These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Recent progress with the DNA repair mutants of Chinese hamster ovary cells. Thompson LH, Salazar EP, Brookman KW, Collins CC, Stewart SA, Busch DB, Weber CA. J Cell Sci Suppl; 1987; 6():97-110. PubMed ID: 3477565 [Abstract] [Full Text] [Related]
3. Assignment of a human DNA-repair gene associated with sister-chromatid exchange to chromosome 19. Siciliano MJ, Carrano AV, Thompson LH. Mutat Res; 1986 Aug; 174(4):303-8. PubMed ID: 3736579 [Abstract] [Full Text] [Related]
4. Genetic complementation between UV-sensitive CHO mutants and xeroderma pigmentosum fibroblasts. Thompson LH, Mooney CL, Brookman KW. Mutat Res; 1985 Aug; 150(1-2):423-9. PubMed ID: 4000167 [Abstract] [Full Text] [Related]
8. Correction of a nucleotide-excision-repair mutation by human chromosome 19 in hamster-human hybrid cells. Thompson LH, Mooney CL, Burkhart-Schultz K, Carrano AV, Siciliano MJ. Somat Cell Mol Genet; 1985 Jan; 11(1):87-92. PubMed ID: 3919454 [Abstract] [Full Text] [Related]
9. Isolation of the functional human excision repair gene ERCC5 by intercosmid recombination. Mudgett JS, MacInnes MA. Genomics; 1990 Dec; 8(4):623-33. PubMed ID: 2276736 [Abstract] [Full Text] [Related]
10. Molecular cloning and biological characterization of the human excision repair gene ERCC-3. Weeda G, van Ham RC, Masurel R, Westerveld A, Odijk H, de Wit J, Bootsma D, van der Eb AJ, Hoeijmakers JH. Mol Cell Biol; 1990 Jun; 10(6):2570-81. PubMed ID: 2111438 [Abstract] [Full Text] [Related]
15. A CHO-cell strain having hypersensitivity to mutagens, a defect in DNA strand-break repair, and an extraordinary baseline frequency of sister-chromatid exchange. Thompson LH, Brookman KW, Dillehay LE, Carrano AV, Mazrimas JA, Mooney CL, Minkler JL. Mutat Res; 1982 Aug; 95(2-3):427-40. PubMed ID: 6889677 [Abstract] [Full Text] [Related]
16. The Chinese hamster FANCG/XRCC9 mutant NM3 fails to express the monoubiquitinated form of the FANCD2 protein, is hypersensitive to a range of DNA damaging agents and exhibits a normal level of spontaneous sister chromatid exchange. Wilson JB, Johnson MA, Stuckert AP, Trueman KL, May S, Bryant PE, Meyn RE, D'Andrea AD, Jones NJ. Carcinogenesis; 2001 Dec; 22(12):1939-46. PubMed ID: 11751423 [Abstract] [Full Text] [Related]
20. Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19. Thompson LH, Bachinski LL, Stallings RL, Dolf G, Weber CA, Westerveld A, Siciliano MJ. Genomics; 1989 Nov; 5(4):670-9. PubMed ID: 2591959 [Abstract] [Full Text] [Related] Page: [Next] [New Search]