المؤلفون: Nilsson, Elisabeth C, Long, Yun Chau, Martinsson, Sofia, Glund, Stephan, Garcia-Roves, Pablo, Svensson, L Thomas, Andersson, Leif, Zierath, Juleen R, Mahlapuu, Margit

المصدر: J Biol Chem. 281(11):7244-52

مصطلحات موضوعية: Animals, Biological Markers/metabolism, Gene Expression Regulation, Glucose/metabolism, Glycogen/metabolism, Lipid Metabolism, Lipids/chemistry, Mice, Inbred C57BL, Knockout, Transgenic, Models, Biological, Multienzyme Complexes/*metabolism, Muscle, Skeletal/*metabolism, Nucleic Acid Hybridization, Oligonucleotide Array Sequence Analysis, Oxygen/metabolism, Phenotype, Protein Isoforms, Protein Kinases/*genetics/*physiology, Protein-Serine-Threonine Kinases/*metabolism, RNA/metabolism, RNA, Complementary/metabolism, Reverse Transcriptase Polymerase Chain Reaction, Transcription, Genetic

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-22452
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=16410251&dopt=Citation

المؤلفون: Andrée Houbion, Patricia Renard, Catherine Demazy, Martine Raes, Aurélia De Pauw, Sébastien Vankoningsloo, Christophe Lecocq, Marie Piens, Audrey Gilson, Thierry Arnould

المساهمون: FUNDP - SBIO_URBC (unité de recherche en biologie cellulaire), UCL - SSS/IREC/FATH - Pôle de Pharmacologie et thérapeutique

المصدر: Journal of Lipid Research, Vol. 46, no. 6, p. 1133-49 (2005)
Journal of Lipid Research, Vol 46, Iss 6, Pp 1133-1149 (2005)

مصطلحات موضوعية: Monosaccharide Transport Proteins - metabolism, Time Factors, Glucose uptake, Mitochondria - metabolism, pathology, Muscle Proteins, Fatty Acids - metabolism, DNA - metabolism, Biochemistry, Phosphatidylinositol 3-Kinases, chemistry.chemical_compound, Mice, Endocrinology, GSK-3, Adipocyte, Adipocytes, Muscles - enzymology, Enzyme Inhibitors, Luciferases, Cells, Cultured, peroxisome proliferator-activated receptor γ, Glucose Transporter Type 4, Microscopy, Confocal, muscle carnitine palmitoyl transferase-1, Reverse Transcriptase Polymerase Chain Reaction, Muscles, Carnitine O-Palmitoyltransferase - biosynthesis, Fatty Acids, Calcium - metabolism, Cell Differentiation, AMP-dependent kinase, Mitochondria, Protein Transport, Retinoid X Receptor alpha - metabolism, Phenotype, Triglycerides - metabolism, PPAR gamma - metabolism, Carbohydrate Metabolism, Enzyme Inhibitors - pharmacology, medicine.drug, Protein Binding, medicine.medical_specialty, Oxygen - metabolism, Cell Membrane - metabolism, Monosaccharide Transport Proteins, Blotting, Western, Down-Regulation, QD415-436, Protein Serine-Threonine Kinases, Biology, Transfection, Models, Biological, Proto-Oncogene Proteins, Internal medicine, 3T3-L1 Cells, medicine, Animals, RNA, Messenger, Carnitine, Phosphatidylinositol, carbohydrate-responsive element binding protein, Protein-Serine-Threonine Kinases - metabolism, Triglycerides, phosphatidylinositol 3-kinase/Akt1/glycogen synthase kinase 3β, Muscle Proteins - metabolism, Proto-Oncogene Proteins - metabolism, Retinoid X Receptor alpha, Carnitine O-Palmitoyltransferase, Triglyceride, Cell Membrane, Phosphatidylinositol 3-Kinases - metabolism, Glucose transporter, Adipocytes - cytology, Lipid metabolism, DNA, Cell Biology, Lipid Metabolism, Oxygen, PPAR gamma, Glucose, chemistry, Microscopy, Fluorescence, Glucose - metabolism, pharmacokinetics, RNA, Messenger - metabolism, Calcium, Proto-Oncogene Proteins c-akt, Luciferases - metabolism

