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On the other hand, in mice which underwent laparotomy immediately before assay, the TD50 was reduced significantly though not to the same extent as in WBI mice.
The mean number of tumour cells required for 50% successful takes (TD50) in these mice was found to be not significantly different from that in normal controls but highly significantly greater than in WBI mice.
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She is currently a post doctoral researcher in the Laboratory of Knowledge Management in Bioinformatics (WBI), Humboldt-Universität, Berlin, Germany.
Some of the corpora I present here are included in the WBI repository (http://corpora.informatik.hu-berlin.de), which provides their full visualization using the Stav/Brat annotation tool.
The statistical design of these studies is elaborated in order to show equivalence between APBI and whole breast irradiation (WBI) in term of local control.
An accelerated prescription for whole brain irradiation (WBI) in the treatment of brain metastases has been reported to provide favourable survival in good performance status patients.
Thus, accelerated partial breast irradiation (APBI) has been promoted in phase I-III trials designed to test the feasibility and equivalence with the standard Whole breast irradiation (WBI) in properly selected low risk early breast cancer patients after BCS.
Exposure to a higher dose (13Gy) of WBI resulted in 100% mortality in both Rad21+/− and WT littermates by day 8 post-treatment (Fig. 3B).
Here we show that treatment of either WT or Fus1 KO mice with PM prior to 9 Gy WBI resulted in improved survival compared to mice treated with WBI alone.
In the cobas® DNA Sample Preparation kit, Proteinase K, WBI (wash buffer I) and WBI (wash buffer II) were prepared according to the manufacturer's instructions.
WBI resulted in a two-fold increase in serum Rspo1 concentrations by day 3.5 (Fig 1A and 1B).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com