ライフサイエンスコーパス: cress

1 , human) and Arabidopsis thaliana (AT, thale cress).

2 SION 1 (TOC1) in Arabidopsis thaliana (thale cress).

3 e gene exchange between Arabidopsis and salt cress.

4 usion protein of Arabidopsis thaliana (thale cress) 4-coumaroyl-CoA ligase (At4CL1) and Vitis vinifer

5 Cress accumulated specific polyphenols at low vermicompo

6 Efficient transformation of salt cress allows for simple gene exchange between Arabidopsi

7 n of T-DNA-tagged mutant collections of salt cress, already in progress, will open the door to a new

8 Salt cress, although salt and cold tolerant, is not exception

9 ipt expression changes in germinating garden cress and Arabidopsis (Arabidopsis thaliana) seeds sugge

10 uorescence and EM studies on root cells from cress and maize.

11 ntly lower intron densities in yeasts, thale cress and mice.

12 garlic 140 mg/100 g.The Phe amount in garden cress and sunflower seed microgreen was 150 mg and 140 m

13 hydroxycinnamoyl transferase (HCT) in thale cress (Arabidopsis thaliana) and alfalfa (Medicago sativ

14 Previously, we have shown that thale cress (Arabidopsis thaliana) engineered to express two g

15 Here, we report on whole-mount ExM of thale cress (Arabidopsis thaliana) root tissues (PlantEx), ach

16 eat (Triticum aestivum cv Augusta) and thale cress (Arabidopsis thaliana), whereas the pattern of exp

17 cies including rice (Oryza sativa) and thale cress (Arabidopsis thaliana).

18 Stomata of salt cress are distributed on the leaf surface at higher dens

19 Leaves of salt cress are more succulent-like, have a second layer of pa

20 e, mouse, chicken, dog, worm, fly, rice, and cress, as well as those for a wide variety of other spec

21 In miniaturized biotests with garden cress, (-)-beflubutamid showed at least 1000x higher her

22 rized six PAT1s (Arabidopsis thaliana (thale cress), Citrus sinensis (sweet orange), Pistacia vera (p

23 Roots of salt cress develop both an extra endodermis and cortex cell l

24 la halophila (Thellungiella salsuginea; salt cress), displays extreme tolerance to high salinity, low

25 Several enterovirus genotypes and CRESS DNA genomes were associated with ICD relative to h

26 BdDV-1 is the first-described CRESS DNA mycovirus of zoosporic true fungi, with a dist

27 of all viral reads, followed by 9 to 17% for CRESS DNA virus sequences.

28 The remaining unclassified CRESS DNA virus was related to smacoviruses but possesse

29 he 3'-end of the Rep ORF in the unclassified CRESS DNA virus.

30 ce smacovirus species, ten of the identified CRESS DNA viruses are assigned to the genera Porprismaco

31 s circular Rep-encoding single-stranded DNA (CRESS DNA) viral genomes, were identified.

32 ps of circular Rep-encoding single-stranded (CRESS) DNA viruses and their related plasmids (pCRESS).

33 ated protein (Rep) encoding single-stranded (CRESS) DNA viruses detected in the faeces of Zambian non

34 ly of circular Rep-encoding single-stranded (CRESS) DNA viruses found in the human ororespiratory tra

35 monas reinhardtii, closely resembles that of CRESS-DNA viruses and other HUH endonucleases.

36 The CRESS-DNA viruses emerged via recombination between such

37 e show that the replication machinery of the CRESS-DNA viruses evolved, on three independent occasion

38 A genomes have evolved via parvoviruses from CRESS-DNA viruses.

39 d circular Rep-encoding single-stranded DNA (CRESS-DNA) virus, were also detected in nasal swabs, pos

40 articular, the circular, Rep-encoding ssDNA (CRESS-DNA) viruses show high diversity and abundance in

41 , circular Rep-encoding single-stranded DNA (CRESS-DNA) viruses, and densoviruses, and more partial g

42 Analysis of salt cress expressed sequence tags provides evidence for the

43 tire proteomes: human, mouse, rat, mouse-ear cress, fruit fly, the S. pombe yeast, the E. coli bacter

44 Salt cress is an extremophile native to harsh environments an

45 Field cress (Lepidium campestre L.), despite its potential as

46 ere studied by following individual roots of cress (Lepidium sativum L.) through reorientation and cl

47 chemical and biological potential of garden cress (Lepidium sativum L.) to receive valuable plant ex

48 ation occur during the germination of garden cress (Lepidium sativum).

49 ain a circular Rep-encoding single-stranded (CRESS)-like DNA virus, which we named Bd DNA virus 1 (Bd

50 The rice and thale cress MMGs have total lengths of 346 562 and 358 041 bp,

51 with alpha-linolenic acid (ALA) rich Garden cress oil (GCO) and assess their modulatory effect on li

52 a noticeably higher level in unstressed salt cress plants and are induced rapidly under stress.

53 mine ITCs in broccoli, white cabbage, garden cress, radish, horseradish and papaya.

54 Hybridizations of salt cress RNA targets to an Arabidopsis whole-genome oligonu

55 l properties and the aggregation behavior of cress seed mucilage (CSM)-beta-lactoglobulin (Blg) compl

56 ay datasets, one from an experiment of thale cress seedlings and the other from an experiment of maiz

57 ffected differently shoot and root length of cress seedlings in germination tests highlighting its co

58 days and do not demonstrate any toxicity for cress seeds during their growth.

59 Garden cress seeds were undergone for different processing meth

60 mitochondrial DNA segments (NUMTs) in thale cress strongly affected the frequency evaluation of the

61 veral ethyl methanesulfonate mutants of salt cress that have reduced salinity tolerance, which provid

62 Salt cress (Thellungiella halophila) is a small winter annual

63 anate-forming protein (TFP) from field-penny cress, Thlaspi arvense (Brassicaceae), is a representati

64 BAC clones to allow the chromosomes of field cress to be identified reliably.

65 This analysis suggests two CRESS virus families (Naryaviridae and Nenyaviridae) inf

66 The trio supplements five CRESS virus families already known to infect eukaryotes,

67 dy known to infect eukaryotes, extending the CRESS virus host range to protozoa.

68 Phylogenetic analysis implies CRESS viruses infecting multicellular life have evolved

69 e circular Rep-encoding single-stranded DNA (CRESS) viruses of high prevalence in healthy humans.