ライフサイエンスコーパス: nude rat

1 vivo PET of Abl-expressing human tumors in a nude rat.

2 tumor cells were implanted into the brain of nude rats.

3 eal melanoma spheroids were implanted in six nude rats.

4 oblastomas were implanted into the brains of nude rats.

5 out the entire 24-hour period in LAN-exposed nude rats.

6 s were elevated in LAN-exposed tumor-bearing nude rats.

7 carcinoma tumor was grown in each of 10 male nude rats.

8 shown using a Du145 tumor xenograft model in nude rats.

9 ft tumors (length, approximately 23 mm) in 6 nude rats.

10 or suprachoroidal space of 26 WAG/RijHsd-rnu nude rats.

11 erior suprachoroidal space of 11 WAG/Nij-rnu nude rats.

12 d orthotopically implanted prostate tumor in nude rats.

13 asting at least 18 weeks in SCID mice and in nude rats.

14 tion in soft agar, and no tumor formation in nude rats.

15 lls into 8.5-mm calvarial defects created in nude rats.

16 minutes after the induction of MI in athymic nude rats.

17 on from Tie2/lacZ mice to background mice or nude rats.

18 n tumor cell line enhances tumorigenicity in nude rats.

19 d growth of human melanoma tumors growing in nude rats.

20 ommodation of hamster cardiac transplants in nude rats.

21 r as compared with CD4+ T cell-reconstituted nude rats.

22 implanted into the common carotid artery in nude rats.

23 coronary artery in male Hsd:RH-rnu (athymic nude) rats.

24 was transplanted into ischemic myocardium of nude rats 10 minutes after ligation of the left anterior

25 urface in carotid arteries of statin-treated nude rats (20+/-3 versus 4+/-1 cells/mm surface length,

26 es) but was still more rapid than in control nude rats (3.3 +/- 0.5 days).

27 irst xenografts in CD8+ T cell-reconstituted nude rats (9 +/- 2 days), indicating that the CD8+ T cel

28 re tumor volume for at least a month in both nude rat and severe combined immunodeficiency (SCID) mou

29 Of the six models evaluated, nude rats and gerbils immunosuppressed with dexamethason

30 ere implanted subcutaneously in the dorsa of nude rats and harvested after 1 and 3 months.

31 Using nude rats and MCF7 cells expressing different rat comple

32 eroids were implanted in the choroids of six nude rats and six severe combined immunodeficiency mice.

33 tilage defect (n = 5 each) on the femur of a nude rat, and the quality of the repaired tissue was eva

34 t--NICD-transduced cells generated tumors in nude rats--and was associated with the loss of markers a

35 ing rat 9L or human U87 deltaEGFR gliomas in nude rats at various times (8 h to 8 days) and at variou

36 n tumors with this system is demonstrated in nude rats bearing cerebral implants of human U87 glioma.

37 In a xenograft model, nude rats bearing DHFR-HSV1 TK-transduced HCT-8 tumors a

38 Nude rats bearing either s.c. low VEGF (V-) or high VEGF

39 Nude rats bearing human head and neck cancer and non-sma

40 n this study, we report that tumor growth in nude rats bearing human steroid receptor-negative MCF-7

41 in the portal vein or the hepatic artery of nude rats bearing intrahepatic LoVo colon carcinomas cou

42 taining activity both in cell culture and in nude rats bearing intrahepatic xenografts.

43 selected for further dynamic PET studies in nude rats bearing subcutaneous RG2TK+ and RG2 tumors.

44 stereotactically injected these clones into nude rat brains (six animals were injected per clone).

45 ive antibodies present in the serum of naive nude rats, but there was also an IgM response to MCF7 tu

46 alysis of recipient sera of both control and nude rats by ELISA, for the binding of IgG or IgM to gui

47 ngrafted orthotopically in immunocompromised nude rats by targeting and ablating pleomorphic cells th

48 We have reconstituted nude rats carrying an accommodated xenograft with syngen

49 t stem cells to enhance functional repair of nude rat critically sized femoral defects.