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7a612efc2df745f58c9cf3cf0cbcd37
https://doi.org/10.1194/jlr.M400464-JLR200

المؤلفون: Arisa Higa, Raphael Pineau, Michael Hallett, Stéphanie Lhomond, Olivier Pluquet, Marion Bouchecareilh, Anne Vital, Sandrine Loriot, Gaelle Cubel, Jann N. Sarkaria, Maylis Delugin, Hugues Loiseau, Wenting Wu, Nicolas Dejeans, Keith Anderson, Sara J. C. Gosline, Frédéric Saltel, Martin E. Fernandez-Zapico, Fausto J. Rodriguez, C. Combe, Jean Rosenbaum, Eric Chevet, Nathalie Dugot-Senant, Saïd Taouji

المساهمون: Physiopathologie du cancer du foie, Université Bordeaux Segalen - Bordeaux 2-Institut National de la Santé et de la Recherche Médicale (INSERM), DIPI (DIPI), ENISE, Ecosystèmes aquatiques et changements globaux (UR EABX), Institut national de recherche en sciences et technologies pour l'environnement et l'agriculture (IRSTEA), Centre de Recherche sur la Matière Divisée (CRMD), Université d'Orléans (UO)-Centre National de la Recherche Scientifique (CNRS), CHU Bordeaux [Bordeaux], Department of Health and Human Services, National Institutes of Health [Bethesda] (NIH), Institut de biologie et chimie des protéines [Lyon] (IBCP), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Centre National de la Recherche Scientifique (CNRS), Oncogenesis Stress Signaling (OSS), Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-CRLCC Eugène Marquis (CRLCC), This work was supported by an Avenir program (INSERM), grants from the Institut National du Cancer (INCa), Ligue contre le cancer, a Marie Curie International Reintegration Grant (E. Chevet), a grant from the Mayo Clinic Cancer Centre (M.E. Fernandez-Zapico), a grant from Institut Fédératif de Recherche 66 (O. Pluquet). O. Pluquet was supported by fellowships from INSERM and Association pour la Recherche contre le Cancer. M. Bouchecareilh was supported from a fellowship from le Conseil Régional d'Aquitaine and la Fondation pour la Recherche Française (FRM). Human glioblastoma samples were collected through the Bordeaux Tumor Bank (JP Merlio, CHU Bordeaux, France) funded by the Cancéropôle Grand Sud-Ouest and by a CEREPEG project grant (PHRC 2003, H. Loiseau) or through the Mayo Clinic Department of Clinical Pathology and funded by the Mayo Clinic SPORE in Brain Cancer P50 CA108961 (Rochester)., The authors thank M. Moenner (Université Bordeaux 1, Bordeaux, France) for precious help and fruitful discussions, S. Manié (UMR CNRS 5286, INSERM 1052, Cancer Research Center of Lyon, Lyon, France), and the Chevet lab for critical reading of the manuscript. The authors also thank Dr S. Gery (University of California, Los Angeles, CA) for the gift of pcDNA3.1-hPER1 expression vector and Dr U. Albrecht (Freiburg, Switzerland) for providing us with the pPER1-Luc vector., Centre National de la Recherche Scientifique (CNRS)-Université d'Orléans (UO), Diagnostics et imageries des procédés industriels (ENISE-DIPI), Ecole Nationale d'Ingénieurs de Saint Etienne (ENISE), Université de Rennes (UR)-CRLCC Eugène Marquis (CRLCC)

المصدر: Cancer Research
Cancer Research, American Association for Cancer Research, 2013, 73 (15), pp.4732-4743. ⟨10.1158/0008-5472.CAN-12-3989⟩
Cancer Research, 2013, 73 (15), pp.4732-4743. ⟨10.1158/0008-5472.CAN-12-3989⟩

