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 spretus diverged from Mus musculus over one million

6 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

7 CAS RNA are unspliced in Mus musculus 129SvJ/Mus castaneous (CAS) hybrid female ES cells.

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

9 of complex human societies, we analyzed 829 Mus specimens from 43 archaeological contexts in Southwe

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

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

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

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

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

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

16 er distinctive difference between Acomys and Mus lies in the macrophage-produced arginase 1 is found

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

18 re expressed at similar levels in Acomys and Mus, but there are significant differences.

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

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

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

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

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

34 90% sequence identity, that Danio rerio and Mus musculus alphaE-catenin have striking functional dif

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

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

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

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

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

40 small secreted proteins in Homo sapiens and Mus musculus.

41 time information from both Homo sapiens and Mus musculus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

63 (5%) for Arabidopsis thaliana, 1456 (4%) for Mus musculus and 614 (4%) for Drosophila melanogaster.

64 5% for Can f 1, 90% for Fel d 1, and 83% for Mus m 1.

65 8 targets and 6511 functional categories for Mus musculus.

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

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

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

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

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

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

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

73 along the Mus lineage after divergence from Mus caroli.

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

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

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

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

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

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

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

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

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

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

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

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

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

87 rity and deficient sprouting angiogenesis in Mus musculus.

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

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

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

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

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

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

94 ch as collagens are more highly expressed in Mus, but likely more important is the higher expression

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

96 e macrophage-produced arginase 1 is found in Mus whereas arginase 2 is found in Acomys.

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

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

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

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

101 d target of rapamycin signalling pathways in Mus Musculus.

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

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

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

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

106 e expression (Serpine 1, Plau, and Timp1) in Mus as compared to Acomys (p < .05).

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

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

109 n-associated enzymes and kinases, whereas in Mus immuno-modulation proteins characteristic of inflamm

110 Following wounding in Mus the complement and coagulation cascades, PPAR signal

111 retroviruses presently targeted by ZFP809 in Mus musculus.

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

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

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

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

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

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

118 ular senescence in non-regenerating mammals (Mus and Rattus).

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

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

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

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

123 s following SCI as compared to C57BL/6 mice (Mus), which similar to all mammals studied to date exhib

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

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

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

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

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

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

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

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

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

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

134 the urinary protein fraction in house mice (Mus spp.) and rats (Rattus spp.).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

198 convergent extension of the cochlear duct of Mus musculus.

199 been detected in several tissue extracts of Mus musculus.

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

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

202 resentative of the major taxonomic groups of Mus.

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

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

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

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

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

208 ith several other closely related species of Mus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

225 he genomes of Rattus norvegicus (brown rat), Mus spretus (Algerian mouse), and Apodemus sylvaticus (w

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

245 Standard Mus musculus laboratory mice lack a functional XPR1 rece

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

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

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

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

250 melanogaster and the house mouse subspecies Mus musculus castaneus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

272 nts of the evolutionary translocation in the Mus lineage.

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

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

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

276 evelopment in guinea pigs and members of the Mus genus, animals that navigate particularly small home

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

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

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

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

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

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

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

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

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

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

287 een involved in genetic conflicts throughout Mus evolution.

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

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

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

291 (Bmp2, GDNF, and Shh) in Acomys compared to Mus (p < .05).

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

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

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

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

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

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

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

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

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