ライフサイエンスコーパス: inbred mouse strain

1 +) T cells compared to a resistant classical inbred mouse strain.

2 translational studies utilize only a single inbred mouse strain.

3 a consistent manner, equivalent to any other inbred mouse strain.

4 pe apolipoprotein(a) have been created in an inbred mouse strain.

5 bility in the genetically predisposed 129/Sv inbred mouse strain.

6 ction of previous wake duration varies among inbred mouse strains.

7 study compared fear extinction in a panel of inbred mouse strains.

8 ss between the Large (LG/J) and Small (SM/J) inbred mouse strains.

9 etory phenotypes varied considerably in four inbred mouse strains.

10 issues, such as colon and lung, of different inbred mouse strains.

11 brain samples of a panel of BXD recombinant inbred mouse strains.

12 as not achieved in three (A/J, AKR/J, CBA/J) inbred mouse strains.

13 ted with resistance to Bacillus anthracis in inbred mouse strains.

14 n platelet integrin alpha2beta1 levels among inbred mouse strains.

15 ic basis for several trait differences among inbred mouse strains.

16 set collected from F2 intercross studies of inbred mouse strains.

17 ularization in the BXD series of recombinant inbred mouse strains.

18 ed for each marker and tested on a set of 48 inbred mouse strains.

19 ntitative phenotype that varies widely among inbred mouse strains.

20 th saccharin preference in a large number of inbred mouse strains.

21 ative gene expression data, which vary among inbred mouse strains.

22 P markers were designed and typed against 54 inbred mouse strains.

23 largely congruent with the known history of inbred mouse strains.

24 processing between these two closely related inbred mouse strains.

25 n APP YAC transgene was transferred to three inbred mouse strains.

26 regulatory variation in 69 genes across four inbred mouse strains.

27 ze in vitro differentiated Th1 cells from 16 inbred mouse strains.

28 ssed in eight brain regions obtained from 14 inbred mouse strains.

29 x cardiovascular traits in two commonly used inbred mouse strains.

30 characteristics can be very different among inbred mouse strains.

31 r3 alleles and Sac phenotypes in recombinant inbred mouse strains.

32 th with lifespan, even among closely related inbred mouse strains.

33 /6, BALB/c, RIII, AKR, DBA/2, I, A/J and C3H inbred mouse strains.

34 r in striatal regions in AXB/BXA recombinant inbred mouse strains.

35 of lung eosinophilia, we tested 15 different inbred mouse strains.

36 6J mice and in 11 of the AXB/BXA recombinant inbred mouse strains.

37 gh exploitation of genetic differences among inbred mouse strains.

38 efting in the AXB and BXA set of recombinant inbred mouse strains.

39 lytropic env genes present in the genomes of inbred mouse strains.

40 n treatment) is inherited in A/J and C3H/HeJ inbred mouse strains.

41 and neuropathology they produce in panels of inbred mouse strains.

42 scle disease in CD-1 mice as well as several inbred mouse strains.

43 to induce immune responses in corresponding inbred mouse strains.

44 ally by C57BL/6 CTLs stimulated by different inbred mouse strains.

45 e results would at least generalize to other inbred mouse strains.

46 this finding was replicated in a study of 98 inbred mouse strains.

47 recently, been limited to a small number of inbred mouse strains.

48 mponents in dendritic cells from recombinant inbred mouse strains.

49 GWAS) cannot be productively performed using inbred mouse strains.

50 g can distinguish hair shafts from different inbred mouse strains.

51 (healer of ear wounds) and SM/J (nonhealer) inbred mouse strains.

52 ic variation in hematopoietic function among inbred mouse strains.

53 of thirteen classical and four wild-derived inbred mouse strains.

54 ve mouse hot spot in F1 hybrids derived from inbred mouse strains.

55 d a wide range of pulmonary metastasis among inbred mouse strains.

56 bility phenotype of four previously untested inbred mouse strains.

57 lymorphic APOBEC3 alleles found in different inbred mouse strains.

58 induced CNV in the BXD series of recombinant inbred mouse strains.

59 -1-induced disease, we examined 14 different inbred mouse strains.

