ライフサイエンスコーパス: Strongyloides stercoralis

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

2 spartic protease precursor from the nematode Strongyloides stercoralis.

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

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

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

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

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

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

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

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

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

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

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

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

15 Infections with Strongyloides stercoralis are of considerable public hea

16 Strongyloides stercoralis causes chronic asymptomatic in

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

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

19 Strongyloides stercoralis hyperinfection causes high mor

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

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

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

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

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

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

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

27 Strongyloides stercoralis infection is associated with d

28 Donor-derived Strongyloides stercoralis infection occurs rarely after

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

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

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

32 Strongyloides stercoralis is a soil-transmitted helminth

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

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

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

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

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

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

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

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

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

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