandrasekar G, et al. (2015) DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling. American Journal of Human Genetics. 96: 81-92
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