ライフサイエンスコーパス: Fischer rat

1 female Lewis relative to the histocompatible Fischer rat.

2 tion was performed in (DPPIV)-deficient F344-Fischer rats.

3 xual receptivity in adult, regularly cycling Fischer rats.

4 putamen (CPu) and nucleus accumbens (NAc) of Fischer rats.

5 with more pronounced effect in Lewis than in Fischer rats.

6 Fos protein levels in the caudate/putamen of Fischer rats.

7 adenovirally transduced into MSCs from male Fischer rats.

8 car of a 1-week-old myocardial infarction in Fischer rats.

9 adenocarcinoma nodules were implanted in 250 Fischer rats.

10 rcinoma (1.1-1.4 cm) was implanted in female Fischer rats.

11 e-a dose that induced CPP in male and female Fischer rats.

12 were implanted subcutaneously in 132 female Fischer rats.

13 own within the mammary fat pads of 19 female Fischer rats.

14 ors (1.3-1.5 cm) were implanted in 48 female Fischer rats.

15 ) were implanted subcutaneously in 84 female Fischer rats.

16 detected in the bile and urine samples from Fischer rats.

17 e points after 70% hepatectomy in adult male Fischer rats.

18 rmed in young (4 months) and old (24 months) Fischer rats.

19 partly the defecation response in Lewis and Fischer rats.

20 drug-preferring Lewis rats and absent in the Fischer rats.

21 dividing cells in 13- to 14-week-old, intact Fischer rats.

22 by a metabolism study of 166Hox@C82(OH)y in Fischer rats.

23 ralateral brainstem of adult Charles-derived Fischer rats.

24 F2 intercross population bred from Lewis and Fischer rats.

25 lanted into the liver of an inbred strain of Fischer rats.

26 lanted into the right cerebral hemisphere of Fischer rats.

27 disease progression and death in susceptible Fischer rats and BALB/c mice challenged with LT.

28 IL-12 coadministered to Fischer rats and C57BL/6 mice at the time of S3 vaccinat

29 Tissue distribution studies in normal Fischer rats and Fischer rats implanted intracranially w

30 disease progression and death in susceptible Fischer rats and increased survival in BALB/c mice after

31 avioral responses to psychoactive drugs than Fischer rats and they fail to show biochemical adaptatio

32 tereotactically implanted into the brains of Fischer rats, and 2 weeks later biodistribution studies

33 cal displacement SCI was performed in female Fischer rats, and behavior was assessed for 8 weeks.

34 gglutinin B (rHag B), using the conventional Fischer rat as the experimental animal model.

35 THRP) in cerebral tissue was studied in male Fischer rats at 4, 12 and 24 months of age during euthyr

36 Fischer rats bearing 9L s.c. tumors were given injection

37 Cardiomyocytes from neonatal Fischer rats (both sexes) or medium were injected into t

38 d deficits in PPI in both Sprague-Dawley and Fischer rats but had no effect in Lewis rats.

39 tyrosine hydroxylase compared to that of the Fischer rat by blot immunolabeling procedures.

40 sacral spinal cord (L6-S1) in both Lewis and Fischer rats compared with non stress groups.

41 on showed a commodity-by-strain interaction: Fischer rats defended consumption with greater vigor whe

42 ted in athymic mice bearing s.c. tumors from Fischer rat embryo fibroblasts transfected with erbB2.

43 Relative to Lewis rats, Fischer rats exhibit greater avoidance of a saccharin cu

44 Lewis and Fischer rats exhibited lower startle reactivity than Spr

45 Germ-free Fischer rats fed a diet containing 5% sucrose were infec

46 postlabeling in liver, kidney, and uterus of Fischer rats given TAM or TOR in the diet for 18 months.

47 Since Lewis and Fischer rats have opposite susceptibility to experimenta

48 border zone of subacute infarcted syngeneic Fischer rat hearts and compared with medium-injected con

49 tribution studies in normal Fischer rats and Fischer rats implanted intracranially with 9L gliosarcom

50 /kg Salmonella enteritidis endotoxin to male Fischer rats induced a drastic but transient activation

51 duced suppression of saccharin intake by the Fischer rats is not likely mediated by differences in se

52 Compared to Fischer rats, Lewis rats acquired cocaine self-administr

53 induced complete remission in the syngeneic Fischer rat model of NK-cell leukemia.

