ライフサイエンスコーパス: Norway rat

1 sory and auditory areas than the wild-caught Norway rat.

2 studied a relatively short-lived mammal: the Norway rat.

3 marrow cells into lethally irradiated Brown Norway rats.

4 N-gamma-untreated chimeras, Lewis, and Brown Norway rats.

5 number in IFN-gamma-treated Lewis and Brown Norway rats.

6 acheal blood vessels of unanesthetized brown Norway rats.

7 diazoxide significantly lowered IOP in Brown Norway rats.

8 determined in euthanatized, pigmented Brown Norway rats.

9 aser photocoagulation of the retina in Brown-Norway rats.

10 esthetized and mechanically ventilated Brown Norway rats.

11 B breakdown in streptozotocin-diabetic Brown Norway rats.

12 placed within the vitreous chamber of Brown-Norway rats.

13 leral vein, as previously described in Brown Norway rats.

14 adult (YA; 8 months) male Fischer344 x Brown Norway rats.

15 to an episcleral vein in 20 adult male Brown-Norway rats.

16 w pathways and produce elevated IOP in Brown Norway rats.

17 ert inflammation or fibrosis) in adult Brown Norway rats.

18 c abdominal aorta allografts from male Brown-Norway rats.

19 t autoimmune interstitial nephritis in Brown Norway rats.

20 in the liver of Fischer 344, Lewis and Brown Norway rats.

21 PDT was performed in 36 Brown-Norway rats 2 weeks after laser induction of CNV.

22 esent experiment, huddles composed of infant Norway rats (2- or 8-day-olds), which produce heat endog

23 cattle (174/1,156, 15%), dogs (2/212, 0.9%), Norway rats (2/318, 0.6%), farmed swine (267/648, 41.2%)

24 s and are active in a disease relevant brown Norway rat acute OVA model of Th2-driven lung inflammati

25 ae from 30 hamsters (xenografts) or 23 Brown-Norway rats (allografts) were implanted and wrapped in t

26 preservation of livers from fed donor Brown Norway rats and 67% (8/12) survivors with donor livers f

27 bdominal aorta was harvested from male Brown Norway rats and exposed to 0, 200, or 500 ng/ml of IGF-I

28 d in an experimental glaucoma model in Brown Norway rats and in a spontaneous model of glaucoma in th

29 Brown Norway rats are pretreated with a Lewis bone marrow infu

30 in the thoracic aorta of 36-month-old Brown Norway rats are tetraploid compared with 8% in their 3-m

31 obust retina-to-vSPVZ projection develops in Norway rats around the end of the second postnatal week

32 We therefore evaluated the Brown Norway rat as an alternative small animal model for pneu

33 Fischer-Brown Norway rats at 10 months of age were hindlimb unloaded f

34 IOP was measured in awake Brown Norway rats before surgery and every other day after sal

35 al retinal detachments were created in Brown-Norway rats by injecting 10% hyaluronic acid into the su

36 Retinal detachments were created in Brown Norway rats by injecting 10% hyaluronic acid into the su

37 IOP was raised in brown Norway rats by injecting hypertonic saline into the limb

38 IOP was raised in Brown Norway rats by injecting hypertonic saline into the limb

39 Retinal detachments were created in Brown Norway rats by injection of 1% hyaluronic acid into the

40 helium (RPE) separation was created in Brown-Norway rats by subretinal injection of 1% hyaluronic aci

41 Retinal-RPE separation was created in Brown Norway rats by subretinal injection of 1% hyaluronic aci

42 d-type C57BL mice, IL-6(-/-) mice, and Brown Norway rats by subretinal injection of 1% hyaluronic aci

43 RD was induced in adult Brown Norway rats by subretinal injection of sodium hyaluronat

44 hat an HCV-related hepacivirus discovered in Norway rats can establish high-titer hepatotropic infect

45 Heterotopic brown Norway rat cardiac isografts were removed on postoperati

46 We have established Lewis anti-Brown Norway rat CD4+ T-cell lines and confirmed their reactiv

47 performed in Lewis rat recipients from Brown-Norway rat donors.

48 Three chimeras, 3 Lewis, and 2 Brown Norway rats each received intravenous injections of gamm

49 Brown Norway rats, exhibiting substantial age-dependent lipofu

50 ment organ culture and decrease IOP in Brown Norway rat eyes.

51 The laboratory Norway rat had a larger percentage of dorsolateral corte

52 e drug to induce a similar survival of Brown Norway rat heart allografts with an equal suppression of

53 lograft rejection, Lewis recipients of Brown Norway rat heart grafts were left untreated for the firs

54 Lewis rats received full-mismatched Brown Norway rat hindlimb transplants.

55 ERGs were recorded from anaesthetized Brown Norway rats in response to brief full-field flashes pres

56 from all layers of the barrel field in Brown Norway rats in vivo showed that bimodal stimulation (sim

57 Thus, the Brown Norway rat is an appealing alternative small animal mode

58 te that the kidney of the normotensive Brown Norway rat is inherently much more susceptible to hypert

59 from both eyes of anaesthetized adult Brown-Norway rats (ketamine: xylazine: acepromazine, 55: 5: 1

60 f sensory cortex in four rodents: laboratory Norway rats (Long Evans; Rattus norvegicus), wild-caught

61 cytolysis of LT-sensitive (Fischer and Brown-Norway) rat macrophages.

