Masoud Shekarabi - Publications

Affiliations: 
Neuroscience McGill (Montreal Neuorological Institute) 
Area:
Neurobiology of Diseases

21/36 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Robinson JA, Guenthner G, Warfield R, Kublin JR, Smith MD, Shekarabi M, Miller AD, Burdo TH. Atrophy and death of non-peptidergic and peptidergic nociceptive neurons in SIV infection. The American Journal of Pathology. PMID 32246920 DOI: 10.1016/J.Ajpath.2020.03.004  0.347
2019 Mohseni Ahooyi T, Torkzaban B, Shekarabi M, Tahrir FG, Decoppet EA, Cotto B, Langford D, Amini S, Khalili K. Perturbation of synapsins homeostasis through HIV-1 Tat-mediated suppression of BAG3 in primary neuronal cells. Cell Death & Disease. 10: 473. PMID 31209204 DOI: 10.1038/S41419-019-1702-2  0.421
2018 Mohseni Ahooyi T, Shekarabi M, Torkzaban B, Langford TD, Burdo TH, Gordon J, Datta PK, Amini S, Khalili K. Dysregulation of Neuronal Cholesterol Homeostasis upon Exposure to HIV-1 Tat and Cocaine Revealed by RNA-Sequencing. Scientific Reports. 8: 16300. PMID 30390000 DOI: 10.1038/S41598-018-34539-9  0.313
2017 Ahooyi TM, Shekarabi M, Decoppet EA, Langford TD, Khalili K. Network Analysis of Hippocampal Neurons by Microelectrode Array in the Presence of HIV-1 Tat and Cocaine. Journal of Cellular Physiology. PMID 29206302 DOI: 10.1002/Jcp.26322  0.306
2017 Shekarabi M, Zhang J, Khanna AR, Ellison DH, Delpire E, Kahle KT. WNK Kinase Signaling in Ion Homeostasis and Human Disease. Cell Metabolism. 25: 285-299. PMID 28178566 DOI: 10.1016/J.Cmet.2017.01.007  0.328
2016 Auer RN, Laganière JL, Robitaille YO, Richardson J, Dion PA, Rouleau GA, Shekarabi M. 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. PMID 27230413 DOI: 10.1038/Modpathol.2016.90  0.414
2013 Salin-Cantegrel A, Shekarabi M, Rasheed S, Charron FM, Laganière J, Gaudet R, Dion PA, Lapointe JY, Rouleau GA. Potassium-chloride cotransporter 3 interacts with Vav2 to synchronize the cell volume decrease response with cell protrusion dynamics. Plos One. 8: e65294. PMID 23724134 DOI: 10.1371/Journal.Pone.0065294  0.452
2012 Shekarabi M, Moldrich RX, Rasheed S, Salin-Cantegrel A, Laganière J, Rochefort D, Hince P, Huot K, Gaudet R, Kurniawan N, Sotocinal SG, Ritchie J, Dion PA, Mogil JS, Richards LJ, et al. 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. PMID 22423107 DOI: 10.1523/Jneurosci.3679-11.2012  0.434
2011 Jarjour AA, Durko M, Luk TL, Marçal N, Shekarabi M, Kennedy TE. Autocrine netrin function inhibits glioma cell motility and promotes focal adhesion formation. Plos One. 6: e25408. PMID 21980448 DOI: 10.1371/Journal.Pone.0025408  0.602
2011 Rivière JB, Ramalingam S, Lavastre V, Shekarabi M, Holbert S, Lafontaine J, Srour M, Merner N, Rochefort D, Hince P, Gaudet R, Mes-Masson AM, Baets J, Houlden H, Brais B, et al. 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. PMID 21820098 DOI: 10.1016/J.Ajhg.2011.06.013  0.36
2011 Salin-Cantegrel A, Rivière JB, Shekarabi M, Rasheed S, Dacal S, Laganière J, Gaudet R, Rochefort D, Lesca G, Gaspar C, Dion PA, Lapointe JY, Rouleau GA. Transit defect of potassium-chloride Co-transporter 3 is a major pathogenic mechanism in hereditary motor and sensory neuropathy with agenesis of the corpus callosum. The Journal of Biological Chemistry. 286: 28456-65. PMID 21628467 DOI: 10.1074/Jbc.M111.226894  0.419
2011 Shekarabi M, Salin-Cantegrel A, Laganière J, Gaudet R, Dion P, Rouleau GA. Cellular expression of the K+-Cl- cotransporter KCC3 in the central nervous system of mouse. Brain Research. 1374: 15-26. PMID 21147077 DOI: 10.1016/J.Brainres.2010.12.010  0.417
