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Nature Protocols
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September 3, 2011
Investigating protein-protein interactions in living cells using fluorescence lifetime imaging microscopy
Yuansheng Sun, Richard N Day, Ammasi Periasamy
Nature Protocols
|
September 30, 2016
A simple approach for measuring FRET in fluorescent biosensors using two-photon microscopy
Richard N Day, Wen Tao, Kenneth W Dunn
The Journal of Biological Chemistry
|
December 17, 2013
Vinculin phosphorylation at Tyr1065 regulates vinculin conformation and tension development in airway smooth muscle tissues
Youliang Huang, Richard N Day, Susan J Gunst
Journal of Biomedical Optics
|
July 8, 2008
Characterization of an improved donor fluorescent protein for Forster resonance energy transfer microscopy
Richard N Day, Cynthia F Booker, Ammasi Periasamy
The Journal of Biological Chemistry
|
January 18, 2003
Conformation of CCAAT/enhancer-binding protein alpha dimers varies with intranuclear location in living cells
Fred Schaufele, Xia Wang, Xiaowei Liu, et al.
Journal of Biomedical Optics
|
February 9, 2013
Unraveling transcription factor interactions with heterochromatin protein 1 using fluorescence lifetime imaging microscopy and fluorescence correlation spectroscopy
Amanda P Siegel, Nicole M Hays, Richard N Day
Biotechniques
|
March 25, 2005
Quantitative imaging of protein interactions in the cell nucleus
Ty C Voss, Ignacio A Demarco, Richard N Day
Plos One
|
December 23, 2021
Direct visualization by FRET-FLIM of a putative mechanosome complex involving Src, Pyk2 and MBD2 in living MLO-Y4 cells
Richard N Day, Kathleen H Day, Fredrick M Pavalko
Biophysical Journal
|
July 9, 2015
Inferring diffusion dynamics from FCS in heterogeneous nuclear environments
Konstantinos Tsekouras, Amanda P Siegel, Richard N Day, et al.
Journal of Microscopy
|
November 1, 2007
Characterization of spectral FRET imaging microscopy for monitoring nuclear protein interactions
Ye Chen, Joshua P Mauldin, Richard N Day, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 43) with videos related to
Sort By:
Page
of 5
Nature Protocols
|
September 3, 2011
Investigating protein-protein interactions in living cells using fluorescence lifetime imaging microscopy
Yuansheng Sun, Richard N Day, Ammasi Periasamy
Nature Protocols
|
September 30, 2016
A simple approach for measuring FRET in fluorescent biosensors using two-photon microscopy
Richard N Day, Wen Tao, Kenneth W Dunn
The Journal of Biological Chemistry
|
December 17, 2013
Vinculin phosphorylation at Tyr1065 regulates vinculin conformation and tension development in airway smooth muscle tissues
Youliang Huang, Richard N Day, Susan J Gunst
Journal of Biomedical Optics
|
July 8, 2008
Characterization of an improved donor fluorescent protein for Forster resonance energy transfer microscopy
Richard N Day, Cynthia F Booker, Ammasi Periasamy
The Journal of Biological Chemistry
|
January 18, 2003
Conformation of CCAAT/enhancer-binding protein alpha dimers varies with intranuclear location in living cells
Fred Schaufele, Xia Wang, Xiaowei Liu, et al.
Journal of Biomedical Optics
|
February 9, 2013
Unraveling transcription factor interactions with heterochromatin protein 1 using fluorescence lifetime imaging microscopy and fluorescence correlation spectroscopy
Amanda P Siegel, Nicole M Hays, Richard N Day
Biotechniques
|
March 25, 2005
Quantitative imaging of protein interactions in the cell nucleus
Ty C Voss, Ignacio A Demarco, Richard N Day
Plos One
|
December 23, 2021
Direct visualization by FRET-FLIM of a putative mechanosome complex involving Src, Pyk2 and MBD2 in living MLO-Y4 cells
Richard N Day, Kathleen H Day, Fredrick M Pavalko
Biophysical Journal
|
July 9, 2015
Inferring diffusion dynamics from FCS in heterogeneous nuclear environments
Konstantinos Tsekouras, Amanda P Siegel, Richard N Day, et al.
Journal of Microscopy
|
November 1, 2007
Characterization of spectral FRET imaging microscopy for monitoring nuclear protein interactions
Ye Chen, Joshua P Mauldin, Richard N Day, et al.
Page
of 5