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1 ence in rabbits (based on survival following ocular infection).
2 ne model of naturally-acquired P. aeruginosa ocular infection.
3 y to delay its clearance from the eye during ocular infection.
4 of infected mice between days 1 and 5 after ocular infection.
5 fic effector T (T(eff)) cells induced during ocular infection.
6 oss lymphoid and extralymphoid tissues after ocular infection.
7 mice than in BALB/c and CBA/J mice following ocular infection.
8 ndicating the critical role of HVEM in HSV-1 ocular infection.
9 le of CXCL10 during the acute phase of HSV-1 ocular infection.
10 d disease occurs in humans following primary ocular infection.
11 imulation in susceptibility to P. aeruginosa ocular infection.
12 nd enteric washes and were protected against ocular infection.
13 for the treatment of symptomatic adenoviral ocular infection.
14 TMCs) and an IFNAR1-deficient mouse model of ocular infection.
15 A1 (sncRNA1) encoded within LAT during HSV-1 ocular infection.
16 and disease progression in a murine model of ocular infection.
17 the conjunctiva did not result in successful ocular infection.
18 ymphotropic dissemination of HSV-1 following ocular infection.
19 ding virulence and immune responses to viral ocular infection.
20 n models: mouse footpad infection and rabbit ocular infection.
21 s into immunopathological responses to viral ocular infection.
22 tics in order to gain effective control over ocular infection.
23 SE by acyclovir treatment provided 4 d after ocular infection.
24 of either receptor attenuates disease after ocular infection.
25 against herpes simplex virus type 1 (HSV-1) ocular infection.
26 ls of testican-1 after P. aeruginosa-induced ocular infection.
27 ratitis (AK) is a rare but sight-threatening ocular infection.
28 al wild-type adenoviral serotypes that cause ocular infections.
29 unoglobulin for treatment and prophylaxis of ocular infections.
30 therapy for the treatment of adenoviral (Ad) ocular infections.
31 monas aeruginosa are the leading isolates in ocular infections.
32 ence showing excellent potency in the war on ocular infections.
33 f this antiviral drug in treating adenoviral ocular infections.
34 visual outcomes in endophthalmitis and other ocular infections.
35 teria are the major contributor of bacterial ocular infections.
36 was aimed to review the bacterial profile of ocular infections.
37 ibility pattern among patients with external ocular infections.
38 s hospital infections and community-acquired ocular infections.
39 ibacterials used for empirical management of ocular infections.
40 marily on innate immunity to protect against ocular infections.
41 n be a vector for transmission of adenovirus ocular infections.
42 live attenuated vaccines against genital and ocular infections.
43 is known about the role of magA in secondary ocular infections.
44 lens could be used as a treatment for fungal ocular infections.
45 differentiate Fusarium spp. responsible for ocular infections.
46 he role of NK cells in the modulation of CMV ocular infection, 9.0 x 10(2) plaque-forming units of th
48 simplex virus type 1 (HSV-1) during primary ocular infection and after reactivation of latent infect
50 n four districts, we incorporated testing of ocular infection and serology into routine trachoma impa
54 Pneumococcus is also a major cause of human ocular infections and is commonly isolated in cases of b
56 ed in the eyes of control mice after primary ocular infection, and near-normal histology with few tac
57 ease in HSV-1-infected mice.IMPORTANCE HSV-1 ocular infections are the leading cause of corneal blind
58 s conducted among 160 patients with external ocular infections at Borumeda hospital, Northeast Ethiop
60 s latent HSV infection in the mouse model of ocular infection but has no impact on the maintenance of
62 ratory tract suspected to be responsible for ocular infections but no well-described case of D. pigru
64 are highly antibiotic resistant, and primary ocular infection by ESBL E coli has rarely been reported
65 ns of DCs to the protection afforded against ocular infection by immunization against HSV-1 and their
66 t sncRNA1 has a protective role during acute ocular infection by modulating the innate immune respons
69 ion of neutrophils during primary chlamydial ocular infection by using the guinea pig model of Chlamy
70 -associated MRSA is an important pathogen of ocular infections; CA-MRSA and HA-MRSA ocular infections
71 arises during Pseudomonas aeruginosa-induced ocular infection can trigger tissue damage resulting in
74 ulation approach to suppress the severity of ocular infections caused by herpes simplex virus infecti
75 e overlapping functions.IMPORTANCE Recurring ocular infections caused by HSV-1 can cause corneal scar
77 ility (meeting release criteria) and safety (ocular infection, corneal perforation, or graft detachme
78 y and duration of Chlamydia trachomatis (Ct) ocular infections decrease with age, suggesting developm
