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 tal methylation differences are inherited by recombinant inbred lines.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

33 Recombinant inbred lines derived from an advanced interc

34 Recombinant inbred lines derived from Col and Cvi were u

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

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

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

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

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

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

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

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

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

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

45 Recombinant inbred lines developed from the maize (Zea m

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

75 In a recombinant inbred line mapping population, copy number

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

96 A recombinant inbred line population derived from a cross

97 In a recombinant inbred line population derived from a cross

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

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

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

101 Using a recombinant inbred line population developed from a lett

102 Screening a recombinant inbred line population developed from PI2152

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

104 1 (Tsushima, Japan) x Kas-1 (Kashmir, India) recombinant inbred line population of Arabidopsis thalia

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

106 Using a recombinant inbred line population, a separate quantitat

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

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

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

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

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

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

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

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

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

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

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

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

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

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

121 Analysis of recombinant inbred lines provides evidence that the majo

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

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

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

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

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

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

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

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

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

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

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

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

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

135 2A and ahFAD2B) to oil quality traits in two recombinant inbred line (RIL) populations.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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