ライフサイエンスコーパス: Mus

1 Mus m 1, Der p 1, and Bla g 1 were detected in 60%, 35%,

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

3 Mus musculus exhibits five alleles of Prdm9; human popul

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

5 Mus spicilegus is an Eastern European wild mouse species

6 Mus spretus diverged from Mus musculus over one million

7 Bla g 1, Can f 1, Fel d 1, Der f 1, Der p 1, Mus m 1, and Rat n 1) in dust vacuumed from nearly 7000

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

9 We identified Fv1 in 3 of the 4 Mus subgenera; its absence from Coelomys and 1 of 3 spec

10 nd to isolate methylation perturbations in a Mus musculusxMus caroli hybrid.

11 plification, both present in the genome of a Mus hybrid model, thus making it an ideal system to eval

12 riant recently isolated from the spleen of a Mus spicilegus mouse neonatally inoculated with Moloney

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

14 omal clones) to map sequence variation among Mus spretus (SPRET/Ei and SPRET/Glasgow) and Mus musculu

15 c mite allergens (DM), Fel d 1, Can f 1, and Mus m 1.

16 particles that propagated to human 293T and Mus dunni cells.

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

18 ila melanogaster, Caenorhabditis elegans and Mus musculus.

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

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

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

22 5 from cow's milk, Equ c 1 from horses, and Mus m 1 from mice, all of them representing major allerg

23 ic subgroup: Mus cervicolor isolate M813 and Mus spicilegus endogenous retrovirus HEMV.

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

25 abnormalities in Drosophila melanogaster and Mus musculus.

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

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

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

29 rged species of house mice (Mus musculus and Mus domesticus) as a natural mapping experiment to ident

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

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

32 rom 45 different strains of Mus musculus and Mus spretus revealed extensive polymorphism involving al

33 hat are polymorphic between Mus musculus and Mus spretus, we used The Jackson Laboratory (TJL) inters

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

35 ice using two mouse strains A/J (Par1/-) and Mus spretus (Par1/+).

36 90% sequence identity, that Danio rerio and Mus musculus alphaE-catenin have striking functional dif

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

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

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

40 time information from both Homo sapiens and Mus musculus.

41 small secreted proteins in Homo sapiens and Mus musculus.

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

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

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

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

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

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

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

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

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

51 Transfer of certain Mus domesticus-derived Y chromosomes (Sry(DOM) alleles,

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

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

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

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

56 lope precursor protein (gPr80(env)) than did Mus dunni fibroblasts, which are resistant to virus-indu

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

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

59 in Microtus is more extensive than in either Mus or in Rattus, consistent with the elevated rate of s

60 cal process gene ontology category in either Mus or Rattus.

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

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

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

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

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

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

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

68 (5%) for Arabidopsis thaliana, 1456 (4%) for Mus musculus and 614 (4%) for Drosophila melanogaster.

69 5% for Can f 1, 90% for Fel d 1, and 83% for Mus m 1.

70 the murine species Mus terricolor (formerly Mus dunni) is reported and compared with the published s

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

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

73 d strain with excellent hearing derived from Mus castaneus, CAST/EiJ.

74 SPRET/Ei is an inbred strain derived from Mus spretus that has approximately 1% sequence differenc

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

76 along the Mus lineage after divergence from Mus caroli.

77 lus castaneus and nucleotide divergence from Mus famulus and Rattus norvegicus to compare rates of ad

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

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

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

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

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

83 from diverse murid species of murine genera Mus, Rattus, Apodemus, Diplothrix, Hybomys, Mastomys, an

84 hensive sampling of taxa of the mouse (genus Mus), spanning a phylogenetic distance of 10 Myr.

85 en species or subspecies of the rodent genus Mus and two outgroup species were compared.

86 us musculus were representative of the genus Mus.

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

88 In Mus spretus, the chloride channel 4 gene Clcn4-2 is X-li

89 in this pathway is the recent acquisition in Mus of male-specific Fmo3 gene repression.

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

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

92 rmacology in Peromyscus and chemogenetics in Mus, we show that vasopressin inhibits nest building but

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

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

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

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

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

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

99 d target of rapamycin signalling pathways in Mus Musculus.

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

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

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

103 ormation of large multinucleated syncytia in Mus dunni cells.

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

105 retroviruses presently targeted by ZFP809 in Mus musculus.

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

107 ypothesis that the Progonomys clade includes Mus, the lineage separation event in the Siwalik fossil

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

109 ts of an industrial settlement on inhabitant Mus spretus mice.

110 After intraperitoneal injection of XMRV into Mus pahari mice, XMRV proviral DNA could be detected in

111 y common inbred strains and in some Japanese Mus molossinus mice but in none of the other wild mouse

112 ed by the backcross of (lean C57BL/6J x lean Mus spretus) x C57BL/6J, provides an excellent model of

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

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

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

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

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

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

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

120 ated beta-globin genes of Indian house mice (Mus castaneus) in conjunction with experimental studies

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

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

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

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

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

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

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

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

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

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

131 , which is unable to infect laboratory mice (Mus sp.) without the aid of powerful immunosuppressants.

