Zobrazeno 1 - 10
of 28
pro vyhledávání: '"S. F. Stinson"'
Publikováno v:
Xenobiotica. 32:339-347
1. The single-dose plasma pharmacokinetics of O(2)-vinyl 1-(pyrrolidin-1-yl)diazen-1-ium-1,2-diolate (V-PYRRO/NO) following intravenous (i.v.) and intraperitoneal (i.p.) bolus administration to the male C57BL/6 mouse was studied in an effort to chara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::816ffe94c3f794c05924941236fa1aed
https://doi.org/10.1080/00498250110102665
https://doi.org/10.1080/00498250110102665
Autor:
M S, Chua, E, Kashiyama, T D, Bradshaw, S F, Stinson, E, Brantley, E A, Sausville, M F, Stevens
Publikováno v:
Cancer research. 60(18)
2-(4-Amino-3-methylphenyl)benzothiazole (DF 203, NSC 674495) is a candidate antitumor agent with potent and selective activity against human-derived tumor cell lines in vitro and in vivo. Only sensitive cell lines (e.g., MCF-7) were able to accumulat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df666f2231bc34f22f7c0cacf1d3a17e
https://pubmed.ncbi.nlm.nih.gov/11016648
https://pubmed.ncbi.nlm.nih.gov/11016648
Publikováno v:
Biochemical pharmacology. 57(11)
The tricyclic compound 2,5-bis(5-hydroxymethyl-2-thienyl)furan (NSC 652287) has shown a highly selective pattern of differential cytotoxic activity in the tumor cell lines comprising the National Cancer Institute (NCI) Anticancer Drug Screen. The mec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2db5271a4b17c156b6efdafd96402aa4
https://pubmed.ncbi.nlm.nih.gov/10230772
https://pubmed.ncbi.nlm.nih.gov/10230772
Autor:
F, Arguello, M, Alexander, J A, Sterry, G, Tudor, E M, Smith, N T, Kalavar, J F, Greene, W, Koss, C D, Morgan, S F, Stinson, T J, Siford, W G, Alvord, R L, Klabansky, E A, Sausville
Publikováno v:
Blood. 91(7)
Flavopiridol is a novel semisynthetic flavone derivative of the alkaloid rohitukine. Flavopiridol is known to inhibit potently the activity of multiple cyclin-dependent kinases. We have assessed its effects on normal and malignant cells in preclinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b0968500375ee8f92ae51f56d9aa50ab
https://pubmed.ncbi.nlm.nih.gov/9516149
https://pubmed.ncbi.nlm.nih.gov/9516149
Publikováno v:
IARC scientific publications. (111)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f82f4d033b559ba15126b1071ad226a6
https://pubmed.ncbi.nlm.nih.gov/8082911
https://pubmed.ncbi.nlm.nih.gov/8082911
Autor:
S F, Stinson, M C, Alley, W C, Kopp, H H, Fiebig, L A, Mullendore, A F, Pittman, S, Kenney, J, Keller, M R, Boyd
Publikováno v:
Anticancer research. 12(4)
A panel of 60 human tumor cell lines is currently being used in the U.S. National Cancer Institute's in vitro anticancer drug screen. The panel is organized into 7 subpanels; 6 leukemia/lymphoma lines comprise one subpanel, and 54 other lines are org
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2301e7e1db52d956f5f1d1783257d5de
https://pubmed.ncbi.nlm.nih.gov/1503399
https://pubmed.ncbi.nlm.nih.gov/1503399
Autor:
L, Wu, A M, Smythe, S F, Stinson, L A, Mullendore, A, Monks, D A, Scudiero, K D, Paull, A D, Koutsoukos, L V, Rubinstein, M R, Boyd
Publikováno v:
Cancer research. 52(11)
Disease-oriented panels of human tumor cell lines used by the National Cancer Institute for large-scale in vitro anticancer drug screening were evaluated for multidrug-resistant phenotype at the functional (in vitro drug sensitivity) and molecular le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2b32d3aee985474d242b688c59fe7799
https://pubmed.ncbi.nlm.nih.gov/1350507
https://pubmed.ncbi.nlm.nih.gov/1350507
Autor:
W. A. Harrison, James B. McMahon, S F Stinson, J. B. Pierce, John P. Bader, V L Narayanan, Owen S. Weislow, M. R. Boyd, R. J. Schultz, C. F. Midelfort
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 88(15)
Oxathiin carboxanilide (OC), NSC 615985, a compound originally synthesized as a potential fungicide, was demonstrated to be highly active in preventing human immunodeficiency virus (HIV)-induced cell killing and in inhibiting HIV reproduction. Virus-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8205e08916c4be87fc6eb46a5bb82ce7
https://pubmed.ncbi.nlm.nih.gov/1713689
https://pubmed.ncbi.nlm.nih.gov/1713689
Autor:
S. F. Stinson, M. B. Sporn
Publikováno v:
Journal of Microscopy. 109:329-335
SUMMARY The feasibility of using an automated image analyser to evaluate quantitatively hyperplasia caused by N-butyl-N-(4-hydroxybutyl) nitrosamine in bladder epithelium was studied. The number of cells per unit length of epithelium was counted manu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec56e9955d2248c4eb44f3a304840683
https://doi.org/10.1111/j.1365-2818.1977.tb01146.x
https://doi.org/10.1111/j.1365-2818.1977.tb01146.x
Publikováno v:
Clinical Chemistry. 17:1050-1054
A direct o-toluidine method for serum glucose is described as an alternative to the usual Cu—neocuproine method used with the Technicon SMA 12/60 AutoAnalyzer. Routine operation of the machine is simplified: the number of reagents and manifold line
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f56a0887fc519b44c4184950cd3d0fc
https://doi.org/10.1093/clinchem/17.10.1050
https://doi.org/10.1093/clinchem/17.10.1050