ライフサイエンスコーパス: house mice

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

2 tions in maintaining subspecies integrity in house mice.

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

4 ibuting to the evolution of recombination in house mice.

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

6 in six bilateral discrete skeletal traits in house mice.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

26 EE-housed mice expressed elevated FosB/DeltaFosB immunostai

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

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

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

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

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

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

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

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

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

36 Housing mice in an enriched environment from P21 until a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

55 House mice offer a powerful system to reconstruct the ev

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

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

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

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

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

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

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

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

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

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

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

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

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

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

70 House mice were the most common mammal species captured

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

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

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

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

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

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

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

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