ライフサイエンスコーパス: laboratory mouse

1 the primary community data resource for the laboratory mouse.

2 ource for gene expression information in the laboratory mouse.

3 ource of gene expression information for the laboratory mouse.

4 ource of gene expression information for the laboratory mouse.

5 variety of additional information about the laboratory mouse.

6 y, polymorphism and molecular data about the laboratory mouse.

7 genomic and phenotypic information about the laboratory mouse.

8 effort to produce a dense genetic map of the laboratory mouse.

9 athered from the studies performed using the laboratory mouse.

10 y used model organism for human disease, the laboratory mouse.

11 genomic, genetic and biological data on the laboratory mouse.

12 ication of phenotype-associated genes in the laboratory mouse.

13 netic, genomic and biological data about the laboratory mouse.

14 d for their inability to infect cells of the laboratory mouse.

15 ry community model organism database for the laboratory mouse.

16 utors to natural phenotypic variation in the laboratory mouse.

17 s the known genetic variation present in the laboratory mouse.

18 ontaneous copy number variation (CNV) in the laboratory mouse.

19 ropathy represents a founder mutation in the laboratory mouse.

20 on the genetics, genomics and biology of the laboratory mouse.

21 , a model organism database resource for the laboratory mouse.

22 and transcriptome data now available for the laboratory mouse.

23 ystem, a community database resource for the laboratory mouse.

24 te a definitive set of information about the laboratory mouse.

25 ) is the community database resource for the laboratory mouse, a key model organism for interpreting

26 ) is the community database resource for the laboratory mouse, a key model organism for interpreting

27 ent of a community database resource for the laboratory mouse, a key model organism for interpreting

28 ity model organism database resource for the laboratory mouse, a premier animal model for the study o

29 genomic and phenotypic information about the laboratory mouse, a primary animal model for studying hu

30 genomic and phenotypic information about the laboratory mouse, a primary animal model for studying hu

31 ryonic stem cells from the 129 strain of the laboratory mouse and mostly crossed to non-129 strains.

32 ely 30-40%) compared with that in the common laboratory mouse and rat ( approximately 1-3%) and may p

33 us and H. bilis infections are widespread in laboratory mouse and rat colonies.

34 oth similarities and differences between the laboratory mouse and rat were observed.

35 ry community model organism database for the laboratory mouse and serves as the source for key biolog

36 he community model organism database for the laboratory mouse and the authoritative source for phenot

37 te a definitive set of information about the laboratory mouse and to build and implement the data and

38 te a definitive set of information about the laboratory mouse and to build and implement the data and

39 s to explore the phylogenetic history of the laboratory mouse and to examine the functional consequen

40 hypothesis that common inbred strains of the laboratory mouse are derived from a limited ancestral ge

41 for cancer genetics researchers who use the laboratory mouse as a model system for understanding hum

42 se, is designed to facilitate the use of the laboratory mouse as a model system for understanding hum

43 Amino acids implicated previously in laboratory mouse attenuation generally did not vary amon

44 m for detecting genetic contamination in the laboratory mouse based on assaying single-nucleotide pol

45 d a high-resolution map of the origin of the laboratory mouse by generating 25,400 phylogenetic trees

46 t microbiome differed significantly from its laboratory mouse counterpart and was transferred to and

47 tis elegans, Drosophila melanogaster and the laboratory mouse, exist for the Foxo family of transcrip

48 g exposure of mice to the MLVs restricted by laboratory mouse Fv1, and suggests a mechanism for Fv1 r

49 hat matches patients' clinical phenotypes to laboratory mouse gene knockouts, we were able to strongl

50 a chance occurrence, we surveyed the Jackson Laboratory Mouse Genome Database for knockout mouse stra

51 hile all 31 P-MLV ERVs map to the 95% of the laboratory mouse genome derived from P-MLV-infected M. m

52 wild mice and are embedded in the 5% of the laboratory mouse genome derived from the Asian Mus muscu

53 The amount of variation found in the inbred laboratory mouse genome has increased to 71 M SNPs and 1

54 A dense map of genetic variation in the laboratory mouse genome will provide insights into the e

55 For many years the laboratory mouse has been used as the standard model for

56 erm motility and ATP production and that the laboratory mouse has comparatively low values in these t

57 The laboratory mouse has emerged as a primary model organism

58 Here we show that standard laboratory mouse husbandry has profound effects on the i

59 cteristics data to facilitate the use of the laboratory mouse in translational research for human hea

60 ogenetic origin of the genome of most extant laboratory mouse inbred strains.

