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المؤلفون: Karl Persson, Agnès Llored, Matteo De Chiara, Agurtzane Irizar, Simon Stenberg, Gianni Liti, Eric Gilson, Benjamin Barré, Jia-Xing Yue, Joseph Schacherer, Melania D’Angiolo, Jonas Warringer, Roberto Marangoni
المساهمون: Institut de Recherche sur le Cancer et le Vieillissement (IRCAN), Université Nice Sophia Antipolis (... - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UCA)
المصدر: Nature
Nature, Nature Publishing Group, 2020, 587 (7834), pp.420-425. ⟨10.1038/s41586-020-2889-1⟩مصطلحات موضوعية: [SDV]Life Sciences [q-bio], Lineage (evolution), Loss of Heterozygosity, yeast, Paradoxus, Genome, 0302 clinical medicine, MESH: Genetic Fitness, MESH: Genetic Introgression, Homologous Recombination, MESH: Phylogeny, Phylogeny, MESH: Evolution, Molecular, MESH: Reproduction, Asexual, 0303 health sciences, Multidisciplinary, biology, MESH: Genomic Instability, MESH: Genomics, Fungal genetics, Genomics, Reproductive isolation, MESH: Crosses, Genetic, MESH: Saccharomyces cerevisiae, Meiosis, yeast, Alpechin, genomic introgression, MESH: Genome, Fungal, Genome, Fungal, Mitosis, Alpechin, Introgression, Saccharomyces cerevisiae, Genetic Introgression, Genomic Instability, Evolution, Molecular, MESH: Homologous Recombination, Saccharomyces, 03 medical and health sciences, Reproduction, Asexual, Saccharomyces paradoxus, Crosses, Genetic, 030304 developmental biology, MESH: Loss of Heterozygosity, MESH: Saccharomyces, MESH: Fertility, genomic introgression, MESH: Mitosis, biology.organism_classification, MESH: Meiosis, Fertility, Evolutionary biology, Genetic Fitness, 030217 neurology & neurosurgery
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المؤلفون: Marion Blin, Caroline Brossas, Gaël A. Millot, Mélanie Schmidt, Viola Nähse, Marie-Noëlle Prioleau, Michelle Debatisse, Benoît Le Tallec
المساهمون: Dynamique de l'information génétique : bases fondamentales et cancer (DIG CANCER), Centre National de la Recherche Scientifique (CNRS)-Institut Curie [Paris]-Sorbonne Université (SU), Centre de Recherche en Cancérologie de Marseille (CRCM), Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut Paoli-Calmettes, Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Aix Marseille Université (AMU), Institute for Cancer Research [Oslo], Oslo University Hospital [Oslo], Institute of Clinical Medicine [Oslo], Faculty of Medicine [Oslo], University of Oslo (UiO)-University of Oslo (UiO), Stabilité Génétique et Oncogenèse (UMR 8200), Université Paris-Sud - Paris 11 (UP11)-Institut Gustave Roussy (IGR)-Centre National de la Recherche Scientifique (CNRS), Institut Jacques Monod (IJM (UMR_7592)), Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS), Hub Bioinformatique et Biostatistique - Bioinformatics and Biostatistics HUB, Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), The M.D. team is supported by the Agence Nationale de la Recherche (grant ANR-13-BSV6-0008-01/FRA-Dom), the Association pour la Recherche sur le Cancer (grant Subvention Libre Sl220130607073), and the Institut National du Cancer (grants INCa subventions 2013-103 and PLBIO17-194). The M.N.P. team is supported by the Association pour la Recherche sur le Cancer (grant Labellisation PGA120150202272) and the Agence Nationale de la Recherche (grant ANR-15-CE12-0004-01). M.B. was supported by fellowships from the Ministère de l’Enseignement Supérieur et de la Recherche and the Ligue contre le cancer., We thank S. Lambert and O. Hyrien for critical reading of the manuscript. The authors would like to acknowledge