ライフサイエンスコーパス: Mus musculus

1 ween closely related house mouse subspecies (Mus musculus).

2 show the same pattern of results with mice (Mus musculus).

3 mental duplication, R2d, in the house mouse (Mus musculus).

4 n a nonhibernating species, the house mouse (Mus musculus).

5 ed in the submaxillary glands of house mice (Mus musculus).

6 ncreases in response to wakefulness in mice (Mus musculus).

7 SCN from neurogenesis to adulthood in mice (Mus musculus).

8 ms are currently supported: Homo sapiens and Mus musculus.

9 pursued this further by knocking out Iop1 in Mus musculus.

10 time information from both Homo sapiens and Mus musculus.

11 , Peromyscus maniculatus, and the lab mouse, Mus musculus.

12 convergent extension of the cochlear duct of Mus musculus.

13 been detected in several tissue extracts of Mus musculus.

14 ection in natural populations of house mice, Mus musculus.

15 small secreted proteins in Homo sapiens and Mus musculus.

16 response properties of the laboratory mouse, Mus musculus.

17 ulosis, Rattus norvegicus, Homo sapiens, and Mus musculus.

18 the X and Y chromosomes of the house mouse, Mus musculus.

19 ila melanogaster, Caenorhabditis elegans and Mus musculus.

20 abnormalities in Drosophila melanogaster and Mus musculus.

21 rthologous to an H2a histone pseudogene from Mus musculus.

22 han a dozen cell types from Homo sapiens and Mus musculus.

23 retroviruses presently targeted by ZFP809 in Mus musculus.

24 d target of rapamycin signalling pathways in Mus Musculus.

25 the C57BL/6J strain of the laboratory mouse Mus musculus.

26 ression of TRPM1 on the dendrites of DBCs in mus musculus.

27 of wild-caught mice from three subspecies of Mus musculus.

28 is thaliana (14.0% of cytosines methylated), Mus musculus (7.6%), and Escherichia coli (2.3%).

29 ths, Drosophila, Caenorhabditis elegans, and Mus musculus, a complete signaling system can be genetic

30 -associated ribonuclease genes of the rodent Mus musculus, a finding that may have implications with

31 These novel findings suggest that Mus musculus, a nontraditional animal host of hantavirus

32 sely with the stop codon of the house mouse, Mus musculus, a species known to have a single copy of S

33 he nerve agent antidote HI-6 in complex with Mus musculus AChE covalently inhibited by the nerve agen

34 d behavior and neurochemistry in adult mice (Mus musculus) after neonatal depletion of monoaminergic

35 7, had specific activating mutations in the Mus musculus allele in 23 of 26 carcinomas.

36 erase, human alpha2,3-sialyltransferase, and Mus musculus alpha2,6-sialyltransferase were transiently

37 90% sequence identity, that Danio rerio and Mus musculus alphaE-catenin have striking functional dif

38 (5%) for Arabidopsis thaliana, 1456 (4%) for Mus musculus and 614 (4%) for Drosophila melanogaster.

39 Despite cell cycle re-entry in Mus musculus and A. cahirinus, efficient cell cycle prog

40 rhabditis elegans, Drosophila, Homo sapiens, Mus musculus and Arabidopsis species as well as all the

41 ies including human, Caenorhabditis elegans, Mus musculus and Arabidopsis thaliana.

42 egans, Drosophila melanogaster, Danio rerio, Mus musculus and Arabidopsis thaliana.

43 ors conserved across species as divergent as Mus musculus and Caenorhabditis elegans.

44 the long telomeres (20 to 50 kb) typical of Mus musculus and did not show telomere shortening during

45 homology with orthologous proteins found in Mus musculus and Drosophila melanogaster.

46 Ca(2+)-calmodulin binding site in the mouse Mus musculus and found that removal of (3) alters respon

47 eptor cilia) and Drosophila melanogaster, to Mus musculus and Homo sapiens (in which they are found i

48 evisiae, Caenorhabditis elegans, Drosophila, Mus musculus and Homo sapiens.

