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1 istory of LINE-1 dynamics in the deer mouse, Peromyscus.
2 tes produce the majority of LINE-1 copies in Peromyscus.
3 re sequence of the BC1 gene within the genus Peromyscus.
4 nsposable element found throughout the genus Peromyscus.
5 igs had similar responses to caffeine as did Peromyscus.
6 ies of the ecologically diverse rodent genus Peromyscus.
7 no acids under lineage-specific selection in Peromyscus.
8 halamus (PVN) in new world mice of the genus Peromyscus.
9 ss II E beta sequence diversity in the genus Peromyscus.
10 or from fathers to offspring was examined in Peromyscus.
11 to account for evolution of MHC diversity in Peromyscus.
12 ert present in multiple species of the genus Peromyscus.
14 ting that mys was present in the ancestor of Peromyscus and has been active through much of the evolu
15 ic mechanisms underlie hybrid inviability in Peromyscus and hence have a role in the establishment an
17 in the independently derived HBA-T3 genes of Peromyscus and Rattus have been attributed to positive s
18 and mouse but also following the deer mouse (Peromyscus) and hamster split, with no evidence of incre
23 rent data suggests that both cospeciation of Peromyscus-borne hantaviruses with their specific rodent
24 f mice belonging to the genera Onychomys and Peromyscus by generating 100 random topologies and estim
26 s issue in the territorial California mouse (Peromyscus californicus) because males of this species a
27 Brains were collected from male and female Peromyscus californicus, Peromyscus leucopus, Peromyscus
29 4 animal species from four different groups (Peromyscus deer mice, Drosophila flies, mosquitoes, and
31 than Mus we examined the distribution of the Peromyscus ESTs across the rat genome finding markers on
32 Here we show that sperm of deer mice (genus Peromyscus) form motile aggregations, then we use this s
35 lected from vegetation, and from the rodents Peromyscus gossypinus (cotton mouse), Neotoma floridana
36 n rat (Sigmodon hispidus), and cotton mouse (Peromyscus gossypinus) in Georgia and Florida, belonged
37 ties and infections in the reservoir rodents Peromyscus gossypinus, Sigmodon hispidus, and Neotoma fl
38 e LINE-1 lineage seen in the muroid rodents, Peromyscus has at least two LINE-1 lineages whose most r
40 y's worth of detailed descriptive studies of Peromyscus in the wild, coupled with emerging genetic an
41 rising therefore that the natural history of Peromyscus is among the best studied of any small mammal
42 uggest that the evolution of cytochrome b in Peromyscus is chiefly governed by purifying selection.
51 c ehrlichiosis (HGE), C3H/HeJ, C3H-SCID, and Peromyscus leucopus mice were infected with an HGE agent
53 sequential captures of a single free-living Peromyscus leucopus mouse and were examined for differen
54 The earliest seroreactive sample was from a Peromyscus leucopus mouse collected in June 1986 in Conn
56 scapularis ticks and from white-footed mice (Peromyscus leucopus) and 1 isolate from an Ixodes dentat
57 laboratory population of white-footed mice (Peromyscus leucopus) deprived of water for biologically
61 we hypothesized that male white-footed mice (Peromyscus leucopus) would reduce brain size in response
62 rferi) by immunizing wild white-footed mice (Peromyscus leucopus), a reservoir host species, with eit
63 mples were collected from white-footed mice (Peromyscus leucopus), eastern chipmunks (Tamias striatus
64 acklegged ticks (Ixodes scapularis) on mice (Peromyscus leucopus), we fit the extended model to the b
65 all mammals, such as the white-footed mouse (Peromyscus leucopus), which currently inhabit the region
69 rom male and female Peromyscus californicus, Peromyscus leucopus, Peromyscus maniculatus, and Peromys
71 oci in the genome of the white-footed mouse, Peromyscus leucopus, were examined for the presence or a
73 obtained from the following Nevada rodents: Peromyscus maniculatus (17 isolates), Tamias minimus (11
74 odent species Peromyscus polionotus (PO) and Peromyscus maniculatus (BW) yield parent-of-origin effec
75 and vital rate CV were negatively related in Peromyscus maniculatus (Wagner, 1845), but the relations
76 nce of coinfection in rodents, predominantly Peromyscus maniculatus and N. mexicana, that inhabit the
77 eotoma neomexicana) and two species of mice (Peromyscus maniculatus and P. boylii) decreased in the c
78 vious analysis of L1 sequences in deer mice, Peromyscus maniculatus and P. leucopus, revealed two act
79 es Peromyscus polionotus and the polyandrous Peromyscus maniculatus yield progeny with parent-of-orig
80 rat (Rattus norvegicus) and the deer mouse (Peromyscus maniculatus) are attributable to a relaxation
83 d strain of Sin Nombre virus from deer mice (Peromyscus maniculatus) by i.m. inoculation of 4- to 6-w
84 example, survivorship studies of deer mice (Peromyscus maniculatus) have demonstrated that thermogen
85 Reithrodontomys megalotis, and one omnivore: Peromyscus maniculatus) in the Smoke Creek Desert of nor
86 n genes in natural populations of deer mice (Peromyscus maniculatus) that are adapted to different el
89 e the range of its reservoir (the deer mouse Peromyscus maniculatus), an investigation sought to dete
90 ds, soil, earthworms (Lumbricus), deer mice (Peromyscus maniculatus), and eggs of European starlings
91 on in its natural reservoir, the deer mouse (Peromyscus maniculatus), despite a strong host immune re
92 y inoculating them into groups of deer mice (Peromyscus maniculatus), hamsters, and Swiss Webster mic
93 ses from one such reservoir, the deer mouse (Peromyscus maniculatus), infected with Sin Nombre virus.
