ライフサイエンスコーパス: intercross

1 sequence length polymorphic markers in an F2 intercross.

2 F(2) rats generated from an SR/JrHsd x SHRSP intercross.

3 h some unexpected differences from the B x A intercross.

4 geny from an Itgb2(tm1Bay) (PL/J x C57BL/6J) intercross.

5 r's yeast from a multiparent 12th generation intercross.

6 ession data from a cohort of F2 female mouse intercross.

7 ntified in a B6-Tulp1(tm1Pjn/tm1Pjn) x AKR/J intercross.

8 at this block on albumin excretion in an F2 intercross.

9 re accurately than is possible with standard intercrosses.

10 re generated from Aqp11 +/sjds and Aqp11 +/- intercrosses.

11 e 2 congenic strains and three additional F2 intercrosses.

12 correlated with body weight in two of the F2 intercrosses.

13 to analyze individual embryos from Asah1 +/- intercrosses.

14 ygous offspring were observed from PINCH1+/- intercrosses.

15 more than do conventional backcrosses and F2 intercrosses.

16 pressure QTLs detected in equivalent genetic intercrosses.

17 ood pressure QTLs in equivalent (Dahl S x R)-intercrosses.

18 sis occurs in the F2 generation following F1 intercrosses.

19 utcrossing to C57BL/10J, and backcrossing or intercrossing.

20 allelic chimeric mice without further strain intercrossing.

21 Here, we have intercrossed 129S1/SvImJ, which carries the Xce(a) allel

22 egnancy influence genomic DNA methylation by intercrossing 2 inbred mouse strains, C57BL/6N and C3H/H

23 ncreasingly complex genetic structure: an F2 intercross, a heterogeneous stock (HS) formed by crossin

24 g the F(10) generation of the LG,SM advanced intercross (AI) line.

25 te-selective Smad2/Smad3 double knockouts by intercrossing AlbCre/Smad2(f/f) (S2HeKO) and Smad3-defic

26 expression between sexes, and the use of an intercross allowed analysis of the genetic control of se

27 e through application to a set of four mouse intercrosses among five inbred strains, with data on HDL

28 brid male sterility is known to occur in all intercrosses among members of the Anopheles gambiae comp

29 will facilitate transfer of useful genes and intercrossing among the beans.

30 linkage analyses on the progeny of a B6CBAF1 intercross and a CBAxB6CBAF1 backcross were performed.

31 ved (avg. spacing 1.77 cM) in a single large intercross and anchored in the rat genomic sequence (avg

32 We compared a classical intercross and three CSS intercrosses to examine the gen

33 g chromosomes with no significant QTL in the intercross and, in some cases (CSS-1, CSS-17), effects t

34 arbitrary sequence of selfing, backcrossing, intercrossing and haploid-doubling steps that includes m

35 on as new allelic combinations arose through intercrossing and inbreeding to create new stable geneti

36 over multigenotype crosses, such as the F(2) intercross, and multiple QTL models.

37 the major loci previously identified in this intercross, and with SSLPs covering chromosomes 12 and 1

38 gregating populations including backcrosses, intercrosses, and natural populations.

39 clinically affected are 90% greater for F(2) intercross animals injected in the summercompared to tho

40 ock-out, and knock-in mouse models and their intercrosses are more recent developments that mirror de

41 Furthermore, we used genetic intercrosses as well as pharmacological agents to link t

42 generated from G alpha(12)+/- G alpha(13)+/- intercrosses, at least one intact G alpha(12) allele is

43 using C57Bl/6 (B6), 129S6/SvEvTac (129), and intercross (B6 x 129)F2 mice on a low- or high-fat diet.

44 Linkage analysis in F2 intercross (B6 x MSM) progeny identified several MSM loc

45 mouse population from a C57BL/6J and CASA/Rk intercross (B6CASAF2).

