ライフサイエンスコーパス: musculus

1 from neurogenesis to adulthood in mice (Mus musculus).

2 closely related house mouse subspecies (Mus musculus).

3 w the same pattern of results with mice (Mus musculus).

4 al duplication, R2d, in the house mouse (Mus musculus).

5 nonhibernating species, the house mouse (Mus musculus).

6 n the submaxillary glands of house mice (Mus musculus).

7 ases in response to wakefulness in mice (Mus musculus).

8 ion of TRPM1 on the dendrites of DBCs in mus musculus.

9 sent a broad sampling of diversity within M. musculus.

10 ild-caught mice from three subspecies of Mus musculus.

11 re currently supported: Homo sapiens and Mus musculus.

12 ued this further by knocking out Iop1 in Mus musculus.

13 n rate (centimorgans per megabase) within M. musculus.

14 mouse subspecies, M. m. castaneus and M. m. musculus.

15 of recombination rate segregating within M. musculus.

16 romyscus maniculatus, and the lab mouse, Mus musculus.

17 e information from both Homo sapiens and Mus musculus.

18 ergent extension of the cochlear duct of Mus musculus.

19 n detected in several tissue extracts of Mus musculus.

20 on in natural populations of house mice, Mus musculus.

21 ll secreted proteins in Homo sapiens and Mus musculus.

22 le coding region that was present only in M. musculus.

23 onse properties of the laboratory mouse, Mus musculus.

24 is, Rattus norvegicus, Homo sapiens, and Mus musculus.

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

26 melanogaster, Caenorhabditis elegans and Mus musculus.

27 itis elegans, Drosophila melanogaster, and M.musculus.

28 rmalities in Drosophila melanogaster and Mus musculus.

29 a dozen cell types from Homo sapiens and Mus musculus.

30 oviruses presently targeted by ZFP809 in Mus musculus.

31 rget of rapamycin signalling pathways in Mus Musculus.

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

33 S. cerevisiae, C. elegans, D. rerio, and M. musculus.

34 haliana (14.0% of cytosines methylated), Mus musculus (7.6%), and Escherichia coli (2.3%).

35 Drosophila, Caenorhabditis elegans, and Mus musculus, a complete signaling system can be genetically

36 ociated ribonuclease genes of the rodent Mus musculus, a finding that may have implications with resp

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

38 erve agent antidote HI-6 in complex with Mus musculus AChE covalently inhibited by the nerve agent sa

39 had specific activating mutations in the Mus musculus allele in 23 of 26 carcinomas.

40 e, human alpha2,3-sialyltransferase, and Mus musculus alpha2,6-sialyltransferase were transiently co-

41 sequence identity, that Danio rerio and Mus musculus alphaE-catenin have striking functional differe

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

43 Despite cell cycle re-entry in Mus musculus and A. cahirinus, efficient cell cycle progress

44 ditis elegans, Drosophila, Homo sapiens, Mus musculus and Arabidopsis species as well as all the euka

45 including human, Caenorhabditis elegans, Mus musculus and Arabidopsis thaliana.

46 s, Drosophila melanogaster, Danio rerio, Mus musculus and Arabidopsis thaliana.

47 ology with orthologous proteins found in Mus musculus and Drosophila melanogaster.

48 2+)-calmodulin binding site in the mouse Mus musculus and found that removal of (3) alters response w

49 la melanogaster, Caenorhabditis elegans, Mus musculus and Homo Sapiens.

50 iae, Caenorhabditis elegans, Drosophila, Mus musculus and Homo sapiens.

51 hila melanogaster, Arabidopsis thaliana, Mus musculus and Homo sapiens.

52 t patterns produced by speciation between M. musculus and M. domesticus are visible in the genomes of

53 itic worms in two species of house mice (Mus musculus and M. domesticus) and in their natural hybrids

54 hich are largely genetic hybrids between Mus musculus and M. domesticus, have become available.

55 nly in M. musculus or exclusively in both M. musculus and M. domesticus, indicative of recent integra

56 at differ between wild-derived strains of M. musculus and M. domesticus, we identified several physic

57 osome between two species of house mice, Mus musculus and M. domesticus.

