ライフサイエンスコーパス: deer mice

1 onse that fails to clear the virus occurs in deer mice.

2 disease were observed in any of the infected deer mice.

3 Nombre virus (SNV) from chronically infected deer mice.

4 99 case patients reported indoor exposure to deer mice.

5 cted in seven different organs of sacrificed deer mice.

6 was used for expression and immunization of deer mice against SNV-G1.

7 However, two deer mice and all hamsters and Swiss Webster mice inocul

8 ve phosphorylation pathways in high-altitude deer mice and by concomitant changes in the expression o

9 Hopi Hoekstra studied an intercross between deer mice and old-field mice that differ in their mating

10 Deer mice are also susceptible to Andes hantavirus (ANDV

11 Deer mice are the principal reservoir hosts of Sin Nombr

12 mice, we sacrificed experimentally infected deer mice at eight time points from day 21 to day 217 po

13 RT-PCR) in the blood of ELISA-positive adult deer mice but not in the blood of ELISA-positive juvenil

14 Deer mice can be experimentally infected with Sin Nombre

15 s most HCPS cases in South America; however, deer mice clear ANDV.

16 agent of HPS in North America, propagated in deer mice develop HPS, which is characterized by thrombo

17 results suggest that sperm from promiscuous deer mice discriminate among relatives and thereby coope

18 ecies from four different groups (Peromyscus deer mice, Drosophila flies, mosquitoes, and Nasonia was

19 he lungs or cardiac tissue from SNV-infected deer mice, even at the time of peak viral antigen expres

20 Male deer mice exposed to BPA or ethinyl estradiol (EE) throu

21 nfection of P. maniculatus, we examined wild deer mice for localization of viral antigens and nucleic

22 Here we show that sperm of deer mice (genus Peromyscus) form motile aggregations, t

23 Most ANDV-infected deer mice had seroconverted 14 days after inoculation, b

24 er inoculation, but none of the SNV-infected deer mice had.

25 We demonstrate that highland deer mice have an enhanced thermogenic capacity under hy

26 Immunohistochemical analysis of SNV-infected deer mice identified viral antigens within lung, liver,

27 cular helper phenotype in some ANDV-infected deer mice, including activation of the interleukin 4 (IL

28 dentified elevated immune gene expression in deer mice infected with ANDV and suggested maturation to

29 enhanced thermogenic performance of highland deer mice is largely attributable to an increased capaci

30 the 1-hydroxyethyl radical (HER) by rat and deer mice liver microsomal systems.

31 We studied cryptically colored deer mice living on the Nebraska Sand Hills and show tha

32 humans (n = 20; 11 positive, 9 negative) and deer mice (n = 6; 4 positive, 2 negative).

33 bias in seropositivity was detected in adult deer mice, no significant sex bias in seropositivity was

34 wever, in T cells from persistently infected deer mice, only TGF-beta(1) was expressed by all lines,

35 small, simple burrows of its sister species, deer mice (P. maniculatus).

36 Deer mice (Peromyscus maniculatus) are the natural reser

37 ouse-adapted strain of Sin Nombre virus from deer mice (Peromyscus maniculatus) by i.m. inoculation o

38 For example, survivorship studies of deer mice (Peromyscus maniculatus) have demonstrated tha

39 cated globin genes in natural populations of deer mice (Peromyscus maniculatus) that are adapted to d

40 Male deer mice (Peromyscus maniculatus) were maintained on lo

41 Data from naturally infected deer mice (Peromyscus maniculatus) were used to investig

42 ied biosolids, soil, earthworms (Lumbricus), deer mice (Peromyscus maniculatus), and eggs of European

43 evaluated by inoculating them into groups of deer mice (Peromyscus maniculatus), hamsters, and Swiss

44 es not cause disease in chronically infected deer mice (Peromyscus maniculatus), the natural host.

45 the tandemly duplicated beta-globin genes of deer mice (Peromyscus maniculatus), which contribute to

46 strains of house mice (Mus musculus) and of deer mice (Peromyscus maniculatus).

47 (SNV), which is carried asymptomatically by deer mice (Peromyscus maniculatus).

48 A previous analysis of L1 sequences in deer mice, Peromyscus maniculatus and P. leucopus, revea

49 etween high- and low-altitude populations of deer mice, Peromyscus maniculatus.

50 ere relatively weak in T cells isolated from deer mice, regardless of acute or persistent infection.

51 Deer mice remain infected despite a helper T cell respon

52 Infection of deer mice results in persistence without conspicuous pat

53 conducted on wild-caught, naturally infected deer mice showed a similar pattern of intermittent posit

54 The T cells from acutely infected deer mice synthesized a broad spectrum of cytokines, inc

55 adaptive variation in this complex trait in deer mice that are native to different elevations.

56 gen levels within the kidney were highest in deer mice that did not have antibodies to SNV but contai

57 field, we show that the light coat color of deer mice that recently colonized the light-colored soil

58 the genetic architecture of parental care in deer mice to discover an important contribution of vasop

59 role in SNV persistence and immune escape in deer mice, we measured the prevalence of virus quasispec

60 address Sin Nombre (SN) virus persistence in deer mice, we sacrificed experimentally infected deer mi

61 nal to the mass of the animal, with juvenile deer mice weighing less than 11 g most likely to be anti

62 distribution, and immune gene expression in deer mice were examined.

63 Ten juvenile deer mice were identified that had initially tested posi

64 elium in both species, but positive cells in deer mice were rare.

65 lizing antibodies were routinely detected in deer mice which maintained virus RNA in the blood and lu

66 serial blood samples from naturally infected deer mice, which were sequentially analyzed for SNV dive

67 However, infection of deer mice with a heterologous hantavirus, Andes virus, r

68 to transmit infection by cohousing infected deer mice with seronegative cage mates, we observed only

69 We infected deer mice with SNV or ANDV to identify differences in ho

70 virus through inoculation of cells or naive deer mice with the secreta or excreta of infected mice w