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hal.structure.identifierlp2n-04,lp2n-12
dc.contributor.authorCOGNET, Laurent
hal.structure.identifierPolarité cellulaire, Migration et cancer
dc.contributor.authorLEDUC, Cécile
hal.structure.identifierlp2n-04,lp2n-12
dc.contributor.authorLOUNIS, Brahim
dc.date.accessioned2023-05-12T10:19:04Z
dc.date.available2023-05-12T10:19:04Z
dc.date.issued2014-05-27
dc.identifier.issn1367-5931
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/181026
dc.description.abstractEnResolving the movement of individual molecules in living cells by single particle tracking methods has allowed many molecular behaviors to be deciphered over the past three decades. These methods have increasingly benefited from advances in microscopy of single nano-objects such as fluorescent dye molecules, proteins or nanoparticles as well as tiny absorbing metal nanoparticles. In parallel to these efforts aiming at tracking ever smaller and more photostable nano-objects in living cells, the development of localization-based super-resolution imaging provided means to increase the number of single molecules tracked on a single cell. In this review we will present the most recent advances in the field.
dc.language.isoen
dc.publisherElsevier
dc.title.enAdvances in live-cell single-particle tracking and dynamic super-resolution imaging
dc.typeArticle de revue
dc.identifier.doi10.1016/j.cbpa.2014.04.015
dc.subject.halPhysique [physics]/Physique [physics]/Biophysique [physics.bio-ph]
bordeaux.journalCurrent Opinion in Chemical Biology
bordeaux.page78-85
bordeaux.volume20C
bordeaux.hal.laboratoriesLaboratoire Photonique, Numérique et Nanosciences (LP2N) - UMR 5298*
bordeaux.institutionUniversité de Bordeaux
bordeaux.institutionCNRS
bordeaux.peerReviewedoui
hal.identifierhal-00997350
hal.version1
hal.origin.linkhttps://hal.archives-ouvertes.fr//hal-00997350v1
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