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FLIM Publications

  • Error Analysis Of The Rapid Lifetime Determination Method For Double-Exponential Decays And New Windowing Schemes
    Anal. Chem.1999, 71,947-952
  • Dynamic Imaging Using Fluorescence Resonance Energy Transfer
    Biotechniques Vol. 32 No. 6 (2002)
  • Nanosecond Fluorescence Resonance Energy Transfer-Fluorescence Lifetime Imaging Microscopy To Localize The Protein Interactions In A Single Living Cell
    Journal Of Microscopy, Vol. 205, Pt 1 January 2002, Pp. 3-14
  • Fluorescence Lifetime Imaging (FLIM) Of Green Fluorescent Fusion Proteins In Living Cells
    Methods In Molecular Biology, Vol. 183: Green Fluorescent Protein: Applications And Protocals
  • Time-Gated Fluorescence Microscopy For Clinical Imaging
    USA Microscopy And Analyses, March 1995 19
  • Time-Resolved Fluorescence Lifetime Imaging Microscopy Using A Picosecond Pulsed Tunable Dye Laser System
    Rev. Sci. Instrum. 67 (10), October 1996
  • Protein localization in living cells and tissues using FRET and FLIM
    Differentiation (2003) 71:528–541


  • Error Analysis Of The Rapid Lifetime Determination Method For Double-Exponential Decays And New Windowing Schemes
      Kristin K. Sharman

    ABSTRACT: The rapid lifetime determination method (RLD) is a mathematical technique for extremely rapid evaluations of lifetimes in exponential decays. It has been applied in luminescence microscopy and single-molecule lifetime evaluation....
    Anal. Chem.1999, 71,947-952
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    Dynamic Imaging Using Fluorescence Resonance Energy Transfer
      Masilamani Elangovan

    ABSTRACT: Recently, fluorescnce resonance energy transfer (FRET) and fluorescnce lifetime imaging microscopy (FLIM) have been the buzzwords for monitoring protein-protein interactions in living cells....
    Biotechniques Vol. 32 No. 6 (2002)
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    Nanosecond Fluorescence Resonance Energy Transfer-Fluorescence Lifetime Imaging Microscopy To Localize The Protein Interactions In A Single Living Cell
      Masilamani Elangovan

    ABSTRACT: Visualizing and quantifying protein-protein interactions is a recent trend in biomedical imaging. The current advances in fluorescnce microscopy, coupled with the development of new fluorescent probes such as green fluorescent proteins, allow fluorescent resonance energy transfer (FRET) to be used to study protein interactions in living spectrums....
    Journal Of Microscopy, Vol. 205, Pt 1 January 2002, Pp. 3-14
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    Fluorescence Lifetime Imaging (FLIM) Of Green Fluorescent Fusion Proteins In Living Cells
      Ammasi Periasamy

    ABSTRACT: Fluorescence microscopy is an exception al tool for looling inside cells and tissues. Recent advances in fluorescence microscopy, including improved optics, sensitive fluorescent dyes, and high-sensitivity cameras, coupled with technological advances in computes and sophisticated software now permit quantitative measurement and noninvasive acquisition of spectroscopic information from a single living cell....
    Methods In Molecular Biology, Vol. 183: Green Fluorescent Protein: Applications And Protocals
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    Time-Gated Fluorescence Microscopy For Clinical Imaging
      Assami Periasamy

    ABSTRACT: Fluorescence microscopy has been an essential tool for generations of biologists, allowing the examination of details of individual living or fixed cells. The development of a large number of fluorescnece dyes and the ability to attach them to specific molecular cell constituents allows real-time observation and quantification of the activities of these constituents in cells and tissues....
    USA Microscopy And Analyses, March 1995 19
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    Time-Resolved Fluorescence Lifetime Imaging Microscopy Using A Picosecond Pulsed Tunable Dye Laser System
      Ammasi Periasamy

    ABSTRACT: The design and implementation of a time-resolved fluorescence lifetime imaging microscope (TRFLIM) for the biomedical sciences are described. The measurement of fluorescence lifetimes offers many benefits, among which is that they are independent of local signal intensity and concentration of the fluorophore and they provide visualization of the molecular environment in a single living cell.
    Rev. Sci. Instrum. 67 (10), October 1996
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    Protein localization in living cells and tissues using FRET and FLIM
    Ye Chen . James D. Mills. Ammasi Periasamy

    Abstract: Interacting proteins assemble into molecular machines that control cellular homeostasis in living cells. While the in vitro screening methods have the advantage of providing direct access to the genetic information encoding unknown protein partners, they do not allow direct access to interactions of these protein partners in their natural environment inside the living cell. Using wide-.eld, confocal, or two-photon (2p) .uorescence resonance energy transfer (FRET) microscopy, ..........
    Differentiation (2003) 71:528–541
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