-
1
-
-
0026793462
-
Metabolism and functions of trypanothione in the Kinetoplastida
-
Fairlamb, A. H.; Cerami, A. Metabolism and functions of trypanothione in the Kinetoplastida. Annu. Rev. Microbiol. 1992, 46, 695-729.
-
(1992)
Annu. Rev. Microbiol.
, vol.46
, pp. 695-729
-
-
Fairlamb, A.H.1
Cerami, A.2
-
2
-
-
0022002912
-
Trypanothione: A novel bis(glutathionyl)spermidine cofactor for glutathione reductase in trypanosomatids
-
Fairlamb, A. H.; Blackburn, P.; Ulrich, P.; Chait, B. T.; Cerami, A. Trypanothione: a novel bis(glutathionyl)spermidine cofactor for glutathione reductase in trypanosomatids. Science 1985, 227, 1485-1487.
-
(1985)
Science
, vol.227
, pp. 1485-1487
-
-
Fairlamb, A.H.1
Blackburn, P.2
Ulrich, P.3
Chait, B.T.4
Cerami, A.5
-
3
-
-
0023051830
-
Purification and characterization of trypanothione reductase from Crithidia fasciculata, a newly discovered member of the family of disulfide-containing flavoprotein reductases
-
Shames, S. L.; Fairlamb, A. H.; Cerami, A.; Walsh, C. T. Purification and characterization of trypanothione reductase from Crithidia fasciculata, a newly discovered member of the family of disulfide-containing flavoprotein reductases. Biochemistry 1986, 25, 3519-3526.
-
(1986)
Biochemistry
, vol.25
, pp. 3519-3526
-
-
Shames, S.L.1
Fairlamb, A.H.2
Cerami, A.3
Walsh, C.T.4
-
4
-
-
0023150396
-
Trypanothione reductase from Trypanosoma cruzi. Purification and characterization of the crystalline enzyme
-
Krauth-Siegel, R. L.; Enders, B.; Henderson, G. B.; Fairlamb, A. H.; Schirmer, R. H. Trypanothione reductase from Trypanosoma cruzi. Purification and characterization of the crystalline enzyme. Eur. J. Biochem. 1987, 164, 123-128.
-
(1987)
Eur. J. Biochem.
, vol.164
, pp. 123-128
-
-
Krauth-Siegel, R.L.1
Enders, B.2
Henderson, G.B.3
Fairlamb, A.H.4
Schirmer, R.H.5
-
5
-
-
0030221261
-
Charge is the major discriminating factor for glutathione reductase versus trypanothione reductase inhibitors
-
Faerman, C. H.; Savvides, S. N.; Strickland, C.; Breidenbach, M. A.; Ponasik, J. A.; Ganem, B.; Ripoll, D.; Krauth-Siegel, R. L.; Karplus, P. A. Charge is the major discriminating factor for glutathione reductase versus trypanothione reductase inhibitors. Bioorg. Med. Chem. 1996, 4, 1247-1253.
-
(1996)
Bioorg. Med. Chem.
, vol.4
, pp. 1247-1253
-
-
Faerman, C.H.1
Savvides, S.N.2
Strickland, C.3
Breidenbach, M.A.4
Ponasik, J.A.5
Ganem, B.6
Ripoll, D.7
Krauth-Siegel, R.L.8
Karplus, P.A.9
-
6
-
-
0030997915
-
Glutathione reductase turned into trypanothione reductase: Structural analysis of an engineered change in substrate specificity
-
Stoll, V. S.; Simpson, S. J.; Krauth-Siegel, R. L.; Walsh, C. T.; Pai, E. F. Glutathione reductase turned into trypanothione reductase: structural analysis of an engineered change in substrate specificity. Biochemistry 1997, 36, 6437-6447.
