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3 s recently shown promise in the treatment of protozoal and fungal diseases, most notably, leishmanias
4 extensively as a drug target for bacterial, protozoal and fungal infections, and also for neoplastic
8 to opportunistic organisms-bacterial, viral, protozoal, and others-and such infections may be more se
10 , we now show that the mitogenic property of protozoal antigen preparations is in part attributable t
11 ered mammalian, plant, yeast, bacterial, and protozoal cells in seconds to minutes via a nonendocytic
12 ion (16%) while increasing local groundwater protozoal contamination (87-306%), with the largest incr
14 ecessary to improve the staining quality for protozoal cysts fixed in STF to a level comparable to th
15 ia risk: agents against amoebiasis and other protozoal diseases (106 genes, p=0.00046, pcorrected =0.
16 r the treatment of leishmaniasis, a group of protozoal diseases that includes visceral leishmaniasis,
19 12, TNF-alpha, and NO induced by E. coli and protozoal DNA were strongly correlated (r2 > 0.9) with t
22 In agreement with its unique capacity as a protozoal dsRNA virus to survive and transmit through ex
25 0)LEYEF(184)), which define the fungal/viral/protozoal family of metal-dependent RNA triphosphatases.
27 activity, was caused by the decrease in the protozoal grazing due to the higher inhibition of ciliat
28 ecology of bioengineered systems to include protozoal grazing, especially under perturbation scenari
29 be involved in host immune modulation during protozoal infection and may be useful as vaccine adjuvan
32 % with TGF-beta1, even in the face of active protozoal infection; and epithelial cell necrosis monito
33 ndependent methods for bacterial, viral, and protozoal infections (eg, polymerase chain reaction [PCR
34 eutics against HIV/AIDS-associated bacterial/protozoal infections and neoplasms, we investigated whet
36 D2 sequencing diagnosed 5 cases of invasive protozoal infections due to Toxoplasma gondii (n = 3), T
39 e crucial for immunity to many bacterial and protozoal infections, whereas Th2 cells, which make IL-4
44 nomegaly that follows a variety of viral and protozoal infections; this finding raises the question o
47 bacterial (Clostridium difficile), and three protozoal (one Giardia lamblia, two Cryptosporidium) inf
48 iviridae, along with several other groups of protozoal or fungal viruses, including Leishmania RNA vi
50 However, we and others have observed that protozoal parasite antigens can induce the proliferation
57 alus microplus ticks efficiently acquire the protozoal pathogen Babesia equi during acute and persist
59 yptosporidium parvum is a minimally invasive protozoal pathogen of intestinal epithelium that results
60 ope to provide an understanding of the human-protozoal pathogen-microbiome interaction and to specula
62 ccines targeting intracellular bacterial and protozoal pathogens are notoriously ineffective at gener
64 xamined for a range of bacterial, viral, and protozoal pathogens using traditional and molecular micr
68 d evaluated infection with 2 disease-causing protozoal pathogens, Toxoplasma gondii and Sarcocystis n
71 ila was by means of lytic enzymes within the protozoal phagosome, not by initial spore germination fo
75 w tested this class of analogs against other protozoal species: T. cruzi (Chagas disease), Leishmania
76 udied as a potential anti-cancer and/or anti-protozoal target; however, very little is known about th
81 idence indicates that at least some of these protozoal viruses can likewise enhance the pathogenicity
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