ライフサイエンスコーパス: inbred strain of mice

1 s a polygenic trait that varies widely among inbred strains of mice ().

2 ed skin and reach draining lymph nodes in an inbred strain of mice.

3 matory responses in two genetically distinct inbred strains of mice.

4 en increases lung tumor multiplicity in some inbred strains of mice.

5 s from sequences recently reported for other inbred strains of mice.

6 feration and immunodeficiency in susceptible inbred strains of mice.

7 that they have not been identified in other inbred strains of mice.

8 using immunocompetent and immunocompromised inbred strains of mice.

9 nensis can cause progressive disease in most inbred strains of mice.

10 l to determine copy number variation between inbred strains of mice.

11 nensis can cause progressive disease in most inbred strains of mice.

12 o the more complex tetrabranched peptides in inbred strains of mice.

13 ata on commonly used and genetically diverse inbred strains of mice.

14 ensive map of DNA variation among the common inbred strains of mice.

15 NA gene sequencing in a panel of 110 diverse inbred strains of mice.

16 We compared vascular remodeling among 5 inbred strains of mice.

17 ally with clearance of colonization in three inbred strains of mice.

18 differences in regional DNA content between inbred strains of mice.

19 immunogenicity of PvRMC-CSP in groups of six inbred strains of mice.

20 causes progressive cutaneous lesions in most inbred strains of mice.

21 de polymorphisms across the genomes of eight inbred strains of mice.

22 sis using an intercross of PERA/Ei and I/LnJ inbred strains of mice.

23 elopment of latent inhibition in a number of inbred strains of mice.

24 esent study we applied this model to various inbred strains of mice.

25 n, allelic variants were typed among several inbred strains of mice.

26 Transplant rejection was compared in two inbred strains of mice: 129, which apparently use perfor

27 Three inbred strains of mice (A/J, BALB/c, and C57BL/6) that w

28 transfer of 8 mAbs to WI-1 into 3 different inbred strains of mice also did not improve the course o

29 s leading to acute heart injury in different inbred strains of mice also suggest that this response h

30 nnective tissue disease patients and certain inbred strains of mice and are thought to be pathogenic.

31 f high-fat and low-fat diets on males of two inbred strains of mice and discovered that C57BL/6J but

32 ng of the unique variation patterns found in inbred strains of mice and how they have arisen through

33 ble trait exhibiting sixfold variation among inbred strains of mice and is used here to identify gene

34 7BL/6J (B6), BALB/cJ (BALB), and DBA/2J (D2) inbred strains of mice and resistant FVB-Tg(Ela-KRAS(G12

35 ata on commonly used and genetically diverse inbred strains of mice and their derivatives.

36 by methyl-donor deficiency among individual inbred strains of mice and to investigate the underlying

37 ith naturally occurring hepatitis in certain inbred strains of mice, and in A/JCr mice it has been li

38 eptide-specific CD8(+) T cells, varies among inbred strains of mice, and is not mediated by tradition

39 ces alternatively spliced transcripts across inbred strains of mice, and its splicing pattern cosegre

40 In this study different inbred strains of mice appeared to control and contain a

41 Most inbred strains of mice are susceptible to Leishmania ama

42 Inbred strains of mice are valuable tools for determinin

43 oss (Ahl) is a non-syndromic trait in common inbred strains of mice associated with the Ahl locus on

44 Two inbred strains of mice (BALB/c and C57BL/6) were vaccina

45 Little or no mortality develops in most inbred strains of mice, but C3H and FVB/N mice exhibit f

46 The 50% lethal doses differed among inbred strains of mice, but within a given mouse strain,

47 Retroviruses induce leukemia in inbred strains of mice by activating cellular proto-onco

48 However, in more commonly used inbred strains of mice (C57BL/6, FVB/N) that were hemizy

49 In two inbred strains of mice, C57BL/6 and 129Sv, the majority

50 Variation between inbred strains of mice can be used to identify modifier

51 ucted with three F1 hybrids made using three inbred strains of mice (DBA/2J and C3H/HeJ, DCC-suscepti

52 However, several inbred strains of mice derived from wild mice, including

53 C57BL/6J (B6) and AKR/J (AKR) inbred strains of mice develop a comparable degree of ob

54 Inbred strains of mice differ in susceptibility to ather

55 Similarly, inbred strains of mice differ in their susceptibility to

56 In this study, we demonstrate that inbred strains of mice differ significantly in the rate

57 Various inbred strains of mice exhibit dramatic differences in s

58 Inbred strains of mice exhibit substantial differences i

59 ple sclerosis patients and spleen cells from inbred strains of mice, expressing different H-2 haploty

60 Here we show, by using inbred strains of mice, F1 hybrids, and segregating popu

61 haracterize hypothalamic transcriptome in 99 inbred strains of mice from the Hybrid Mouse Diversity P

