-
1
-
-
7844232347
-
Indolequinones and cyclopropamitosenes as novel bioreductive anticancer agents. Metabolism and chemosensitivity studies
-
Some of the results herein have been presented in preliminary form: Ross, D.; Beall, H. D.; Bourne, J. T.; Bolton, E. M.; Cotterill, A. S.; Swann, E.; Moody, C. J. Indolequinones and cyclopropamitosenes as novel bioreductive anticancer agents. Metabolism and chemosensitivity studies. Proc. Am. Assoc. Cancer Res. 1996, 37, 295. Beall, H. D.; Griffin, A. M.; Poulet, C.; Swann, E.; Moody, C. J.; Ross, D. Bioactivation of novel indolequinones, mitosenes and cyclopropamitosenes by NAD-(P)H:quinone oxidoreductase (NQO1): structure-metabolism and structure-cytotoxicity studies. Proc. Am. Assoc. Cancer Res. 1997, 38, 6612. Beall, H. D.; Hudnott, A. R.; Winski, S.; Siegel, D.; Swann, E.; Ross, D.; Moody, C. J. Indolequinone antitumor agents: relationship between quinone structure and rate of metabolism by recombinant human NQO1. Bioorg. Med. Chem. Lett. 1998, 8, 545-548.
-
(1996)
Proc. Am. Assoc. Cancer Res.
, vol.37
, pp. 295
-
-
Ross, D.1
Beall, H.D.2
Bourne, J.T.3
Bolton, E.M.4
Cotterill, A.S.5
Swann, E.6
Moody, C.J.7
-
2
-
-
7844223234
-
Bioactivation of novel indolequinones, mitosenes and cyclopropamitosenes by NAD-(P)H:quinone oxidoreductase (NQO1): Structure-metabolism and structure-cytotoxicity studies
-
Some of the results herein have been presented in preliminary form: Ross, D.; Beall, H. D.; Bourne, J. T.; Bolton, E. M.; Cotterill, A. S.; Swann, E.; Moody, C. J. Indolequinones and cyclopropamitosenes as novel bioreductive anticancer agents. Metabolism and chemosensitivity studies. Proc. Am. Assoc. Cancer Res. 1996, 37, 295. Beall, H. D.; Griffin, A. M.; Poulet, C.; Swann, E.; Moody, C. J.; Ross, D. Bioactivation of novel indolequinones, mitosenes and cyclopropamitosenes by NAD-(P)H:quinone oxidoreductase (NQO1): structure-metabolism and structure-cytotoxicity studies. Proc. Am. Assoc. Cancer Res. 1997, 38, 6612. Beall, H. D.; Hudnott, A. R.; Winski, S.; Siegel, D.; Swann, E.; Ross, D.; Moody, C. J. Indolequinone antitumor agents: relationship between quinone structure and rate of metabolism by recombinant human NQO1. Bioorg. Med. Chem. Lett. 1998, 8, 545-548.
-
(1997)
Proc. Am. Assoc. Cancer Res.
, vol.38
, pp. 6612
-
-
Beall, H.D.1
Griffin, A.M.2
Poulet, C.3
Swann, E.4
Moody, C.J.5
Ross, D.6
-
3
-
-
0032478053
-
Indolequinone antitumor agents: Relationship between quinone structure and rate of metabolism by recombinant human NQO1
-
Some of the results herein have been presented in preliminary form: Ross, D.; Beall, H. D.; Bourne, J. T.; Bolton, E. M.; Cotterill, A. S.; Swann, E.; Moody, C. J. Indolequinones and cyclopropamitosenes as novel bioreductive anticancer agents. Metabolism and chemosensitivity studies. Proc. Am. Assoc. Cancer Res. 1996, 37, 295. Beall, H. D.; Griffin, A. M.; Poulet, C.; Swann, E.; Moody, C. J.; Ross, D. Bioactivation of novel indolequinones, mitosenes and cyclopropamitosenes by NAD-(P)H:quinone oxidoreductase (NQO1): structure-metabolism and structure-cytotoxicity studies. Proc. Am. Assoc. Cancer Res. 1997, 38, 6612. Beall, H. D.; Hudnott, A. R.; Winski, S.; Siegel, D.; Swann, E.; Ross, D.; Moody, C. J. Indolequinone antitumor agents: relationship between quinone structure and rate of metabolism by recombinant human NQO1. Bioorg. Med. Chem. Lett. 1998, 8, 545-548.
