The bethe approximation to the three-state chiral clock model

1987 ◽  
Vol 66 (2) ◽  
pp. 227-235 ◽  
Author(s):  
M. Siegert ◽  
H. U. Everts
1986 ◽  
Author(s):  
Robert P. Frueholz ◽  
James C. Camparo
Keyword(s):  

2021 ◽  
Vol 103 (23) ◽  
Author(s):  
Flavio Ronetti ◽  
Daniel Loss ◽  
Jelena Klinovaja
Keyword(s):  

2021 ◽  
Vol 103 (19) ◽  
Author(s):  
Naveen Nishad ◽  
M. Santhosh ◽  
G. J. Sreejith
Keyword(s):  

Polymer ◽  
2009 ◽  
Vol 50 (17) ◽  
pp. 4257-4269 ◽  
Author(s):  
Douglas B. Adolf ◽  
Robert S. Chambers ◽  
Matthew A. Neidigk

2001 ◽  
Vol 356 (1415) ◽  
pp. 1717-1724 ◽  
Author(s):  
Louis W. Morgan ◽  
Jerry F. Feldman ◽  
Deborah Bell-Pedersen

Recent work on circadian clocks in Neurospora has primarily focused on the frequency ( frq ) and white–collar ( wc ) loci. However, a number of other genes are known that affect either the period or temperature compensation of the rhythm. These include the period (no relationship to the period gene of Drosophila ) genes and a number of genes that affect cellular metabolism. How these other loci fit into the circadian system is not known, and metabolic effects on the clock are typically not considered in single–oscillator models. Recent evidence has pointed to multiple oscillators in Neurospora , at least one of which is predicted to incorporate metabolic processes. Here, the Neurospora clock–affecting mutations will be reviewed and their genetic interactions discussed in the context of a more complex clock model involving two coupled oscillators: a FRQ/WC–based oscillator and a ‘ frq –less’ oscillator that may involve metabolic components.


2012 ◽  
Vol 112 (6) ◽  
pp. 063924 ◽  
Author(s):  
Raymond P. H. Wu ◽  
Veng-cheong Lo ◽  
Haitao Huang

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