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Models of slipped mono- and dinucleotide repeats have been limited to heteroduplexes that contain a repeat sequence in the absence of its complementary strand [for example, a (CA 4 slip-out without a complementary (TG) n tract].
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This recent hypothesis however remains controversial and many authors remain in favor of the previous model of slipped mispairing [31].
Here we determined that models of slipped-DNA junctions can assume multiple interconverting isoforms that can be differentially recognized by structure-specific DNA-binding proteins, and we reveal that the junction conformation can affect DNA repair, determining whether slip-outs are correctly repaired or lead to expansion mutations.
A phenomenological model of slip patterning in fatigued metals is developed.
Toda et al. (2016) examine surface ruptures aligned parallel to each other near the Mashiki town and Nishihara village and present a model of slip partitioning.
It is shown that deformation twinning is a natural outgrowth of the present model of slip when the material is deformed in a particular regime of temperature and stress.
Green patches 1A 1B correspond to alternative models of coseismic slip on MHT during the 1833 AD earthquake.
Many models of stick-slip behaviour in non-biological systems employ rules in which the strain is increased only when all sites are stable (inactive) and hence the system is in a quiescent state [59], [60], [61].
The 'Spectral analysis and synthesis of earthquake slip' section describes the details of the stochastic source modelling of earthquake slip distribution.
In this work, we use density-functional theory (DFT) calculations to, systematically study the all-dimension relaxed atomic models of Mg crystal slip, with a special focus on the "subslip modes" in prismatic and pyramidal slip systems.
Figure 9 shows best fit models of the simulated slip distribution with a superposition of spatial basis functions.
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