ライフサイエンスコーパス: house mice

1 rated, mirroring the situation found here in house mice.

2 symbiont strains between laboratory and wild house mice.

3 hat may underlie environmental adaptation in house mice.

4 e, and sometimes becoming dispensable, as in house mice.

5 nsible for the early stages of speciation in house mice.

6 an intensively monitored population of wild house mice.

7 tions in maintaining subspecies integrity in house mice.

8 n rate both within and between subspecies of house mice.

9 ibuting to the evolution of recombination in house mice.

10 it flies, pipefish, wild mallards, and feral house mice.

11 in six bilateral discrete skeletal traits in house mice.

12 eas concurrently (MPO/VTA) of castrated male house mice.

13 ex vivo gamma oscillations in conventionally housed mice.

14 rced similar barcode distributions across co-housed mice.

15 a vaccination are better recapitulated in co-housed mice.

16 n the absence of societal factors, in single-housed mice.

17 ts of bright light on this cell type in dark-housed mice.

18 eric lymph from germ-free and conventionally housed mice.

19 s of CIT treatment were attenuated in single-housed mice.

20 -regulated, in isolated relative to socially housed mice.

21 )-one, and allopregnanolone similar to group-housed mice.

22 oused mice showed less bite wounds than pair housed mice.

23 sed to 30% of the values calculated in group-housed mice.

24 btypic T cell immunity was compromised in co-housed mice.

25 This task is accessible to group-housed mice 24 h per day, enabling high-throughput longi

26 resistance to anticoagulant rodenticides in house mice and a new missense mutation Ala72Val in the M

27 eting microbiotas from wild-derived lines of house mice and other mouse species (Mus and Peromyscus s

28 Continued efforts to study wild house mice and to create new inbred strains from wild po

29 and IL-6 are produced only in conventionally housed mice and both cytokines directly promote Breg cel

30 chy status established within cages of group-housed mice and the expression of the stress peptide PAC

31 Heligmosomoides bakeri, a model parasite of house mice, and Heligmosomoides polygyrus, a closely rel

32 cause the genomes of these recently diverged house mice are highly collinear, observed differences in

33 First, we show that house mice are highly polyandrous: 47% of 682 litters we

34 these reasons and because they are mammals, house mice are well suited to serve as models for human

35 populations have the potential to strengthen house mice as a model system.

36 ounding effect of the interaction between co-housed mice, as well as facilitate the identification of

37 dismutase (SOD2) in four treatment groups of house mice assayed by RNase protection at 20 months of a

38 We showed that housing mice at 35.5 degrees C rather than 23 degrees C

39 Adipocyte-specific activation of Ikbkb or housing mice at thermoneutrality attenuated improvements

40 Our findings show that once male house mice become territorial and socially dominant, the

41 Here we show that resistant house mice can also originate from selection on vkorc1 p

42 Most male B6D2F1 hybrid house mice continue to copulate after castration (contin

43 At the Natufian site of Ain Mallaha, house mice displaced less commensal wild mice during per

44 ast Asia, which is also where X-MLV-infected house mice evolved.

45 in regions of socially isolated versus group-housed mice exposed to the contextual fear conditioning

46 EE-housed mice expressed elevated FosB/DeltaFosB immunostai

47 fferentiation of cultured NPCs from standard-housed mice expressing wild-type PS1 or PS1 variants are

48 f size and shape of the mandibular molars in house mice from an F2 intercross population generated fr

49 ice evolved the largest body size among wild house mice from around the world.

50 ome sequencing of museum-stored specimens of house mice from one secondary subspecies (M. m.

51 otide variation in the adult globin genes of house mice from South America.

52 c surveys of hemoglobin (Hb) polymorphism in house mice from South Asia and the Middle East have reve

53 Normally housed mice had a dispersed, salt-and-pepper whisker map

54 Individually housed mice, however, had high nest scores, low body wei

55 udies of the primary reproductive barrier in house mice-hybrid male sterility-have been restricted to

56 eveal the earliest known commensal niche for house mice in long-term forager settlements 15,000 y ago

57 House mice in the wild consist of at least three distinc

58 ulatory divergence in temperate and tropical house mice in two metabolic tissues under two thermal co

59 ating a diverse dataset of single- and multi-housed mice in complex setups.

60 By housing mice in 20-h light/dark cycles, incongruous with

61 mice find waste products aversive, and that housing mice in a way that facilitates spatial segregati

62 Housing mice in an enriched environment from P21 until a

63 treatment enhanced serotonin release in pair-housed mice, it did not significantly alter uptake rate.

64 correlate with male reproductive success of house mice living in competitive conditions.

65 of urinary protein and VOCs of wild-derived house mice living in large seminatural enclosures to com

66 igated the regulation of chemical signals of house mice living in seminatural social conditions.