80 en of ocular infections; CA-MRSA and HA-MRSA ocular infections differ demographically and clinically,
81 The rare descriptions, in the literature, of ocular infections due to Pasteurella multocida include:
82 ch has targeted immune mechanisms in primary ocular infections, events that could impact chronic resp
89 d treatment of Staphylococcus aureus-induced ocular infection in both rats and rabbits compared to go
99 ainst the Zika virus (ZIKV), in general, and ocular infection, in particular, has never been investig
100 he role of neutrophils in primary chlamydial ocular infection, indicates a previously unappreciated r
104 l as well as molecular investigation on HAdV ocular infections is rather absent in Greece, which has
105 ), a subgroup D virus associated with severe ocular infections, is unable to use CAR efficiently to i
106 icroflora isolates, 0.80 (CI, 0.54-0.94) for ocular infection isolates, and 1.0 (CI, 0.45-1.0) for st
108 ied a potential target for modulation during ocular infection, macrophage migration inhibitory factor
110 nanosuspension's potential for comprehensive ocular infection management by reducing treatment freque
112 anti-HSV-1 mechanisms of murine IFN-beta in ocular infection, mice were transduced with an adenovira
114 st to provide evidence that in P. aeruginosa ocular infection, mouse strains favoring development of
118 ollowing herpes simplex virus type 1 (HSV-1) ocular infection of C57BL/6 mice, activated CD8(+) T cel
121 Conversely, forced expression of CD80 by ocular infection of mice with a recombinant HSV-1 exacer
122 dministration begun at different times after ocular infection of mice with HSV could influence the se
127 lactic Delta41Delta29 vaccination on primary ocular infection of NIH inbred mice with HSV-1 McKrae, a
138 the many problems associated with recurrent ocular infection, reducing virus reactivation should be
142 ing IL-18 to the cornea of mice before HSV-1 ocular infection resulted in reduced angiogenesis and di
144 IL-10(-/-) animals depleted of nTregs before ocular infection showed more severe SK lesions as compar
145 r System, Central Nervous System Infections, Ocular Infections, Soft Tissue Infections of the Head an
146 r System, Central Nervous System Infections, Ocular Infections, Soft Tissue Infections of the Head an
148 DeltasncRNA1 virus were more susceptible to ocular infection than their wild-type (WT) counterparts.
149 osa keratitis (or pink eye) is a challenging ocular infection that causes serious complications due t
150 C. trachomatis infection causes trachoma, an ocular infection that leads to blindness, and sexually t
151 nduced fungal keratitis is a rare but severe ocular infection that may result in significant vision i
152 tible C57BL/6J (B6) mouse to resistant after ocular infection through modulation of the inflammatory
157 moral immunity in herpes simplex virus (HSV) ocular infections was studied in immunoglobulin mu chain
159 potheses, guinea pigs with primary C. caviae ocular infections were depleted of neutrophils by using
164 participants with symptomatic ocular or peri-ocular infections who were enrolled using a consecutive
166 implex virus type 1 (HSV-1) during the acute ocular infection with and without AED treatment focusing
167 scertain the disease pattern of trachoma and ocular infection with C trachomatis in a trachoma hypere
168 ll households were examined for trachoma and ocular infection with C. trachomatis at baseline, and 6
170 s where trachoma is mesoendemic suggest that ocular infection with Chlamydia trachomatis can be elimi
173 tibiotic treatment could reduce trachoma and ocular infection with Chlamydia trachomatis in hyperende
175 reventable blindness, is produced by chronic ocular infection with Chlamydia trachomatis, an obligate
179 erpetic stromal keratitis (HSK) that follows ocular infection with herpes simplex virus (HSV) is sugg
185 f immunization strategies to protect against ocular infection with herpes simplex virus 1 (HSV-1) mus
188 infiltrates in the cornea of mice following ocular infection with herpes simplex virus 1 (HSV-1).
192 plicated in the modulation of the outcome of ocular infection with herpes simplex virus type 1 (HSV-1
193 Treatment was begun at different times after ocular infection with HSV and the outcome was assessed c
198 sion was up-regulated (10- to 20-fold) after ocular infection with HSV, an event that involved the pr
199 e between VEGF-A and sVR-1 that occurs after ocular infection with HSV, which causes prominent neovas
204 e are highly susceptible to HSV-1 infection, ocular infection with HSV-IL-4 resulted in 100% survival
208 s potential importance, the role of IL-12 in ocular infection with P. aeruginosa remains unexplored a
211 study was conducted to determine whether the ocular infection with this recombinant virus induces opt
212 prevalent among staphylococcal isolates from ocular infections, with many strains demonstrating multi
213 vation.IMPORTANCE HSV-1 is a common cause of ocular infections worldwide and a significant cause of p