58 in a previous F(2) intercross between M. m. musculus and M. m. domesticus and found three shared aut

59 xtensive regulatory divergence between M. m. musculus and M. m. domesticus, largely attributable to c

60 rt in an orthologous locus exclusively in M. musculus and M. pahari.

61 Despite the value of utilizing M. musculus and M. spretus for quantitative trait locus (QT

62 recently diverged species of house mice (Mus musculus and Mus domesticus) as a natural mapping experi

63 ral use of interspecific crosses between Mus musculus and Mus spretus for the detection of strong gen

64 sis of Nod2 from 45 different strains of Mus musculus and Mus spretus revealed extensive polymorphism

65 in our set that are polymorphic between Mus musculus and Mus spretus, we used The Jackson Laboratory

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

67 (examples are provided for Homo sapiens/Mus musculus and Plasmodium falciparum/Plasmodium vivax comp

68 0% sequence identity among Homo sapiens, Mus musculus and Rattus norvegicus.

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

70 induction is conserved in both the mouse Mus musculus and the cricket Gryllus bimaculatus, which is a

71 data of two other vertebrates, the mouse Mus musculus and the puffer fish Tetraodon nigroviridis, pro

72 romyces cerevisiae, circadian rhythms in Mus musculus and the root clock in Arabidopsis thaliana.

73 ve ever lived and include blue (Balaenoptera musculus) and fin (Balaenoptera physalus) whales.

74 entified in humans (Homo sapiens), mice (Mus musculus) and flies (Drosophila melanogaster), together

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

76 s), chimpanzee (Pan troglodytes), mouse (Mus musculus) and rat (Rattus norvegicus) for evidence of ge

77 related rodents, including house mouse (Mus musculus) and rat (Rattus norvegicus), did not support e

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

79 ovement sensors to blue whales (Balaenoptera musculus), and by recording the direction and size of th

80 d opossum (Didelphis virginiana), mouse (Mus musculus), and human (Homo sapiens) to determine if thei

81 at have cytosine methylation (H. sapiens, M. musculus, and A. thaliana) than in organisms that do not

82 la melanogaster, Caenorhabditis elegans, Mus musculus, and Arabidopsis thaliana, and investigated sta

83 ring methylated genomes of Homo sapiens, Mus musculus, and Danio rerio with nonmethylated genomes of

84 la melanogaster, Caenorhabditis elegans, Mus musculus, and Homo sapiens PPI networks.

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

86 ition comparing Drosophila melanogaster, Mus musculus, and Homo sapiens.

87 itis elegans, Drosophila, Gallus gallus, Mus musculus, and Homo sapiens.

88 re length differences among Homo sapiens, M. musculus, and M. spretus.

89 d model organisms, the laboratory mouse, Mus musculus, and the fruit fly, Drosophila melanogaster, wi

90 large samples of wild Mus domesticus and M. musculus, and we found low levels of nucleotide diversit

91 in the following genomes: Homo sapiens, Mus musculus, Arabidopsis thaliana, and Caenorhabditis elega

92 mparison of eight species: Homo sapiens, Mus musculus, Arabidopsis thaliana, Caenorhabditis elegans,

93 ns have been truncated on chromosome 7 in M. musculus as compared with the X-linked loci from seven o

94 ogous genes in strains and subspecies of Mus musculus as well as other species of Mus using a PCR-bas

95 capable of inducing key promoters of the Mus musculus Bdnf gene.

96 even eukaryotic organisms (Homo sapiens, Mus musculus, Bos taurus, Rattus norvegicus, Danio rerio, Ga

97 tially similar in size to those of mice (Mus musculus) but that, subsequently, bat digits greatly len

98 rred the protein-protein interactions in Mus musculus by using two approaches: i) identifying mouse o

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

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

101 ertebrate and invertebrate model systems Mus musculus, Caenorhabditis elegans, and Drosophila melanog

102 Mice (Mus musculus) carrying a hypomorphic allele of Ppp2r5delta,

103 strain and the evolutionarily divergent Mus musculus castaneus (CAST/Ei) strain as a mapping partner

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

105 ism data from the house mouse subspecies Mus musculus castaneus and nucleotide divergence from Mus fa

106 mJ, which carries the Xce(a) allele, and Mus musculus castaneus EiJ, which carries the Xce(c) allele,

107 ucture of the suppressive allele in wild Mus musculus castaneus suggests selective advantage.