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 545-548
-
-
Beall, H.D.1
Hudnott, A.R.2
Winski, S.3
Siegel, D.4
Swann, E.5
Ross, D.6
Moody, C.J.7
-
4
-
-
77957000392
-
DT Diapborase
-
Ernster, L. DT Diapborase. Methods Enzymol. 1967, 10, 309-317.
-
(1967)
Methods Enzymol.
, vol.10
, pp. 309-317
-
-
Ernster, L.1
-
5
-
-
0002117840
-
DT Diaphorase: A historical review
-
Ernster, L. DT Diaphorase: a historical review. Chem. Scripta 1987, 27A, 1-13.
-
(1987)
Chem. Scripta
, vol.27 A
, pp. 1-13
-
-
Ernster, L.1
-
6
-
-
0025142668
-
DT Diaphorase; purification, properties and function
-
Lind, C.; Cadenas, E.; Hochstein, P.; Ernster, L. DT Diaphorase; purification, properties and function. Methods Enzymol. 1990, 186, 287-301.
-
(1990)
Methods Enzymol.
, vol.186
, pp. 287-301
-
-
Lind, C.1
Cadenas, E.2
Hochstein, P.3
Ernster, L.4
-
7
-
-
0023724493
-
Human dioxin-inducible cytosolic NAD(P)H-menadione oxidoreductase - CDNA sequence and localization of gene to chromosome-16
-
Jaiswal, A. K.; McBride, O. W.; Adesnik, M.; Nebert, D. W. Human dioxin-inducible cytosolic NAD(P)H-menadione oxidoreductase - cDNA sequence and localization of gene to chromosome-16. J. Biol. Chem. 1988, 263, 13572-13578.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 13572-13578
-
-
Jaiswal, A.K.1
McBride, O.W.2
Adesnik, M.3
Nebert, D.W.4
-
8
-
-
0029068515
-
The three-dimensional structure of NAD(P)H:quinone reductase, a flavoprotein involved in cancer chemoprotection and chemotherapy: Mechanism of the two-electron reduction
-
Li, R.; Bianchet, M. A.; Talalay, P.; Amzel, L. M. The three-dimensional structure of NAD(P)H:quinone reductase, a flavoprotein involved in cancer chemoprotection and chemotherapy: mechanism of the two-electron reduction. Proc. Natl. Acad. Sci. U.S.A. 1995, 92, 8846-8850.
-
(1995)
Proc. Natl. Acad. Sci. U.S.A.
, vol.92
, pp. 8846-8850
-
-
Li, R.1
Bianchet, M.A.2
Talalay, P.3
Amzel, L.M.4
-
9
-
-
0027295491
-
DT-Diaphorase in activation and detoxicification of quinones
-
Ross, D.; Siegel, D.; Beall, H.; Prakash, A. S.; Mulcahy, R. T.; Gibson, N. W. DT-Diaphorase in activation and detoxicification of quinones. Cancer Metast. Rev. 1993, 12, 83-101.
-
(1993)
Cancer Metast. Rev.
, vol.12
, pp. 83-101
-
-
Ross, D.1
Siegel, D.2
Beall, H.3
Prakash, A.S.4
Mulcahy, R.T.5
Gibson, N.W.6
-
10
-
-
0028610410
-
Bioactivation of quinones by DT-diaphorase, molecular, biochemical, and chemical studies
-
Ross, D.; Beall, H.; Traver, R. D.; Siegel, D.; Phillips, R. M.; Gibson, N. W. Bioactivation of quinones by DT-diaphorase, molecular, biochemical, and chemical studies. Oncol. Res. 1994, 6, 493-500.
-
(1994)
Oncol. Res.
, vol.6
, pp. 493-500
-
-
Ross, D.1
Beall, H.2
Traver, R.D.3
Siegel, D.4
Phillips, R.M.5
Gibson, N.W.6
-
11
-
-
0029997868
-
Enzymology of bioreductive drug activation
-
Ross, D.; Beall, H. D.; Siegel, D.; Traver, R. D.; Gustafson, D. L. Enzymology of bioreductive drug activation. Br. J. Cancer 1996, 74 (Suppl. XXVII), S1-S8.
