Zobrazeno 1 - 10
of 314
pro vyhledávání: '"Arlett, C"'
Autor:
Lehmann, A. R., Kirk-Bell, S., Arlett, C. F., Paterson, M. C., Lohman, P. H. M., De Weerd-Kastelein, E. A., Bootsma, D.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1975 Jan 01. 72(1), 219-223.
Externí odkaz:
https://www.jstor.org/stable/64309
Autor:
Badie, C., Iliakis, G., Foray, N., Alsbeih, G., Cedervall, B., Chavaudra, N., Pantelias, G., Arlett, C., Malaise, E. P.
Publikováno v:
Radiation Research, 1995 Oct 01. 144(1), 26-35.
Externí odkaz:
https://www.jstor.org/stable/3579232
Autor:
Ulus-Senguloglu, G1, Arlett, C F2, Plowman, P N3, Parnell, J1, Patel, N1, Bourton, E C1, Parris, C N1
Publikováno v:
British Journal of Cancer. 10/23/2012, Vol. 107 Issue 9, p1506-1513. 8p. 1 Color Photograph, 2 Charts, 6 Graphs.
Publikováno v:
Bulletin (Association for Tropical Biology), 1962 Jan 01(1), 96-98.
Externí odkaz:
https://www.jstor.org/stable/45132451
Publikováno v:
International Journal of Radiation Biology. Dec99, Vol. 75 Issue 12, p1589-1595. 7p. 8 Graphs.
Autor:
Arlett, C. F.1, Lehmann, A. R.1
Publikováno v:
Annual Review of Genetics. 1978, Vol. 12, p95-115. 21p.
Autor:
Broughton, B. C., Thompson, A. F., Harcourt, S. A., Vermeulen, W., Hoeijmakers, J. H. J., Botta, E., Stefanini, M., King, M. D., Weber, C. A., Cole, J., Arlett, C. F., Lehmann, A. R.
Xeroderma pigmentosum (XP) and Cockayne syndrome (CS) are quite distinct genetic disorders that are associated with defects in excision repair of UV-induced DNA damage. A few patients have been described previously with the clinical features of both
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8ca6f55209346691751d667cd962a066
https://europepmc.org/articles/PMC1801309/
https://europepmc.org/articles/PMC1801309/
Autor:
Stefanini, M., Vermeulen, W., Weeda, G., Giliani, S., Nardo, T., Mezzina, M., Sarasin, A., Harper, J. I., Arlett, C. F., Hoeijmakers, J. H. J., Lehmann, A. R.
The sun-sensitive, cancer-prone genetic disorder xeroderma pigmentosum (XP) is associated in most cases with a defect in the ability to carry out excision repair of UV damage. Seven genetically distinct complementation groups (i.e., A-G) have been id
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8be57c258a46304d1497127e20f0b1fb
https://hdl.handle.net/11379/565972
https://hdl.handle.net/11379/565972