-
(1997)
Biochemistry
, vol.36
, pp. 6437-6447
-
-
Stoll, V.S.1
Simpson, S.J.2
Krauth-Siegel, R.L.3
Walsh, C.T.4
Pai, E.F.5
-
7
-
-
0035865881
-
2- and 3-substituted 1,4-naphthoquinone derivatives as subversive substrates of trypanothione reductase and lipoamide dehydrogenase from Trypanosoma cruzi: Synthesis and correlation between redox cycling activities and in vitro cytotoxicity
-
Salmon-Chemin, L.; Buisine, E.; Yardley, V.; Kohler, S.; Debreu, M. A.; Landry, V.; Sergheraert, C.; Croft, S. L.; Krauth-Siegel, R. L.; Davioud-Charvet, E. 2- and 3-substituted 1,4-naphthoquinone derivatives as subversive substrates of trypanothione reductase and lipoamide dehydrogenase from Trypanosoma cruzi: synthesis and correlation between redox cycling activities and in vitro cytotoxicity. J. Med. Chem. 2001, 44, 548-565.
-
(2001)
J. Med. Chem.
, vol.44
, pp. 548-565
-
-
Salmon-Chemin, L.1
Buisine, E.2
Yardley, V.3
Kohler, S.4
Debreu, M.A.5
Landry, V.6
Sergheraert, C.7
Croft, S.L.8
Krauth-Siegel, R.L.9
Davioud-Charvet, E.10
-
8
-
-
0000876731
-
Lipoamide dehydrogenase, glutathione reductase, thioredoxin reductase, and mercuric ion reductase, a family of flavoenzyme transhydrogenases
-
CRC Press: Boca Raton, FL
-
Williams, C. H., Jr. Lipoamide Dehydrogenase, Glutathione Reductase, Thioredoxin Reductase, and Mercuric Ion Reductase, a Family of Flavoenzyme Transhydrogenases. Chemistry and Biochemistry of Flavoenzymes; CRC Press: Boca Raton, FL, 1992; pp 121-211.
-
(1992)
Chemistry and Biochemistry of Flavoenzymes
, pp. 121-211
-
-
Williams Jr., C.H.1
-
9
-
-
0033977079
-
Trypanosomes lacking trypanothione reductase are avirulent and show increased sensitivity to oxidative stress
-
Krieger, S.; Schwarz, W.; Ariyanayagam, M. R.; Fairlamb, A. H.; Krauth-Siegel, R. L.; Clayton, C. Trypanosomes lacking trypanothione reductase are avirulent and show increased sensitivity to oxidative stress. Mol. Microbiol. 2000, 35, 542-552.
-
(2000)
Mol. Microbiol.
, vol.35
, pp. 542-552
-
-
Krieger, S.1
Schwarz, W.2
Ariyanayagam, M.R.3
Fairlamb, A.H.4
Krauth-Siegel, R.L.5
Clayton, C.6
-
10
-
-
0036833868
-
Enzymes of the trypanothione metabolism as targets for antitrypanosomal drug development
-
Schmidt, A.; Krauth-Siegel, R. L. Enzymes of the trypanothione metabolism as targets for antitrypanosomal drug development. Curr. Top. Med. Chem. 2002, 2, 1239-1259.
-
(2002)
Curr. Top. Med. Chem.
, vol.2
, pp. 1239-1259
-
-
Schmidt, A.1
Krauth-Siegel, R.L.2
-
11
-
-
0038646796
-
Thiol-based redox metabolism of protozoan parasites
-
Müller, S.; Liebau, E.; Walter, R. D.; Krauth-Siegel, R. L. Thiol-based redox metabolism of protozoan parasites. Trends Parasitol. 2003, 19, 320-328.
-
(2003)
Trends Parasitol.
, vol.19
, pp. 320-328
-
-
Müller, S.1
Liebau, E.2
Walter, R.D.3
Krauth-Siegel, R.L.4
-
12
-
-
13444280474
-
Dithiol proteins as guardians of the intracellular redox milieu in parasites: Old and new drug targets in trypanosomes and malaria-causing Plasmodia
-
Krauth-Siegel, R. L.; Bauer, H.; Schirmer, R. H. Dithiol proteins as guardians of the intracellular redox milieu in parasites: Old and new drug targets in trypanosomes and malaria-causing Plasmodia. Angew. Chem., Int. Ed. 2005, 44, 690-715.
