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 genes of agronomic interest such as pest and herbicide resistance.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

23 Herbicide resistance has also become a major problem, in

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

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

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

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

28 Dinitroaniline herbicide resistance in the invasive weed goosegrass was

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

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

31 Metabolic herbicide resistance in weedy plant species first became

32 Herbicide resistance in wild grasses is widespread in th

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

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

35 Herbicide resistance is an important trait often introdu

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

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

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

39 aining exclusively the initially nonselected herbicide resistance marker.

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

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

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

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

44 Herbicide-resistance mutations were introduced into SuR

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

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

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

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

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

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

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

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

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