46 d a humanized mouse model of HD, Hu97/18, by intercrossing BACHD and YAC18 mice with knockout of the

47 An intercross between atherosclerosis susceptible (C57BL/6J

48 bility locus on chromosome 19 revealed in an intercross between atherosclerosis-susceptible C57BL6 an

49 ale F(2) mice (n=266) were generated from an intercross between B6.Apoe(-/-) and BALB.Apoe(-/-) mice

50 HC) was performed in wan/wan mice from an F2 intercross between C3H/HeJ(+/wan) and CAST/Ei(+/+) F1 hy

51 FeJ strain, F2 Eya1(bor/bor) mutants from an intercross between C3HeB/FeJ-Eya1(bor/+) and C57BL/6J sh

52 Using an intercross between C57BL/6J (B6) and C3H/HeJ (C3H) apoE(

53 A team led by Hopi Hoekstra studied an intercross between deer mice and old-field mice that dif

54 In an intercross between F1(BBDP x F344) rats, we identified a

55 Using an F2 intercross between H. cydno and H. pachinus, we first ma

56 somatic tissues of 334 mice derived from an intercross between inbred mouse strains C57BL/6J and C3H

57 inants and mechanisms underlying MetS, an F2 intercross between Lyon hypertensive and Lyon normotensi

58 cross with QTL identified in a previous F(2) intercross between M. m. musculus and M. m. domesticus a

59 uivalent to the Kauai population-an advanced intercross between Red Junglefowl and domestic layer bir

60 e expression and metabolic traits in a mouse intercross between strains C57BL/6J and C3H/HeJ.

61 t locus (QTL) analysis of schooling in an F2 intercross between strongly schooling marine and weakly

62 and validation of network connections: an F2 intercross between the C57BL/6 J and C3H/HeJ mouse strai

63 position traits in the F(3) generation of an intercross between the Large (LG/J) and Small (SM/J) inb

64 F(2) (n = 1181) population resulting from an intercross between the M16 and ICR lines of mice.

65 Using an intercross between the two divergent chicken lines, 16 a

66 titative trait locus (QTL) analysis using an intercross between the two strains carrying the apoE-/-

67 We created an intercross between these lines, and in the F2 progeny, w

68 F2 male mice created by an intercross between these two strains exhibit a 60% incid

69 s performed with 8-month-old progeny from an intercross between these two strains.

70 mice in the F(2) generation produced from an intercross between two inbred strains (C57BL/6J and AKR/

71 l muscle mass of 1,867 mice from an advanced intercross between two inbred strains (LG/J and SM/J); t

72 ntified that underlie serum IGF-I in a mouse intercross between two inbred strains.

73 solation in house mice, we conducted an F(2) intercross between wild-derived inbred strains from Mus

74 key reproductive barrier, we conducted an F2 intercross between wild-derived inbred strains from two

75 veying viability of Egfrtm1Mag mutants using intercrosses between 129S6/SvEvTAC-Egfrtm1Mag and nine S

76 Moreover, intercrosses between Atmin(Gpg6/+) and Vangl2(Lp/+) mice

77 Intercrosses between B and three CSSs (CSS-3, CSS-11, an

78 By analysis of backcrosses and intercrosses between C3H or CBA and resistant B6 mice, w

79 c linkage maps constructed from experimental intercrosses between closely related house mouse subspec

80 F1 offspring from intercrosses between F0 animals that carry embryonic let

81 We use genetic mapping in large F(2) intercrosses between Gough Island mice and WSB/EiJ to id

82 Intercrosses between inbred lines provide a traditional

83 Using genetic intercrosses between Nf1 +/- and class I (A)-PI-3K-defic

84 on-complementation of aganglionosis in mouse intercrosses between Ret null and the Ednrb hypomorphic

85 nduced pituitary tumorigenesis in reciprocal intercrosses between the genetically related ACI and Cop

86 ote mutations that reduce the probability of intercrossing between populations carrying different rea

87 Intercrossing between wild-type and Faah-/- mice rescued

88 We investigated the effects of intercross breeding designs on the utility of such lines

89 Heterozygous intercross breeding of the mutant mice yielded the expec

90 found among progeny of A1cf and Ago2 mutant intercrosses but not in backcrosses and without fetal lo

91 assic complement pathway in atherogenesis by intercrossing C1q-deficient mice (C1qa-/-) with low-dens

92 through only four (backcross case) or nine (intercross case) independent standard normal random vari

93 g 2-deficient (Gcm2-deficient) background by intercrossing CasR- and Gcm2-deficient mice.

