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Francine Grondin

Researcher at Université de Sherbrooke

Publications -  18
Citations -  997

Francine Grondin is an academic researcher from Université de Sherbrooke. The author has contributed to research in topics: Furin & Proprotein convertase. The author has an hindex of 12, co-authored 18 publications receiving 923 citations.

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Journal ArticleDOI

Evidence that Furin Is an Authentic Transforming Growth Factor-β1-Converting Enzyme

TL;DR: It is demonstrated for the first time that furin is an authentic and adaptive TGF-beta1-converting enzyme whereas other members of the PC family might substitute or supplement furin activity.
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Hypoxia-enhanced expression of the proprotein convertase furin is mediated by hypoxia-inducible factor-1: impact on the bioactivation of proproteins.

TL;DR: It is demonstrated herein that the levels of fur mRNA, encoding furin, are remarkably increased upon hypoxic challenge, and a new facet of the physiological consequences of hypoxia/HIF-1 is unveiled, through enhanced furin-induced proteolytic processing/activation of proproteins known to be involved in tumorigenesis.
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Cross-talk between the p42/p44 MAP Kinase and Smad Pathways in Transforming Growth Factor β1-induced Furin Gene Transactivation

TL;DR: The findings clearly show that the activation of the p42/p44 MAPK pathway is involved in fur gene expression and led us to propose a co-operative model whereby TGFβ1-induced receptor activation stimulates not only a Smad pathway but also a parallel p42-p44MAPK pathway that targets Smad2 for an increased nuclear translocation and enhanced fur gene transactivation.
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Some effects of chitosan on liver function in the rat.

TL;DR: The results taken collectively indicate that the 7.5% chitosan formula maintained adequate cholesterol homeostasis in rats, despite a greatly increased intake of cholesterol.
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Hypoxia-inducible Factor Mediates Hypoxic and Tumor Necrosis Factor α-induced Increases in Tumor Necrosis Factor-α Converting Enzyme/ADAM17 Expression by Synovial Cells

TL;DR: It is reported that low oxygen concentrations and TNFα enhance TACE mRNA levels in synovial cells through direct binding of hypoxia-inducible factor-1 (HIF-1) to the 5′ promoter region, which suggests a mechanism by which TACE is increased in RA-affected joints.