62 accumulation of lipofuscin in the aged Brown Norway rat makes it a suitable small animal model for th

63 Retinal imaging was performed in 16 brown norway rats (N = 16 EYES; X = 372 G).

64 Brown Norway rats (N = 16) received unilateral episcleral vein

65 IOP was unilaterally elevated in Brown Norway rats (N = 26) by injection of hypertonic saline a

66 Brown-Norway rats (n = 30) were injected intravitreally with a

67 In Brown-Norway rats, nicotine inhibits several parameters of all

68 P was achieved manometrically in adult Brown Norway rats (nine experimental groups; n=4-7 in each; 10

69 uptake by the abdominal aorta of male Brown Norway rats occurred within 30 min.

70 rticles significantly inhibited RVP in Brown Norway rats one month after administration compared to n

71 by 24 h after sporozoite challenge in Brown Norway rats previously immunized with irradiated Plasmod

72 Elevation of IOP in Brown Norway rats produced increased expression of ET(B) recep

73 ong triplicated alpha-globin paralogs of the Norway rat (Rattus norvegicus) and the deer mouse (Perom

74 m the nest and placed in a cool environment, Norway rat (Rattus norvegicus) pups emit ultrasonic voca

75 s, 1 striped skunk (Mephitis mephitis) and 1 Norway rat (Rattus norvegicus) were seropositive for ant

76 Norway rats (Rattus norvegicus) are hosts for various mi

77 invasive species, we examined the impacts of Norway rats (Rattus norvegicus) introduced to the Aleuti

78 In contrast, infant Norway rats (Rattus norvegicus) produce heat endogenousl

79 Norway rats (Rattus norvegicus) were introduced to the F

80 In adult Norway rats (Rattus norvegicus), which are nocturnal, th

81 (Long Evans; Rattus norvegicus), wild-caught Norway rats (Rattus norvegicus), wild-caught California

82 or component of the behavioral repertoire of Norway rats (Rattus norvegicus).

83 Fischer 344 x Brown Norway rats received fractionated whole-brain irradiatio

84 Brown Norway rats received intravitreal injections of azurocid

85 ere performed between Lewis donors and Brown Norway rat recipients.

86 The present study, in male Fischer Brown Norway rats, seeks to determine the location and functio

87 Two groups of Brown-Norway rats (sensitized and control) were exposed to aer

88 meras, 21 additional Lewis rats, and 6 Brown Norway rats served as controls.

89 EW rats that have been sensitized with Brown Norway rat skin grafts on day -7.

90 ed in each of the following tissues of Brown Norway rats: the renal cortex, renal outer medulla, live

91 s sensitive enough to be used in awake Brown Norway rats, though instrument fluctuation may limit its

92 from Lewis rats were transplanted into Brown Norway rats to induce liver rejection in untreated recip

93 Brown Norway rat trachea were transplanted into the greater om

94 Donor allografts from Brown Norway rats treated with University of Wisconsin (UW) so

95 PDT was performed in Brown-Norway rats using laser light at a wavelength of 689 nm,

96 Diabetes was induced in Brown Norway rats using streptozotocin, and retinal vascular p

97 s old) and middle-aged (13 months old) Brown Norway rats via Silastic implants to suppress endogenous

98 The Brown Norway rat was recently described as a bubonic plague mo

99 ct of diazoxide on IOP in anesthetized Brown Norway rats was measured with a rebound tonometer.

100 ta transplantation from Dark Agouti to Brown Norway rats was performed.

101 adult, middle age, and old Fischer 344 Brown Norway rats were compared.

102 However, when Lewis, Wistar Furth, or Brown Norway rats were immunized using a similar protocol, no

103 Donor lungs from Brown Norway rats were implanted into Lewis recipients and wer

104 To test this hypothesis, male Norway rats were inoculated with Seoul virus and regulat

105 The kidneys of Brown-Norway rats were orthotopically transplanted into bilate

106 Fourteen adult male Brown-Norway rats were studied under anesthesia (ketamine/xyla

107 Left lungs of Brown Norway rats were transplanted into four groups of Lewis

108 Kidneys from normotensive Brown Norway rats were transplanted into unilaterally nephrect

109 effects of nicotine on allergy/asthma, Brown Norway rats were treated with nicotine and sensitized an

110 Sixteen adult Brown Norway rats were-administered unilateral episcleral vein

111 allogeneic tracheal grafts (Lewis and Brown Norway rats) were harvested at 2 and 4 weeks using each

112 Experimental CNV was induced in the Brown-Norway rat with a diode laser.

113 nterventions, such as the treatment of Brown Norway rats with agents resulting in polyclonal B cell s

114 PDT was performed in monkey and Brown Norway rats with laser-induced CNV.

115 cynomolgus macaques, BALB/c mice, and brown Norway rats with LcrV-derived peptides, rV10, but not rL