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1 t and one missense mutation Ser149Ile in the Norway rat.
2 es use three species: human, house mouse, or Norway rat.
3 sory and auditory areas than the wild-caught Norway rat.
4 studied a relatively short-lived mammal: the Norway rat.
5 w pathways and produce elevated IOP in Brown Norway rats.
6 c abdominal aorta allografts from male Brown-Norway rats.
7 t autoimmune interstitial nephritis in Brown Norway rats.
8 in the liver of Fischer 344, Lewis and Brown Norway rats.
9  marrow cells into lethally irradiated Brown Norway rats.
10 N-gamma-untreated chimeras, Lewis, and Brown Norway rats.
11  number in IFN-gamma-treated Lewis and Brown Norway rats.
12 acheal blood vessels of unanesthetized brown Norway rats.
13 B breakdown in streptozotocin-diabetic Brown Norway rats.
14 ert inflammation or fibrosis) in adult Brown Norway rats.
15 diazoxide significantly lowered IOP in Brown Norway rats.
16  determined in euthanatized, pigmented Brown Norway rats.
17 aser photocoagulation of the retina in Brown-Norway rats.
18 esthetized and mechanically ventilated Brown Norway rats.
19  placed within the vitreous chamber of Brown-Norway rats.
20 leral vein, as previously described in Brown Norway rats.
21 adult (YA; 8 months) male Fischer344 x Brown Norway rats.
22 to an episcleral vein in 20 adult male Brown-Norway rats.
23                PDT was performed in 36 Brown-Norway rats 2 weeks after laser induction of CNV.
24 esent experiment, huddles composed of infant Norway rats (2- or 8-day-olds), which produce heat endog
25 cattle (174/1,156, 15%), dogs (2/212, 0.9%), Norway rats (2/318, 0.6%), farmed swine (267/648, 41.2%)
26 s and are active in a disease relevant brown Norway rat acute OVA model of Th2-driven lung inflammati
27 ae from 30 hamsters (xenografts) or 23 Brown-Norway rats (allografts) were implanted and wrapped in t
28  preservation of livers from fed donor Brown Norway rats and 67% (8/12) survivors with donor livers f
29 bdominal aorta was harvested from male Brown Norway rats and exposed to 0, 200, or 500 ng/ml of IGF-I
30 d in an experimental glaucoma model in Brown Norway rats and in a spontaneous model of glaucoma in th
31 fects from wood mice can substitute those of Norway rats and that both species contributed to negativ
32                     Differences between wild Norway rats and their laboratory counterparts were first
33                                        Brown Norway rats are pretreated with a Lewis bone marrow infu
34  in the thoracic aorta of 36-month-old Brown Norway rats are tetraploid compared with 8% in their 3-m
35 obust retina-to-vSPVZ projection develops in Norway rats around the end of the second postnatal week
36             We therefore evaluated the Brown Norway rat as an alternative small animal model for pneu
37                                Fischer-Brown Norway rats at 10 months of age were hindlimb unloaded f
38              IOP was measured in awake Brown Norway rats before surgery and every other day after sal
39 al retinal detachments were created in Brown-Norway rats by injecting 10% hyaluronic acid into the su
40    Retinal detachments were created in Brown Norway rats by injecting 10% hyaluronic acid into the su
41                      IOP was raised in brown Norway rats by injecting hypertonic saline into the limb
42                      IOP was raised in Brown Norway rats by injecting hypertonic saline into the limb
43    Retinal detachments were created in Brown Norway rats by injection of 1% hyaluronic acid into the
44 helium (RPE) separation was created in Brown-Norway rats by subretinal injection of 1% hyaluronic aci
45  Retinal-RPE separation was created in Brown Norway rats by subretinal injection of 1% hyaluronic aci
46 d-type C57BL mice, IL-6(-/-) mice, and Brown Norway rats by subretinal injection of 1% hyaluronic aci
47                RD was induced in adult Brown Norway rats by subretinal injection of sodium hyaluronat
48 hat an HCV-related hepacivirus discovered in Norway rats can establish high-titer hepatotropic infect
49                            Heterotopic brown Norway rat cardiac isografts were removed on postoperati
50         We have established Lewis anti-Brown Norway rat CD4+ T-cell lines and confirmed their reactiv
51 performed in Lewis rat recipients from Brown-Norway rat donors.
