Marc Tramier

发表

OPTIMAL CONTROL FOR MULTIDIMENSIONAL MICROSCOPY

Julien Roul, Otmane Bouchareb, Olivier Chanteux, 2017 .

multi-functional modules driving method including a multi-wavelength imaging device and steering system corresponding

Julien Roul, Marc Tramier, Jacques Pecreaux, 2014 .

Quantitative comparison of different fluorescent protein couples for fast FRET-FLIM acquisition.

Marc Tramier, Maïté Coppey-Moisan, Sergi Padilla-Parra, 2009, Biophysical journal.

Time-domain fluorescence lifetime imaging microscopy: a quantitative method to follow transient protein-protein interactions in living cells.

Marc Tramier, Maïté Coppey-Moisan, Sergi Padilla-Parra, 2015, Cold Spring Harbor protocols.

Low-intensity two-dimensional imaging of fluorescence lifetimes in living cells

Valentina Emiliani, Marc Tramier, Klaus Kemnitz, 2003 .

Supplmentary Material Spatio-Temporal Analysis of Cell Response to a Rigidity Gradient : A Quantitative Study by Multiple Optical Tweezers

Marc Tramier, Maïté Coppey-Moisan, S. Hénon, 2008 .

Quantitative FRET analysis by fast acquisition time domain FLIM at high spatial resolution in living cells.

Marc Tramier, Maïté Coppey-Moisan, Sergi Padilla-Parra, 2008, Biophysical journal.

Sensitivity of CFP/YFP and GFP/mCherry pairs to donor photobleaching on FRET determination by fluorescence lifetime imaging microscopy in living cells

Marc Tramier, Maïté Coppey-Moisan, M. Tramier, 2006, Microscopy research and technique.

827Spatio-Temporal Quantification of FRET in Living Cells by Fast Time-Domain FLIM: A Comparative Study of Non-Fitting Methods

Aymeric Leray, Julien Roul, Marc Tramier, 2013, PloS one.

Spatiotemporal analysis of cell response to a rigidity gradient: a quantitative study using multiple optical tweezers.

Marc Tramier, Christiane Durieux, Maïté Coppey-Moisan, 2009, Biophysical journal.

Picosecond-hetero-FRET microscopy to probe protein-protein interactions in live cells.

Marc Tramier, Klaus Kemnitz, Christiane Durieux, 2002, Biophysical journal.