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 690-715
-
-
Krauth-Siegel, R.L.1
Bauer, H.2
Schirmer, R.H.3
-
13
-
-
0032866917
-
Rational drug design using trypanothione reductase as a target for anti-trypanosomal and anti-leishmanial drug leads
-
Austin, S. E.; Khan, M. O.; Douglas, K. T. Rational drug design using trypanothione reductase as a target for anti-trypanosomal and anti-leishmanial drug leads. Drug Des. Discovery 1999, 16, 5-23.
-
(1999)
Drug Des. Discovery
, vol.16
, pp. 5-23
-
-
Austin, S.E.1
Khan, M.O.2
Douglas, K.T.3
-
14
-
-
0033927095
-
Target-based drug discovery for malaria, leishmaniasis, and trypanosomiasis
-
Werbovetz, K. A. Target-based drug discovery for malaria, leishmaniasis, and trypanosomiasis. Curr. Med. Chem. 2000, 7, 835-860.
-
(2000)
Curr. Med. Chem.
, vol.7
, pp. 835-860
-
-
Werbovetz, K.A.1
-
15
-
-
0037963699
-
Parasite-specific trypanothione reductase as a drug target molecule
-
Krauth-Siegel, R. L.; Inhoff, O. Parasite-specific trypanothione reductase as a drug target molecule. Parasitol. Res. 2003, 90 (Suppl. 2), S77-S85.
-
(2003)
Parasitol. Res.
, vol.90
, Issue.SUPPL. 2
-
-
Krauth-Siegel, R.L.1
Inhoff, O.2
-
16
-
-
0030057025
-
Crystal structure of the Trypanosoma cruzi trypanothione reductase-mepacrine complex
-
Jacoby, E. M.; Schlichting, I.; Lantwin, C. B.; Kabsch, W.; Krauth-Siegel, R. L. Crystal structure of the Trypanosoma cruzi trypanothione reductase-mepacrine complex. Proteins 1996, 24, 73-80.
-
(1996)
Proteins
, vol.24
, pp. 73-80
-
-
Jacoby, E.M.1
Schlichting, I.2
Lantwin, C.B.3
Kabsch, W.4
Krauth-Siegel, R.L.5
-
17
-
-
3142719178
-
Two interacting binding sites for quinacrine derivatives in the active site of trypanothione reductase: A template for drug design
-
Saravanamuthu, A.; Vickers, T. J.; Bond, C. S.; Peterson, M. R.; Hunter, W. N.; Fairlamb, A. H. Two interacting binding sites for quinacrine derivatives in the active site of trypanothione reductase: a template for drug design. J. Biol. Chem. 2004, 279, 29493-29500.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 29493-29500
-
-
Saravanamuthu, A.1
Vickers, T.J.2
Bond, C.S.3
Peterson, M.R.4
Hunter, W.N.5
Fairlamb, A.H.6
-
18
-
-
0023728105
-
The behavior and significance of slow-binding enzyme inhibitors
-
Morrison, J. F.; Walsh, C. T. The behavior and significance of slow-binding enzyme inhibitors. Adv Enzymol. Relat. Areas Mol. Biol. 1988, 61, 201-301.
-
(1988)
Adv Enzymol. Relat. Areas Mol. Biol.
, vol.61
, pp. 201-301
-
-
Morrison, J.F.1
Walsh, C.T.2
-
19
-
-
0034649656
-
2,2′:6′,2″-Terpyridineplatinum(II) complexes are irreversible inhibitors of Trypanosoma cruzi trypanothione reductase but not of human glutathione reductase
-
Bonse, S.; Richards, J. M.; Ross, S. A.; Lowe, G.; Krauth-Siegel, R. L. (2,2′:6′,2″-Terpyridine)platinum(II) complexes are irreversible inhibitors of Trypanosoma cruzi trypanothione reductase but not of human glutathione reductase. J. Med. Chem. 2000, 43, 4812-4821.
