학술논문
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'학술논문'
에서 검색결과 266건 | 목록
1~20
Academic Journal
Tran Mau-Them, F.; Guibaud, L.; Duplomb, L.; Keren, B.; Lindstrom, K.; Marey, I.; Mochel, F.; van den Boogaard, M. J.; Oegema, R.; Nava, C.; Masurel, A.; Jouan, T.; Jansen, F. E.; Au, M.; Chen, Agnes H.; Cho, M.; Duffourd, Y.; Lozier, E.; Konovalov, F.; Sharkov, A.; Korostelev, S.; Urteaga, B.; Dickson, P.; Vera, M.; Martínez-Agosto, Julián A.; Begemann, A.; Zweier, M.; Schmitt-Mechelke, T.; Rauch, A.; Philippe, C.; van Gassen, K.; Nelson, S.; Graham, J. M.; Friedman, J.; Faivre, L.; Lin, H. J.; Thauvin-Robinet, C.; Vitobello, A.
Genetics in Medicine. 21:1008-1014
Academic Journal
El It F; UMR1231 Inserm, Génétique des anomalies du développement (GAD), université de Bourgogne Franche-Comté, Dijon, France - FHU TRANSLAD, CHU Dijon, Dijon, France.; Faivre L; UMR1231 Inserm, Génétique des anomalies du développement (GAD), université de Bourgogne Franche-Comté, Dijon, France - FHU TRANSLAD, CHU Dijon, Dijon, France - Centre de référence des anomalies du développement et syndromes malformatifs, CHU Dijon, Dijon, France.; Thauvin-Robinet C; UMR1231 Inserm, Génétique des anomalies du développement (GAD), université de Bourgogne Franche-Comté, Dijon, France - FHU TRANSLAD, CHU Dijon, Dijon, France - Centre de référence des anomalies du développement et syndromes malformatifs, CHU Dijon, Dijon, France.; Vitobello A; UMR1231 Inserm, Génétique des anomalies du développement (GAD), université de Bourgogne Franche-Comté, Dijon, France - FHU TRANSLAD, CHU Dijon, Dijon, France - Unité fonctionnelle innovation en diagnostic génomique des maladies rares, CHU Dijon, Dijon, France.; Duplomb L; UMR1231 Inserm, Génétique des anomalies du développement (GAD), université de Bourgogne Franche-Comté, Dijon, France - FHU TRANSLAD, CHU Dijon, Dijon, France.
Publisher: EDK Country of Publication: France NLM ID: 8710980 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1958-5381 (Electronic) Linking ISSN: 07670974 NLM ISO Abbreviation: Med Sci (Paris) Subsets: MEDLINE
Academic Journal
Thevenon, J; Duplomb, L; Phadke, S; Eguether, T; Saunier, A; Avila, M; Carmignac, V; Bruel, A. L; St Onge, J; Duffourd, Y; Pazour, G. J; FRANCO, BRUNELLA; Attie Bitach, T; Masurel Paulet, A; Rivière, J. B; Cormier Daire, V; Philippe, C; Faivre, L; Thauvin Robinet, C.
Clinical Genetics. 90:509-517
Academic Journal
Journal of Biological Chemistry. 274:24685-24693
Academic Journal
Jego, G.; Lanneau, D.; de Thonel, A.; Berthenet, K.; Hazoumé, A.; Droin, N.; Hamman, A.; Girodon, F.; Bellaye, P.-S.; Wettstein, G.; Jacquel, A.; Duplomb, L.; Le Mouël, A.; Papanayotou, C.; Christian, E.; Bonniaud, P.; Lallemand-Mezger, V.; Solary, E.; Garrido, C.
Leukemia. 28:1676-1686
Academic Journal
Baud'huin, M.E.; Duplomb, L.; Teletchea, S.; Lamoureux, F.; Ruiz-Velasco, C.; Maillasson, M.; Redini, F.; Heymann, M-F.; Heymann, D.
