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1 t secondary sites colonized by T. gondii and succumb to infection.
2 ox Consequently, Eros-deficient mice quickly succumb to infection.
3 igeminal ganglia in mice that may ultimately succumb to infection.
4 st patients treated with chemotherapy do not succumb to infection.
5 Within 36 h, all infected mice succumbed to infection.
6 ed animals experienced rapid weight loss and succumbed to infection.
7 t, as neonatal animals lacking either factor succumbed to infection.
8 infected animals that received vehicle alone succumbed to infection.
9 increase in circulating monocytes, and they succumbed to infection.
10 ivity accelerated virus control, 50% of mice succumbed to infection.
11 ens compared with wild-type mice and rapidly succumbed to infection.
12 ly controlled parasite growth but eventually succumbed to infection.
13 sistant background recruited neutrophils and succumbed to infection.
14 of HSV-2, whereas most 5BlacZ-immunized mice succumbed to infection.
15 rvival, the reconstituted animals eventually succumbed to infection.
16 widespread virus-induced liver pathology and succumbed to infection.
17 mice: many micro MT and RAG1 mice eventually succumbed to infection.
18 ly lethal, only 50% of NiVM-infected animals succumbed to infection.
19 ls alone developed a progressive disease and succumbed to infection.
20 ice expressing the lower level of beta S all succumbed to infection.
21 e, ILC-deficient Raggammac(-/-) mice rapidly succumbed to infection.
22 tance when investigating how organisms avoid succumbing to infection.
26 nfected with larger doses of influenza, they succumbed to infection before the immune response was in
27 Animals became viremic within 4 days and succumbed to infection between 8 and 9 days, and a petec
28 hours and then rapidly decreased as animals succumbed to infection between days 5 and 8 after exposu
29 ich only one FAS2 allele was disrupted, also succumbed to infection, but mortality was not observed u
32 rium strain C5, 100% of the ICAM-1(-/-) mice succumbed to infection, compared to 30% of wild-type mic
33 , all monkeys that had received transfusions succumbed to infection concurrently with control monkeys
34 expression in T cells (GR(lck-Cre)) rapidly succumb to infection despite displaying parasite burdens
35 devoid of T cells failed to control VACV and succumbed to infection despite a marked increase in NK c
36 impaired parasite control and caused mice to succumb to infection during late acute/early chronic sta
37 robust immune response, C3.SW-H2(b)/SnJ mice succumbed to infection early and were similarly suscepti
38 ntaining Ifnar-deficient hematopoietic cells succumbed to infection early, whereas Ifnar-deficient mi
40 iking features were observed in animals that succumbed to infection, including high viral titers in a
41 t terminal stages of disease in animals that succumbed to infection, indicating substantial consumpti
42 y 120, a time when nonvaccinated guinea pigs succumbed to infection, low levels of IFN-gamma mRNA wer
46 hat survives infection than in a strain that succumbs to infection suggests that immune-mediated mech
47 the hcl1 mutant took significantly longer to succumb to infection than mice infected with the wild-ty
49 itions of lethal T. cruzi challenge, WT mice succumbed to infection whereas IFNAR(-/-) mice were ulti
50 ice developed pneumonia and splenomegaly and succumbed to infection, whereas wild-type mice cleared t
51 ith K3995 exhibited intestinal pathology and succumbed to infection, while none of those infected wit
52 es TNF-alpha, IL-6, or CC chemokine ligand 2 succumb to infection with A/Vietnam/1203/04 (H5N1) virus
55 protein of CDV vaccine strain Onderstepoort succumbed to infection with a more recent wild-type stra
58 mally (i.d.) or intranasally (i.n.) with LVS succumbed to infection with doses 2 log units less than
59 contrast to wild-type (wt) animals, rapidly succumbed to infection with either the avirulent ME49 st
61 ntrols receiving a 20% protein diet, rapidly succumbed to infection with Mycobacterium tuberculosis.
62 serum, had an increased parasite burden, and succumbed to infection with T. gondii within 20 days.
63 NK cell depletion both CD8(-/-) and WT mice succumbed to infection with the same kinetics as TAP-1(-
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