ライフサイエンスコーパス: Mus musculus

1 acaca mulatta), pig (Sus scrofa), and mouse (Mus musculus).

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

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

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

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

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

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

8 s thaliana), rice (Oryza sativa), and mouse (Mus musculus).

9 Odocoileus spp) to standard laboratory mice (Mus musculus).

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

11 a comparison of tissues in Homo sapiens and Mus musculus.

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

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

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

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

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

17 8 targets and 6511 functional categories for Mus musculus.

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

19 convergent extension of the cochlear duct of Mus musculus.

20 been detected in several tissue extracts of Mus musculus.

21 s, Drosophila melanogaster, Danio rerio, and Mus musculus.

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

23 small secreted proteins in Homo sapiens and Mus musculus.

24 response properties of the laboratory mouse, Mus musculus.

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

26 ablation with single-cell RNA-sequencing in Mus musculus.

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

28 ila melanogaster, Caenorhabditis elegans and Mus musculus.

29 rity and deficient sprouting angiogenesis in Mus musculus.

30 s, supported by Wnt1-Cre lineage analysis in Mus musculus.

31 time information from both Homo sapiens and Mus musculus.

32 abnormalities in Drosophila melanogaster and Mus musculus.

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

34 retroviruses presently targeted by ZFP809 in Mus musculus.

35 d target of rapamycin signalling pathways in Mus Musculus.

36 oth Xist129 and XistCAS RNA are unspliced in Mus musculus 129SvJ/Mus castaneous (CAS) hybrid female E

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

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

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

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

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

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

43 7, had specific activating mutations in the Mus musculus allele in 23 of 26 carcinomas.

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

45 90% sequence identity, that Danio rerio and Mus musculus alphaE-catenin have striking functional dif

46 n two pairs of species: (i) Homo sapiens and Mus musculus and (ii) Saccharomyces cerevisiae and Schiz

47 (5%) for Arabidopsis thaliana, 1456 (4%) for Mus musculus and 614 (4%) for Drosophila melanogaster.

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

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

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

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

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

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

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

55 s from Bombyx mori, Drosophila melanogaster, Mus musculus and Homo sapiens bound G4 structures in BmP

56 rom three species, namely, Escherichia coli, Mus musculus and Homo sapiens, and compared using random

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

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

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

60 nting distinct neocortical neuron classes in Mus musculus and interneuron developmental states in Hom

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

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

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

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

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

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

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

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

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

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

71 enomes were syntenic with that of the murids Mus musculus and Rattus norvegicus.

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

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

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

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

76 es in hamsters (Mesocricetus auratus), mice (Mus musculus) and cynomolgus macaques (Macaca fascicular

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

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

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

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

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

82 ry systems: the pig (Sus scrofa), the mouse (Mus musculus), and 2 frogs (Xenopus laevis and Xenopus t

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

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

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

86 The method was applied to colonic crypts in Mus musculus, and enabled detection of mutant subclones

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

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

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

90 zosaccharomyces pombe, Arabidopsis thaliana, Mus musculus, and Homo sapiens.

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

92 proteomics at 10 ages across the lifespan of Mus musculus, and integrated these findings with data fr

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

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

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

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

97 Laboratory mice (Mus musculus) are typically housed in simple cages consi

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

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

100 To assess B cell breadth, Mus musculus (BALB/c) Ab-secreting cells elicited by a c

101 ced during exercise in male mice induces the Mus musculus Bdnf gene and promotes learning and memory

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

103 d proteomic analyses of skin from Acomys and Mus musculus before and after wounding.

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

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

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

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

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

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

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

111 irus, MmuPV1, which infects laboratory mice (Mus musculus), can cause infections in the female cervic

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

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

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

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

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

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

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

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

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

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

122 melanogaster and the house mouse subspecies Mus musculus castaneus.

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

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

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

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

127 Laboratory mice (Mus musculus) communicate a variety of social messages t

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

129 ing drastically different lifestyles such as Mus musculus, Danio rerio, Oryzias latipes and Xiphophor

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

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

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

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

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

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

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

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

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

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

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

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

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

143 nd morphometric variation in the house mice (Mus musculus domesticus) from the Orkney archipelago.

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

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

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

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

148 scribed in the western European house mouse (Mus musculus domesticus), clarifying their role in semio

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

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

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

152 XY C57BL/6J (B6) mice harboring a Mus musculus domesticus-type Y chromosome (Y (POS) ), kn

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

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

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

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

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

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

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

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

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

162 adaptation and initiation of inflammation in Mus musculus embryonic fibroblasts.

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

164 Systems genetics in laboratory mice (Mus musculus) enables data-driven discovery of biologica

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

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

167 Mus musculus exhibits five alleles of Prdm9; human popul

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

169 Male mice Mus musculus fed a high-fat diet rich in SFAs developed

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

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

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

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

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

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

176 10 eukaryotic model organisms: Homo sapiens, Mus musculus, Gallus gallus, Rattus norvegicus, Arabidop

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

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

179 developing naked mole rats compared to mice (Mus musculus), gerbils (Meriones unguiculatus), and Dama

180 life spans and body sizes, including mouse (Mus musculus), goat (Capra hircus), Audouin's gull (Laru

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

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

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

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

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

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

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

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

189 The mouse (Mus musculus) is an extensively used model of human dise

190 The mouse (Mus musculus) is the dominant organism used to investiga

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

192 Here we present the structure of a CCC, the Mus musculus K(+)-Cl(-) cotransporter (KCC) KCC4, in lip

193 Standard Mus musculus laboratory mice lack a functional XPR1 rece

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

195 ticle cryo-electron microscopy structures of Mus musculus LRRC8A in complex with the inhibitor DCPIB

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

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

198 tive regulator of the type I IFN response in Mus musculus macrophages.

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

200 esent the X-ray structure of the apo form of Mus musculus MICU2 at 2.5- angstrom resolution.

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

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

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

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

205 d data integration for Homo sapiens (human), Mus musculus (mouse), Rattus norvegicus (rat), Danio rer

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

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

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

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

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

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

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

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

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

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

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

217 time search behavior of Escherichia coli and Mus musculus MUTYH WT and wedge variant orthologs on DNA

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

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

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

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

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

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

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

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

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

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

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

229 characterized a skin cancer model, in which Mus musculus papillomavirus 1 (MmuPV1) infection caused

230 ss the discovery of a murine papillomavirus, Mus musculus papillomavirus 1 (MmuPV1), and how its expe

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

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

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

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

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

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

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

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

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

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

241 The house mouse (Mus musculus) represents the extreme of globalization of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

260 -derived inbred strains representing several Mus musculus subspecies.

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

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

263 esent cryo-electron microscopy structures of Mus musculus TASK2 in lipid nanodiscs in open and closed

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

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

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

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

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

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

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

271 we used a piezoelectric system validated for Mus musculus to monitor sleep in both species.

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

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

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

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

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

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

278 Using the mouse model (Mus musculus), we demonstrated that rather than being dr

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

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

281 ings from posterior parietal cortex in mice (Mus musculus), we show that drift is systematically cons

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

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

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

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

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

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

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

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

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

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

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

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

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

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

296 as broadly distributed throughout the CNS in Mus musculus, with FGFR1 exhibiting the greatest heterog

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

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

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

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