Detection of Unique Antigenic Lesions in the Uracil DNA Glycosylase from Bloom’s Syndrome
Author:
Publisher
Springer US
Link
http://link.springer.com/content/pdf/10.1007/978-1-4684-1327-4_36.pdf
Reference37 articles.
1. Arenaz, P. and Sirover, M.A., 1983, Isolation and characterization of monoclonal antibodies to the uracil DNA glycosylase from human placenta, Proc. Natl. Acad. Sci., USA, 80:5822.
2. Bessman, M.J., Lehman, I.R., Adler, J., Zimmerman, S.B., Simns, E.S., and Kornberg, A., 1958, Enzymatic synthesis of DNA. III. The incorporation of purine and pyrimidine analogues into DNA. Proc. Natl. Acad. Sci., USA, 44:633.
3. Bloom, D., 1966, The syndrome of congenital telangiectatic erythema and stunted growth, J. Pediatrics, 68:103.
4. Bryant, E.M., Hoehn, H., and Martin, G.M., 1979, Normalization of sister chromatid exchange frequencies in Bloom’s syndrome by euploid cell hybridization. Nature, 279:795.
5. Chaganti, R.S.K., Schonberg, S. and German, J., 1979, A many fold increase in sister chromatid exchanges in Bloom’s syndrome lymphocytes. Proc. Natl. Acad. Sci., USA, 71:4508.
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