108 l population of the Eastern house mouse, Mus musculus castaneus We performed simulations to assess th

109 wo subspecies: M. musculus domesticus and M. musculus castaneus.

110 pulated by the virus-infected subspecies Mus musculus castaneus.

111 anogaster and the house mouse subspecies Mus musculus castaneus.

112 ons/deletions among 20 inbred strains of Mus musculus, chosen to enable interpretation of the molecul

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

114 ile in the closely related mouse species Mus musculus, Clcn4-2 has been translocated to chromosome 7.

115 ting thermal lability is conserved among Mus musculus, Danio rerio, Drosophila melanogaster and Caeno

116 rmation with previously published mouse (Mus musculus) data and identified a subset of seven microRNA

117 single M. domesticus-derived and a single M. musculus-derived Sry allele (B6-Y(POS,RIII) and B6-Y(AKR

118 ta indicate that CDK3 is not required for M. musculus development and suggest that any functional rol

119 We estimate that M. domesticus and M. musculus diverged <500,000 years ago.

120 with estimated divergence rates between Mus musculus domesticus and either M. m. musculus or M. m. c

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

122 which represent the other two subspecies: M. musculus domesticus and M. musculus castaneus.

123 the two European house mouse subspecies, Mus musculus domesticus and M.m.musculus, sharing a hybrid z

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

125 ncompatible paternal allele arose in the Mus musculus domesticus lineage and that incompatible strain

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

127 n both Ins2 and Ins1 gene regions in the Mus musculus domesticus populations.

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

129 We investigated the contribution of the M. musculus domesticus Y chromosome to hybrid male sterilit

130 r introgression between the house mouse (Mus musculus domesticus) and the Algerian mouse (Mus spretus

131 e subcomponent 1 (vkorc1) of house mice (Mus musculus domesticus) can cause resistance to anticoagula

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

133 ion data from chromosome 7 in the mouse (Mus musculus domesticus) genome detected a recently reported

134 MV RNA in a common European house mouse (Mus musculus domesticus) in Africa.

135 ess cells derived from the common mouse (Mus musculus domesticus) were fused to cytoplasts prepared f

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

137 s from two inbred strains of house mice (Mus musculus domesticus).

138 bspecies pair: Mus musculus musculus and Mus musculus domesticus.

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

140 finding methods on six model organisms, Mus musculus, Drosophila melanogaste, Arabidopsis thaliana,

141 y in the transcriptomes of Homo sapiens, Mus musculus, Drosophila melanogaster and Caenorhabditis ele

142 is currently available for Homo sapiens, Mus musculus, Drosophila melanogaster and Caenorhabditis ele

143 the information content of Homo sapiens, Mus musculus, Drosophila melanogaster, Caenorhabditis elegan

144 ce sites from five species-Homo sapiens, Mus musculus, Drosophila melanogaster, Caenorhabditis elegan

145 nced eukaryotic proteomes (Homo sapiens, Mus musculus, Drosophila melanogaster, Caenorhabditis elegan

146 We find in Mus musculus, each AKT isoform has a unique expression patte

147 recombination-based gene targeting using Mus musculus embryonic stem cells has greatly impacted biome

148 y the Mus dunni endogenous virus and the Mus musculus endogenous retrovirus.

149 Mus musculus enjoys pride of place at the center of contempo

150 Mus musculus exhibits five alleles of Prdm9; human populatio

151 In particular, the C-terminal domain of M. musculus Exo70 adopts a new orientation relative to the

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

153 bility using four different M. spretus by M. musculus F1 backcrosses.

154 evolutionary distances, X-linked genes in M. musculus fall into the same strata as orthologous genes

155 scherichia coli (strain K12, MG1655) and Mus musculus (female BALB/c mouse).

156 ng 19,000 expressed sequence tags of the Mus musculus FGO cDNA library.

