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1 ert present in multiple species of the genus Peromyscus.
2 istory of LINE-1 dynamics in the deer mouse, Peromyscus.
3 tes produce the majority of LINE-1 copies in Peromyscus.
4 re sequence of the BC1 gene within the genus Peromyscus.
5 nsposable element found throughout the genus Peromyscus.
6 igs had similar responses to caffeine as did Peromyscus.
7 ies of the ecologically diverse rodent genus Peromyscus.
8 no acids under lineage-specific selection in Peromyscus.
9 halamus (PVN) in new world mice of the genus Peromyscus.
10 ss II E beta sequence diversity in the genus Peromyscus.
11 or from fathers to offspring was examined in Peromyscus.
12 to account for evolution of MHC diversity in Peromyscus.
13  that two sister species of deer mice (genus Peromyscus)(5) show different responses to the same loom
14                        Using pharmacology in Peromyscus and chemogenetics in Mus, we show that vasopr
15 ting that mys was present in the ancestor of Peromyscus and has been active through much of the evolu
16 ic mechanisms underlie hybrid inviability in Peromyscus and hence have a role in the establishment an
17             R1alpha localizes to midpiece in Peromyscus and is differentially expressed in mature spe
18                                 Whereas both Peromyscus and Mus pups produce ultrasonic vocalizations
19 in the independently derived HBA-T3 genes of Peromyscus and Rattus have been attributed to positive s
20 evelopment in eight taxa of deer mice (genus Peromyscus) and compare them with laboratory mice (C57BL
21 and mouse but also following the deer mouse (Peromyscus) and hamster split, with no evidence of incre
22                                              Peromyscus animals show biallelic expression of Rasgrf1
23             A more divergent rodent species (Peromyscus) appears to lack a similar repeat structure b
24                         Rodents of the genus Peromyscus are among the most common North American mamm
25                            Mice of the genus Peromyscus are found in nearly every habitat from Alaska
26  4% infection rate with a recently described Peromyscus Betacoronavirus with high similarity to HCoV-
27 rent data suggests that both cospeciation of Peromyscus-borne hantaviruses with their specific rodent
28 f mice belonging to the genera Onychomys and Peromyscus by generating 100 random topologies and estim
29                             California mice (Peromyscus californicus) are unusual; fathers participat
30 s issue in the territorial California mouse (Peromyscus californicus) because males of this species a
31    To test this hypothesis, California mice (Peromyscus californicus) offspring were exposed through
32 sponses to social stress in California mice (Peromyscus californicus), a model species for studying s
33   In free-living monogamous California mice (Peromyscus californicus), males administered three T-inj
34 behavior in male and female California mice (Peromyscus californicus).
35 that in monogamous Peromyscus polionotus and Peromyscus californicus, but not in polygamous Peromyscu
36   Brains were collected from male and female Peromyscus californicus, Peromyscus leucopus, Peromyscus
37 , Peromyscus maniculatus, and was designated Peromyscus CMV (PCMV).
38 4 animal species from four different groups (Peromyscus deer mice, Drosophila flies, mosquitoes, and
39                           Whereas Rattus and Peromyscus each have three adult alpha-globin genes (HBA
40 than Mus we examined the distribution of the Peromyscus ESTs across the rat genome finding markers on
41  Here we show that sperm of deer mice (genus Peromyscus) form motile aggregations, then we use this s
42                                  Because the Peromyscus genome organization resembles the Rattus geno
43 , and describe their utility for mapping the Peromyscus genome.
44 lected from vegetation, and from the rodents Peromyscus gossypinus (cotton mouse), Neotoma floridana
45 otton rats (Sigmodon hispidus), cotton mice (Peromyscus gossypinus) and oldfield mice (Peromyscus pol
46 n rat (Sigmodon hispidus), and cotton mouse (Peromyscus gossypinus) in Georgia and Florida, belonged
47 ties and infections in the reservoir rodents Peromyscus gossypinus, Sigmodon hispidus, and Neotoma fl
48 e LINE-1 lineage seen in the muroid rodents, Peromyscus has at least two LINE-1 lineages whose most r
49                                     Although Peromyscus has been studied extensively under both field
50           In the North American rodent genus Peromyscus, highland deer mice (Peromyscus maniculatus)
51 y's worth of detailed descriptive studies of Peromyscus in the wild, coupled with emerging genetic an
52 rising therefore that the natural history of Peromyscus is among the best studied of any small mammal
53 uggest that the evolution of cytochrome b in Peromyscus is chiefly governed by purifying selection.
