ライフサイエンスコーパス: Strongyloides

1 for diagnoses related to tuberculosis, HBV, Strongyloides, and schistosomiasis, may improve outcomes

2 testing of serum from the deceased donor for Strongyloides antibodies by enzyme-linked immunosorbent

3 lin (Ig) G or IgG4 antibody to a recombinant Strongyloides antigen (NIE) and was compared with an NIE

4 ood mononuclear cells (PBMC) to mitogens and Strongyloides antigen.

5 ri, Yersinia enterocolitica, adenovirus, and Strongyloides fulleborni in samples collected from anima

6 as9 genome editing in parasites of the genus Strongyloides, generating both knock-outs and knock-ins,

7 Soil-transmitted nematodes, including the Strongyloides genus, cause one of the most prevalent neg

8 Parasitic nematode worms of the genus Strongyloides have an alternation of many asexual, all-f

9 two renal allograft recipients who developed Strongyloides hyperinfection syndrome after receipt of o

10 two renal transplant patients who developed Strongyloides hyperinfection syndrome are reported in ca

11 parasite-specific IgE and IgG4 antibodies in Strongyloides-infected patients.

12 Moreover, treatment of Strongyloides infection resulted in a significant revers

13 donors and recipients should be screened for Strongyloides infection, so that appropriate treatment c

14 systemic cytokine profile characteristic of Strongyloides infection, we measured the circulating lev

15 ause of the potential for serious disease in Strongyloides infections, there is need for improved dia

16 Exploiting the unique Strongyloides life cycle, we compare the transcriptomes

17 Rhabditophanes sp. and Strongyloides ratti are placed as sister taxa, probably

18 w that infection with the parasitic nematode Strongyloides ratti induced upregulation of the coinhibi

19 The parasitic nematode Strongyloides ratti reproduces by both parthenogenesis a

20 ragment which specifically bound to HSP60 of Strongyloides sp. and was applied in the development of

21 ction was a heat shock protein 60 (HSP60) of Strongyloides sp. The selected scFv was applied in serod

22 tion with Schistosoma mansoni, Trichuris, or Strongyloides species and P. falciparum infection.

23 Here we compare the genomes of four Strongyloides species, including the human pathogen Stro

24 G4/IgE ratio was seen in those infected with Strongyloides stercoralis (P < 0.05) and when all helmin

25 first case of mixed pulmonary infection with Strongyloides stercoralis and Blastomyces dermatitidis.

26 ge larva (L1, L3i) of the parasitic nematode Strongyloides stercoralis and compared the results to Ca

27 xplore the ability of eosinophils to present Strongyloides stercoralis antigen in naive and immunized

28 Purified eosinophils were exposed to soluble Strongyloides stercoralis antigens, and the expression o

29 Infections with Strongyloides stercoralis are of considerable public hea

30 Strongyloides stercoralis causes chronic asymptomatic in

31 Strongyloides stercoralis hyperinfection causes high mor

32 Protective immunity to larval Strongyloides stercoralis in mice has been shown to be d

33 effector cells in the secondary response to Strongyloides stercoralis in mice.

34 e and adaptive protective immunity to larval Strongyloides stercoralis in mice.

35 e and adaptive protective immunity to larval Strongyloides stercoralis in mice.

36 trophils and complement to kill the parasite Strongyloides stercoralis in vitro.

37 uals with LTB and with or without coexistent Strongyloides stercoralis infection before and after ant

38 Strongyloides stercoralis infection is associated with d

39 Donor-derived Strongyloides stercoralis infection occurs rarely after

40 ciated inflammatory response in asymptomatic Strongyloides stercoralis infection, we measured the pla

41 and standardized assay for the diagnosis of Strongyloides stercoralis infection.

42 Protective immunity to Strongyloides stercoralis infective larvae in mice has b

43 Strongyloides stercoralis is a soil-transmitted helminth

44 (+) T cell responses in human infection with Strongyloides stercoralis is not well defined.

45 ), a retrovirus, and the intestinal parasite Strongyloides stercoralis was investigated in persons in

46 to the infective third-stage larvae (L3) of Strongyloides stercoralis was shown to be dependent on i

47 library prepared from the infective stage of Strongyloides stercoralis were characterized.

48 testinal parasites Entamoeba histolytica and Strongyloides stercoralis were predictors of LBW despite

49 stoma duodenale and Necator americanus], and Strongyloides stercoralis).

50 e (Ss-RIOK-2) encoding gene (Ss-riok-2) from Strongyloides stercoralis, a medically important parasit

51 Nonspecific cues for Strongyloides stercoralis, a nematode that infects human

52 L3) in several nematode parasites, including Strongyloides stercoralis, Ancylostoma spp., and Necator

53 sed based on comparisons between C. elegans, Strongyloides stercoralis, and Haemonchus contortus.

54 Results: Schistosoma mansoni, hookworm, Strongyloides stercoralis, and Mansonella perstans were

55 , Ascaris lumbricoides, Trichuris trichiura, Strongyloides stercoralis, and Necator americanus.

56 loides species, including the human pathogen Strongyloides stercoralis, and their close relatives tha

57 e frequent appearance of infections, such as Strongyloides stercoralis, commonly found in the develop

58 um, Entamoeba histolytica, Balantidium coli, Strongyloides stercoralis, cytomegalovirus, and adenovir

59 a, Mansonella perstans, Onchocerca volvulus, Strongyloides stercoralis, or Wuchereria bancrofti.

60 Rs, one each from Caenorhabditis elegans and Strongyloides stercoralis, were distinct from the coelom

61 he direct development of infective larvae of Strongyloides stercoralis, which may facilitate hyperinf

62 patients (n=21) than in uninfected (n=3) and Strongyloides stercoralis-infected patients (n=4), and g

63 spartic protease precursor from the nematode Strongyloides stercoralis.

64 ecator americanus), Trichuris trichiura, and Strongyloides stercoralis.

65 Infection with the parasite Strongyloides venezuelensis and injections of IL-3, each

66 bute to expulsion of the intestinal nematode Strongyloides venezuelensis during primary infection.

67 basophils in mice infected with the nematode Strongyloides venezuelensis exhibits a strong positive c

68 binatorial library against total proteins of Strongyloides venezuelensis.