60 tly less hippocampal neurogenesis than other inbred mouse strains [1] and do not perform well in lear

61 We report that females of some substrains of inbred mouse strain 129 are resistant to systemic plague

62 In the present study, we tested 12 inbred mouse strains (129/J, A/J, AKR/J, BALB/cJ, C3H/He

63 is a major contributor to AHL in nine other inbred mouse strains-129P1/ReJ, A/J, BALB/cByJ, BUB/BnJ,

64 cortex, and olfactory bulb) of 10 different inbred mouse strains (129S1/SvImJ, A/J, AKR/J, BALB/cByJ

65 We describe the origins and relationships of inbred mouse strains, 90 years after the generation of t

66 strains (Lewis and Fischer 344) or a pair of inbred mouse strains (A/J and C57BL/6J); (2) which of th

67 hology associated with R. parkeri infection, inbred mouse strains (A/J, BALB/c, C3H/HeJ, and C3H/HeN)

68 RORgamma(+) Treg proportions varied between inbred mouse strains, a trait transmitted by the mother

69 we screened reciprocal backcrosses of three inbred mouse strains, A/J, NOD/LtJ and SKH2/J, with age-

70 audi chabaudi AS in early gestation, several inbred mouse strains abort at midgestation.

71 erin 23 gene (Cdh23(c.753A)), common to many inbred mouse strains, accelerates age-related hearing lo

72 -sensitive C57BL/6J and the normotensive A/J inbred mouse strains after they were provided with water

73 When homozygous, the Mor1 allele from the inbred mouse strain AKR/J diminishes the severity of the

74 etabolomic analysis performed using multiple inbred mouse strains, along with knowledge-based filteri

75 Inbred mouse strains also have highly variable plasma VW

76 ucture of the Naip array among commonly used inbred mouse strains, although these gross structural di

77 mbers can be significantly different between inbred mouse strains, analogous to the haplotype differe

78 served in crosses between females of the DDK inbred mouse strain and many non-DDK males.

79 t derived from DBA/2J (D2) and C57BL/6J (B6) inbred mouse strains and (B6xD2)F2 hybrid mice derived f

80 ernative splice products is observed between inbred mouse strains and appears to correlate with an in

81 ere to quantify gravity receptor function in inbred mouse strains and compare vestibular and auditory

82 iting in RNA samples isolated from different inbred mouse strains and dissected brain regions, as wel

83 Polymorphisms among inbred mouse strains and feral species suggest that muta

84 We surveyed inbred mouse strains and found that for the majority tes

85 We surveyed 120 inbred mouse strains and found that the frequency of adu

86 Although blood neutrophil numbers in inbred mouse strains and individual human subjects are t

87 Hundreds of inbred mouse strains and intercross populations have bee

88 e EMPReSSslim pipeline which is performed on inbred mouse strains and knock-out lines arising from th

89 hese assays are ubiquitously performed using inbred mouse strains and mutations placed on inbred gene

90 ng inflammation and toxicity across multiple inbred mouse strains and to use genome-wide association

91 These peptides were expressed in diverse inbred mouse strains and were recognized preferentially

92 cal F1 hybrids (between the DDK and C57BL/6J inbred mouse strains) and C57BL/6J males at markers link

93 mice, that contain the nuclear DNA from one inbred mouse strain, and the mtDNA from a different inbr

94 cells was quantified in the C57BL/6J and A/J inbred mouse strains, and in 25 recombinant inbred strai

95 ved potency for delivery across a variety of inbred mouse strains, and in cynomolgus macaques and hum

96 onsumption across a panel of BXD recombinant inbred mouse strains, and that share a genomic region th

97 kinetic differences, was seen with six other inbred mouse strains, and was not observed using carboxy

98 Inbred mouse strains are an invaluable resource for mode

99 ly mirrored in a murine genetic model, where inbred mouse strains are differentially susceptible to H

100 a variety of species, macrophages from most inbred mouse strains are nonpermissive for intracellular

101 st several days of infection.IMPORTANCE Most inbred mouse strains are relatively resistant to orthopo

102 Most inbred mouse strains are resistant to infection by L. pn

103 bestos fibers are clearly reduced in the 129 inbred mouse strain as compared with typical fibrogenesi

104 These data reveal limitations to the use of inbred mouse strains as preclinical models at vaccine de

105 To identify variants between inbred mouse strains at a single nucleotide resolution,

106 dogenes in the mouse reference genome and 18 inbred mouse strains (available via the mouse.pseudogene