94 d into a single strain by "endoreduplication intercross." Chemically synthesized genomes like Sc2.0 a

95 analysis in F2 rats derived from a bHR x bLR intercross confirmed that these regions harbored genes a

96 The intercross data reveal locus heterogeneity of the En1 mo

97 approach is illustrated through a mouse F(2) intercross data set.

98 fied by other network analyses of this mouse intercross data-set, but all have been previously associ

99 tal parasite infections of advanced mosquito intercrosses demonstrated a strong association between t

100 chromosome 19 in a leptin-deficient obese F2 intercross derived from C57BL/6 (B6) and BTBR T+ tf/J (B

101 We found that intercrossing Dnd1+/KO heterozygotes to generate a compl

102 MHC genes controlling EBA susceptibility, we intercrossed EBA-susceptible MRL/MpJ with EBA-resistant

103 In this article, motivated by a mosquito intercross experiment involving two selected lines that

104 es are further illustrated with data from an intercross experiment to identify QTL contributing to va

105 Intercross experiments demonstrate that susceptibility i

106 gly, although diabetes was evident in the F1 intercross expressing rat insulin promoter (RIP)-TNF, of

107 The AR trial phenotype of BALB/cJ x SWR/J intercross F(1) and F(2) mice was consistent with BALB/c

108 Genome-wide mapping conducted with 60 intercross F(2) animals linked two loci to the number of

109 9(+/-) mice were generated, but heterozygous intercrosses failed to yield Mrad9(-/-) pups, since embr

110 We intercrossed female and male F(1) adult control (C) and

111 specks revealed a compact network of highly intercrossed filaments, whereas pyrin domain (PYD) or ca

112 to hepcidin independently of each other, we intercrossed Hjv(-/-) and Bmp6(-/-) mice and compared th

113 sis were determined in C57BL/6J, BALB/cJ, F1 intercross identical with C57BL/6J X 129S3/SvIM, and 129

114 s analysis performed on F2 C57; Eln(+/-)x129 intercrosses identified highly significant peaks on chro

115 onents of this autoimmune disorder, we first intercrossed IL-2-deficient mice with mice lacking CD28

116 binant inbred lines derived from an advanced intercross, in which multiple generations of mating have

117 By studying two intercrosses, in which the DCC trait segregates, a singl

118 ption and preference in F2 rats generated by intercrossing inbred P and nonpreferring rats.

119 uantitative trait locus (QTL) analysis of an intercross involving the inbred mouse strains NZB/BlNJ a

120 he JNK2 isoform in metabolic homeostasis, we intercrossed Jnk1(-/-) and Jnk2(-/-) mice and examined b

121 n this family segregated either in 1:2:1 (F2 intercross-like segregation) or 1:1 ratio (backcross-lik

122 fixed effects model using simulated advanced intercross line (AIL) data.

123 econd was the 10th generation of an advanced intercross line (AIL) derived from a broiler-layer cross

124 in mice, we used a 34th generation advanced intercross line (AIL) derived from two inbred strains (S

125 , we feed 1154 mice of an autoimmunity-prone intercross line (AIL) three different diets.

126 We generated a large (n = 815) advanced intercross line of mice (G(4)) derived from a line selec

127 An F34 advanced intercross line of mice (Wustl:LG,SM-G34) was generated

128 position in a large (n = 645) mouse advanced intercross line originating from a cross between C57BL/6

129 n of this four-way autoimmune-prone advanced intercross line were immunized with a fragment of murine

130 Ae. aegypti were mapped in an F(3) advanced intercross line.

131 ed in the F(2) and again in an F(5) advanced intercross line.

