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Thus, we observe some convergence between previous behavioral studies of various mouse populations and our initial characterization of the DO.
Burgeoning mouse populations and exchange among scientists have led to the re-emergence of many of these agents.
A great deal of the experimental work in nutritional epigenetics is conducted with inbred mouse populations and the measurement of methylation levels of particular pieces of their idiosyncratic genomes.
The increased genetic diversity in the DO introduced by novel allele combinations provides a wide spectrum of behavior extending far beyond that of historical genetic mouse populations, and holds great promise for the genetic dissection of complex behavioral traits.
We compared measures of sequence diversity within mouse populations and divergence from the rat at these loci and in regions flanking them to the patterns around ARs and PC exons.
However, recent work in the field shows that both Hbb alleles are present in wild mouse populations and suggests that these alleles are maintained by balancing selection (Storz et al. 2007).
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However, the few animals living in such areas might or might not represent a noticeable fraction of the overall wood mouse population and might possibly disperse to more adequate areas whenever available.
Our data indicate that a CNV found in the largest extant mouse RI panel, a large inbred strain panel, an outbred laboratory mouse population and wild-caught mice causes an eQTL for Glo1.
Altered patterns of transgene expression within a mouse population and with age can affect results (Lopez et al., 2011).
Here, we experimentally reduced nematode infection in a wild mouse population and measured the effects on other non-target parasites.
Bonhomme et al. [ 7] used minisatellites to study house mouse population and provided a migration map for them.
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