the Cell and Tissue Imaging Platform – PICT-IBiSA (member of France-Bioimaging) of the Genetics and Developmental Biology Department (UMR3215/U934) of Institut Curie for help with light microscopy, the Flow Cytometry Platform Imagoseine of Institut Jacques Monod, Université Paris Diderot, and the Imaging and Cytometry Platform (PFIC) of Institut Gustave Roussy for assistance with cell sorting., ANR-13-BSV6-0008,FRA-Dom,Chorégraphie des domaines de la chromatine au cours de la différenciation: réorganisation des profils de réplication et des sites fragiles communs(2013), Institut Curie [Paris]-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Aix Marseille Université (AMU)-Institut Paoli-Calmettes, Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), Institut de biologie de l'ENS Paris (UMR 8197/1024) (IBENS), Département de Biologie - ENS Paris, École normale supérieure - Paris (ENS Paris)-École normale supérieure - Paris (ENS Paris)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Institut Curie-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Université de Lorraine (UL), Centre National de la Recherche Scientifique (CNRS)-Université Paris Diderot - Paris 7 (UPD7), Université Paris Descartes - Faculté de Chirurgie Dentaire (UPD5 Odontologie), Université Paris Descartes - Paris 5 (UPD5), Institut Curie
المصدر: Nature Structural and Molecular Biology
Nature Structural and Molecular Biology, Nature Publishing Group, 2019, 26 (1), pp.58-66. ⟨10.1038/s41594-018-0170-1⟩
Nature Structural and Molecular Biology, 2019, 26 (1), pp.58-66. ⟨10.1038/s41594-018-0170-1⟩مصطلحات موضوعية: DNA Replication, MESH: Genomic Instability / physiology, Transcription, Genetic, [SDV]Life Sciences [q-bio], Mitosis, [SDV.CAN]Life Sciences [q-bio]/Cancer, Endogeny, Biology, Genomic Instability, 03 medical and health sciences, 0302 clinical medicine, Structural Biology, Transcription (biology), MESH: Transcription, Genetic / genetics, MESH: DNA Replication / genetics, Animals, Humans, MESH: Animals, MESH: Chromosome Fragile Sites / genetics, MESH: Genomic Instability / genetics, Molecular Biology, Gene, 030304 developmental biology, Genome stability, 0303 health sciences, Replication timing, MESH: Humans, MESH: Mitosis / physiology, Chromosome Fragile Sites, Chromosomal fragile site, Promoter, Cell biology, MESH: Mitosis / genetics, MESH: Chromosome Fragile Sites / physiology, Fragile sites, MESH: DNA Replication / physiology, Transcription, Origin selection, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, 030217 neurology & neurosurgery
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المؤلفون: Arnaud Echard, Hugo Wioland, Frédérique Cuvelier, Guillaume Romet-Lemonne, Tamara Advedissian, Jian Bai
المساهمون: Trafic membranaire et Division cellulaire - Membrane Traffic and Cell Division, Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), Collège Doctoral, Sorbonne Université (SU), Institut Jacques Monod (IJM (UMR_7592)), Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Work in the A.E. laboratory has been supported by Institut Pasteur, CNRS, and the Agence Nationale de la Recherche (ANR) (AbsCystem and RedoxActin). J.B. was supported by the Pasteur-Paris University (PPU) international PhD program and received a fellowship from Fondation ARC pour la Recherche sur le Cancer (DOC20180507410). H.W. has been supported by a postdoctoral fellowship from the Fondation ARC pour la Recherche sur le Cancer. T.A. has been supported by a postdoctoral fellowship from the Fondation pour la Recherche Médicale (FRM SPF201809006907) and the ANR (Cytosign)., ANR-15-CE13-0001,AbsCyStem,Régulation de l'abscission dans les cellules animales(2015), ANR-19-CE13-0018,RedoxActin,Régulation du cytosquelette d'actine par le contrôle de son oxydation(2019), Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), Collège doctoral [Sorbonne universités], Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP)
