ライフサイエンスコーパス: whole-body irradiation

1 ute dose-limiting side effects of thorax and whole body irradiation.

2 s acid-beta-galactosidase activity following whole body irradiation.

3 ecovered from pancytopenia within 4 weeks of whole body irradiation.

4 proliferation in tongues of mice exposed to whole-body irradiation.

5 ival when irradiated, as did mice exposed to whole-body irradiation.

6 rine and in vivo using C3H mice subjected to whole-body irradiation.

7 o DNA interstrand cross-links (ICLs) but not whole-body irradiation.

8 e effect was seen only in mice that received whole-body irradiation 1 day before tumor implantation.

9 Recipient pigs underwent whole body irradiation (100 cGy), thymic irradiation (70

10 unological tolerance, including splenectomy, whole body irradiation (300 cGy) or cyclophosphamide (80

11 i-CD4 and anti-CD8 mAbs, followed by 3 Gy of whole body irradiation, 7 Gy of thymic irradiation, and

12 at the p53-mediated pathological response to whole-body irradiation, a prototypical genotoxic carcino

13 CD4 and anti-CD8 mAbs, then received 3 Gy of whole body irradiation and 7 Gy of thymic irradiation pr

14 teen SLA(dd) miniature swine received 1.5 Gy whole body irradiation and class I-mismatched (SLA(gg) )

15 ting of depleting CD4 and CD8 mAb's and 3 Gy whole-body irradiation and 7 Gy thymic irradiation, led

16 otoxic host treatment as provided by 100-cGy whole-body irradiation and relatively high levels of mar

17 in second-set rejection was tested by donor whole-body irradiation and replacement of donor B10 live

18 and natural killer (NK) cell depletion, 3 Gy whole body irradiation, and 7 Gy thymic irradiation.

19 h depleting anti-CD4 and anti-CD8 mAbs, 3-Gy whole body irradiation, and 7-Gy thymic irradiation, fol

20 anti-CD4 and CD8 monoclonal antibodies, 3 Gy whole-body irradiation, and 7 Gy thymic irradiation.

21 olve immune factors, as strains subjected to whole-body irradiation are significantly more susceptibl

22 Whole-body irradiation at the minimal lethal dose causes

23 tion of the host with either chemotherapy or whole-body irradiation augmented the therapeutic efficac

24 and corroborated in other models, including whole-body irradiation/bone-marrow transplantation.

25 g anti-CD4 and anti-CD8 mAbs on day -5, 3 Gy whole body irradiation (day 0), and 15x10(6) fully MHC-m

26 four female) received a suberythemal dose of whole body irradiation from ultraviolet-A-emitting fluor

27 dose of 7.5 Gy with 1 of 3 radiation schemes-whole-body irradiation, half-body shielding (HBS), or 1-

28 ion across MHC barriers without the need for whole body irradiation in miniature swine.

29 is strategy presents many of the benefits of whole-body irradiation, including the provision of high

30 Interestingly, following whole-body irradiation, mice lacking RIP140 exhibited im

31 After whole body irradiation of mice, both naive and memory CD

32 himerism require recipient conditioning with whole body irradiation or a cytoablative regimen to crea

33 he significant increase in DeltaR2 2 d after whole-body irradiation (P = 0.0022) and HBS (P = 0.0003)

34 eceived a nonmyeloablative regimen including whole body irradiation, pharmacological immunosuppressio

35 d antibody and CTLA4Ig, a low dose (3 Gy) of whole body irradiation, plus fully major histocompatibil

36 provided before exposure to a lethal dose of whole-body irradiation protected WT mice from DNA damage

37 blood vitamin D(3) concentrations 24 h after whole-body irradiation showed that the incremental incre

38 ogenic survival assays and in vivo sublethal whole body irradiation tests showed that Nrf2 deletion i

39 In C3H mice given 5-Gy whole-body irradiation, there was a significant inductio

40 , two cynomolgus monkeys were conditioned by whole body irradiation (total dose 300 cGy) 6 and 5 days

41 lonal antibodies (mAbs) on day -5, plus 3 Gy whole body irradiation (WBI) and 7 Gy thymic irradiation

42 Abs administered on day -5, followed by 3-Gy whole body irradiation (WBI) and 7-Gy thymic irradiation

43 Abs administered on day -5, followed by 3-Gy whole body irradiation (WBI) and 7-Gy thymic irradiation

44 ed when hosts were exposed to 1 Gy (100 cGy) whole body irradiation (WBI) and infused with 40 x 10(6)

45 for the development of viable mitigators of whole body irradiation (WBI) due to the possibility of u

46 ngle components of the conditioning regimen--whole body irradiation (WBI), antithymocyte globulin (AT

47 ese regimens generally include some level of whole body irradiation (WBI), which is thought to facili

48 CD154 monoclonal antibody (mAb) and either a whole body irradiation (WBI)- or cyclophosphamide (CPP)-

49 r cells) into splenectomized preconditioned (whole body irradiation (WBI)-based) baboons, intended to

50 syngeneic bone marrow transplants (BMT) with whole body irradiation (WBI).

51 ng regimen by: fractionating or reducing the whole-body irradiation (WBI) dosage; adding deoxyspergua

52 We depleted the bone marrow by including whole-body irradiation (WBI) of 6 Gy as part of a total

53 This is especially true for whole-body irradiation, where even moderate nonlethal do

54 especially exposure to alkylating agents and whole body irradiation, which cause substantial germ cel

55 RPC consisted of whole body irradiation with 400 R (day 0); some recipien

56 Whole-body irradiation with ocular shielding induced bon

57 ndrome susceptible mouse model, we show that whole-body irradiation with protons are more effective i