2008 Salin-Cantegrel A, Shekarabi M, Holbert S, Dion P, Rochefort D, Laganière J, Dacal S, Hince P, Karemera L, Gaspar C, Lapointe JY, Rouleau GA. HMSN/ACC truncation mutations disrupt brain-type creatine kinase-dependant activation of K+/Cl- co-transporter 3. Human Molecular Genetics. 17: 2703-11. PMID 18566107 DOI: 10.1093/Hmg/Ddn172  0.364
2008 Shekarabi M, Girard N, Rivière JB, Dion P, Houle M, Toulouse A, Lafrenière RG, Vercauteren F, Hince P, Laganiere J, Rochefort D, Faivre L, Samuels M, Rouleau GA. Mutations in the nervous system--specific HSN2 exon of WNK1 cause hereditary sensory neuropathy type II. The Journal of Clinical Investigation. 118: 2496-505. PMID 18521183 DOI: 10.1172/Jci34088  0.361
2007 Salin-Cantegrel A, Rivière JB, Dupré N, Charron FM, Shekarabi M, Karéméra L, Gaspar C, Horst J, Tekin M, Deda G, Krause A, Lippert MM, Willemsen MA, Jarrar R, Lapointe JY, et al. Distal truncation of KCC3 in non-French Canadian HMSN/ACC families. Neurology. 69: 1350-5. PMID 17893295 DOI: 10.1212/01.Wnl.0000291779.35643.15  0.302
2005 Shekarabi M, Moore SW, Tritsch NX, Morris SJ, Bouchard JF, Kennedy TE. Deleted in colorectal cancer binding netrin-1 mediates cell substrate adhesion and recruits Cdc42, Rac1, Pak1, and N-WASP into an intracellular signaling complex that promotes growth cone expansion. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 3132-41. PMID 15788770 DOI: 10.1523/Jneurosci.1920-04.2005  0.649
2004 Bouchard JF, Moore SW, Tritsch NX, Roux PP, Shekarabi M, Barker PA, Kennedy TE. Protein kinase A activation promotes plasma membrane insertion of DCC from an intracellular pool: A novel mechanism regulating commissural axon extension. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 3040-50. PMID 15044543 DOI: 10.1523/Jneurosci.4934-03.2004  0.617
2002 Li X, Meriane M, Triki I, Shekarabi M, Kennedy TE, Larose L, Lamarche-Vane N. The adaptor protein Nck-1 couples the netrin-1 receptor DCC (deleted in colorectal cancer) to the activation of the small GTPase Rac1 through an atypical mechanism. The Journal of Biological Chemistry. 277: 37788-97. PMID 12149262 DOI: 10.1074/Jbc.M205428200  0.678
2002 Shekarabi M, Kennedy TE. The netrin-1 receptor DCC promotes filopodia formation and cell spreading by activating Cdc42 and Rac1. Molecular and Cellular Neurosciences. 19: 1-17. PMID 11817894 DOI: 10.1006/Mcne.2001.1075  0.663
1997 Shekarabi M, Bourbonnière M, Dagenais A, Nalbantoglu J. Transcriptional regulation of amyloid precursor protein during dibutyryl cyclic AMP-induced differentiation of NG108-15 cells Journal of Neurochemistry. 68: 970-978. PMID 9048742 DOI: 10.1046/J.1471-4159.1997.68030970.X  0.338
1997 Bourbonnière M, Shekarabi M, Nalbantoglu J. Enhanced expression of amyloid precursor protein in response to dibutyryl cyclic AMP is not mediated by the transcription factor AP-2 Journal of Neurochemistry. 68: 909-916. PMID 9048735 DOI: 10.1046/J.1471-4159.1997.68030909.X  0.315
Low-probability matches (unlikely to be authored by this person)
2011 Hamdan FF, Gauthier J, Araki Y, Lin DT, Yoshizawa Y, Higashi K, Park AR, Spiegelman D, Dobrzeniecka S, Piton A, Tomitori H, Daoud H, Massicotte C, Henrion E, Diallo O, ... ... Shekarabi M, et al. Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability. American Journal of Human Genetics. 88: 306-16. PMID 21376300 DOI: 10.1016/J.Ajhg.2011.03.011  0.29
2016 Roehm PC, Shekarabi M, Wollebo HS, Bellizzi A, He L, Salkind J, Khalili K. Inhibition of HSV-1 Replication by Gene Editing Strategy. Scientific Reports. 6: 23146. PMID 27064617 DOI: 10.1038/Srep23146  0.286
