Research
Epitranscriptomics & Cancer Adaptation : A.David

Activities

Our research work focuses on the contribution of post-transcriptional mechanisms on cancer cell adaptation, in particular RNA epigenetic & translational control.

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Zotero public

Added by mollevi
Group name EquipeVC
Item Type Note
Note The following values have no corresponding Zotero field:
auth-address: *INSERM, U1183, Institut de Recherche en Medecine regenerative et Biotherapie, Montpellier F-34295, France; Universite de Montpellier, UMR 1183, Montpellier F-34295, France; CNRS, FRE 3689 - Universite de Montpellier, Centre d'etudes d'agents Pathogenes et Biotechnologies pour la Sante (CPBS), Montpellier F-34293, France; Institut de Recherche en Cancerologie de Montpellier, Montpellier F-34298, France; Sanofi Aventis, Drug Disposition Domain, Montpellier F-34184, France; Faculty of Medicine and Dentistry, Department of Medical Chemistry and Biochemistry, Palacky University, Olomouc, Czech Republic; CNRS 5203 - INSERM 1191, Institut de Genomique Fonctionnelle, Montpellier F-34094, France; Departement de chirurgie digestive, CHU Saint Eloi, Montpellier F-34295, France; Departement d'anatomopathologie, CHU Gui de Chauliac, Montpellier F-34295, France; and. *INSERM, U1183, Institut de Recherche en Medecine regenerative et Biotherapie, Montpellier F-34295, France; Universite de Montpellier, UMR 1183, Montpellier F-34295, France; **CHU Montpellier, Institut de Recherche en Medecine regenerative et Biotherapie, Montpellier F-34295, France. *INSERM, U1183, Institut de Recherche en Medecine regenerative et Biotherapie, Montpellier F-34295, France; Universite de Montpellier, UMR 1183, Montpellier F-34295, France; sabine.gerbal-chaloin@inserm.fr.
alt-title: Toxicological sciences : an official journal of the Society of Toxicology
number: 1
accession-num: 26259606
Tags _EndnoteXML import
Date Added 2018/11/14 - 12:10:52
Date Modified 2018/11/14 - 12:10:52
Parent item Analysis of Glycogen Synthase Kinase Inhibitors That Regulate Cytochrome P450 Expression in Primary Human Hepatocytes by Activation of beta-Catenin, Aryl Hydrocarbon Receptor and Pregnane X Receptor Signaling


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