-
(2000)
J. Med. Chem.
, vol.43
, pp. 4812-4821
-
-
Bonse, S.1
Richards, J.M.2
Ross, S.A.3
Lowe, G.4
Krauth-Siegel, R.L.5
-
20
-
-
0033602511
-
Cytotoxicity of (2,2′:6′,2″-terpyridine)platinum(II) complexes to Leishmania donovani, Trypanosoma cruzi, and Trypanosoma brucei
-
Lowe, G.; Droz, A. S.; Vilaivan, T.; Weaver, G. W.; Tweedale, L.; Pratt, J. M.; Rock, P.; Yardley, V.; Croft, S. L. Cytotoxicity of (2,2′:6′, 2″-terpyridine)platinum(II) complexes to Leishmania donovani, Trypanosoma cruzi, and Trypanosoma brucei. J. Med. Chem. 1999, 42, 999-1006.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 999-1006
-
-
Lowe, G.1
Droz, A.S.2
Vilaivan, T.3
Weaver, G.W.4
Tweedale, L.5
Pratt, J.M.6
Rock, P.7
Yardley, V.8
Croft, S.L.9
-
21
-
-
0001231790
-
Further advances in the chemistry of Mannich bases
-
Tramontini, M.; Angiolini, L. Further advances in the chemistry of Mannich bases. Tetrahedron 1990, 46, 1791-1837.
-
(1990)
Tetrahedron
, vol.46
, pp. 1791-1837
-
-
Tramontini, M.1
Angiolini, L.2
-
22
-
-
0032482080
-
Modern variants of the Mannich reaction
-
Arend, M.; Westermann, B.; Risch, N. Modern variants of the Mannich reaction. Angew. Chem., Int. Ed. 1998, 37, 1045-1070.
-
(1998)
Angew. Chem., Int. Ed.
, vol.37
, pp. 1045-1070
-
-
Arend, M.1
Westermann, B.2
Risch, N.3
-
23
-
-
0024001880
-
Mannich bases in polymer chemistry
-
Tramontini, M.; Angiolini, L.; Ghedini, N. Mannich bases in polymer chemistry. Polym. Rev. 1988, 29, 771-788.
-
(1988)
Polym. Rev.
, vol.29
, pp. 771-788
-
-
Tramontini, M.1
Angiolini, L.2
Ghedini, N.3
-
24
-
-
10744226522
-
Mechanism-based inactivation of thioredoxin reductase from Plasmodium falciparum by Mannich bases. Implication for cytotoxicity
-
Davioud-Charvet, E.; McLeish, M. J.; Veine, D. M.; Giegel, D.; Arscott, L. D.; Andricopulo, A. D.; Becker, K.; Muller, S.; Schirmer, R. H.; Williams, C. H., Jr.; Kenyon, G. L. Mechanism-based inactivation of thioredoxin reductase from Plasmodium falciparum by Mannich bases. Implication for cytotoxicity. Biochemistry 2003, 42, 13319-13330.
-
(2003)
Biochemistry
, vol.42
, pp. 13319-13330
-
-
Davioud-Charvet, E.1
McLeish, M.J.2
Veine, D.M.3
Giegel, D.4
Arscott, L.D.5
Andricopulo, A.D.6
Becker, K.7
Muller, S.8
Schirmer, R.H.9
Williams Jr., C.H.10
Kenyon, G.L.11
-
25
-
-
0000286075
-
Synthesis of 1,4-dien-3-ones and 2-cyclopentenones
-
Kjeldsen, G.; Knudsen, J. S.; Ravn-Petersen, L. S.; Torssel, K. B. Synthesis of 1,4-dien-3-ones and 2-cyclopentenones. Tetrahedron 1983, 39, 2237-2239.
