ライフサイエンスコーパス: inbred

1 pression of the drl2-Mo17 allele in the Mo17 inbred.

2 ion population, comprising 279 diverse maize inbreds.

3 been described in two Iowa Stiff Stalk (SS) inbreds.

4 zygous), Virunga Mountain Gorilla (78.12 %), inbred Abyssinian cat (62.63 %), Tasmanian devil, domest

5 the well-characterized Utah 30th generation inbred accession--and grew 183 plants in the glasshouse

6 rogeny and lifetime-accumulated mortality of inbred adults.

7 icken experimental populations were used, as inbred and as genetically distant as possible.

8 in laboratory mice, partly because they are inbred and genetically homogeneous, can be genetically m

9 fects ID and the potential for purging using inbred and outbred Drosophila melanogaster larvae expose

10 Second, via tracking survival in inbred and outbred families, we demonstrate that inbred

11 In this study, we demonstrate that inbred and outbred mice recovering from a septic event a

12 iP protein gave high antibody titers in both inbred and outbred mice.

13 We discovered that both inbred and outbred rats could shorten the duration of SW

14 uma.SIGNIFICANCE STATEMENT Our evidence that inbred and outbred rats learn to control the duration of

15 xual development and population viability of inbred and outbred zebrafish (Danio rerio).

16 Finally, NAT pairs in 368 diverse maize inbreds and 19 segregating populations were specifically

17 Here, two genomes for Mo17 (a modern maize inbred) and mexicana are assembled using a meta-assembly

18 opulation sequence data from 488 recombinant inbred Arabidopsis thaliana genomes, we identified 6502

19 matography analyses demonstrate that the two inbreds are highly differentiated in their metabolite pr

20 d trait is robust as it improves yield in an inbred as well as in a panel of hybrids, at several loca

21 omosomally anchored the nuclear genome of an inbred B. pendula individual.

22 ntal gradient from four maize genotypes (the inbreds B73 and Mo17, and the reciprocal hybrids B73 x M

23 erformed using 14-day-old maize seedlings of inbreds B73, Mo17, Oh43, PH207 and B37 under control, co

24 obust MSI, this capacity was impaired in the inbred BTBR T+tf/J mouse model of idiopathic autism.

25 larval stage also increased the lifespan of inbred but not outbred adults, suggesting that the benef

26 rized by a missense mutation in Cacna1a, and inbred C3H/HeOuJ.

27 d qMotor in SOD1(G93A) transgenic mice in an inbred C57BL/6J background, hereafter called iSOD1(G93A)

28 20 times more frequent in clean wild-derived inbred CAST/EiJ mice than in C57BL/6J mice.

29 ring loss disrupts high-frequency hearing in inbred CD-1 mice.

30 g ASE in F1 reciprocal crosses of two highly inbred chicken lines (Fayoumi and Leghorn).

31 In addition, a highly inbred (complete major histocompatibility complex [MHC]

32 xperimental nerve injury is increased in the inbred DA strain compared with the PVG strain and is ass

33 the whole-genome sequencing and assembly of inbred derivatives of its two wild parents, P. axillaris

34 ple stages of metazoan development, using 80 inbred Drosophila wild isolates, identifying thousands o

35 ed and outbred families, we demonstrate that inbred families have reduced larval survival and that th

36 n, which comprises 25 biparental recombinant inbred families.

37 s, expression QTL analysis and heterogeneous inbred family validation.

38 The inbred Fischer 344 rat is being evaluated for testing no

39 entration at the higher water temperature in inbred fish but not in outbred fish.

40 ome is sequenced from adult flies from lines inbred for 20 generations.

41 ining extensive genetic variation from eight inbred founder strains.

42 rg719Trp (RW/+), VM/+ mice with an identical inbred genetic background lacked hallmarks of HCM such a

43 inbred mouse strains and mutations placed on inbred genetic backgrounds.

44 stone formation, we utilized 95th-generation inbred genetic hypercalciuric stone-forming rats.

45 han previously seen in MARV-infected mice or inbred guinea pigs.

46 wo loci having repulsion linkage between two inbreds, heterosis in the hybrid can appear as a single

47 in some cases, via the production of highly inbred (i.e., self-fertilized) offspring.

