Picosecond-hetero-FRET microscopy to probe protein-protein interactions in live cells.
about
Wide-Field Multi-Parameter FLIM: long-term minimal invasive observation of proteins in living cellsAn improved cerulean fluorescent protein with enhanced brightness and reduced reversible photoswitching.Quantitative analysis of energy transfer between fluorescent proteins in CFP-GBP-YFP and its response to Ca2+.Tracking the interactions of rRNA processing proteins during nucleolar assembly in living cells.Dynamic interaction of amphiphysin with N-WASP regulates actin assembly.Multi-dimensional time-correlated single photon counting (TCSPC) fluorescence lifetime imaging microscopy (FLIM) to detect FRET in cellsDetectors for single-molecule fluorescence imaging and spectroscopy.Dual-color fluorescence lifetime correlation spectroscopy to quantify protein-protein interactions in live cell.The fluorescent protein palette: tools for cellular imaging.Quantum dot-aluminum phthalocyanine conjugates perform photodynamic reactions to kill cancer cells via fluorescence resonance energy transferCofilin, actin and their complex observed in vivo using fluorescence resonance energy transfer.Fluorescence lifetime readouts of Troponin-C-based calcium FRET sensors: a quantitative comparison of CFP and mTFP1 as donor fluorophores.The truncated prelamin A in Hutchinson-Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymers.The L-cysteine desulfurase NFS1 is localized in the cytosol where it provides the sulfur for molybdenum cofactor biosynthesis in humansSpatio-Temporal Quantification of FRET in living cells by fast time-domain FLIM: a comparative study of non-fitting methods [corrected].X-Ray Crystal Structure and Properties of Phanta, a Weakly Fluorescent Photochromic GFP-Like Protein.Live-cell imaging reveals multiple interactions between Epstein-Barr virus nuclear antigen 1 and cellular chromatin during interphase and mitosisCorrelating calcium binding, Förster resonance energy transfer, and conformational change in the biosensor TN-XXL.Phasor imaging with a widefield photon-counting detectorHomodimerization of amyloid precursor protein at the plasma membrane: a homoFRET study by time-resolved fluorescence anisotropy imagingFluorescence lifetime imaging microscopy of intracellular glucose dynamics.Quantitative FRET analysis by fast acquisition time domain FLIM at high spatial resolution in living cells.Quantitative comparison of different fluorescent protein couples for fast FRET-FLIM acquisition.Application of phasor plot and autofluorescence correction for study of heterogeneous cell population.Tracking the green invaders: advances in imaging virus infection in plants.Mapping the disease protein interactome: toward a molecular medicine GPS to accelerate drug and biomarker discovery.FRET microscopy in the living cell: different approaches, strengths and weaknesses.Newly engineered cyan fluorescent proteins with enhanced performances for live cell FRET imaging.Grb14 is a negative regulator of CEACAM3-mediated phagocytosis of pathogenic bacteria.Non fitting based FRET-FLIM analysis approaches applied to quantify protein-protein interactions in live cells.Rab6-interacting protein 1 links Rab6 and Rab11 function.Monitoring protein interactions in the living cell through the fluorescence decays of the cyan fluorescent protein.Multiphoton-FLIM quantification of the EGFP-mRFP1 FRET pair for localization of membrane receptor-kinase interactions.Structural changes of yellow Cameleon domains observed by quantitative FRET analysis and polarized fluorescence correlation spectroscopy.Fluorescence lifetime imaging microscopy (FLIM) to quantify protein-protein interactions inside cells.Photophysics of Clomeleon by FLIM: discriminating excited state reactions along neuronal development.PucC and LhaA direct efficient assembly of the light-harvesting complexes in Rhodobacter sphaeroidesAnalysis of FRET signals in the presence of free donors and acceptors.Homo- and hetero-oligomerization of beta-arrestins in living cells.Accepting from the best donor; analysis of long-lifetime donor fluorescent protein pairings to optimise dynamic FLIM-based FRET experiments.
P2860
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P2860
Picosecond-hetero-FRET microscopy to probe protein-protein interactions in live cells.
description
2002 nî lūn-bûn
@nan
2002 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Picosecond-hetero-FRET microscopy to probe protein-protein interactions in live cells
@nl
Picosecond-hetero-FRET microscopy to probe protein-protein interactions in live cells.
@ast
Picosecond-hetero-FRET microscopy to probe protein-protein interactions in live cells.
@en
type
label
Picosecond-hetero-FRET microscopy to probe protein-protein interactions in live cells
@nl
Picosecond-hetero-FRET microscopy to probe protein-protein interactions in live cells.
@ast
Picosecond-hetero-FRET microscopy to probe protein-protein interactions in live cells.
@en
prefLabel
Picosecond-hetero-FRET microscopy to probe protein-protein interactions in live cells
@nl
Picosecond-hetero-FRET microscopy to probe protein-protein interactions in live cells.
@ast
Picosecond-hetero-FRET microscopy to probe protein-protein interactions in live cells.
@en
P2093
P2860
P1433
P1476
Picosecond-hetero-FRET microscopy to probe protein-protein interactions in live cells
@en
P2093
Christiane Durieux
Isabelle Gautier
Jacques Coppey
Klaus Kemnitz
Sylvie Ravalet
Tristan Piolot
Vincent Mignotte
P2860
P304
P356
10.1016/S0006-3495(02)75357-5
P407
P577
2002-12-01T00:00:00Z