ライフサイエンスコーパス: Microtus

1 e with the origin and radiation of the genus Microtus.

2 angement, and mitochondrial DNA evolution in Microtus.

3 In this study, field voles (Microtus agrestis), bank voles (Clethrionomys glareolus)

4 uals in a natural population of field voles (Microtus agrestis).

5 species (Myodes glareolus, Microtus arvalis, Microtus agrestis, Alexandromys oeconomus) in north-east

6 CNM and Hepatozoon spp. in three species of Microtus and to assess the occurrence of vertical transm

7 e litters of six infected Microtus dams (two Microtus arvalis and one M. oeconomus) and in 3/45 embry

8 xpansion observed in the Iberian common vole Microtus arvalis asturianus shortly after a colonization

9 onitoring data on abundances of common vole (Microtus arvalis), a cyclic agricultural rodent pest.

10 y in whole blood samples of the common vole (Microtus arvalis), taken from 10 ul tail-nick blood samp

11 belonging to four species (Myodes glareolus, Microtus arvalis, Microtus agrestis, Alexandromys oecono

12 elated species of common vole (field mouse), Microtus arvalis.

13 In voles (Microtus), central oxytocin (OT) receptor patterns are a

14 % of pups from three litters of six infected Microtus dams (two Microtus arvalis and one M. oeconomus

15 Paternal and nonpaternal voles (microtus) have different arginine-vasopressin (AVP) and

16 The genus Microtus includes several closely related species of vol

17 Our data suggest that numt translocation in Microtus is more extensive than in either Mus or in Ratt

18 Relative abundance of voles (Microtus mexicanus) increased in exclosure drainages, li

19 ecies of microtines, the polygynous montane (Microtus montanus) and meadow (M. pennsylvanicus) voles

20 ochrogaster) and promiscuous montane voles (Microtus montanus) exhibit remarkable differences in the

21 f pro-social behavior in male prairie voles (Microtus ochragaster), predicting that inhibition of tes

22 1818), Sigmodon hispidus Say & Ord, 1825 and Microtus ochrogaster (Wagner, 1842) was negatively relat

23 atric with cervids, including prairie voles (Microtus ochrogaster) and field mice (Peromyscus spp.).

24 Adult female prairie (Microtus ochrogaster) and meadow (M. pennsylvanicus) vol

25 expression across monogamous prairie voles (Microtus ochrogaster) and promiscuous meadow voles (Micr

26 Monogamous prairie voles (Microtus ochrogaster) and promiscuous montane voles (Mic

27 he formation of pair bonds in prairie voles (Microtus ochrogaster) and zebra finches (Taenioypygia gu

28 Prairie voles (Microtus ochrogaster) are a valuable model for studying

29 Pair-bonded prairie voles (Microtus ochrogaster) are biparental after the birth of

30 Prairie voles (Microtus ochrogaster) are exceptional among rodents in t

31 Prairie voles (Microtus ochrogaster) are monogamous and, like humans, a

32 Prairie voles (Microtus ochrogaster) are monogamous rodents that displa

33 Prairie voles (Microtus ochrogaster) are monogamous rodents that form p

34 Although prairie voles (Microtus ochrogaster) are socially monogamous, males var

35 lished the socially monogamous prairie vole (Microtus ochrogaster) as an animal model with which to i

36 ensory cortex was examined in prairie voles (Microtus ochrogaster) by using electrophysiological reco

37 After pair-bonding, male prairie voles (Microtus ochrogaster) display aggression toward novel fe

38 Male prairie voles (Microtus ochrogaster) display mating-induced pair bondin

39 Prairie voles (Microtus ochrogaster) exhibit a monogamous social struct

40 The prairie vole (Microtus ochrogaster) exhibits parental behavior in both

41 Male prairie voles (Microtus ochrogaster) form a pair bond with a female par

42 e humans, socially monogamous prairie voles (Microtus ochrogaster) form opposite-sex pair bonds, and

43 activity (IR) was compared in prairie voles (Microtus ochrogaster) from Illinois (IL), which are high

44 Studies in prairie voles (Microtus ochrogaster) have shown that although formation

45 Prairie vole pups (Microtus ochrogaster) in laboratory cages prefer hind ni

46 The prairie vole (Microtus ochrogaster) is a highly social, monogamous spe

47 The prairie vole (Microtus ochrogaster) is a socially monogamous rodent sp

48 Here we show, using a prairie vole (Microtus ochrogaster) model of social bonding, how a fun

49 Monogamous prairie voles (Microtus ochrogaster) show mating-induced aggression tow

50 Male prairie voles (Microtus ochrogaster) spontaneously exhibit high levels

51 The authors exposed male prairie voles (Microtus ochrogaster) to novel females in a multitrial s

52 xually nai;ve male and female prairie voles (Microtus ochrogaster) triggers a cascade of physiologica