48 Three inbred ILSXISS strains were fed high-fat or chow diets a

49 unlike mice or rats, which are deliberately inbred in a laboratory to minimize variation between ani

50 Mo17 (IBM) populations of maize recombinant inbreds, indicating that this gene may be agronomically

51 n larger populations even if only moderately inbred individuals are available for addition.

52 Inbreeding depression occurs when inbred individuals experience reduced fitness as a resul

53 Initially, the Pkd1(RC/RC) model was inbred into the C57BL/6 background, minimizing disease v

54 ined, including wild-derived populations and inbred isogenic laboratory strains.

55 The amount of variation found in the inbred laboratory mouse genome has increased to 71 M SNP

56 Most inbred laboratory mouse strains are deficient in Mx1, bu

57 a1c and Tcf7l2 and wild-type females from 30 inbred laboratory strains.

58 Inbred Lewis rats sustain normotension despite a genetic

59 advanced backcross (28.6 cM) and recombinant inbred line (32.3 cM) populations.

60 s) for the interspecific Petunia recombinant inbred line (RIL) population - P. axillaris x P. exserta

61 ou9308's high yield potential, a recombinant inbred line (RIL) population derived from cross of Xieqi

62 basis of high yield potential, a recombinant inbred line (RIL) population derived from the cross betw

63 cessions, Col-0 and Bur-0, and a recombinant inbred line (RIL) population derived from these parents

64 rphisms (SNPs) identified in the recombinant inbred line (RIL) population of ICC 4958 (drought tolera

65 We used 10 different recombination inbred line (RIL) populations genotyped with high-densit

66 e cultivars, such as the sequenced reference inbred line B73.

67 y genome sequence is available for the elite inbred line BTx623, but functional validation of genes r

68 hen introgressed by backcross into the maize inbred line PH09B, the mutant phenotype of vyl lasted mu

69 we generated a draft genome assembly of the inbred line PH207 to complement and compare with the exi

70 f samples in a subtropical maize recombinant inbred line population (CML444 x SC Malawi) subjected in

71 (Lemont) by indica (Teqing) rice recombinant inbred line population and focused on the genetic variat

72 In a recombinant inbred line population derived from a cross between CDC

73 A recombinant inbred line population derived from a cross between the

74 Screening a recombinant inbred line population developed from PI215246 and cv Sa

75 Using a recombinant inbred line population, a separate quantitative trait lo

76 e points from a greenhouse-grown recombinant inbred line population.

77 easurement of gene expression in recombinant inbred line populations has enabled investigation of the

78 from ear, tassel, and leaf of the B73 public inbred line were constructed at four developmental stage

79 -RIL (nested association mapping-recombinant inbred line) populations indicated that the drl loci res

80 y 313.4-Mb genome sequence of a bottle gourd inbred line, USVL1VR-Ls, with a scaffold N50 of 8.7 Mb a

81 ot and shoot tissues of two maize (Zea mays) inbred lines (B73 and Mo17).

82 abidopsis accessions, epigenetic recombinant inbred lines (epiRILs) and also verified in rice.

83 1-2 (ddm1-2)-derived epigenetic recombinant inbred lines (epiRILs) in Arabidopsis thaliana is well s

84 c contribution to heterosis using epigenetic inbred lines (epiRILs) with varying levels and distribut

85 ight-week old male mice from two recombinant inbred lines (LGXSM-6 and LGXSM-33) were subjected to ax

86 ecture of local adaptation using recombinant inbred lines (RIL) derived from a cross between two loca

87 ia as well as in a collection of recombinant inbred lines (RILs) derived from indica Jasmine-type var

88 ter:sweet compounds by analysing recombinant inbred lines (RILs) from an interspecific lettuce mappin

89 gths and widths in Brassica rapa recombinant inbred lines (RILs) throughout ontogeny.

90 By re-sequencing of 138 recombinant inbred lines (RILs), a total of ~0.7 million SNPs were i

91 , as well as in two derivative recombination inbred lines (RILs).

92 e and transcriptome variation in elite maize inbred lines across heterotic pools.