-
(1996)
Br. J. Cancer
, vol.74
, Issue.SUPPL. XXVII
-
-
Ross, D.1
Beall, H.D.2
Siegel, D.3
Traver, R.D.4
Gustafson, D.L.5
-
12
-
-
0028645493
-
Enzyme-directed bioreductive drug development revisited: A commentary on recent progress and future prospects with emphasis on quinone anticancer agents and quinone metabolizing enzymes, particularly DT-diaphorase
-
Workman, P. Enzyme-directed bioreductive drug development revisited: a commentary on recent progress and future prospects with emphasis on quinone anticancer agents and quinone metabolizing enzymes, particularly DT-diaphorase. Oncol. Res. 1994, 6, 461-475.
-
(1994)
Oncol. Res.
, vol.6
, pp. 461-475
-
-
Workman, P.1
-
13
-
-
0027390265
-
The one-electron reduction potential of several substrates can be related to their reduction rates by cytochrome P-450 reductase
-
Butler, J.; Hoey, B. M. The one-electron reduction potential of several substrates can be related to their reduction rates by cytochrome P-450 reductase. Biochim. Biophys. Acta 1993, 1161, 73-78.
-
(1993)
Biochim. Biophys. Acta
, vol.1161
, pp. 73-78
-
-
Butler, J.1
Hoey, B.M.2
-
14
-
-
0018875204
-
Relationship or the single-electron reduction potential of quinones with their reduction by flavoproteins
-
Powis, G.; Appel, P. L. Relationship or the single-electron reduction potential of quinones with their reduction by flavoproteins. Biochem. Pharmacol. 1980, 29, 2567-2572.
-
(1980)
Biochem. Pharmacol.
, vol.29
, pp. 2567-2572
-
-
Powis, G.1
Appel, P.L.2
-
15
-
-
0018830610
-
Anaerobic reduction of nitroimidazoles by reduced flavin mononucleotide and xanthine oxidase
-
Clarke, E. D.; Wardman, P.; Goulding, K. H. Anaerobic reduction of nitroimidazoles by reduced flavin mononucleotide and xanthine oxidase. Biochem. Pharmacol. 1980, 29, 2684-2687.
-
(1980)
Biochem. Pharmacol.
, vol.29
, pp. 2684-2687
-
-
Clarke, E.D.1
Wardman, P.2
Goulding, K.H.3
-
16
-
-
0019956167
-
Nitroimidazoles as anaerobic electron acceptors for xanthine oxidase
-
Clarke, E. D.; Goulding, K. H.; Wardman, P. Nitroimidazoles as anaerobic electron acceptors for xanthine oxidase. Biochem. Pharmacol. 1982, 31, 3237-3242.
-
(1982)
Biochem. Pharmacol.
, vol.31
, pp. 3237-3242
-
-
Clarke, E.D.1
Goulding, K.H.2
Wardman, P.3
-
17
-
-
0024498044
-
DT-diaphorase-catalysed reduction of 1,4-naphthoquinone derivatives and glutathionyl-quinone conjugates
-
Buffington, G. D.; Ollinger, K.; Brunmark, A.; Cadenas, E. DT-diaphorase-catalysed reduction of 1,4-naphthoquinone derivatives and glutathionyl-quinone conjugates. Biochem. J. 1989, 257, 561-571.
-
(1989)
Biochem. J.
, vol.257
, pp. 561-571
-
-
Buffington, G.D.1
Ollinger, K.2
Brunmark, A.3
Cadenas, E.4
-
18
-
-
0027048768
-
Relationship between DT-diaphorase-mediated metabolism of a series of aziridinylbenzoquinones and DNA damage and cytotoxicity
-
Gibson, N. W.; Hartley, J. A.; Butler, J.; Siegel, D.; Ross, D. Relationship between DT-diaphorase-mediated metabolism of a series of aziridinylbenzoquinones and DNA damage and cytotoxicity. Mol. Pharmacol. 1992, 42, 531-536.
-
(1992)
Mol. Pharmacol.