53 Male and female prairie voles (Microtus ochrogaster) were cohabitated with an opposite-

54 Female prairie voles (Microtus ochrogaster) were exposed to 1 hour immobilizat

55 Pair-bonded male prairie voles (Microtus ochrogaster) were infused with a retrograde tra

56 (Microtus pennsylvanicus) and prairie voles (Microtus ochrogaster) were injected with lipopolysacchar

57 The prairie vole (Microtus ochrogaster), a monogamous rodent that forms lo

58 T given developmentally in the prairie vole (Microtus ochrogaster), a socially monogamous rodent, oft

59 of monogamous pair bonding in prairie voles (Microtus ochrogaster), as well as opportunities afforded

60 e highly social and monogamous prairie vole (Microtus ochrogaster), greatly increases partner-directe

61 Prairie voles (Microtus ochrogaster), like humans, are biparental and s

62 In the socially monogamous prairie vole (Microtus ochrogaster), mating induces enduring pair-bond

63 In socially monogamous prairie voles (Microtus ochrogaster), parental behaviors not only occur

64 ch on a monogamous rodent, the prairie vole (Microtus ochrogaster), suggests that these neuropeptides

65 ed to enhance ERalpha in male prairie voles (Microtus ochrogaster), which display high levels of pros

66 Using the prairie vole (Microtus ochrogaster)--a socially monogamous rodent that

67 ced social deficits, using the prairie vole (Microtus ochrogaster)-a socially monogamous rodent that

68 nding) in socially monogamous prairie voles (Microtus ochrogaster).

69 eproductive behaviors in male prairie voles (Microtus ochrogaster).

70 ure in the social, monogamous prairie voles (Microtus ochrogaster).

71 a partner preference in male prairie voles (Microtus ochrogaster).

72 al contact in male and female prairie voles (Microtus ochrogaster).

73 ence (PP) formation in female prairie voles (Microtus ochrogaster).

74 n monogamous mammals, such as prairie voles (Microtus ochrogaster).

75 s, for the socially monogamous prairie vole (Microtus ochrogaster).

76 In prairie voles, Microtus ochrogaster, females exhibit a dramatic increas

77 5-year study of the monogamous prairie vole, Microtus ochrogaster, in Illinois, USA.

78 In monogamous prairie voles, Microtus ochrogaster, males are parental and exhibit a d

79 revious studies have related pair-bonding in Microtus ochrogaster, the prairie vole, with plastic cha

80 ulation dynamics were studied in root voles (Microtus oeconomus).

81 attachment of the "monogamous" prairie vole (Microtus orchrogaster).

82 x chromosome karyotype of the creeping vole (Microtus oregoni) represents a long-standing anomaly, wi

83 In the creeping vole, Microtus oregoni, females are X0 and males are XY.

84 nt 1, individually housed male meadow voles (Microtus pennsylvanicus) and prairie voles (Microtus och

85 ature, whereas closely related meadow voles (Microtus pennsylvanicus) are solitary and polygamous.

86 Female meadow voles (Microtus pennsylvanicus) are territorial during warm mon

87 Nonmonogamous meadow voles (Microtus pennsylvanicus), which exhibit seasonal changes

88 tion, respectively, among male meadow voles (Microtus pennsylvanicus).

89 y inexperienced or experienced meadow voles (Microtus pennsylvanicus).

90 s ochrogaster) and promiscuous meadow voles (Microtus pennsylvanicus).

91 Here we show that male meadow voles, Microtus pennsylvanicus, increase their sperm investment

92 nsmission of food preferences in pine voles (Microtus pinetorum) and whether food items had to be pre

93 The mammalian genus Microtus provides an excellent model for investigating t

94 rbored within the nuclear genome of the vole Microtus rossiaemeridionalis.

95 ally attenuated with a narrow host range for Microtus species only.

96 Numt sequence data from five Microtus species were used to estimate an average rate o

97 he vole community ranged 24-47% depending on Microtus species.

98 The high prevalence of CNM infections in the Microtus spp. community may be a result of a relatively

99 monogamous species pairs of Peromyscus mice, Microtus voles, parid songbirds, dendrobatid frogs, and