Skip to main content
NCBI home page
British Journal of Cancer logoLink to British Journal of Cancer
. 1987 Aug;56(2):173–209. doi: 10.1038/bjc.1987.180

Twenty-eighth annual meeting of the British Association for Cancer Research (in conjunction with the second annual meeting of the Association of Cancer Physicians). April 6-8, 1987, Newcastle-upon-Tyne, UK. Abstracts.

PMCID: PMC2002145  PMID: 3663470

Full text

PDF
173

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Angel P., Pöting A., Mallick U., Rahmsdorf H. J., Schorpp M., Herrlich P. Induction of metallothionein and other mRNA species by carcinogens and tumor promoters in primary human skin fibroblasts. Mol Cell Biol. 1986 May;6(5):1760–1766. doi: 10.1128/mcb.6.5.1760. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bargmann C. I., Hung M. C., Weinberg R. A. Multiple independent activations of the neu oncogene by a point mutation altering the transmembrane domain of p185. Cell. 1986 Jun 6;45(5):649–657. doi: 10.1016/0092-8674(86)90779-8. [DOI] [PubMed] [Google Scholar]
  3. Berthois Y., Katzenellenbogen J. A., Katzenellenbogen B. S. Phenol red in tissue culture media is a weak estrogen: implications concerning the study of estrogen-responsive cells in culture. Proc Natl Acad Sci U S A. 1986 Apr;83(8):2496–2500. doi: 10.1073/pnas.83.8.2496. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bonnevie-Nielsen V., Tager H. S. Glucagon receptors on isolated hepatocytes and hepatocyte membrane vesicles. Discrete populations with ligand- and environment-dependent affinities. J Biol Chem. 1983 Sep 25;258(18):11313–11320. [PubMed] [Google Scholar]
  5. Burridge K. Changes in cellular glycoproteins after transformation: identification of specific glycoproteins and antigens in sodium dodecyl sulfate gels. Proc Natl Acad Sci U S A. 1976 Dec;73(12):4457–4461. doi: 10.1073/pnas.73.12.4457. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cifone M. A., Fidler I. J. Increasing metastatic potential is associated with increasing genetic instability of clones isolated from murine neoplasms. Proc Natl Acad Sci U S A. 1981 Nov;78(11):6949–6952. doi: 10.1073/pnas.78.11.6949. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Clarke R., Van den Berg H. W., Kennedy D. G., Murphy R. F. Oestrogen receptor status and the response of human breast cancer cell lines to a combination of methotrexate and 17-beta oestradiol. Br J Cancer. 1985 Mar;51(3):365–369. doi: 10.1038/bjc.1985.48. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Deacon J. M., Holliday S. B., Ahmed I., Jenkins T. C. Experimental pharmacokinetics of RSU-1069 and its analogues: high tumor/plasma ratios. Int J Radiat Oncol Biol Phys. 1986 Jul;12(7):1087–1090. doi: 10.1016/0360-3016(86)90232-4. [DOI] [PubMed] [Google Scholar]
  9. Double J. A., Bibby M. C., Loadman P. M. Pharmacokinetics and anti-tumour activity of LM985 in mice bearing transplantable adenocarcinomas of the colon. Br J Cancer. 1986 Oct;54(4):595–600. doi: 10.1038/bjc.1986.214. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Downes C. S., Ord M. J., Mullinger A. M., Collins A. R., Johnson R. T. Novobiocin inhibition of DNA excision repair may occur through effects on mitochondrial structure and ATP metabolism, not on repair topoisomerases. Carcinogenesis. 1985 Sep;6(9):1343–1352. doi: 10.1093/carcin/6.9.1343. [DOI] [PubMed] [Google Scholar]
  11. Evan G. I., Hancock D. C. Studies on the interaction of the human c-myc protein with cell nuclei: p62c-myc as a member of a discrete subset of nuclear proteins. Cell. 1985 Nov;43(1):253–261. doi: 10.1016/0092-8674(85)90030-3. [DOI] [PubMed] [Google Scholar]
  12. Koch G., Smith M., Twentyman P., Wright K. Identification of a novel calcium-binding protein (CP22) in multidrug-resistant murine and hamster cells. FEBS Lett. 1986 Jan 20;195(1-2):275–279. doi: 10.1016/0014-5793(86)80176-4. [DOI] [PubMed] [Google Scholar]
