ライフサイエンスコーパス: musculus

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

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

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

4 closely related house mouse subspecies (Mus musculus).

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

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

7 aliana), rice (Oryza sativa), and mouse (Mus musculus).

8 such as endangered blue whales (Balaenoptera musculus).

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

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

11 oviruses presently targeted by ZFP809 in Mus musculus.

12 rget of rapamycin signalling pathways in Mus Musculus.

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

14 omparison of tissues in Homo sapiens and Mus musculus.

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

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

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

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

19 re currently supported: Homo sapiens and Mus musculus.

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

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

22 rosophila melanogaster, Danio rerio, and Mus musculus.

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

24 of recombination rate segregating within M. musculus.

25 rgets and 6511 functional categories for Mus musculus.

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

27 ergent extension of the cochlear duct of Mus musculus.

28 n detected in several tissue extracts of Mus musculus.

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

30 ll secreted proteins in Homo sapiens and Mus musculus.

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

32 onse properties of the laboratory mouse, Mus musculus.

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

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

35 ation with single-cell RNA-sequencing in Mus musculus.

36 rated by laboratory-reared conditions for M. musculus.

37 and deficient sprouting angiogenesis in Mus musculus.

38 the flagellated protist T. brucei and in M. musculus.

39 upported by Wnt1-Cre lineage analysis in Mus musculus.

40 e information from both Homo sapiens and Mus musculus.

41 rmalities in Drosophila melanogaster and Mus musculus.

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

43 Xist129 and XistCAS RNA are unspliced in Mus musculus 129SvJ/Mus castaneous (CAS) hybrid female ES ce

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

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

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

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

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

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

50 o pairs of species: (i) Homo sapiens and Mus musculus and (ii) Saccharomyces cerevisiae and Schizosac

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

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

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

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

55 2+)-calmodulin binding site in the mouse Mus musculus and found that removal of (3) alters response w

56 (AUC: 0.930, 0.923 and 0.944 for E. coli, M. musculus and H. sapiens, respectively).

57 om Bombyx mori, Drosophila melanogaster, Mus musculus and Homo sapiens bound G4 structures in BmPOUM2

58 three species, namely, Escherichia coli, Mus musculus and Homo sapiens, and compared using randomized

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

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

61 g distinct neocortical neuron classes in Mus musculus and interneuron developmental states in Homo sa

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

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

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

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

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

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

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

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

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

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

72 0% sequence identity among Homo sapiens, Mus musculus and Rattus norvegicus.

73 es were syntenic with that of the murids Mus musculus and Rattus norvegicus.

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

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

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

77 n hamsters (Mesocricetus auratus), mice (Mus musculus) and cynomolgus macaques (Macaca fascicularis),

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

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

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

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

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

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

84 ystems: the pig (Sus scrofa), the mouse (Mus musculus), and 2 frogs (Xenopus laevis and Xenopus tropi

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

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

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

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

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

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

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

92 ccharomyces pombe, Arabidopsis thaliana, Mus musculus, and Homo sapiens.

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

94 eomics at 10 ages across the lifespan of Mus musculus, and integrated these findings with data from t

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

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

97 ramework, we found that A. cahirinus, lab M. musculus, and wild M. musculus were primarily nocturnal,

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

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

100 Laboratory mice (Mus musculus) are typically housed in simple cages consistin

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

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

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

104 during exercise in male mice induces the Mus musculus Bdnf gene and promotes learning and memory form

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

106 oteomic analyses of skin from Acomys and Mus musculus before and after wounding.

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

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

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

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

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

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

113 , MmuPV1, which infects laboratory mice (Mus musculus), can cause infections in the female cervicovag

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

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

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

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

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

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

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

121 anogaster and the house mouse subspecies Mus musculus castaneus.

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

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

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

125 Laboratory mice (Mus musculus) communicate a variety of social messages throu

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

127 drastically different lifestyles such as Mus musculus, Danio rerio, Oryzias latipes and Xiphophorus m

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

129 The overall structure of M. musculus dCTPase is highly similar to enzymes from the a

130 Comparison of M. musculus dCTPase with homologs from a diverse range of m

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

146 bed in the western European house mouse (Mus musculus domesticus), clarifying their role in semiochem

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

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

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

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

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

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

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

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

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

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

157 tation and initiation of inflammation in Mus musculus embryonic fibroblasts.

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

159 Systems genetics in laboratory mice (Mus musculus) enables data-driven discovery of biological ne

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

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

162 . cahirinus sleep significantly more than M. musculus, exhibit nearly three times more REM, and sleep

163 Mus musculus exhibits five alleles of Prdm9; human populatio

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

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

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

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

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

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

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

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

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

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

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

175 loping naked mole rats compared to mice (Mus musculus), gerbils (Meriones unguiculatus), and Damarala

176 e spans and body sizes, including mouse (Mus musculus), goat (Capra hircus), Audouin's gull (Larus au

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

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

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

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

181 tures of an active mammalian dCTPase from M. musculus in complex with the nonhydrolyzable substrate a

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

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

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

185 of rare Antarctic blue whales (Balaenoptera musculus intermedia) in relation to the swarm characteri

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

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

188 The mouse (Mus musculus) is an extensively used model of human disease

189 The mouse (Mus musculus) is the dominant organism used to investigate t

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

191 e we present the structure of a CCC, the Mus musculus K(+)-Cl(-) cotransporter (KCC) KCC4, in lipid n

192 Standard Mus musculus laboratory mice lack a functional XPR1 receptor

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

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

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

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

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

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

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

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

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

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

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

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

205 ta integration for Homo sapiens (human), Mus musculus (mouse), Rattus norvegicus (rat), Danio rerio (

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

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

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

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

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

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

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

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

214 search behavior of Escherichia coli and Mus musculus MUTYH WT and wedge variant orthologs on DNA tig

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

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

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

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

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

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

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

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

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

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

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

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

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

228 lis), fin (B. physalus), and blue whales (B. musculus) over a decade, based on daily detections of th

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

230 racterized a skin cancer model, in which Mus musculus papillomavirus 1 (MmuPV1) infection caused cSCC

231 he discovery of a murine papillomavirus, Mus musculus papillomavirus 1 (MmuPV1), and how its experime

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

233 ptera physalus) and blue whale (Balaenoptera musculus) peroxisome proliferator-activated receptor gam

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

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

236 23% of Arabidopsis thaliana, and 28% of Mus musculus proteins are mostly disordered.

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

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

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

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

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

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

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

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

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

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

247 .5 kb lambda genome, and a representative M. musculus sequence (the 16.3 kb mitochondrial genome), at

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

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

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

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

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

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

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

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

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

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

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

259 ived inbred strains representing several Mus musculus subspecies.

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

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

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

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

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

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

266 We also included wild M. musculus to control for alterations generated by laborat

267 sed a piezoelectric system validated for Mus musculus to monitor sleep in both species.

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

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

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

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

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

273 Using the mouse model (Mus musculus), we demonstrated that rather than being driven

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

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

276 from posterior parietal cortex in mice (Mus musculus), we show that drift is systematically constrai

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

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

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

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

281 t A. cahirinus, lab M. musculus, and wild M. musculus were primarily nocturnal, but exhibited distinc

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

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

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

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

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

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

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

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

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

291 roadly distributed throughout the CNS in Mus musculus, with FGFR1 exhibiting the greatest heterogenei

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

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

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

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

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

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

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

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

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