ライフサイエンスコーパス: recombinant inbred line

1 s technique was demonstrated by genotyping a recombinant inbred line.

2 the task of generating populations of highly recombinant inbred lines.

3 oxA, were evaluated on a population of wheat recombinant inbred lines.

4 3A-specific markers on 95 single-chromosome recombinant inbred lines.

5 ponse to benzaldehyde, using a population of recombinant inbred lines.

6 restriction fragment length polymorphisms of recombinant inbred lines.

7 ed 38% of the phenotypic variation among the recombinant inbred lines.

8 sses and backcrosses and using La-er x Col-0 recombinant inbred lines.

9 e top of chromosome 1 by RFLP analysis of F8 recombinant inbred lines.

10 lex disease phenotypes within a panel of rat recombinant inbred lines.

11 allele cosegregated with 2,4-D resistance in recombinant inbred lines.

12 tal methylation differences are inherited by recombinant inbred lines.

13 to a large panel of Drosophila melanogaster recombinant inbred lines.

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

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

16 g QTL mapping with a new advanced intercross-recombinant inbred line (AI-RIL) population, we show tha

17 ese contigs on the Landsberg erecta/Columbia recombinant inbred lines allowed positioning of the cont

18 peed in a reporter-modified Bay-0 x Shakdara recombinant inbred line and localized heritable variatio

19 mouse strains, C57BL/6J and DBA/2J, several recombinant inbred lines and cerebellar mutant strains.

20 traits in parallel sets of F(2) hybrids plus recombinant inbred lines and generated nearly isogenic l

21 alysis with two sets of Arabidopsis thaliana recombinant inbred lines and have identified 14 QVE (qua

22 The difference persisted in hybrids and recombinant inbred lines and was mapped to a single expr

23 solution phenotypes, a mapping population of recombinant inbred lines, and a dense single-nucleotide

24 ased sex ratio was observed in 24 of the 221 recombinant inbred lines, and subsequent tests attribute

25 For those organisms where recombinant inbred lines are available for mapping, the

26 form to study hundreds of rice landraces and recombinant inbred lines at two sites, from 2019 to 2021

27 we identify are not specific to the Col-Cvi recombinant inbred lines but have an epigenetic state th

28 llers per plant of hybrid rice (derived from recombinant inbred lines) by comprehensively evaluating

29 The resistant parents and their recombinant inbred lines carrying either ARG4 or ARG5 ar

30 o be an intermediate of transposition) in 98 recombinant inbred lines constructed from a line exhibit

31 isition by physiological comparison of maize recombinant inbred lines contrasting in RCA grown under

32 Two indica rice genotypes, FL478, a recombinant inbred line derived from a population develo

33 ent of FRL2-Ler, but not of FRL2-Col, into a recombinant inbred line derived from these plants restor

34 we mapped tiller and biomass QTLs with ~ 250 recombinant inbred lines derived from a 'Francis' by 'Ro

35 sis of the editing efficiency in a sample of recombinant inbred lines derived from a cross between Co

36 ve trait loci (QTL) for total fitness in 398 recombinant inbred lines derived from a cross between lo

37 t loci analysis was performed using a set of recombinant inbred lines derived from a cross between th

38 ments were reliably scored and mapped in 100 recombinant inbred lines derived from a cross between th

39 Using oligonucleotide array data from 30 recombinant inbred lines derived from a cross of Columbi

40 Recombinant inbred lines derived from an advanced interc

41 Recombinant inbred lines derived from Col and Cvi were u

42 We produced 1,636 MAGIC maize recombinant inbred lines derived from eight genetically

43 the variance in Al tolerance observed among recombinant inbred lines derived from Landsberg erecta (

44 ee QTL for each behavioral trait in a set of recombinant inbred lines derived from the laboratory sto

45 ingenin accumulation in rice (Oryza sativa), recombinant inbred lines derived from the Nipponbare and

46 sposable element markers, in a population of recombinant inbred lines derived from the Oregon and 2b

47 A population of recombinant inbred lines derived from the tetraploid dur

48 behavior was assessed in a population of 98 recombinant inbred lines derived from these two strains