107 re very long, in the size range reported for inbred mouse strains (averaging 46 kb per chromosome end

108 adenovirus vector to immunize 26 recombinant inbred mouse strains (AXB and BXA) derived from A/J and

109 8%) T lymphocytes differ significantly among inbred mouse strains: B220% is high in C57BL/6J (B6) and

110 ance to Coccidioides immitis infection among inbred mouse strains: B6 mice are susceptible, while DBA

111 The very closely related inbred mouse strains BALB/cJ and BALB/cByJ differ substa

112 Two inbred mouse strains, BALB/c and CBA/Ca, were infected w

113 Mndal is highly polymorphic among inbred mouse strains, because it is absent in 10 of 24 s

114 ced leakage as early as 15 to 25 min in some inbred mouse strains, but not in others, whereas PA or L

115 me and caspase-1 in macrophages from certain inbred mouse strains, but the mechanism by which this oc

116 , higher than values previously estimated in inbred mouse strains by a larger bore microneedle manome

117 ogen B. gibsoni, we infected the susceptible inbred mouse strains C.B-17.scid and DBA/2 with a clinic

118 Mice of the inbred mouse strain C3H/HeJ have been shown to be homozy

119 The inbred mouse strain C3H/HeJ is prone to absence seizures

120 In two inbred mouse strains, C3H/2Ibg (C3H) and DBA/2Ibg (DBA/2

121 nitor differentiation from the marrow of two inbred mouse strains, C3H/HeJ (C3H) and C57BL6J (B6).

122 The common inbred mouse strain C57BL/6J (B6) restricts L. pneumophi

123 The inbred mouse strain C57BL/6J is widely used in models of

124 s from a second-generation intercross of the inbred mouse strains C57BL/6 and FVB/N.

125 Inbred mouse strains C57BL/6J (B6) and C3H/HeJ (C3H) dif

126 Inbred mouse strains C57BL/6J (B6) and C3H/HeJ (C3H) exh

127 Using the inbred mouse strains C57BL/6J (B6) and C3H/HeJ (C3H), wh

128 elated traits in a segregating cross between inbred mouse strains C57BL/6J (B6) and DBA/2J (DBA).

129 334 mice derived from an intercross between inbred mouse strains C57BL/6J and C3H/HeJ.

130 ZIKV exposure in four genetically divergent inbred mouse strains (C57BL/6J, 129S1/SvImJ, FVB/NJ, and

131 assessing 331 back-cross (N2) progeny of two inbred mouse strains, C57BL/6 and FVB/N, previously show

132 n lung tissue from two genetically divergent inbred mouse strains, C57BL/6J and CAST/EiJ, both in une

133 e genomic DNA methylation by intercrossing 2 inbred mouse strains, C57BL/6N and C3H/HeN, and analyzin

134 iet (HCD), we quantified food-intake in four inbred mouse strains: C57Bl/6J (B6), NOD/LtJ (NOD), 129S

135 We applied these methods to two inbred mouse strains: C57BL/6J and DBA/2J.

136 with varying susceptibilities for different inbred mouse strains; C57BL/6N are highly susceptible wh

137 he heme biosynthetic pathway) activity among inbred mouse strains can be attributed to variation in t

138 recent whole-genome resequencing study of 15 inbred mouse strains captured a significant fraction of

139 and related traits in an intercross between inbred mouse strains CAST/Ei and C57BL/6J.

140 Interestingly, several inbred mouse strains commonly used in behavioral, anatom

141 Numerous inbred mouse strains comprise models for human diseases

142 Inbred mouse strains contain numerous endogenous proviru

143 e we report a dense set of genotypes from 94 inbred mouse strains containing 10.77 million genotypes

144 ose at The Jackson Laboratory in 1993 in the inbred mouse strain DBA/1LacJ.

