Serge Gravel

Chronic PMA treatment of Jurkat T lymphocytes results in decreased protein tyrosine phosphorylation and inhibition of CD3‐ but not Ti‐dependent antibody‐triggered Ca2+ signaling

P. Giguère, T. Fülöp, G. Dupuis, 2000, Journal of leukocyte biology.

Molecular diagnosis of muscular diseases in outpatient clinics

P. Jacques, S. Lévesque, F. Thuriot, 2020, Neurology: Genetics.

Molecular Diagnosis of Pompe Disease in the Genomic Era: Correlation with Acid Alpha-Glucosidase Activity in Dried Blood Spots

S. Lévesque, F. Thuriot, Elaine Gravel, 2021, Journal of clinical medicine.

Discovery of a novel and potent series of thieno[3,2-b]pyridine-based inhibitors of c-Met and VEGFR2 tyrosine kinases.

M. Robert, A. Macleod, A. Vaisburg, 2008, Bioorganic & medicinal chemistry letters.

A Canadian perspective

P. Jacques, S. Lévesque, F. Thuriot, 2020 .

Glutaric Aciduria Type 3: Three Unrelated Canadian Cases, with Different Routes of Ascertainment.

Thomas M. Kitzler, P. Waters, Y. Trakadis, 2018, JIMD reports.

Methylmalonyl-coA epimerase deficiency: A new case, with an acute metabolic presentation and an intronic splicing mutation in the MCEE gene

S. Lévesque, F. Thuriot, P. Waters, 2016, Molecular genetics and metabolism reports.

HSD10 mitochondrial disease: p.Leu122Val variant, mild clinical phenotype, and founder effect in French‐Canadian patients from Quebec

S. Lévesque, B. Maranda, P. Waters, 2019, Molecular genetics & genomic medicine.

Wide Spectrum of DUOX2 Deficiency: From Life-Threatening Compressive Goiter in Infancy to Lifelong Euthyroidism.

S. Lévesque, G. Szinnai, K. Heinimann, 2019, Thyroid : official journal of the American Thyroid Association.