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1  house mice (Mus musculus) and of deer mice (Peromyscus maniculatus).
2 ch is carried asymptomatically by deer mice (Peromyscus maniculatus).
3 en forest and prairie ecotypes of deer mice (Peromyscus maniculatus).
4 n the closely related promiscuous deer mice (Peromyscus maniculatus).
5 - and low-altitude populations of deer mice, Peromyscus maniculatus.
6  low-altitude haplogroups of the deer mouse, Peromyscus maniculatus.
7  obtained from the following Nevada rodents: Peromyscus maniculatus (17 isolates), Tamias minimus (11
8 in the reproductive physiology of deer mice (Peromyscus maniculatus), a rodent species with an except
9 creases in aerobic performance in deer mice (Peromyscus maniculatus) adapted to the hypoxic environme
10 e the range of its reservoir (the deer mouse Peromyscus maniculatus), an investigation sought to dete
11 nce of coinfection in rodents, predominantly Peromyscus maniculatus and N. mexicana, that inhabit the
12 eotoma neomexicana) and two species of mice (Peromyscus maniculatus and P. boylii) decreased in the c
13 vious analysis of L1 sequences in deer mice, Peromyscus maniculatus and P. leucopus, revealed two act
14 ior, across two sister species of deer mice (Peromyscus maniculatus and P. polionotus) with divergent
15                     High-altitude deer mice (Peromyscus maniculatus) and low-altitude white-footed mi
16 ilfered by 10 species, including deer mice ((Peromyscus maniculatus) and southern red-backed voles (M
17 ds, soil, earthworms (Lumbricus), deer mice (Peromyscus maniculatus), and eggs of European starlings
18 eromyscus californicus, Peromyscus leucopus, Peromyscus maniculatus, and Peromyscus polionotus, and d
19 rampelinus ("singing mice"), the deer mouse, Peromyscus maniculatus, and the lab mouse, Mus musculus.
20 us (CMV) was isolated from its natural host, Peromyscus maniculatus, and was designated Peromyscus CM
21  rat (Rattus norvegicus) and the deer mouse (Peromyscus maniculatus) are attributable to a relaxation
22                                   Deer mice (Peromyscus maniculatus) are the natural reservoirs of Si
23                 We have used the deer mouse (Peromyscus maniculatus) as a model to test this hypothes
24                  Using omnivorous deer mice (Peromyscus maniculatus) as a model, we examine how varyi
25 ry and in male deer mice from the subspecies Peromyscus maniculatus bairdii.
26 odent species Peromyscus polionotus (PO) and Peromyscus maniculatus (BW) yield parent-of-origin effec
27 d strain of Sin Nombre virus from deer mice (Peromyscus maniculatus) by i.m. inoculation of 4- to 6-w
28 idus and the LINE-1 active outgroup species, Peromyscus maniculatus, by PCR of a pro-pol region has a
29 transmitted by the North American deer mouse Peromyscus maniculatus, can cause infection in humans th
30 on in its natural reservoir, the deer mouse (Peromyscus maniculatus), despite a strong host immune re
31 y inoculating them into groups of deer mice (Peromyscus maniculatus), hamsters, and Swiss Webster mic
32                              The deer mouse, Peromyscus maniculatus, has been identified as the prima
33  example, survivorship studies of deer mice (Peromyscus maniculatus) have demonstrated that thermogen
34 rodent genus Peromyscus, highland deer mice (Peromyscus maniculatus) have greater thermogenic maximal
35 r species of mice, Peromyscus polionotus and Peromyscus maniculatus, have large and heritable differe
36 Reithrodontomys megalotis, and one omnivore: Peromyscus maniculatus) in the Smoke Creek Desert of nor
37 ses from one such reservoir, the deer mouse (Peromyscus maniculatus), infected with Sin Nombre virus.
38                                   Deer mice (Peromyscus maniculatus) live at both low and high altitu
39 ariant of Epas1 in North American deer mice (Peromyscus maniculatus) on the control of breathing and
40 climate and urbanization affect body size of Peromyscus maniculatus (PEMA), an abundant rodent found
41 ty and abundance scenarios for a deer mouse (Peromyscus maniculatus) population, parameterized with d
42 trast, in the highly promiscuous deer mouse, Peromyscus maniculatus, sperm are significantly more lik
43 n genes in natural populations of deer mice (Peromyscus maniculatus) that are adapted to different el
44 e disease in chronically infected deer mice (Peromyscus maniculatus), the natural host.
45 romyscus californicus, but not in polygamous Peromyscus maniculatus, the disruption of pair bonds alt
46  was highly associated with the abundance of Peromyscus maniculatus, the reservoir of Sin Nombre viru
47  in enabling highland and lowland deer mice (Peromyscus maniculatus) to sustain aerobic thermogenesis
48 s), rat (Rattus norvegicus), and deer mouse (Peromyscus maniculatus), to identify rapidly evolving ge
49 and vital rate CV were negatively related in Peromyscus maniculatus (Wagner, 1845), but the relations
50 ng forest and prairie ecotypes of deer mice (Peromyscus maniculatus), we characterized the genetic ba
51  a single, widespread species of deer mouse (Peromyscus maniculatus), we identified 21 polymorphic in
52                              Male deer mice (Peromyscus maniculatus) were maintained on long or short
53      Data from naturally infected deer mice (Peromyscus maniculatus) were used to investigate vertica
54 y duplicated beta-globin genes of deer mice (Peromyscus maniculatus), which contribute to adaptive di
55 rent responses to the same looming stimulus: Peromyscus maniculatus, which occupies densely vegetated
56 xperiment, we observed individual deer mice (Peromyscus maniculatus) with known personality traits pr
57 es Peromyscus polionotus and the polyandrous Peromyscus maniculatus yield progeny with parent-of-orig