Rainer Heintzmann

Summary

Affiliation: King's College London
Country: UK

Publications

  1. ncbi New effects in polynucleotide release from cationic lipid carriers revealed by confocal imaging, fluorescence cross-correlation spectroscopy and single particle tracking
    Svitlana Berezhna
    Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Goettingen, Germany
    Biochim Biophys Acta 1669:193-207. 2005
  2. ncbi High-resolution image reconstruction in fluorescence microscopy with patterned excitation
    Rainer Heintzmann
    Randall Division of Cell and Molecular Biophysics, Kings College London, London SE1 1UL, UK
    Appl Opt 45:5037-45. 2006
  3. ncbi Breaking the resolution limit in light microscopy
    Rainer Heintzmann
    Brief Funct Genomic Proteomic 5:289-301. 2006
  4. ncbi Structured illumination microscopy of a living cell
    Liisa M Hirvonen
    Randall Division of Cell and Molecular Biophysics, King s College London, New Hunt s House, London, UK
    Eur Biophys J 38:807-12. 2009
  5. ncbi Breaking the resolution limit in light microscopy
    Rainer Heintzmann
    Randall Division of Cell and Molecular Biophysics, King's College London, London SE1 1UL, United Kingdom
    Methods Cell Biol 81:561-80. 2007
  6. ncbi Dynamic speckle illumination microscopy with wavelet prefiltering
    Cathie Ventalon
    Boston University, Department of Biomedical Engineering, Boston, Massachusetts 02215, USA
    Opt Lett 32:1417-9. 2007
  7. ncbi Three-dimensional FRET reconstruction microscopy for analysis of dynamic molecular interactions in live cells
    Adam D Hoppe
    Department of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, USA
    Biophys J 95:400-18. 2008
  8. ncbi Fluorescence lifetime imaging in an optically sectioning programmable array microscope (PAM)
    Quentin S Hanley
    Department of Molecular Biology, Max Planck Institute for Biophysical Chemistry, Gottingen, Germany
    Cytometry A 67:112-8. 2005
  9. ncbi Resolution enhancement by subtraction of confocal signals taken at different pinhole sizes
    Rainer Heintzmann
    Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Gottingen, Germany
    Micron 34:293-300. 2003
  10. ncbi Saturated patterned excitation microscopy with two-dimensional excitation patterns
    Rainer Heintzmann
    Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, Göttingen 37077, Germany
    Micron 34:283-91. 2003

Collaborators

  • Thomas M Jovin
  • JEROME C MERTZ
  • Quentin S Hanley
  • Liisa M Hirvonen
  • Adam D Hoppe
  • Cathie Ventalon
  • Svitlana Berezhna
  • Kai Wicker
  • Ondrej Mandula
  • Joel A Swanson
  • Spencer L Shorte
  • Michael Jahnz
  • Ashok Deniz
  • Stephan Schaefer
  • Guido Boese
  • Petra Schwille

Detail Information

Publications11

  1. ncbi New effects in polynucleotide release from cationic lipid carriers revealed by confocal imaging, fluorescence cross-correlation spectroscopy and single particle tracking
    Svitlana Berezhna
    Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Goettingen, Germany
    Biochim Biophys Acta 1669:193-207. 2005
    ....
  2. ncbi High-resolution image reconstruction in fluorescence microscopy with patterned excitation
    Rainer Heintzmann
    Randall Division of Cell and Molecular Biophysics, Kings College London, London SE1 1UL, UK
    Appl Opt 45:5037-45. 2006
    ..We investigate the influence of some data processing strategies on unwanted effects such as residual patterning and local deviations from linearity in the reconstructed intensity...
  3. ncbi Breaking the resolution limit in light microscopy
    Rainer Heintzmann
    Brief Funct Genomic Proteomic 5:289-301. 2006
    ..Key concepts such as the point spread function and the Abbe limit, which are necessary for an in depth understanding of the presented methods, are described without requiring extensive mathematical training...
  4. ncbi Structured illumination microscopy of a living cell
    Liisa M Hirvonen
    Randall Division of Cell and Molecular Biophysics, King s College London, New Hunt s House, London, UK
    Eur Biophys J 38:807-12. 2009
    ..Here we demonstrate that with the help of a spatial light modulator, this technique can be used for imaging slowly moving structures in living cells...
  5. ncbi Breaking the resolution limit in light microscopy
    Rainer Heintzmann
    Randall Division of Cell and Molecular Biophysics, King's College London, London SE1 1UL, United Kingdom
    Methods Cell Biol 81:561-80. 2007
  6. ncbi Dynamic speckle illumination microscopy with wavelet prefiltering
    Cathie Ventalon
    Boston University, Department of Biomedical Engineering, Boston, Massachusetts 02215, USA
    Opt Lett 32:1417-9. 2007
    ..The resultant gain in sectioning strength leads to a fundamentally improved scaling law for the out-of-focus background rejection...
  7. ncbi Three-dimensional FRET reconstruction microscopy for analysis of dynamic molecular interactions in live cells
    Adam D Hoppe
    Department of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, USA
    Biophys J 95:400-18. 2008
    ..These results verify previous observations that Cdc42 signaling is localized to the advancing margins of forming phagosomes in macrophages...
  8. ncbi Fluorescence lifetime imaging in an optically sectioning programmable array microscope (PAM)
    Quentin S Hanley
    Department of Molecular Biology, Max Planck Institute for Biophysical Chemistry, Gottingen, Germany
    Cytometry A 67:112-8. 2005
    ..The PAM can be used in sectioning and nonsectioning modes, thereby constituting a useful platform for fluorescence lifetime imaging...
  9. ncbi Resolution enhancement by subtraction of confocal signals taken at different pinhole sizes
    Rainer Heintzmann
    Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, 37077 Gottingen, Germany
    Micron 34:293-300. 2003
    ..A comparison of 2D and 3D experimental data analysed with subtractive imaging, the equivalent Fourier-space processing of the confocal data only, and Fourier-space weighted averaging is presented...
  10. ncbi Saturated patterned excitation microscopy with two-dimensional excitation patterns
    Rainer Heintzmann
    Max Planck Institute for Biophysical Chemistry, Am Fassberg 11, Göttingen 37077, Germany
    Micron 34:283-91. 2003
    ..For higher resolution, an increased number of detected photons and of raw data images are required. A potential method for substantially decreasing the required number of raw images in PEM and SPEM is discussed...
  11. ncbi Saturated patterned excitation microscopy--a concept for optical resolution improvement
    Rainer Heintzmann
    Max Planck Institute for Biophysical Chemistry, Gottingen, Germany
    J Opt Soc Am A Opt Image Sci Vis 19:1599-609. 2002
    ..The effects of photon noise are included in the simulations...