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1 be recovered from inoculated C3H/HeNCrlBR or white-footed mice.
2 as used to detect granulocytic ehrlichiae in white-footed mice and in a dog inhabiting the area surro
3 ocytic Ehrlichia infections in humans, dogs, white-footed mice, and ticks.
4                         A high percentage of white-footed mice are infected or have been infected nat
5     Furthermore, given the important role of white-footed mice as seed predators and dispersers, and
6                                              White-footed mice from a field site infected laboratory-
7 immunity against E. phagocytophila precludes white-footed mice from further maintenance of this agent
8   Infection with Ehrlichia phagocytophila in white-footed mice is transient and followed by a strong
9    Using selected lines from a population of white-footed mice known to vary genetically in reproduct
10 are determined by interactions among acorns, white-footed mice, moths, deer, and ticks.
11 ce (Peromyscus maniculatus) and low-altitude white-footed mice (P. leucopus) were born and raised in
12 olates from Ixodes scapularis ticks and from white-footed mice (Peromyscus leucopus) and 1 isolate fr
13 aximal oxygen uptake ( VO2max ) than lowland white-footed mice (Peromyscus leucopus) at a level of hy
14 mbers of an outbred laboratory population of white-footed mice (Peromyscus leucopus) deprived of wate
15 ted in hantavirus antibody- and PCR-positive white-footed mice (Peromyscus leucopus) from Indiana and
16                                  We examined white-footed mice (Peromyscus leucopus) from Minnesota f
17 ence the demographics and physical traits of white-footed mice (Peromyscus leucopus) using a 39-year
18 s of brain tissue, we hypothesized that male white-footed mice (Peromyscus leucopus) would reduce bra
19 nt (Borrelia burgdorferi) by immunizing wild white-footed mice (Peromyscus leucopus), a reservoir hos
20                  Samples were collected from white-footed mice (Peromyscus leucopus), eastern chipmun
21                                              White-footed mice, Peromyscus leucopus, were captured in
22 a single infection with E. phagocytophila in white-footed mice provided only partial protection again
23 trial, we show that oral vaccination of wild white-footed mice resulted in outer surface protein A-sp
24  Infection with Anaplasma phagocytophilum in white-footed mice results in partial protection against
25                                 In contrast, white-footed mice were retrieved equally rarely by Calif