Patent life cycle: New evidence

2014 ◽  
Vol 88 ◽  
pp. 313-324 ◽  
Author(s):  
Lubica Hikkerova ◽  
Niaz Kammoun ◽  
Jean-Sébastien Lantz
Keyword(s):  
Parasite ◽  
2013 ◽  
Vol 20 ◽  
pp. 15 ◽  
Author(s):  
Balu Alagar Venmathi Maran ◽  
Seong Yong Moon ◽  
Susumu Ohtsuka ◽  
Sung-Yong Oh ◽  
Ho Young Soh ◽  
...  
Keyword(s):  

Parasitology ◽  
1993 ◽  
Vol 107 (3) ◽  
pp. 237-247 ◽  
Author(s):  
W. Schlimme ◽  
M. Burri ◽  
K. Bender ◽  
B. Betschart ◽  
H. Hecker

SummaryNucleosome filaments of two stages of the life-cycle of Trypanosoma brucei brucei, namely bloodstream forms and procyclic culture forms, were investigated by electron microscopy. Chromatin of bloodstream forms showed a salt-dependent condensation. The level of condensation was higher than that shown by chromatin from procyclic culture forms, but 30 nm fibres as formed in rat liver chromatin preparations were not found. Analysis of histones provided new evidence for the existence of H1-like proteins, which comigrated in the region of the core histones in SDS–PAGE and in front of the core histones in Triton acid urea gels. Differences were found between the H1-like proteins of the two trypanosome stages as well as between the core histones in their amount, number of bands and banding pattern. It can be concluded that T. b. brucei contains a full set of histones, including H1-like proteins, and that the poor condensation of its chromatin is not due to the absence of H1, but most probably due to histone–DNA interaction being weak. It is obvious that structural and functional differences of the chromatin exist not only between T. b. brucei and higher eukaryotes, but also between various stages of the life-cycle of the parasite. It is therefore not adequate to investigate the chromatin only of the procyclic culture forms as a model for all stages of the life-cycle of T. b. brucei.


Author(s):  
Thomas J Kniesner ◽  
W. Kip Viscusi ◽  
James P Ziliak

AbstractOur research presents new evidence on the age pattern of the implicit value of life revealed from workers' differential wages and job safety pairings. Although aging reduces the number of years of life expectancy, aging can affect the value of life through an effect on planned life-cycle consumption. The elderly could, a priori, have the highest implicit value of life if there is a life-cycle plan to defer consumption until old age. We find that largely due to the age pattern of consumption, which is non-constant, the implicit value of life rises and falls over the lifetime in a way that the value for the elderly is higher than the average over all ages or for the young. There are important health policy implications of our empirical results. Because there may be age-specific benefits of programs to save statistical lives, instead of valuing the lives of the elderly at less than the young, health policymakers should more correctly value the lives of the elderly at as much as twice the young because of relatively greater consumption lost when accidental death occurs.


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