, vol.42
, pp. 531-536
-
-
Gibson, N.W.1
Hartley, J.A.2
Butler, J.3
Siegel, D.4
Ross, D.5
-
19
-
-
0029121481
-
NAD(P)H:quinone oxidoreductase (DT-diaphorase) as a target for bioreductive antitumor quinones: Quinone cytotoxicity and selectivity in human lung and breast cancer cell lines
-
Beall, H. D.; Murphy, A. M.; Siegel, D.; Hargreaves, R. H. J.; Butler, J.; Ross, D. NAD(P)H:quinone oxidoreductase (DT-diaphorase) as a target for bioreductive antitumor quinones: quinone cytotoxicity and selectivity in human lung and breast cancer cell lines. Mol. Pharmacol. 1995, 48, 499-504.
-
(1995)
Mol. Pharmacol.
, vol.48
, pp. 499-504
-
-
Beall, H.D.1
Murphy, A.M.2
Siegel, D.3
Hargreaves, R.H.J.4
Butler, J.5
Ross, D.6
-
20
-
-
0025893246
-
The role of NAD(P)H-quinone reductase (EC 1.6.99.2, DT-diaphorase) in the reductive bioactivation of the novel indoloquinone antitumor agent EO9
-
Walton, M. I.; Smith, P. J.; Workman, P. The role of NAD(P)H-quinone reductase (EC 1.6.99.2, DT-diaphorase) in the reductive bioactivation of the novel indoloquinone antitumor agent EO9. Cancer Commun. 1991, 3, 199-206.
-
(1991)
Cancer Commun.
, vol.3
, pp. 199-206
-
-
Walton, M.I.1
Smith, P.J.2
Workman, P.3
-
21
-
-
0026724635
-
The sensitivity of human tumor-cells to quinone bioreductive drugs - What role for DT-diaphorase
-
Robertson, N.; Stratford, I. J.; Houlbrook, S.; Carmichael, J.; Adams, G. E. The sensitivity of human tumor-cells to quinone bioreductive drugs - what role for DT-diaphorase. Biochem. Pharmacol. 1992, 44, 409-412.
-
(1992)
Biochem. Pharmacol.
, vol.44
, pp. 409-412
-
-
Robertson, N.1
Stratford, I.J.2
Houlbrook, S.3
Carmichael, J.4
Adams, G.E.5
-
22
-
-
0028101349
-
Factors affecting sensitivity to EO9 in rodent and human tumor-cells in vitro - DT-diaphorase activity and hypoxia
-
Robertson, N.; Haigh, A.; Adams, G. E.; Stratford, I. J. Factors affecting sensitivity to EO9 in rodent and human tumor-cells in vitro - DT-diaphorase activity and hypoxia. Eur. J. Cancer 1994, 30A, 1013-1019.
-
(1994)
Eur. J. Cancer
, vol.30 A
, pp. 1013-1019
-
-
Robertson, N.1
Haigh, A.2
Adams, G.E.3
Stratford, I.J.4
-
23
-
-
0028272417
-
Cyclopropamitosenes, novel bioreductive anticancer agents; mechanism of action and enzymic reduction
-
Moody, C. J.; O'Sullivan, N.; Stratford, I. J.; Stephens, M. A.; Workman, P.; Bailey, S. M.; Lewis, A. Cyclopropamitosenes, novel bioreductive anticancer agents; mechanism of action and enzymic reduction. Anti-Cancer Drugs 1994, 5, 367-372.
-
(1994)
Anti-Cancer Drugs
, vol.5
, pp. 367-372
-
-
Moody, C.J.1
O'Sullivan, N.2
Stratford, I.J.3
Stephens, M.A.4
Workman, P.5
Bailey, S.M.6
Lewis, A.7
-
24
-
-
0028236801
-
Cyclopropamitosenes, novel bioreductive anticancer agents. Synthesis of 7-methoxycyclopropamitosene and related indolequinones
-
Cotterill, A. S.; Hartopp, P.; Jones, G. B.; Moody, C. J.; Norton, C. L.; O'Sullivan, N.; Swarm, E. Cyclopropamitosenes, novel bioreductive anticancer agents. Synthesis of 7-methoxycyclopropamitosene and related indolequinones. Tetrahedron 1994, 50, 7657-7674.