54                    The results indicate that Peromyscus is the first taxonomic group reported to have
55                        The deer mouse (genus Peromyscus) is the most abundant mammal in North America
56             The elasticity of vital rates of Peromyscus leucopus (Rafinesque, 1818), Sigmodon hispidu
57 isolates, and 5 geographically corresponding Peromyscus leucopus (white-footed mouse) isolates.
58                                              Peromyscus leucopus and M. ochrogaster showed plasticity
59                        The cricetine rodents Peromyscus leucopus and P. maniculatus are key reservoir
60                          Further analysis of Peromyscus leucopus blood and tissue samples demonstrate
61                    The northern expansion of Peromyscus leucopus in southern Quebec provides an oppor
62 ri use Ixodes scapularis ticks as vector and Peromyscus leucopus mice as major reservoir host.
63                           Blood samples from Peromyscus leucopus mice captured at an enzootic site in
64 c ehrlichiosis (HGE), C3H/HeJ, C3H-SCID, and Peromyscus leucopus mice were infected with an HGE agent
65 c with sera obtained from naturally infected Peromyscus leucopus mice, a major reservoir.
66  sequential captures of a single free-living Peromyscus leucopus mouse and were examined for differen
67  The earliest seroreactive sample was from a Peromyscus leucopus mouse collected in June 1986 in Conn
68                      Sera from NY-1-positive Peromyscus leucopus neutralized NY-1 and SN at titers of
69 scapularis ticks and from white-footed mice (Peromyscus leucopus) and 1 isolate from an Ixodes dentat
70 e ( VO2max ) than lowland white-footed mice (Peromyscus leucopus) at a level of hypoxia that matches
71  laboratory population of white-footed mice (Peromyscus leucopus) deprived of water for biologically
72 ntibody- and PCR-positive white-footed mice (Peromyscus leucopus) from Indiana and Oklahoma.
73               We examined white-footed mice (Peromyscus leucopus) from Minnesota for infection with t
74 to feed to repletion on either white-footed (Peromyscus leucopus) or DBA/2 (Mus musculus) mice.
75 cs and physical traits of white-footed mice (Peromyscus leucopus) using a 39-year dataset from Maine,
76 we hypothesized that male white-footed mice (Peromyscus leucopus) would reduce brain size in response
77 rferi) by immunizing wild white-footed mice (Peromyscus leucopus), a reservoir host species, with eit
78 mples were collected from white-footed mice (Peromyscus leucopus), eastern chipmunks (Tamias striatus
79 acklegged ticks (Ixodes scapularis) on mice (Peromyscus leucopus), we fit the extended model to the b
80 all mammals, such as the white-footed mouse (Peromyscus leucopus), which currently inhabit the region
81 nherbivorous mouse species (Mus musculus and Peromyscus leucopus).
82 eservoir, the ubiquitous white-footed mouse (Peromyscus leucopus).
83                   The white-footed deermouse Peromyscus leucopus, a long-lived rodent, is a key reser
84                 The wild white-footed mouse, Peromyscus leucopus, is commonly used for photoperiod st
85 rom male and female Peromyscus californicus, Peromyscus leucopus, Peromyscus maniculatus, and Peromys
86                           White-footed mice, Peromyscus leucopus, were captured in southern Connectic
87 oci in the genome of the white-footed mouse, Peromyscus leucopus, were examined for the presence or a
88 ifics and a closely related lowland species, Peromyscus leucopus.
89 a wild population of the white-footed mouse, Peromyscus leucopus.
90  obtained from the following Nevada rodents: Peromyscus maniculatus (17 isolates), Tamias minimus (11
91 odent species Peromyscus polionotus (PO) and Peromyscus maniculatus (BW) yield parent-of-origin effec
92 climate and urbanization affect body size of Peromyscus maniculatus (PEMA), an abundant rodent found
93 and vital rate CV were negatively related in Peromyscus maniculatus (Wagner, 1845), but the relations
94 nce of coinfection in rodents, predominantly Peromyscus maniculatus and N. mexicana, that inhabit the
95 eotoma neomexicana) and two species of mice (Peromyscus maniculatus and P. boylii) decreased in the c
96 vious analysis of L1 sequences in deer mice, Peromyscus maniculatus and P. leucopus, revealed two act
97 ior, across two sister species of deer mice (Peromyscus maniculatus and P. polionotus) with divergent
98 ry and in male deer mice from the subspecies Peromyscus maniculatus bairdii.