132 and a more highly recombinant F(8) advanced intercross line.

133 ly developed F(11) generation mouse advanced intercross lines (AIL) to fine map Pas1-3 quantitative t

134 ly detected in this vector using F6 advanced intercross lines (AIL).

135 The novel approach of advanced intercross lines (AILs) generates many more recombinatio

136 derived from inbred lines, such as advanced intercross lines and heterogeneous stocks, can be used t

137 is thaliana (multiparent advanced generation intercross lines) in controlled conditions simulating fo

138 lectron transfer dissociation (ETD)-MS/MS of intercross-linked peptides (two peptides connected with

139 multaneous binding to one GNP) and DC-SIGNR (intercross-linking with multiple GNPs), via a combined h

140 We conclude that, in this intercross, loci of atherosclerosis susceptibility are i

141 sis thaliana multiparent advanced generation intercross (MAGIC) lines.

142 Arabidopsis multiparent advanced generation intercross (MAGIC) mapping population, derived from 19 r

143 sions of the multiparent advanced generation intercross (MAGIC) population showed that significant na

144 al stiffness in six-week old F2 (Dahl S x R)-intercross male and female rats characterized for abdomi

145 Genome-wide analysis of 200 F2-intercross male rats detects two QTLs with highly signif

146 groups have developed multi-parent advanced intercross mapping panels in different model organisms i

147 on Resource (DSPR), a multiparental advanced intercross mapping population.

148 to, rather than a replacement for, classical intercross mapping.

149 Intercross matings show that hem6 can suppress the porph

150 modifier screen through F1 backcross and F1 intercross matings.

151 er loss of Mbd2 increases lymphomagenesis by intercrossing Mbd2 deficient mice with p53 deficient and

152 were found to be different in female BS x BS intercross mice as compared with females from the three

153 We therefore surmise that LG/J by SM/J intercross mice can be used to dissect the genetic basis

154 ion restricted cohorts of (B10.S x SJL/J) F2 intercross mice in an effort to identify such linkages.

155 n the susceptibility of (B10.S x SJL/J) F(2) intercross mice to experimental allergic encephalomyelit

156 s deleted in macrophages and neutrophils, we intercrossed mice carrying a loxP-flanked (floxed) IL-4R

157 We intercrossed mice heterozygous for a (7.18) Rb transloca

158 that were preserved in the iWAT of B6x129 F1-intercrossed mice, with an imbalance favoring the 129-de

159 ficient) CaR(-/-) mice (Pth(-/-)CaR(-/-)) by intercrossing mice heterozygous for the null CaR allele

160 analysis on F2 (B6.Rag1(-/-) x NOD.Rag1(-/-) intercross) mice.

161 We intercrossed mouse mammary tumor virus (MMTV)-c-neu tran

162 ogy was rescued and viable mice generated by intercrossing MRTF-B mutants with mice expressing Cre re

163 We analyzed an F(2) intercross (n = 282 mice) between mouse strains resistan

164 were detected in the F(2) generation of the intercross (n = 510), where no maternal genetic effect v

165 ive phenotypes in a large BALB/cN x C57BL/6N intercross (n = 795) and identified three to eight genom

166 rive from 8 founder inbred strains by serial intercrossing (n>60), resulting in fine-grained genetic

167 atically pair the recombinant gametes of two intercrossed natural genomes into an array of diploid hy

168 Intercrossing Nf1(+/-) mice and mice deficient in class

169 Similar to the Swiss-derived intercrosses, nine congenic strains, derived from 129S6/

170 hscy, 1,160 F(2) mice were produced from an intercross of (C57BL/6-hscy x CAST/EiJ) F(1) hybrids, an

171 An intercross of 2 transgenic lines produced offspring with

172 ls could also be recovered following a blind intercross of G1 progeny, yielding several new white-eye

173 The intercross of hR120GCryAB cardiomyopathic animals with m

174 ns affecting mouse skeletal morphology in an intercross of LG/J and SM/J inbred strains (N = 1040), u

175 our methods to data on gut length in a large intercross of mice carrying the Sox10Dom mutation, a mod

176 or an ordinal trait, dead fetuses, in a F(2) intercross of mice.

