Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: A third repair gene on human chromosome 19
Open Access
- 1 November 1989
- Vol. 5 (4) , 670-679
- https://doi.org/10.1016/0888-7543(89)90107-9
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- Mammalian DNA repair — use of mutants hypersensitive to cytotoxic agentsTrends in Genetics, 1988
- Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19qHuman Genetics, 1987
- A simple and ranid method for preparing yeast chromosomes for Pulse Field Gel ElectrophoresisNucleic Acids Research, 1987
- Transforming growth factor β gene maps to human chromosome 19 long arm and to mouse chromosome 7Somatic Cell and Molecular Genetics, 1986
- Electrophoretic Separations of Large DNA Molecules by Periodic Inversion of the Electric FieldScience, 1986
- Toward early diagnosis of myotonic dystrophy:construction and characterization of a somatic cell hybrid with a single human der(19) chromosomeCytogenetic and Genome Research, 1986
- Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybridsCytogenetic and Genome Research, 1986
- Rapid detection of DNA-damaging agents using repair-deficient CHO cellsMutation Research/Environmental Mutagenesis and Related Subjects, 1984
- The cDNA for the β-subunit of human chorionic gonadotropin suggests evolution of a gene by readthrough into the 3′-untranslated regionNature, 1980
- The chromosomes of CHO, an aneuploid Chinese hamster cell line: G-band, C-band, and autoradiographic analysesChromosoma, 1973