ライフサイエンスコーパス: herbicide resistance

1 riers to advances in understanding metabolic herbicide resistance.

2 genetic background for a quick evolution of herbicide resistance.

3 ch hybridization may foster the evolution of herbicide resistance.

4 notype specificity and measurable changes in herbicide resistance.

5 genes of agronomic interest such as pest and herbicide resistance.

6 rice, recovering novel candidate alleles for herbicide resistance.

7 ricultural fields are well-characterized for herbicide resistance.

8 the selection of numerous genes involved in herbicide resistance.

9 due to their involvement in non-target-site herbicide resistance.

10 important implications for the management of herbicide resistance.

11 chinensis developed significantly increased herbicide resistance, accompanied by the selection of nu

12 olvement for each known MoA based on the new Herbicide Resistance Action Committee classification.

13 lications using TadDE are shown: introducing herbicide resistance alleles in OsALS and creating synon

14 sess the impact of HR cultivated rice on the herbicide resistance and population structure of weedy r

15 f rapid adaptation for important traits like herbicide resistance and stress tolerance and the effect

16 er understand weediness and the evolution of herbicide resistance and to devise new management strate

17 s biotic and abiotic stress tolerance (e.g., herbicide resistance) and sex determination.

18 ied cropping strategies aimed at controlling herbicide resistance, and estimated resulting weed densi

19 -active assessment of adaptive potential for herbicide resistance, and provides compelling evidence o

20 evance of these results to the management of herbicide resistance are discussed.

21 Most studies of herbicide resistance are performed reactively and focus

22 d provides significant new insights into the herbicide resistance as well as the origin and adaptive

23 This mechanism of synthetic auxin herbicide resistance assigns an in planta function to th

24 with a 35S enhancer tetramer and glufosinate herbicide resistance (BAR) on the mobile Ds-ATag element

25 hereas transgenic cotton with Bt protein and herbicide resistance (BtHr) did not affect herbicide use

26 ted gene flow (PMGF) is capable of spreading herbicide resistance, but the extent of PMGF has not yet

27 We report the genetic engineering of herbicide resistance by stable integration of the petuni

28 ow that the mutated gene is the cause of the herbicide resistance by using it to transform maize and

29 case of the eccDNA, demonstrate how evolved herbicide resistance can generate new insights into plan

30 Results demonstrate that herbicide resistance can spread between adjacent field p

31 edesign of plant cell walls, and deciphering herbicide resistance evolution can lead to the next gene

32 review to current understanding of metabolic herbicide resistance evolution in weedy plant species.

33 tors and provides another unique example for herbicide resistance evolution.

34 I then develop how one would use herbicide-resistance evolution as a model for studying e

35 ng-term management as numerous weeds evolved herbicide resistance following recurrent-selection with

36 Furthermore, an N-terminal portion of the herbicide resistance gene 5-enolpyruvylshikimate-3-phosp

37 s and a donor DNA construct comprising a pat herbicide resistance gene cassette flanked by short stre

38 ialaphos to test for the presence of the bar herbicide resistance gene on a cotransformed plasmid; al

39 e the pCK2 plastid vector also carried a bar herbicide resistance gene that, due to the choice of its

40 erted-repeat ends surrounding the selectable herbicide resistance gene, bar.

41 necessary to complement a non-functional pat herbicide resistance gene.

42 circumvent the potential risk of antibiotic/herbicide-resistance gene transfer into neighboring plan

43 Antibiotic and herbicide resistance genes have been used in transgene t

44 oncerns related to the use of antibiotic and herbicide resistance genes in the production of transgen

45 sformation are based on either antibiotic or herbicide resistance genes.