62 ALB.B (both H2b) and related CXB recombinant inbred strains of mice has been studied to determine the

63 Over 450 inbred strains of mice have been described, providing a

64 In this respect, common inbred strains of mice have played a crucial role, and r

65 that two complementary experimental models: inbred strains of mice (i.e. C57BL/6 and C3H/HeJ), and a

66 seeking," we compared the performance of 14 inbred strains of mice in five tests: activity in a nove

67 In contrast, common inbred strains of mice, including BALB/c and C57BL/6, ar

68 c cardiac calcinosis (DCC) occurs in certain inbred strains of mice, including DBA/2 and C3H/He, and

69 ted cardiomyopathy that occurs among certain inbred strains of mice, involves myocardial injury, necr

70 The 129S1/SvImJ (129/Sv) inbred strain of mice is an excellent model for studying

71 The DBA/2J inbred strain of mice is used extensively in hearing res

72 lsivity measures, 5CSRTT performance, in two inbred strains of mice known to differ in alcohol intake

73 ng nematode Trichuris muris, the majority of inbred strains of mice launch a Th2-type immune response

74 e action in 1) a panel of 41 BXD recombinant inbred strains of mice (n = 13.7 +/- .8 per strain; n =

75 Inbred strains of mice offer promising models for unders

76 However, the availability of different inbred strains of mice offers an excellent model system

77 ence in bleomycin-induced lung damage in two inbred strains of mice [parental generation: C57BL/6J (f

78 lity of numerous congenic and H2 recombinant inbred strains of mice produced earlier by Snell, Stimpf

79 nations of genetic loci in MRL/MpJ and SJL/J inbred strains of mice regulate bone strength and bone d

80 Inbred strains of mice show varying degrees of susceptib

81 Examination of 12 inbred strains of mice showed differences in dental fluo

82 ions of virus yields from infected brains of inbred strains of mice showed that E1A null and CR3Delta

83 A survey of 15 inbred strains of mice showed that some mouse strains re

84 We had reported earlier that inbred strains of mice such as BALB/cJ could survive a c

85 f circadian behavior observed among multiple inbred strains of mice suggest that the inherent contrib

86 In the 129 family of inbred strains of mice, teratomas initiate around embryo

87 the F1 genetic vaccine were obtained in all inbred strains of mice tested, but Ab levels were less t

88 Thus, the use of inbred strains of mice that are hemizygous for the Drd2

89 ntributing to atherogenesis, we have studied inbred strains of mice that are susceptible (C57BL/6J) a

90 s were tested in an elevated zero-maze for 8 inbred strains of mice that are used widely in biomedica

91 with experimental studies of Hb function in inbred strains of mice that carry the alternative Hbb(d)

92 the less potent S-baclofen enantiomer in two inbred strains of mice that display low sociability and/

93 we examined five cognitive functions in two inbred strains of mice, the stress-resilient strain C57B

94 11, we analyzed the immune response of three inbred strains of mice to antigen immunization using two

95 The use of inbred strains of mice to dissect the genetic complexity

96 the highly variable plasma VWF levels among inbred strains of mice to identify 2 major regulators, M

97 A haplotype map was developed in four inbred strains of mice used in our complex-trait mapping

98 in (UCP1) in fat tissues of A/J and C57BL/6J inbred strains of mice varied in a regional-specific man

99 Inbred strains of mice vary in their susceptibility to C

100 iously that hemopoietic stem cells of common inbred strains of mice vary widely in cycling activity a

101 Inbred strains of mice vary widely in onset and severity

102 A long-established inbred strain of mice was divergently selected for body

103 Susceptibility to WNV disease in inbred strains of mice was mapped to a nonsense mutation

104 Diversity Panel data, which consisted of 100 inbred strains of mice, we identified 97 DMCs that were

105 NKT cell number and function among different inbred strains of mice, we investigated whether the role

106 gment length polymorphisms among recombinant inbred strains of mice, we localized the beta3 subunit g

107 roral infection with Toxoplasma gondii among inbred strains of mice, we performed studies to examine

108 d WSR selected lines and DBA/2J and C57BL/6J inbred strains of mice were exposed to ethanol vapor or

109 Hamsters, guinea pigs, cotton rats, and nine inbred strains of mice were inoculated intranasally with

110 Forty inbred strains of mice were tested (in most cases using

111 Recent research characterizing infection of inbred strains of mice with a murine gamma-herpesvirus,

112 We treated eight different inbred strains of mice with N-nitroso-tris-chloroethylur

113 these findings by challenging 12 additional inbred strains of mice with rabbit anti-mouse glomerular

114 tions of opioid receptor subtypes in certain inbred strains of mice with varying sensitivities to the

115 diated leukocytes, studies were conducted in inbred strains of mice with well-characterized MHC antig

116 We challenged several inbred strains of mice with Y. pestis and found that BAL

117 We explored this issue in inbred strains of mice, with a special focus on the low