49 osophila melanogaster, Arabidopsis thaliana, Mus musculus and Homo sapiens.

50 ophila melanogaster, Caenorhabditis elegans, Mus musculus and Homo Sapiens.

51 arasitic worms in two species of house mice (Mus musculus and M. domesticus) and in their natural hyb

52 e, which are largely genetic hybrids between Mus musculus and M. domesticus, have become available.

53 hromosome between two species of house mice, Mus musculus and M. domesticus.

54 two recently diverged species of house mice (Mus musculus and Mus domesticus) as a natural mapping ex

55 general use of interspecific crosses between Mus musculus and Mus spretus for the detection of strong

56 sis using an interspecific backcross between Mus musculus and Mus spretus inbred strains.

57 nalysis of Nod2 from 45 different strains of Mus musculus and Mus spretus revealed extensive polymorp

58 kers in our set that are polymorphic between Mus musculus and Mus spretus, we used The Jackson Labora

59 we tested two nonherbivorous mouse species (Mus musculus and Peromyscus leucopus).

60 hods (examples are provided for Homo sapiens/Mus musculus and Plasmodium falciparum/Plasmodium vivax

61 ng 80% sequence identity among Homo sapiens, Mus musculus and Rattus norvegicus.

62 TG2 exacerbates alpha-synuclein toxicity in Mus musculus and Saccharomyces cerevisiae.

63 ell induction is conserved in both the mouse Mus musculus and the cricket Gryllus bimaculatus, which

64 nce data of two other vertebrates, the mouse Mus musculus and the puffer fish Tetraodon nigroviridis,

65 ccharomyces cerevisiae, circadian rhythms in Mus musculus and the root clock in Arabidopsis thaliana.

66 s identified in humans (Homo sapiens), mice (Mus musculus) and flies (Drosophila melanogaster), toget

67 ive studies of inbred strains of house mice (Mus musculus) and of deer mice (Peromyscus maniculatus).

68 genetic maps of individual homologous mouse (Mus musculus) and rat (Rattus norvegicus) chromosomal re

69 piens), chimpanzee (Pan troglodytes), mouse (Mus musculus) and rat (Rattus norvegicus) for evidence o

70 from related rodents, including house mouse (Mus musculus) and rat (Rattus norvegicus), did not suppo

71 ith genetic analyses in dysbindin-null mice (Mus musculus) and the genome of schizophrenia patients.

72 inted opossum (Didelphis virginiana), mouse (Mus musculus), and human (Homo sapiens) to determine if

73 ophila melanogaster, Caenorhabditis elegans, Mus musculus, and Arabidopsis thaliana, and investigated

74 egypti) and three vertebrates (Homo sapiens, Mus musculus, and Brachydanio rerio) and sequenced from

75 omparing methylated genomes of Homo sapiens, Mus musculus, and Danio rerio with nonmethylated genomes

76 ophila melanogaster, Caenorhabditis elegans, Mus musculus, and Homo sapiens PPI networks.

77 ree distinct open reading frames in Xenopus, Mus musculus, and Homo sapiens.

78 position comparing Drosophila melanogaster, Mus musculus, and Homo sapiens.

79 habditis elegans, Drosophila, Gallus gallus, Mus musculus, and Homo sapiens.

80 aenorhabditis elegans, Arabidopsis thaliana, Mus musculus, and humans.

81 om Old World rodents (Clethrionomys species, Mus musculus, and Rattus species).

82 rized model organisms, the laboratory mouse, Mus musculus, and the fruit fly, Drosophila melanogaster

83 lets in the following genomes: Homo sapiens, Mus musculus, Arabidopsis thaliana, and Caenorhabditis e

84 c comparison of eight species: Homo sapiens, Mus musculus, Arabidopsis thaliana, Caenorhabditis elega

85 ins of mice, spanning a genetic continuum of Mus musculus as a prelude to uncovering complex traits a

86 thologous genes in strains and subspecies of Mus musculus as well as other species of Mus using a PCR

87 is capable of inducing key promoters of the Mus musculus Bdnf gene.