49 Most frequently, recombinant inbred lines derived from two isogenic paren

50 bdominal and sternopleural bristles among 98 recombinant inbred lines, derived from two homozygous la

51 multi-parent population comprising over 500 recombinant inbred lines, descended from sixteen histori

52 A recombinant inbred line design was used to map QTL for t

53 QTL mapping with recombinant inbred lines detected 12 major QTL for 11 of

54 thermal infrared imaging in a population of recombinant inbred lines developed from a cross between

55 Recombinant inbred lines developed from the maize (Zea m

56 eveloped 25 families composed of ~200 random recombinant inbred lines each from crosses between a com

57 t life span was examined for a population of recombinant inbred lines, each of which had been crossed

58 aborative Cross (CC) is a panel of eight-way recombinant inbred lines: eight diverse parental strains

59 e base resolution methylomes from epigenetic recombinant inbred lines (epiRIL), we show that epiallel

60 n natural Arabidopsis accessions, epigenetic recombinant inbred lines (epiRILs) and also verified in

61 ened an Arabidopsis population of epigenetic recombinant inbred lines (epiRILs) for resistance agains

62 methylation 1-2 (ddm1-2)-derived epigenetic recombinant inbred lines (epiRILs) in Arabidopsis thalia

63 ta from a large panel of isogenic epigenetic recombinant inbred lines (epiRILs) to derive a recombina

64 Multi-parent crosses of recombinant inbred lines exist in many species for fine-

65 sociation mapping population, composed of 25 recombinant inbred line families derived from diverse in

66 ow that there is genetic variation among the recombinant inbred lines for parameters of the reaction

67 ineum and in Arabidopsis thaliana epigenetic recombinant inbred lines found no evidence in support of

68 n mapping (NAM) population, comprising 4,998 recombinant inbred lines from 25 biparental families, an

69 esistance on soybean chromosome 13 using 184 recombinant inbred lines from a 'Wyandot' x PI 567324 cr

70 Between 110 and 176 F6 recombinant inbred lines from a mapping population deriv

71 d in regions very close to the centromere in recombinant inbred lines from an intermated B73 x Mo17 p

72 ts, and natural accession and populations of recombinant inbred lines from over 800 separate experime

73 Using a population of recombinant inbred lines from resistant and susceptible

74 yping array was developed and applied to 741 recombinant inbred lines from six mapping populations.

75 nerate a SNP-based genetic map by genotyping recombinant inbred lines from the intermated B73 x Mo17

76 ism and photosynthesis in the flag leaves of recombinant inbred lines from wheat cultivars Seri M82 a

77 number, and to analyze marker segregation in recombinant inbred lines generated from an interstrain c

78 Here, we used 219 soybean accessions and 152 recombinant inbred lines genotyped with high-density mar

79 The high amylose high protein recombinant inbred line (HAHP_101) was enriched in essen

80 er rosette leaf number at flowering in RILs (Recombinant Inbred Lines) harboring the SG allele.

81 Recently, we have reported on two recombinant inbred lines (I and V) and the location of a

82 The use of well-structured recombinant inbred lines in combination with "omics" ana

83 lyzing the distributions of COs in panels of recombinant inbred lines in relation to TE polymorphism

84 s in vivo was demonstrated by characterizing recombinant inbred lines, including Oh43, which has a po

85 Quantitative trait loci analysis of recombinant inbred lines indicates that multiple loci in

86 markers has been developed using intermated recombinant inbred lines (IRILs) from the intermated B73

87 parental population with a limited number of recombinant inbred lines, it is unnecessary to genotype

88 t knees of eight-week old male mice from two recombinant inbred lines (LGXSM-6 and LGXSM-33) were sub

89 iation for flowering time with a set of 5000 recombinant inbred lines (maize Nested Association Mappi

90 In the Arabidopsis multiparent recombinant inbred line mapping population, a limited nu

91 In a recombinant inbred line mapping population, copy number

92 n each of 1141 genes in one or more of three recombinant inbred line mapping populations, thus provid

93 in Arabidopsis using map-based cloning with recombinant inbred lines, natural variation transcriptom

94 nbred, as well as between high and low eEF1A recombinant inbred lines obtained from their cross.

