Lethal and kinetic effects of DDMP (2,4-diamino-5-(3′,4′-dichlorophenyl)-6-methylpyrimidine)-Reference-Cited by-同舟云学术

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Lethal and kinetic effects of DDMP (2,4-diamino-5-(3′,4′-dichlorophenyl)-6-methylpyrimidine)

Published:1980-01 Issue:1 Volume:16 Page:147-157
ISSN:0014-2964
Container-title:European Journal of Cancer (1965)
language:en
Short-container-title:European Journal of Cancer (1965)

Author:

Hill Bridget T.,Whelan R.D.H.

Publisher

Elsevier BV

Subject

General Medicine

Reference38 articles.

1. Studies concerned with overcoming resistance to methotrexate: a comparison of the effects of methotrexate and 2,4-diamino-5-(3′-4′-dichlotophenyl-)-6-methyl pyrimidine (BW 51097) on the colony-forming ability of L5178Y cells;Hill;Brit. J. Cancer,1973

2. Attempts to overcome methotrexate resistance: the value of drug-resistant cell lines;Hill,1976

3. Diamino dichlorophenyl pyrimidines in mouse leukemia;Burchenal;Cancer Res.,1952

4. Effect of 2,4-diamino pyrimidines on mouse sarcoma 180;Clarke;Cancer Res.,1952

5. Effects of various compounds on the Ehrlich ascites carcinoma;Sugiura;Cancer Res.,1953

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1. Differential patterns of anti-tumour drug responses and mechanisms of resistance in a series of independently-derived VP-16-resistant human tumour cell lines;International Journal of Cancer;1988-09-15

2. Characterization of a continuous cell line in culture established from a Krukenberg tumour of the ovary arising from a primary gastric adenocarcinoma;European Journal of Cancer and Clinical Oncology;1988-09

3. Establishment and characterisation of three new human ovarian carcinoma cell lines and initial evaluation of their potential in experimental chemotherapy studies;International Journal of Cancer;1987-02-15

4. Establishment of an etoposide-resistant human epithelial tumour cell lineIn vitro: Characterization of patterns of cross-resistance and drug sensitivities;International Journal of Cancer;1984-05-15

5. Identification of differential drug responses and mechanism(s) of resistance in vincristine-resistant cell lines developed either by exposure to the drug or to fractionated radiation;Cancer Treatment Reviews;1984-03

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