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1 ), hepatitis B (0.7), hepatitis C (0.5), and Strongyloides (0.5) infections were significantly lower
2 L; -0.25 [95% CI, -.49 to -.02]; P = .04) or Strongyloides (2.34 vs 2.69 mmol/L; -0.32 [95% CI, -.53
3 minths such as Schistosoma, Nippostrongylus, Strongyloides, and Heligmosomoides potentially mitigatin
4  for diagnoses related to tuberculosis, HBV, Strongyloides, and schistosomiasis, may improve outcomes
5 testing of serum from the deceased donor for Strongyloides antibodies by enzyme-linked immunosorbent
6 lin (Ig) G or IgG4 antibody to a recombinant Strongyloides antigen (NIE) and was compared with an NIE
7 gyloides-specific IgG to the recombinant NIE-Strongyloides antigen and/or to a soluble extract of S.
8 ood mononuclear cells (PBMC) to mitogens and Strongyloides antigen.
9 tic and infectious diseases (Toxocara canis, strongyloides, filariasis, cysticercosis, fasciola, tric
10 s-specific TaqMan probe assay that conflates Strongyloides fuelleborni fuelleborni with Strongyloides
11 ri, Yersinia enterocolitica, adenovirus, and Strongyloides fulleborni in samples collected from anima
12 as9 genome editing in parasites of the genus Strongyloides, generating both knock-outs and knock-ins,
13    Soil-transmitted nematodes, including the Strongyloides genus, cause one of the most prevalent neg
14        Parasitic nematode worms of the genus Strongyloides have an alternation of many asexual, all-f
15 two renal allograft recipients who developed Strongyloides hyperinfection syndrome after receipt of o
16  two renal transplant patients who developed Strongyloides hyperinfection syndrome are reported in ca
17 2.80 mmol/L, -0.25 [-0.49,-0.02] p=0.04) and Strongyloides infected (2.34 vs 2.69mmol/L, -0.32 [-0.53
18 parasite-specific IgE and IgG4 antibodies in Strongyloides-infected patients.
19                       Moreover, treatment of Strongyloides infection resulted in a significant revers
20              Eleven of 46 (23.9%) tested for Strongyloides infection while 17 of 46 (37%) tested for
21 donors and recipients should be screened for Strongyloides infection, so that appropriate treatment c
22  systemic cytokine profile characteristic of Strongyloides infection, we measured the circulating lev
23 ause of the potential for serious disease in Strongyloides infections, there is need for improved dia
24                        Exploiting the unique Strongyloides life cycle, we compare the transcriptomes
25 ies that included data for the prevalence of Strongyloides or Schistosoma antibodies in serum or the
26                       Rhabditophanes sp. and Strongyloides ratti are placed as sister taxa, probably
27  of sRNAs in the Clade IV parasitic nematode Strongyloides ratti by comparing two genetically identic
28 w that infection with the parasitic nematode Strongyloides ratti induced upregulation of the coinhibi
29  RA signaling impaired worm expulsion during Strongyloides ratti infection, indicating functional imp
30                                              Strongyloides ratti is a common parasitic nematode of wi
31                       The parasitic nematode Strongyloides ratti reproduces by both parthenogenesis a
32 neously infected with the parasitic helminth Strongyloides ratti were investigated to understand mech
33 previously identified in the rodent parasite Strongyloides ratti.
34 ragment which specifically bound to HSP60 of Strongyloides sp. and was applied in the development of
35 ction was a heat shock protein 60 (HSP60) of Strongyloides sp. The selected scFv was applied in serod
36 tion with Schistosoma mansoni, Trichuris, or Strongyloides species and P. falciparum infection.
37          Here we compare the genomes of four Strongyloides species, including the human pathogen Stro
38 OT) candidates and recipients, we quantified Strongyloides-specific IgG to the recombinant NIE-Strong
39                       DIP-1 is found only in Strongyloides spp. and selectively interacts with DAF-12
40      The gastrointestinal parasitic nematode Strongyloides spp. has a unique life cycle that alternat
41  not been found before and may also apply to Strongyloides spp. that infect people, which will affect
42 en stimulation in individuals with LTB with (Strongyloides stercoralis (+)LTB(+)) or without S. sterc
43 G4/IgE ratio was seen in those infected with Strongyloides stercoralis (P < 0.05) and when all helmin
44 ionship between a soil-transmitted helminth, Strongyloides stercoralis (Ss), and T2DM, we examined an
45 first case of mixed pulmonary infection with Strongyloides stercoralis and Blastomyces dermatitidis.
46 ge larva (L1, L3i) of the parasitic nematode Strongyloides stercoralis and compared the results to Ca
47               The human-parasitic threadworm Strongyloides stercoralis and hookworm Ancylostoma ceyla
48 hermosensory neurons of the human threadworm Strongyloides stercoralis and show that they display uni
49 xplore the ability of eosinophils to present Strongyloides stercoralis antigen in naive and immunized
50 Purified eosinophils were exposed to soluble Strongyloides stercoralis antigens, and the expression o
51                              Infections with Strongyloides stercoralis are of considerable public hea
52                                              Strongyloides stercoralis causes chronic asymptomatic in
53 ctious stage of parasitic species, including Strongyloides stercoralis Here, we identified a parasite
54                                              Strongyloides stercoralis hyperinfection causes high mor
55                Protective immunity to larval Strongyloides stercoralis in mice has been shown to be d
56  effector cells in the secondary response to Strongyloides stercoralis in mice.