157 dae), including the blue whale (Balaenoptera musculus), fin whale (B. physalus), sei whale (B. boreal

158 n vertebrates but is notably absent from Mus musculus Findings highlight unexpected KCNE gene diversi

159 oxo5), Homo sapiens FKHR-L1 (FoxO3a) and Mus musculus FKHR2 (Foxo3).

160 d IFNA gene families from H. sapiens and Mus musculus, for the analysis of both whole and partial gen

161 Male mice (Mus musculus) from 15 standard inbred strains were exposed t

162 y portion of the cochlear nerve of mice (Mus musculus) generates a robust phase-locked response to th

163 for the D. melanogaster, H. sapiens, and M. musculus genomes.

164 tory inferred from a set of house mouse (Mus musculus) genomes.

165 M. musculus has a single IGFL family member that is located

166 Laboratory mice (Mus musculus) have long telomeres, although a related mouse

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

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

169 tructures of their complexes with mouse (Mus musculus) importin-alpha show preferential binding to th

170 ic mRNA expression between M. spretus and M. musculus in F1 mouse skin.

171 tigated whether placing a group of mice (Mus musculus) in nest shavings during the 180-min separation

172 The approach was applied to Mus musculus, in which the experimentally identified interac

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

174 line of retrotransposed genes specific to M. musculus is documented.

175 Laboratory mouse, Mus musculus, is one of the most important animal tools in b

176 Standard Mus musculus laboratory mice lack a functional XPR1 receptor

177 cell types in five GABAergic Cre mouse (Mus musculus) lines, and identified two new amacrine cell ty

178 an individual male blue whale (Balaenoptera musculus, Linnaeus 1758) using the earplug as a natural

179 Mus musculus lymphoid cell lines EL4 and L1-2 and Mus dunni

180 ust forward as the rostral extrinsic muscle, musculus (m.) nasalis, contracts to pull the pad and ini

181 in M. musculus we sequenced this locus in M. musculus, M. hortulanus, M. spretus, M. caroli, and M. p

182 musculus subspecies--M. m. domesticus, M. m. musculus, M. m. castaneus and the hybrid M. m. molossinu

183 50% of the total variation identified in M. musculus may be recovered in intrasubspecific crosses.

184 e-footed (Peromyscus leucopus) or DBA/2 (Mus musculus) mice.

185 M. musculus (Mm) and M. spretus TIN2s were >95% identical,

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

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

188 erility is asymmetric: F1 males with a M. m. musculus mother are sterile or nearly so while F1 males

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

190 s (worm), Drosophila melanogaster (fly), Mus musculus (mouse)).

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

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

193 s between wild-derived inbred strains of Mus musculus musculus and M. m. domesticus in which sterilit

194 Regulatory divergence between Mus musculus musculus and M. m. domesticus was characterized

195 of mice captured in a hybrid zone between M. musculus musculus and M. m. domesticus.

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

197 rains from two subspecies of house mice, Mus musculus musculus and Mus musculus domesticus.

198 tory mouse genome derived from the Asian Mus musculus musculus and, in one case, in the <1% derived f

199 ernal genome was derived from the inbred Mus musculus musculus CzechII/Ei strain.

200 In house mice, the contribution of the Mus musculus musculus X chromosome to hybrid male sterility

201 The Mus musculus myosin-18A gene is expressed as two alternative

202 l patch clamp recordings of GFP-encoding Mus musculus nAChRs transfected into HEK 293 cells to assess

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

204 Tgfb1-linked skin tumor susceptibility in M. musculus NIH/Ola x (M. spretus x M. musculus NIH/Ola)F1

205 ic linkage analysis of three independent Mus musculus NIH/Ola x (Mus spretus x M. musculus NIH/Ola)F1

206 ty in M. musculus NIH/Ola x (M. spretus x M. musculus NIH/Ola)F1 backcross mice depends on interactio

207 ent Mus musculus NIH/Ola x (Mus spretus x M. musculus NIH/Ola)F1 backcrosses, to identify a skin tumo

208 pecific backcross [outbred Mus spretus X Mus musculus (NIH/Ola)].

209 The Mus musculus non-selective cation channel gene mNSC1 was use

210 species - H. sapiens, R. norvegicus, and M. musculus - obtained from the piRBase and show that piRNA

211 d elements were identified either only in M. musculus or exclusively in both M. musculus and M. domes

212 een Mus musculus domesticus and either M. m. musculus or M. m. castaneus.

