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1 in a model rodent system, the North American deer mouse.
2 ng a model rodent system, the North American deer mouse.
3 here are 25,000 copies of ID elements in the deer mouse, 1,500 copies in the gerbil (both cricetid ro
4  an eastern gray squirrel, a chipmunk, and a deer mouse, and 4 water samples from New York.
5 tion into the functional significance of the deer mouse beta-globin polymorphism was motivated by the
6 ence of individual ID elements in gerbil and deer mouse further confirms BC1 as a master gene in ID a
7                                          The deer mouse (genus Peromyscus) is the most abundant mamma
8                             For decades, the deer mouse has contributed to our understanding of popul
9 ntribute to adaptive functional variation in deer mouse hemoglobin (Hb).
10 um revealed that high-altitude adaptation of deer mouse hemoglobin involves parallel functional diffe
11                        Using an experimental deer mouse infection model in an outdoor laboratory, we
12 rred outside the range of its reservoir (the deer mouse Peromyscus maniculatus), an investigation sou
13 arried and transmitted by the North American deer mouse Peromyscus maniculatus, can cause infection i
14 f the Norway rat (Rattus norvegicus) and the deer mouse (Peromyscus maniculatus) are attributable to
15                             We have used the deer mouse (Peromyscus maniculatus) as a model to test t
16 nt personality and abundance scenarios for a deer mouse (Peromyscus maniculatus) population, paramete
17 tent infection in its natural reservoir, the deer mouse (Peromyscus maniculatus), despite a strong ho
18  cell responses from one such reservoir, the deer mouse (Peromyscus maniculatus), infected with Sin N
19 (Mus musculus), rat (Rattus norvegicus), and deer mouse (Peromyscus maniculatus), to identify rapidly
20  analyses in a single, widespread species of deer mouse (Peromyscus maniculatus), we identified 21 po
21 ence of rat and mouse but also following the deer mouse (Peromyscus) and hamster split, with no evide
22 na and S. xerampelinus ("singing mice"), the deer mouse, Peromyscus maniculatus, and the lab mouse, M
23                                          The deer mouse, Peromyscus maniculatus, has been identified
24       In contrast, in the highly promiscuous deer mouse, Peromyscus maniculatus, sperm are significan
25 en high- and low-altitude haplogroups of the deer mouse, Peromyscus maniculatus.
26 ylogenetic history of LINE-1 dynamics in the deer mouse, Peromyscus.
27  Sin Nombre (SN) hantavirus is maintained in deer mouse populations is unclear.
28 latus) by i.m. inoculation of 4- to 6-wk-old deer mouse pups.
29            Furthermore, transfer of a set of deer mouse-specific Hif-2a amino acids to house mouse Hi
30                                        Other deer mouse tissues, including kidney, were negative; in
31 SARS-CoV-2 RNA in six species, including the deer mouse, Virginia opossum, raccoon, groundhog, Easter
32     We have determined that infection of the deer mouse with its homologous hantavirus, Sin Nombre vi