ライフサイエンスコーパス: X-irradiation

1 an be restored to almost 50% of wild-type by X irradiation.

2 m E. coli organisms subjected to both UV and X irradiation.

3 uced following early gestational exposure to x-irradiation.

4 l, respectively, before their co-exposure to X-irradiation.

5 res chronic administration and is blocked by x-irradiation.

6 g NES mutants exhibit reduced survival after X-irradiation.

7 chemotherapeutic agents, UV irradiation, and X-irradiation.

8 nd to colocalize spatially after UV- but not x-irradiation.

9 was blocked by ablation of neurogenesis with X-irradiation.

10 of the cell cycle and following exposure to X-irradiation.

11 ((60)Co) gamma-radiation or 600 cGy, 250 kVp x-irradiation.

12 ons had been produced using ethidium bromide/X-irradiation.

13 PSA, after infantile (PND 2-15) exposure to x-irradiation.

14 y exposed to O, 12, or 21-Gy single doses of x-irradiation.

15 e progenitor cells several generations after X-irradiation.

16 erved in normal syncytial embryos exposed to X-irradiation.

17 d by exposure of the spinal cord to 40 Gy of X-irradiation.

18 ming growth factor-beta1 protected them from x-irradiation.

19 ked in developing chick limb buds exposed to X-irradiation.

20 cellular components of the lesion site with x-irradiation.

21 Rat cortical neurons were treated with x-irradiation 7 d after isolation to test for the role o

22 viable cell than that observed after 0.5 Gy x-irradiation, a dose that causes the same level of toxi

23 After X-irradiation, a lower proportion of the p53-null than w

24 results, showing substantial deficits after x-irradiation alone, encourage the hypothesis that hippo

25 elated with an increased hypersensitivity to X-irradiation and a DNA DSB repair deficit in synchroniz

26 hypoxia, both protect cells from killing by X-irradiation and are present in solid tumors but not in

27 Using the taiep rat and a combination of X-irradiation and cell transplantation, it has been poss

28 adult, or aged adult rat sciatic nerves into X-irradiation and ethidium bromide-induced demyelinated

29 of 128 WG-RH hybrid cell lines generated by X-irradiation and fusion has been tested for the retenti

30 dly resistant to several stresses, including X-irradiation and inhibition of protein synthesis.

31 e adult rat spinal cord were demyelinated by x-irradiation and intraspinal injections of ethidium bro

32 Both X-irradiation and thalidomide-induced phocomelia have be

33 that this increase was a consequence of the X-irradiation and to highlight the significance of remye

34 s have been described for cells that survive x-irradiation, and suggest random genetic damage is a co

35 as arrested in mice using low-dose, targeted x-irradiation, and the effects of irradiation were assay

36 hippocampal lesions, and infant exposure to X-irradiation, and they add strongly to these earlier de

37 Using X-irradiation as a model cytotoxic agent we investigated

38 oduction is required for cell survival after x-irradiation but not under unstressed conditions.

39 the cytotoxicity of the DNA damaging agents X-irradiation, cisplatin or bleomycin was p53-independen

40 luoxetine, and ablation of neurogenesis with x-irradiation completely blocked the effects of chronic

41 lity to rapidly phosphorylate HDM2 following X-irradiation, confirming a role for ATM in its phosphor

42 to three subsequent cell divisions following X-irradiation, confirming that X-rays induce cell death

43 ellular constituents at the lesion site with x-irradiation delivered within a critical time window af

44 Single-dose x-irradiation destroys reactive glia at the damage site

45 proximodistal patterning is unaffected after X-irradiation does not support the predictions of the pr

46 Selective exposure to x-irradiation during infancy, from postnatal days (PND)

47 ersistent demyelination in rodent CNS in the X-irradiation/ethidium bromide (X-EB) model.

48 constituted cells were transplanted into the X-irradiation/ethidium bromide lesioned dorsal columns o

49 production during a smog chamber isoprene-NO x irradiation experiment.

50 s to 6-aminonicotinamide prior to 3- or 6-Gy x-irradiation induced a supra-additive cell kill, indica

51 X-irradiation-induced DNA damage perturbs the G(1), S, a

52 etaphase/anaphase transition after extensive X-irradiation-induced DNA damage, whereas Grp/Chk1, but

53 m of the retinoblastoma gene product blocked x-irradiation-induced neuronal death.

54 Indeed, studies of X-irradiation-induced phocomelia have served as one of t

55 s and lineage tracing in chick, we show that X-irradiation-induced phocomelia is fundamentally not a

56 ert culture dish method is used to show that X-irradiation induces medium-mediated bystander effects

57 on between radiation inducible TNF-alpha and X-irradiation occurs selectively within the tumor vessel

58 Specifically, focal X irradiation of the hippocampus or genetic ablation of

59 e mice of differing ages to a single dose of X-irradiation of 1-4 Gy.

60 X-irradiation of a restricted region of mouse brain cont

61 e technique of ionizing neutral compounds by X-irradiation of cryogenic Ar matrices to radicals embed

62 Sublethal X-irradiation of frogs decreased leukocyte numbers in th

63 X-irradiation of heterozygous CAUT line seeds results in

64 X-irradiation of hippocampal neurons induced p53 immunor

65 X-irradiation of mature seeds produced aneuploid albino

66 mbiguously distinguished DNA SSBs induced by X-irradiation of mouse leukemia L1210 cells from DNA DSB

67 We have reported in a separate article that x-irradiation of sectioned adult rat spinal cord resulte

68 by either total body X-irradiation (TBI) or X-irradiation of the chest (CI) with 62.5, 125, 250, or

69 Rats received localized X-irradiation of the heart with an image-guided irradiat

70 The preparative regimen consisted of X-irradiation of the host liver and mitotic stimulation

71 X-irradiation of the rat thymocytes induced apoptosis, l

72 ed study of the potential effect of paternal x-irradiation on progeny seems justified.

73 d intervention in certain cellular events by x-irradiation prevents the onset of degeneration and thu

74 inhibited by exposing the brain to 40 Gy of X-irradiation prior to cuprizone intoxication and this r

75 to show that cells die at a fixed time after X-irradiation rather than from a specific cell cycle poi

76 These results, showing alleviation of x-irradiation-related deficits in short-term memory by D

77 istration of analog II prior to fractionated X-irradiation significantly diminished the number and de

78 ll cycle, and their differential response to X-irradiation suggest that they may perform different fu

79 g progenitors, followed by either total body X-irradiation (TBI) or X-irradiation of the chest (CI) w

80 After X-irradiation, the endothelial leukocyte adhesion molecu

81 l populations, we used low-dose, whole-brain x-irradiation to eliminate proliferating dentate granule

82 the effects of random DNA breaks induced by X-irradiation to site-specific I-CreI endonuclease-induc

83 t specific times before or after SE, or used x-irradiation to suppress neurogenesis.

84 is regulated by a variety of factors such as x-irradiation, ultraviolet radiation, steroids, growth f

85 The response of neurons to x-irradiation was compared with that of astrocytes that

86 X-irradiation was used to provoke loss of the FCA allele

87 mocytes, as well as their toxicities without X-irradiation, was successfully evaluated using this met

88 e if the occlusive effects of Ad.Egr-TNF and X-irradiation were specific for tumor vessels, non-tumor

89 asts sharply to the situation observed after x-irradiation, where peak levels of gamma-H2AX foci were

90 Da protein was not significantly affected by X-irradiation, while the abundance of the 73 and the 62

91 Following X-irradiation with 9.5 Gy, cells were imaged every 3 min

92 X-irradiation yielded similar results.