213 a melanogaster, G. gallus, Homo sapiens, Mus musculus or Rattus norvegicus and identifies the specifi

214 igra x maximowiczii) expressing a mouse (Mus musculus) ornithine (Orn) decarboxylase (odc) cDNA.

215 melanogaster, Danio rerio, Homo sapiens, Mus musculus, Oryza sativa, Solanum lycopersicum and Zea may

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

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

218 Mus musculus papillomavirus 1 (MmuPV1/MusPV1) induces persis

219 tk6 allele inherited from the susceptible M. musculus parent was overexpressed in normal cells and pr

220 fly (Drosophila melanogaster) and mouse (Mus musculus) phenotypes.

221 the Class I HDAC isoforms in protecting Mus musculus primary cortical neurons from oxidative death.

222 23% of Arabidopsis thaliana, and 28% of Mus musculus proteins are mostly disordered.

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

224 been clearly demonstrated in house mice (Mus musculus), raising concerns about mouse models of human

225 f divergence among three rodents, mouse (Mus musculus), rat (Rattus norvegicus), and deer mouse (Pero

226 bditis elegans, Drosophila melanogaster, Mus musculus, Rattus norvegicus and Homo sapiens).

227 nine eukaryotic organisms: Homo sapiens, Mus musculus, Rattus norvegicus, Arabidopsis thaliana, Droso

228 seven supported organisms (Homo sapiens, Mus musculus, Rattus norvegicus, Drosophila melanogaster, Da

229 supports seven organisms (Homo sapiens, Mus musculus, Rattus novegicus, Drosophila melanogaster, Dan

230 mice and in the house mouse subspecies ofMus musculus Receptor usage and envelope (env) sequence vari

231 ivo, we deleted the Phlp1 gene in mouse (Mus musculus) retinal rod photoreceptor cells and measured t

232 R), C. fumiferana ultraspiracle (CfUSP), Mus musculus retinoid X receptor (MmRXR) to either GAL4 DNA

233 is elegans, Drosophila melanogaster, and Mus musculus revealed no sequence homology.

234 t the DNA sequence and gene structure of Mus musculus RNase 6 and examine the expression pattern and

235 M. musculus RNase 6 has a limited expression pattern compar

236 om incorporation into proteins, a mouse (Mus musculus) Se-Cys lyase (SL) was expressed in the cytosol

237 .5 kb lambda genome, and a representative M. musculus sequence (the 16.3 kb mitochondrial genome), a

238 subspecies, Mus musculus domesticus and M.m.musculus, sharing a hybrid zone, provides an opportunity

239 , Macaca mulatta, Rattus norvegicus, and Mus musculus) showed a human-like mtDNA transcription patter

240 equencies of M. domesticus alleles on the M. musculus side of the hybrid zone.

241 rity of segments derived from domesticus and musculus sources.

242 n resulting in assortative mating in the Mus musculus species complex.

243 In CXCR3-deficient mice (Mus musculus), SPTB-associating cytokines were not acutely i

244 f cave fish, gecko (Gekko gekko), mouse (Mus musculus), squirrel (Sciurus carolinensis), and human.

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

246 In both cases, presence of the M. musculus Sry(RIII) allele corrected abnormal testis deve

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

248 nal M. spretus strains and one additional M. musculus strain generating 40.1 kb of sequence data.

249 t mutation in the CDK3 gene from several Mus musculus strains commonly used in the laboratory.

250 osses between M. spretus and susceptible Mus musculus strains have been used to map locations of gene

251 eously measuring gene signatures of both Mus musculus (stromal) and Homo sapiens (epithelial) tissue

252 -expressed genes are highly amplified in Mus musculus subspecies and in two further species from the

253 n to the cDNAs, which represent those of the musculus subspecies of Mus musculus, we also report the

254 tellite variant repeat mapping by PCR in Mus musculus subspecies suggested that mouse minisatellites

255 cestry, the genetic contributions of the Mus musculus subspecies--M. m. domesticus, M. m. musculus, M

256 ived inbred strains representing several Mus musculus subspecies.