93 identified in earlier studies with the same inbred lines and associated with biometrical, physiologi

94 es of several commonly used maize (Zea mays) inbred lines and has been anecdotally linked to enhanced

95 ragenotypic variability), we used Drosophila inbred lines and measured the spontaneous locomotor beha

96 mine the level of genetic diversity in INERA inbred lines and patterns of relationships of these inbr

97 ints of floral transition of almost 30 maize inbred lines and show that tropical lines exhibit a dela

98 F1 progeny of such inbred lines are often more vigorous than their parents,

99 ated how the genetic divergence of the maize inbred lines B73 and Mo17 and their F1 hybrid progeny is

100 criptomic divergence of the maize (Zea mays) inbred lines B73 and Mo17 and their reciprocal F1 hybrid

101 me shotgun (WGS) sequences for the two maize inbred lines B73 and Mo17 using k-mer analysis to quanti

102 onmental conditions in hybrid progeny of the inbred lines B73 and Mo17.

103 g two whole-genome de novo assemblies of the inbred lines B73 and PH207.

104 are not specific to the Col-Cvi recombinant inbred lines but have an epigenetic state that is inhere

105 Recombinant inbred lines derived from Col and Cvi were used to exami

106 We produced 1,636 MAGIC maize recombinant inbred lines derived from eight genetically diverse foun

107 Inbred lines derived from T. mirus with a dominant d-rDN

108 r castaneus map, and a map constructed using inbred lines derived predominantly from M. m. domesticus

109 lines and patterns of relationships of these inbred lines developed from two sources; and (3) examine

110 Distantly related maize (Zea mays) inbred lines display an exceptional degree of genomic di

111 Arabidopsis thaliana epigenetic recombinant inbred lines found no evidence in support of any role fo

112 of DNA methylation in five maize (Zea mays) inbred lines found that while DNA methylation levels for

113 AM) population, comprising 4,998 recombinant inbred lines from 25 biparental families, and in an asso

114 Using a population of recombinant inbred lines from resistant and susceptible parents, the

115 A training population made up of 384 inbred lines from the Ames Panel was phenotyped by extra

116 d 219 soybean accessions and 152 recombinant inbred lines genotyped with high-density markers and phe

117 rom 368 diverse temperate and tropical maize inbred lines in this study.

118 urally dispersing populations of recombinant inbred lines of Arabidopsis thaliana segregating early a

119 this issue by exposing a set of recombinant inbred lines of Arabidopsis thaliana to a simulated glob

120 llocation among floral whorls in recombinant inbred lines of Brassica rapa in multiple environments t

121 of reproduction over ontogeny in recombinant inbred lines of Brassica rapa in the field and glasshous

122 In this study we determined that two inbred lines of chicken differing in their genetic backg

123 in Mozambique was compared among recombinant inbred lines of common bean (Phaseolus vulgaris) having

124 riptomic response to cold was studied in two inbred lines of contrasting cold-tolerance.

125 variation of defensin genes was examined in inbred lines of Leghorn and Fayoumi chickens, and a dupl

126 l coma recovery) in the unrelated, sequenced inbred lines of the Drosophila melanogaster Genetic Refe

127 s at 1, 2, and 4 wk of age in the sequenced, inbred lines of the Drosophila melanogaster Genetic Refe

128 ariation in gene expression in the sequenced inbred lines of the Drosophila melanogaster Genetic Refe

129 a recovery time, in the unrelated, sequenced inbred lines of the Drosophila melanogaster Genetic Refe

130 ter stages of development in 197 recombinant inbred lines of two different maize (Zea mays) populatio

131 eate large numbers of mutant embryos without inbred lines opens exciting new possibilities for studyi

132 lly expressed genes between the two parental inbred lines significantly exceeded those of parent vers

133 d the number of active genes in the parental inbred lines significantly independent of treatment.

