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Journal Abstract Search

337 related items for PubMed ID: 16498675

  • 1. Setup and characterization of a multiphoton FLIM instrument for protein-protein interaction measurements in living cells.
    Waharte F, Spriet C, Héliot L.
    Cytometry A; 2006 Apr; 69(4):299-306. PubMed ID: 16498675
    [Abstract] [Full Text] [Related]

  • 2. A flow cytometric method to detect protein-protein interaction in living cells by directly visualizing donor fluorophore quenching during CFP-->YFP fluorescence resonance energy transfer (FRET).
    He L, Olson DP, Wu X, Karpova TS, McNally JG, Lipsky PE.
    Cytometry A; 2003 Oct; 55(2):71-85. PubMed ID: 14505312
    [Abstract] [Full Text] [Related]

  • 3. Sensitivity of CFP/YFP and GFP/mCherry pairs to donor photobleaching on FRET determination by fluorescence lifetime imaging microscopy in living cells.
    Tramier M, Zahid M, Mevel JC, Masse MJ, Coppey-Moisan M.
    Microsc Res Tech; 2006 Nov; 69(11):933-9. PubMed ID: 16941642
    [Abstract] [Full Text] [Related]

  • 4. High-precision FLIM-FRET in fixed and living cells reveals heterogeneity in a simple CFP-YFP fusion protein.
    Millington M, Grindlay GJ, Altenbach K, Neely RK, Kolch W, Bencina M, Read ND, Jones AC, Dryden DT, Magennis SW.
    Biophys Chem; 2007 May; 127(3):155-64. PubMed ID: 17336446
    [Abstract] [Full Text] [Related]

  • 5. The use of fluorescence microscopy to visualise homotypic interactions of tomato spotted wilt virus nucleocapsid protein in living cells.
    Snippe M, Borst JW, Goldbach R, Kormelink R.
    J Virol Methods; 2005 Apr; 125(1):15-22. PubMed ID: 15737412
    [Abstract] [Full Text] [Related]

  • 6. Characterization of two-photon excitation fluorescence lifetime imaging microscopy for protein localization.
    Chen Y, Periasamy A.
    Microsc Res Tech; 2004 Jan 01; 63(1):72-80. PubMed ID: 14677136
    [Abstract] [Full Text] [Related]

  • 7. Imaging protein molecules using FRET and FLIM microscopy.
    Wallrabe H, Periasamy A.
    Curr Opin Biotechnol; 2005 Feb 01; 16(1):19-27. PubMed ID: 15722011
    [Abstract] [Full Text] [Related]

  • 8. Fluorescence resonance energy transfer of GFP and YFP by spectral imaging and quantitative acceptor photobleaching.
    Dinant C, van Royen ME, Vermeulen W, Houtsmuller AB.
    J Microsc; 2008 Jul 01; 231(Pt 1):97-104. PubMed ID: 18638193
    [Abstract] [Full Text] [Related]

  • 9. Detection of the interaction between SNAP25 and rabphilin in neuroendocrine PC12 cells using the FLIM/FRET technique.
    Lee JD, Chang YF, Kao FJ, Kao LS, Lin CC, Lu AC, Shyu BC, Chiou SH, Yang DM.
    Microsc Res Tech; 2008 Jan 01; 71(1):26-34. PubMed ID: 17886343
    [Abstract] [Full Text] [Related]

  • 10. Quantitative FRET analysis with the EGFP-mCherry fluorescent protein pair.
    Albertazzi L, Arosio D, Marchetti L, Ricci F, Beltram F.
    Photochem Photobiol; 2009 Jan 01; 85(1):287-97. PubMed ID: 18764891
    [Abstract] [Full Text] [Related]

  • 11. In-depth fluorescence lifetime imaging analysis revealing SNAP25A-Rabphilin 3A interactions.
    Lee JD, Huang PC, Lin YC, Kao LS, Huang CC, Kao FJ, Lin CC, Yang DM.
    Microsc Microanal; 2008 Dec 01; 14(6):507-18. PubMed ID: 18986604
    [Abstract] [Full Text] [Related]

  • 12. Protein localization in living cells and tissues using FRET and FLIM.
    Chen Y, Mills JD, Periasamy A.
    Differentiation; 2003 Dec 01; 71(9-10):528-41. PubMed ID: 14686950
    [Abstract] [Full Text] [Related]

  • 13. Isolation of FRET-positive cells using single 408-nm laser flow cytometry.
    van Wageningen S, Pennings AH, van der Reijden BA, Boezeman JB, de Lange F, Jansen JH.
    Cytometry A; 2006 Apr 01; 69(4):291-8. PubMed ID: 16498686
    [Abstract] [Full Text] [Related]

  • 14. A feasible add-on upgrade on a commercial two-photon FLIM microscope for optimal FLIM-FRET imaging of CFP-YFP pairs.
    Xu L, Wang L, Zhang Z, Huang ZL.
    J Fluoresc; 2013 May 01; 23(3):543-9. PubMed ID: 23456419
    [Abstract] [Full Text] [Related]

  • 15. Optimized protocol of a frequency domain fluorescence lifetime imaging microscope for FRET measurements.
    Leray A, Riquet FB, Richard E, Spriet C, Trinel D, Héliot L.
    Microsc Res Tech; 2009 May 01; 72(5):371-9. PubMed ID: 19084885
    [Abstract] [Full Text] [Related]

  • 16. Concatenation of cyan and yellow fluorescent proteins for efficient resonance energy transfer.
    Shimozono S, Hosoi H, Mizuno H, Fukano T, Tahara T, Miyawaki A.
    Biochemistry; 2006 May 23; 45(20):6267-71. PubMed ID: 16700538
    [Abstract] [Full Text] [Related]

  • 17. Imaging FRET standards by steady-state fluorescence and lifetime methods.
    Domingo B, Sabariegos R, Picazo F, Llopis J.
    Microsc Res Tech; 2007 Dec 23; 70(12):1010-21. PubMed ID: 17722057
    [Abstract] [Full Text] [Related]

  • 18. Cyan and yellow super fluorescent proteins with improved brightness, protein folding, and FRET Förster radius.
    Kremers GJ, Goedhart J, van Munster EB, Gadella TW.
    Biochemistry; 2006 May 30; 45(21):6570-80. PubMed ID: 16716067
    [Abstract] [Full Text] [Related]

  • 19. A novel fluorescence lifetime imaging system that optimizes photon efficiency.
    Colyer RA, Lee C, Gratton E.
    Microsc Res Tech; 2008 Mar 30; 71(3):201-13. PubMed ID: 18008362
    [Abstract] [Full Text] [Related]

  • 20. Correlated fluorescence lifetime and spectral measurements in living cells.
    Spriet C, Trinel D, Waharte F, Deslee D, Vandenbunder B, Barbillat J, Héliot L.
    Microsc Res Tech; 2007 Feb 30; 70(2):85-94. PubMed ID: 17152071
    [Abstract] [Full Text] [Related]

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