المصدر: Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, 2020, 117 (8), pp.4169-4179. ⟨10.1073/pnas.1911629117⟩
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2020, 117 (8), pp.4169-4179. ⟨10.1073/pnas.1911629117⟩
Proc Natl Acad Sci U S Aمصطلحات موضوعية: MESH: Oxidation-Reduction, Cell division, MESH: Drosophila, Mixed Function Oxygenases, MESH: Endosomal Sorting Complexes Required for Transport, Drosophila Proteins, MESH: Animals, Cytoskeleton, 0303 health sciences, Multidisciplinary, Chemistry, Microfilament Proteins, 030302 biochemistry & molecular biology, cytoskeleton, Biological Sciences, MESH: Mixed Function Oxygenases, Chromatin, Cell biology, MESH: Methionine Sulfoxide Reductases, Midbody, Drosophila, Oxidation-Reduction, actin, MESH: Cytokinesis, MESH: Drosophila Proteins, Aurora B kinase, Mitosis, cytokinesis, [SDV.BC]Life Sciences [q-bio]/Cellular Biology, macromolecular substances, MESH: Actins, Cell Line, MESH: Chromatin, MESH: Microfilament Proteins, 03 medical and health sciences, Abscission, Animals, Humans, Actin, 030304 developmental biology, MESH: Humans, Endosomal Sorting Complexes Required for Transport, MESH: Mitosis, abscission checkpoint, Actins, MESH: Cell Line, oxidoreduction, Methionine Sulfoxide Reductases, MESH: HeLa Cells, Cytokinesis, HeLa Cells
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5139df330b93d415d9a12ca7d187948c
https://doi.org/10.1073/pnas.1911629117 -
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المؤلفون: Richard, Guy-Franck
المساهمون: Génétique des génomes - Genetics of Genomes (UMR 3525), Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), Work in the G.-F.R. laboratory is generously funded by the Institut Pasteur and the Centre National de la Recherche Scientifique (CNRS).
المصدر: Cells
Cells, Vol 10, Iss 1019, p 1019 (2021)
Cells, 2021, 10 (5), pp.1019. ⟨10.3390/cells10051019⟩مصطلحات موضوعية: MESH: Trinucleotide Repeats, DNA Repair, Genotype, MESH: Mice, Transgenic, QH301-705.5, [SDV]Life Sciences [q-bio], MutS, Mitosis, Mice, Transgenic, Saccharomyces cerevisiae, Review, DNA Mismatch Repair, microsatellites, MESH: Genotype, Mice, Trinucleotide Repeats, Schizosaccharomyces, MESH: Trinucleotide Repeat Expansion, MutS Proteins, Animals, Humans, MESH: Animals, Biology (General), MESH: Mice, MESH: MutS Proteins, MutL, MESH: DNA Repair, Recombination, Genetic, MESH: Humans, MESH: MutL Proteins, MESH: DNA, DNA, MESH: Mitosis, MESH: Saccharomyces cerevisiae, MESH: Meiosis, Meiosis, mismatch repair, MESH: Schizosaccharomyces, MESH: DNA Mismatch Repair, MutL Proteins, MESH: Recombination, Genetic, MESH: Microsatellite Repeats, Trinucleotide Repeat Expansion, Microsatellite Repeats
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المؤلفون: Sabine Quitard, Mohamed Lala Bouali, Mira Kuzmić, Pascal Verdier-Pinard, Pierre-Henri Puech, Danièle Salaun, Daniel Isnardon, Stéphane Audebert, Ali Badache, Aurélie Mangon, Sylvie Thuault
