244
D. Lloyd
145. E.L. Salgado, D.B. Murray, D. Lloyd, Some antidepressants (Li+, monoamine oxidase type-A
inhibitors) perturb the ultradian clock in Saccharomyces cerevisiae. Biol. Rhythm Res. 33,
351–361 (2002)
146. K. Sasidharan, M. Tomita, M.A. Aon, D. Lloyd, D.B. Murray, The time-structure of yeast
metabolism in vivo. Adv. Exp. Med. Biol. 736, 359–379 (2012)
147. A.D. Satroutdinov, H. Kuriyama, H. Kobayashi, Oscillatory metabolism of Saccharomyces
cerevisiae in continuous culture. FEMS Microbiol. Lett. 98, 261–268 (1992)
148. E.E. Sel’kov, Two alternative self-oscillating stationary states in thiol metabolism-two
alternative, types of cell division-normal and malignant ones. Biophysika 15, 1065–1073
(1970)
149. R.M. Shymko, R.R. Klevecz, Cell division gated by oscillatory timekeeping and critical size,
in Biomathematics and Cell Kinetics, ed. by Rotenberg (Elsevier/North Holland Biomedical
Press, Amsterdam, 1981), pp. 329–348
150. S.J. Silverman, A.A. Petti, N. Slavov, L. Parsond, R. Briehof, S.Y. Thiberge, D. Zenklusen,
S.J. Gandhi, D.R. Larson, R.H. Singer, D.P. Botstein, Metabolic cycling in single yeast cells
from unsynchronized steady-state populations limited on glucose or phosphate. Proc. Nat.
Acad. Sci. USA 107, 6946–6995 (2010)
151. N. Slavov, D. Botstein, Coupling among growth rate response, metabolic cycle and cell
division cycle in yeast. Mol. Biol. Cell 22, 1997–2009 (2011)
152. N. Slavov, J. Macinskas, A. Caudy, D. Botstein, Metabolic cycling without cell division in
respiring yeast. Proc. Nat. Acad. Sci. USA 108, 19090–19095 (2011)
153. H.Y. Sohn, D.B. Murray, H. Kuriyama, Ultradian oscillation of Saccharomyces cerevisiae
during aerobic continuous culture: hydrogen sulfide mediates population synchrony. Yeast
16, 1185–1190 (2000)
154. A. Stefanovska, Coupled oscillators—complex but not complicated cardiovascular and brain
interactions. IEEE Eng. Med. Biol. Mag. 26, 25–29 (2007)
155. A. Stefanovska, P.T. Clemson, Suprunenko, An introduction to chronotaxis systems—systems
far from equilibrium that adjust their clocks, in Self-organization in Complex Systems: The
Past, the Present and the Future of Synergetics, ed. by A. Pelster, G. Wunner (Springer, Berlin,
2013)
156. H.S. Thoke, L.F. Olsen, L. Duelund, R.P. Stock, T. Heimburg, L.A. Bagatolli, Is a constant
low-entropy process at the root of glycolytic oscillations? J. Biol. Phys. 44, 419–431 (2018)
157. V. Ticcinelli, T. Stankovski, P. McClintock, A. Stefanovsky, Aging of the couplings between
cardiac, respiratory and myogenic activity in humans. IEEE Eng. Med. Biol. Soc. (2015).
https://doi.org/10.1109/EMBC.2015.7320093
158. D.C. Wallace, Mitochondria and cancer. Nat. Rev. Cancer 12, 685–698 (2012)
159. D.C. Wallace, Mitochondrial DNA in human variation and disease. Cell 163, 33–38 (2015)
160. H.N. Xu, J. Tchou, M. Feng, H. Zhao, L.Z. Li, Optical redox imaging indices discriminate
human breast cancer from normal tissues. J. Biomed. Opt. 21(11), 114003 (2016)
161. H.N. Xu, H. Zhao, K. Chellappa, J.G. Davis, S. Nioka, J.A. Baur, L.Z. Li, Optical Redox
imaging of fixed unstained muscle slides reveals useful biological information. Mol. Imaging
Biol. 21(3), 417–425 (2019)
162. F.E. Yates, Fractal applications in biology: scaling time in biochemical networks: (Numerical
Methods). Meth. Enzymol. 219, 636–676 (1992)
163. F.E. Yates, L.B. Yates, Ultradian rhythms as the dynamic signatures of life, in Ultradian
Rhythms from Molecules to Mind, A New Vision of Life, ed. by D. Lloyd, E.L. Rossi (Springer,
Dordrecht, 2008), pp. 249–260
164. K. Zand, T. Pham, A. Davila Jr., D.C. Wallace, P.J. Burke, Nanofluidic platform for single
mitochondria analysis using fluorescence microscopy. Anal. Chem. 85(12), 6018–6025 (2013)
