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1 FP mutant to colonize the nasopharynx of the chinchilla.
2 th the nasopharynx and the middle ear of the chinchilla.
3 t to both colonize and cause otitis media in chinchillas.
4 to the left and right middle ear cavities of chinchillas.
5 otitis media, to inoculate the middle ear of chinchillas.
6 pathogenesis of experimental otitis media in chinchillas.
7 tem efferent neurons were performed in young chinchillas.
8 BDNF transcripts were found in the untreated chinchillas.
9  auditory nerve response properties in adult chinchillas.
10  cells were recorded in the same cochleae in chinchillas.
11 s would protect against NTHi otitis media in chinchillas.
12 f type 6A-, 19A-, and 19F-challenged placebo chinchillas.
13 fection following transbullar inoculation of chinchillas.
14 ing of luciferase-producing NTHI in infected chinchillas.
15 esis were inoculated into the middle ears of chinchillas.
16                                 Although the chinchilla 3D aVOR gain changed with both frequency and
17 cantly compared to untreated chinchillas and chinchillas 4 weeks after treatment.
18 neurons in the lateral lemniscus (LL) of the chinchilla, a species with pronounced low-frequency sens
19 th nerve input, ADN cells were recorded from chinchillas after bilateral semicircular canal occlusion
20 rynges, eustachian tubes, and middle ears of chinchillas after intranasal and transbullar challenges.
21  this paradox and report that the mouse, and chinchilla, AN are mechanically sensitive, and minute me
22 f NTHi-specific bactericidal antibody in the chinchilla and also affords a reduction in the incidence
23 histochemical studies were done in the adult chinchilla and rat vestibular brainstem; diaphorase hist
24 elevated significantly compared to untreated chinchillas and chinchillas 4 weeks after treatment.
25 of sound localization in auditory neurons of chinchillas and guinea pigs of both sexes, and show how
26 esent in the vestibular ganglia of untreated chinchillas and trkB mRNA levels did not change followin
27 ishes that cochlear frequency selectivity in chinchillas (and probably in mammals in general) is full
28  The V(BM) simulation results for gerbil and chinchilla are consistent with in vivo cochlea measureme
29 al ILD sensitivity (in single neurons of the chinchilla auditory midbrain) remain robust under stimul
30 m-identification (Wiener kernel) analyses of chinchilla auditory nerve fiber responses to Gaussian no
31 re computed from existing records of cat and chinchilla auditory-nerve fibers on the basis of their c
32 align with each other, we predicted that the chinchilla aVOR would be relatively low in gain and isot
33       Here, we demonstrated that recombinant chinchilla beta defensin-1 specifically interacted with
34  the parent strain to killing by recombinant chinchilla beta-defensin 1.
35 homolog of human beta-defensin 3, designated chinchilla beta-defensin-1 (cBD-1), and found by Norther
36 essing in auditory nerve (AN) fibers of male chinchillas between two prevalent hearing loss etiologie
37 d protocols to induce the differentiation of chinchilla bone marrow precursor cells into DCs, which r
38                      Depleting complement in chinchillas by use of cobra venom factor (CoVF) rendered
39 chlear fluid model was developed for gerbil, chinchilla, cat, and human, featuring an active "push-pu
40 curred in 38%, 62%, 0, and 78% of vaccinated chinchillas challenged with types 6B, 6A, 19F, and 19A,
41 voviridae) in the genomes of the long-tailed chinchilla (Chinchilla lanigera) and the degu (Octodon d
42 genic PCho transferase (licD) mutant using a chinchilla (Chinchilla lanigera) model of otitis media.
43 responses to noise-vocoded tone complexes in chinchillas (Chinchilla laniger) using a stimulus genera
44                                              Chinchillas (Chinchilla laniger) were trained to discrim
45                                       In the chinchilla, co-administration of GM and EA can produce h
46 li at the organ of Corti (OoC) in the intact chinchilla cochlea at sites with characteristic frequenc
47 air cell (IHC) depolarization throughout the chinchilla cochlea were inferred from responses of audit
48 er responses to tones at a basal site of the chinchilla cochlea with characteristic frequency approxi
49 f our experiments on guinea pig, gerbil, and chinchilla cochleas, regardless of the sex of the animal
50                                              Chinchillas colonized by strains with the ChoP(+) phenot
51 19 per milliliter of nasal lavage fluid than chinchillas colonized with predominantly the ChoP(-) var
52 biotic delivery to the middle ear in healthy chinchillas compared with current tympanostomy tubes, wi
53 eustachian tube and inducing otitis media in chinchillas compromised by an ongoing viral upper respir
54                                          The chinchilla crista ampullaris was studied in 10 samples,
55 ceptor subunit, NR-1 was investigated in the chinchilla cristae ampullaris and utricular maculae at t
56     These data are the first to characterize chinchilla DCs and their functional properties.
57                                           As chinchilla DCs have not been described, we adapted well-
58 thermore, they suggest an important role for chinchilla DCs in the development of protective immunity
59                                    In vitro, chinchilla DCs readily internalized LB1, upregulated exp
60                        We found that SNHL in chinchillas degraded peripheral temporal coding in backg
61                                              Chinchillas discriminated either a harmonic tone complex
62 ntral nucleus of the inferior colliculus (of chinchilla) effectively encode ILDs despite complete dec
63 ns were evaluated on the cell surface in the chinchilla eustachian tube (ET) lumen of a cohort challe
64                                           As chinchillas' eyes are afoveate and never align with each
65                In contrast, the lateral-eyed chinchilla faces different adaptive demands and thus enl
66  in the vestibular end organs and ganglia of chinchillas following gentamicin ototoxicity.