المساهمون: Centre de Recherche en Cancérologie de Marseille (CRCM), Aix Marseille Université (AMU)-Institut Paoli-Calmettes, Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Institut Paoli-Calmettes, Fédération nationale des Centres de lutte contre le Cancer (FNCLCC), Adhésion et Inflammation (LAI), Aix Marseille Université (AMU)-Assistance Publique - Hôpitaux de Marseille (APHM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Turing Center for Living Systems, ANR-16-CE11-0008,flexiplex,Fonctions émergentes d'un inhibiteur de p53: une organisation macromoléculaire flexible pour des fonctions biologiques distinctes(2016)
المصدر: Journal of Cell Biology
Journal of Cell Biology, 2021, 220 (12), ⟨10.1083/jcb.202012002⟩مصطلحات موضوعية: MESH: Myosin Type I, [SDV]Life Sciences [q-bio], Amino Acid Motifs, Mitosis, Spindle Apparatus, Biology, medicine.disease_cause, Microtubules, 03 medical and health sciences, MESH: Amino Acid Motifs, Myosin Type I, 0302 clinical medicine, Microtubule, MESH: Intracellular Signaling Peptides and Proteins, Cell cortex, MESH: Phosphoprotein Phosphatases, medicine, Phosphoprotein Phosphatases, MESH: Protein Binding, Humans, MESH: Spindle Apparatus, Actin, 030304 developmental biology, 0303 health sciences, Mutation, Gene knockdown, MESH: Humans, MESH: Microtubules, Intracellular Signaling Peptides and Proteins, Cell Biology, MESH: Mitosis, Cell biology, Spindle apparatus, Repressor Proteins, MESH: Microtubule-Associated Proteins, HEK293 Cells, MESH: Repressor Proteins, MESH: HEK293 Cells, Cancer cell, MESH: HeLa Cells, Microtubule-Associated Proteins, 030217 neurology & neurosurgery, HeLa Cells, Protein Binding
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2a9dda92c75dd137b294fb690ec092d
https://pubmed.ncbi.nlm.nih.gov/34705028 -
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المؤلفون: Nicola Festuccia, Alexandra Tachtsidi, Inma Gonzalez, Thaleia Papadopoulou, Agnès Dubois, Pablo Navarro, Elphège P. Nora, Michel Cohen-Tannoudji, Sandrine Vandormael-Pournin, Benoit G. Bruneau, Nick D.L. Owens
المساهمون: Epigénomique, Prolifération et Identité Cellulaire - Epigenomics, Proliferation and the Identity of Cells (EPIC), Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), Collège Doctoral, Sorbonne Université (SU), Embryon précoce de mammifères et cellules souches, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), University of California [San Francisco] (UC San Francisco), University of California (UC), This work was supported by recurrent funding from the Institut Pasteur, the CNRS, and Revive (Investissement d’Avenir, ANR-10-LABX-73). E.P.N. was supported by EMBO (ALTF523-2013), HSFP, and the Roddenberry Stem Cell Center at Gladstone. N.O. is supported by Revive. P.N. acknowledges financial support from the Fondation Schlumberger (FRM FSER 2017), the Agence Nationale de la Recherche (ANR 16 CE120004 01 MITMAT), the Ligue contre le Cancer (LNCC EL2018 NAVARRO) and the European Research Council (ERC-CoG-2017 BIND)., ANR-10-LABX-0073,REVIVE,Stem Cells in Regenerative Biology and Medicine(2010), ANR-16-CE12-0004,MitMAT,Mémoire mitotique de l'activité transcriptionnelle dans les cellules ES(2016), European Project: 773083,ERC-CoG-2017,BIND(2018), Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), Collège doctoral [Sorbonne universités], Embryon précoce de mammifères et cellules souches - Early Mammalian Development & Stem Cell Biology, Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS)-Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), University of California [San Francisco] (UCSF), University of California, Epigénétique des Cellules Souches - Epigenetics of Stem Cells, Génétique fonctionnelle de la Souris, Génétique Fonctionnelle de la Souris, ANR-10-LABX-0073/10-LABX-0073,REVIVE,Stem Cells in Regenerative Biology and Medicine(2010), European Project
