ライフサイエンスコーパス: deer mice

1 of breathing and metabolism in high-altitude deer mice.

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

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

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

5 99 case patients reported indoor exposure to deer mice.

6 cted in seven different organs of sacrificed deer mice.

7 pas1, including high-altitude populations of deer mice.

8 obic performance in hypoxia in high-altitude deer mice.

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

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

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

12 ide insight into high-altitude adaptation in deer mice and evolution at the Epas1 locus.

13 n, genome structure and genetic diversity in deer mice and likely facilitate local adaptation across

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

15 In the two most abundant species, deer mice and southern red-backed voles, risky behaviour

16 More exploratory deer mice and those with lower body condition were more

17 pproaches: the genetic basis of burrowing in deer mice and transcriptomic analyses of division of lab

18 Deer mice are also susceptible to Andes hantavirus (ANDV

19 Deer mice are the principal reservoir hosts of Sin Nombr

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

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

22 protein is highly enriched in high-altitude deer mice, but its functional significance is unknown.

23 Deer mice can be experimentally infected with Sin Nombre

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

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

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

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

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

29 genetic cross between two sister species of deer mice exhibiting large, innate differences in the ac

30 ng gestation and found that lowland-ancestry deer mice expand their placenta and maternal blood space

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

32 In two repeated experiments, deer mice fed for 4 weeks on controlled diets that varie

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

34 Deer mice from controlled crosses between high- and low-

35 eucopus raised in the laboratory and in male deer mice from the subspecies Peromyscus maniculatus bai

36 across neonatal development in eight taxa of deer mice (genus Peromyscus) and compare them with labor

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

38 Here we find that two sister species of deer mice (genus Peromyscus)(5) show different responses

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

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

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

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

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

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

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

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

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

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

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

50 foraging within mature forests; in contrast, deer mice occur in high densities across forest types an

51 In contrast, deer mice only demonstrated consistent behavioural respo

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

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

54 ocial behavior, across two sister species of deer mice (Peromyscus maniculatus and P. polionotus) wit

55 adaptive increases in aerobic performance in deer mice (Peromyscus maniculatus) adapted to the hypoxi

56 High-altitude deer mice (Peromyscus maniculatus) and low-altitude whit

57 Deer mice (Peromyscus maniculatus) are the natural reser

58 Using omnivorous deer mice (Peromyscus maniculatus) as a model, we examin

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

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

61 h American rodent genus Peromyscus, highland deer mice (Peromyscus maniculatus) have greater thermoge

62 Deer mice (Peromyscus maniculatus) live at both low and

63 -altitude variant of Epas1 in North American deer mice (Peromyscus maniculatus) on the control of bre

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

65 plasticity in enabling highland and lowland deer mice (Peromyscus maniculatus) to sustain aerobic th

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

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

68 n a field experiment, we observed individual deer mice (Peromyscus maniculatus) with known personalit

69 adaptation in the reproductive physiology of deer mice (Peromyscus maniculatus), a rodent species wit

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

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

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

73 Using forest and prairie ecotypes of deer mice (Peromyscus maniculatus), we characterized the

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

75 urs, than in the closely related promiscuous deer mice (Peromyscus maniculatus).

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

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

78 ences between forest and prairie ecotypes of deer mice (Peromyscus maniculatus).

79 oodrats (Neotoma fuscipes; primary prey) and deer mice (Peromyscus spp.; alternative prey).

80 83.5% were pilfered by 10 species, including deer mice ((Peromyscus maniculatus) and southern red-bac

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

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

83 Highland-ancestry deer mice produce even larger placentas and maternal blo

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

85 Deer mice remain infected despite a helper T cell respon

86 The patterns observed in deer mice resemble developmental plasticity observed in

87 Infection of deer mice results in persistence without conspicuous pat

88 omparisons of forest and prairie ecotypes of deer mice revealed 13 inversions that contribute to diff

89 High-altitude deer mice show evidence of natural selection on the Epas

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

91 sence of sera from bonded and bond-disrupted deer mice showed that in monogamous Peromyscus polionotu

92 Genes associated with fetal growth in deer mice significantly overlap with genes involved in h

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

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

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

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

97 In highland deer mice, the enhanced thermogenic VO2max in hypoxia is

98 In deer mice, these lower frequency "cries" are predominant

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

100 etween high- and low-altitude populations of deer mice to disrupt linkages between genetic loci so th

101 We acclimated lowland- and highland-ancestry deer mice to normoxia or hypoxia (12.3% O(2)) during ges

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

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

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

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

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

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

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

109 We examined high-altitude deer mice, which have evolved a high capacity for aerobi

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

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

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

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

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