ライフサイエンスコーパス: post inoculation

1 tion), preceding cognitive deficits (4 weeks post-inoculation).

2 f the wheat bran particles after 20 and 40 h post inoculation.

3 cultivar IP18292 with a ~tenfold peak at 9 h post inoculation.

4 318 functional direct target genes at 14 hr post inoculation.

5 s significantly increased between 8-12 weeks post inoculation.

6 ted leaves was isolated at 3, 14 and 28 days post inoculation.

7 mixed with S. intermedius (P < 10-6) 7 days post-inoculation.

8 uantified infection load on day 8 and day 15 post-inoculation.

9 either kept constant or decreased after 72h post-inoculation.

10 ioamnionitis and fetal pathology at 72 hours post-inoculation.

11 he severity of disease from 42 until 84 days post-inoculation.

12 wer in the Sp-a(-/-) mice at all time points post-inoculation.

13 rongly and similarly induced 3 hrs and 1 day post-inoculation.

14 tected in TCV-hp-inoculated leaves at 2 days post-inoculation.

15 d to expand in both ecotypes through 10 days post-inoculation.

16 and pathogenicity level was recorded 4-days-post-inoculation.

17 e was evaluated at 3, 9, 11, 13, and 14 days post-inoculation.

18 be recovered from heart tissue 3 and 5 days post-inoculation.

19 applied every hour for 3 days, starting 1-h post-inoculation.

20 icular helper (cTfh) T cell responses 7 days post-inoculation.

21 Importantly, ototopical post-inoculation administration of a PDE4 inhibitor supp

22 ations were maintained for at least 4 months post inoculation, although the levels decreased as the c

23 nd IBD in mdr1a-/- mice within 6 to 17 weeks post-inoculation and before the expected onset of sponta

24 h mucosal IL-33 release in the first 8 hours post-inoculation and divergent CD8(+) and circulating T

25 II insert was stable for at least 18-30 days post-inoculation and had little effect on WSMV CP accumu

26 ensitized during the acute infection (3-days post inoculation) and then chronically underwent challen

27 emonstrated no viral replication or shedding post-inoculation, and all bats displayed strong secondar

28 s (BIGs), 462 were induced at or before 36 h post-inoculation, and may be involved in resistance to t

29 ociated with distinct immune responses early post-inoculation, and may provide a correlate of protect

30 ter studies indicated that as early as 1 day post-inoculation, both transcription factor genes were u

31 ats, and evaluated them 1, 2, 4 and 16 weeks post-inoculation by immunohistochemistry and immunofluor

32 xon terminals in the hippocampus from 1 week post-inoculation, concomitant with mild dopaminergic deg

33 Beginning 4 or 5 days post inoculation, cynomolgus macaques were treated once

34 crosis and limited chlorosis within 5-6 days post-inoculation (d.p.i.), which can lead to systemic ne

35 ignificantly shorter duration of shedding in post-inoculation day 10 subgroup and lower cumulative sh

36 Within 1 day post inoculation, diversity was reduced >35-fold with ex

37 e collected at 30, 60, 90, 105, and 120 days post inoculation (dpi) or at the onset of clinical signs

38 ss multiple size ranges took place at 2 days post inoculation (DPI), with higher viral RNA load found

39 eaf samples collected at 0, 1, 3, and 8 days post inoculation (DPI).

40 inical evaluation was conducted up to 7 days post inoculation (dpi).

41 gs per group were necropsied at 3 and 5 days post inoculation (dpi).

42 uc, and their tissues were assayed 3-21 days post-inoculation (dpi) for luciferase protein production

43 accumulation at 7 but not at 14 and 21 days post-inoculation (dpi) on the non-inoculated leaves of C

44 expressed genes (DEGs) in rice roots, 1 day post-inoculation (dpi) with H. seropedicae.

45 %), or remdesivir (80%), is initiated 5 days post-inoculation (dpi) with MARV, no animals survive whe

46 At 21 days post-inoculation (dpi), a 76% reduction of linamarin con

47 Seven days post-inoculation (dpi), we identified 7,627 transcripts

48 nts (from one day pre-inoculation to 57-days post-inoculation [dpi]) using direct injection mass spec

49 at the termination of the trials 25-29 days post-inoculation (Flec: 2.2 (2.4), Veh: 4.2 (4.2), P < 0

50 s were circular in profile and within 3 days post-inoculation had developed a brightly fluorescent le

51 Falpha and KC/GRO) was observed at two hours post-inoculation; however, cytokines returned to baselin

52 ponding to defined stages between 1 and 72 h post inoculation (hpi).

53 gen-processing pathways were induced at 24 h post-inoculation (hpi) and/or 48 hpi, while apoptosis an

54 ified as being modulated by TTEs within 12 h post-inoculation (hpi), 20% of which represented transcr

55 nsis adhered to passing nematodes within 8 h post-inoculation (hpi), formed an infection peg between

56 ly stage of pathogen establishment (48 hours post inoculation, hpi) to a late stage of symptom expres

57 rly response to fungus infection in RF (24 h post-inoculation-HPI), being 68-fold and 53-fold more ex

58 loss of differential gene expression at 24 h post inoculation in med15b.D mutants, suggesting that tr

59 ant viruses were rapidly eliminated 1-7 days post-inoculation in competition experiments with WT.