52         Three chimeras, 3 Lewis, and 2 Brown Norway rats each received intravenous injections of gamm
53                                        Brown Norway rats, exhibiting substantial age-dependent lipofu
54                                              Norway rats express MUPs in urine but information about
55 ment organ culture and decrease IOP in Brown Norway rat eyes.
56                               The laboratory Norway rat had a larger percentage of dorsolateral corte
57                                          The Norway rat has important impacts on our life.
58 e drug to induce a similar survival of Brown Norway rat heart allografts with an equal suppression of
59 lograft rejection, Lewis recipients of Brown Norway rat heart grafts were left untreated for the firs
60                                              Norway rat hepacivirus (NrHV) infection in rats shares H
61       We infected a panel of CC strains with Norway rat hepacivirus and identified several that faile
62                                              Norway rat hepacivirus is of particular interest, as it
63 utility for reverse genetic studies, and the Norway rat hepacivirus mouse model will facilitate studi
64                                              Norway rat hepacivirus, closely related to HCV, causes c
65    Lewis rats received full-mismatched Brown Norway rat hindlimb transplants.
66  ERGs were recorded from anaesthetized Brown Norway rats in response to brief full-field flashes pres
67 from all layers of the barrel field in Brown Norway rats in vivo showed that bimodal stimulation (sim
68 odenticide treatments (to control introduced Norway rats) increased Manx shearwater breeding success.
69               Young-adult male Fischer Brown Norway rats, injected with the inhibitory opsin archaerh
70                              Thus, the Brown Norway rat is an appealing alternative small animal mode
71 te that the kidney of the normotensive Brown Norway rat is inherently much more susceptible to hypert
72  from both eyes of anaesthetized adult Brown-Norway rats (ketamine: xylazine: acepromazine, 55: 5: 1
73 f sensory cortex in four rodents: laboratory Norway rats (Long Evans; Rattus norvegicus), wild-caught
74 cytolysis of LT-sensitive (Fischer and Brown-Norway) rat macrophages.
75 accumulation of lipofuscin in the aged Brown Norway rat makes it a suitable small animal model for th
76    Retinal imaging was performed in 16 brown norway rats (N = 16 EYES; X = 372 G).
77                                        Brown Norway rats (N = 16) received unilateral episcleral vein
78       IOP was unilaterally elevated in Brown Norway rats (N = 26) by injection of hypertonic saline a
79                                        Brown-Norway rats (n = 30) were injected intravitreally with a
80                                     In Brown-Norway rats, nicotine inhibits several parameters of all
81 P was achieved manometrically in adult Brown Norway rats (nine experimental groups; n=4-7 in each; 10
82  uptake by the abdominal aorta of male Brown Norway rats occurred within 30 min.
83 rticles significantly inhibited RVP in Brown Norway rats one month after administration compared to n
84  by 24 h after sporozoite challenge in Brown Norway rats previously immunized with irradiated Plasmod
85                    Elevation of IOP in Brown Norway rats produced increased expression of ET(B) recep
86 ong triplicated alpha-globin paralogs of the Norway rat (Rattus norvegicus) and the deer mouse (Perom
87 m the nest and placed in a cool environment, Norway rat (Rattus norvegicus) pups emit ultrasonic voca
88 s, 1 striped skunk (Mephitis mephitis) and 1 Norway rat (Rattus norvegicus) were seropositive for ant
89                                              Norway rats (Rattus norvegicus) are hosts for various mi
90 invasive species, we examined the impacts of Norway rats (Rattus norvegicus) introduced to the Aleuti
91                          In contrast, infant Norway rats (Rattus norvegicus) produce heat endogenousl
92                  Eleven years after invasive Norway rats (Rattus norvegicus) were eradicated from Haw
93                                              Norway rats (Rattus norvegicus) were introduced to the F
94                                     In adult Norway rats (Rattus norvegicus), which are nocturnal, th
95 (Long Evans; Rattus norvegicus), wild-caught Norway rats (Rattus norvegicus), wild-caught California
96 or component of the behavioral repertoire of Norway rats (Rattus norvegicus).