-
(1983)
Tetrahedron
, vol.39
, pp. 2237-2239
-
-
Kjeldsen, G.1
Knudsen, J.S.2
Ravn-Petersen, L.S.3
Torssel, K.B.4
-
26
-
-
28544432677
-
Polymerization of substituted divinyl ketones with cycle formation
-
Matsoyan, S. G.; Avetyan, M. G. Polymerization of substituted divinyl ketones with cycle formation. Zh. Obshch. Khim. 1960, 30, 2431-2432.
-
(1960)
Zh. Obshch. Khim.
, vol.30
, pp. 2431-2432
-
-
Matsoyan, S.G.1
Avetyan, M.G.2
-
27
-
-
0029019365
-
Acyclic O- and N- substituted pentadienyl cations: Structural characterization, cyclization and computational results
-
Howell, J. A. S.; O'Leary, P. J.; Yates, P. C.; Goldschmidt, Z.; Gottlieb, H. E.; Hezroni-Langerman, D. Acyclic O- and N- substituted pentadienyl cations: structural characterization, cyclization and computational results. Tetrahedron 1995, 51, 7231-7246.
-
(1995)
Tetrahedron
, vol.51
, pp. 7231-7246
-
-
Howell, J.A.S.1
O'Leary, P.J.2
Yates, P.C.3
Goldschmidt, Z.4
Gottlieb, H.E.5
Hezroni-Langerman, D.6
-
28
-
-
0001126635
-
The reaction of some nuclear substituted acyclic conjugated styryl ketones and related Mannich bases with ethanethiol
-
Dimmock, J. R.; Smith, L. M.; Smith, P. J. The reaction of some nuclear substituted acyclic conjugated styryl ketones and related Mannich bases with ethanethiol. Can. J. Chem. 1980, 58, 984-991.
-
(1980)
Can. J. Chem.
, vol.58
, pp. 984-991
-
-
Dimmock, J.R.1
Smith, L.M.2
Smith, P.J.3
-
29
-
-
0025330154
-
Deamination and thiolation of Mannich bases derived from conjugated styryl ketones
-
Dimmock, J. R.; Jonnalagadda, S. S.; Reid, R. S.; Arteca, G. A.; Mezey, P. G. Deamination and thiolation of Mannich bases derived from conjugated styryl ketones. Pharmazie 1990, 45, 252-255.
-
(1990)
Pharmazie
, vol.45
, pp. 252-255
-
-
Dimmock, J.R.1
Jonnalagadda, S.S.2
Reid, R.S.3
Arteca, G.A.4
Mezey, P.G.5
-
30
-
-
0042858330
-
r thioredoxin reductase from Drosophila melanogaster
-
r thioredoxin reductase from Drosophila melanogaster. J. Biol. Chem. 2003, 278, 33020-33028.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 33020-33028
-
-
Bauer, H.1
Massey, V.2
Arscott, L.D.3
Schirmer, R.H.4
Ballou, D.A.5
Williams Jr., C.H.6
-
31
-
-
0034532221
-
Enetic characterization of glutathione reductase from the malarial parasite Plasmodium falciparum. Comparison with the human enzyme
-
Böhme, C. C.; Arscott, L. D.; Becker, K.; Schirmer, R. H.; Williams, C. H., Jr. Enetic characterization of glutathione reductase from the malarial parasite Plasmodium falciparum. Comparison with the human enzyme. J. Biol. Chem. 2000, 275, 37317-37323.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 37317-37323
-
-
Böhme, C.C.1
Arscott, L.D.2
Becker, K.3
Schirmer, R.H.4
Williams Jr., C.H.5
-
32
-
-
0019883230
-
Lipoamide dehydrogenase from pig heart. Pyridine nucleotide induced changes in monoalkylated two-electron reduced enzyme
-
Thorpe, C.; Williams, C. H., Jr. Lipoamide dehydrogenase from pig heart. Pyridine nucleotide induced changes in monoalkylated two-electron reduced enzyme. Biochemistry 1981, 20, 1507-1513.