145 The inbred mouse strains DBA/2J and C57BL/6J exhibit contras

146 loned and characterized the Lv locus from an inbred mouse strain (DBA/2J) that has three times the no

147 of mammary cancer, we identified previously inbred mouse strains (DBA/2J, NZB/B1NJ, and I/LnJ) that

148 Among inbred mouse strains, DBA/2 mice are unique because of t

149 of the plt locus, we find that commonly used inbred mouse strains demonstrate at least three differen

150 ysaccharide (LPS) responder and nonresponder inbred mouse strains demonstrated that a single genetic

151 CMV (MCMV) infection varies among different inbred mouse strains depending on NK cell effector funct

152 , a powerful genetic resource of recombinant inbred mouse strains derived from eight diverse founder

153 Inbred mouse strains differ in susceptibility to anti-GB

154 Inbred mouse strains differ in their ability to demonstr

155 Here, we exploited robust inbred mouse strain differences in Pavlovian fear extinc

156 M9-dependent histone modifications using two inbred mouse strains differing only in their PRDM9 zinc

157 Certain inbred mouse strains display progression to lymphoma dev

158 Inbred mouse strains display significant differences in

159 Inbred mouse strains display variable sensitivity to LeT

160 The collection of classical inbred mouse strains displays heritable variation in a l

161 isease, show remarkably wide variation among inbred mouse strains (eg, C57BL/6 and BALB/c), resulting

162 These data indicate that inbred mouse strains exhibit differences in receptor fun

163 The observations reinforce the notion that inbred mouse strains exhibit differences in their pathol

164 Interestingly, inbred mouse strains exhibit dramatic differences in the

165 Inbred mouse strains exhibit significant differences in

166 Macrophages from different inbred mouse strains exhibit striking differences in the

167 Inbred mouse strains exhibit striking differences in the

168 Ac1-16 peptide-specific T helper cells from inbred mouse strains expressing identical k haplotype-de

169 ANCA NCGN severity was investigated using 13 inbred mouse strains, F1 and F2 hybrids, bone marrow chi

170 C57BL/6 is the most commonly used inbred mouse strain for biomedical research, but widespr

171 of the extinction-impaired 129S1/SvImJ (S1) inbred mouse strain for multiple behavioral, autonomic,

172 FVB/N is considered an ideal inbred mouse strain for transgenic mouse production beca

173 y metastasis that can be assayed in multiple inbred mouse strains for further use in identification o

174 We used a family of recombinant inbred mouse strains for interval mapping and to examine

175 Accordingly, we screened 38 inbred mouse strains for susceptibility to MPXV.

176 ested dendritic cells derived from different inbred mouse strains for their abilities to be infected

177 in a reference population of BXD recombinant inbred mouse strains for which extensive single-nucleoti

178 ses for these traits in a set of recombinant inbred mouse strains formed from the cross of LG/J with

179 Strain-dependent differences exist in four inbred mouse strains frequently used for genetic manipul

180 which next generation sequence data from 17 inbred mouse strains had been aligned, we identify and i

181 Earlier studies showed that inbred mouse strains had different susceptibility to cer

182 Marked genetic variance in inbred mouse strains has been observed for sucrose intak

183 High-density SNP screening of panels of inbred mouse strains has been proposed as a method to ac

184 Atherosclerosis in inbred mouse strains has been widely studied by using an

185 gate protective immune responses, the use of inbred mouse strains has proven invaluable.

186 phenotypes of the available BxD recombinant inbred mouse strains have been determined.

187 Although inbred mouse strains have been the premier model organis

188 Detailed studies of seven inbred mouse strains have now revealed three strains (C5

189 A catalog of the genetic variation among inbred mouse strains, however, is required to enable pow

190 We show that inbred mouse strains (i.e., C3H and C57) with varying al

191 Analysis of multiple inbred mouse strains identified 117 antigens recognized

192 Linkage analysis using inbred mouse strains identified a locus on chromosome 7

193 Genetic analyses of inbred mouse strains identified loci affecting different

194 transcriptomes of Kupffer cells derived from inbred mouse strains identified strain-specific environm

195 Sequence analysis of 15 standard inbred mouse strains identifies six Mpdz haplotypes that

196 moter was cloned from both the C3H and DBA/2 inbred mouse strains in an attempt to identify polymorph

197 Previous data have shown differences among inbred mouse strains in sensory gating of auditory evoke

198 Wide differences among inbred mouse strains in susceptibility to develop compon

199 Similar to the generation of inbred mouse strains in the last century, we suggest a w

200 bolites in liver extracts obtained from four inbred mouse strains in the study of acetaminophen-induc

201 hat the pattern of angiogenic response among inbred mouse strains in this ex vivo assay differs from

202 al) seizures were determined in 16 different inbred mouse strains in two different laboratories.