134 00 years has produced elite maize (Zea mays) inbred lines that combine to produce high-yielding hybri

135 ng of seedling RNA from 503 maize (Zea mays) inbred lines to characterize the maize pan-genome, we id

136 because genetic variation among wild-derived inbred lines was much lower than predicted from a neutra

137 INERA and 41 exotic (temperate and tropical) inbred lines were characterized using 1057 SNP markers t

138 ve tissues from 27 genetically diverse maize inbred lines were deeply sequenced to identify genes exh

139 closely examined beta-costic acid-deficient inbred lines were found to harbor Zmtps21 pseudogenes la

140 ed differentially to stress between parental inbred lines were identified.

141 on tests on the maize-282-diverse-panel (282 inbred lines) under normal (25 degrees C) and chilling (

142 We also identify, in recombinant inbred lines, a locus that affects maternal hatching, a

143 notypes, a mapping population of recombinant inbred lines, and a dense single-nucleotide polymorphism

144 using an independent population of backcross inbred lines, derived from the same parents, which allow

145 s demonstrated by characterizing recombinant inbred lines, including Oh43, which has a point mutation

146 In further comparisons of 60 diverse inbred lines, non-syntenic genes were six times more lik

147 ments from seedlings in a variety of Pioneer inbred lines, routinely recovering healthy, fertile T0 p

148 tential hybrids derived from 210 recombinant inbred lines, selection of the top 10 hybrids predicted

149 duction fixes recombinant haploid genomes in inbred lines, shaving years off the breeding process.

150 lone establishes systemic infection in maize inbred lines, sorghum (Sorghum bicolor), and green foxta

151 -induced volatiles among 26 maize (Zea mays) inbred lines, we conducted a nested association mapping

152 conditions in three Brachypodium distachyon inbred lines, we describe the identification and the mai

153 Exploiting wild accessions and recombinant inbred lines, we reveal extensive phenotypic variation i

154 l root length' (TRL) were predicted for 2431 inbred lines, which had previously been genotyped by seq

155 numerous previously non-transformable maize inbred lines.

156 gene variants present in the many available inbred lines.

157 ompared with B73 and Tx601 maize susceptible inbred lines.

158 ed representation sequencing of 14,129 maize inbred lines.

159 ata obtained by RT-qPCR technique from maize inbred lines.

160 ified using eRD-GWAS on a panel of 369 maize inbred lines.

161 by crossing B73 and each of the three other inbred lines.

162 genetic diversity in a diverse set of maize inbred lines; (2) determine the level of genetic diversi

163 TL) in the Intermated B73 x Mo17 recombinant inbred maize (Zea mays) population using pyrolysis molec

164 on, comparative optical mapping of two other inbred maize lines revealed a prevalence of deletions in

165 more than 2.5-fold across a diverse group of inbred maize lines were resolved.

166 y (AS) panel consisting of 74 diverse set of inbred maize lines were screened for seedling root trait

167 isms determining divergent cold-tolerance of inbred maize lines.

168 We employed a SEFL paradigm in inbred male and female C57BL/6 mice that combines acute

169 5 trans-loci were identified in shoots of an inbred mapping population of Brassica rapa (IMB211 x R50

170 Recombinant inbred mapping populations derived from three different

171 pecies of Ebola virus (ZEBOV) primarily used inbred mice and guinea pigs to model disease.

172 show that B cells and serum antibodies from inbred mice demonstrate a reproducible ID hierarchy to t

173 aborative Cross (CC), a large panel of newly inbred mice that captures 90% of the known variation amo

174 n tumors derived from a panel of recombinant inbred mice to identify a network of co-expressed genes

175 red the retinal pathology of Crb1(rd8/rd8)/J inbred mice with that of two Crb1(rd8/rd8) lines backcro

176 irus induces diabetes in restricted lines of inbred mice, the susceptibility genes to virus-induced d

177 ularly important for model organisms such as inbred mice, where LD extends much further than in human

178 ctional difference not apparent in classical inbred mice.

179 hypertrophy and fibrosis in a large panel of inbred mice.

180 in an inbred strain but fully lethal in non-inbred mice.

181 tes that cause different disease symptoms in inbred mice.

182 kinetics, plaque size, and pathogenicity in inbred mice.

183 t that received cecal microbes from C57BL/6J inbred mice; however, durability of choline diet-depende

184 Genetic (inbred) models of this disorder in rats have been used t

185 Using an inbred mouse neuronal phenotypic screen, we find that CA

186 mRNA) sequencing datasets from a recombinant inbred mouse panel.

