Jean Pierre Julien, PhD

Affiliations: 
 
Area:
neurodegeneration
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"Jean Pierre Julien"
Mean distance: 17.16 (cluster 32)
 
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Publications

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Dutta K, Thammisetty SS, Boutej H, et al. (2020) Mitigation of ALS pathology by neuron-specific inhibition of nuclear factor kappa B signaling. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience
Dutta K, Patel P, Rahimian R, et al. (2016) Withania somnifera Reverses Transactive Response DNA Binding Protein 43 Proteinopathy in a Mouse Model of Amyotrophic Lateral Sclerosis/Frontotemporal Lobar Degeneration. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics
Millecamps S, Robertson J, Lariviere R, et al. (2006) Defective axonal transport of neurofilament proteins in neurons overexpressing peripherin. Journal of Neurochemistry. 98: 926-38
Sasaki T, Gotow T, Shiozaki M, et al. (2006) Aggregate formation and phosphorylation of neurofilament-L Pro22 Charcot-Marie-Tooth disease mutants. Human Molecular Genetics. 15: 943-52
Veglianese P, Lo Coco D, Bao Cutrona M, et al. (2006) Activation of the p38MAPK cascade is associated with upregulation of TNF alpha receptors in the spinal motor neurons of mouse models of familial ALS. Molecular and Cellular Neurosciences. 31: 218-31
Kriz J, Beaulieu JM, Julien JP, et al. (2005) Up-regulation of peripherin is associated with alterations in synaptic plasticity in CA1 and CA3 regions of hippocampus. Neurobiology of Disease. 18: 409-20
Nguyen MD, Shu T, Sanada K, et al. (2004) A NUDEL-dependent mechanism of neurofilament assembly regulates the integrity of CNS neurons. Nature Cell Biology. 6: 595-608
Zhang G, Spencer PH, Jin LQ, et al. (2004) The single neurofilament subunit of lamprey may need another element for filament assembly. The Journal of Comparative Neurology. 471: 188-200
Lariviere RC, Julien JP. (2004) Functions of intermediate filaments in neuronal development and disease. Journal of Neurobiology. 58: 131-48
Larivière RC, Beaulieu JM, Nguyen MD, et al. (2003) Peripherin is not a contributing factor to motor neuron disease in a mouse model of amyotrophic lateral sclerosis caused by mutant superoxide dismutase. Neurobiology of Disease. 13: 158-66
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