ライフサイエンスコーパス: common bean

1 0.94 Mb of sequence from Phaseolus vulgaris (common bean).

2 ification of macrosynteny between cowpea and common bean.

3 stablishment of root nodule symbiosis in the common bean.

4 eotide resolution methylomes for soybean and common bean.

5 ernational genome-sequencing project for the common bean.

6 n and the establishment of root symbiosis in common bean.

7 learly indicate a Mesoamerican origin of the common bean.

8 pper or tomato, but not to a CMV strain from common bean.

9 nto genetic improvement programs in Nigerian common beans.

10 wo varieties (Negro 8025 and Bayo Madero) of common beans.

11 eotide polymorphisms to investigate 417 wild common bean accessions and a representative sample of 16

12 soform, alpha AI-2, present in seeds of wild common bean accessions, and of two homologs, alpha AI-Pa

13 Cowpea and common bean added 4.6-5.2 g protein/d and 4-5 g indigest

14 We compared the genome for the common bean against the soybean genome to find changes i

15 elated to soybean such as pigeonpea, cowpea, common bean and others could provide a valuable and dive

16 0.23 +/- 0.21, and 0.26 +/- 0.31 for cowpea, common bean, and control, respectively), nor did the cha

17 a wide range of applications in soybean and common bean, and they have implications for improvement

18 we assessed the past and recent evolution of common bean, and traced the diversification of patterns

19 lletotrichum lindemuthianum, causal agent of common bean anthracnose.

20 Cultivated common beans are the primary protein source for millions

21 lve the ongoing debate on the origins of the common bean by investigating the nucleotide diversity at

22 ellite repeats, CentPv1 and CentPv2, and the common bean centromere-specific histone H3 (PvCENH3) wer

23 ybean), Lotus japonicus, Phaseolus vulgaris (common bean), Cicer arietinum (chickpea) and Cajanus caj

24 The single orthologous region in common bean contains approximately the same number of pa

25 train from common bean systemically infected common bean cv. Othello.

26 We also located putative areas of common bean domestication in Mesoamerica, in the Oaxaca

27 These results suggest that common bean extracts may be used as a source of anti-inf

28 is that complementary feeding with cowpea or common bean flour would reduce growth faltering and EED

29 ing and characterising some popular Nigerian common beans for their nutritive value based on seed coa

30 mapping would best be practised within each common bean gene pool.

31 gh transcriptome analysis, we identified 114 common bean genes that coexpressed with AP2-1 and propos

32 uences have evolved independently within the common bean genome, and provide insight into centromere

33 nd and gain a more in-depth knowledge of the common bean genome, the ends of a number of bacterial ar

34 nd an estimated 3- to 5-fold coverage of the common bean genome.

35 The diversity of 24 wild common bean genotypes from throughout the geographic ran

36 ate a conventional and a specific transgenic common beans, grown in greenhouse or under field conditi

37 Flavonoids and saponins from common beans have been widely studied due to their bioac

38 we show that RabA2, a monomeric GTPase from common bean, is required for the progression of the infe

39 proteins of some legumes, such as chickpea, common bean, lentil, lupin, pea, and soybean, by using t

40 localization was earlier observed in the CMS common bean line containing orf239 in the mitochondrial

41 Results suggest that peptides present in common bean NDF contributed to the antiproliferative eff

42 tudy was to characterize peptides present in common bean non-digestible fractions (NDF) produced afte

43 action of alpha AI-1 present in seeds of the common bean, of a different isoform, alpha AI-2, present

44 S-associated mitochondrial DNA sequence from common bean, orf239, was introduced into the tobacco nuc

45 ast, a double sitA mntH mutant was Fix(+) on common bean (Phaseoli vulgaris), a member of the phaseol

46 s involved in a viral resistance response in common bean (Phaseolus vulgaris cv. Othello) were identi

47 acterization of a group 6 LEA protein from a common bean (Phaseolus vulgaris L.) (PvLEA6) by circular

48 We have constructed a common bean (Phaseolus vulgaris L.) bacterial artificial

49 ymes, and chlorophyll content was studied in common bean (Phaseolus vulgaris L.) exposed to excess Mn

50 Wild common bean (Phaseolus vulgaris L.) is distributed throu

51 Among cultivated plants, common bean (Phaseolus vulgaris L.) is the most importan

52 Common bean (Phaseolus vulgaris L.) is the most importan

53 Common bean (Phaseolus vulgaris L.), the staple crop of

54 n-coding genes of a Mesoamerican genotype of common bean (Phaseolus vulgaris L., BAT93).

