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dc.contributor.authorHendry, Jolyon H
dc.date.accessioned2010-11-08T10:52:44Z
dc.date.available2010-11-08T10:52:44Z
dc.date.issued1987-02
dc.identifier.citationLack of differential sparing of late ischaemic atrophy and early epidermal healing, after dose fractionation of mouse tails down to 2.6 Gy per fraction. 1987, 8 (2):153-60 Radiother Oncolen
dc.identifier.issn0167-8140
dc.identifier.pmid3562894
dc.identifier.urihttp://hdl.handle.net/10541/114929
dc.description.abstractLong-term atrophy of irradiated mouse tails began after about 5 months, and the incidence rose steadily to the end of the lifespan. The major associated histological change was atherosclerosis in the single tail artery. The incidence of the ischaemic atrophy was dependent on the size of the irradiated volume. The probability of ischaemic atrophy assessed at 3 years after irradiation was little dependent on the dose. The fractionation effect was described by alpha/beta congruent to 30 Gy, which was not lower than the range of values applicable for healing of the early epidermal reactions on the tail. Hence the general finding of a sparing of late effects in tissues using low doses per fraction was not observed in these experiments using dose fractions down to 2.6 Gy and the present endpoints.
dc.language.isoenen
dc.subject.meshAnimals
dc.subject.meshAtrophy
dc.subject.meshMice
dc.subject.meshRadiation Dosage
dc.subject.meshRadiation Injuries, Experimental
dc.subject.meshTail
dc.subject.meshTime Factors
dc.subject.meshWound Healing
dc.titleLack of differential sparing of late ischaemic atrophy and early epidermal healing, after dose fractionation of mouse tails down to 2.6 Gy per fraction.en
dc.typeArticleen
dc.contributor.departmentDepartment of Radiobiology, Paterson Institute for Cancer Research, Christie Hospital and Holt Radium Institute, Manchester M20 9BX, U.K.en
dc.identifier.journalRadiotherapy and Oncologyen
html.description.abstractLong-term atrophy of irradiated mouse tails began after about 5 months, and the incidence rose steadily to the end of the lifespan. The major associated histological change was atherosclerosis in the single tail artery. The incidence of the ischaemic atrophy was dependent on the size of the irradiated volume. The probability of ischaemic atrophy assessed at 3 years after irradiation was little dependent on the dose. The fractionation effect was described by alpha/beta congruent to 30 Gy, which was not lower than the range of values applicable for healing of the early epidermal reactions on the tail. Hence the general finding of a sparing of late effects in tissues using low doses per fraction was not observed in these experiments using dose fractions down to 2.6 Gy and the present endpoints.


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