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Gene expression response of mice after a single dose of (137)cs as an internal emitter.
We have profiled global gene expression in blood of male C57BL/6 mice injected with (137)CsCl. We extracted RNA from the blood of control or (137)CsCl-injected mice at 2, 3, 5, 20 or 30 days after exposure. Gene expression was measured using Agilent Whole Mouse Genome Microarrays, and the data was a...
Exposure to Electrical Contact Currents and the Risk of Childhood Leukemia.
Abstract The objectives of this study were to examine the association between contact current exposure and the risk of childhood leukemia and to investigate the relationship between residential contact currents and magnetic fields. Indoor and outdoor contact voltage and magnetic-fiel...
Acceleration of diabetic wound healing by low-dose radiation is associated with peripheral mobilization of bone marrow stem cells.
We investigated the effect of repeated low-dose radiation exposure (75 mGy X ray) on skin wound healing in a rat model of diabetes. A skin wound was made on the backs of diabetic and age-matched control rats 60 days after diabetes was induced by a single injection of streptozotocin. Rats with skin w...
Roles of Stem Cells in Tissue Turnover and Radiation Carcinogenesis.
Abstract Radiation research has its foundation on the target and hit theories, which assume that the initial stochastic deposition of energy on a sensitive target in a cell determines the final biological outcome. This assumption is rather static in nature but forms the foundation of...
Response to Dr. Simmons
The initiator motif is preferentially used as the core promoter element in ionizing radiation-responsive genes.
We analyzed the promoters of 217 radiation-responsive human genes, compiled from microarray databases available in the literature. Using the DBTSS database, the transcriptional start sites were determined, and the core promoter elements, such as the TATA-box, initiator (Inr), GC-box and CCAAT-box, w...
Comments on the Responses of Utteridge et al. (Radiat. Res. 159, 277–278, 2003) to Letters about their Paper (Radiat. Res. 158, 357–364, 200...
The proliferative response of mouse jejunal crypt cells to radiation-induced cell depletion is not mediated exclusively by transforming grow...
We have tested this hypothesis by comparing the repopulation response of wild-type and Tgfa-null mice, using the microcolony assay. Mice were exposed whole-body to (137)Cs gamma rays at a dose of approximately 1.6 Gy/min. Single doses and equal doses separated by 4 and 54 h were given. The rightward...
Cancer predisposition, radiosensitivity and the risk of radiation-induced cancers: biological aspects and computational modeling.
Thyroid cancer after scalp irradiation: a reanalysis accounting for uncertainty in dosimetry.