1,161 research outputs found
A study of characteristics of intercity transportation systems. Phase 1: Definition of transportation comparison methodology
Decision making in early transportation planning must be responsive to complex value systems representing various policies and objectives. The assessment of alternative transportation concepts during the early initial phases of the system life cycle, when supportive research and technology development activities are defined, requires estimates of transportation, environmental, and socio-economic impacts throughout the system life cycle, which is a period of some 40 or 50 years. A unified methodological framework for comparing intercity passenger and freight transportation systems is described and is extended to include the comparison of long term transportation trends arising from implementation of the various R & D programs. The attributes of existing and future transportation systems are reviewed in order to establish measures for comparison, define value functions, and attribute weightings needed for comparing alternative policy actions for furthering transportation goals. Comparison criteria definitions and an illustrative example are included
Cooperative Chiral Order in Copolymers of Chiral and Achiral Units
Polyisocyanates can be synthesized with chiral and achiral pendant groups
distributed randomly along the chains. The overall chiral order, measured by
optical activity, is strongly cooperative and depends sensitively on the
concentration of chiral pendant groups. To explain this cooperative chiral
order theoretically, we map the random copolymer onto the one-dimensional
random-field Ising model. We show that the optical activity as a function of
composition is well-described by the predictions of this theory.Comment: 13 pages, including 3 postscript figures, uses REVTeX 3.0 and
epsf.st
Theory of Chiral Order in Random Copolymers
Recent experiments have found that polyisocyanates composed of a mixture of
opposite enantiomers follow a chiral ``majority rule:'' the chiral order of the
copolymer, measured by optical activity, is dominated by whichever enantiomer
is in the majority. We explain this majority rule theoretically by mapping the
random copolymer onto the random-field Ising model. Using this model, we
predict the chiral order as a function of enantiomer concentration, in
quantitative agreement with the experiments, and show how the sharpness of the
majority-rule curve can be controlled.Comment: 13 pages, including 4 postscript figures, uses REVTeX 3.0 and
epsf.st
P16-52. HIV-activated human plasmacytoid DCs induce Tregs through an indoleamine 2,3-dioxygenase-dependent mechanism
International audiencen.
Dynamical scaling of the DNA unzipping transition
We report studies of the equilibrium and the dynamics of a general set of
lattice models which capture the essence of the force-induced or mechanical DNA
unzipping transition. Besides yielding the whole equilibrium phase diagram in
the force vs temperature plane, which reveals the presence of an interesting
re-entrant unzipping transition for low T, these models enable us to
characterize the dynamics of the process starting from a non-equilibrium
initial condition. The thermal melting of the DNA strands displays a model
dependent time evolution. On the contrary, our results suggest that the
dynamical mechanism for the unzipping by force is very robust and the scaling
behaviour does not depend on the details of the description we adopt.Comment: 6 pages, 4 figures, A shorter version of this paper appeared in Phys.
Rev. Lett. 88, 028102 (2002
Chiral molecule adsorption on helical polymers
We present a lattice model for helicity induction on an optically inactive
polymer due to the adsorption of exogenous chiral amine molecules. The system
is mapped onto a one-dimensional Ising model characterized by an on-site
polymer helicity variable and an amine occupancy one. The equilibrium
properties are analyzed at the limit of strong coupling between helicity
induction and amine adsorption and that of non-interacting adsorbant molecules.
We discuss our results in view of recent experimental results
Lifelongα-tocopherol supplementation increases the median life span of C57BL/6 mice in the cold but has only minor effects on oxidative damage
The effects of dietary antioxidant supplementation on oxidative stress and life span are confused. We maintained C57BL/6 mice at 7 ± 2°C and supplemented their diet with α-tocopherol from 4 months of age. Supplementation significantly increased (p = 0.042) median life span by 15% (785 days, n = 44) relative to unsupplemented controls (682 days, n = 43) and also increased maximum life span (oldest 10%, p = 0.028). No sex or sex by treatment interaction effects were observed on life span, with treatment having no effect on resting or daily metabolic rate. Lymphocyte and hepatocyte oxidative DNA damage and hepatic lipid peroxidation were unaffected by supplementation, but hepatic oxidative DNA damage increased with age. Using a cDNA macroarray, genes associated with xenobiotic metabolism were significantly upregulated in the livers of female mice at 6 months of age (2 months supplementation). At 22 months of age (18 months supplementation) this response had largely abated, but various genes linked to the p21 signaling pathway were upregulated at this time. We suggest that α-tocopherol may initially be metabolized as a xenobiotic, potentially explaining why previous studies observe a life span extension generally when lifelong supplementation is initiated early in life. The absence of any significant effect on oxidative damage suggests that the life span extension observed was not mediated via any antioxidant properties of α-tocopherol. We propose that the life span extension observed following α-tocopherol supplementation may be mediated via upregulation of cytochrome p450 genes after 2 months of supplementation and/or upregulation of p21 signaling genes after 18 months of supplementation. However, these signaling pathways now require further investigation to establish their exact role in life span extension following α-tocopherol supplementation
Sequence randomness and polymer collapse transitions
Contrary to expectations based on Harris' criterion, chain disorder with
frustration can modify the universality class of scaling at the theta
transition of heteropolymers. This is shown for a model with random two-body
potentials in 2D on the basis of exact enumeration and accurate Monte Carlo
results. When frustration grows beyond a certain finite threshold, the
temperature below which disorder becomes relevant coincides with the theta one
and scaling exponents definitely start deviating from those valid for
homopolymers.Comment: 4 pages, 4 eps figure
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