67 f the animals in each group, and all treated chinchillas had sterile MEF at 24 h.
68     Here we reveal that NTHI P5 binds to the chinchilla homologue of CEACAM1 and that rabbit anti-hum
69 ilms formed by NTHI in the middle ear of the chinchilla in an experimental otitis media model, and in
70 wecA, lsgB, and siaA mutants survived in the chinchilla, inducing culture-positive middle ear effusio
71 these strains had persistence defects in the chinchilla infection model for otitis media, as well as
72 y potential glutamatergic connections of the chinchilla inferior colliculus (IC).
73 noise-vocoded tone complexes in chinchillas (Chinchilla laniger) using a stimulus generalization para
74                                 Chinchillas (Chinchilla laniger) were trained to discriminate IIRN[+]
75 n the genomes of the long-tailed chinchilla (Chinchilla lanigera) and the degu (Octodon degus).
76 ransferase (licD) mutant using a chinchilla (Chinchilla lanigera) model of otitis media.
77 the aVOR of a lateral-eyed, afoveate mammal (Chinchilla lanigera).
78 course of efferent fiber and SGN loss in the chinchilla may make it a practical model for studying me
79 y expressed Gly-Gly peptide-encoding gene in chinchilla middle ear effusions.
80  thickness and biomass for biofilms grown on chinchilla middle ear epithelial cells.
81 ast, LPS of ex vivo organisms recovered from chinchilla middle ear exudates was sialylated.
82 moniae caused a significant attenuation in a chinchilla middle ear infection model and a minor attenu
83 ot arcT, of an OM isolate is required during chinchilla middle ear infection.
84 ae (NTHI) can form biofilms during human and chinchilla middle ear infections.
85 f rbsB impaired bacterial persistence in the chinchilla middle ear, similar to our previous results w
86 HI forms biofilms in vitro as well as in the chinchilla middle ear, suggesting that biofilm formation
87                                 Furthermore, chinchilla middle ears challenged with the sapA mutant d
88 nal pathway, increases NTHI virulence in the chinchilla model for otitis media infections.
89 siaB mutants, show attenuated virulence in a chinchilla model of experimental otitis media (EOM).
90 an ex vivo middle ear (ME) aspirate from the chinchilla model of experimental otitis media is insuffi
91 on on pathogenesis and disease severity in a chinchilla model of experimental otitis media.
92                               Studies in the chinchilla model of middle ear infection demonstrated th
93 cts various aspects of NTHI virulence in the chinchilla model of nasopharyngeal colonization and otit
94    Furthermore, these data indicate that the chinchilla model of nasopharyngeal colonization provides
95 ession is upregulated in the middle ear in a chinchilla model of nontypeable Haemophilus influenzae (
96                                       In the chinchilla model of NTHi infection, we observed consiste
97 ession in one specific anatomical niche of a chinchilla model of NTHI-induced otitis media.
98 e bactericidal antibody or protection in the chinchilla model of OM.
99  The nuclease mutant formed a biofilm in the chinchilla model of otitis media and demonstrated a prop
100 ly attenuated in its ability to survive in a chinchilla model of otitis media compared with the paren
101 infection with Haemophilus influenzae in the chinchilla model of otitis media results in the formatio
102            Analyses of a modA2 strain in the chinchilla model of otitis media show a clear selection
103          In vivo infection studies using the chinchilla model of otitis media showed a direct correla
104       In vitro and in vivo studies using the chinchilla model of otitis media were performed using a
105                                    We used a chinchilla model of otitis media, which has previously b
106    Various types of MEEs and biofilms in the chinchilla model were identified, which showed comparabl
107                                          The chinchilla model will likely be extremely useful to test
108 ponse of biofilms and MEEs in the OM-induced chinchilla model, the standard model for human OM.
109 nasopharynx and invade the middle ear in the chinchilla model.
110 enge of the middle ear were evaluated in the chinchilla model.
111 transbullar inoculation was evaluated in the chinchilla model.
112 -di-GMP), flagella, and quorum sensing--in a chinchilla model.
113 eduction in pneumococcal colonization in the chinchilla model.
114 es for their relative protective efficacy in chinchilla models of otitis media.
115                Herein, we describe mouse and chinchilla models of RSV infection of the nasopharynx an
116 y of immunogens derived from this adhesin in chinchilla models support the continued development of P
117  vivo, LB1-activated DCs trafficked from the chinchilla nasal cavity primarily to the nasal-associate
118 or P5), is essential for colonization of the chinchilla nasopharynx and infection of the middle ear.
