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Wednesday 22 Nov

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François Gros-Louis

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Principal area
Regenerative medecine
Address
Hôpital de l'Enfant-Jésus
1401, 18e Rue, Local R-211 LOEX / CMDGT
Québec (Québec)
CANADA G1J 1Z4

Phone
+1 418-990-8255, poste 61708
Fax
Email
francois.gros-louis@fmed.ulaval.ca

Research project(s) recognized by Université Laval (in French)

Other active research project(s)

No active project

Recent publications (see all publication from this researcher)

Pare B, Gros-Louis F. Potential skin involvement in ALS: revisiting Charcot's observation - a review of skin abnormalities in ALS. Reviews in the neurosciences,  2017. 28: 551-572
Ohta Y, Soucy G, Phaneuf D, Audet JN, Gros-Louis F, Rouleau GA, Blasco H, Corcia P, Andersen PM, Nordin F, Yamashita T, Abe K, Julien JP. Sex-dependent effects of chromogranin B P413L allelic variant as disease modifier in amyotrophic lateral sclerosis. Human molecular genetics,  2016. 25: 4771-4786
Pare B, Deschenes LT, Pouliot R, Dupre N, Gros-Louis F. An Optimized Approach to Recover Secreted Proteins from Fibroblast Conditioned-Media for Secretomic Analysis. Frontiers in cellular neuroscience,  2016. 10: 70
Beaudet MJ, Yang Q, Cadau S, Blais M, Bellenfant S, Gros-Louis F, Berthod F. High yield extraction of pure spinal motor neurons, astrocytes and microglia from single embryo and adult mouse spinal cord. Scientific reports,  2015. 5: 16763
Pare B, Touzel-Deschenes L, Lamontagne R, Lamarre MS, Scott FD, Khuong HT, Dion PA, Bouchard JP, Gould P, Rouleau GA, Dupre N, Berthod F, Gros-Louis F. Early detection of structural abnormalities and cytoplasmic accumulation of TDP-43 in tissue-engineered skins derived from ALS patients. Acta neuropathologica communications,  2015. 3: 5
Paré B, Berthod F, Gros-Louis F. The relation between ALS and the skin: a novel human in vitro model to identify new biomarkers Journal of molecular biomarkers & diagnosis,  2015. 6: 1000e121
Saxena S, Roselli F, Singh K, Leptien K, Julien JP, Gros-Louis F, Caroni P. Neuroprotection through excitability and mTOR required in ALS motoneurons to delay disease and extend survival. Neuron,  2013. 80: 80-96
Kabashi E, El Oussini H, Bercier V, Gros-Louis F, Valdmanis PN, McDearmid J, Mejier IA, Dion PA, Dupre N, Hollinger D, Sinniger J, Dirrig-Grosch S, Camu W, Meininger V, Loeffler JP, Rene F, Drapeau P, Rouleau GA, Dupuis L. Investigating the contribution of VAPB/ALS8 loss of function in amyotrophic lateral sclerosis. Human molecular genetics,  2013. 22: 2350-60
Berthod F, Gros-Louis F. In vivo and in vitro models to study amyotrophic lateral sclerosis (Chapter 4) In: Maurer M, ed.  Amyotrophic Lateral Sclerosis : InTech, 2012. p.81-124.
Daoud H, Valdmanis PN, Gros-Louis F, Belzil V, Spiegelman D, Henrion E, Diallo O, Desjarlais A, Gauthier J, Camu W, Dion PA, Rouleau GA. Resequencing of 29 candidate genes in familial and sporadic ALS patients Archives of neurology,  2011. 68: 
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