67 Strikingly, co-housed mice maintained colonization resistance after tre

68 f the duplicated beta-globin genes of Indian house mice (Mus castaneus) in conjunction with experimen

69 sed to novel (strange) males, was studied in house mice (Mus domesticus) differing in t-complex genot

70 red (from full-sib matings) and outbred wild house mice (Mus domesticus) in large, seminatural enclos

71 Here we show in wild house mice (Mus domesticus) that urinary MUPs play an im

72 Preferences for male odors by female house mice (Mus domesticus) were examined with respect t

73 netically heterogeneous laboratory strain of house mice (Mus domesticus).

74 d types of parasitic worms in two species of house mice (Mus musculus and M. domesticus) and in their

75 one between two recently diverged species of house mice (Mus musculus and Mus domesticus) as a natura

76 epoxide reductase subcomponent 1 (vkorc1) of house mice (Mus musculus domesticus) can cause resistanc

77 uences and short-read RNA-Seq data from wild house mice (Mus musculus domesticus) collected along a l

78 Here, we show that natural selection within house mice (Mus musculus domesticus) drives deterministi

79 se genetic and morphometric variation in the house mice (Mus musculus domesticus) from the Orkney arc

80 mice (C57BL6/J strain) and free-living, wild house mice (Mus musculus domesticus).

81 trains to females from two inbred strains of house mice (Mus musculus domesticus).

82 reported here, now identified from commensal house mice (Mus musculus group) by sequencing this segme

83 ailed extensive studies of inbred strains of house mice (Mus musculus) and of deer mice (Peromyscus m

84 The major urinary proteins (MUPs) of house mice (Mus musculus) bind and stabilize the release

85 House mice (Mus musculus) have spread globally as a resu

86 Exposing female house mice (Mus musculus) to male urinary scent accelera

87 timing has not been clearly demonstrated in house mice (Mus musculus), raising concerns about mouse

88 amily produced in the submaxillary glands of house mice (Mus musculus).

89 component of the urinary protein fraction in house mice (Mus spp.) and rats (Rattus spp.).

90 n of the X chromosome between two species of house mice, Mus musculus and M. domesticus.

91 erived inbred strains from two subspecies of house mice, Mus musculus musculus and Mus musculus domes

92 alancing selection in natural populations of house mice, Mus musculus.

93 House mice offer a powerful system to reconstruct the ev

94 ) and publicly available genome sequences of house mice previously characterized as M. m.

95 With recently diverged subspecies, house mice provide a powerful system for understanding t

96 scorpion venom induces pain in many mammals (house mice, rats, humans) by activating the voltage-gate

97 th reproductively nonresponsive and long day-housed mice release less GnRH following castration than

98 of the microbiota, but the microbiotas of co-housed mice remained more similar to each other compared

99 nduced humoral responses were dampened in co-housed mice, resulting in poor control upon challenge.

100 wild-type (WT) and Rag1-knockout (Rag1(-/-)) house mice revealed widespread fitness advantages for na

101 Trio housed mice showed less bite wounds than pair housed mic

102 We use house mice (subspecies: Mus musculus domesticus) from re

103 stems from controlled laboratory studies in house mice, the combined influence of ecological factors

104 In house mice, the contribution of the Mus musculus musculu

105 At weanling age in normally housed mice, the LP contains a population of Rag-express

106 out the genetics of hybrid male sterility in house mice, they have been restricted to F1 sterility or

107 eliable scalar timing in a sizable sample of house mice, thus validating the peak-interval procedure

108 Stowaway transport of house mice to Cyprus can be inferred as early as 10,800

109 al dynamics in long-term settlements allowed house mice to establish durable commensal populations th

110 We exposed three-week old male house mice to female urine or water (control) for ca.

111 ly, we performed scans for selection in wild house mice to identify genomic signatures of rapid adapt

112 arge panel of pedigreed, genetically admixed house mice to study patterns of recombination rate varia

113 Here we show that exposure of dark-housed mice to light induces a gene program in cortical

114 m monitoring the voluntary behavior of group-housed mice under seminaturalistic conditions.

115 orough assessment of their existence in wild house mice using a panel of evaluation criteria.

116 een associated with hybrid sterility in male house mice via spermatogenic failure at the pachytene st

117 haracterization of reproductive isolation in house mice, we conducted an F(2) intercross between wild

118 House mice were the most common mammal species captured

119 Individually housed mice were challenged orally with C. jejuni 11168,

120 Although SPF and co-housed mice were comparably susceptible to acute influen

121 When castrated long day-housed mice were provided with long day levels of testos

122 Pair-housed mice were significantly more responsive to CIT tr

123 atment with antibiotics, whereas most singly housed mice were susceptible to E. coli.

124 ts differ from those previously described in house mice, where a single protein induces female attrac

125 in was approximately 50% lower than in group-housed mice whereas 3alpha-hydroxysteroid oxidoreductase

126 his was applied to wild-stock outbred female house mice, which nest socially and often rear offspring

127 hances the contextual fear response in group housed mice, which suggests that social isolation alters

128 el for the origin and radiation of commensal house mice whose main features are an origin in west-cen

129 re evaluated using laboratory populations of house mice with known evolutionary histories.

130 or in oral antibiotic-treated conventionally housed mice with depleted intestinal microbiomes that gr