54 /partial hepatectomy (PH) in a DPPIV- mutant Fischer rat model.

55 to the wall of the abdominal aorta in female Fischer rats (n=22 in each group).

56 Among the traits studied in Lewis and Fischer rats, one seemed most amenable to quantitative t

57 Male Fischer rats showed a significantly attenuated HPA axis

58 Fischer rat SMCs were stably transfected with a cDNA for

59 Fischer rat SMCs were transduced in vitro with a retrovi

60 We used Fischer rat smooth muscle cells (SMCs) overexpressing MM

61 t in Wistar rats (allogeneic) as compared to Fischer rats (syngeneic).

62 We investigated the ability of Fischer rat T9 glioblastoma cells transduced with cDNA g

63 dose-related responding to cocaine, although Fischer rats tended to show higher response rates.

64 In Fischer rats, there was no increase in 5-HT (6% +/- 7: P

65 EG), or both, were transplanted in the adult Fischer rat thoracic (T9) spinal cord 1 week after a mod

66 In Fischer rat thyroid (FRT) cells, which express low level

67 regulates ENaC in two epithelial cell lines (Fischer rat thyroid and H441); small interfering RNA (si

68 Moreover, TSA increased ENaC current in Fischer rat thyroid and kidney collecting duct epithelia

69 Fischer rat thyroid cells expressing CFTR and a halide-s

70 luorometric measurements of iodide influx in Fischer rat thyroid cells expressing DeltaF508-CFTR show

71 ASK-3 channels were transiently expressed in Fischer rat thyroid cells, and their function was studie

72 pha, beta, and gammaENaC were coexpressed in Fischer rat thyroid epithelia to generate apical Na(+) c

73 ryonic kidney 293 cells but had no effect in Fischer rat thyroid epithelia.

74 to inhibit ENaC in both Xenopus oocytes and Fischer rat thyroid epithelia.

75 KS-WNK1 and the epithelial Na(+) channel in Fischer rat thyroid epithelial cells also stimulates Na(

76 conducted on TASK-3 transiently expressed in Fischer rat thyroid epithelial monolayers; channel funct

77 hs old; n=10) and aged (20 months old; n=10) Fischer rats underwent cardiac micro-CT imaging as well

78 9+/-3 g) and 9 adult (199+/-5 g) male inbred Fischer rats underwent ligation of the left internal and

79 denocarcinomas implanted in the flanks of 48 Fischer rats was treated with a single 5- or 15-Gy dose

80 Fischer rats were divided into: MCA tumor bearing fed ch

81 sociation between iron loading and high TGs, Fischer rats were fed chow containing 1% carbonyl iron.

82 Water-deprived Lewis and Fischer rats were given 5 min access to 0.15% saccharin

83 Adult, regularly cycling female Fischer rats were injected daily with 10 mg/kg fluoxetin

84 Six-to 27-month-old Fischer rats were injected intraperitoneally with BrdU t

85 R3230 mammary adenocarcinomas in Fischer rats were treated with either RF ablation (n = 4

86 rmed subcutaneous tumors when implanted into Fischer rats, whereas control T9 cells did.

87 on was reduced by 52% in Lewis compared with Fischer rats while colonic motor response to CRF injecte

88 rasympathetic nucleus in Lewis compared with Fischer rats while similar Fos expression was observed i

89 Biodistribution studies in normal Fischer rats with [18F]16 and [18F]17 showed high uptake

90 of monoclonal antibodies by immunization of Fischer rats with enzymatically dispersed nonparenchymal

91 Among 20 Fischer rats with implanted FN13762 tumors in the liver,

92 Fischer rats with one-week-old myocardial infarcts were

93 34 senescent, male and female, normotensive Fischer rats with transthoracic Doppler echocardiography