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1 train (McKrae) that does not require corneal scarification.
2 an avirulent HSV-1 strain (RE) after corneal scarification.
3 virulent HSV-1 strain McKrae without corneal scarification.
4 se characterized by progressive interstitial scarification.
5 arvesting autologous flaps and postoperative scarification.
6 re inoculated with S aureus 2 days before VV scarification.
7 ough disrupted epidermis in a process called scarification.
8 sions, and higher skin virus levels after VV scarification.
9 FU) of adenovirus type 5 (Ad5) after corneal scarification.
10 oculated in both eyes with Ad5 after corneal scarification.
11 PF), results from aberrant wound healing and scarification.
12 noculated with Fusarium solani after corneal scarification.
13 munocompromised mice by the route of corneal scarification.
14 of Candida albicans after unilateral corneal scarification.
15  positive control) were killed 2 hours after scarification.
16 both eyes with HSV-1 McKrae after epithelial scarification.
17 he licensed vaccinia vaccine administered by scarification.
18 ved dendritic cells in the dermis after VACV scarification.
19                However, 23.5% who had tattoo/scarification, 29.6% who used injection drug, 33.3% who
20 e that cutaneous vaccinia virus infection by scarification activates dermal lymphatic capillary junct
21       Topical application without concurrent scarification also resulted in transgene delivery to 20%
22 ACAM2000 and Dryvax are administered by skin scarification and can cause progressive vaccinia, with s
23                                              Scarification and intradermal vaccine recipients who dev
24 n-1 double-KO mice were infected via corneal scarification and monitored for clinical signs of infect
25 unilateral laser-induced trabecular meshwork scarification and ocular hypertension, were observed wit
26                   Infection required corneal scarification and replication-competent virus, and the s
27                   Naive, sham-infected (post scarification), and McKrae-infected C57BL/6 corneas serv
28 ual activity, non-professional tattooing and scarification, and needle sharing.
29     Uninoculated mice that underwent corneal scarification (apoptosis positive control) were killed 2
30 r associations with incarceration, religious scarification, being stuck or cut with a bloody object,
31 uence seed germination probabilities through scarification, breaking dormancy, and preventing rotting
32 ity of a standard smallpox vaccine, given by scarification (by bifurcated needle), to induce primary
33 k conditions with three seed pre-treatments (scarification, drying and cold).
34 irulent strains of HSV-1, even after corneal scarification, had lower virus titers in the eye, had le
35 ermal inoculation of vaccinia virus (VV), or scarification, has been used effectively for the inducti
36 scular delivery and percutaneous delivery by scarification-impact several immune effectors.
37               Topical delivery after corneal scarification in both mouse and rat resulted in lacZ exp
38 5x10(5) plaque-forming units) by 15 puncture scarification in double-blind fashion.
39 in digested and undigested seeds proves that scarification in the gut is not strictly required for ge
40 riate logistic regression showed that tattoo/scarification, injection drug use, history of blood tran
41 e and behaviors by inmates such as tattooing/scarification, injection drugs use, sharing of shaving e
42     What was unappreciated was the role that scarification itself plays in generating protective immu
43                                              Scarification of individuals with atopic skin disease or
44 OP was induced in 11 rhesus monkeys by laser scarification of the trabecular meshwork.
45  of SKH1 mice (Crl:SKH1-Hrhr) with MmuPV1 by scarification on their tail resulted in three clinical o
46  avirulent HSV-1 strain RE following corneal scarification or (ii) the virulent HSV-1 strain McKrae w
47       Mice were immunized with rVV by dermal scarification or i.p. injection to determine the contrib
48  pulmonary pathology observed between dermal scarification or i.p. vaccinated mice was not reflected
49        The latter was administered either by scarification or intramuscularly.
50 led 'physical dormancy' often require either scarification or passage through an animal gut (replete
51  days (OR = 2.9; 95% CI: 1.3-6.6), religious scarification (OR = 2.8; 95% CI: 1.2-7.0), having been s
52 ntroduced into patients via a process called scarification, performed with a bifurcated needle contai
53                             These effects of scarification presumably reflect the unique immunologica
54 n with or without virus, suggesting that the scarification process itself is a major contributor to i
55                       By a wide margin, skin scarification provided the greatest protection.
56                                         Skin scarification (s.s.) with vaccinia virus (VACV) is essen
57 s (VACV) to superficially injured skin (skin scarification, s.s.).
58  infections and indicate that the process of scarification should be critically considered during the
59 e, utilized mass immunization using the skin scarification (SS) route.
60 een hours after inoculation of the cornea by scarification, staining was found in the scarified epith
61 s study, we applied vaccinia virus (VACV) by scarification to IL-1R1 knockout mice (IL-1R1(-/-)) and
62         Smallpox vaccine was administered by scarification using 15 skin punctures in the deltoid reg
63  lesions developed in a higher proportion of scarification vaccinees.
64                          Dryvax challenge by scarification was conducted in 36 healthy subjects who h
65 irculating, memory CD8(+) T cells primed via scarification were functionally superior and conferred e
66 ed that VACV infection and replication after scarification were limited to the epidermal layer of wil
67 duced in immunosuppressed mice after surface scarification, which resulted in infection and clinical
68 te were inoculated in each eye after corneal scarification with 1.5 x 10(6) plaque-forming units per
69 response occurs within the first 2 min after scarification with or without virus, suggesting that the
70 ganglia for LATs 1 and 8 weeks after corneal scarification with ribonucleotide reductase-deficient HS
71                       Rabbits vaccinated via scarification with the three attenuated derivatives (SCH
72                Treatment at the time of tail scarification with vaccinia virus did not block vaccinat
73                                    Following scarification with VV, both transgenic and wild-type mic