Peter J Verveer

Summary

Country: Germany

Publications

  1. ncbi request reprint High-resolution three-dimensional imaging of large specimens with light sheet-based microscopy
    Peter J Verveer
    Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany
    Nat Methods 4:311-3. 2007
  2. doi request reprint Quantitative microscopy and systems biology: seeing the whole picture
    Peter J Verveer
    Department of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, Otto Hahn Strasse 11, 44227, Dortmund, Germany
    Histochem Cell Biol 130:833-43. 2008
  3. ncbi request reprint Global analysis of time correlated single photon counting FRET-FLIM data
    Hernan E Grecco
    Department of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, Otto Hahn Strasse 11, 44227 Dortmund, Germany
    Opt Express 17:6493-508. 2009
  4. ncbi request reprint An acylation cycle regulates localization and activity of palmitoylated Ras isoforms
    Oliver Rocks
    Department of Structural Biology, Max Planck Institute for Molecular Physiology, Otto Hahn Strasse 11, 44227 Dortmund, Germany
    Science 307:1746-52. 2005
  5. ncbi request reprint Growth factor-induced MAPK network topology shapes Erk response determining PC-12 cell fate
    Silvia D M Santos
    European Molecular Biology Laboratory EMBL, Cell Biology and Biophysics, Meyerhofstrasse 1, D 69117 Heidelberg, Germany
    Nat Cell Biol 9:324-30. 2007
  6. doi request reprint FRET in cell biology: still shining in the age of super-resolution?
    Hernan E Grecco
    Department of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, Otto Hahn Strasse 11, D 44227 Dortmund, Germany
    Chemphyschem 12:484-90. 2011
  7. ncbi request reprint Red-edge anisotropy microscopy enables dynamic imaging of homo-FRET between green fluorescent proteins in cells
    Anthony Squire
    Cell Biology and Cell Biophysics Program, European Molecular Biology Laboratory, Meyerhofstrasse 1, D 69117 Heidelberg, Germany
    J Struct Biol 147:62-9. 2004
  8. ncbi request reprint Imaging sites of receptor dephosphorylation by PTP1B on the surface of the endoplasmic reticulum
    Fawaz G Haj
    Cancer Biology Program, Division of Hematology Oncology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA 02115, USA
    Science 295:1708-11. 2002
  9. pmc Cdt1 associates dynamically with chromatin throughout G1 and recruits Geminin onto chromatin
    Georgia Xouri
    Laboratory of General Biology, School of Medicine, University of Patras, Patras, Greece
    EMBO J 26:1303-14. 2007

Collaborators

Detail Information

Publications9

  1. ncbi request reprint High-resolution three-dimensional imaging of large specimens with light sheet-based microscopy
    Peter J Verveer
    Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, Meyerhofstrasse 1, 69117 Heidelberg, Germany
    Nat Methods 4:311-3. 2007
    ..The ability to rapidly image large samples at high resolution with minimal photodamage provides new opportunities especially for the study of subcellular processes in large living specimens...
  2. doi request reprint Quantitative microscopy and systems biology: seeing the whole picture
    Peter J Verveer
    Department of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, Otto Hahn Strasse 11, 44227, Dortmund, Germany
    Histochem Cell Biol 130:833-43. 2008
    ..Combined with computational approaches they allow us to obtain insights in the reaction-diffusion processes that determine biological function on the scale of cells...
  3. ncbi request reprint Global analysis of time correlated single photon counting FRET-FLIM data
    Hernan E Grecco
    Department of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, Otto Hahn Strasse 11, 44227 Dortmund, Germany
    Opt Express 17:6493-508. 2009
    ..The proposed method is efficient and robust, and can be routinely applied to analyze FRET-FLIM data acquired in intact cells...
  4. ncbi request reprint An acylation cycle regulates localization and activity of palmitoylated Ras isoforms
    Oliver Rocks
    Department of Structural Biology, Max Planck Institute for Molecular Physiology, Otto Hahn Strasse 11, 44227 Dortmund, Germany
    Science 307:1746-52. 2005
    ..The de/reacylation cycle also initiates Ras activation at the Golgi by transport of PM-localized Ras guanosine triphosphate. Different de/repalmitoylation kinetics account for isoform-specific activation responses to growth factors...
  5. ncbi request reprint Growth factor-induced MAPK network topology shapes Erk response determining PC-12 cell fate
    Silvia D M Santos
    European Molecular Biology Laboratory EMBL, Cell Biology and Biophysics, Meyerhofstrasse 1, D 69117 Heidelberg, Germany
    Nat Cell Biol 9:324-30. 2007
    ..These results show that growth factor context determines the topology of the MAPK signalling network and that the resulting dynamics govern cell fate...
  6. doi request reprint FRET in cell biology: still shining in the age of super-resolution?
    Hernan E Grecco
    Department of Systemic Cell Biology, Max Planck Institute of Molecular Physiology, Otto Hahn Strasse 11, D 44227 Dortmund, Germany
    Chemphyschem 12:484-90. 2011
    ..Herein we review the major applications in biological FRET imaging and we discuss the possibilities and challenges in the super-resolution era...
  7. ncbi request reprint Red-edge anisotropy microscopy enables dynamic imaging of homo-FRET between green fluorescent proteins in cells
    Anthony Squire
    Cell Biology and Cell Biophysics Program, European Molecular Biology Laboratory, Meyerhofstrasse 1, D 69117 Heidelberg, Germany
    J Struct Biol 147:62-9. 2004
    ....
  8. ncbi request reprint Imaging sites of receptor dephosphorylation by PTP1B on the surface of the endoplasmic reticulum
    Fawaz G Haj
    Cancer Biology Program, Division of Hematology Oncology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA 02115, USA
    Science 295:1708-11. 2002
    ..Most of the RTKs activated at the cell surface showed interaction with PTP1B after internalization, establishing that RTK activation and inactivation are spatially and temporally partitioned within cells...
  9. pmc Cdt1 associates dynamically with chromatin throughout G1 and recruits Geminin onto chromatin
    Georgia Xouri
    Laboratory of General Biology, School of Medicine, University of Patras, Patras, Greece
    EMBO J 26:1303-14. 2007
    ..We propose that dynamic Cdt1-chromatin associations and the recruitment of Geminin to chromatin provide spatio-temporal control of the licensing process...