D. Lloyd
145. E.L. Salgado, D.B. Murray, D. Lloyd, Some antidepressants (Li+, monoamine oxidase type-A
inhibitors) perturb the ultradian clock in Saccharomyces cerevisiae. Biol. Rhythm Res. 33,
351–361 (2002)
146. K. Sasidharan, M. Tomita, M.A. Aon, D. Lloyd, D.B. Murray, The time-structure of yeast
metabolism in vivo. Adv. Exp. Med. Biol. 736, 359–379 (2012)
147. A.D. Satroutdinov, H. Kuriyama, H. Kobayashi, Oscillatory metabolism of Saccharomyces
cerevisiae in continuous culture. FEMS Microbiol. Lett. 98, 261–268 (1992)
148. E.E. Sel’kov, Two alternative self-oscillating stationary states in thiol metabolism-two
alternative, types of cell division-normal and malignant ones. Biophysika 15, 1065–1073
(1970)
149. R.M. Shymko, R.R. Klevecz, Cell division gated by oscillatory timekeeping and critical size,
in Biomathematics and Cell Kinetics, ed. by Rotenberg (Elsevier/North Holland Biomedical
Press, Amsterdam, 1981), pp. 329–348
150. S.J. Silverman, A.A. Petti, N. Slavov, L. Parsond, R. Briehof, S.Y. Thiberge, D. Zenklusen,
S.J. Gandhi, D.R. Larson, R.H. Singer, D.P. Botstein, Metabolic cycling in single yeast cells
from unsynchronized steady-state populations limited on glucose or phosphate. Proc. Nat.
Acad. Sci. USA 107, 6946–6995 (2010)
151. N. Slavov, D. Botstein, Coupling among growth rate response, metabolic cycle and cell
division cycle in yeast. Mol. Biol. Cell 22, 1997–2009 (2011)
152. N. Slavov, J. Macinskas, A. Caudy, D. Botstein, Metabolic cycling without cell division in
respiring yeast. Proc. Nat. Acad. Sci. USA 108, 19090–19095 (2011)
153. H.Y. Sohn, D.B. Murray, H. Kuriyama, Ultradian oscillation of Saccharomyces cerevisiae
during aerobic continuous culture: hydrogen sulfide mediates population synchrony. Yeast
16, 1185–1190 (2000)
154. A. Stefanovska, Coupled oscillators—complex but not complicated cardiovascular and brain
interactions. IEEE Eng. Med. Biol. Mag. 26, 25–29 (2007)
155. A. Stefanovska, P.T. Clemson, Suprunenko, An introduction to chronotaxis systems—systems
far from equilibrium that adjust their clocks, in Self-organization in Complex Systems: The
Past, the Present and the Future of Synergetics, ed. by A. Pelster, G. Wunner (Springer, Berlin,
2013)
156. H.S. Thoke, L.F. Olsen, L. Duelund, R.P. Stock, T. Heimburg, L.A. Bagatolli, Is a constant
low-entropy process at the root of glycolytic oscillations? J. Biol. Phys. 44, 419–431 (2018)
157. V. Ticcinelli, T. Stankovski, P. McClintock, A. Stefanovsky, Aging of the couplings between
cardiac, respiratory and myogenic activity in humans. IEEE Eng. Med. Biol. Soc. (2015).
https://doi.org/10.1109/EMBC.2015.7320093
158. D.C. Wallace, Mitochondria and cancer. Nat. Rev. Cancer 12, 685–698 (2012)
159. D.C. Wallace, Mitochondrial DNA in human variation and disease. Cell 163, 33–38 (2015)
160. H.N. Xu, J. Tchou, M. Feng, H. Zhao, L.Z. Li, Optical redox imaging indices discriminate
human breast cancer from normal tissues. J. Biomed. Opt. 21(11), 114003 (2016)
161. H.N. Xu, H. Zhao, K. Chellappa, J.G. Davis, S. Nioka, J.A. Baur, L.Z. Li, Optical Redox
imaging of fixed unstained muscle slides reveals useful biological information. Mol. Imaging
Biol. 21(3), 417–425 (2019)
162. F.E. Yates, Fractal applications in biology: scaling time in biochemical networks: (Numerical
Methods). Meth. Enzymol. 219, 636–676 (1992)
163. F.E. Yates, L.B. Yates, Ultradian rhythms as the dynamic signatures of life, in Ultradian
Rhythms from Molecules to Mind, A New Vision of Life, ed. by D. Lloyd, E.L. Rossi (Springer,
Dordrecht, 2008), pp. 249–260
164. K. Zand, T. Pham, A. Davila Jr., D.C. Wallace, P.J. Burke, Nanofluidic platform for single
mitochondria analysis using fluorescence microscopy. Anal. Chem. 85(12), 6018–6025 (2013)