88 om seven eukaryotic organisms (Homo sapiens, Mus musculus, Bos taurus, Rattus norvegicus, Danio rerio

89 initially similar in size to those of mice (Mus musculus) but that, subsequently, bat digits greatly

90 inferred the protein-protein interactions in Mus musculus by using two approaches: i) identifying mou

91 Mus spretus (SPRET/Ei and SPRET/Glasgow) and Mus musculus (C3H/HeJ, BALB/cJ, 129/J, DBA/2J, NIH, FVB/

92 , we show that a laboratory strain of mouse (Mus musculus, C57BL/6J) robustly pursues, captures, and

93 he vertebrate and invertebrate model systems Mus musculus, Caenorhabditis elegans, and Drosophila mel

94 NA poly(A) tails; Caenorhabditis elegans and Mus musculus CAF1, transcription factor CCR4-associated

95 Mice (Mus musculus) carrying a hypomorphic allele of Ppp2r5del

96 bred strain and the evolutionarily divergent Mus musculus castaneus (CAST/Ei) strain as a mapping par

97 een C57BL/6J-kat2J/+ and an inbred strain of Mus musculus castaneus (CAST/Ei).

98 oss between wild-derived inbred strains from Mus musculus castaneus and M. m. domesticus.

99 performed an intersubspecific backcross with Mus musculus castaneus and mapped microsatellite markers

100 orphism data from the house mouse subspecies Mus musculus castaneus and nucleotide divergence from Mu

101 /SvImJ, which carries the Xce(a) allele, and Mus musculus castaneus EiJ, which carries the Xce(c) all

102 structure of the suppressive allele in wild Mus musculus castaneus suggests selective advantage.

103 tural population of the Eastern house mouse, Mus musculus castaneus We performed simulations to asses

104 cific crosses of 129/SvEv mice with CAST/Ei (Mus musculus castaneus).

105 s mammary carcinoma model in female (FVB/N x Mus musculus castaneus)F1 mice.

106 In an intercross involving Mus musculus castaneus, jcpk was precisely mapped 0.2 cM

107 le animals of M. musculus inbred strains and Mus musculus castaneus.

108 a populated by the virus-infected subspecies Mus musculus castaneus.

109 melanogaster and the house mouse subspecies Mus musculus castaneus.

110 The t-haplotype is a chromosomal region in Mus musculus characterized by meiotic drive such that he

111 ertions/deletions among 20 inbred strains of Mus musculus, chosen to enable interpretation of the mol

112 replication-dependent histone genes found on Mus musculus chromosome 13.

113 to free-running Drosophila melanogaster and Mus musculus circadian models.

114 A ligases from human (Homo sapiens), murine (Mus musculus), clawed toad (Xenopus laevis) and the yeas

115 , while in the closely related mouse species Mus musculus, Clcn4-2 has been translocated to chromosom

116 romoting thermal lability is conserved among Mus musculus, Danio rerio, Drosophila melanogaster and C

117 information with previously published mouse (Mus musculus) data and identified a subset of seven micr

118 tent with estimated divergence rates between Mus musculus domesticus and either M. m. musculus or M.

119 thod to data from the hybridizing subspecies Mus musculus domesticus and M. m.

120 een the two European house mouse subspecies, Mus musculus domesticus and M.m.musculus, sharing a hybr

121 he Y chromosomes from certain populations of Mus musculus domesticus are introduced into the mouse st

122 Their genomes are overwhelmingly Mus musculus domesticus in origin, and the remainder is

123 A LINE-1 element, LIC105, was found in the Mus musculus domesticus inbred strain, C57BL/6J.

124 he incompatible paternal allele arose in the Mus musculus domesticus lineage and that incompatible st

125 On average, 92% of the genome is of Mus musculus domesticus origin, and the distribution of

126 ng on both Ins2 and Ins1 gene regions in the Mus musculus domesticus populations.

