Please use this identifier to cite or link to this item: http://tailieuso.udn.vn/handle/TTHL_125/7718
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dc.contributor.advisorMolla, Annie, Dr.-
dc.contributor.authorLe, Ly Thuy Tram-
dc.date.accessioned2018-03-05T08:33:27Z-
dc.date.available2018-03-05T08:33:27Z-
dc.date.issued2013-09-18-
dc.date.submitted2013-10-22-
dc.identifier.urihttp://tailieuso.udn.vn/handle/TTHL_125/7718-
dc.descriptionDoctoral thesic. Major: Biologie Cellulaire; 144 pagesen
dc.description.tableofcontentsChapter 1: Cell cycle and its regulation; Chapter 2: Aurora kinases; Chapter 3: Aurora kinase inhibitors and anti-cancer therapies.en
dc.language.isoenen
dc.publisherUniversity of Joseph Fourier, Franceen
dc.sourceUniversity of Science and Technology - The University of Danangen
dc.subjectCanceren
dc.subjectMitotic kinasesen
dc.subjectKinase inhibitoren
dc.subjectHistone H3 phosphorylationen
dc.subjectChromosome compactionen
dc.titleBenzo[E]pyridoindolones, nouveaux inhibiteurs de kinases hydrosolubles a fort potentiel anti-proliferatifen
dc.title.alternativeBenzo[E]pyridoindolones, những chất mới ức chế kinases hòa tan trong nước với hoạt tính kháng phân bào mạnhen
dc.typePh.D Thesisen
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