المصدر: eLife
eLife, 2019, 8, ⟨10.1101/563619⟩
eLife, eLife Sciences Publication, 2019, 8, ⟨10.1101/563619⟩
eLife, Vol 8 (2019)مصطلحات موضوعية: 0301 basic medicine, Nucleosome organization, CCCTC-Binding Factor, Cell division, Mouse, MESH: DNA Replication, [SDV.BC.BC]Life Sciences [q-bio]/Cellular Biology/Subcellular Processes [q-bio.SC], chemistry.chemical_compound, Mice, 0302 clinical medicine, MESH: Animals, MESH: CCCTC-Binding Factor, Biology (General), MESH: Embryonic Stem Cells, Cells, Cultured, 0303 health sciences, Cultured, General Neuroscience, General Medicine, Chromosomes and Gene Expression, MESH: Gene Expression Regulation, 3. Good health, Cell biology, Nucleosomes, Medicine, nucleosome positioning, MESH: Cells, Cultured, Research Article, DNA Replication, Transcriptional Activation, chromosomes, replication, QH301-705.5, Science, Cells, Biology, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, MESH: Nucleosomes, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], transcription factors, Genetics, Nucleosome, Animals, Mitosis, Transcription factor, Gene, MESH: Mice, mouse, Embryonic Stem Cells, 030304 developmental biology, mitosis, General Immunology and Microbiology, fungi, DNA replication, MESH: Mitosis, Stem Cell Research, CTCF, pluripotency, 030104 developmental biology, [SDV.BDD.EO]Life Sciences [q-bio]/Development Biology/Embryology and Organogenesis, chemistry, Gene Expression Regulation, gene expression, MESH: Transcriptional Activation, Generic health relevance, Biochemistry and Cell Biology, 030217 neurology & neurosurgery, DNA
وصف الملف: application/pdf
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المؤلفون: Thomas, James A., Baker, Nicola, Hutchinson, Sebastian, Dominicus, Caia, Trenaman, Anna, Glover, Lucy, Alsford, Sam, Horn, David
المساهمون: London School of Hygiene and Tropical Medicine (LSHTM), University of York [York, UK], Institut Pasteur [Paris], The Francis Crick Institute [London], University of Dundee, We thank Philippa Radley for assistance with assembly of tagging constructs, Richard Wheeler (Uni. of Oxford) for advice on ImageJ analysis and Achim Schnaufer (Uni. of Edinburgh) for the ATP-synthase antibody, Institut Pasteur [Paris] (IP)
المصدر: PLoS Neglected Tropical Diseases
PLoS Neglected Tropical Diseases, Public Library of Science, 2018, 12 (11), pp.e0006980. ⟨10.1371/journal.pntd.0006980⟩
PLoS Neglected Tropical Diseases, Vol 12, Iss 11, p e0006980 (2018)
PLoS Neglected Tropical Diseases, 2018, 12 (11), pp.e0006980. ⟨10.1371/journal.pntd.0006980⟩مصطلحات موضوعية: Physiology, [SDV]Life Sciences [q-bio], RC955-962, Melarsoprol, MESH: Melarsoprol, Biochemistry, Arctic medicine. Tropical medicine, Medicine and Health Sciences, Cell Cycle and Cell Division, MESH: Trypanocidal Agents, Energy-Producing Organelles, Protozoans, Chromosome Biology, Pharmaceutics, Eukaryota, MESH: Mitochondrial Proteins, Trypanocidal Agents, Mitochondria, Electrophysiology, Nucleic acids, Cell Processes, MESH: Pentamidine, Cellular Structures and Organelles, Public aspects of medicine, RA1-1270, Research Article, Trypanosoma, MESH: Mitochondria, Trypanosoma brucei brucei, Mitosis, Suramin, Bioenergetics, DNA replication, Membrane Potential, MESH: Cell Biology, Mitochondrial Proteins, Drug Therapy, parasitic diseases, Trypanosoma Brucei, Genetics, Humans, MESH: Suramin, Pentamidine, MESH: Humans, MESH: Nifurtimox, Organisms, Biology and Life Sciences, MESH: Trypanosoma brucei brucei, Cell Biology, DNA, MESH: Mitosis, Parasitic Protozoans, Kinetoplasts, Trypanosomiasis, African, MESH: Trypanosomiasis, African, Nifurtimox, Lysosomes, Trypanosoma Brucei Gambiense, MESH: Lysosomes