177 Using an intercross of Pak 1(-/-) mice with Nf1(+/-) mice, we det

178 a quantitative trait locus analysis using an intercross of PERA/Ei and I/LnJ inbred strains of mice.

179 otyped >3100 hearts from a second-generation intercross of the inbred mouse strains C57BL/6 and FVB/N

180 exes in a population of mice derived from an intercross of the Large and Small inbred strains.

181 F(3) population of mice originating from an intercross of the LG/J (Large) and SM/J (Small) inbred s

182 arly growth in mice using a three-generation intercross of the Small (SM/J) and Large (LG/J) inbred m

183 nic mouse strains by performing a reciprocal intercross of the strains HcB-8 and HcB-23, phenotyped f

184 Through linkage analysis of a cross-intercross of these two parental strains, this trait was

185 Here, we studied an F2 intercross of two outbred lines of rats selected for tam

186 library of an F2 population derived from an intercross of var. hallii and filipes.

187 Using F(2) population of the intercross of wild-type and chr15 consomic strain, we co

188 rabidopsis thaliana individuals derived from intercrosses of 30 parents in a half diallel mating sche

189 Homozygous null mice were produced from intercrosses of heterozygous null mice at the expected M

190 Successive generational intercrosses of mTerc(-/-)MMT mice produced cohorts with

191 Intercrosses of Nmt1+/- mice yielded no viable homozygot

192 Intercrosses of Pol epsilon-, Pol delta-, and mismatch r

193 rdbp(+/-)) mice are fertile and healthy, but intercrosses of Tardbp(+/-) mice yielded no viable homoz

194 Interval mapping in the F(2) generation from intercrosses of the LG/J and SM/J strains revealed 33 QT

195 nant inbred line population derived from the intercrossing of 19 accessions.

196 Intercrossing of heterozygous TAFI mice produced offspri

197 n embryonic stem cells and/or time-consuming intercrossing of mice with a single mutation.

198 a(-/-) embryonic stem (ES) cells through the intercrossing of p38alpha(+/-) mice.

199 The intercrossing of Par-1a(-/-) with Par-1b(-/-) mice revea

200 Arthritic male (DA x ACI)F2 intercross offspring (n = 143) were analyzed separately

201 tides of RNA-seq reads from the livers of F2 intercross offspring and parental rats.

202 Intercross offspring were genotyped, and linkage analysi

203 P overexpression, so FVBxF1 backcross and F2 intercross offspring were produced.

204 imately 30% smaller than that from GPR4(+/+) intercrosses on N3 and N5 C57BL/6 genetic backgrounds.

205 in the second generation (F2) of the F1 X F1 intercross or backcrosses to the parental strains.

206 netic Reference Panel (DGRP) and an advanced intercross outbred population derived from a subset of D

207 ) is a newly developed multifounder advanced intercross panel consisting of >1600 recombinant inbred

208 om the same parental cross: the IBM advanced intercross population and a conventional recombinant inb

209 gene expression data from an MRL/MpJ x SM/J intercross population and predicted a previously unchara

210 e Panel (DGRP) and a large outbred, advanced intercross population derived from 40 DGRP lines (Flylan

211 ative trait locus GWA on an outbred advanced intercross population derived from extreme DGRP lines, a

212 squito Aedes albopictus and examined an F(1) intercross population for quantitative trait loci (QTL)

213 e mandibular molars in house mice from an F2 intercross population generated from crossing the Large

214 he DGRP and a DGRP-derived outbred, advanced intercross population identified candidate genes and gen

215 A multiparent advanced-generation intercross population of maize has been developed to hel

216 otypes derived from a multiparental advanced-intercross population, mapping three moderate-effect loc

217 uantitative trait variation in a large yeast intercross population.