127 hed sequence for the common laboratory mouse Mus musculus domesticus strain C57BL/6J.

128 Mus musculus domesticus Y chromosomes (YDOM Chrs) vary i

129 n for introgression between the house mouse (Mus musculus domesticus) and the Algerian mouse (Mus spr

130 ctase subcomponent 1 (vkorc1) of house mice (Mus musculus domesticus) can cause resistance to anticoa

131 We use house mice (subspecies: Mus musculus domesticus) from remote Gough Island to pro

132 riation data from chromosome 7 in the mouse (Mus musculus domesticus) genome detected a recently repo

133 f LCMV RNA in a common European house mouse (Mus musculus domesticus) in Africa.

134 NA-less cells derived from the common mouse (Mus musculus domesticus) were fused to cytoplasts prepar

135 In laboratory mice (Mus musculus domesticus), alpha(1)-PI occurs in multiple

136 males from two inbred strains of house mice (Mus musculus domesticus).

137 omal boundary (PAB) in the laboratory mouse (Mus musculus domesticus, C57BL/6) such that the 5' three

138 of the western European form of house mouse, Mus musculus domesticus, in central Belgium.

139 ies of house mice, Mus musculus musculus and Mus musculus domesticus.

140 e subspecies pair: Mus musculus musculus and Mus musculus domesticus.

141 oRNA finding methods on six model organisms, Mus musculus, Drosophila melanogaste, Arabidopsis thalia

142 ology in the transcriptomes of Homo sapiens, Mus musculus, Drosophila melanogaster and Caenorhabditis

143 GUI is currently available for Homo sapiens, Mus musculus, Drosophila melanogaster and Caenorhabditis

144 of the information content of Homo sapiens, Mus musculus, Drosophila melanogaster, Caenorhabditis el

145 splice sites from five species-Homo sapiens, Mus musculus, Drosophila melanogaster, Caenorhabditis el

146 equenced eukaryotic proteomes (Homo sapiens, Mus musculus, Drosophila melanogaster, Caenorhabditis el

147 We find in Mus musculus, each AKT isoform has a unique expression p

148 ous recombination-based gene targeting using Mus musculus embryonic stem cells has greatly impacted b

149 ed by the Mus dunni endogenous virus and the Mus musculus endogenous retrovirus.

150 Mus musculus enjoys pride of place at the center of cont

151 Mus musculus exhibits five alleles of Prdm9; human popul

152 Here, we present the crystal structure of Mus musculus Exo70 at 2.25 A resolution.

153 e, Escherichia coli (strain K12, MG1655) and Mus musculus (female BALB/c mouse).

154 lyzing 19,000 expressed sequence tags of the Mus musculus FGO cDNA library.

155 ad in vertebrates but is notably absent from Mus musculus Findings highlight unexpected KCNE gene div

156 R (foxo5), Homo sapiens FKHR-L1 (FoxO3a) and Mus musculus FKHR2 (Foxo3).

157 rized IFNA gene families from H. sapiens and Mus musculus, for the analysis of both whole and partial

158 Male mice (Mus musculus) from 15 standard inbred strains were expos

159 10 eukaryotic model organisms: Homo sapiens, Mus musculus, Gallus gallus, Rattus norvegicus, Arabidop

160 uency portion of the cochlear nerve of mice (Mus musculus) generates a robust phase-locked response t

161 history inferred from a set of house mouse (Mus musculus) genomes.