-
(1981)
Biochemistry
, vol.20
, pp. 1507-1513
-
-
Thorpe, C.1
Williams Jr., C.H.2
-
33
-
-
0033537705
-
Thioredoxin reductase from Plasmodium falciparum: Evidence for interaction between the C-terminal cysteine residues and the active site disulfide-dithiol
-
Wang, P. F.; Arscott, L. D.; Gilberger, T. W.; Müller, S.; Williams, C. H., Jr. Thioredoxin reductase from Plasmodium falciparum: evidence for interaction between the C-terminal cysteine residues and the active site disulfide-dithiol. Biochemistry 1999, 38, 3187-3196.
-
(1999)
Biochemistry
, vol.38
, pp. 3187-3196
-
-
Wang, P.F.1
Arscott, L.D.2
Gilberger, T.W.3
Müller, S.4
Williams Jr., C.H.5
-
34
-
-
10644295071
-
Flavoprotein disulfide reductases: Advances in chemistry and function
-
Argyrou, A.; Blanchard, J. S. Flavoprotein disulfide reductases: advances in chemistry and function. Prog. Nucleic Acid Res. Mol. Biol. 2004, 78, 89-142.
-
(2004)
Prog. Nucleic Acid Res. Mol. Biol.
, vol.78
, pp. 89-142
-
-
Argyrou, A.1
Blanchard, J.S.2
-
35
-
-
0028598280
-
Compared reactivities of trypanothione and glutathione in conjugation reactions
-
Moutiez, M.; Meziane-Cherif, D.; Aumercier, M.; Sergheraert, C.; Tartar, A. Compared reactivities of trypanothione and glutathione in conjugation reactions. Chem. Pharm. Bull. 1994, 42, 2641-2644.
-
(1994)
Chem. Pharm. Bull.
, vol.42
, pp. 2641-2644
-
-
Moutiez, M.1
Meziane-Cherif, D.2
Aumercier, M.3
Sergheraert, C.4
Tartar, A.5
-
36
-
-
0025118967
-
Molecular and cellular aspects of thiol-disulfide exchange
-
Gilbert, H. F. Molecular and cellular aspects of thiol-disulfide exchange. Adv. Enzymol. Relat. Areas Mol. Biol. 1990, 63, 69-172.
-
(1990)
Adv. Enzymol. Relat. Areas Mol. Biol.
, vol.63
, pp. 69-172
-
-
Gilbert, H.F.1
-
37
-
-
0029944732
-
Reversal of doxorubicin, etoposide, vinblastine, and taxol resistance in multidrug resistant human sarcoma cells by a polymer of spermine
-
Gosland, M. P.; Gillespie, M. N.; Tsuboi, C. P.; Tofiq, S.; Olson, J. W.; Crooks, P. A.; Aziz, S. M. Reversal of doxorubicin, etoposide, vinblastine, and taxol resistance in multidrug resistant human sarcoma cells by a polymer of spermine. Cancer Chemother. Pharmacol. 1996, 37, 593-600.
-
(1996)
Cancer Chemother. Pharmacol.
, vol.37
, pp. 593-600
-
-
Gosland, M.P.1
Gillespie, M.N.2
Tsuboi, C.P.3
Tofiq, S.4
Olson, J.W.5
Crooks, P.A.6
Aziz, S.M.7
-
38
-
-
0032714228
-
Inhibition of P-glycoprotein by D-alpha-tocopheryl polyethylene glycol 1000 succinate (TPGS)
-
Dintaman, J. M.; Silverman, J. A. Inhibition of P-glycoprotein by D-alpha-tocopheryl polyethylene glycol 1000 succinate (TPGS). Pharm. Res. 1999, 16, 1550-1556.
-
(1999)
Pharm. Res.
, vol.16
, pp. 1550-1556
-
-
Dintaman, J.M.1
Silverman, J.A.2
-
39
-
-
0026098498
-
Cloning, sequencing, overproduction and purification of trypanothione reductase from Trypanosoma cruzi
-
Sullivan, F. X.; Walsh, C. T. Cloning, sequencing, overproduction and purification of trypanothione reductase from Trypanosoma cruzi. Mol. Biochem. Parasitol. 1991, 44, 145-147.