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

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

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

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

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

137 In contrast, Gairdner's shrew-mice (Mus pahari) do express functional XPR1.

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

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

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

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

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

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

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

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

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

147 The mouse Mus spretus has been used to assess the biological respo

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

149 musculus domesticus) and the Algerian mouse (Mus spretus), using samples from the ranges of sympatry

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

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

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

153 s and bedroom floors and analyzed for mouse (Mus m 1), dust mite (Der p 1), cockroach (Bla g 1), and

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

176 response properties of the laboratory mouse, Mus musculus.

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

178 Cells of Mus minutoides, an African pygmy mouse of the subgenus N

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

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

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

182 convergent extension of the cochlear duct of Mus musculus.

183 been detected in several tissue extracts of Mus musculus.

184 MV), found in a single copy in the genome of Mus spicilegus, was remarkable for characteristics that

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

186 resentative of the major taxonomic groups of Mus.

187 These data demonstrate infection of Mus pahari by XMRV, potential cell tropism of the virus,

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

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

190 To determine if the polytropic proviruses of Mus spretus contain functional genes, we inoculated neon

191 tral rodent lineage before the separation of Mus and Rattus.

192 cy, Smcx, Zfy, and Zfx from seven species of Mus confirmed that the strata in Mus musculus were repre

193 of Mus musculus as well as other species of Mus using a PCR-based assay.

194 ith several other closely related species of Mus.

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

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

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

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

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

200 itochondrial organisms, and for the study of Mus genus origins.

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

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

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

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

205 These data support the use of Mus pahari as a model for XMRV pathogenesis and as a pla

206 ls from MoMLV-inoculated mice were plated on Mus dunni cells and mink cells, since these cells do not

207 ween C57BL/6J (B6) and either C3H/HeJ (H) or Mus spretus (SPRET) occurred in four zones (A-D); zone A

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

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

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

211 ari could serve as a model for XMRV, primary Mus pahari fibroblasts and mice were infected with cell-

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

234 -derived inbred strains representing several Mus musculus subspecies.

235 The Asian wild mouse species Mus caroli harbors an endogenous retrovirus (McERV) that

236 Cells from the Asian wild mouse species Mus castaneus are resistant to infection by the polytrop

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

238 Cells from the Asian mouse species Mus pahari show a unique pattern of susceptibility to th

239 e mitochondrial genome of the murine species Mus terricolor (formerly Mus dunni) is reported and comp

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

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

242 telomeres, although a related mouse species, Mus spretus, has human-sized telomeres.

243 Standard Mus musculus laboratory mice lack a functional XPR1 rece

244 ine leukemia virus (MLV) ecotropic subgroup: Mus cervicolor isolate M813 and Mus spicilegus endogenou

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

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

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

248 melanogaster and the house mouse subspecies Mus musculus castaneus.

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

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

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

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

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

254 ha-globin genes (HBA-T1, HBA-T2 and HBA-T3), Mus has only two copies.

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

256 esembles the Rattus genome more closely than Mus we examined the distribution of the Peromyscus ESTs

257 ecies showed weaker avoidance responses than Mus to 10 mM caffeine.

258 It has been reported elsewhere that Mus spretus SEG mice resist plague and develop an immune

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

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

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

262 a set to characterize TE variants across the Mus lineage, and to infer neutral and selective processe

263 thylamine production arose de novo along the Mus lineage after divergence from Mus caroli.

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

265 endogenous retrovirus family defined by the Mus dunni endogenous virus and the Mus musculus endogeno

266 C57BL/6J (B6) mice containing the Mus domesticus poschiavinus Y chromosome, YPOS, develop

267 e been widely used as the 12 Ma date for the Mus/Rattus split or a more basal split, conclusive paleo

268 Ts were specific to only one location in the Mus genome and spanned introns of an appropriate size fo

269 nts of the evolutionary translocation in the Mus lineage.

270 7, had specific activating mutations in the Mus musculus allele in 23 of 26 carcinomas.

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

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

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

274 is a relatively recent introduction into the Mus germ line but is representative of a relatively ance

275 was acquired shortly after the origin of the Mus genus.

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

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

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

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

280 The position of M. pahari at the base of the Mus phylogenetic tree indicates that XPR1-mediated susce

281 Mice of the Mus spretus species are resistant to tumour development,

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

283 in the Siwalik fossil record represents the Mus/Arvicanthis split.

284 They provide an evolutionary outgroup to the Mus/Rattus lineage and serve as an intermediary between

285 e most genetically distant strain within the Mus mus species and many trait variations relevant to co

286 een involved in genetic conflicts throughout Mus evolution.

287 hat Fv1 has had an antiviral role throughout Mus evolution predating exposure of mice to the MLVs res

288 ere identified using the BLASTX algorithm to Mus and Rattus, and 34 - 54% of all ESTs could be assign

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

290 rosatellite scan together with outcrosses to Mus spretus and M. castaneous followed by a subsequent t

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

292 To determine whether Mus pahari could serve as a model for XMRV, primary Mus

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

294 five X-linked loci in large samples of wild Mus domesticus and M. musculus, and we found low levels

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

296 y in >95% of pachynemas of Mus m. musculus x Mus m. domesticus sterile F1 males.

297 e performed RNA sequencing in Mus musculus x Mus spretus cells with complete skewing of X inactivatio

298 interspecific mouse crosses (Mus musculus x Mus spretus) identified the gene encoding Aurora2 (Stk6

299 of three independent Mus musculus NIH/Ola x (Mus spretus x M. musculus NIH/Ola)F1 backcrosses, to ide

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