Richard Day

Summary

Affiliation: Indiana University
Country: USA

Publications

  1. pmc The fluorescent protein palette: tools for cellular imaging
    Richard N Day
    Department of Cellular and Integrative Physiology, Indiana University School of Medicine, 635 Barnhill Dr, Indianapolis, IN 46202, USA
    Chem Soc Rev 38:2887-921. 2009
  2. pmc Unraveling transcription factor interactions with heterochromatin protein 1 using fluorescence lifetime imaging microscopy and fluorescence correlation spectroscopy
    Amanda P Siegel
    Indiana University School of Medicine, Department of Cellular and Integrative Physiology, 635 Barnhill Drive, Indianapolis, IN 46202, USA
    J Biomed Opt 18:25002. 2013
  3. pmc Measuring protein interactions using Förster resonance energy transfer and fluorescence lifetime imaging microscopy
    Richard N Day
    Department of Cellular and Integrative Physiology, Indiana University School of Medicine, 635 Barnhill Dr, Indianapolis, IN 46202, USA Electronic address
    Methods 66:200-7. 2014
  4. pmc Strengths and weaknesses of recently engineered red fluorescent proteins evaluated in live cells using fluorescence correlation spectroscopy
    Amanda P Siegel
    Department of Cellular and Integrative Physiology, Indiana University School of Medicine, 635 Barnhill Dr, MS 333, Indianapolis, IN 46202, USA
    Int J Mol Sci 14:20340-58. 2013
  5. pmc Monitoring biosensor activity in living cells with fluorescence lifetime imaging microscopy
    Julia M Hum
    Department of Cellular and Integrative Physiology, Indiana University School of Medicine, 635 Barnhill Dr, MS 333, Indianapolis, IN 46202, USA
    Int J Mol Sci 13:14385-400. 2012
  6. pmc Fluorescent proteins for FRET microscopy: monitoring protein interactions in living cells
    Richard N Day
    Department of Cellular and Integrative Physiology, Indiana University School of Medicine, Indianapolis, IN, USA
    Bioessays 34:341-50. 2012

Collaborators

  • Michael W Davidson
  • Amanda P Siegel
  • Julia M Hum
  • Nicole M Hays
  • Michelle A Baird
  • Fredrick M Pavalko

Detail Information

Publications6

  1. pmc The fluorescent protein palette: tools for cellular imaging
    Richard N Day
    Department of Cellular and Integrative Physiology, Indiana University School of Medicine, 635 Barnhill Dr, Indianapolis, IN 46202, USA
    Chem Soc Rev 38:2887-921. 2009
    ....
  2. pmc Unraveling transcription factor interactions with heterochromatin protein 1 using fluorescence lifetime imaging microscopy and fluorescence correlation spectroscopy
    Amanda P Siegel
    Indiana University School of Medicine, Department of Cellular and Integrative Physiology, 635 Barnhill Drive, Indianapolis, IN 46202, USA
    J Biomed Opt 18:25002. 2013
    ..The functional significance of these interactions is discussed...
  3. pmc Measuring protein interactions using Förster resonance energy transfer and fluorescence lifetime imaging microscopy
    Richard N Day
    Department of Cellular and Integrative Physiology, Indiana University School of Medicine, 635 Barnhill Dr, Indianapolis, IN 46202, USA Electronic address
    Methods 66:200-7. 2014
    ..The results demonstrate that the basic region and leucine zipper (BZip) domain of C/EBPα is sufficient for the interaction with HP1α in regions of heterochromatin. ..
  4. pmc Strengths and weaknesses of recently engineered red fluorescent proteins evaluated in live cells using fluorescence correlation spectroscopy
    Amanda P Siegel
    Department of Cellular and Integrative Physiology, Indiana University School of Medicine, 635 Barnhill Dr, MS 333, Indianapolis, IN 46202, USA
    Int J Mol Sci 14:20340-58. 2013
    ..The assays developed here aim to enable the rapid evaluation of new red FPs and their smooth adaptation to live cell spectroscopic microscopy and nanoscopy. ..
  5. pmc Monitoring biosensor activity in living cells with fluorescence lifetime imaging microscopy
    Julia M Hum
    Department of Cellular and Integrative Physiology, Indiana University School of Medicine, 635 Barnhill Dr, MS 333, Indianapolis, IN 46202, USA
    Int J Mol Sci 13:14385-400. 2012
    ..Importantly, the factors required for the accurate determination and reproducibility of lifetime measurements are described in detail...
  6. pmc Fluorescent proteins for FRET microscopy: monitoring protein interactions in living cells
    Richard N Day
    Department of Cellular and Integrative Physiology, Indiana University School of Medicine, Indianapolis, IN, USA
    Bioessays 34:341-50. 2012
    ..We then discuss the selection of FPs for the different FRET methods, identifying the most useful FP candidates for FRET microscopy. The recent success in expanding the FP color palette offers the opportunity to explore new FRET pairs...