Cytokine & Growth Factor Reviews. 24:401-409
Academic Journal
Saidi, S; Bouri, F; Lencel, P; Duplomb, L; Baud'huin, M; Delplace, S; Leterme, D; Miellot, F; Heymann, D; Hardouin, P; Palmer-Lourenco, Gaby; Magne, David
Cytokine, Vol. 53, No 3 (2011) pp. 347-54
Academic Journal
Journal of Biological Chemistry. 284:31704-31713
Academic Journal
Durand M; INSERM, UMR1231, Team HSP-Pathies Labellisée « Ligue Nationale Contre Le Cancer » and Labex LipSTIC, Dijon, 21000, France.; University of Burgundy, Medical Sciences Faculty, Dijon, 21078, France.; Cabaud Gibouin V; INSERM, UMR1231, Team HSP-Pathies Labellisée « Ligue Nationale Contre Le Cancer » and Labex LipSTIC, Dijon, 21000, France.; University of Burgundy, Medical Sciences Faculty, Dijon, 21078, France.; Duplomb L; INSERM, UMR1231, Equipe GAD, University of Burgundy, Dijon, 21078, France.; Salmi L; INSERM, UMR1231, Team HSP-Pathies Labellisée « Ligue Nationale Contre Le Cancer » and Labex LipSTIC, Dijon, 21000, France.; University of Burgundy, Medical Sciences Faculty, Dijon, 21078, France.; Caillot M; INSERM, U1245, Normandy University, Caen, 14000, France.; Sola B; INSERM, U1245, Normandy University, Caen, 14000, France.; Camus V; Department of Hematology, Centre Henri Becquerel, Rouen, 76000, France.; Jardin F; Department of Hematology, Centre Henri Becquerel, Rouen, 76000, France.; Garrido C; INSERM, UMR1231, Team HSP-Pathies Labellisée « Ligue Nationale Contre Le Cancer » and Labex LipSTIC, Dijon, 21000, France.; University of Burgundy, Medical Sciences Faculty, Dijon, 21078, France.; Georges François Leclerc Cancer Centre, CGFL, Dijon, France.; Jego G; INSERM, UMR1231, Team HSP-Pathies Labellisée « Ligue Nationale Contre Le Cancer » and Labex LipSTIC, Dijon, 21000, France. gaetan.jego@u-bourgogne.fr.; University of Burgundy, Medical Sciences Faculty, Dijon, 21078, France. gaetan.jego@u-bourgogne.fr.; INSERM, UMR1231, Université Bourgogne, 7 Boulevard Jeanne d'Arc, Dijon, 21078, France. gaetan.jego@u-bourgogne.fr.
Publisher: BioMed Central Country of Publication: England NLM ID: 8308647 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-9966 (Electronic) Linking ISSN: 03929078 NLM ISO Abbreviation: J Exp Clin Cancer Res Subsets: MEDLINE
Academic Journal
Cellular and Molecular Life Sciences. 09 2007 64(18):2334-2350
Academic Journal
Garret P; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Laboratoire CERBA, Saint-Ouen l'Aumône, France.; Ebstein F; Universitätsmedizin Greifswald, Institut für Medizinische Biochemie und Molekularbiologie, Greifswald, Germany.; Delplancq G; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Dozieres-Puyravel B; AP-HP, Hôpital Robert Debré, Service de Neurologie pédiatrique, Paris, France.; Boughalem A; Laboratoire CERBA, Saint-Ouen l'Aumône, France.; Auvin S; AP-HP, Hôpital Robert Debré, Service de Neurologie pédiatrique, Paris, France.; UMR1141 INSERM, Université Paris Diderot, Paris, France.; Duffourd Y; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Klafack S; Universitätsmedizin Greifswald, Institut für Medizinische Biochemie und Molekularbiologie, Greifswald, Germany.; Zieba BA; Universitätsmedizin Greifswald, Institut für Medizinische Biochemie und Molekularbiologie, Greifswald, Germany.; Mahmoudi S; Service de Pédiatrie, Centre Hospitalier René-Dubos, Pontoise, France.; Singh KK; Department of Biochemistry and Biomedical Sciences, Stem Cell and Cancer Research Institute, McMaster University, Hamilton, Canada.; Duplomb L; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Thauvin-Robinet C; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Centre de Référence Maladies Rares 'déficience intellectuelle', centre de génétique, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Costa JM; Laboratoire CERBA, Saint-Ouen l'Aumône, France.; Krüger E; Universitätsmedizin Greifswald, Institut für Medizinische Biochemie und Molekularbiologie, Greifswald, Germany.; Trost D; Laboratoire CERBA, Saint-Ouen l'Aumône, France.; Verloes A; UMR1141 INSERM, Université Paris Diderot, Paris, France.; Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.; Faivre L; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Centre de Référence Maladies Rares 'Anomalies du développement et syndromes malformatifs', centre de génétique, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Vitobello A; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.
Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE
Academic Journal
Cellular and Molecular Life Sciences (CMLS). Sept, 2007, Vol. 64 Issue 18, p2334, 17 p.
Academic Journal
Avila, M.; Gigot, N.; Aral, B.; Callier, P.; Gautier, E.; Thevenon, J.; Pasquier, L.; Lopez, E.; Gueneau, L.; Duplomb, L.; Goldenberg, A.; Baumann, C.; Cormier, V.; Marlin, S.; Masurel-Paulet, A.; Huet, F.; Attié-Bitach, T.; Faivre, L.; Thauvin-Robinet, C.
Human Mutation. Nov 01, 2011 32(11):1332-1333
Periodical
Obesity, Fitness & Wellness Week. October 21, 2017, p871
Academic Journal
Biochemical and Biophysical Research Communications. 323:49-51
Academic Journal
Aymeric Masson; Julien Paccaud; Martina Orefice; Estelle Colin; Outi Mäkitie; Valérie Cormier-Daire; Raissa Relator; Sourav Ghosh; Jean-Marc Strub; Christine Schaeffer-Reiss; Carlo Marcelis; David A. Koolen; Rolph Pfundt; Elke de Boer; Lisenka E.L.M. Vissers; Thatjana Gardeitchik; Lonneke A.M. Aarts; Tuula Rinne; Paulien A. Terhal; Nienke E. Verbeek; Linda C. Zuurbier; Astrid S. Plomp; Marja W. Wessels; Stella A. de Man; Arjan Bouman; Lynne M. Bird; Reem Saadeh-Haddad; Maria J. Guillen Sacoto; Richard Person; Catherine Gooch; Anna C.E. Hurst; Michelle L. Thompson; Susan M. Hiatt; Rebecca O. Littlejohn; Elizabeth R. Roeder; Mari Mori; Scott Hickey; Jesse M. Hunter; Kristy Lee; Khaled Osman; Rana Halloun; Ruxandra Bachmann-Gagescu; Anita Rauch; Dagmar Wieczorek; Konrad Platzer; Johannes Luppe; Laurence Duplomb-Jego; Fatima El It; Yannis Duffourd; Frédéric Tran Mau-Them; Celine Huber; Christopher T. Gordon; Fulya Taylan; Riikka E. Mäkitie; Alice Costantini; Helena Valta; Stephen Robertson; Gemma Poke; Michel Francoise; Andrea Ciolfi; Marco Tartaglia; Nina Ekhilevitch; Rinat Zaid; Michael A. Levy; Jennifer Kerkhof; Haley McConkey; Julian Delanne; Martin Chevarin; Valentin Vautrot; Valentin Bourgeois; Sylvie Nguyen; Nathalie Marle; Patrick Callier; Hana Safraou; Angela Morgan; David J. Amor; Michael Hildebrand; David Coman; Marion Aubert Mucca; Julien Thevenon; Fanny Laffargue; Frédéric Bilan; Céline Pebrel-Richard; Grace Yoon; Michelle M. Axford; Luis A. Pérez-Jurado; Marta Sevilla-Porras; Douglas Black; Christophe Philippe; Bekim Sadikovic; Christel Thauvin-Robinet; Laurence Olivier-Faivre; Michela Ori; Quentin Thomas; Antonio Vitobello
Journal of Clinical Investigation.