2019 Shekarabi M, Robinson JA, Smith MD, Burdo TH. SIV-mediated synaptic dysfunction is associated with an increase in synapsin site 1 phosphorylation and impaired PP2A activity. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 31270156 DOI: 10.1523/Jneurosci.0178-19.2019  0.284
2013 Shekarabi M, Lafrenière RG, Gaudet R, Laganière J, Marcinkiewicz MM, Dion PA, Rouleau GA. Comparative analysis of the expression profile of Wnk1 and Wnk1/Hsn2 splice variants in developing and adult mouse tissues. Plos One. 8: e57807. PMID 23451271 DOI: 10.1371/Journal.Pone.0057807  0.275
2004 Rivière JB, Verlaan DJ, Shekarabi M, Lafrenière RG, Bénard M, Der Kaloustian VM, Shbaklo Z, Rouleau GA. A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family. Annals of Neurology. 56: 572-5. PMID 15455397 DOI: 10.1002/Ana.20237  0.274
2012 Shekarabi M, Dion PA, Rouleau GA. Letter to the editors: comment on "hereditary sensory and autonomic neuropathy II due to novel mutation in the HSN2 gene in Mexican families". Journal of Neurology. 259: 565-6. PMID 21847616 DOI: 10.1007/S00415-011-6206-7  0.263
2009 Rivière JB, Dion P, Shekarabi M, Girard N, Faivre L, Lafrenière RG, Samuels M, Rouleau GA. [Mutations in the HSN2 exon of WNK1 cause hereditary sensory neuropathy type II]. Mã©Decine Sciences : M/S. 25: 235-8. PMID 19361385 DOI: 10.1051/Medsci/2009253235  0.261
2018 Kearns AC, Robinson JA, Shekarabi M, Liu F, Qin X, Burdo TH. Caspase-1-associated immune activation in an accelerated SIV-infected rhesus macaque model. Journal of Neurovirology. PMID 29611111 DOI: 10.1007/S13365-018-0630-8  0.247
2019 Abu-Baker A, Kharma N, Perreault J, Grant A, Shekarabi M, Maios C, Dona M, Neri C, Dion PA, Parker A, Varin L, Rouleau GA. RNA-Based Therapy Utilizing Oculopharyngeal Muscular Dystrophy Transcript Knockdown and Replacement. Molecular Therapy. Nucleic Acids. 15: 12-25. PMID 30831428 DOI: 10.1016/J.Omtn.2019.02.003  0.238
2020 Torkzaban B, Natarajaseenivasan K, Mohseni Ahooyi T, Shekarabi M, Amini S, Langford TD, Khalili K. The lncRNA LOC102549805 (U1) modulates neurotoxicity of HIV-1 Tat protein. Cell Death & Disease. 11: 835. PMID 33033233 DOI: 10.1038/s41419-020-03033-4  0.23
2021 Shekarabi M, Robinson JA, Burdo TH. Isolation and Culture of Dorsal Root Ganglia (DRG) from Rodents. Methods in Molecular Biology (Clifton, N.J.). 2311: 177-184. PMID 34033086 DOI: 10.1007/978-1-0716-1437-2_14  0.226
1997 Bourbonnière M, Shekarabi M, Nalbantoglu J. Determination of molecular weights of nucleic acid-binding proteins by UV photo-crosslinking and SDS-PAGE Biotechniques. 23: 60-62. PMID 9232228 DOI: 10.2144/97231Bm11  0.204
2019 Bagheri Y, Babaha F, Falak R, Yazdani R, Azizi G, Sadri M, Abolhassani H, Shekarabi M, Aghamohammadi A. IL-10 induces TGF-β secretion, TGF-β receptor II upregulation, and IgA secretion in B cells. European Cytokine Network. 30: 107-113. PMID 31957700 DOI: 10.1684/ecn.2019.0434  0.114
2020 Samei A, Fallahpour M, Bolouri MR, Mahmoudi AR, Nasri F, Seif F, Khoshmirsafa M, Batooli H, Shekarabi M, Falak R. Evaluating the Immunoreactivity of Ailanthus Altissima (The Tree of Heaven) Pollen Extract in Atopic Patients. Iranian Journal of Allergy, Asthma, and Immunology. 19: 132-138. PMID 32372626 DOI: 10.18502/ijaai.v19i2.2763  0.079
2015 Shekarabi M. Potential Application of Novel DNA Editing Techniques in Translational Neuroscience. Basic and Clinical Neuroscience. 6: 4-5. PMID 27375845  0.02
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