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International Journal of Cancer|April 15, 2011
Prolonged expression of the γ-H2AX DNA repair biomarker correlates with excess acute and chronic toxicity from radiotherapy treatmentEmma C Bourton, Piers N Plowman, Daniel Smith, et al.The British Journal of Dermatology|February 12, 1998
Induction of mutagenic DNA damage in human fibroblasts after exposure to artificial tanning lampsA Woollons, P H Clingen, M L Price, et al.The British Journal of Dermatology|May 1, 1991
Abnormal erythemal response and elevated T lymphocyte HRPT mutant frequency in Cockayne's syndromeP G Norris, C F Arlett, J Cole, et al.The British Journal of Radiology|August 1, 1990
An instance of clinical radiation morbidity and cellular radiosensitivity, not associated with ataxia-telangiectasiaP N Plowman, B A Bridges, C F Arlett, et al.Drug Safety|April 19, 2017
Patient Reporting in the EU: Analysis of EudraVigilance DataMarin Banovac, Gianmario Candore, Jim Slattery, et al.Pharmacoepidemiology and Drug Safety|October 25, 2020
What are the patients' and health care professionals' understanding and behaviors towards adverse drug reaction reporting and additional monitoring?Justina Januskiene, Andrej Segec, Jim Slattery, et al.International Journal of Radiation Biology|December 1, 1988
Comparative human cellular radiosensitivity: I. The effect of SV40 transformation and immortalisation on the gamma-irradiation survival of skin derived fibroblasts from normal individuals and from ataxia-telangiectasia patients and heterozygotesC F Arlett, M H Green, A Priestley, et al.Mutation Research|December 1, 1975
A comparison of the 8-azaguanine and ouabain-resistance systems for the selection of induced mutant Chinese hamster cellsC F Arlett, D Turnbull, S A Harcourt, et al.Journal of the American Academy of Dermatology|November 1, 1993
Xeroderma pigmentosum-Cockayne syndrome complex in two patients: absence of skin tumors despite severe deficiency of DNA excision repairR J Scott, P Itin, W J Kleijer, et al.Lancet (London, England)|June 20, 1992
Growth retardation and immunodeficiency in a patient with mutations in the DNA ligase I geneA D Webster, D E Barnes, C F Arlett, et al.Pageof 23