203 One example is the NOD inbred mouse strain, in which MZ B cell expansion has be

204 tigen sensitization and challenge of the A/J inbred mouse strain induced AHR, eosinophilic airway inf

205 n silico whole-genome association mapping of inbred mouse strains involving hundreds of thousands of

206 The BALB/cJ inbred mouse strain is a useful model system for testing

207 The SWXL-4 recombinant inbred mouse strain is unusually sensitive to recurrent

208 Age-related hearing loss (AHL) in common inbred mouse strains is a genetically complex quantitati

209 sociation mapping in model organisms such as inbred mouse strains is a promising approach for the ide

210 ence in H. capsulatum susceptibility between inbred mouse strains is attributable to the genotype at

211 fine structure of sequence variation across inbred mouse strains is needed.

212 adiotherapy and from radiation studies using inbred mouse strains, it is hypothesized that individual

213 ypothesis, we examined GSK-3 activity in two inbred mouse strains known to be susceptible (C57BL/6J)

214 erent target sequence preferences of the two inbred mouse strain mA3 alleles, but examination of alle

215 pond to the F1 plasmid, suggesting that some inbred mouse strains may exhibit exaggerated responses t

216 e of memory retention, and they suggest that inbred mouse strains may provide a diversity of phenotyp

217 perturbations on the gut microbiota of five inbred mouse strains, mice deficient for genes relevant

218 t peritoneal macrophages from a wild-derived inbred mouse strain, MOLF/Ei, are hyporesponsive to CpG

219 Inbred mouse strains MRL and LG share the ability to ful

220 QTL) analysis of an intercross involving the inbred mouse strains NZB/BlNJ and SM/J revealed QTL for

221 for further genetic analysis, we screened 17 inbred mouse strains of various Bcg and H-2 genotypes fo

222 erve as an immunodominant focus in different inbred mouse strains or are there structural constraints

223 However, experiments with a particular inbred mouse strain performed in different laboratories

224 Inbred mouse strains provide a relatively stable and res

225 Isogenic inbred mouse strains provide a valuable approach to eluc

226 Inbred mouse strains provide the foundation for mouse ge

227 Retroviral insertional mutagenesis in inbred mouse strains provides a powerful method for canc

228 etween the two healing phenotypes for common inbred mouse strains (r=0.92) and RI mouse lines (r=0.86

229 Differences in AHR affinity between inbred mouse strains reflect variations in CYP1 inducibi

230 cerevisiae induced an acute inflammation in inbred mouse strains resembling human Ps and PsA-like di

231 mesticus Sry alleles, onto the C57BL/6J (B6) inbred mouse strain results in abnormal testis developme

232 The inbred mouse strain RIII has long been known for sheddin

233 -susceptible BALB/c substrain, identified in inbred mouse strain screening.

234 NON/Lt and NZO/Hl are inbred mouse strains selected for IGT and polygenic obes

235 ALS/Lt and ALR/Lt are inbred mouse strains selected for susceptibility and res

236 teractions between iNKT-cells and DCs in two inbred mouse strains should raise a cautionary note abou

237 Inbred mouse strains show a wide range of noise sensitiv

238 Whereas most inbred mouse strains show an intermediate level of inter

239 1) backcrosses involving the DDK and C57BL/6 inbred mouse strains show transmission ratio distortion

240 susceptibilities to LT in the larger set of inbred mouse strains showed a lack of correlation betwee

241 Inbred mouse strains showed clear variability in their r

242 uction of pathogenic mutations into a single inbred mouse strain sometimes fails to mimic human disea

243 Data obtained with inbred mouse strains suggested an association between a

244 /2)F(1) x C57BL/6 mice and B x D recombinant inbred mouse strains suggested tentative associations of

245 Analysis of macrophages from recombinant inbred mouse strains support the model that macropinocyt

246 resistance to obesity, two obesity-resistant inbred mouse strains, SWR/J and A/J, were compared to 3

247 rformed quantitative trait locus analysis in inbred mouse strains that carry the same hypomorphic all

248 bdas > 10, purported linkage at 1q41-42, and inbred mouse strains that consistently develop lupus.

