Fanconi's anaemia: correlation of genetic complementation group with psoralen/UVA response
- 1 January 1988
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 78 (1) , 51-54
- https://doi.org/10.1007/bf00291234
Abstract
The correlation found by Moustacchi (1987) between cellular response to a crosslinking challenge and genetic heterogeneity in Fanconi's anaemia is confirmed for an earlier set of complementation groups (Zakrzewski and Sperling 1980). This allows the matching of the two independently established complementation groupings and better characterization of their DNA repair-related biochemical properties.Keywords
This publication has 26 references indexed in Scilit:
- REVIEWBiological Chemistry Hoppe-Seyler, 1986
- Identification of two complementation groups in Fanconi anemiaSomatic Cell and Molecular Genetics, 1985
- Regulation of DNA ligase activity by poly(ADP-ribose)Nature, 1982
- Analysis of heterogeneity in Fanconi's anemia patients of different ethnic originHuman Genetics, 1982
- Rejoining of DNA double‐strand breaks in human fibroblasts and its impairment in one ataxia telangiectasia and two fanconi strainsJournal of Supramolecular Structure and Cellular Biochemistry, 1981
- Specific cellular defects in patients with Fanconi anemiaJournal of Cellular Physiology, 1979
- Deficiency of DNA ligase activity in Fanconi's anemiaHuman Genetics, 1978
- Cross-link repair in human cells and its possible defect in Fanconi's anemia cellsJournal of Molecular Biology, 1977
- Clinical and cytogenetic observations during a six-year period in an adult with Fanconi's anaemiaAnnals of Hematology, 1977
- Frequency and distribution of sister-chromatid exchanges in a case of Fanconi's anemiaHuman Genetics, 1975