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

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

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

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

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

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

193 translational studies utilize only a single inbred mouse strain.

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

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

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

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

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

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

200 Genetic analyses of inbred mouse strains identified loci affecting different

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

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

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

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

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

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

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

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

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

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

211 otropic ERV subgroup largely confined to the inbred mouse Y chromosome.envvariations define three E-M

212 In 23 inbreds of domesticated maize chosen to represent the ge

213 ions of germinating seeds from two different inbreds of maize (Zea mays) seeds, B73 and Mo17.

214 at maternal care improves the performance of inbred offspring more than that of outbred offspring.

215 When relatives mate, their inbred offspring often suffer a reduction in fitness-rel

216 e earliest maize from San Marcos was already inbred, opening the possibility for Tehuacan maize culti

217 le parent during larval development and (ii) inbred or outbred offspring.

218 individuals from three genetic backgrounds (inbred - outbred) into a novel environment at three foun

219 p between Wolbachia and mtDNA, using a large inbred panel of Drosophila simulans.

220 ch SAM size variation within a diverse maize inbred panel.

221 of gene expression in the relevant tissue in inbred parental samples, which are not always available

222 tive genes in F1-hybrids compared with their inbred parents.

223 dulating (nod-) and nodulating (nod+) sister inbred peanut lines, E4/E5 and E7/E6, and their nod+ par

224 -quality genome assembly for the elite maize inbred PH207 expands our knowledge of the breadth of nat

225 For example, the Pioneer inbred PHH5G is recalcitrant to biolistic and Agrobacter

226 lleles, and subsequent phenotypic changes in inbred plants, inbreeding may alter plant-insect interac

227 ere, using a novel approach for screening an inbred population of laboratory animals, we identified t

228 ceptible) were used to develop a recombinant inbred population with future goals of identifying genom

229 ffects are likely to be most acute in small, inbred populations exhibiting environmental sex determin

230 y in response to male skews and declines for inbred populations occurred at lower male skews than for

231 g can uncover rich genetic diversity even in inbred populations, and introduces a novel strategy to d

232 ions are predicted to be expressed in small, inbred populations, reducing both individual fitness and

233 purging deleterious alleles from threatened inbred populations.

234 e been conducted in Arabidopsis thaliana, an inbred primarily self-fertilizing species that should ha

235 ation of renal water reabsorption, using the inbred rat strain SHR-A3 as an animal model with disrupt

236 male and male mice from the same recombinant inbred (RI) strain have the same genomic components exce

237 ced lung collagen content in BXD recombinant inbred (RI) strains and identified significant linkage o

238 The highly resistant recombinant inbred RIL 46 and moderately resistant RIL 48 were selec

239 ates ZEBOV infection of primates better than inbred rodent models, is useful for dissecting key event

240 nsive CNV exists within Fayette, a released, inbred SCN-resistant soybean cultivar with a high copy n

241 d genome-wide association analyses using the inbred, sequenced lines of the Drosophila melanogaster G

242 sticity for three quantitative traits in the inbred, sequenced lines of the Drosophila melanogaster G

243 Though all three accessions are inbred seven generations, each accession still possesses

244 However, these inbred species do not show some of the important feature

245 that this approach is even more relevant in inbred species such as rice (Oryza sativa L.), which are

246 cts have been successful in many haploid and inbred species, the assembly of noninbred or rearranged

247 Furthermore, use of an inbred strain allows for investigation into epigenetic m

248 defects, which are partially penetrant in an inbred strain but fully lethal in non-inbred mice.