-
(1994)
Tetrahedron
, vol.50
, pp. 7657-7674
-
-
Cotterill, A.S.1
Hartopp, P.2
Jones, G.B.3
Moody, C.J.4
Norton, C.L.5
O'Sullivan, N.6
Swarm, E.7
-
25
-
-
0027996508
-
Cyclopropamitosenes, novel bioreductive anticancer agents. Synthesis, electrochemistry and biological activity of 7-substituted cyclopropamitosenes and related indolequinones
-
Cotterill, A. S.; Moody, C. J.; Mortimer, R. J.; Norton, C. L.; O'Sullivan, N.; Stephens, M. A.; Stradiotto, N. R.; Stratford, I. J.; Swann, E. Cyclopropamitosenes, novel bioreductive anticancer agents. Synthesis, electrochemistry and biological activity of 7-substituted cyclopropamitosenes and related indolequinones. J. Med. Chem. 1994, 37, 3834-3843.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3834-3843
-
-
Cotterill, A.S.1
Moody, C.J.2
Mortimer, R.J.3
Norton, C.L.4
O'Sullivan, N.5
Stephens, M.A.6
Stradiotto, N.R.7
Stratford, I.J.8
Swann, E.9
-
26
-
-
15144357021
-
Indolequinone Antitumor Agents: Reductive Activation and Elimination from (5-Methoxy-1,2-dimethyl-4,7-dioxo-indol-3-yl)methyl Derivatives and Hypoxia-Selective Cytotoxicity in vitro
-
Naylor, M. A.; Swann, E.; Everett, S. A.; Jaffar, M.; Nolan, J.; Robertson, N.; Lockyer, S. D.; Patel, K. B.; Dennis, M. F.; Stratford, M. R. L.; Wardman, P.; Adams, G. E.; Moody, C. J.; Stratford, I. J. Indolequinone Antitumor Agents: Reductive Activation and Elimination from (5-Methoxy-1,2-dimethyl-4,7-dioxo-indol-3-yl)methyl Derivatives and Hypoxia-Selective Cytotoxicity in vitro. J. Med. Chem. 1998, 41, 2720-2731.
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2720-2731
-
-
Naylor, M.A.1
Swann, E.2
Everett, S.A.3
Jaffar, M.4
Nolan, J.5
Robertson, N.6
Lockyer, S.D.7
Patel, K.B.8
Dennis, M.F.9
Stratford, M.R.L.10
Wardman, P.11
Adams, G.E.12
Moody, C.J.13
Stratford, I.J.14
-
27
-
-
0022536981
-
Preparation and antitumor activity of 7-substituted 1,2-aziridinomitomycins
-
Iyengar, B. S.; Remers, W. A.; Bradner, W. T. Preparation and antitumor activity of 7-substituted 1,2-aziridinomitomycins. J. Med. Chem. 1986, 29, 1864-1868.
-
(1986)
J. Med. Chem.
, vol.29
, pp. 1864-1868
-
-
Iyengar, B.S.1
Remers, W.A.2
Bradner, W.T.3
-
28
-
-
0002855270
-
-
Wilman, D. E. V., Ed.; Blackie and Son Ltd.: Glasgow
-
Franck, R. W.; Tomasz, M. In Chemistry of Antitumor Agents; Wilman, D. E. V., Ed.; Blackie and Son Ltd.: Glasgow, 1990; pp 379-393.
-
(1990)
Chemistry of Antitumor Agents
, pp. 379-393
-
-
Franck, R.W.1
Tomasz, M.2
-
29
-
-
0002890787
-
N-H Insertion reactions of rhodium carbenoids: A modified Bischler indole synthesis
-
Moody, C. J.; Swann, E. N-H Insertion reactions of rhodium carbenoids: a modified Bischler indole synthesis. Synlett 1998, 135-136.
-
(1998)
Synlett
, pp. 135-136
-
-
Moody, C.J.1
Swann, E.2
-
30
-
-
7844242846
-
Synthesis of 5-hydroxyindoles. I. Derivatives of 2-phenyl-5-hydroxyindole
-
Raileanu, D.; Nenitzescu, C. D. Synthesis of 5-hydroxyindoles. I. Derivatives of 2-phenyl-5-hydroxyindole. Rev. Roumaine Chim. 1965, 10, 339-353.
-
(1965)
Rev. Roumaine Chim.
