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This role of PTP1B in protecting mice against irradiation injury is a relevant issue of the present work and we reasoned that perhaps strategies to improve transient PTP1B activity in the course of irradiation will have beneficial effects.
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In addition, high dose re-irradiation will have extensive side effects.
One can hope that more sophisticated irradiation techniques such as conformal radiotherapy, intensity-modulated radiotherapy or proton beam irradiation will cause less cognitive damage.
Since the LINAC is the instrument used for radiotherapy treatment, these in vivo samples will have the same irradiation source as our preliminary study, which is important in order to compare data.
It suggests that cyanurate (triagine ring) will have a resistance against irradiation but oxazolidinon will lose the resistance after heavy irradiation.
Such patients will have received a total body irradiation of 450 millisievert (mSv) and may have suffered from side effects such as nausea, sialoadenitis, loss of taste, or reduced spermatogenesis.
Also recurrent patients will have a chance of re-irradiation with proton therapy.
Although, with breath-hold IMPT, the mean heart dose could be reduced to almost zero, the question arises whether all left-sided breast cancer patients will have clinically relevant benefit from proton irradiation.
Calculated dosimetry indicates that the microtumor irradiation from the 213Bi-mAbs with the specific activity obtained in this study will have its main origin from surrounding, non-targeted 213Bi-mAbs in the i.p. fluid.
Corollaries (with emphasis on cancer) are: mutations of circadian clock genes will be associated with altered rates of cancer; circadian "clock gene" and protein expression levels will be altered in tumors; mutant mice with disrupted circadian clock genes will have altered (increased) cancer incidence under basal aging conditions, following gamma-irradiation, and in cancer-prone models.
mutations of circadian clock genes will be associated with altered rates of cancer; circadian "clock gene" and protein expression levels will be altered in tumors; mutant mice with disrupted circadian clock genes will have altered (increased) cancer incidence under basal aging conditions, following gamma-irradiation, and in cancer-prone models.
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