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Items: 1 to 20 of 111


Three-color spectral FRET microscopy localizes three interacting proteins in living cells.

Sun Y, Wallrabe H, Booker CF, Day RN, Periasamy A.

Biophys J. 2010 Aug 9;99(4):1274-83. doi: 10.1016/j.bpj.2010.06.004.


Measuring protein interactions using Förster resonance energy transfer and fluorescence lifetime imaging microscopy.

Day RN.

Methods. 2014 Mar 15;66(2):200-7. doi: 10.1016/j.ymeth.2013.06.017. Epub 2013 Jun 24.


Characterization of an improved donor fluorescent protein for Forster resonance energy transfer microscopy.

Day RN, Booker CF, Periasamy A.

J Biomed Opt. 2008 May-Jun;13(3):031203. doi: 10.1117/1.2939094.


Monitoring dynamic protein interactions with photoquenching FRET.

Demarco IA, Periasamy A, Booker CF, Day RN.

Nat Methods. 2006 Jul;3(7):519-24.


Characterization of an orange acceptor fluorescent protein for sensitized spectral fluorescence resonance energy transfer microscopy using a white-light laser.

Sun Y, Booker CF, Kumari S, Day RN, Davidson M, Periasamy A.

J Biomed Opt. 2009 Sep-Oct;14(5):054009. doi: 10.1117/1.3227036.


FRET by fluorescence polarization microscopy.

Piston DW, Rizzo MA.

Methods Cell Biol. 2008;85:415-30.


Monitoring protein interactions in living cells with fluorescence lifetime imaging microscopy.

Sun Y, Hays NM, Periasamy A, Davidson MW, Day RN.

Methods Enzymol. 2012;504:371-91. doi: 10.1016/B978-0-12-391857-4.00019-7. Review.


Fluorescence resonance energy transfer microscopy: a mini review.

Periasamy A.

J Biomed Opt. 2001 Jul;6(3):287-91. Review.


Fluorescence resonance energy transfer-based stoichiometry in living cells.

Hoppe A, Christensen K, Swanson JA.

Biophys J. 2002 Dec;83(6):3652-64.


Improving the spectral analysis of Fluorescence Resonance Energy Transfer in live cells: application to interferon receptors and Janus kinases.

Krause CD, Digioia G, Izotova LS, Pestka S.

Cytokine. 2013 Oct;64(1):272-85. doi: 10.1016/j.cyto.2013.05.026. Epub 2013 Jun 21.


Fluorescent proteins for FRET microscopy: monitoring protein interactions in living cells.

Day RN, Davidson MW.

Bioessays. 2012 May;34(5):341-50. doi: 10.1002/bies.201100098. Epub 2012 Mar 7. Review. Erratum in: Bioessays. 2012 Jun;34(6):521.


N-way FRET microscopy of multiple protein-protein interactions in live cells.

Hoppe AD, Scott BL, Welliver TP, Straight SW, Swanson JA.

PLoS One. 2013 Jun 6;8(6):e64760. doi: 10.1371/journal.pone.0064760. Print 2013.


A practical method for monitoring FRET-based biosensors in living animals using two-photon microscopy.

Tao W, Rubart M, Ryan J, Xiao X, Qiao C, Hato T, Davidson MW, Dunn KW, Day RN.

Am J Physiol Cell Physiol. 2015 Dec 1;309(11):C724-35. doi: 10.1152/ajpcell.00182.2015. Epub 2015 Sep 2. Review.


Imaging protein interactions with bioluminescence resonance energy transfer (BRET) in plant and mammalian cells and tissues.

Xu X, Soutto M, Xie Q, Servick S, Subramanian C, von Arnim AG, Johnson CH.

Proc Natl Acad Sci U S A. 2007 Jun 12;104(24):10264-9. Epub 2007 Jun 5.


Quantification of protein interaction in living cells by two-photon spectral imaging with fluorescent protein fluorescence resonance energy transfer pair devoid of acceptor bleed-through.

Kim J, Li X, Kang MS, Im KB, Genovesio A, Grailhe R.

Cytometry A. 2012 Feb;81(2):112-9. doi: 10.1002/cyto.a.21150. Epub 2011 Nov 10.


Characterization of spectral FRET imaging microscopy for monitoring nuclear protein interactions.

Chen Y, Mauldin JP, Day RN, Periasamy A.

J Microsc. 2007 Nov;228(Pt 2):139-52.

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