249 We have identified genetic differences in inbred mouse strains that determine whether their cultur

250 From comparative microRNA profiling between inbred mouse strains that display profound differences i

251 aborative Cross (CC), a panel of recombinant inbred mouse strains that exhibit a range of disease man

252 CTT-1 was expressed by independently derived inbred mouse strains that express H2b.

253 emiological studies can be overcome by using inbred mouse strains that harbor mutation(s) in genes in

254 nes encoding these proteins are defective in inbred mouse strains that serve as models of Hermansky-P

255 In inbred mouse strains the rate of thymic involution and t

256 ntry of phenotypic information obtained from inbred mouse strains, the phenotypic and genotypic infor

257 In transferring this system to inbred mouse strains, the third bit of good fortune was

258 ough urinary Mup protein levels vary between inbred mouse strains, this difference is most pronounced

259 mouse strain, and the mtDNA from a different inbred mouse strain to examine the genome-wide nuclear D

260 The studies reported here screened 8 inbred mouse strains to determine whether genetic factor

261 a genetic correlation of the sensitivity of inbred mouse strains to different assays of nociception

262 Susceptibility of inbred mouse strains to EAE is in part determined by maj

263 transcription factors between crosses of two inbred mouse strains to elucidate the regulatory mechani

264 ing cis-regulatory variation in wild-derived inbred mouse strains to explore the mechanisms underlyin

265 surgically induced hindlimb ischemia between inbred mouse strains to identify key microRNAs involved

266 The response of inbred mouse strains to infection with Leishmania major

267 MTX, we directly compared the responses of 4 inbred mouse strains to MTX in the air-pouch model of ac

268 Resistance or susceptibility of inbred mouse strains to the parasite Leishmania major co

269 The differing responses of inbred mouse strains to the same pathogen reflect variat

270 tinal ganglion cell (RGC) function in common inbred mouse strains using the pattern electroretinogram

271 l processes relevant to behavior and because inbred mouse strains vary in their responses to tests of

272 basis for this susceptibility, a panel of 36 inbred mouse strains was used to model genetic diversity

273 Using publicly available data from inbred mouse strains, we conducted a genome-wide associa

274 nd nine of its metabolites in plasma from 13 inbred mouse strains, we correlated strain-specific diff

275 In the BXD series of recombinant inbred mouse strains, we have mapped the regions respons

276 study, structural changes in glomeruli of 24 inbred mouse strains were characterized in male mice at

277 To get around this problem, inbred mouse strains were developed, leading to identifi

278 Seven inbred mouse strains were immunized against human factor

279 ed to analyze the median survival data after inbred mouse strains were infected with C. albicans, whi

280 otransformation systems prepared from the 15 inbred mouse strains were measured.

281 Allelic gene differences exist among inbred mouse strains which control structure and tissue-

282 eron (IFN-gamma) and interleukin-4 (IL-4) in inbred mouse strains which differ in their susceptibilit

283 as well as the NMDA receptor-deficient 129S6 inbred mouse strain, which also lacks tolerance, exhibit

284 es of BAT protein function occur in a single inbred mouse strain, which has limited the understanding

285 e studied the C3H/HeJ (C3H) and C57BL/6 (B6) inbred mouse strains, which differ in their susceptibili

286 developmental disorders typically use single inbred mouse strains, which fail to capture the genetic

287 and molecular traits in more than 100 unique inbred mouse strains, which were fed a diet rich in fat

288 Inbred mouse strains with age-related hearing loss (AHL)

289 Infection of inbred mouse strains with Borrelia burgdorferi results i

290 cells (ECs) were isolated from the aorta of inbred mouse strains with different susceptibilities to

291 immunoreactivity in the taste tissue of two inbred mouse strains with different Tas1r3 haplotypes an

292 ulin resistance, and glucose metabolism in 3 inbred mouse strains with differing susceptibilities to

293 Here, we used inbred mouse strains with distinct amounts of cerebellar

294 as1r3 gene and its flanking regions from six inbred mouse strains with high and low saccharin prefere

295 Three inbred mouse strains with known secretory phospholipase

296 for 5 days (12-hour light/dark cycle) in two inbred mouse strains with low (A/J) and high (DBA/2J) hy

297 a combination of behavioural analysis of six inbred mouse strains with quantitative gene expression p

298 Comparing variability among inbred mouse strains with respect to a specific phenotyp

299 al lymphocytic activation molecule (Slam) in inbred mouse strains, with the Slam haplotype 1 expresse

300 Mvwf6-7) using a backcross approach with the inbred mouse strains WSB/EiJ and C57BL/6J.