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Biophysical Journal|June 10, 2008
Quantitative FRET analysis by fast acquisition time domain FLIM at high spatial resolution in living cellsSergi Padilla-Parra, Nicolas Audugé, Maïté Coppey-Moisan, et al.Cold Spring Harbor Protocols|June 3, 2015
Time-domain fluorescence lifetime imaging microscopy: a quantitative method to follow transient protein-protein interactions in living cellsSergi Padilla-Parra, Nicolas Audugé, Marc Tramier, et al.Methods in Molecular Biology (Clifton, N.J.)|October 11, 2013
Quantitative study of protein-protein interactions in live cell by dual-color fluorescence correlation spectroscopySergi Padilla-Parra, Nicolas Audugé, Maïté Coppey-Moisan, et al.Microscopy Research and Technique|May 28, 2011
Dual-color fluorescence lifetime correlation spectroscopy to quantify protein-protein interactions in live cellSergi Padilla-Parra, Nicolas Audugé, Maïté Coppey-Moisan, et al.Plos One|July 23, 2013
Spatio-Temporal Quantification of FRET in living cells by fast time-domain FLIM: a comparative study of non-fitting methods [corrected]Aymeric Leray, Sergi Padilla-Parra, Julien Roul, et al.Methods and Applications in Fluorescence|February 8, 2020
Automated screening of AURKA activity based on a genetically encoded FRET biosensor using fluorescence lifetime imaging microscopyFlorian Sizaire, Gilles Le Marchand, Jacques Pécréaux, et al.Frontiers in Molecular Biosciences|May 22, 2024
Actin cytoskeleton differently regulates cell surface organization of GPI-anchored proteins in polarized epithelial cells and fibroblastsStéphanie Lebreton, Simona Paladino, Mickaël Lelek, et al.Nature Communications|September 15, 2016
A FRET biosensor reveals spatiotemporal activation and functions of aurora kinase A in living cellsGiulia Bertolin, Florian Sizaire, Gaëtan Herbomel, et al.Nucleic Acids Research|May 14, 2019
Chromatin condensation fluctuations rather than steady-state predict chromatin accessibilityNicolas Audugé, Sergi Padilla-Parra, Marc Tramier, et al.Microscopy Research and Technique|August 31, 2006
Sensitivity of CFP/YFP and GFP/mCherry pairs to donor photobleaching on FRET determination by fluorescence lifetime imaging microscopy in living cellsMarc Tramier, Morad Zahid, Jean-Claude Mevel, et al.Pageof 5