50 In vivo conditioning in nude rats did not confer TLR4 expression in hESC-EC.

51 Direct injection of G207 into nude rat flank tumors suppressed tumor growth significan

52 decline was addressed by irradiating athymic nude rats followed 2 days later by intrahippocampal tran

53 or 13 d and then implanted subcutaneously in nude rats for 4 and 8 wk.

54 (HF-US) was used to measure tumor volume in nude rats for up to 2 weeks.

55 i-PMN) and antimacrophage antibodies, 80% of nude rats formed tumors, whereas only 40% of the rats de

56 d potent and durable antitumor activity in a nude rat HCT-116 tumor xenograft model and exhibited goo

57 of H2122-PPAR(gamma) cells into the lungs of nude rats inhibited tumor growth and metastasis in vivo

58 odel, that immunocompetent, but not athymic, nude rats injected intraperitoneally with xenogeneic end

59 premalignancy and (b) an in vivo orthotopic nude rat lung cancer model to evaluate response to epige

60 We used a nude rat model of a full-thickness articular cartilage d

61 ted this composite onto the infarct bed in a nude rat model of cardiac infarction.

62 drug-response monitoring and prediction in a nude rat model of human sarcoma by AAVP imaging.

63 ) were injected into the myocardium of adult nude rats (n=20).

64 o the left ventricular myocardium of athymic nude rats (NDRs) versus immunocompetent Sprague-Dawley r

65 d to track uveal melanoma growth in the same nude rat or SCID mouse for up to a month.

66 l method to measure tumor volume in the same nude rat over time in this orthotopic xenograft model of

67 can be quantified noninvasively in the same nude rat over time using a portable, high-resolution, hi

68 In vivo trials using the nude rat PCNSL model demonstrated significantly improved

69 Adoptive transfer of these XAb into naive nude rats provoked hyperacute xenograft rejection (38 +/

70 CD8+ T cell-reconstituted nude rats rejected their grafts later (19.4 +/- 5.8 days

71 roidal space of 20, 17, and 16 WAG/RijHs-rnu nude rats, respectively.

72 B-cell lines into the caudate nucleus of the nude rat resulted in lethal CNS tumor burden manifested

73 plantation of the engineered cell lines into nude rats reveals that stably integrated genes are expre

74 l of meningeal leukemia was developed in the nude rat, rnu/rnu, using the human-derived acute lymphob

75 Thus, our data in nude rats show rejection times and intragraft features o

76 , and one of them was serially propagated in nude rats six times over a period of 10 months.

77 iation-induced cognitive impairment, athymic nude rats subjected to head only irradiation (10 Gy) wer

78 choroidal melanoma orthotopic xenografts in nude rats that reproduce the PAS staining patterns assoc

79 etumumab in human cancer xenograft models in nude rats to assess effects on both tumor cells and the

80 Twenty-three nude rats underwent successful left anterior descending

81 even Dunning R3327-AT prostate tumor-bearing nude rats were immobilized in custom-fabricated whole-bo

82 Transgenic nude rats were protected from disease manifestations.

83 eck and 10 HT29 colorectal carcinoma-bearing nude rats were studied.

84 Male nude rats were subcutaneously inoculated in the shoulder

85 comparing discordant xenograft responses of nude rats, which lack T cell receptor (TCR)-alpha/beta+

86 To study this, we inoculated 30 nude rats with HER2-positive cells derived from a brain

87 ved grafting into the spinal cord of athymic nude rats with no signs of overgrowth and with a very si

88 bcutaneous cancer esophageal xenografts, and nude rats with orthotopic esophageal cancers in four stu

89 Sixty nude rats with subcutaneously implanted HNSCC xenografts

90 therapy in human cancer xenograft tumors in nude rats without increased toxicity.

91 efficacy of the DOT1L inhibitor EPZ5676 in a nude rat xenograft model of DNMT3A-mutant AML.

92 -CHC imaging experiments were performed with nude rats xenografted with the BE (2)-C-sensitive and -r

93 Similar CpG treatment of athymic nude rats yielded no neuroprotection, further suggesting