46 Herbicide resistance has also become a major problem, in

47 Herbicide resistance has been observed in Chloris trunca

48 Herbicide resistance has been studied for more than 60 y

49 Despite its multi-faceted nature, herbicide resistance has rarely been researched in a hol

50 Plants with incorporated pest resistance and herbicide resistance help meet these needs through incre

51 Documenting the diversity of mechanisms for herbicide resistance in agricultural weeds is helpful fo

52 dy in tobacco plastids to achieve high-level herbicide resistance in both vegetative tissues and repr

53 The evolution of herbicide resistance in crop weeds presents one of the g

54 ection pressure, leading to the evolution of herbicide resistance in hundreds of weed species.

55 pport agriculture by reversing pesticide and herbicide resistance in insects and weeds, and control d

56 e now revealing the genes endowing metabolic herbicide resistance in plants.

57 oplastic glutamine synthetase (GS2) produces herbicide resistance in the glufosinate-resistant Palmer

58 Dinitroaniline herbicide resistance in the invasive weed goosegrass was

59 r with a bar gene as a selectable marker for herbicide resistance in the plant cells.

60 gene amplification conferring field-evolved herbicide resistance in weed populations.

61 bicides has led to the repeated evolution of herbicide resistance in weeds.

62 Metabolic herbicide resistance in weedy plant species first became

63 Herbicide resistance in wild grasses is widespread in th

64 fluorescent markers instead of antibiotic or herbicide resistance increases the applicability to othe

65 different types of transgenes, for example, herbicide resistance, insect resistance, crop quality an

66 Herbicide resistance is a growing concern in this specie

67 ackgrass (Alopecurus myosuroides), for which herbicide resistance is a major economic issue.

68 Herbicide resistance is a recurrent evolutionary event t

69 Herbicide resistance is an important trait often introdu

70 In vector pMHB11, expression of herbicide resistance is dependent on conversion of an AC

71 strates and discuss our findings in terms of herbicide resistance management.

72 rge fragment of genetic material including a herbicide resistance marker gene, a 30 kb yeast genomic

73 aining exclusively the initially nonselected herbicide resistance marker.

74 Little is known about how the evolution of herbicide resistance may impact plant-herbivore interact

75 This occurrence of gene amplification as an herbicide resistance mechanism in a naturally occurring

76 The vast array of herbicide-resistance mechanisms for generalist (NTSR) an

77 Multiple-herbicide resistance (MHR) in black-grass (Alopecurus my

78 for understanding the molecular basis of the herbicide resistance mutations and cross resistance amon

79 n for local adaptation, multiple target-site herbicide resistance mutations of barnyard grasses, and

80 Given the observed frequency of herbicide resistance mutations, we calculate that there

81 Herbicide-resistance mutations were introduced into SuR

82 ver putative loci involved in nontarget-site herbicide resistance (NTSR) and to examine evolutionary

83 the genomic/genetic basis of non-target site herbicide resistance (NTSR).

84 etraploidization to the gene sources for the herbicide resistance of L. chinensis.

85 The evolution of herbicide resistance on contemporary timescales in turn

86 ates, with both agricultural populations and herbicide resistance only recently emerging in Canada.

87 Arabidopsis based on systemic expression of herbicide resistance or proherbicide sensitivity genes,

88 nes and, in the case of hr-ALS, enhanced the herbicide resistance phenotype.

89 cid substitution at Pro-196 of ALS confers a herbicide-resistance phenotype that can be used as a sel

90 Antimicrobial resistance (AMR) and herbicide resistance pose threats to society, necessitat

91 gation in the T1 generation was confirmed by herbicide resistance screening.

92 a resistance technology will augment current herbicide resistance technologies and extend their effec

93 n to a new climatic niche and acquisition of herbicide resistance, thereby fostering the establishmen

94 he ACETOLACTATE SYNTHASE gene, which confers herbicide resistance to Clearfield rice.

95 t the potency and expected durability of the herbicide resistance trait are examined.

96 k was established linking viral infection to herbicide resistance, transcriptome sequencing showed a

97 revealed that French teosintes have acquired herbicide resistance via the introgression of a mutant h

98 Moreover, in an environment of increasing herbicide resistance, with a shortage in new herbicide c