99 es Peromyscus polionotus and the polyandrous Peromyscus maniculatus yield progeny with parent-of-orig
100 creases in aerobic performance in deer mice (Peromyscus maniculatus) adapted to the hypoxic environme
101                     High-altitude deer mice (Peromyscus maniculatus) and low-altitude white-footed mi
102 ilfered by 10 species, including deer mice ((Peromyscus maniculatus) and southern red-backed voles (M
103  rat (Rattus norvegicus) and the deer mouse (Peromyscus maniculatus) are attributable to a relaxation
104                                   Deer mice (Peromyscus maniculatus) are the natural reservoirs of Si
105                 We have used the deer mouse (Peromyscus maniculatus) as a model to test this hypothes
106                  Using omnivorous deer mice (Peromyscus maniculatus) as a model, we examine how varyi
107 d strain of Sin Nombre virus from deer mice (Peromyscus maniculatus) by i.m. inoculation of 4- to 6-w
108  example, survivorship studies of deer mice (Peromyscus maniculatus) have demonstrated that thermogen
109 rodent genus Peromyscus, highland deer mice (Peromyscus maniculatus) have greater thermogenic maximal
110 Reithrodontomys megalotis, and one omnivore: Peromyscus maniculatus) in the Smoke Creek Desert of nor
111                                   Deer mice (Peromyscus maniculatus) live at both low and high altitu
112 ariant of Epas1 in North American deer mice (Peromyscus maniculatus) on the control of breathing and
113 ty and abundance scenarios for a deer mouse (Peromyscus maniculatus) population, parameterized with d
114 n genes in natural populations of deer mice (Peromyscus maniculatus) that are adapted to different el
115  in enabling highland and lowland deer mice (Peromyscus maniculatus) to sustain aerobic thermogenesis
116                              Male deer mice (Peromyscus maniculatus) were maintained on long or short
117      Data from naturally infected deer mice (Peromyscus maniculatus) were used to investigate vertica
118 xperiment, we observed individual deer mice (Peromyscus maniculatus) with known personality traits pr
119 in the reproductive physiology of deer mice (Peromyscus maniculatus), a rodent species with an except
120 e the range of its reservoir (the deer mouse Peromyscus maniculatus), an investigation sought to dete
121 ds, soil, earthworms (Lumbricus), deer mice (Peromyscus maniculatus), and eggs of European starlings
122 on in its natural reservoir, the deer mouse (Peromyscus maniculatus), despite a strong host immune re
123 y inoculating them into groups of deer mice (Peromyscus maniculatus), hamsters, and Swiss Webster mic
124 ses from one such reservoir, the deer mouse (Peromyscus maniculatus), infected with Sin Nombre virus.
125 e disease in chronically infected deer mice (Peromyscus maniculatus), the natural host.
126 s), rat (Rattus norvegicus), and deer mouse (Peromyscus maniculatus), to identify rapidly evolving ge
127 ng forest and prairie ecotypes of deer mice (Peromyscus maniculatus), we characterized the genetic ba
128  a single, widespread species of deer mouse (Peromyscus maniculatus), we identified 21 polymorphic in
129 y duplicated beta-globin genes of deer mice (Peromyscus maniculatus), which contribute to adaptive di
130 en forest and prairie ecotypes of deer mice (Peromyscus maniculatus).
131 n the closely related promiscuous deer mice (Peromyscus maniculatus).
132  house mice (Mus musculus) and of deer mice (Peromyscus maniculatus).
133 ch is carried asymptomatically by deer mice (Peromyscus maniculatus).
134 eromyscus californicus, Peromyscus leucopus, Peromyscus maniculatus, and Peromyscus polionotus, and d
135 rampelinus ("singing mice"), the deer mouse, Peromyscus maniculatus, and the lab mouse, Mus musculus.
136 us (CMV) was isolated from its natural host, Peromyscus maniculatus, and was designated Peromyscus CM
137 idus and the LINE-1 active outgroup species, Peromyscus maniculatus, by PCR of a pro-pol region has a
138 transmitted by the North American deer mouse Peromyscus maniculatus, can cause infection in humans th
139                              The deer mouse, Peromyscus maniculatus, has been identified as the prima
140 r species of mice, Peromyscus polionotus and Peromyscus maniculatus, have large and heritable differe
141 trast, in the highly promiscuous deer mouse, Peromyscus maniculatus, sperm are significantly more lik
142 romyscus californicus, but not in polygamous Peromyscus maniculatus, the disruption of pair bonds alt
143  was highly associated with the abundance of Peromyscus maniculatus, the reservoir of Sin Nombre viru
144 rent responses to the same looming stimulus: Peromyscus maniculatus, which occupies densely vegetated
145 - and low-altitude populations of deer mice, Peromyscus maniculatus.
146  low-altitude haplogroups of the deer mouse, Peromyscus maniculatus.