162 both orangutan (Pongo pygmaeus) and murine (Mus musculus) genomic DNAs, both encoded on single exons

163 e, now identified from commensal house mice (Mus musculus group) by sequencing this segment can be or

164 lus gallus), rat (Rattus norvegicus), mouse (Mus musculus), hamster (Mesocricetus auratus), green mon

165 Laboratory mice (Mus musculus) have long telomeres, although a related mo

166 alobacter halobium, Drosphilia melanogaster, Mus musculus, Homo sapiens, mitochondria of M. musculus,

167 his study, we report the characterization of Mus musculus (house mouse) Neil3 (MmuNeil3) as an active

168 directly from mammalian tissues excised from Mus musculus (house mouse).

169 al structures of their complexes with mouse (Mus musculus) importin-alpha show preferential binding t

170 nvestigated whether placing a group of mice (Mus musculus) in nest shavings during the 180-min separa

171 The approach was applied to Mus musculus, in which the experimentally identified int

172 E elements in the genomes of Mus spretus and Mus musculus inbred strains and wild-caught animals.

173 he crystal structure for the death domain of Mus musculus IRAK-4 to 1.7 A resolution.

174 Laboratory mouse, Mus musculus, is one of the most important animal tools

175 Standard Mus musculus laboratory mice lack a functional XPR1 rece

176 lion cell types in five GABAergic Cre mouse (Mus musculus) lines, and identified two new amacrine cel

177 Mus musculus lymphoid cell lines EL4 and L1-2 and Mus du

178 es studied included four major subspecies of Mus musculus (M. m. castaneus, M. m. musculus, M. m. mol

179 white-footed (Peromyscus leucopus) or DBA/2 (Mus musculus) mice.

180 arker density method was then applied to the Mus musculus microsatellite linkage map.

181 n and flanking tRNAs were sequenced from 139 Mus musculus mitochondrial DNAs (mtDNAs) from mice colle

182 USP) or RXR from Locusta migratoria (LmRXR), Mus musculus (MmRXR) or Homo sapiens (HsRXR) to the VP16

183 In a murine (Mus musculus) model of HCPS (infection of NZB/BLNJ mice

184 of both the first and second PHR domains of Mus musculus (mouse) Phr1 (MYC binding protein 2, Mycbp2

185 egans (worm), Drosophila melanogaster (fly), Mus musculus (mouse)).

186 ruses found in wild mouse species, including Mus musculus, Mus spretus, and Mus spicelegus, as well a

187 icus) were fused to cytoplasts prepared from Mus musculus, Mus spretus, or rat (Rattus norvegicus), a

188 f skin tumor susceptibility in interspecific Mus musculus/Mus spretus hybrid mice and have identified

189 the first upper molar of hybrid mice between Mus musculus musculus and M. m.

190 cross between wild-derived inbred strains of Mus musculus musculus and M. m. domesticus in which ster

191 Regulatory divergence between Mus musculus musculus and M. m. domesticus was character

192 d strains from two subspecies of house mice, Mus musculus musculus and Mus musculus domesticus.

193 been restricted to a single subspecies pair: Mus musculus musculus and Mus musculus domesticus.

194 boratory mouse genome derived from the Asian Mus musculus musculus and, in one case, in the <1% deriv

195 paternal genome was derived from the inbred Mus musculus musculus CzechII/Ei strain.

196 In house mice, the contribution of the Mus musculus musculus X chromosome to hybrid male steril

197 us spretus, and 32% showed variation between Mus musculus musculus-derived standard laboratory inbred

198 The Mus musculus myosin-18A gene is expressed as two alterna

199 cell patch clamp recordings of GFP-encoding Mus musculus nAChRs transfected into HEK 293 cells to as

200 tion of TG2 alone is insufficient to protect Mus musculus neurons from oxidative death.

201 enetic linkage analysis of three independent Mus musculus NIH/Ola x (Mus spretus x M. musculus NIH/Ol

202 terspecific backcross [outbred Mus spretus X Mus musculus (NIH/Ola)].

