II. Sister chromatid exchanges
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[1] J. B. Rattner,et al. An investigation of human sperm pronuclear chromosome "gaps" using scanning electron microscopy. , 1986, Cytogenetics and cell genetics.
[2] A. Carrano,et al. Determination of the baseline sister chromatid exchange frequency in human and mouse peripheral lymphocytes using monoclonal antibodies and very low doses of bromodeoxyuridine. , 1986, Cytogenetics and cell genetics.
[3] G. Sutherland,et al. Heritable fragile sites on human chromosomes. XI. Factors affecting expression of fragile sites at 10q25, 16q22, and 17p12. , 1984, American journal of human genetics.
[4] C. Harrison,et al. The fragile X: a scanning electron microscope study. , 1983, Journal of medical genetics.
[5] G. Croci. BrdU-sensitive fragile site on long arm of chromosome 16. , 1983, American journal of human genetics.
[6] R. Painter. A replication model for sister-chromatid exchange. , 1980, Mutation research.
[7] Chung-Cheng Liu,et al. Type II DNA topoisomerases: Enzymes that can unknot a topologically knotted DNA molecule via a reversible double-strand break , 1980, Cell.
[8] A. Krey. Non-Intercalative Binding to DNA , 1980 .
[9] S. Wolff,et al. New Giemsa method for the differential staining of sister chromatids , 1974, Nature.
[10] S. Latt. Localization of Sister Chromatid Exchanges in Human Chromosomes , 1974, Science.
[11] E. Delain,et al. Mécanisme d'action des diamidines trypanocides. Importance de la composition en bases dans l'association berenil-polynucléotides. , 1970 .