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Proceedings of the National Academy of Sciences of the United States of America|June 1, 1983
Expression of human myeloid-associated surface antigens in human-mouse myeloid cell hybridsA H Geurts van Kessel, P A Tetteroo, A E von dem Borne, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1991
Structural and functional conservation of two human homologs of the yeast DNA repair gene RAD6M H Koken, P Reynolds, I Jaspers-Dekker, et al.
Cell|August 24, 1990
A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndromeG Weeda, R C van Ham, W Vermeulen, et al.
Experimental Cell Research|April 1, 1987
Localization of a gene involved in complementation of the defect in xeroderma pigmentosum group A cells on human chromosome 1W Keijzer, M Stefanini, D Bootsma, et al.
Carcinogenesis|December 1, 1991
Characterization of the mouse homolog of the XPBC/ERCC-3 gene implicated in xeroderma pigmentosum and Cockayne's syndromeG Weeda, L Ma, R C van Ham, et al.
Tsitologiia|January 1, 1996
[The dual function of the proliferating cell nuclear antigen (PCNA) in the response of human cells to UV damages]L V Solov'eva, M P Svetlova, R Hancock, et al.
Mutation Research|May 1, 1985
A ninth complementation group in xeroderma pigmentosum, XP IE Fischer, W Keijzer, H W Thielmann, et al.
The Journal of Experimental Medicine|July 1, 1983
c-sis is translocated from chromosome 22 to chromosome 9 in chronic myelocytic leukemiaJ Groffen, N Heisterkamp, J R Stephenson, et al.
The EMBO Journal|September 1, 1993
Evidence for a repair enzyme complex involving ERCC1 and complementing activities of ERCC4, ERCC11 and xeroderma pigmentosum group FA J van Vuuren, E Appeldoorn, H Odijk, et al.
Bailliere'S Clinical Haematology|October 1, 1992
Translocation t(6;9) in acute non-lymphocytic leukaemia results in the formation of a DEK-CAN fusion geneM von Lindern, M Fornerod, N Soekarman, et al.
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