95 ablished naturally dispersing populations of recombinant inbred lines of Arabidopsis thaliana segrega

96 We address this issue by exposing a set of recombinant inbred lines of Arabidopsis thaliana to a si

97 We apply the method to data from a panel of recombinant inbred lines of Arabidopsis thaliana, descen

98 and rosette leaf number were measured in 100 recombinant inbred lines of Arabidopsis thaliana, grown

99 nd biomass allocation among floral whorls in recombinant inbred lines of Brassica rapa in multiple en

100 s and onset of reproduction over ontogeny in recombinant inbred lines of Brassica rapa in the field a

101 Using recombinant inbred lines of Brassica rapa, we examined t

102 n the field in Mozambique was compared among recombinant inbred lines of common bean (Phaseolus vulga

103 (locomotor reactivity) in a population of 98 recombinant inbred lines of Drosophila melanogaster and

104 tabolic rate, and free-flight performance in recombinant inbred lines of Drosophila melanogaster.

105 f published plant height data involving 3502 recombinant inbred lines of maize planted in multiple di

106 e Cross (CC) is a genetic reference panel of recombinant inbred lines of mice, designed for the disse

107 We find analogous results in recombinant inbred lines of the Bayreuth x Shahdara cros

108 h leaf at later stages of development in 197 recombinant inbred lines of two different maize (Zea may

109 is of earleaf samples in a subtropical maize recombinant inbred line population (CML444 x SC Malawi)

110 panel of 383 diverse cowpea accessions and a recombinant inbred line population (RIL) were SNP genoty

111 ols Mo accumulation in rice grain by using a recombinant inbred line population and a backcross intro

112 a japonica (Lemont) by indica (Teqing) rice recombinant inbred line population and focused on the ge

113 o17 (IBM) population, an advanced intercross recombinant inbred line population derived from a cross

114 A recombinant inbred line population derived from a cross

115 In a recombinant inbred line population derived from a cross

116 ng of natural accessions, we have analyzed a recombinant inbred line population derived from crosses

117 e flowering time gene SNPs in an independent recombinant inbred line population derived from the inte

118 Using AFLP technology and a recombinant inbred line population derived from the sorg

119 Using a recombinant inbred line population developed from a lett

120 Screening a recombinant inbred line population developed from PI2152

121 oot architectures within a Col-0 x Catania-1 recombinant inbred line population identified several lo

122 1 (Tsushima, Japan) x Kas-1 (Kashmir, India) recombinant inbred line population of Arabidopsis thalia

123 Inheritance studies in a recombinant inbred line population of wheat-Ae. peregrin

124 Analysis of a Ler x Sha recombinant inbred line population revealed a single maj

125 were identified by crossing a Columbia x C24 recombinant inbred line population to diploid A. arenosa

126 Using a recombinant inbred line population, a separate quantitat

127 Here, a recombinant inbred line population, originating from a c

128 In mapping this intermated recombinant inbred line population, we have contributed

129 gle time point microarray experiments from a recombinant inbred line population.

130 ced intercross population and a conventional recombinant inbred line population.

131 ing was performed using the IBM (B73 x Mo17) recombinant inbred line population.

132 ally occurring ecotypes and in the Ler x Col recombinant inbred line population.

133 me traits in the Landsberg erecta x Columbia recombinant inbred line population.

134 opmental time points from a greenhouse-grown recombinant inbred line population.

135 se within the Arabidopsis thaliana Kas x Tsu recombinant inbred line population.

136 s (Arabidopsis thaliana) Bayreuth x Shahdara recombinant inbred line population.

137 representing parents and descendants of two recombinant inbred line populations derived from two wee

138 throughput measurement of gene expression in recombinant inbred line populations has enabled investig

139 it locus analyses for seed longevity, in six recombinant inbred line populations, revealed five loci:

140 on (DOG), earlier identified in the same six recombinant inbred line populations.