-
(1991)
Mol. Biochem. Parasitol.
, vol.44
, pp. 145-147
-
-
Sullivan, F.X.1
Walsh, C.T.2
-
40
-
-
0024521456
-
Trypanothione reductase from Trypanosoma cruzi. Catalytic properties of the enzyme and inhibition studies with trypanocidal compounds
-
Jockers-Scherübl, M. C.; Schirmer, R. H.; Krauth-Siegel, R. L. Trypanothione reductase from Trypanosoma cruzi. Catalytic properties of the enzyme and inhibition studies with trypanocidal compounds. Eur. J. Biochem. 1989, 180, 267-272.
-
(1989)
Eur. J. Biochem.
, vol.180
, pp. 267-272
-
-
Jockers-Scherübl, M.C.1
Schirmer, R.H.2
Krauth-Siegel, R.L.3
-
41
-
-
0029861640
-
Efficient technique for screening drugs for activity against Trypanosoma cruzi using parasites expressing beta-galactosidase. Antimicrob
-
Buckner, F. S.; Verlinde, C. L.; La Flamme, A. C.; Van Voorhis, W. C. Efficient technique for screening drugs for activity against Trypanosoma cruzi using parasites expressing beta-galactosidase. Antimicrob. Agents Chemother. 1996, 40, 2592-2597.
-
(1996)
Agents Chemother.
, vol.40
, pp. 2592-2597
-
-
Buckner, F.S.1
Verlinde, C.L.2
La Flamme, A.C.3
Van Voorhis, W.C.4
-
42
-
-
0024948840
-
Continuous cultivation of Trypanosoma brucei blood stream forms in a medium containing a low concentration of serum protein without feeder cell layers
-
Hirumi, H.; Hirumi, K. Continuous cultivation of Trypanosoma brucei blood stream forms in a medium containing a low concentration of serum protein without feeder cell layers. J. Parasitol. 1989, 75, 985-989.
-
(1989)
J. Parasitol.
, vol.75
, pp. 985-989
-
-
Hirumi, H.1
Hirumi, K.2
-
43
-
-
0019395570
-
Chloroquine sensitivity of isolates of Plasmodium falciparum adapted to in vitro culture
-
Ponnudurai, T.; Leeuwenberg, A. D.; Meuwissen, J. H. Chloroquine sensitivity of isolates of Plasmodium falciparum adapted to in vitro culture. Trop. Geogr. Med. 1981, 33, 50-54.
-
(1981)
Trop. Geogr. Med.
, vol.33
, pp. 50-54
-
-
Ponnudurai, T.1
Leeuwenberg, A.D.2
Meuwissen, J.H.3
-
44
-
-
0017311840
-
Human malaria parasites in continuous culture
-
Trager, W.; Jensen, J. B. Human malaria parasites in continuous culture. Science 1976, 193, 673-675.
-
(1976)
Science
, vol.193
, pp. 673-675
-
-
Trager, W.1
Jensen, J.B.2
-
45
-
-
3342962349
-
Novel azasterols as potential agents for treatment of leishmaniasis and trypanosomiasis
-
Lorente, S. O.; Rodrigues, J. C.; Jimenez Jimenez, C.; Joyce-Menekse, M.; Rodrigues, C.; Croft, S. L.; Yardley, V.; de Luca-Fradley, K.; Ruiz-Perez, L. M.; Urbina, J.; de Souza, W.; Gonzalez Pacanowska, D.; Gilbert, I. H. Novel azasterols as potential agents for treatment of leishmaniasis and trypanosomiasis. Antimicrob. Agents Chemother. 2004, 48, 2937-2950.
-
(2004)
Antimicrob. Agents Chemother.
