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1 iation profile persisting for at least 12 mo postirradiation.
2 ase with maximal activity detected at 10 min postirradiation.
3 ry form of tumor stem or clonogen cell death postirradiation.
4 raction with the DNA damage response pathway postirradiation.
5 fraction of apoptotic cells within 24 hours postirradiation.
6 lated one or more of these surface molecules postirradiation.
7 proteins was increased at least 5-fold 14 h postirradiation.
8 e11 is required for normal cellular survival postirradiation.
9 ss of heavily damaged basal cells within 4 d postirradiation.
10 ar foci was observed and persisted until 2 h postirradiation.
11 activity in the lung between 3 and 30 weeks postirradiation.
12 survival than when incubated at 30 degrees C postirradiation.
13 ival whether incubated at 30 or 40 degrees C postirradiation.
14 ion) whether incubated at 30 or 40 degrees C postirradiation.
15 ndent manner, which persisted through 7 days postirradiation.
16 repair is observed following the first 1.5 h postirradiation.
17 ese enzymes do not form double-strand breaks postirradiation and are substantially more radioresistan
19 The goal of this study was to use serial (postirradiation and follow-up) volumetric intravascular
20 lethality, and delayed T-cell reconstitution postirradiation and hematopoietic stem cell transplantat
21 ST) that met the following criteria: on both postirradiation and six-month follow-up IVUS imaging, >
22 lete blood counts were monitored for 60 days postirradiation and the durations of neutropenia (absolu
23 lete blood counts were monitored for 60 days postirradiation and the durations of neutropenia (NEUT;
24 ar to those of p21-/- tumors (2-fold at 24 h postirradiation) and improved radiocurability of p21+/+
25 MCL-1 association with genomic DNA increased postirradiation, and the protein colocalized with 53BP1
26 em cell survival was found at 1 and 4 months postirradiation, and transplanted cells showed robust mi
29 maintenance of chromosomes protein 1 (SMC1), postirradiation bromodeoxyuridine incorporation to evalu
31 duced by ionizing radiation during the first postirradiation cell cycle of tumor cells, suggesting a
35 ippocampal-dependent cognitive task 4 months postirradiation, compared to their irradiated surgical c
37 Cs, primarily CD11b+ myelomonocytes, and the postirradiation development of functional tumor vasculat
40 se kinetics parallel those of D. radiodurans postirradiation genome reconstitution, suggesting that D
41 tic material over time (10-12 cell divisions postirradiation) has two relevant outcomes: (a) cell dea
42 evels of apoptosis were observed at 24 hours postirradiation in aerobic and hypoxic NH32 cells, a p53
43 formed at radiation-induced clusters during postirradiation incubation and also in a dose-dependent
44 thesis that DNA repair occurring immediately postirradiation is by a recA-independent single-strand a
47 f acentric chromosome fragments at the first postirradiation mitosis, and an increased radiosensitivi
50 e DNA circles were formed in the first 1.5 h postirradiation, several hours before the onset of detec
51 exneri M90T, incubated at 37 or 40 degrees C postirradiation, shows up to 30-fold higher survival tha
53 e a role for ceramide in mediating the rapid postirradiation translocation and inhibition of PKCalpha
56 yte recruitment normally observed at 2 hours postirradiation was blunted by the xanthine oxidase inhi
57 in ceramide production seen was at 4 minutes postirradiation, with a 46% reduction in ceramide levels
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