1 In contrast, when corneas were
scarified,
allowing virus access to other cell surfaces,
2 orneas of 6-week-old female BALB/c mice were
scarified and inoculated with HSV-1 17Syn(+) (high pheno
3 k-old) and aged (1- to 2-year-old) mice were
scarified and inoculated with P. aeruginosa.
4 ains of mice (BALB/c, A/J, and C57BL/6) were
scarified and inoculated with S. aureus strain 8325-4.
5 Corneas of BALB/c mice were
scarified and topically inoculated with 10(5) or 10(6) c
6 Corneas of BALB/c mice were
scarified and topically inoculated with 10(6) colony-for
7 Corneas of young and aged A/J mice were
scarified and topically inoculated with a log phase S. a
8 nd BALB/c mice were infected with HSV on the
scarified cornea and subjected to clinical, histologic,
9 The
scarified cornea keratitis model was modified to study P
10 counterparts were infected topically on the
scarified cornea with 2.5 x 10(5) PFU of HSV-1 strain RE
11 The effect of ETA on adherence to
scarified corneal epithelium was assessed in an in vitro
12 poptosis was detected only in the uninfected
scarified corneas and the HSV-1-infected congenic contro
13 Scarified corneas of 6-week-old female BALB/c mice were
14 lity to inhibit P. aeruginosa binding to the
scarified corneas of adult (6 weeks to 6 months of age)
15 Scarified corneas of adult B6, TLR5(-/-), Camp(-/-) (cat
16 Scarified corneas of adult BALB/c mice were topically in
17 Scarified corneas of BALB/c and C57BL/6J mice were topic
18 Scarified corneas of BALB/c mice were topically inoculat
19 Scarified corneas of female BALB/c mice were inoculated
20 Scarified corneas of immunocompetent or cyclophosphamide
21 The
scarified corneas of TLR2(-/-) mice, TLR4(-/-) mice, and
22 In
scarified corneas, P. aeruginosa PAO-A1 (LasA negative)
23 SV-1 inoculation and in uninfected mice with
scarified corneas.
24 nfection of, and spread from intact, but not
scarified,
corneas.
25 by scarification, staining was found in the
scarified epithelium of the cornea and in the unscarifie
26 s assessed ex vivo by topical inoculation of
scarified porcine or human corneas with A. nidulans stra
27 of 10(5) plaque-forming units [PFU]) in the
scarified rabbit cornea and stromal keratitis induced by
28 ated with spermidine (50 mM), and applied to
scarified rabbit corneas.
29 s with Staphylococcus aureus were applied to
scarified rabbit eyes.
30 Histopathology revealed bacteria in
scarified regions of the corneas and, for 8325-4 and DU1
31 mbranes with improved salt rejection without
scarifying the membrane permeability, which provides a n
32 Following their recovery, VV-
scarified TNFR1-/- mice were fully protected against cha
33 e following RSV challenge compared with mice
scarified with rVV expressing either wild-type or secret
34 Mice
scarified with rVV expressing the membrane-anchored G pr
35 BALB/c mice
scarified with vaccinia virus (VV) expressing the secret
36 influx following RSV challenge than do mice
scarified with VV expressing the membrane-anchored form.
37 Although mice
scarified with VV-Ftm(-) developed a slight increase in