James I. Morgan

Developmental Neurobiology St Jude, Garden Grove, CA, United States 
"James Morgan"
Mean distance: 16.58 (cluster 11)
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Pattarini R, Rong Y, Shepherd KR, et al. (2012) Long-lasting transcriptional refractoriness triggered by a single exposure to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyrimidine. Neuroscience. 214: 84-105
Wei P, Rong Y, Li L, et al. (2009) Characterization of trans-neuronal trafficking of Cbln1. Molecular and Cellular Neurosciences. 41: 258-73
Iscru E, Serinagaoglu Y, Schilling K, et al. (2009) Sensorimotor enhancement in mouse mutants lacking the Purkinje cell-specific Gi/o modulator, Pcp2(L7). Molecular and Cellular Neurosciences. 40: 62-75
Wei P, Smeyne RJ, Bao D, et al. (2007) Mapping of Cbln1-like immunoreactivity in adult and developing mouse brain and its localization to the endolysosomal compartment of neurons. The European Journal of Neuroscience. 26: 2962-78
Pattarini R, Smeyne RJ, Morgan JI. (2007) Temporal mRNA profiles of inflammatory mediators in the murine 1-methyl-4-phenyl-1,2,3,6-tetrahydropyrimidine model of Parkinson's disease. Neuroscience. 145: 654-68
Wang T, Morgan JI. (2007) The Purkinje cell degeneration (pcd) mouse: an unexpected molecular link between neuronal degeneration and regeneration. Brain Research. 1140: 26-40
Wang T, Parris J, Li L, et al. (2006) The carboxypeptidase-like substrate-binding site in Nna1 is essential for the rescue of the Purkinje cell degeneration (pcd) phenotype. Molecular and Cellular Neurosciences. 33: 200-13
Rong Y, Wang T, Morgan JI. (2004) Identification of candidate Purkinje cell-specific markers by gene expression profiling in wild-type and pcd(3J) mice. Brain Research. Molecular Brain Research. 132: 128-45
Tomomura M, Rice DS, Morgan JI, et al. (2001) Purification of Purkinje cells by fluorescence-activated cell sorting from transgenic mice that express green fluorescent protein. The European Journal of Neuroscience. 14: 57-63
Soares HD, Chen SC, Morgan JI. (2001) Differential and prolonged expression of Fos-lacZ and Jun-lacZ in neurons, glia, and muscle following sciatic nerve damage. Experimental Neurology. 167: 1-14
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