Masoud Shekarabi

Affiliations: 
Neuroscience McGill (Montreal Neuorological Institute) 
Area:
Neurobiology of Diseases
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"Masoud Shekarabi"
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Publications

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Robinson JA, Guenthner G, Warfield R, et al. (2020) Atrophy and death of non-peptidergic and peptidergic nociceptive neurons in SIV infection. The American Journal of Pathology
Mohseni Ahooyi T, Torkzaban B, Shekarabi M, et al. (2019) Perturbation of synapsins homeostasis through HIV-1 Tat-mediated suppression of BAG3 in primary neuronal cells. Cell Death & Disease. 10: 473
Mohseni Ahooyi T, Shekarabi M, Torkzaban B, et al. (2018) Dysregulation of Neuronal Cholesterol Homeostasis upon Exposure to HIV-1 Tat and Cocaine Revealed by RNA-Sequencing. Scientific Reports. 8: 16300
Ahooyi TM, Shekarabi M, Decoppet EA, et al. (2017) Network Analysis of Hippocampal Neurons by Microelectrode Array in the Presence of HIV-1 Tat and Cocaine. Journal of Cellular Physiology
Shekarabi M, Zhang J, Khanna AR, et al. (2017) WNK Kinase Signaling in Ion Homeostasis and Human Disease. Cell Metabolism. 25: 285-299
Auer RN, Laganière JL, Robitaille YO, et al. (2016) KCC3 axonopathy: neuropathological features in the central and peripheral nervous system. Modern Pathology : An Official Journal of the United States and Canadian Academy of Pathology, Inc
Salin-Cantegrel A, Shekarabi M, Rasheed S, et al. (2013) Potassium-chloride cotransporter 3 interacts with Vav2 to synchronize the cell volume decrease response with cell protrusion dynamics. Plos One. 8: e65294
Shekarabi M, Moldrich RX, Rasheed S, et al. (2012) Loss of neuronal potassium/chloride cotransporter 3 (KCC3) is responsible for the degenerative phenotype in a conditional mouse model of hereditary motor and sensory neuropathy associated with agenesis of the corpus callosum. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 3865-76
Jarjour AA, Durko M, Luk TL, et al. (2011) Autocrine netrin function inhibits glioma cell motility and promotes focal adhesion formation. Plos One. 6: e25408
Rivière JB, Ramalingam S, Lavastre V, et al. (2011) KIF1A, an axonal transporter of synaptic vesicles, is mutated in hereditary sensory and autonomic neuropathy type 2. American Journal of Human Genetics. 89: 219-30
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