119  ability of M. catarrhalis to survive in the chinchilla nasopharynx over a 3-day period.
120  ability of M. catarrhalis to persist in the chinchilla nasopharynx were upregulated in the mesR muta
121 onic antigen blocks NTHI colonization of the chinchilla nasopharynx, providing the first demonstratio
122  exhibit a reduced ability to survive in the chinchilla nasopharynx.
123 s and theta cells) were identified in intact chinchillas, no direction-specific activity was seen aft
124                                      Using a chinchilla OM infection model, we demonstrated that H. p
125 tC of NTHI strain 2019 were evaluated in the chinchilla OM model.
126 otypes within serogroups was measured in the chinchilla otitis media (OM) model because several serot
127 arcD and arcT are potentially essential in a chinchilla otitis media (OM) model.
128 zed middle ear inflammatory responses in the chinchilla otitis media model after injecting a very sma
129 of H. influenzae attenuated virulence in the chinchilla otitis media model of noninvasive disease.
130        We conclude from these studies that a chinchilla otitis media model provides a means to evalua
131                            LOS purified from chinchilla-passed NTHi 86-028NP had increased PCho conte
132 m; diaphorase histochemistry was done in the chinchilla periphery.
133 or LPD-LB1(f)2,1,3 to adenovirus-compromised chinchillas, prior to intranasal challenge with nontypea
134 following intranasal challenge; however, the chinchilla proved to be more permissive than the mouse.
135 l clusters in the cochlear nerve root of the chinchilla provide the simplest example of this structur
136 r otolithic organs, and Scarpa's ganglia) in chinchilla, rat, and guinea pig were examined for immuno
137 ips between fecal pellet diameters from ashy chinchilla rats (Abrocoma cinerea) and mean annual rainf
138                                              Chinchillas received three monthly subcutaneous injectio
139                                  Fifty-eight chinchillas received three subcutaneous or intramuscular
140 8 and 51%, respectively, in the P6-immunized chinchillas relative to the sham-immunized cohort.
141 ory epithelial cells, in colonization of the chinchilla respiratory tract as well as a requirement fo
142 ances into the endolymph or perilymph of the chinchilla's cochlea and then used scanning laser interf
143 reactivity of a panel of high-titered immune chinchilla sera to the 8- to 10-mer peptides representin
144 ly sensitive to the bactericidal activity of chinchilla serum and thus did not survive.
145 mals formerly immunized with PE-PilA, and in chinchillas, signs of otitis media were significantly re
146 IRN[-] test stimuli were more variable among chinchillas, suggesting that IIRN[-] did not evoke simil
147 ithelium with morphophysiological studies in chinchilla suggests that the labeled population consists
148 te outer-face ribbons being more numerous in chinchilla than in squirrel monkey, afferent discharge p
149 pithelium lining the uppermost airway of the chinchilla, the established rodent host for the study of
150       In the vestibular ganglia of untreated chinchillas, the level of expression of BDNF mRNA is low
151 d in a sensitized background provided by the chinchilla (Tyrc-ch) mutation, which uncovers a phenotyp
152 ession of the sap operon within sites of the chinchilla upper airway upon infection.
153 ease in children and experimental disease in chinchillas, we found a hierarchical pattern of immunodo
154                                 In 11 normal chinchillas, we recorded binocular 3D eye movements in d
155    A total of 48 research-grade, young adult chinchillas weighing 500 g were used for 2 series of ani
156                                  Young adult chinchillas were atraumatically inoculated with Moraxell
157                                              Chinchillas were challenged with NTHI variant population
158                                              Chinchillas were exposed to an impulse noise at 155 dB p
159                                              Chinchillas were given tetravalent vaccine composed of p
160                                              Chinchillas were immunized subcutaneously with either th
161            Data from a second study, wherein chinchillas were immunized with LB1 or lipoprotein D, ea
162                                              Chinchillas were immunized with P6 and challenged 10 day
163                                         When chinchillas were immunized with recombinant P1 (rP1) obt
164  To test this hypothesis, the middle ears of chinchillas were infected with either a strain of GAS ca
165                                              Chinchillas were infected with nontypeable Haemophilus i
166                                              Chinchillas were infected with S. pneumoniae TIGR4 and e
167  time course of efferent fiber and SGN loss, chinchillas were injected with GM (125 mg/kg IM) followe
168                          Both middle ears of chinchillas were inoculated with one of the three pneumo
169                                              Chinchillas were passively immunized here with serum spe
170                                              Chinchillas were psychophysically trained and tested bef
171 dle ear fluids sequentially recovered from a chinchilla with an ongoing NTHI-induced otitis media (OM
172  media (OM) after intranasal immunization of chinchillas with an NTHI P5-derived synthetic peptide im
173 ingle auditory nerve fibers were measured in chinchillas with complete cochlear de-efferentation prod
174 ys post-transbullar challenge, the number of chinchillas with middle ear fluid and the incidence of N
175 ech sentence in noise from anesthetized male chinchillas with normal hearing (NH) or noise-induced he
176                                              Chinchillas with psychophysical evidence of chronic tinn

 
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