60 l RNA levels peak in the heart tissue 7 days post-inoculation in multiple different murine genetic ba

61 Resistance at 7 days post-inoculation in these accessions was characterized b

62 vaccinated animals obtained at 3- or 5- days post inoculation, in contrast to lungs of control animal

63 At 24 h post inoculation, intestines of each passage (F1), were

64 rease in viral population diversity at day 3 post inoculation is associated with a tenfold reduced le

65 ited increased resistance to BPH only at 3 d post-inoculation of Xoo, while the Xoo infection did not

66 va from plants with CBSD as early as 28 days post inoculation on a susceptible and a tolerant cultiva

67 mock-infected corneas were compared at 1 day post inoculation (p.i.) with a murine gene microarray.

68 in the late infection/effector phase, 9 days post inoculation (p.i.), without significant differences

69 rimary human hepatocytes (PHHs) over 32 days post-inoculation (p.i.) and modified our in-vivo agent-b

70 After a 5-day post-inoculation period, infected presumed motoneurons w

71 gy, and cytokine profiles at 6 and 19 months post inoculation (pi).

72 T. brucei DNA was detected in 85% of post-inoculation (PI) faecal samples (n = 114/134) by qP

73 raesuis at acute (8 hours (h), 24 h and 48 h post-inoculation (pi)) and chronic stages (21 days (d) p

74 RNA was detected in multiple tissues 21 days post-inoculation (pi).

75 ollow-up examination was done up to 24 weeks post-inoculation(PI).

76 ation were the first events observed (1 week post-inoculation), preceding cognitive deficits (4 weeks

77 jection with PRV, the animals survived 4-day post-inoculation prior to sacrifice and tissue processin

78 endpoint would be HCV clearance by 24 weeks post-inoculation, recognizing that the prevention of chr

79 (IAV)-infected ferrets at a fixed timepoint post-inoculation represents a frequent component of risk

80 nset of cognitive deficits, at 1 and 4 weeks post-inoculation, respectively.

81 leaves displaying HR lesions at 90 and 168 h post-inoculation, salicylate accumulation was detected p

82 s, this has been achieved as soon as 6-month post-inoculation, suggesting this sample type is a candi

83 sease model with treatment initiation 5 days post inoculation, supporting further assessment of remde

84 erm potentiation more efficiently at 4 weeks post-inoculation than pramipexole, which partially rescu

85 kinetics, with peak viral titers 48 to 72 h post-inoculation that increased by 2 to 4 log(10) PFU/ex

86 Dg93 mRNA is abundant in nodules at 4 weeks post inoculation, the earliest time assayed, and steady-

87 1 and Sgt1, is triggered between 16 and 20 h post inoculation, the same time frame that haustoria of

88 Later on, at 16 weeks post-inoculation, there was a deregulation of proteins i

89 the spinal cords of these animals at 8-12 h post inoculation; this returned to background by 72 h.

90 We used the number of days post inoculation to clinical disease to calculate the in

91 ionally, feces were collected for seven days post-inoculation to determine the effect on gut bacteria

92 Within 30 days post-inoculation, tumors in KO mice were larger than tho

93 Post-inoculation, volunteers were quarantined in functio

94 osure to bacteria during pregnancy. 3-5 days post inoculation, we assessed the presence of bacterial

95 paroscopic evaluations for four weeks and at post-inoculation week 8, to monitor upper tract infectio

96 istinct murine models of IPA on days 2 and 3 post inoculation when infection is established and activ

97 enylpropanoid genes analysed occurred at 48h post-inoculation, when decay symptoms started to appear,

98 post-challenge with virulent PEDV at 21 days post-inoculation, whereas 50% of mock-challenged piglets

99 roducing visible symptoms within 3 to 4 days post-inoculation, which led to complete fruit rot and mu

100 viral loads, antibody titers rose by day 15 post-inoculation, while in participants with low or unde

101 y in nodule development, between 12 and 96 h post inoculation with Bradyrhizobium japonicum.

102 mes higher than that in wild-type plants 6 h post inoculation with the virulent powdery mildew Golovi

103 otyledons of R and S plants at 48- and 120-h post-inoculation with LM using UPLC-QTOF/MS.

104 At 6 days post-inoculation with nod signal, ENOD40 expression was

105 transcripts were transiently upregulated 1 d post-inoculation with Pgt, but not in mock-inoculated pl

106 After 6 wk post-inoculation with Rhizophagus irregularis, root deve

107 ed with R(11) -mediated resistance at 7 days post-inoculation with rust, and uncovered the potential

108 MCA detects skin PrP(Sc) as early as 2 weeks post inoculation (wpi) in hamsters and 4 wpi in Tg40h mi