Research Grants18

  1. SPECIFIC REPRESSION OF PROLACTIN GENE EXPRESSION
    Richard Day; Fiscal Year: 2009
    ..Discovering how nuclear architecture controls gene expression will be the cornerstone for understanding how genomes work. ..
  2. SPECIFIC REPRESSION OF PROLACTIN GENE EXPRESSION
    Richard Day; Fiscal Year: 1999
    ..Continuing on this theme, the final aim will investigate the association of Pit-1 and its protein partners with the nuclear matrix. ..
  3. SPECIFIC REPRESSION OF PROLACTIN GENE EXPRESSION
    Richard N Day; Fiscal Year: 2010
    ..Discovering how nuclear architecture controls gene expression will be the cornerstone for understanding how genomes work. ..
  4. SPECIFIC REPRESSION OF PROLACTIN GENE EXPRESSION
    Richard Day; Fiscal Year: 2009
    ..Discovering how nuclear architecture controls gene expression will be the cornerstone for understanding how genomes work. ..
  5. SPECIFIC REPRESSION OF PROLACTIN GENE EXPRESSION
    Richard Day; Fiscal Year: 2007
    ..abstract_text> ..
  6. SPECIFIC REPRESSION OF PROLACTIN GENE EXPRESSION
    Richard Day; Fiscal Year: 2005
    ..abstract_text> ..
  7. SPECIFIC REPRESSION OF PROLACTIN GENE EXPRESSION
    Richard Day; Fiscal Year: 2004
    ..abstract_text> ..
  8. SPECIFIC REPRESSION OF PROLACTIN GENE EXPRESSION
    Richard Day; Fiscal Year: 2003
    ..abstract_text> ..
  9. SPECIFIC REPRESSION OF PROLACTIN GENE EXPRESSION
    Richard Day; Fiscal Year: 2002
    ..Continuing on this theme, the final aim will investigate the association of Pit-1 and its protein partners with the nuclear matrix. ..
  10. SPECIFIC REPRESSION OF PROLACTIN GENE EXPRESSION
    Richard Day; Fiscal Year: 2001
    ..Continuing on this theme, the final aim will investigate the association of Pit-1 and its protein partners with the nuclear matrix. ..
  11. SPECIFIC REPRESSION OF PROLACTIN GENE EXPRESSION
    Richard Day; Fiscal Year: 2000
    ..Continuing on this theme, the final aim will investigate the association of Pit-1 and its protein partners with the nuclear matrix. ..
  12. SPECIFIC REPRESSION OF PROLACTIN GENE EXPRESSION
    Richard Day; Fiscal Year: 2006
    ..abstract_text> ..
  13. SPECIFIC REPRESSION OF PROLACTIN GENE EXPRESSION
    Richard N Day; Fiscal Year: 2010
    ..Discovering how nuclear architecture controls gene expression will be the cornerstone for understanding how genomes work. ..