257 Of 3 groups of Mus musculus Swiss male mice, the first was inoculated intra

258 Additionally ML lengthening due to musculus syringealis ventralis (VS) shortening is intrin

259 tically diverse organisms: Homo sapiens, Mus musculus, Takifugu rubripes, Ciona intestinalis, Caenorh

260 ippocampus) and a non-locomotor head muscle (musculus temporalis) in a receptive female rat during se

261 es identified in the genome of the mouse Mus musculus that are highly divergent orthologs of the prim

262 eration of splenic T cells isolated from Mus musculus that were stimulated with either T-cell recepto

263 Twenty mice (Mus musculus), the second filial generation offspring from a

264 In mice (Mus musculus) they die at peri-implantation due to the misex

265 we characterized the ABC superfamily in Mus musculus through in silico gene identification and mappi

266 ll secreted proteins in Homo sapiens and Mus musculus using a novel database searching strategy.

267 d a forward genetic screen in the mouse (Mus musculus) using ENU mutagenesis.

268 finches (Taeniopygia guttata), and mice (Mus musculus) utilizing fluorescent immunohistochemistry wit

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

270 The house mouse, Mus musculus, was established in the early 1900s as one of t

271 To study the evolution of mNSC1 in M. musculus we sequenced this locus in M. musculus, M. hort

272 eration (Acomys cahirinus) and scarring (Mus musculus), we found that both species exhibited an acute

273 ativa), human (Homo sapiens), and mouse (Mus musculus), we found that these organisms primarily opera

274 sent those of the musculus subspecies of Mus musculus, we also report the coding regions of the beta

275 caspase-8 as a model of wound healing in Mus musculus, we analyzed the signaling components responsib

276 irements for the maturation barricade in Mus musculus, we discovered that the exosome complex is a vi

277 musculus, we find evidence for an increase in the rate o

278 e it has thus far been observed mainly in M. musculus, we refer to this family as MMIDL.

279 cies of Mus confirmed that the strata in Mus musculus were representative of the genus Mus.

280 imalia; phylum, Chordata; genus/species, Mus musculus) were infected with influenza virus A/PR/8/34 w

281 -mo-old C57BL/6J mice (Animalia Chordata Mus musculus) were randomly divided into 2 groups (n = 65 ea

282 L/6J (C57) and DBA/2J (DBA) inbred mice (Mus musculus) were tested on a task of simple odor discrimin

283 the crystal structure of the hinge from Mus musculus, which like its bacterial counterpart is charac

284 al oligonucleotide microarray containing Mus musculus whole-genome probes to assess the biological ef

285 s thaliana, Drosophila melanogaster, and Mus musculus, whole-genome expression arrays have enabled re

286 SB hot spots in four major subspecies of Mus musculus with different Prdm9 alleles and in their F1 hy

287 ions of severe combined immunodeficiency Mus musculus with the bacterium Borrelia hermsii.

288 rossed LRRK2 R1441G BAC transgenic mice (Mus musculus) with tau P301S mutant transgenic mice and char

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

290 also identified a homologous gene on the Mus musculus X chromosome (MMUX) (mUtp14a) that is the stric

291 wo-locus incompatibilities between the M. m. musculus X chromosome and M. m. domesticus autosomal all

292 -derived strains in which males with a M. m. musculus X chromosome and M. m. domesticus Y chromosome

293 Introgression of the M. musculus X chromosome into a wild-derived M. domesticus

294 ify one relatively narrow interval on the M. musculus X chromosome involved in hybrid male sterility.

295 nterval in the proximal portion of the M. m. musculus X chromosome is associated with both overexpres

296 ith gene expression in normal skin from a M. musculus x M. spretus backcross to generate a network vi

297 the sex body in >95% of pachynemas of Mus m. musculus x Mus m. domesticus sterile F1 males.

298 in mouse, we performed RNA sequencing in Mus musculus x Mus spretus cells with complete skewing of X

299 mapping in interspecific mouse crosses (Mus musculus x Mus spretus) identified the gene encoding Aur

300 m. domesticus Y and an interval on the M. m. musculus X that resulted in abnormal sperm morphology.