وصف الملف: application/pdf
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المؤلفون: Patrick Weber, Nadia Benaroudj, Frederick Saul, Sarah Dubrac, Annie Landier, Bénédicte Beaudeau, Raléb Taher, Mounira Kebouchi, Ahmed Haouz, Mathieu Picardeau
المساهمون: Biologie des Spirochètes / Biology of Spirochetes, Institut Pasteur [Paris], Cristallographie (Plateforme) - Crystallography (Platform), Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), Biologie des Bactéries pathogènes à Gram-positif, This work was supported by the Institut Pasteur and Agence National de la Recherche Grant ANR-08-MIE-018., M. K., R. T., A. L., B. B., and P. W. performed experiments. F. S., A. H., S. D., M. P., and N. B. conceived, performed, and analyzed experiments. N. B. conceived and coordinated the study and wrote the paper. All authors approved the final version of the manuscript.We acknowledge SOLEIL for provision of synchrotron radiation facilities, and we thank the staff of beamline PROXIMA 1 for assistance. We are grateful to Gerald Murray and Ben Adler for providing the perR mutant. We thank Gouzel Karimova, Isabelle Michaud-Soret, and Victor Duarte for critically reading the manuscript and for helpful discussions., ANR-08-MIEN-0018,LEPTOVIR,Les leptospires : de la génétique à la pathogénèse(2008), Institut Pasteur [Paris] (IP), Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)
المصدر: Journal of Biological Chemistry 2 (293), 497-509. (2018)
Journal of Biological Chemistry
Journal of Biological Chemistry, American Society for Biochemistry and Molecular Biology, 2018, 293 (2), pp.497-509. ⟨10.1074/jbc.M117.804443⟩
Journal of Biological Chemistry, 2018, 293 (2), pp.497-509. ⟨10.1074/jbc.M117.804443⟩مصطلحات موضوعية: MESH: Signal Transduction, 0301 basic medicine, MESH: Leptospira interrogans, [SDV]Life Sciences [q-bio], Mutant, Regulatory site, Metal Binding Site, Cell Cycle Proteins, spirochaetes, Biochemistry, Peroxide, chemistry.chemical_compound, Metalloprotein, oxidative stress, structural biology, spirochetes, MESH: Bacterial Proteins, Leptospira, chemistry.chemical_classification, biology, Chemistry, régulation transcriptionnelle, [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology, transcription regulation, Leptospira interrogans, Protein Binding, Signal Transduction, Repressor, Mitosis, PerR, reactive oxygen species (ROS), Microbiology, 03 medical and health sciences, MESH: Cell Cycle Proteins, Bacterial Proteins, métalloprotéine, MESH: Protein Binding, microbiologie, Molecular Biology, Binding Sites, metalloprotein, stress oxydatif, Cell Biology, MESH: Mitosis, biology.organism_classification, 030104 developmental biology, MESH: Binding Sites, Structural biology
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22a1791136e69ce8ef074b3acbc923a3
http://prodinra.inra.fr/record/427975 -
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المؤلفون: Maillet, Vanessa, Boussetta, Nadia, Leclerc, Jocelyne, Fauveau, Veronique, Foretz, Marc, Viollet, Benoit, Couty, Jean-Pierre, Celton-Morizur, Séverine, Perret, Christine, Desdouets, Chantal
المساهمون: Viollet, Benoit, Institut Cochin (IC UM3 (UMR 8104 / U1016)), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Université Sorbonne Paris Cité (USPC), Université Paris Diderot - Paris 7 (UPD7), This study was supported by grants from INSERM, Agence Nationale de la Recherche (ANR-2010-BLANC-1123-02). V.M. was a recipient of a La Ligue Nationale Contre le Cancer (LNCC) grant.