141 ng maize NAM-RIL (nested association mapping-recombinant inbred line) populations indicated that the

142 Genetic analysis of recombinant inbred lines produced from a triploid identi

143 Analysis of recombinant inbred lines provides evidence that the majo

144 e report that, in Arabidopsis accessions and recombinant inbred lines, reducing Hsp90 function produc

145 is difference in insect susceptibility using recombinant inbred lines resulted in the discovery of th

146 GWAS and analysis of recombinant inbred lines reveal multiple genetic regions

147 g-by-sequencing-(GBS) derived markers to map recombinant inbred line (RIL) and doubled haploid (DH) p

148 hn loci were then determined using two maize recombinant inbred line (RIL) mapping populations.

149 (QTL) from previous Ler x Col and Cvi x Ler recombinant inbred line (RIL) mapping studies, no additi

150 ship of alphaS aggregation, we constructed a Recombinant Inbred Line (RIL) panel derived from a cross

151 rphisms (SNPs) for the interspecific Petunia recombinant inbred line (RIL) population - P. axillaris

152 x US96UC23 (Lactuca serriola) (L. serriola) recombinant inbred line (RIL) population and USDA germpl

153 In this study, we used the recombinant inbred line (RIL) population between Landsbe

154 facility was used to measure WUE(plant) in a recombinant inbred line (RIL) population created between

155 eed germination responses to priming using a recombinant inbred line (RIL) population derived from a

156 MS), and cell wall composition (CWC) using a recombinant inbred line (RIL) population derived from a

157 ng, we constructed a new advanced intercross recombinant inbred line (RIL) population derived from a

158 nism of Xieyou9308's high yield potential, a recombinant inbred line (RIL) population derived from cr

159 AMF colonization of a worldwide crop from a Recombinant Inbred Line (RIL) population derived from So

160 Two accessions, Col-0 and Bur-0, and a recombinant inbred line (RIL) population derived from th

161 ing genetic basis of high yield potential, a recombinant inbred line (RIL) population derived from th

162 rT) sequencing - were employed to genotype a recombinant inbred line (RIL) population developed from

163 iosynthesis in melon rind and flesh, using a Recombinant Inbred Line (RIL) population from the cross

164 otide polymorphisms (SNPs) identified in the recombinant inbred line (RIL) population of ICC 4958 (dr

165 FPs were enumerated between two parents of a recombinant inbred line (RIL) population segregating for

166 says (KASP) and analyzed in two F(6)-derived recombinant inbred line (RIL) populations derived from t

167 Two sorghum recombinant inbred line (RIL) populations, BTx623/BTx642

168 2A and ahFAD2B) to oil quality traits in two recombinant inbred line (RIL) populations.

169 One mapping population of recombinant inbred line (RIL) used in this study was der

170 netic architecture of local adaptation using recombinant inbred lines (RIL) derived from a cross betw

171 Two hundred forty-six recombinant inbred lines (RIL) derived from a cross betw

172 VL677-PMS and four introgressed PM resistant recombinant inbred lines (RIL, USVL531-PMR x USVL677-PMS

173 An analysis of 48 Ler/Cvi recombinant inbred lines (RILs) and a further 30 Ler/Col

174 at is, parents, F(1)'s, F(2)'s, backcrosses, recombinant inbred lines (RILs) and a triple test cross

175 Quantitative trait locus (QTL) studies with recombinant inbred lines (RILs) and near-isogenic lines

176 e, we present epigenomic analyses of soybean recombinant inbred lines (RILs) and their parents.

177 number of different population designs, but recombinant inbred lines (RILs) are among the most effec

178 Cape Verde Islands by Landsberg erecta (CvL) recombinant inbred lines (RILs) at 12 degrees , 22 degre

179 ngle feature polymorphism (SFP) detection in recombinant inbred lines (RILs) can capitalize on the hi

180 Recombinant inbred lines (RILs) can serve as powerful to

181 We evaluated recombinant inbred lines (RILs) carrying resistance from

182 h-density genetic map of a population of 210 recombinant inbred lines (RILs) derived from a cross bet

183 asis for their allometric relationship using recombinant inbred lines (RILs) derived from a natural p

184 Using a panel of Recombinant Inbred Lines (RILs) derived from a single na

185 data to generate detailed haplotypes for 148 recombinant inbred lines (RILs) derived from Arabidopsis