مصطلحات موضوعية: Cancer Research, Endoribonuclease activity, [SDV]Life Sciences [q-bio], Circadian clock, MESH: Base Sequence, MESH: Period Circadian Proteins/metabolism, Mice, 0302 clinical medicine, RNA interference, MESH: Glioblastoma/metabolism, MESH: Reverse Transcriptase Polymerase Chain Reaction, MESH: Animals, RNA Processing, Post-Transcriptional, MESH: Gene Expression Regulation, Neoplastic/physiology, Oligonucleotide Array Sequence Analysis, Regulation of gene expression, 0303 health sciences, Reverse Transcriptase Polymerase Chain Reaction, Period Circadian Proteins, MESH: Protein-Serine-Threonine Kinases/genetics, Cell biology, Gene Expression Regulation, Neoplastic, Oncology, MESH: Endoribonucleases/metabolism, 030220 oncology & carcinogenesis, MESH: Glioblastoma/genetics, RNA Interference, PER1, MESH: RNA Processing, Post-Transcriptional, endocrine system, MESH: Xenograft Model Antitumor Assays, XBP1, Molecular Sequence Data, MESH: RNA Interference, MESH: Endoribonucleases/genetics, [SDV.CAN]Life Sciences [q-bio]/Cancer, Protein Serine-Threonine Kinases, Biology, Transfection, Article, 03 medical and health sciences, Endoribonucleases, MESH: Unfolded Protein Response/physiology, Animals, Humans, Gene silencing, MESH: Protein-Serine-Threonine Kinases/metabolism, RNA, Messenger, MESH: Mice, 030304 developmental biology, MESH: RNA, Messenger, MESH: Period Circadian Proteins/genetics, MESH: Humans, MESH: Molecular Sequence Data, Base Sequence, MESH: Transfection, Xenograft Model Antitumor Assays, Molecular biology, MESH: Oligonucleotide Array Sequence Analysis, Unfolded Protein Response, Unfolded protein response, Glioblastoma

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bfc10e690b81b99ff91f9bf2ddd7579
https://hal.archives-ouvertes.fr/hal-02400356

المؤلفون: Bernard Gallez, Pierre Danhier, Yu-Chih Nien, Ines Batinic-Haberle, Mark W. Dewhirst, Eui Jung Moon, Pierre Sonveaux, Paolo E. Porporato, Thies Schroeder

المساهمون: UCL - SSS/IREC/FATH - Pôle de Pharmacologie et thérapeutique, UCL - SSS/IREC - Institut de recherche expérimentale et clinique

المصدر: Proceedings of the National academy of sciences of the United States of America, Vol. 107, no. 47, p. 20477-20482 (2010)

مصطلحات موضوعية: Vascular Endothelial Growth Factor A, MAPK/ERK pathway, chemistry.chemical_compound, Mice, Extracellular Signal-Regulated MAP Kinases - metabolism, 0302 clinical medicine, Neoplasms, Extracellular Signal-Regulated MAP Kinases, chemistry.chemical_classification, 0303 health sciences, Multidisciplinary, NADPH oxidase, biology, Reverse Transcriptase Polymerase Chain Reaction, Biological Sciences, Cell Hypoxia - physiology, Immunohistochemistry, DNA Primers - genetics, Cell Hypoxia, 3. Good health, Vascular endothelial growth factor, NADPH Oxidase - metabolism, Vascular endothelial growth factor A, Hypoxia-Inducible Factor 1 - metabolism, 030220 oncology & carcinogenesis, Female, Hypoxia-Inducible Factor 1, Lactic Acid - blood, Pyruvate dehydrogenase kinase, Neoplasms - metabolism, therapy, Blotting, Western, Reactive Oxygen Species - metabolism, Enzyme-Linked Immunosorbent Assay, Protein Serine-Threonine Kinases, 03 medical and health sciences, Cell Line, Tumor, Animals, Humans, Lactic Acid, Protein-Serine-Threonine Kinases - metabolism, DNA Primers, 030304 developmental biology, Reactive oxygen species, Analysis of Variance, Tumor hypoxia, Vascular Endothelial Growth Factor A - metabolism, NADPH Oxidases, Pyruvate Dehydrogenase Acetyl-Transferring Kinase, Hyperthermia, Induced, Tumor Oxygenation, Molecular biology, Gene Expression Regulation, chemistry, Gene Expression Regulation - physiology, biology.protein, Cancer research, Reactive Oxygen Species

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c483da9bbab0739059fbe16d5b6ef826
https://hdl.handle.net/2078.1/88185