203 The Mus musculus non-selective cation channel gene mNSC1 was

204 phila melanogaster, G. gallus, Homo sapiens, Mus musculus or Rattus norvegicus and identifies the spe

205 us nigra x maximowiczii) expressing a mouse (Mus musculus) ornithine (Orn) decarboxylase (odc) cDNA.

206 ila melanogaster, Danio rerio, Homo sapiens, Mus musculus, Oryza sativa, Solanum lycopersicum and Zea

207 Mus spretus diverged from Mus musculus over one million years ago.

208 ) is correlated to the capture rate of field Mus musculus (p = 0.011, r = 0.037); but surprisingly it

209 Mus musculus papillomavirus 1 (MmuPV1/MusPV1) induces pe

210 The Mus musculus Pax3 mutation Spd (Splotch-delayed, Pax3Spd

211 ruitfly (Drosophila melanogaster) and mouse (Mus musculus) phenotypes.

212 s of the Class I HDAC isoforms in protecting Mus musculus primary cortical neurons from oxidative dea

213 cum, 23% of Arabidopsis thaliana, and 28% of Mus musculus proteins are mostly disordered.

214 orvegicus (r = 0.246, p = 0.01; N = 110) and Mus musculus (r = 0.21, p = 0.0026; N = 203) genes.

215 not been clearly demonstrated in house mice (Mus musculus), raising concerns about mouse models of hu

216 ls of divergence among three rodents, mouse (Mus musculus), rat (Rattus norvegicus), and deer mouse (

217 rhaebditis elegans, Drosophila melanogaster, Mus musculus, Rattus norvegicus and Homo sapiens).

218 rom nine eukaryotic organisms: Homo sapiens, Mus musculus, Rattus norvegicus, Arabidopsis thaliana, D

219 the seven supported organisms (Homo sapiens, Mus musculus, Rattus norvegicus, Drosophila melanogaster

220 ntly supports seven organisms (Homo sapiens, Mus musculus, Rattus novegicus, Drosophila melanogaster,

221 in vivo, we deleted the Phlp1 gene in mouse (Mus musculus) retinal rod photoreceptor cells and measur

222 CfEcR), C. fumiferana ultraspiracle (CfUSP), Mus musculus retinoid X receptor (MmRXR) to either GAL4

223 bditis elegans, Drosophila melanogaster, and Mus musculus revealed no sequence homology.

224 esent the DNA sequence and gene structure of Mus musculus RNase 6 and examine the expression pattern

225 y from incorporation into proteins, a mouse (Mus musculus) Se-Cys lyase (SL) was expressed in the cyt

226 gh level of similarity to mammalian genes: a Mus musculus serine/threonine kinase, a rat tricarboxyla

227 ytes, Macaca mulatta, Rattus norvegicus, and Mus musculus) showed a human-like mtDNA transcription pa

228 ction resulting in assortative mating in the Mus musculus species complex.

229 his way, 64% showed length variation between Mus musculus spp. and Mus spretus, and 32% showed variat

230 e inter-specific backcross panel (C57BL/6J x Mus musculus spretus) has localized Bft to the central p

231 In CXCR3-deficient mice (Mus musculus), SPTB-associating cytokines were not acute

232 ts of cave fish, gecko (Gekko gekko), mouse (Mus musculus), squirrel (Sciurus carolinensis), and huma

233 tored in B6 T(Orl)/+ XY(AKR) mice carrying a Mus musculus Sry transgene.

234 ing a broad phylogenetic range: house mouse (Mus musculus), stickleback fish (Gasterosteus aculeatus)

235 point mutation in the CDK3 gene from several Mus musculus strains commonly used in the laboratory.