186 Recombinant inbred lines (RILs) derived from B73 x M017

187 In this study, 223 recombinant inbred lines (RILs) derived from crossing an

188 and Australia as well as in a collection of recombinant inbred lines (RILs) derived from indica Jasm

189 In this study, 185 F(12)-recombinant inbred lines (RILs) derived from two US rice

190 fifteen heat stress indices (HIs) among 200 recombinant inbred lines (RILs) derived from WH711 x WH1

191 dvanced intercross panel consisting of >1600 recombinant inbred lines (RILs) designed for the genetic

192 roteomic evidence, investigating a subset of recombinant inbred lines (RILs) developed by the Austral

193 he maize NAM population, consisting of 5,000 recombinant inbred lines (RILs) from 25 families represe

194 y (GWAS) was conducted using a subset of 408 Recombinant Inbred Lines (RILs) from a Multi-Parent Adva

195 atios of bitter:sweet compounds by analysing recombinant inbred lines (RILs) from an interspecific le

196 We use F5 recombinant inbred lines (RILs) generated from a cross b

197 ng with a maize population consisting of 515 recombinant inbred lines (RILs) grown in Texas and a hyb

198 rait loci (QTL) influencing recombination in recombinant inbred lines (RILs) is proposed that relies

199 d sugarcane aphid (SCA) was performed in two recombinant inbred lines (RILs) of sorghum, resistant (R

200 We developed a population of recombinant inbred lines (RILs) originating from a cross

201 A careful analysis of two maize recombinant inbred lines (RILs) relative to their inbred

202 s12 against a set of P. sojae isolates using recombinant inbred lines (RILs) that contain recombinati

203 red leaf lengths and widths in Brassica rapa recombinant inbred lines (RILs) throughout ontogeny.

204 Seq used phenotypically contrasting bulks of recombinant inbred lines (RILs) to identify Pm5e-linked

205 By re-sequencing of 138 recombinant inbred lines (RILs), a total of ~0.7 million

206 Here we report a population of recombinant inbred lines (RILs), derived from the two ec

207 osophila community consisting of two sets of recombinant inbred lines (RILs), each derived from an ad

208 mated males and females from a panel of 144 recombinant inbred lines (RILs).

209 er) accessions of Arabidopsis thaliana using recombinant inbred lines (RILs).

210 i (QTLs) in constructed populations, such as recombinant inbred lines (RILs).

211 he 21 945 potential hybrids derived from 210 recombinant inbred lines, selection of the top 10 hybrid

212 The limited number of recombinant events in recombinant inbred lines suggests that for a biparental

213 ected significant phenotypic variation among recombinant inbred lines that comprise the mapping popul

214 mined whether ileitis in SAMP1/YitFc mice, a recombinant-inbred line that spontaneously develops ilei

215 Using RFLP analysis in recombinant inbred lines, the ferrochelatase-I gene was

216 We used maize (Zea mays) recombinant inbred lines to map a quantitative trait loc

217 o overcome variability in the assay, we used recombinant inbred lines to map this phenotype.

218 leracea We used transgressive segregation in recombinant inbred lines to test if this apparent specie

219 ing lifespan that segregate among a panel of recombinant inbred lines using a dense molecular marker

220 In the development of recombinant inbred lines using Samba Mahsuri and IR36 am

221 L linkage analysis using the A x B and B x A recombinant inbred lines verified Aod3 and confirmed lin

222 ic variation present in the wild, a panel of recombinant inbred lines was created from two heterozygo

223 for Drosophila longevity in a population of recombinant inbred lines was investigated by estimating

224 Exploiting wild accessions and recombinant inbred lines, we reveal extensive phenotypic

225 By testing a total of 25 BXD recombinant inbred lines, we were able to map a chromoso

226 A total of 156 Bambara groundnut (BGN) recombinant inbred lines were analysed for physicochemic

227 A set of recombinant inbred lines were assayed for ovariole numbe

228 Ninety-eight recombinant inbred lines were constructed from two paren

229 red the process in a set of Zea mays (maize) recombinant inbred lines with machine vision and compare

230 , and life history in a set of Brassica rapa recombinant inbred lines within and across field and gre