  13. Kärre K., Ljunggren H. G., Piontek G., Kiessling R. Selective rejection of H-2-deficient lymphoma variants suggests alternative immune defence strategy. Nature. 1986 Feb 20;319(6055):675–678. doi: 10.1038/319675a0. [DOI] [PubMed] [Google Scholar]
  14. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  15. Langdon S. P., Hickman J. A. Correlation between the molecular weight and potency of polar compounds which induce the differentiation of HL-60 human promyelocytic leukemia cells. Cancer Res. 1987 Jan 1;47(1):140–144. [PubMed] [Google Scholar]
  16. McFerran N. V., Quigley T. P. Towards an automated two-dimensional gel analysis system. Biochem Soc Trans. 1984 Dec;12(6):1000–1005. doi: 10.1042/bst0121000. [DOI] [PubMed] [Google Scholar]
  17. McGown A. T., Ward T. H., Fox B. W. Comparative studies of the uptake of daunorubicin in sensitive and resistant P388 cell lines by flow cytometry and biochemical extraction procedures. Cancer Chemother Pharmacol. 1983;11(2):113–116. doi: 10.1007/BF00254258. [DOI] [PubMed] [Google Scholar]
  18. Neulat-Duga I., Sheppel A., Marty C., Lacroux F., Pourrat J., Caverivière P., Delsol G. Metastases of human tumor xenografts in nude mice. Invasion Metastasis. 1984;4(4):209–224. [PubMed] [Google Scholar]
  19. Ormerod E. J., Everett C. A., Hart I. R. Enhanced experimental metastatic capacity of a human tumor line following treatment with 5-azacytidine. Cancer Res. 1986 Feb;46(2):884–890. [PubMed] [Google Scholar]
  20. Roscoe J. P., Claisse P. J. A sequential in vivo-in vitro study of carcinogenesis induced in the rat brain by ethylnitrosourea. Nature. 1976 Jul 22;262(5566):314–316. doi: 10.1038/262314a0. [DOI] [PubMed] [Google Scholar]
  21. Saffhill R. In vitro reaction of N-n-butyl-N-nitrosourea and n-butyl methanesulphonate with guanine and thymine bases of DNA. Carcinogenesis. 1984 May;5(5):621–625. doi: 10.1093/carcin/5.5.621. [DOI] [PubMed] [Google Scholar]
  22. Saffhill R., Margison G. P., O'Connor P. J. Mechanisms of carcinogenesis induced by alkylating agents. Biochim Biophys Acta. 1985 Dec 17;823(2):111–145. doi: 10.1016/0304-419x(85)90009-5. [DOI] [PubMed] [Google Scholar]
  23. Subramani S., Rubnitz J. Recombination events after transient infection and stable integration of DNA into mouse cells. Mol Cell Biol. 1985 Apr;5(4):659–666. doi: 10.1128/mcb.5.4.659. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Talmadge J. E., Donovan P. A., Hart I. R. Inhibition of cellular division of a murine macrophage tumor by macrophage-activating agents. Cancer Res. 1982 May;42(5):1850–1855. [PubMed] [Google Scholar]
  25. Taniguchi K., Kärre K., Klein G. Lung colonization and metastasis by disseminated B16 melanoma cells: H-2 associated control at the level of the host and the tumor cell. Int J Cancer. 1985 Oct 15;36(4):503–510. doi: 10.1002/ijc.2910360415. [DOI] [PubMed] [Google Scholar]
  26. Taylor D., Hochstein P. Inhibition by adriamycin of a metmyoglobin reductase from beef heart. Biochem Pharmacol. 1978;27(16):2079–2082. doi: 10.1016/0006-2952(78)90073-4. [DOI] [PubMed] [Google Scholar]
  27. Törnqvist M., Mowrer J., Jensen S., Ehrenberg L. Monitoring of environmental cancer initiators through hemoglobin adducts by a modified Edman degradation method. Anal Biochem. 1986 Apr;154(1):255–266. doi: 10.1016/0003-2697(86)90524-5. [DOI] [PubMed] [Google Scholar]
  28. Valerie K., de Riel J. K., Henderson E. E. Genetic complementation of UV-induced DNA repair in Chinese hamster ovary cells by the denV gene of phage T4. Proc Natl Acad Sci U S A. 1985 Nov;82(22):7656–7660. doi: 10.1073/pnas.82.22.7656. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Workman P., Walton M. I. Pharmacology of the mixed-function radio- and chemosensitizers CB 1954 and RSU 1069. Int J Radiat Oncol Biol Phys. 1984 Aug;10(8):1307–1310. doi: 10.1016/0360-3016(84)90337-7. [DOI] [PubMed] [Google Scholar]

Articles from British Journal of Cancer are provided here courtesy of Cancer Research UK

RESOURCES