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1 ch is carried asymptomatically by deer mice (Peromyscus maniculatus).
2 house mice (Mus musculus) and of deer mice (Peromyscus maniculatus).
3 - and low-altitude populations of deer mice, Peromyscus maniculatus.
4 low-altitude haplogroups of the deer mouse, Peromyscus maniculatus.
5 obtained from the following Nevada rodents: Peromyscus maniculatus (17 isolates), Tamias minimus (11
6 e the range of its reservoir (the deer mouse Peromyscus maniculatus), an investigation sought to dete
7 nce of coinfection in rodents, predominantly Peromyscus maniculatus and N. mexicana, that inhabit the
8 eotoma neomexicana) and two species of mice (Peromyscus maniculatus and P. boylii) decreased in the c
9 vious analysis of L1 sequences in deer mice, Peromyscus maniculatus and P. leucopus, revealed two act
10 ds, soil, earthworms (Lumbricus), deer mice (Peromyscus maniculatus), and eggs of European starlings
11 eromyscus californicus, Peromyscus leucopus, Peromyscus maniculatus, and Peromyscus polionotus, and d
12 rampelinus ("singing mice"), the deer mouse, Peromyscus maniculatus, and the lab mouse, Mus musculus.
13 us (CMV) was isolated from its natural host, Peromyscus maniculatus, and was designated Peromyscus CM
14 rat (Rattus norvegicus) and the deer mouse (Peromyscus maniculatus) are attributable to a relaxation
17 odent species Peromyscus polionotus (PO) and Peromyscus maniculatus (BW) yield parent-of-origin effec
18 d strain of Sin Nombre virus from deer mice (Peromyscus maniculatus) by i.m. inoculation of 4- to 6-w
19 idus and the LINE-1 active outgroup species, Peromyscus maniculatus, by PCR of a pro-pol region has a
20 on in its natural reservoir, the deer mouse (Peromyscus maniculatus), despite a strong host immune re
21 y inoculating them into groups of deer mice (Peromyscus maniculatus), hamsters, and Swiss Webster mic
23 example, survivorship studies of deer mice (Peromyscus maniculatus) have demonstrated that thermogen
24 r species of mice, Peromyscus polionotus and Peromyscus maniculatus, have large and heritable differe
25 Reithrodontomys megalotis, and one omnivore: Peromyscus maniculatus) in the Smoke Creek Desert of nor
26 ses from one such reservoir, the deer mouse (Peromyscus maniculatus), infected with Sin Nombre virus.
27 trast, in the highly promiscuous deer mouse, Peromyscus maniculatus, sperm are significantly more lik
28 n genes in natural populations of deer mice (Peromyscus maniculatus) that are adapted to different el
30 was highly associated with the abundance of Peromyscus maniculatus, the reservoir of Sin Nombre viru
31 s), rat (Rattus norvegicus), and deer mouse (Peromyscus maniculatus), to identify rapidly evolving ge
32 and vital rate CV were negatively related in Peromyscus maniculatus (Wagner, 1845), but the relations
35 y duplicated beta-globin genes of deer mice (Peromyscus maniculatus), which contribute to adaptive di
36 es Peromyscus polionotus and the polyandrous Peromyscus maniculatus yield progeny with parent-of-orig
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