218 are opposite to those observed in the B x A intercross population.

219 data from a multiparent advanced generation intercross population.

220 eference Panel (DGRP) and replicate advanced intercross populations derived from the most and least a

221 thanol/sucrose in the F2 offspring of a B6D2 intercross positively correlates with Ucn immunoreactivi

222 Additional analysis of F2 intercross progeny confirms a highly significant effect

223 n effects influence EAE, using reciprocal F2 intercross progeny generated between EAE-susceptible SJL

224 QTL mapping using 87 F(2) intercross progeny identified two significant chromosome

225 lionosis as a quantitative trait in Sox10Dom intercross progeny to investigate the contribution of st

226 ymorphism-based genome scan in Sox10Dom/+ F1 intercross progeny.

227 n-MHC locations by analysis of backcross and intercross progeny.

228 We have intercrossed Rassf1a-knockout mice with mice lacking the

229 random mating, we constructed a new advanced intercross recombinant inbred line (RIL) population deri

230 ted B73 x Mo17 (IBM) population, an advanced intercross recombinant inbred line population derived fr

231 Using QTL mapping with a new advanced intercross-recombinant inbred line (AI-RIL) population,

232 t of early 2-cell embryos from the Asah1 +/- intercrosses rescued Asah1-/- embryos, and enabled their

233 tlSl-20J mice display a white belly spot and intercrossing results in an embryonic lethal phenotype i

234 We intercrossed Ret and Sema3d double null heterozygotes to

235 Analysis of a Ggcx(+/-) intercross revealed a partial developmental block with o

236 The B x A intercross revealed significant quantitative trait loci

237 An intercross revealed that Mom2R encodes a recessive embry

238 r 150 offspring or embryos from heterozygous intercrosses revealed an absence of Asah1(-/-) individua

239 Directed intercrosses revealed that these phenotypes are heritabl

240 be a new approach, called recombinant inbred intercross (RIX) mapping, that extends the power of reco

241 The recombinant inbred intercrosses (RIX) generated from CC recombinant inbred

242 er, total genome-analysis of an F2[Dahl RxS]-intercross selected for contrasting parental strain susc

243 en after genetic background is controlled by intercrossing strains.

244 To this end, we used an intercross strategy in mice to map modifiers of muscular

245 the design and analysis of traditional F(2) intercross studies allows high-confidence prediction of

246 ed test in a real data set collected from F2 intercross studies of inbred mouse strains.

247 The present intercross study was executed to replicate the earlier f

248 Our inability to predict the results of CSS intercrosses suggests that additional complexity will be

249 We intercrossed SwissOF1-En1+/- and C57Bl/6 mice to obtain

250 test for a possible genetic interaction, we intercrossed Tbx1(+/-) and Pitx2(+/-) mice.

251 Intercrossing TFPI(+/-)/mTF(+/-)/hTF+/- mice generated c

252 By intercrossing the congenic lines to create hybrid F1 emb

253 nd the doubly deficient CA IV/XIV KO mice by intercrossing the individual null mice.

254 the chromosome 10 locus in F2 mice from this intercross, the observations now reported suggest that p

255 research in these two areas and propose that intercrossing them and increasing funding to guide resea

256 ertional mutagenesis screen was performed by intercrossing these mice with those carrying a Sleeping

257 By intercrossing these mutants, we show that the stabilitie

258 finding significant differences in RD, an F1 intercross to determine rd3 QTLs that influence this inh

259 n of IFN signature genes in NZW, as shown by intercross to mice with an Ifnar1 knockout.

