Zobrazeno 1 - 10
of 44
pro vyhledávání: '"René Gagnon"'
Autor:
François Normand-Lauzière, Frédérique Frisch, Sébastien M Labbé, Patrick Bherer, René Gagnon, Stephen C Cunnane, André C Carpentier
Publikováno v:
PLoS ONE, Vol 5, Iss 6, p e10956 (2010)
It has been proposed that abnormal postprandial plasma nonesterified fatty acid (NEFA) metabolism may participate in the development of tissue lipotoxicity and type 2 diabetes (T2D). We previously found that non-diabetic offspring of two parents with
Externí odkaz:
https://doaj.org/article/ac7a9a3922b84b06a274292f9f62fb91
Autor:
Topwe Milongwe Mwene-Mbeja, Claude Spino, Donald Poirier, Emery Kalonda Mutombo, Jenny Roy, Kanyinda Mulowayi, Kasongo Kaseya, Marsi Mbayo Kitambala, René Gagnon
Publikováno v:
Clinical Microbiology and Research. :1-5
The main objective of this study was to extract the essential oils from Clerodendrum formicarum and Syzygium cordatum in order to determine the anticancer activity and establish the chemical constituents of that kind of essential oils. Hence, we have
Autor:
René Gagnon
Publikováno v:
Terrains. 16:77-97
Quelles traces laisse le passage d’un anthropologue ou d’un ethnologue dans une communauté ? De quelle façon la population sous observation reste-t-elle marquée ? Et l’observateur, lui, garde-t-il des marques ? L’article suivant et son ann
Publikováno v:
Practical Medicinal Chemistry with Macrocycles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf8e126ef102b613a5910d4ee92c0627
https://doi.org/10.1002/9781119092599.ch19
https://doi.org/10.1002/9781119092599.ch19
Autor:
René Gagnon
Publikováno v:
Rabaska: Revue d'ethnologie de l'Amérique française. 17:332
Publikováno v:
Analogue-Based Drug Discovery III
Publikováno v:
Current Medicinal Chemistry. 20:280-288
Fabry disease is an X-linked, multisystemic lysosomal storage disorder due to alpha-galactosidase A deficiency. It is characterized by the accumulation of glycosphingolipids, mainly globotriaosylceramide (Gb(3)), in biological fluids, vascular endoth
Publikováno v:
Clinica Chimica Acta. 414:273-280
Fabry disease is a complex, multisystemic and clinically heterogeneous disease, with elevated excretion of globotriaosylceramide (Gb(3)) and globotriaosylsphingosine (lyso-Gb(3)) accumulating in biological fluids caused by deficiency of the enzyme, l
Autor:
Frédérique Frisch, Janneke de Wal, André C. Carpentier, René Gagnon, Sébastien M. Labbé, Stephen Greentree, Jaap Twisk, Harald Petry, Daniel Gaudet, Diane Brisson
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 97:1635-1644
Lipoprotein lipase-deficient (LPLD) individuals display marked chylomicronemia and hypertriglyceridemia associated with increased pancreatitis risk. The aim of this study was to determine the effect of i.m. administration of an adeno-associated viral
Autor:
Sarah P. Young, Yan An, Haoyue Zhang, Joe T.R. Clarke, David S. Millington, René Gagnon, Bruno Maranda, Christiane Auray-Blais, Pamela Lavoie
Publikováno v:
Clinica Chimica Acta. 413:771-778
Mucopolysaccharidoses are complex lysosomal storage disorders caused by any of eleven different enzyme deficiencies resulting in the accumulation of substrates, mainly glycosaminoglycans (GAGs), in various tissues and biological fluids.We developed a