55 e inhibitor (alpha AI) protects seeds of the common bean (Phaseolus vulgaris) against predation by ce

56 A new study reports the genome of common bean (Phaseolus vulgaris) and genome-wide reseque

57 n attached primary monofoliate leaves of the common bean (Phaseolus vulgaris) and in early Arabidopsi

58 itrogen fixing symbiosis established between common bean (Phaseolus vulgaris) and Rhizobium etli.

59 identified in this study in closely related common bean (Phaseolus vulgaris) and soybean (Glycine ma

60 Alpha-TIP was purified from seed meal of the common bean (Phaseolus vulgaris) by membrane fractionati

61 We conducted a comprehensive analysis of common bean (Phaseolus vulgaris) centromeric satellite D

62 sets of wild and domesticated accessions of common bean (Phaseolus vulgaris) from Mesoamerica.

63 ajectories of leaf area and leaf mass in the common bean (Phaseolus vulgaris) grown in two contrastin

64 s compared among recombinant inbred lines of common bean (Phaseolus vulgaris) having four distinct ro

65 the organization of genetic variation of the common bean (Phaseolus vulgaris) in its centres of domes

66 a similar trimer is formed in planta by the common bean (Phaseolus vulgaris) NF-Y subunits, revealin

67 m sativum), clover (Trifolium pratense), and common bean (Phaseolus vulgaris) nodules.

68 report that RNAi-mediated down-regulation of common bean (Phaseolus vulgaris) PI3K severely impaired

69 Soybean (Glycine max) and common bean (Phaseolus vulgaris) share a paleopolyploidy

70 Common bean (Phaseolus vulgaris) symbiotically associate

71 haride (LPS), we identified 2,606 genes from common bean (Phaseolus vulgaris) that are differentially

72 e cluster found in soybean (Glycine max) and common bean (Phaseolus vulgaris) that is associated with

73 s found upstream of the G564 ortholog in the Common Bean (Phaseolus vulgaris), indicating that the re

74 cation event and the orthologous region from common bean (Phaseolus vulgaris), Pv5.

75 tural modeling in SimRoot indicates that, in common bean (Phaseolus vulgaris), reduced root secondary

76 t APETALA2 (AP2) transcription factor in the common bean (Phaseolus vulgaris)-Rhizobium etli symbiosi

77 t promotes the development of halo blight in common bean (Phaseolus vulgaris).

78 ne function studies in soybean as well as in common bean (Phaseolus vulgaris).

79 maize (Zea mays), peppers (Capsicum annuum), common beans (Phaseolus vulgaris), and cotton (Gossypium

80 aseolin is the major seed storage protein of common bean, Phaseolus vulgaris L., accounting for up to

81 The I locus of the common bean, Phaseolus vulgaris, controls the developmen

82 Cytoplasmic male sterility in the common bean plant is associated with a dominant mitochon

83 The basal root growth angle of an individual common bean plant, which determines the orientation and

84 al regulatory role of the miR172 node in the common bean-rhizobia symbiosis.

85 mulation and degradation of phaseolin in the common bean seed are not yet sufficiently known.

86 mmetric introgression events occurring among common bean subpopulations in Mesoamerica and across hem

87 hese eight CMV strains, only the strain from common bean systemically infected common bean cv. Othell

88 mprovement of symbiotic nitrogen fixation in common bean, the most important grain legume for human c

89 terility (cms) has been characterized in the common bean, this system would be valuable for investiga

90 illustrated by examples from wheat, barley, common bean, tomato, and pepper.

91 We expressed a common bean UPS1 transporter in cortex and endodermis ce

92 ctional properties of bean powders from four common bean varieties was investigated.

93 The polyphenols and phaseolin interaction in common bean varieties was studied.

94 These data confirm that common bean was domesticated at least twice, in Mesoamer

95 ing the genetic spatial patterns of the wild common bean, we documented the existence of several gene

96 Reference methylomes for both soybean and common bean were constructed, providing resources for in

97 rage on quality, four national accessions of common bean were submitted to two treatments, a conventi

98 v. syringae B728a is a resident on leaves of common bean, where it utilizes several well-studied viru

99 lic rich extracts obtained from two kinds of common beans, white kidney beans (WKB) and round purple