, vol.10
, pp. 339-353
-
-
Raileanu, D.1
Nenitzescu, C.D.2
-
31
-
-
0030747303
-
2-Cyclopropylindoloquinones and their analogues as bioreductively activated antitumor agents: Structure-activity in vitro and efficacy in vivo
-
Naylor, M. A.; Jaffar, M.; Nolan, J.; Stephens, M. A.; Butler, S.; Patel, K. B.; Everett, S. A.; Adams, G. E.; Stratford, I. J. 2-Cyclopropylindoloquinones and their analogues as bioreductively activated antitumor agents: structure-activity in vitro and efficacy in vivo. J. Med. Chem. 1997, 40, 2335-2346.
-
(1997)
J. Med. Chem.
, vol.40
, pp. 2335-2346
-
-
Naylor, M.A.1
Jaffar, M.2
Nolan, J.3
Stephens, M.A.4
Butler, S.5
Patel, K.B.6
Everett, S.A.7
Adams, G.E.8
Stratford, I.J.9
-
32
-
-
0031656599
-
Indolequinone bioreductive drugs: Kinetic factors which influence selectivity for hypoxia
-
Everett, S. A.; Naylor, M. A.; Nolan, J.; Patel, K. B.; Wardman, P. Indolequinone bioreductive drugs: kinetic factors which influence selectivity for hypoxia. Anti-Cancer Drug Des. 1998, 13, 635-653.
-
(1998)
Anti-Cancer Drug Des.
, vol.13
, pp. 635-653
-
-
Everett, S.A.1
Naylor, M.A.2
Nolan, J.3
Patel, K.B.4
Wardman, P.5
-
33
-
-
0027717389
-
PH-Dependent inactivation of DT-diaphorase by mitomycin C and porfiromycin
-
Siegel, D.; Beall, H.; Kasai, M.; Arai, H.; Gibson, N. W.; Ross, D. pH-Dependent inactivation of DT-diaphorase by mitomycin C and porfiromycin. Mol. Pharmacol. 1993, 44, 1128-1134.
-
(1993)
Mol. Pharmacol.
, vol.44
, pp. 1128-1134
-
-
Siegel, D.1
Beall, H.2
Kasai, M.3
Arai, H.4
Gibson, N.W.5
Ross, D.6
-
34
-
-
0031021280
-
Characterization of a polymorphism in NAD(P)H:quinone oxidoreductase (DT-diaphorase)
-
Traver, R. D.; Siegel, D.; Beall, H. D.; Phillips, R. M.; Gibson, N. W.; Franklin, W. A.; Ross, D. Characterization of a polymorphism in NAD(P)H:quinone oxidoreductase (DT-diaphorase). Br. J. Cancer 1997, 75, 69-75.
-
(1997)
Br. J. Cancer
, vol.75
, pp. 69-75
-
-
Traver, R.D.1
Siegel, D.2
Beall, H.D.3
Phillips, R.M.4
Gibson, N.W.5
Franklin, W.A.6
Ross, D.7
-
35
-
-
84988052209
-
An improved preparation of enaminones from 1,3-diketones and ammonium acetate or amine acetates
-
Baraldi, P. G.; Simoni, D.; Manfredini, S. An improved preparation of enaminones from 1,3-diketones and ammonium acetate or amine acetates. Synthesis 1983, 902-903.
-
(1983)
Synthesis
, pp. 902-903
-
-
Baraldi, P.G.1
Simoni, D.2
Manfredini, S.3
-
36
-
-
0028243181
-
Metabolism of bioreductive antitumor compounds by purified rat and human DT-diaphorases
-
Beall, H. D.; Mulcahy, R. T.; Siegel, D.; Traver, R. D.; Gibson, N. W.; Ross, D. Metabolism of bioreductive antitumor compounds by purified rat and human DT-diaphorases. Cancer Res. 1994, 54, 3196-3201.
-
(1994)
Cancer Res.
, vol.54
, pp. 3196-3201
-
-
Beall, H.D.1
Mulcahy, R.T.2
Siegel, D.3
Traver, R.D.4
Gibson, N.W.5
Ross, D.6
-
37
-
-
0021061819
-
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
-
Mosmann, T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods 1983, 65, 55-63.
-
(1983)
J. Immunol. Methods
, vol.65
, pp. 55-63
-
-
Mosmann, T.1
|