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Heritable disorders of DNA repair: xeroderma pigmentosum and Fanconi's anemia.
Curr Probl Dermatol. 1987;17:182-98. doi: 10.1159/000413483.
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DNA repair defects in genetic diseases in man.
Biochimie. 1978;60(10):1173-4. doi: 10.1016/s0300-9084(79)80351-x.
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The Fritz-Lipmann lecture. DNA repair in human cells. Biochemistry of the hereditary diseases Fanconi's anaemia and Cockayne syndrome.
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Two complementation groups of Fanconi's anemia differ in their phenotypic response to a DNA-crosslinking treatment.
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Human disorders showing increased sensitivity to the induction of genetic damage.
Annu Rev Genet. 1978;12:95-115. doi: 10.1146/annurev.ge.12.120178.000523.
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Cross-link repair in human cells and its possible defect in Fanconi's anemia cells.
J Mol Biol. 1977 Jul 15;113(4):635-49. doi: 10.1016/0022-2836(77)90227-3.
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[Chromosome instability syndromes].
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Complementation studies between Fanconi's anemia cells with different DNA repair characteristics.
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Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogens.
Nature. 1976 Jun 10;261(5560):494-6. doi: 10.1038/261494a0.
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[Chromosome instability syndromes].
Pathol Biol (Paris). 1982 Nov;30(9):802-16.
引用本文的文献
1
A new anticancer platinum compound, (-)-(R)-2-aminomethyl-pyrrolidine(1,1-cyclobutanedicarboxylato) platinum(II): DNA interstrand crosslinking, repair and lethal effects in normal human, Fanconi's anaemia and xeroderma pigmentosum cells.
Br J Cancer. 1993 Jun;67(6):1285-92. doi: 10.1038/bjc.1993.239.
2
Defective replication of psoralen adducts detected at the gene-specific level in xeroderma pigmentosum variant cells.
Mol Cell Biol. 1993 Feb;13(2):1002-12. doi: 10.1128/mcb.13.2.1002-1012.1993.
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