147                             Experiments with Peromyscus mice also demonstrate that exposure to hypoxi
148 ge of two locally camouflaged populations of Peromyscus mice to show that the negative regulator of a
149        Here we examine two sister-species of Peromyscus mice with divergent mating systems.
150 y by studying five North American species of Peromyscus mice, all of them similar in diet (generalist
151 onogamous and nonmonogamous species pairs of Peromyscus mice, Microtus voles, parid songbirds, dendro
152 he clade of Sin Nombre-like viruses found in Peromyscus mice.
153 hat cries result in a more rapid approach by Peromyscus mothers than USVs, suggesting a role for crie
154 unconventional chromatid-cohesion pattern in Peromyscus oocytes, with sister chromatids cohered at a
155 revealed that the HBA-T3 genes of Rattus and Peromyscus originated via independent, lineage-specific
156                                    The 2,906 Peromyscus placenta and testis ESTs described here signi
157 etween the two North American rodent species Peromyscus polionotus (PO) and Peromyscus maniculatus (B
158  in a uniquely variable mainland population (Peromyscus polionotus albifrons), we scored 23 pigment t
159 isrupted deer mice showed that in monogamous Peromyscus polionotus and Peromyscus californicus, but n
160 ere we show that two sister species of mice, Peromyscus polionotus and Peromyscus maniculatus, have l
161 rosses between the monogamous rodent species Peromyscus polionotus and the polyandrous Peromyscus man
162                         Here, we report that Peromyscus polionotus is strikingly precocious with rega
163 om 179 wild and captive-bred old-field mice, Peromyscus polionotus subgriseus, comprising pedigree-ba
164 erated a chromosome-level genome assembly of Peromyscus polionotus subgriseus.
165  Here we show that in nature, oldfield mice (Peromyscus polionotus) build complex burrows with long e
166 ncept, we first RAD sequenced oldfield mice (Peromyscus polionotus) from a known pedigree, finding st
167  we show that the monogamous oldfield mouse (Peromyscus polionotus) has recently evolved a novel cell
168        Here, we focus on the oldfield mouse (Peromyscus polionotus), which occurs in the southeastern
169 e (Peromyscus gossypinus) and oldfield mice (Peromyscus polionotus)] in the presence and absence of m
170 myscus leucopus, Peromyscus maniculatus, and Peromyscus polionotus, and double labeled for the expres
171  escapes, whereas the open field specialist, Peromyscus polionotus, briefly freezes.
172 onogamous species lacking sperm competition, Peromyscus polionotus, sperm indiscriminately group with
173 ups produce ultrasonic vocalizations (USVs), Peromyscus pups also produce a second call type with aco
174   Sequence analysis of cloned ID elements in Peromyscus show most ID elements in this genus arose pri
175 usky-footed wood rats (Neotoma fuscipes) and Peromyscus sp. mice (P. maniculatus and P. truei) were c
176 eri infection in Ixodes scapularis ticks and Peromyscus sp. mice captured from areas around La Crosse
177  wood rats (34% of those tested) and 10 (8%) Peromyscus sp. mice were found to be seropositive, but o
178 d rat blood samples and in 1 of the 10 (10%) Peromyscus sp. specimens.
179                           Samples from other Peromyscus species (P. boylii, P. maniculatus, and P. go
180 ecies, we sequenced 11 of these genes in six Peromyscus species and found evidence for positive selec
181 ylogenetic analysis confirmed that these two Peromyscus species are sister taxa in a clade with P. po
182                            Analyses on three Peromyscus species reveal that the internal satellite co
183 sing five large, captive-bred populations of Peromyscus species that range from promiscuous mating wi
184  We show that the TrimCyp gene found in some Peromyscus species was acquired about 2 million years ag
185 ommon ancestor predates the expansion of the Peromyscus species.
186 las of the POA for males and females of both Peromyscus species.
187  faster in the two vole species than the two Peromyscus spp.
188 robes, while higher trophic level omnivores (Peromyscus spp.) and insectivores (Onychomys arenicola)
189  house mice and other mouse species (Mus and Peromyscus spp.) within germ-free wild-type (WT) and Rag
190 voles (Microtus ochrogaster) and field mice (Peromyscus spp.).
191 otoma fuscipes; primary prey) and deer mice (Peromyscus spp.; alternative prey).
192 ost ID elements in this genus arose prior to Peromyscus subgenus divergence.
193 e groups was associated with a rodent genus, Peromyscus, Tamias, or Spermophilus: The gltA, 16S rRNA
194 vergent selection among different species of Peromyscus that inhabit different thermal environments.
195 triplicated alpha-globin genes in Rattus and Peromyscus, the red blood cells of both rodent species c
196 daia and of sigmodontine genera Sigmodon and PEROMYSCUS: We found that M3 is highly conserved, and th

 
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