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Inherent radiosensitivities were examined using a clonogenic survival assay.
Pretreatment of A375 cells with GrB/scFvMEL significantly sensitized melanoma cells to ionizing radiation assessed using a clonogenic survival assay.
Pretreatment of A375M cells with IκBα/scFvMEL significantly sensitized melanoma cells to ionizing radiation assessed using a clonogenic survival assay.
Survival was determined using a clonogenic survival assay.
Cytotoxicity of CSC samples was determined using a clonogenic survival assay.
We examined the effect of survivin suppression on radiosensitivity using a clonogenic survival assay (14 days after irradiation).
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To explore the possible physiological relevance for acute γ irradiation-induced BRCA1 degradation, we initially tested the cellular survival in response to γ irradiation using a clonogenic cell survival analysis [39].
Using a clonogenic cell survival assay, Hsp90 inhibition significantly sensitised the cells for γ-photon irradiation.
To investigate reproductive abilities of both parental and IRR cells to form large colonies or clones after treatment with ionising radiation, cisplatin and Rac1 inhibitor effects were estimated using a clonogenic cell survival assay.
Twenty-two novel derivatives were synthesized and their cytotoxicities were measured using a clonogenic long-term survival assay.
The complemented Mus81−/− MEFs were used in a clonogenic survival assay to test sensitivity to MMC.
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