ライフサイエンスコーパス: third stage

1 ion of large-input neurons is relayed to the third stage.

2 EF fractionation were further separated in a third stage.

3 lood loss compared with an intervention-free third stage.

4 rticipant from the selected household as the third stage.

5 Initial larval infection with 100 third-stage A. ceylanicum larvae resulted in predominant

6 Vaccination of mice with either third-stage Ancylostoma caninum infective hookworm larva

7 delayed growth following oral infection with third-stage Ancylostoma ceylanicum hookworm larvae.

8 layer of the cuticle of third-stage, molting third-stage, and fourth-stage larvae, the body channels

9 The third stage, based on the inferior temporal and frontal

10 llular traits and molecules pertinent to the third stage, colonization, were also affected.

11 y second or third layer, creating second- or third-stage controlled graphite intercolation compounds,

12 modules separately for the first, second and third stage, each containing both a group of co-expresse

13 ged LMCA aneurysm was observed and immediate third-stage embolisation was performed, but due to compl

14 In the third stage, females increased their reproductive invest

15 ses, host-parasite interactions during early third-stage filarial larva (L3) migration are poorly und

16 CAR gene and expanding these cells, and the third stage focuses on validating knockout efficiency an

17 so show that lin-46 is required prior to the third stage for normal adult cell fates, suggesting that

18 The third stage generates, for the major docking modes, inte

19 f laboratory animals with living irradiated, third-stage hookworm larvae (L3), we examined the antibo

20 The third stage identifies candidate genes for the remaining

21 ted Fontan procedure has been performed as a third stage in 32 patients whose median age was 28.7 mon

22 There is now compelling evidence of a third stage in the immune response, in 'tertiary lymphoi

23 ncer cases and 4,316 controls, followed by a third stage in which 30 single nucleotide polymorphisms

24 The developmentally arrested third stage infective larva of hookworms resumes develop

25 the environment as developmentally arrested third-stage infective larvae (iL3s) that navigate toward

26 3,650 PrCa cases and 3,940 controls and in a third stage involving an additional 16,229 cases and 14,

27 The third stage is myotome boundary formation, where the bou

28 The third stage is normalization, in which a local populatio

29 chitinase gene, expressed in the infective, third-stage (L3) larvae of the human filarial parasite O

30 omparing transcriptomes from linker cells of third-stage (L3) larvae, fourth-stage (L4) larvae, and n

31 s in 3311 clusters from first- and infective third-stage larva (L1, L3i) of the parasitic nematode St

32 As-p18 is not present in the post-infective third-stage larva or adult worm tissues, it appears to b

33 teine protease inhibitors on the survival of third stage larvae (L3), and the molting of L3 to L4 in

34 at contains cyclopoid copepods infected with third stage larvae of D. medinensis, but due to the meth

35 recover and resume development as postdauer third stage larvae, with the same VPC spatial-patterning

36 terning events as in continuously developing third stage larvae.

37 cts of adult hookworms but not the infective third stage larvae.

38 shment of Onchocerca volvulus infection, the third-stage larvae (L3) and the molting L3.

39 l infection is initiated by mosquito-derived third-stage larvae (L3) deposited on the skin that trans

40 Protective immunity in mice to the infective third-stage larvae (L3) of Strongyloides stercoralis was

41 n their exposure to mosquito-borne infective third-stage larvae (L3) of these parasitic helminths.

42 t antigens prepared from Onchocerca volvulus third-stage larvae (L3), molting L3 (mL3), and crude ext

43 ary and challenge infections with B. pahangi third-stage larvae (L3).

44 the ability of H. aspersa to shed infective third-stage larvae (L3s) of A. abstrusus and T. brevior

45 exposed to copepods infected with infectious third-stage larvae (L3s) of either Dracunculus insignis

46 hey were inoculated with H. bakeri infective third-stage larvae (L3s).

47 and antibody responses to infective larval (third-stage larvae [L3] and molting L3 [mL3]), adult fem

48 e body channels and multivesicular bodies of third-stage larvae and the processed material found betw

49 NSG mice were then infected with third-stage larvae and treated for 6 wk with methylpredn

50 enorhabditis elegans, developmental fates of third-stage larvae are determined in part by environment

51 mmunized with irradiated Onchocerca volvulus third-stage larvae developed protective immunity.

52 identified through the analysis of a molting third-stage larvae expressed sequence tag dataset.

53 (FEC) and immunoglobulin A activity against third-stage larvae from Teladorsagia circumcincta, as in

54 asites for at least 15 weeks, with infective third-stage larvae molting and developing into the late

55 and is expressed in microfilariae but not in third-stage larvae or adult worms.

56 expression increased following activation of third-stage larvae with serum and that the highest level

57 mmunized against O. volvulus with irradiated third-stage larvae, and it was observed that Th2 respons

58 rval stages, but also the unembryonated egg, third-stage larvae, and ovaries of adult worms, even tho

59 ation of infectious S. stercoralis infective third-stage larvae, and that these effects require the D

60 oral infection of Heligmosomoides polygyrus third-stage larvae, were given intrarectal saline or tri

61 In addition, autoinfective third-stage larvae, which initiate hyperinfection, were

62 kfly vector Simulium sp. carrying infectious third-stage larvae.

63 cts pertaining to morphogenesis of infective third-stage larvae.

64 t reduction in both molting and viability of third-stage larvae.

65 n), followed by infection with A. ceylanicum third-stage larvae.

66 equence primers to amplify a fragment from a third stage larval cDNA library by polymerase chain reac

67 The generation of second- and third-stage mass spectra in an ESI-ion trap-MS showed si

68 Third-stage mass spectrometry of the PS derivative of E2

69 calized to the basal layer of the cuticle of third-stage, molting third-stage, and fourth-stage larva

70 TECs has recently been extended to include a third stage, namely the post-Aire MHCII(lo) subset as id

71 Ascarosides secreted by the dispersal third-stage nematode LIII larvae promote beetle pupation

72 In the third stage, new epistatic QTL are searched in pairs.

73 adult molt by application of precocene II to third-stage nymphs caused a loss of br mRNA at the preco

74 The third stage of adhesion occurs as additional cells are a

75 t least rostral and caudal subdivisions as a third stage of cortical processing.

76 5 mg BID at second stage on Day 6-10 and the third stage of dorzagliatin 75 mg BID alone on Day 11-15

77 the hypotheses that active management of the third stage of labour lowers the rates of primary postpa

78 eceived oxytocin prophylactically during the third stage of labour.

79 The third stage of pregnancy was estimated from fundal heigh

80 Stalling may also occur at a third stage of translocation (III), just before release

81 TL, the statistical power for the second and third stages of analysis for mapping epistatic QTL can b

82 e NACC cohort associated with the second and third stages of CAA (2.23, 1.50-3.30, P < 0.01), LATE-NC

83 peared and diversified during the second and third stages of oxygenation.

84 e randomly assigned active management of the third stage (prophylactic oxytocic within 2 min of baby'

85 Active management of the third stage reduces the risk of PPH, whatever the woman'

86 ion amount of newly selected yeast F-78 from third-stage selection) on the level of monomeric anthocy

87 In the third stage (stage of refractory status epilepticus), a

88 Therefore, with multicomponent systems, a third stage that involves elemental redistribution withi

89 This selected population provides the third stage (the user) with an odor label that can be us

90 in the percentage of larvae molting from the third stage to the fourth stage was observed with mice i

91 ions and 5 meta-predictors, which was in the third stage used with grid cell-specific meta-predictors

92 Surprisingly, the third stage, which appears to be critical for neural fat