95 s), rat (Rattus norvegicus), and deer mouse (Peromyscus maniculatus), to identify rapidly evolving ge
96 y duplicated beta-globin genes of deer mice (Peromyscus maniculatus), which contribute to adaptive di
99 eromyscus californicus, Peromyscus leucopus, Peromyscus maniculatus, and Peromyscus polionotus, and d
100 rampelinus ("singing mice"), the deer mouse, Peromyscus maniculatus, and the lab mouse, Mus musculus.
101 us (CMV) was isolated from its natural host, Peromyscus maniculatus, and was designated Peromyscus CM
102 idus and the LINE-1 active outgroup species, Peromyscus maniculatus, by PCR of a pro-pol region has a
104 r species of mice, Peromyscus polionotus and Peromyscus maniculatus, have large and heritable differe
105 trast, in the highly promiscuous deer mouse, Peromyscus maniculatus, sperm are significantly more lik
106 was highly associated with the abundance of Peromyscus maniculatus, the reservoir of Sin Nombre viru
109 ge of two locally camouflaged populations of Peromyscus mice to show that the negative regulator of a
111 y by studying five North American species of Peromyscus mice, all of them similar in diet (generalist
113 revealed that the HBA-T3 genes of Rattus and Peromyscus originated via independent, lineage-specific
115 etween the two North American rodent species Peromyscus polionotus (PO) and Peromyscus maniculatus (B
116 ere we show that two sister species of mice, Peromyscus polionotus and Peromyscus maniculatus, have l
117 rosses between the monogamous rodent species Peromyscus polionotus and the polyandrous Peromyscus man
119 om 179 wild and captive-bred old-field mice, Peromyscus polionotus subgriseus, comprising pedigree-ba
120 Here we show that in nature, oldfield mice (Peromyscus polionotus) build complex burrows with long e
121 ncept, we first RAD sequenced oldfield mice (Peromyscus polionotus) from a known pedigree, finding st
122 myscus leucopus, Peromyscus maniculatus, and Peromyscus polionotus, and double labeled for the expres
123 onogamous species lacking sperm competition, Peromyscus polionotus, sperm indiscriminately group with
124 Sequence analysis of cloned ID elements in Peromyscus show most ID elements in this genus arose pri
125 usky-footed wood rats (Neotoma fuscipes) and Peromyscus sp. mice (P. maniculatus and P. truei) were c
126 eri infection in Ixodes scapularis ticks and Peromyscus sp. mice captured from areas around La Crosse
127 wood rats (34% of those tested) and 10 (8%) Peromyscus sp. mice were found to be seropositive, but o
130 ecies, we sequenced 11 of these genes in six Peromyscus species and found evidence for positive selec
131 sing five large, captive-bred populations of Peromyscus species that range from promiscuous mating wi
136 e groups was associated with a rodent genus, Peromyscus, Tamias, or Spermophilus: The gltA, 16S rRNA
137 vergent selection among different species of Peromyscus that inhabit different thermal environments.
138 triplicated alpha-globin genes in Rattus and Peromyscus, the red blood cells of both rodent species c
139 daia and of sigmodontine genera Sigmodon and PEROMYSCUS: We found that M3 is highly conserved, and th
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