Pages that link to "Q53495645"
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The following pages link to Radiation-induced chromatid aberrations in Cockayne syndrome and xeroderma pigmentosum group C fibroblasts in relation to cancer predisposition (Q53495645):
Displaying 12 items.
- Four radiation hypersensitivity cases and their implications for clinical radiotherapy (Q34071802) (← links)
- Radiation-induced chromatid breaks and deficient DNA repair in cancer predisposition (Q34134667) (← links)
- Fluorescent light-induced chromatid breaks distinguish Alzheimer disease cells from normal cells in tissue culture (Q34381547) (← links)
- Retinoid protection against x-ray-induced chromatid damage in human peripheral blood lymphocytes. (Q35609265) (← links)
- Radiation-induced micronucleus induction in lymphocytes identifies a high frequency of radiosensitive cases among breast cancer patients: a test for predisposition? (Q36291731) (← links)
- Minimal ionizing radiation sensitivity in a large cohort of xeroderma pigmentosum fibroblasts (Q40035578) (← links)
- Involvement of cell cycle control in bleomycin-induced mutagen sensitivity (Q40707569) (← links)
- Chromosome aberrations induced in vitro: mechanisms, delayed expression, and intriguing questions (Q40743157) (← links)
- Radiation-induced DNA double-strand breaks and the radiosensitivity of human cells: a closer look (Q41065090) (← links)
- Cytogenetic evidence for differences in DNA incision activity in xeroderma pigmentosum group A, C and D cells after X-irradiation during G2 phase (Q41540645) (← links)
- Chromosomal sensitivity to X-ray irradiation during the G2 phase in lymphocytes of patients with hereditary cutaneous malignant melanoma as compared to healthy controls (Q74615743) (← links)
- Tp53 codon-72 polymorphisms identify different radiation sensitivities to g2-chromosome breakage in human lymphoblast cells (Q82249007) (← links)