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activation of receptor gene transcription. Journal of Pharmacological Sciences , 103 ,
374-382.
Digman,M. A., Dalal, R., Horwitz, A. F., &Gratton, E. (2008).Mapping the number ofmolecules
and brightness in the laser scanning microscope. Biophysical Journal , 94 , 2320-2332.
Foo, Y. H., Naredi-Rainer, N., Lamb, D. C., Ahmed, S., & Wohland, T. (2012). Factors af-
fecting the quantification of biomolecular interactions by fluorescence cross-correlation
spectroscopy. Biophysical Journal , 102 , 1174-1183.
Goedhart, J., van Weeren, L., Adjobo-Hermans, M. J. W., Elzenaar, I., Hink, M. A., &
Gadella, T. W. J., Jr. (2011). Quantitative co-expression of proteins at the single cell
level—Application to a multimeric FRET sensor. PloS One , 6 , e27321.
Goedhart, J., von Stetten, D., Noirclerc-Savoye, M., Lelimousin, M., Joosen, L., Hink, M. A.,
et al. (2012). Structure-guided evolution of cyan fluorescent proteins towards a quantum
yield of 93%. Nature Communications , 3 , 751-759.
Gregor, I., Patra, D., & Enderlein, J. (2005). Optical saturation in fluorescence correlation
spectroscopy under continuous-wave and pulsed excitation. ChemPhysChem , 6 , 164-170.
Hassler, K., Leutenegger, M., Rigler, P., Rao, R., Rigler, R., Giisch, M., et al. (2005). Total
internal reflection fluorescence correlation spectroscopy (TIR-FCS) with low background
and high count-rate per molecule. Optics Express , 13 , 7415-7423.
Haustein, E., & Schwille, P. (2007). Fluorescence correlation spectroscopy: Novel variations
of an established technique. Annual Review of Biophysics and Biophysical Chemistry , 36 ,
151-169.
Heinze, K. G., Jahnz, M., & Schwille, P. (2004). Triple-color coincidence analysis: One step
further in following higher order molecular complex formation. Biophysical Journal , 86 ,
506-516.
Herrick-Davis, K., Grinde, E., Lindsley, T., Cowan, A., & Mazurkiewicz, J. E. (2012). Olig-
omer size of the serotonin 5-HT2C receptor revealed by fluorescence correlation spectros-
copy with photon counting histogram analysis: Evidence for homodimers without
monomers or tetramers. The Journal of Biological Chemistry , 287 , 23604-23614.
Hink, M. A. (2012). Single-molecule microscopy using silicone oil immersion objective
lenses. The Biomedical Scientist , 2012 , 83-85.
Hink, M. A. (in preparation) Fluorescence correlation spectroscopy. In P. Verveer (Vol. Ed.).
Methods in molecular biology. Advanced fluorescence microscopy: Methods and proto-
cols. Amsterdam: Springer.
Hink, M. A., de Vries, S. C., & Visser, A J W G (2011). Fluorescence fluctuation analysis of
receptor kinase dimerization. In Plant kinases. Methods and protocols . In N. Dissmeyer &
A. Schnittger (Eds.), Methods in molecular biology , Vol. 779, (pp. 199-216). Dordrecht:
Humana Press.
Hink, M. A., Shah, K., Russinova, E., de Vries, S. C., &Visser, A J WG (2008). Fluorescence
fluctuation analysis of AtSERK and BRI1 oligomerization. Biophysical Journal , 94 ,
1052-1062.
Kolin, D. L., & Wiseman, P. W. (2007). Advances in image correlation spectroscopy: Mea-
suring number densities, aggregation states, and dynamics of fluorescently labeled mac-
romolecules in cells. Cell Biochemistry and Biophysics , 49 , 141-164.
Koppel, D. E. (1974). Statistical accuracy in fluorescence correlation spectroscopy. Physical
Review A , 10 , 1938-1945.
Kremers, G. J., Goedhart, J., van Munster, E. B., & Gadella, T. W. J., Jr. (2006). Cyan and
yellow super fluorescent proteins with improved brightness, protein folding, and FRET
F ¨ rster radius. Biochemistry , 45 , 6570-6580.
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