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

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