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Profil bibliographique

Luc De Vries

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

47Publications signalées
3205Citations signalées
0Affiliations récentes

Les domaines associés

Protein Kinase Regulation and GTPase SignalingReceptor Mechanisms and SignalingCellular transport and secretionPancreatic function and diabetesIon channel regulation and function

Les publications récentes

Accès ouvert 2021 article OpenAlex

RGS12 and RGS14 GoLoco Motifs Are Gα i Interaction Sites with Guanine Nucleotide Dissociation Inhibitor Activity

Luc De Vries, David Peter Siderovski, Hélène Tronchère, Marilyn G. Farquhar et autres

The regulators of G-protein signaling (RGS) proteins accelerate the intrinsic guanosine triphosphatase activity of heterotrimeric G-protein alpha subunits and are thus recognized as key modulators of G-protein-coupled receptor signaling. RGS12 and RGS14 contain not only the hallmark RGS box responsible for GTPase-accelerating …

us (code pays fourni par la source)

0 citations Carolina Digital Repository (University of North Carolina at Chapel Hill)
Accès ouvert 2018 article OpenAlex

Groene ICT verstevigt basis

Anda Counotte, Frank Hartkamp, Luc De Vries, Denny van der Vlist et autres

Groene ICT, een programma dat in 2008 startte om de negatieve milieueffecten van ict te minimaliseren, slaat de vleugels uit en richt zich nu ook op duurzaamheid en circulaire economie. Steeds meer onderwijsinstellingen sluiten zich aan, waardoor het programma een basis krijgt …

nl (code pays fourni par la source)

0 citations DSpace (Open University in the Netherlands)
2017 article OpenAlex

An internalization assay for Dopamine D2(short) Receptors using Bioluminescence Resonance Energy Transfer (BRET) technology

Luc De Vries, Frédéric Finana, Claudie Cathala, Brice Ronsin et autres

Internalization and subsequent degradation of GPCRs located at the plasmamembrane represent a desired therapeutic approach to eliminate those receptors whose activation leads to unwanted cellular behaviour. In order to follow the trafficking of endocytosed receptors and thus the efficacy of agents directing …

fr (code pays fourni par la source)

1 citation The FASEB Journal
Accès ouvert 2016 article OpenAlex

Pharmacological evaluation of a series of smoothened antagonists in signaling pathways and after topical application in a depilated mouse model

Emilie Lauressergues, Peter Heusler, Fabrice Lestienne, David Troulier et autres

The Hedgehog (HH) pathway has been linked to the formation of basal cell carcinoma (BCC), medulloblastoma, and other cancers. The recently approved orally active drugs vismodegib (GDC-0449) and sonidegib (LDE-225) were not only efficacious for the treatment of advanced or metastatic BCC …

de, fr (code pays fourni par la source)

37 citations Pharmacology Research & Perspectives
Accès ouvert 2015 article OpenAlex

Consequences of combining siRNA-mediated DNA methyltransferase 1 depletion with 5-aza-2′-deoxycytidine in human leukemic KG1 cells

Stéphane Vispé, Arthur Deroide, Emeline Davoine, Cécile Desjobert et autres

// Stéphane Vispé 1 , Arthur Deroide 1 , Emeline Davoine 1 , Cécile Desjobert 1 , Fabrice Lestienne 2 , Lucie Fournier 1 , Natacha Novosad 1 , Sophie Bréand 3 , Jérôme Besse 3 , Florence Busato 4 , Jörg …

fr (code pays fourni par la source)

17 citations Oncotarget
2010 article OpenAlex

Inhibition of Proprotein Convertase Subtilisin/Kexin type 9 (PCSK9) secretion by prodomain overexpression or pefabloc treatment as measured by a luciferase assay

Luc De Vries, Céline Robichon, Claudie Cathala, Michel Perez et autres

Proprotein convertase subtilisin/kexin type 9 (PCSK9) is a secreted protease that acts as a regulator of circulating plasma cholesterol levels by enhancing the endocytosis of the low density lipoprotein receptor (LDL‐R) at the cell surface of hepatocytes. In this study, we show …

fr (code pays fourni par la source)

0 citations The FASEB Journal
2009 article OpenAlex

Discovery of Novel Protease Activated Receptors 1 Antagonists with Potent Antithrombotic Activity in Vivo

Michel Perez, Marie Lamothe, Catherine Maraval, Etienne Mirabel et autres

Protease activated receptors (PARs) or thrombin receptors constitute a class of G-protein-coupled receptors (GPCRs) implicated in the activation of many physiological mechanisms. Thus, thrombin activates many cell types such as vascular smooth muscle cells, leukocytes, endothelial cells, and platelets via activation of …

pl, fr (code pays fourni par la source)

43 citations Journal of Medicinal Chemistry

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