المصدر: Cell Reports
Cell Reports, 2018, 22 (8), pp.1994-2005. ⟨10.1016/j.celrep.2018.01.086⟩
Cell Reports, Vol 22, Iss 8, Pp 1994-2005 (2018)
Cell Reports, Elsevier Inc, 2018, 22 (8), pp.1994-2005. ⟨10.1016/j.celrep.2018.01.086⟩مصطلحات موضوعية: MESH: Signal Transduction, congenital, hereditary, and neonatal diseases and abnormalities, MESH: Enzyme Activation, LKB1, EGFR, Mitosis, AMP-Activated Protein Kinases, Protein Serine-Threonine Kinases, MESH: ErbB Receptors, MESH: Protein-Serine-Threonine Kinases, MESH: Hepatocytes, Mice, MESH: Ploidies, MESH: Cell Proliferation, Animals, MESH: Animals, MESH: Gene Silencing, MESH: Genome, Gene Silencing, skin and connective tissue diseases, liver regeneration, lcsh:QH301-705.5, MESH: Mice, polyploidy, Cell Proliferation, [SDV.MHEP.EM] Life Sciences [q-bio]/Human health and pathology/Endocrinology and metabolism, Genome, Ploidies, MESH: Mitosis, [SDV.MHEP.EM]Life Sciences [q-bio]/Human health and pathology/Endocrinology and metabolism, Enzyme Activation, ErbB Receptors, Liver, lcsh:Biology (General), MESH: Gene Deletion, hepatocytes, MESH: Liver Regeneration, microtubule spindle, mitosis fidelity, Gene Deletion, Signal Transduction, MESH: Liver
وصف الملف: application/pdf
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المؤلفون: Anna Noatynska, Nicolas Tavernier, Lionel Pintard, Monica Gotta, Lisa Martino, Françoise Schwager, Thibaut Léger, Costanza Panbianco, Lucie Van Hove
المساهمون: Institut Jacques Monod (IJM (UMR_7592)), Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS), Department of Cellular Physiology and Metabolism, Faculty of Medicine, University of Geneva, Swiss National Centre for Competence in Research Programme Chemical Biology (NCCR-Chemical Biology), University of Geneva [Switzerland], Fondation Association pour la Recherche sur le Cancer PhD fellowship, French Government, French National Research Agency under grant No. ANR-11-IDEX-0005-01, Swiss National Science Foundation, University of Geneva, French National Research Agency under grant No. ANR-2012-BSV2-0001-01, Foundation for Medical Research 'Equipe Fondation pour la Recherche Médicale' DEQ20140329538, ANR-11-IDEX-0005-02/11-LABX-0071,WHO AM I,Determinants de l’Identité : de la molécule à l’individu(2011)
المصدر: The Journal of cell biology
Journal of Cell Biology
Journal of Cell Biology, Rockefeller University Press, 2015, 208 (6), pp.661-9. ⟨10.1083/jcb.201408064⟩
The Journal of Cell Biology
The Journal of Cell Biology, Vol. 208, No 6 (2015) pp. 661-9مصطلحات موضوعية: Embryo, Nonmammalian, Cell division, Cell Cycle Proteins, MESH: Amino Acid Sequence, environment and public health, 0302 clinical medicine, Sf9 Cells, MESH: Sf9 Cells, MESH: Animals, Phosphorylation, Research Articles, Caenorhabditis elegans, Aurora Kinase A, 0303 health sciences, MESH: Spodoptera, Protein-Serine-Threonine Kinases/metabolism, MESH: Caenorhabditis elegans Proteins, MESH: CDC2 Protein Kinase, Cell biology, MESH: Aurora Kinase A, Larva, 030220 oncology & carcinogenesis, CDC2 Protein Kinase/physiology, biological phenomena, cell phenomena, and immunity, inorganic chemicals, MESH: Enzyme Activation, Molecular Sequence Data, Mitosis, Aurora Kinase A/metabolism, macromolecular substances, [SDV.BC]Life Sciences [q-bio]/Cellular Biology, Protein Serine-Threonine Kinases, Spodoptera, Biology, PLK1, MESH: Protein-Serine-Threonine Kinases, 03 medical and health sciences, Enzyme activator, MESH: Cell Cycle Proteins, Report, MESH: Caenorhabditis elegans, CDC2 Protein Kinase, Animals, Humans, Amino Acid Sequence, ddc:612, Caenorhabditis elegans Proteins, 030304 developmental biology, Cyclin-dependent kinase 1, MESH: Humans, MESH: Molecular Sequence Data, Cell Cycle Proteins/metabolism, MESH: Phosphorylation, Larva/cytology/enzymology, MESH: Embryo, Nonmammalian, Cell Biology, MESH: Mitosis, biology.organism_classification, Enzyme Activation, enzymes and coenzymes (carbohydrates), Caenorhabditis elegans/cytology/enzymology, MESH: Protein Processing, Post-Translational, Caenorhabditis elegans Proteins/metabolism, Protein Processing, Post-Translational, MESH: Larva, Embryo, Nonmammalian/cytology/metabolism
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