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Journal of Fish Biology|December 16, 2016
Feeding ecology of silky sharks Carcharhinus falciformis associated with floating objects in the western Indian OceanJ D Filmalter, P D Cowley, M Potier, et al.
The Biochemical Journal|May 1, 1986
Molecular size of N-acetylglucosaminylphosphotransferase and alpha-N-acetylglucosaminyl phosphodiesterase as determined in situ in Golgi membranes by radiation inactivationY Ben-Yoseph, M Potier, B A Pack, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1982
Oral lecithin and linoleic acid in Friedreich's ataxia: II. Clinical resultsS B Melancon, M Vanasse, G Geoffroy, et al.
The Journal of Clinical Investigation|August 1, 1992
An unusual splicing mutation in the HEXB gene is associated with dramatically different phenotypes in patients from different racial backgroundsB McInnes, M Potier, N Wakamatsu, et al.
Analytical Biochemistry|September 20, 1995
Continuous spectrophotometric assay of human lysosomal cathepsin A/protective protein in normal and galactosialidosis cellsA V Pshezhetsky, M V Vinogradova, M A Elsliger, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|January 1, 1996
Radiation inactivation and in situ renaturation of protein tyrosine kinases reveal a major 50-kDa enzyme as part of a membrane complex present in dividing but not in resting prostatic epithelial cellsL T Nguyen, G Beauregard, S Tessier, et al.
Current Medicinal Chemistry|December 30, 2011
Targeting SKCa channels in cancer: potential new therapeutic approachesA Girault, J-P Haelters, M Potier-Cartereau, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1979
Dicarboxylic amino acid uptake in normal, Friedreich's ataxia, and dicarboxylic aminoaciduria fibroblastsS B Melancon, B Grenier, L Dallaire, et al.
Enzyme|January 1, 1986
Characterization of the mutant N-acetylglucosaminylphosphotransferase in I-cell disease and pseudo-Hurler polydystrophy: complementation analysis and kinetic studiesY Ben-Yoseph, B A Pack, D A Mitchell, et al.
Human Molecular Genetics|February 28, 1998
Cloning of the cDNA and gene encoding mouse lysosomal sialidase and correction of sialidase deficiency in human sialidosis and mouse SM/J fibroblastsS A Igdoura, C Gafuik, C Mertineit, et al.
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