Jean-Yves Lapointe

Affiliations: 
Physics Université de Montréal, Montréal, Canada 
Area:
General Biophysics
Website:
http://en.phys.umontreal.ca/department-directory/vue/lapointe-jean-yves/
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"Jean-Yves Lapointe"
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Raynald Laprade grad student 1984 Université de Montréal
 (Étude des résistances électriques membranaires et transepithéliales chez le tubule contourne proximal de lapin en microperfusion in vitro.)
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Publications

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Coady MJ, Wallendorff B, Lapointe JY. (2017) Characterization of the Transport Activity of SGLT2/MAP17, the Renal Low-Affinity Na+/Glucose Cotransporter. American Journal of Physiology. Renal Physiology. ajprenal.00628.2016
Coady MJ, El Tarazi A, Santer R, et al. (2016) MAP17 Is a Necessary Activator of Renal Na+/Glucose Cotransporter SGLT2. Journal of the American Society of Nephrology : Jasn
Sasseville LJ, Morin M, Coady MJ, et al. (2016) The Human Sodium-Glucose Cotransporter (hSGLT1) Is a Disulfide-Bridged Homodimer with a Re-Entrant C-Terminal Loop. Plos One. 11: e0154589
Sasseville LJ, Longpré JP, Wallendorff B, et al. (2014) The transport mechanism of the human sodium/myo-inositol transporter 2 (SMIT2/SGLT6), a member of the LeuT structural family. American Journal of Physiology. Cell Physiology. 307: C431-41
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
Sasseville LJ, Coady MJ, Blunck R, et al. (2013) FRET Quenching by a Hybrid Voltage Sensor (Hvos) Reveals that the Na/Glucose Cotransporter (SGLT1) Is a Disulfide-Bridged Homodimer with Re-Entrant 12-13 Loop Biophysical Journal. 104: 223a
Longpré JP, Sasseville LJ, Lapointe JY. (2012) Simulated annealing reveals the kinetic activity of SGLT1, a member of the LeuT structural family. The Journal of General Physiology. 140: 361-74
Sasseville LJ, Cuervo JE, Lapointe JY, et al. (2011) The structural pathway for water permeation through sodium-glucose cotransporters. Biophysical Journal. 101: 1887-95
Salin-Cantegrel A, Rivière JB, Shekarabi M, et al. (2011) 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
Longpré JP, Lapointe JY. (2011) Determination of the Na(+)/glucose cotransporter (SGLT1) turnover rate using the ion-trap technique. Biophysical Journal. 100: 52-9
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