236 d crosses between M. spretus and susceptible Mus musculus strains have been used to map locations of

237 ltaneously measuring gene signatures of both Mus musculus (stromal) and Homo sapiens (epithelial) tis

238 rized 3 of the most polymorphic loci both in Mus musculus subspecies and in inbred strains by using m

239 atid-expressed genes are highly amplified in Mus musculus subspecies and in two further species from

240 nisatellite variant repeat mapping by PCR in Mus musculus subspecies suggested that mouse minisatelli

241 d ancestry, the genetic contributions of the Mus musculus subspecies--M. m. domesticus, M. m. musculu

242 -derived inbred strains representing several Mus musculus subspecies.

243 Of 3 groups of Mus musculus Swiss male mice, the first was inoculated i

244 genetically diverse organisms: Homo sapiens, Mus musculus, Takifugu rubripes, Ciona intestinalis, Cae

245 Mus musculus (telomere length >25 kb) and Mus spretus (t

246 genes identified in the genome of the mouse Mus musculus that are highly divergent orthologs of the

247 oliferation of splenic T cells isolated from Mus musculus that were stimulated with either T-cell rec

248 Twenty mice (Mus musculus), the second filial generation offspring fr

249 In mice (Mus musculus) they die at peri-implantation due to the m

250 a plant (Arabidopsis thaliana), and mammals (Mus musculus); this finding is consistent with a role fo

251 udy, we characterized the ABC superfamily in Mus musculus through in silico gene identification and m

252 small secreted proteins in Homo sapiens and Mus musculus using a novel database searching strategy.

253 ormed a forward genetic screen in the mouse (Mus musculus) using ENU mutagenesis.

254 bra finches (Taeniopygia guttata), and mice (Mus musculus) utilizing fluorescent immunohistochemistry

255 analysis of RH genes, the Rh homologue from Mus musculus was characterized.

256 The x-ray crystal structure of CDO from Mus musculus was solved to a nominal resolution of 1.75

257 The house mouse, Mus musculus, was established in the early 1900s as one

258 egeneration (Acomys cahirinus) and scarring (Mus musculus), we found that both species exhibited an a

259 za sativa), human (Homo sapiens), and mouse (Mus musculus), we found that these organisms primarily o

260 epresent those of the musculus subspecies of Mus musculus, we also report the coding regions of the b

261 mal caspase-8 as a model of wound healing in Mus musculus, we analyzed the signaling components respo

262 requirements for the maturation barricade in Mus musculus, we discovered that the exosome complex is

263 species of Mus confirmed that the strata in Mus musculus were representative of the genus Mus.

264 , Animalia; phylum, Chordata; genus/species, Mus musculus) were infected with influenza virus A/PR/8/

265 e, 2-mo-old C57BL/6J mice (Animalia Chordata Mus musculus) were randomly divided into 2 groups (n = 6

266 C57BL/6J (C57) and DBA/2J (DBA) inbred mice (Mus musculus) were tested on a task of simple odor discr

267 lved the crystal structure of the hinge from Mus musculus, which like its bacterial counterpart is ch

268 ercial oligonucleotide microarray containing Mus musculus whole-genome probes to assess the biologica

269 opsis thaliana, Drosophila melanogaster, and Mus musculus, whole-genome expression arrays have enable

270 ed DSB hot spots in four major subspecies of Mus musculus with different Prdm9 alleles and in their F

271 fections of severe combined immunodeficiency Mus musculus with the bacterium Borrelia hermsii.

272 we crossed LRRK2 R1441G BAC transgenic mice (Mus musculus) with tau P301S mutant transgenic mice and

273 Mice (mus musculus) with the ELL2 gene floxed in either exon 1

274 We also identified a homologous gene on the Mus musculus X chromosome (MMUX) (mUtp14a) that is the s

275 n-frame hexamer tandem repeat and RNA from a Mus musculus x M.spretus F1interspecific cross, we show

276 ping of Pem and other loci in three separate Mus musculus x Mus spretus backcross panels, we establis

277 ape in mouse, we performed RNA sequencing in Mus musculus x Mus spretus cells with complete skewing o

278 type mapping in interspecific mouse crosses (Mus musculus x Mus spretus) identified the gene encoding