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 ay a role in the regulation of HPR1 activity in planta, although it was not required for growth under

7 In Nicotiana benthamiana leaf cells and in planta, analysis of reporter mRNAs designed from the

8 nthesis, combined with metabolic engineering in planta, and chemical synthesis indicates several of t

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

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

11 -19-ol and germacrene-d-4-ol were detectable in planta, and gene expression analysis of the biosynthe

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

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

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

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

16 ) is able to hexosylate guanine in vitro and in planta, and SULFOTRANSFERASE 202B1 (SULT202B1) cataly

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

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

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

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

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

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

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

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

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

26 erformed to validate one of the interactions in planta, and virus-induced gene silencing was used for

27 TMV is typically produced in planta, and, as an RNA virus, is highly susceptible t

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

29 cal relationship appears to be very specific in planta, as other fatty acids (FA) desaturases do not

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

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

32 In planta, AtGRXcp expression was elevated in young coty

33 In planta, auxin is the first hormone group that was dis

34 of phases-based activity reporter of kinase) in planta, based on phase separation.

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

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

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

38 -1 knockout mutant background revealed that, in planta, both forms are negative regulators of abscisi

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

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

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

42 In planta, CAX3 null alleles were modestly sensitive to

43 hanced disease susceptibility when expressed in planta, consistent with A. candida CCG proteins being

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

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

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

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

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

49 large aggregates without the cognate Se SSU in planta, harboring active Rubisco that enables plant g

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

51 In planta, however, an excess of BCAAs suppress the expr

52 Cutin influences many biological processes in planta; however, due to its complexity and highly bra

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

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

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

56 ical and biophysical techniques in vitro and in planta, including kinase assays, microscale thermopho

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

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

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

60 In planta, increasing NEDD8 gene dosage is sufficient to

61 Our findings, both in vitro and in planta, indicate that a transition of the N-terminal

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

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

64 on the symbiosis plasmid (pSymA), validated in planta, is associated with high or low-quality symbio

65 ally occurring splice variants (SVs) of JAZ4 in planta, JAZ4.1 and JAZ4.2, and employed biochemical a

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

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

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

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

70 In planta, NatB complex formation was essential for enzy

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

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

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

74 e interaction between cryptochromes and Cop1 in planta, pointing to a common ancestor in which the cr

75 tive kinases in vitro but are phosphorylated in planta, possibly by an unknown kinase.

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

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

78 d by RT-qPCR analysis performed in vitro and in planta, proteomic analysis of the IC secretome and bi

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

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

81 gulate 76% and 87% of TF(1) indirect targets in planta, respectively.

82 In planta, Rubisco deactivated at low irradiance except

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

84 In planta, such monolignol-pCA conjugates become incorpo

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

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

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

88 3aKI and AVR3aEM proteins are equally stable in planta, suggesting that the difference in R3a-mediate

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

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

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

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

93 continue to be trained in silico rather than in planta, the best way to avoid disappointing discrepan

94 We found that, in planta, the constitutively active, GTP-bound AtGPA1(Q

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

96 expression analyses in mutants reveal that, in planta, the majority of these regulators repress the

97 In planta, their biosynthesis is still not fully charact

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

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

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

101 t-RS31 may influence its binding specificity in planta, underscoring the value of combining in vivo a

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

103 In planta, very limited information is available about h

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

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

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

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

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

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

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

111 nal characterization of enzymes in vitro and in planta, we show that geraniol is synthesized through

112 In planta, we show, via temporal additions of DOZ, that

113 ogical relevance of the CaM-based regulation in planta, where stomatal closure, induced by exogenous

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

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

116 ine and 2-phenylethyl-beta-d-glucopyranoside in planta, whereas PtAAS1 likely contributes to the herb

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

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

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

120 f infection structures and was nonpathogenic in planta, which was partially recovered by addition of

121 PRR5 can be O-fucosylated by SPY in planta, while point mutation in the catalytic domain

122 orylation occurs at multiple serine residues in planta, with S258 phosphorylation significantly reduc