, vol.48
, pp. 2937-2950
-
-
Lorente, S.O.1
Rodrigues, J.C.2
Jimenez Jimenez, C.3
Joyce-Menekse, M.4
Rodrigues, C.5
Croft, S.L.6
Yardley, V.7
De Luca-Fradley, K.8
Ruiz-Perez, L.M.9
Urbina, J.10
De Souza, W.11
Gonzalez Pacanowska, D.12
Gilbert, I.H.13
-
46
-
-
0021590709
-
An in-vitro system for determining the activity of compounds against the intracellular amastigote form of Leishmania donovani
-
Neal, R. A.; Croft, S. L. An in-vitro system for determining the activity of compounds against the intracellular amastigote form of Leishmania donovani. J. Antimicrob. Chemother. 1984, 14, 463-475.
-
(1984)
J. Antimicrob. Chemother.
, vol.14
, pp. 463-475
-
-
Neal, R.A.1
Croft, S.L.2
-
47
-
-
0027429249
-
A colorimetric assay for trypanosome viability and metabolic function
-
Ellis, J. A.; Fish, W. R.; Sileghem, M.; McOdimba, F. A colorimetric assay for trypanosome viability and metabolic function. Vet. Parasitol. 1993, 50, 143-149.
-
(1993)
Vet. Parasitol.
, vol.50
, pp. 143-149
-
-
Ellis, J.A.1
Fish, W.R.2
Sileghem, M.3
McOdimba, F.4
-
48
-
-
3843112304
-
Identification and activity of a series of azole-based compounds with lactate dehydrogenase-directed anti-malarial activity
-
Cameron, A.; Read, J.; Tranter, R.; Winter, V. J.; Sessions, R. B.; Brady, R. L.; Vivas, L.; Easton, A.; Kendrick, H.; Croft, S. L.; Barros, D.; Lavandera, J. L.; Martin, J. J.; Risco, F.; Garcia-Ochoa, S.; Gamo, F. J.; Sanz, L.; Leon, L.; Ruiz, J. R.; Gabarro, R.; Mallo, A.; Gomez de las Heras, F. Identification and activity of a series of azole-based compounds with lactate dehydrogenase-directed anti-malarial activity. J. Biol. Chem. 2004, 279, 31429-31439.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 31429-31439
-
-
Cameron, A.1
Read, J.2
Tranter, R.3
Winter, V.J.4
Sessions, R.B.5
Brady, R.L.6
Vivas, L.7
Easton, A.8
Kendrick, H.9
Croft, S.L.10
Barros, D.11
Lavandera, J.L.12
Martin, J.J.13
Risco, F.14
Garcia-Ochoa, S.15
Gamo, F.J.16
Sanz, L.17
Leon, L.18
Ruiz, J.R.19
Gabarro, R.20
Mallo, A.21
Gomez De Las Heras, F.22
more..
-
49
-
-
0018606732
-
Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique
-
Desjardins, R. E.; Canfield, C. J.; Haynes, J. D.; Chulay, J. D. Quantitative assessment of antimalarial activity in vitro by a semiautomated microdilution technique. Antimicrob. Agents Chemother. 1979, 16, 710-718.
-
(1979)
Antimicrob. Agents Chemother.
, vol.16
, pp. 710-718
-
-
Desjardins, R.E.1
Canfield, C.J.2
Haynes, J.D.3
Chulay, J.D.4
-
50
-
-
0037124040
-
Thioredoxin-2 but not thioredoxin-1 is a substrate of thioredoxin peroxidase-1 from Drosophila melanogaster: Isolation and characterization of a second thioredoxin in U. melanogaster and evidence for distinct biological functions of Trx-1 and Trx-2
-
Bauer, H.; Kanzok, S. M.; Schirmer, R. H. Thioredoxin-2 but not thioredoxin-1 is a substrate of thioredoxin peroxidase-1 from Drosophila melanogaster: isolation and characterization of a second thioredoxin in U. melanogaster and evidence for distinct biological functions of Trx-1 and Trx-2. J. Biol. Chem. 2002, 277, 17457-17463.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 17457-17463
-
-
Bauer, H.1
Kanzok, S.M.2
Schirmer, R.H.3
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