ライフサイエンスコーパス: in planta,

1 studies addressing the role of auxin influx in planta, 1-NOA is likely to prove the more useful of t

2 To check this mechanism in planta, a benzyl etherification of nonesterified hydr

3 In planta, all three ZeExp mRNAs are found predominantly

4 hat R. solanacearum is essentially nonmotile in planta, although it can be highly motile in culture.

5 nts and yet did not increase during shedding in planta, although it was detectable at low levels in a

6 induced Arabidopsis plant cells, grew poorly in planta, and did not cause disease symptoms.

7 e fusion protein was assembled and expressed in planta, and functionality was confirmed by gp120 bind

8 CO and HOS1 physically interact in vitro and in planta, and HOS1 regulates CO abundance, particularly

9 ecretome of X. fastidiosa, both in vitro and in planta, and identified LesA as one of the pathogenici

10 severely compromised in its ability to grow in planta, and its growth can be partially rescued by th

11 sight into vascular development in vitro and in planta, and provide much needed markers for early vas

12 ation of BRI1 precedes association with BAK1 in planta, and that BRI1 positively regulates BAK1 phosp

13 free ubiquitin and a CEP12 peptide (GrCEP12) in planta, and that GrCEP12 suppresses resistance gene-m

14 AGB1 each physically interact with PLDalpha1 in planta, and that mutation of the so-called PLDalpha1

15 EPS production was confirmed in planta, and the amounts in bacterial biofilms greatly

16 ependent interbacterial competition activity in planta, and the C-terminal variable region of VgrG2 g

17 led structure, the function of these glycans in planta, and the mechanisms by which they are depolyme

18 d MLA10 can self-associate both in vitro and in planta, and this self-association correlates with the

19 fector genes, which may be reduced in growth in planta, and through gain-of-function assays for the a

20 irectly interacts with the Arabidopsis KDM1C in planta, and use one target gene to exemplify that bot

21 is a focal determinant of Na(+) homeostasis in planta, as either positive or negative modulation of

22 indicating post-translational modifications in planta, as was previously suggested for the S1 protei

23 -spread conidia infect ash and may sporulate in planta, as well as in forest debris.

24 In planta, AtGRXcp expression was elevated in young coty

25 The ipx genes were variably induced in planta; beta-glucuronidase reporter gene expression a

26 In planta, biliverdin IX alpha (BV) is reduced by the pl

27 for X. citri subsp. citri virulence, growth in planta, biofilm formation, catalase activity, LPS pro

28 n the physiological status of green oilseeds in planta, Brassica napus and soybean (Glycine max) seed

29 Type III genes are induced in planta, but host factors affecting the induction are

30 is necessary for natural rubber biosynthesis in planta, but yeast-expressed CPTL2 and CPT3 alone coul

31 In planta, CAX3 null alleles were modestly sensitive to

32 Therefore, in planta, CUS1 can catalyze the esterification of both

33 In planta, disrupting miRNA pairing near the center of t

34 Unexpectedly, in planta, E. coli CPS acts primarily on the sn-1 positi

35 s are uniquely relevant to rapid N signaling in planta, enriched in dynamic N-responsive genes, and r

36 anins, the health-promoting compounds which, in planta, function as colourants determining flower and

37 Following transient expression in planta, HopQ1 was shown to copurify with host 14-3-3

38 Normally, nod gene expression is repressed in planta (i.e. within nodules).

39 ation of (i) compromised fitness of bacteria in planta; (ii) decreased efficiency of type III translo

40 These loci are enriched in genes induced in planta, implicating host adaptation in genome evoluti

41 ccessfully to isolate genes that are induced in planta, including many novel genes potentially involv

42 ndirect effects of BAR-containing transgenes in planta, including modified amino acid levels, have be

43 for phosphorylation and biological functions in planta, including PTI, ET signaling, and plant growth

44 In planta, increasing NEDD8 gene dosage is sufficient to

45 acking dctA1 do not grow to wild-type levels in planta, indicating that transport and utilization of

46 In planta, IPK acts in parallel with the MVA pathway and

47 s during growth of cotyledons and 5th leaves in planta, maintaining approximately 13 mtDNA copies and

48 The Q111D and Q111E enzymes, expressed in planta, may provide a means to better define the role

49 in is proteolytically processed in yeast and in planta, most likely resulting in the production of a

50 ne its importance in detoxifying xenobiotics in planta, mutant plants where the respective gene has b

51 Infection of leaves, detached or in planta, of the coexpressing transgenic plants by toba

52 tations on protein function and localization in planta, on metal-binding properties in vitro and on p

53 s recent progress in understanding SL action in planta, particularly in the context of the regulation

54 and mediates the interaction of BSL1 with R2 in planta, possibly through the formation of a ternary c

55 ce of concatenation of the transforming DNA, in planta, prior to integration, followed by HR between

56 n insight into their capacity for moving Suc in planta, representative members of each clade were fir

57 riate plasmid constructs into tobacco leaves in planta, reproducible expression assays could be condu

58 In planta, Rubisco deactivated at low irradiance except

59 mine the influence of light on oil synthesis in planta, siliques on intact plants in full sunlight or

60 In planta, such monolignol-pCA conjugates become incorpo

61 ction (ORF8), expression of which is induced in planta, suggesting a role in the plant-pathogen inter

62 disease symptoms or bacterial multiplication in planta, suggesting that HopPtoV plays a subtle role i

63 ased when co-expressed with a functional KEG in planta, suggesting that KEG contributes to FDH degrad

64 3aKI and AVR3aEM proteins are equally stable in planta, suggesting that the difference in R3a-mediate

65 ly interacts with Arabidopsis thaliana DDB1A in planta, suggesting that WDR55 may be a novel substrat

66 Ybt was also produced by DC3000 in planta, suggesting that Ybt plays a role in DC3000 pa

67 In planta, syrM is not required for expression of syrA.

68 te-directed mutagenesis of PTOX in vitro and in planta, taking advantage null immutans alleles for th

69 In planta, the high level of expression of a deregulated

70 stemodene-derived products were not detected in planta, these results nevertheless provide a hint at

71 exerting an accurate control of ME activity in planta, through changes in metabolite and substrate c

72 We show that expressing the created enzyme in planta, thus etherifying the para-hydroxyls of lignin

73 we developed SILIP (stable isotope labeling in planta) using tomato plants (Solanum lycopersicum cv.

74 In planta, very limited information is available about h

75 m Arabidopsis and rice transiently expressed in planta, we demonstrate that a urease-UreD-UreF-UreG c

76 To explore these processes in planta, we developed a chemical genetic toolbox of ph

77 In yeast (Saccharomyces cerevisiae) and in planta, we further demonstrated by both coimmunopreci

78 Here, through a forward genetic screen in planta, we identify a conserved amino acid residue th

79 , we show that WIT1 also binds WPP1 and WPP2 in planta, we identify the chaperone heat shock cognate

80 To determine the role of potassium channels in planta, we performed a reverse genetic screen and ide

81 successfully over-express other transcripts in planta, we predict that this system will be generally

82 duced in disease symptoms and multiplication in planta, whereas DC3000 hopB1 mutants produced phenoty

83 ng completely abolished the function of DWF1 in planta, whereas partial loss of calmodulin binding re

84 sed in Psph, elicited a weak HR if expressed in planta, whereas the allele from race 1 did not.

85 function, but not for localization, of HMA4 in planta, whereas the Glu residue is important but not

86 re differentially biochemically orchestrated in planta, whereby for example they afford (+)- and (-)-