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 |
|
Hide low-probability matches. |