61 The laboratory mouse is a premier genetic model for understa

62 hology of cancer in different strains of the laboratory mouse is critical to developing and using mou

63 The laboratory mouse is increasingly a subject for visual sy

64 or genome editing become widely adopted, the laboratory mouse is more important than ever as a model

65 The laboratory mouse is one of the most powerful tools for b

66 The laboratory mouse is the most widely used mammalian model

67 The laboratory mouse is the premier animal model for studyin

68 The laboratory mouse is the premier animal model for studyin

69 The laboratory mouse is the premier model system for studies

70 The laboratory mouse is the primary mammalian species used f

71 The laboratory mouse is the workhorse of immunology, used as

72 The genome of the laboratory mouse is thought to be a mosaic of regions wi

73 he community model organism database for the laboratory mouse, is designed to facilitate the use of t

74 med to be part of the telogen phase, using a laboratory mouse model and newly developed techniques fo

75 The laboratory mouse model of Lyme disease has revealed that

76 d with the published sequence for the common laboratory mouse Mus musculus domesticus strain C57BL/6J

77 Y chromosome) of the C57BL/6J strain of the laboratory mouse Mus musculus.

78 ns the pseudoautosomal boundary (PAB) in the laboratory mouse (Mus musculus domesticus, C57BL/6) such

79 ally well-characterized model organisms, the laboratory mouse, Mus musculus, and the fruit fly, Droso

80 Laboratory mouse, Mus musculus, is one of the most impor

81 midbrain auditory response properties of the laboratory mouse, Mus musculus.

82 Thus, a laboratory mouse (NIH Swiss) X-receptor conferred suscep

83 Yet, the laboratory mouse, obtained after decades of human-driven

84 ength genomic DNA of the recently identified laboratory mouse papillomavirus 1 (MusPV1) was synthesiz

85 to the corresponding regions in prototypical laboratory mouse polytropic proviruses, but the wild mou

86 In contrast to humans, the laboratory mouse possesses long telomeres and, even in e

87 The laboratory mouse provides a model to study pathogenesis.

88 The laboratory mouse serves as an important model system for

89 The laboratory mouse shares the majority of its protein-codi

90 ol, we sought an outbred and immunocompetent laboratory mouse strain in which persistent papillomas c

91 ing molecule MR1, this population is rare in laboratory mouse strains ( approximately 0.1% in lymphoi

92 ze the distribution of both proviruses in 48 laboratory mouse strains and 46 wild-derived strains.

93 havior and responses to neuroactive drugs in laboratory mouse strains and may help to explain individ

94 tly expands the catalogue of fully sequenced laboratory mouse strains and now contains several exampl

95 es Project generated genome sequences for 17 laboratory mouse strains and rich catalogues of variants

96 Most inbred laboratory mouse strains are deficient in Mx1, but conge

97 Most inbred laboratory mouse strains are known to have originated fr

98 /CD2 family haplotype is found in many other laboratory mouse strains but only causes autoimmunity in

99 Laboratory mouse strains carry endogenous copies of the

100 The commonly used conventional laboratory mouse strains do not respond robustly to SAgs

101 Most laboratory mouse strains including C57BL/6J do not produ

102 Our current knowledge of TEs in laboratory mouse strains is limited primarily to those p

103 ole-genome shotgun sequence traces from four laboratory mouse strains mapped against the reference C5

104 tion of recombination in the sequences of 15 laboratory mouse strains sequenced by Perlegen Sciences.

105 Furthermore, SIRPalpha polymorphism in laboratory mouse strains significantly affects the exten

106 million individual sequence traces from four laboratory mouse strains to the C57BL/6J reference genom

107 referentially segregate to the polar body in laboratory mouse strains when the fusion centromeres are

108 Most laboratory mouse strains, including C57BL/6J, carry nons

109 enome genotype imputations for 100 classical laboratory mouse strains, using a novel method.

110 a closely related wild relative to standard laboratory mouse strains.

111 a genetic cross was carried out between two laboratory mouse strains.

112 effort to sequence the genomes of the common laboratory mouse strains.

113 ls is due to the extremely long telomeres in laboratory mouse strains.

114 arrying out EMPReSS protocols on four inbred laboratory mouse strains.

115 this methodology to data about genes in the laboratory mouse that are formally represented in the Mo

116 However, the reliance on the laboratory mouse to identify viable therapies for the hu

117 to reconstruct a phylogenetic history of the laboratory mouse using Wagner parsimony analysis.

118 We did this because the laboratory mouse viruses derive directly from specific E

119 nd integrates expression information for the laboratory mouse, with a particular emphasis on mouse de

120 To describe the subspecies origins of laboratory mouse XP-MLV ERVs and their coevolutionary tr

121 1 receptors, including the X-MLV-restricting laboratory mouse Xpr1(n) and a novel M. m. castaneus all

122 lign with the two mutations that disable the laboratory mouse XPR1.