97 ar functions in other rodents, including the Norway rat, Rattus norvegicus.
98                    It is descended from wild Norway rats, Rattus norvegicus, which despite their name
99                          Fischer 344 x Brown Norway rats received fractionated whole-brain irradiatio
100                                        Brown Norway rats received intravitreal injections of azurocid
101 ere performed between Lewis donors and Brown Norway rat recipients.
102     The present study, in male Fischer Brown Norway rats, seeks to determine the location and functio
103                          Two groups of Brown-Norway rats (sensitized and control) were exposed to aer
104 meras, 21 additional Lewis rats, and 6 Brown Norway rats served as controls.
105                       IOP elevation in Brown Norway rats showed a trend towards decreased expression
106 EW rats that have been sensitized with Brown Norway rat skin grafts on day -7.
107  When compared with Sprague Dawley and Brown Norway rats, SS rats have lower nociceptive thresholds d
108 Further, an isolated heart model using Brown Norway rats subjected to I/R injury was utilized to eval
109 ed in each of the following tissues of Brown Norway rats: the renal cortex, renal outer medulla, live
110 s sensitive enough to be used in awake Brown Norway rats, though instrument fluctuation may limit its
111 lavian vessels was transplanted from a Brown Norway rat to a Lewis rat.
112 from Lewis rats were transplanted into Brown Norway rats to induce liver rejection in untreated recip
113                                        Brown Norway rat trachea were transplanted into the greater om
114                  Donor allografts from Brown Norway rats treated with University of Wisconsin (UW) so
115 lantations were performed on Lewis and Brown Norway rats using a new model designed by our group.
116                   PDT was performed in Brown-Norway rats using laser light at a wavelength of 689 nm,
117                Diabetes was induced in Brown Norway rats using streptozotocin, and retinal vascular p
118 s old) and middle-aged (13 months old) Brown Norway rats via Silastic implants to suppress endogenous
119                                    The Brown Norway rat was recently described as a bubonic plague mo
120                             One eye of Brown-Norway rats was implanted with a cannula tethered to a p
121 ct of diazoxide on IOP in anesthetized Brown Norway rats was measured with a rebound tonometer.
122 ta transplantation from Dark Agouti to Brown Norway rats was performed.
123 and lateral ventricle of anaesthetized Brown-Norway rats were cannulated with fine-gauge needles conn
124 adult, middle age, and old Fischer 344 Brown Norway rats were compared.
125  However, when Lewis, Wistar Furth, or Brown Norway rats were immunized using a similar protocol, no
126 (3 mos) and aged (24 mos) Fisher 344 x Brown Norway rats were immunized with either M. vaccae or vehi
127                       Donor lungs from Brown Norway rats were implanted into Lewis recipients and wer
128                To test this hypothesis, male Norway rats were inoculated with Seoul virus and regulat
129                         The kidneys of Brown-Norway rats were orthotopically transplanted into bilate
130                    Fourteen adult male Brown-Norway rats were studied under anesthesia (ketamine/xyla
131                          Left lungs of Brown Norway rats were transplanted into four groups of Lewis
132              Kidneys from normotensive Brown Norway rats were transplanted into unilaterally nephrect
133 effects of nicotine on allergy/asthma, Brown Norway rats were treated with nicotine and sensitized an
134                          Sixteen adult Brown Norway rats were-administered unilateral episcleral vein
135  allogeneic tracheal grafts (Lewis and Brown Norway rats) were harvested at 2 and 4 weeks using each
136    Experimental CNV was induced in the Brown-Norway rat with a diode laser.
137 hma, treatment of ovalbumin-challenged Brown Norway rats with 0.3 to 30 mg/kg/day of 3c gave a dose-d
138 nterventions, such as the treatment of Brown Norway rats with agents resulting in polyclonal B cell s
139        PDT was performed in monkey and Brown Norway rats with laser-induced CNV.
140  cynomolgus macaques, BALB/c mice, and brown Norway rats with LcrV-derived peptides, rV10, but not rL
141 gated the relationship between small mammal (Norway rat, wood mouse and pygmy shrew) abundance and Ma

 
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