260 and fibromodulin-null heterozygous mice were intercrossed to obtain wild-type (Lum(+/+)Fmod(+/+)), lu

261 The late-generation Tert(+/-) mice were intercrossed to produce genotypically wild-type Tert(+/+

262 backcrosses produced N10F1 rats, which were intercrossed to produce rats that were homozygous for GH

263 x 129)F1 x 129 backcross 1 mice, which were intercrossed to select for homozygosity of particular re

264 Heterozygous Lbr and Dhcr14 mice were intercrossed to test for a digenic phenotype.

265 ompared a classical intercross and three CSS intercrosses to examine the genetic architecture underly

266 plications have extended beyond experimental intercrosses to outbred populations by exploiting long-r

267 nase using biolistics, lentivirus or genetic intercrosses triggered heterologous expression of TRPV1

268 We intercrossed two closely related species of monkeyflower

269 By intercrossing two diverged mouse subspecies over five ge

270 t consists of 32 BXD strains of mice made by intercrossing two progenitor strains--C57BL/6J and DBA/2

271 ltiple generations, and the breeding scheme (intercrossing vs. outcrossing) drastically affected the

272 thyroidism-induced hearing impairment, an F1 intercross was generated between DW/J-Pou1f1dw/+ carrier

273 ld-type to Asah1(+/-) individuals from these intercrosses was 1:2.

274 The average litter size from GPR4(-/-) intercrosses was approximately 30% smaller than that fro

275 mice from a B6-Tulp1(tm1Pjn/tm1Pjn) x AKR/J intercross were genotyped with a panel of single nucleot

276 ifferences in the ONL, F2 progeny from an F1 intercross were measured for ONL thickness.

277 srupted La gene, and the offspring from La+/-intercrosses were analyzed.

278 Embryos from Arhgap29(K326X/+) intercrosses were harvested at various time points.

279 Offspring of LSL-KRAS(G12D) x PDX-1-Cre intercrosses were randomly allocated to a diet supplemen

280 and linkage analysis in a large F2(DA x PVG) intercross, which identified quantitative trait loci reg

281 By utilising a domestic x wild advanced intercross with a combination of classical QTL mapping o

282 erneurons evident in NCAM-EC transgenic mice intercrossed with a reporter line expressing green fluor

283 Floxed beta-catenin (exons 2-6) mice were intercrossed with Albumin-Cre recombinase transgenic mic

284 These were intercrossed with C57BL/6.lpr/lpr and MRL/Mp-lpr/lpr str

285 Nf1+/- mice were intercrossed with conditional Rac1(flox/flox)Mxcre+ (Rac

286 report here that when Foxo1(KR/KR) mice are intercrossed with low density lipoprotein receptor knock

287 rsion of tcfap2a which has subsequently been intercrossed with mice expressing Cre recombinase under

288 ment in vivo, TgE-LMP2A-transgenic mice were intercrossed with mice expressing loxP-flanked Notch1 ge

289 homozygous for a conditional Apc allele were intercrossed with mice transgenic for Cre recombinase un

290 When intercrossed with obese, insulin-resistant, and diabetic

291 al cells (LPCs; IKKalpha/beta(LPC-KO) ) were intercrossed with RIPK1(LPC-KO) or RIPK3(-/-) mice to ex

292 54) exhibit a mild disorder, whereas animals intercrossed with SJL/J mice (F1.Q54) have a severe phen

293 of another CD1-defective strain, as well as intercrosses with C57BL/6 mice, indicated that the impai

294 PPP family phosphatases (e.g. PP2A and PP4), intercrosses with mouse lines that ubiquitously express

295 Intercrossing with Brca1(Delta11), which is homozygous l

296 ion of this gene in any tissue of choice, by intercrossing with mice in which Cre-recombinase express

297 Notably, intercrossing with p53-deficient mice completely rescued

298 ow generated a companion model, Hu128/21, by intercrossing YAC128 and BAC21 mice on the Hdh-/- backgr

299 y variable in F2 XY gonads from B6 and 129S1 intercrosses, yet strong correlations emerged.

300 Blastocysts derived from La+/- intercrosses yielded 38 La+/+ and La+/- embryonic stem (