Academic Journal
L. Libert; C. Abdeddaim; K. Saleh; C. Even; S. Duplomb; J. Dubreuil; A. Rambeau; E. Guiard; Y. Pointreau; N. Olympios-Gerotzortzos; C. Moldovan; E. Lévêque; F. Clatot
ESMO Open
Academic Journal
Montillot C; Université de Bourgogne, 21000 Dijon, France; Inserm Unit 1231, 21000 Dijon, France.; Skutunova E; Université de Bourgogne, 21000 Dijon, France; Inserm Unit 1231, 21000 Dijon, France.; Ayushma; Kusuma School of Biological Sciences, Indian Institute of Technology Delhi (IITD), Hauz Khas, New Delhi 110016, India.; Dubied M; Biogéosciences, UMR 6282 CNRS, EPHE, Université de Bourgogne, 21000 Dijon, France.; Lahmar A; Université de Bourgogne, 21000 Dijon, France; Inserm Unit 1231, 21000 Dijon, France.; Nguyen S; Université de Bourgogne, 21000 Dijon, France; Inserm Unit 1231, 21000 Dijon, France.; Peerally B; Université de Bourgogne, 21000 Dijon, France; Inserm Unit 1231, 21000 Dijon, France.; Prin F; Crick Advanced Light Microscopy Facility, The Francis Crick Institute, London NW1 1AT, UK.; Duffourd Y; Université de Bourgogne, 21000 Dijon, France; Inserm Unit 1231, 21000 Dijon, France; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, Dijon University Hospital, 21000 Dijon, France.; Thauvin-Robinet C; Université de Bourgogne, 21000 Dijon, France; Inserm Unit 1231, 21000 Dijon, France; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, Dijon University Hospital, 21000 Dijon, France; Reference Center for Rare Diseases 'Déficiences intellectuelles de causes rares', Dijon University Hospital, 21000 Dijon, France.; Duplomb L; Université de Bourgogne, 21000 Dijon, France; Inserm Unit 1231, 21000 Dijon, France.; Wang H; DDC Clinic for Special Needs Children, Middlefield, OH 44062, USA.; Ansar M; Jules Gonin Eye Hospital, University of Lausanne, CH-1015 Lausanne, Switzerland; Advanced Molecular Genetics and Genomics Disease Research and Treatment Centre, Dow University of Health Sciences, Karachi, Pakistan.; Faivre L; Université de Bourgogne, 21000 Dijon, France; Inserm Unit 1231, 21000 Dijon, France; Reference Center for Rare Diseases 'Anomalies du Développement et syndromes malformatifs', Dijon University Hospital, 21000 Dijon, France.; Navarro N; Biogéosciences, UMR 6282 CNRS, EPHE, Université de Bourgogne, 21000 Dijon, France; EPHE, PSL University, Paris 75014, France.; Minocha S; Kusuma School of Biological Sciences, Indian Institute of Technology Delhi (IITD), Hauz Khas, New Delhi 110016, India.; Collins SC; Université de Bourgogne, 21000 Dijon, France; Inserm Unit 1231, 21000 Dijon, France.; Yalcin B; Université de Bourgogne, 21000 Dijon, France; Inserm Unit 1231, 21000 Dijon, France. Electronic address: binnaz.yalcin@inserm.fr.
Publisher: Academic Press Country of Publication: United States NLM ID: 9500169 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1095-953X (Electronic) Linking ISSN: 09699961 NLM ISO Abbreviation: Neurobiol Dis Subsets: MEDLINE
Academic Journal
L. Libert; C. Abdeddaim; K. Saleh; C. Even; S. Duplomb; J. Dubreuil; A. Rambeau; E. Guiard; Y. Pointreau; N. Olympios; C. Moldovan; E. Lévêque; F. Clatot
Annals of Oncology. 35:S631
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