249 SPRET/Ei is an inbred strain derived from Mus spretus that has approxim

250 identical to that of any other CC strain or inbred strain for which prior data are available, indica

251 rthermore, we demonstrate that the C3H/HeSnJ inbred strain has late onset cerebellar degeneration due

252 ad coverage of approximately 30-fold from an inbred strain medaka (Oryzias latipes), we observed that

253 sting using multiple genotypes revealed that inbred strain siblings do not cooccupy at higher rates t

254 By using BTBR mice, an inbred strain that displays behavioral traits that refle

255 The castaneous (CAST) mouse, a wild-derived inbred strain, is highly susceptible to orthopoxvirus in

256 tomic data from the mouse hippocampus of six inbred strains (129S1/SvImJ, A/J, C57BL/6J, DBA/1J, DBA/

257 e carry out deep sequencing of 13 additional inbred strains (BUB/BnJ, C57BL/10J, C57BR/cdJ, C58/J, DB

258 cly available genome sequences of 36 popular inbred strains and provide lists for each strain of prot

259 heritable trait by using female rats of six inbred strains and six F1 hybrids.

260 e methylation patterns seen among laboratory inbred strains are also found in a free-living populatio

261 he hybrid mouse diversity panel (HMDP) of 83 inbred strains as a surrogate for human natural immune v

262 enes play an important role when using mouse inbred strains as research models.

263 The inbred strains C57BL/6J and DBA/2J (DBA) display strikin

264 Ethiopian inbred strains exhibited much higher frequencies of wing

265 s to study wild house mice and to create new inbred strains from wild populations have the potential

266 physiology from an array of BXD recombinant inbred strains identified a segment on chromosome 4 cont

267 rom eight inbred strains to females from two inbred strains of house mice (Mus musculus domesticus).

268 kemia viruses (MLVs) are found in the common inbred strains of laboratory mice and in the house mouse

269 s leading to acute heart injury in different inbred strains of mice also suggest that this response h

270 haracterize hypothalamic transcriptome in 99 inbred strains of mice from the Hybrid Mouse Diversity P

271 the less potent S-baclofen enantiomer in two inbred strains of mice that display low sociability and/

272 Diversity Panel data, which consisted of 100 inbred strains of mice, we identified 97 DMCs that were

273 NKT cell number and function among different inbred strains of mice, we investigated whether the role

274 We explored this issue in inbred strains of mice, with a special focus on the low

275 matory responses in two genetically distinct inbred strains of mice.

276 NA gene sequencing in a panel of 110 diverse inbred strains of mice.

277 immunogenicity of PvRMC-CSP in groups of six inbred strains of mice.

278 novel insertions exist in every lab strain, inbred strains of the Drosophila Genetic Reference Panel

279 ency of type I NKT cells in the wild-derived inbred strains PWD/PhJ, SPRET/EiJ, and CAST/EiJ.

280 Female mice of 28 inbred strains received this vaccine at 6, 8, and 12 wee

281 Mouse inbred strains remain essential in science.

282 Here, we cross males from eight inbred strains to females from two inbred strains of hou

283 n the neonatal lung by exposing mice from 36 inbred strains to hyperoxia (95% O2) for 72 h after birt

284 ts, explain phenotypical differences between inbred strains, and increase the amount of interesting g

285 in mice have illustrated differences between inbred strains, but the possibility that mitochondrial g

286 th the use of a panel of MHC-III recombinant inbred strains, we found that the 33-kb Ltab-Ncr3 haplot

287 ipts showed significant variation across the inbred strains, with 22% of the transcriptome varying by

288 mic cerebral infarct volume observed between inbred strains.

289 les from intact and OVX mice from a panel of inbred strains.

290 (LD) that is characteristic of crosses among inbred strains.

291 imarily from comparisons of 6J mice to other inbred strains.

292 sequenced classical and high-priority mouse inbred strains.

293 d to a higher increase in larval survival in inbred than in outbred broods.

294 As inbred trisomic mice also exhibit variable phenotypes, w

295 remodelling-features that were stable in the inbred, variable in the second, but virtually absent in

296 somal regions from the Non-Stiff Stalk maize inbred W22 from a single DNA sequence dataset.

297 s, Sprague Dawley and Long-Evans, and/or the inbred WAG/Rij strain (a rat model of heritable human ab

298 plasticity in TSS usage between tissues and inbreds was uncovered, with approximately 1500 genes sho

299 ilar to the distribution in the B73 parental inbred, whereas that of Mo17 x B73 resembles the Mo17 pa

300 se transcript pairs (NAT pairs) in two maize inbreds with different sensitivity to drought, as well a