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1 (7.8% to 0%), roundworm (33.5% to 6.1%), and whipworm (42.7% to 8.9%).
2 .1% to 1.3%), roundworm (28.4% to 0.9%), and whipworm (51.9% to 31.9%).
3 .3% to 1.9%), roundworm (34.5% to 2.3%), and whipworm (55.5% to 40.3%).
4 4% to 85.2%), roundworm (22.8% to 1.4%), and whipworm (86.8% to 59.5%), while albendazole alone signi
5 0% to 71.8%), roundworm (62.0% to 1.4%), and whipworm (93.1% to 74.5%).
6 ainst evolutionarily distant Trichuris muris whipworm adults.
7 single-species), 5 potential pan-intestinal (whipworm and hookworm) and 6 pan-Phylum Nematoda (intest
8  instigating the host immune response to the whipworm and tissue repair.
9 bacillary band and stichosome, found only in whipworms and related parasites.
10 ts unravel intestinal epithelium invasion by whipworms and reveal specific host-parasite interactions
11 al dwelling nematodes Trichuris trichiura (a whipworm) and Ascaris lumbricoides (a roundworm), respec
12 nsmitted nematodes (STNs), namely hookworms, whipworms, and ascarids, are extremely common parasites,
13 ansmitted helminths or nematodes (hookworms, whipworms, and Ascaris) are roundworms that infect more
14                                              Whipworms are common soil-transmitted helminths that cau
15                                              Whipworms are large metazoan parasites that inhabit mult
16                                    Trichuris whipworms cause disease and morbidity in humans and othe
17                                              Whipworm egg counts were determined for 1,253 members of
18               Using RNA sequencing data from whipworm-infected mice, we describe the regulated T help
19 he continent-scale genetic structure between whipworms infecting humans and baboons relative to those
20 ne caecaloids, the first in-vitro system for whipworm infection and organoid model for live helminths
21 re of pathogen interactions and suggest that whipworm infection is a risk factor for coinfections wit
22 ence for 2 QTL influencing susceptibility to whipworm infection, one located on chromosome 9 (logarit
23 both these aspects using the murine model of whipworm infection, Trichuris muris.
24 low-up study of significant heritability for whipworm infection, we conducted the first genome scan f
25 st-parasite interactions that define chronic whipworm infection.
26 he determinants of genetic predisposition to whipworm infection.
27  located on chromosomes 12 and 13 influenced whipworm infection.
28 roximal colon in response to Trichuris suis (whipworm) infection using 16S rRNA gene-based and whole-
29                                   Trichuris (whipworm) infects 1 billion people worldwide and causes
30 /S protein of Trichuris trichiura, the human whipworm, is a highly immunogenic 47-kDa protein that ha
31 We report a case of human infection with the whipworm of dogs, Trichuris vulpis, in a woman with duod
32 , leishmaniasis, Chagas' disease, roundworm, whipworm, pinworm, Chinese liver fluke, fleas and lice.
33 dies report genomic data on three species of whipworm, soil-transmitted parasitic worms responsible f
34 y, T. vulpis ova resemble those of the human whipworm (T. trichiura) but are nearly twice their size.
35 ic host-parasite interactions that allow the whipworm to establish its multi-intracellular niche.
36            In this study, we used the murine whipworm Trichuris muris to investigate the effect of th
37 he genome-scale metabolic model of the mouse whipworm Trichuris muris.
38 enera pathogenic for humans and animals: the whipworm Trichuris sp., the roundworm Ascaris sp., the f
39 rticular, administration of ova from the pig whipworm Trichuris suis (T. suis; TSO) has been proposed
40                                      The pig whipworm Trichuris suis is important in swine production
41 opical disease trichuriasis is caused by the whipworm Trichuris trichiura, a soil-transmitted helmint
42                              Eggs of the pig whipworm (Trichuris suis ova) have been shown to be safe
43                                          The whipworm (Trichuris suis) secretes prostaglandin E2 to s
44 ike hookworm (Necator americanus) or porcine whipworm (Trichuris suis) show that they are safe and ma
45                                              Whipworm (Trichuris trichiura) infection is a soil-trans
46                    Infection with intestinal whipworms (Trichuris spp.) causes widespread morbidity a
47         The orthologue of p43 from the human whipworm, Trichuris trichiura, exhibits similar lipid-bi
48 lostomaduodenale and Necator americanus, the whipworm Trichuristrichiura, and the large roundworm Asc
49 l trials have been performed mainly with pig whipworm, which was chosen because it is likely to be no