57 e and adaptive protective immunity to larval Strongyloides stercoralis in mice.
58 e and adaptive protective immunity to larval Strongyloides stercoralis in mice.
59 trophils and complement to kill the parasite Strongyloides stercoralis in vitro.
60 with (n = 25) or without (n = 25) coincident Strongyloides stercoralis infection (S. stercoralis-posi
61 uals with LTB and with or without coexistent Strongyloides stercoralis infection before and after ant
62                                              Strongyloides stercoralis infection is a neglected condi
63                                              Strongyloides stercoralis infection is associated with a
64                                              Strongyloides stercoralis infection is associated with d
65                                              Strongyloides stercoralis infection is characterized by
66                                Donor-derived Strongyloides stercoralis infection occurs rarely after
67 ciated inflammatory response in asymptomatic Strongyloides stercoralis infection, we measured the pla
68  and standardized assay for the diagnosis of Strongyloides stercoralis infection.
69 th (Ss+) or without (Ss-) seropositivity for Strongyloides stercoralis infection.
70                       Protective immunity to Strongyloides stercoralis infective larvae in mice has b
71                       The parasitic nematode Strongyloides stercoralis infects an estimated 600 milli
72                       A prevalent feature of Strongyloides stercoralis is a life-long and potentially
73                                              Strongyloides stercoralis is a soil-transmitted helminth
74                                              Strongyloides stercoralis is common among populations wi
75                                              Strongyloides stercoralis is common amongst populations
76                                              Strongyloides stercoralis is considered to be historical
77 (+) T cell responses in human infection with Strongyloides stercoralis is not well defined.
78 Necator americanus, Trichuris trichiura, and Strongyloides stercoralis soil-transmitted helminths ("A
79      The human and canine parasitic nematode Strongyloides stercoralis utilizes an XX/XO sex determin
80 ), a retrovirus, and the intestinal parasite Strongyloides stercoralis was investigated in persons in
81              The prevalence of antibodies to Strongyloides stercoralis was measured in 0-12-year-olds
82  to the infective third-stage larvae (L3) of Strongyloides stercoralis was shown to be dependent on i
83 library prepared from the infective stage of Strongyloides stercoralis were characterized.
84 testinal parasites Entamoeba histolytica and Strongyloides stercoralis were predictors of LBW despite
85 stoma duodenale and Necator americanus], and Strongyloides stercoralis).
86 e (Ss-RIOK-2) encoding gene (Ss-riok-2) from Strongyloides stercoralis, a medically important parasit
87                         Nonspecific cues for Strongyloides stercoralis, a nematode that infects human
88 L3) in several nematode parasites, including Strongyloides stercoralis, Ancylostoma spp., and Necator
89 sed based on comparisons between C. elegans, Strongyloides stercoralis, and Haemonchus contortus.
90      Results: Schistosoma mansoni, hookworm, Strongyloides stercoralis, and Mansonella perstans were
91 , Ascaris lumbricoides, Trichuris trichiura, Strongyloides stercoralis, and Necator americanus.
92 loides species, including the human pathogen Strongyloides stercoralis, and their close relatives tha
93 e frequent appearance of infections, such as Strongyloides stercoralis, commonly found in the develop
94 um, Entamoeba histolytica, Balantidium coli, Strongyloides stercoralis, cytomegalovirus, and adenovir
95 kis), proximal small bowel (Giardia lamblia, Strongyloides stercoralis, Mycobacterium avium-intracell
96 a, Mansonella perstans, Onchocerca volvulus, Strongyloides stercoralis, or Wuchereria bancrofti.
97 Rs, one each from Caenorhabditis elegans and Strongyloides stercoralis, were distinct from the coelom
98 he direct development of infective larvae of Strongyloides stercoralis, which may facilitate hyperinf
99 patients (n=21) than in uninfected (n=3) and Strongyloides stercoralis-infected patients (n=4), and g
100 ting the life cycle of the nematode parasite Strongyloides stercoralis.
101 us pacificus and targeted the human parasite Strongyloides stercoralis.
102 ecator americanus), Trichuris trichiura, and Strongyloides stercoralis.
103 spartic protease precursor from the nematode Strongyloides stercoralis.
104 n behavior of the human-infective threadworm Strongyloides stercoralis.
105 navigation in the human-infective threadworm Strongyloides stercoralis.
106 s Strongyloides fuelleborni fuelleborni with Strongyloides stercoralis.
107                  Infection with the parasite Strongyloides venezuelensis and injections of IL-3, each
108 bute to expulsion of the intestinal nematode Strongyloides venezuelensis during primary infection.
109 basophils in mice infected with the nematode Strongyloides venezuelensis exhibits a strong positive c
110 ive life cycle stages of the rodent parasite Strongyloides venezuelensis.
111 binatorial library against total proteins of Strongyloides venezuelensis.

 
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