-
1
-
-
0037376230
-
Potential for proteasome inhibition in the treatment of cancer
-
Adams J (2003) Potential for proteasome inhibition in the treatment of cancer. Drug Discov Today 8:307-315
-
(2003)
Drug Discov Today
, vol.8
, pp. 307-315
-
-
Adams, J.1
-
2
-
-
2342667387
-
The development of proteasome inhibitors as anticancer drugs
-
Adams J (2004) The development of proteasome inhibitors as anticancer drugs. Cancer Cell 5:417-421
-
(2004)
Cancer Cell
, vol.5
, pp. 417-421
-
-
Adams, J.1
-
3
-
-
0033152760
-
Proteasome inhibitors: A novel class of potent and effective antitumor agents
-
Adams J, Palombella VJ, Sausville EA, Johnson J, Destree A, Lazarus DD, Maas J, Pien CS, Prakash S, Elliott PJ (1999) Proteasome inhibitors: a novel class of potent and effective antitumor agents. Cancer Res 59:2615-2622
-
(1999)
Cancer Res
, vol.59
, pp. 2615-2622
-
-
Adams, J.1
Palombella, V.J.2
Sausville, E.A.3
Johnson, J.4
Destree, A.5
Lazarus, D.D.6
Maas, J.7
Pien, C.S.8
Prakash, S.9
Elliott, P.J.10
-
4
-
-
0000146018
-
Cultivation in a semi-defined medium of animal infective forms of Trypanosoma brucei, T. equiperdum, T. evansi, T. rhodesiense and T. gambiense
-
Baltz T, Baltz D, Giroud C, Crockett J (1985) Cultivation in a semi-defined medium of animal infective forms of Trypanosoma brucei, T. equiperdum, T. evansi, T. rhodesiense and T. gambiense. EMBO J 4:1273-1277
-
(1985)
EMBO J
, vol.4
, pp. 1273-1277
-
-
Baltz, T.1
Baltz, D.2
Giroud, C.3
Crockett, J.4
-
5
-
-
0031010398
-
Covalent modification of the active site threonine of proteasomal β subunits and the Escherichia coli homolog HsIV by a new class of inhibitors
-
Bogyo M, McMaster JS, Gaczynska M, Tortorella D, Goldberg AL, Ploegh H (1997) Covalent modification of the active site threonine of proteasomal β subunits and the Escherichia coli homolog HsIV by a new class of inhibitors. Proc Natl Acad Sci U S A 94:6629-6634
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 6629-6634
-
-
Bogyo, M.1
McMaster, J.S.2
Gaczynska, M.3
Tortorella, D.4
Goldberg, A.L.5
Ploegh, H.6
-
6
-
-
0032103006
-
Substrate binding and sequence preference of the proteasome revealed by active-site-directed affinity probes
-
Bogyo M, Shin S, McMaster JS, Ploegh HL (1998) Substrate binding and sequence preference of the proteasome revealed by active-site-directed affinity probes. Chem Biol 5:307-320
-
(1998)
Chem Biol
, vol.5
, pp. 307-320
-
-
Bogyo, M.1
Shin, S.2
McMaster, J.S.3
Ploegh, H.L.4
-
8
-
-
0030016595
-
Structure and functions of the 20S and 26S proteasomes
-
Coux O, Tanaka K, Goldberg AL (1996) Structure and functions of the 20S and 26S proteasomes. Annu Rev Biochem 65:801-847
-
(1996)
Annu Rev Biochem
, vol.65
, pp. 801-847
-
-
Coux, O.1
Tanaka, K.2
Goldberg, A.L.3
-
9
-
-
4344593765
-
Trypanocidal effect of α′,/β′-epoxyketones indicates that trypanosomes are particularly sensitive to inhibitors of proteasome trypsin-like activity
-
Glenn RJ, Pemberton AJ, Royle HJ, Spackman RW, Smith E, Rivett AJ, Steverding D (2004) Trypanocidal effect of α′,/β′- epoxyketones indicates that trypanosomes are particularly sensitive to inhibitors of proteasome trypsin-like activity. Int J Antimicrob Agents 24:286-289
-
(2004)
Int J Antimicrob Agents
, vol.24
, pp. 286-289
-
-
Glenn, R.J.1
Pemberton, A.J.2
Royle, H.J.3
Spackman, R.W.4
Smith, E.5
Rivett, A.J.6
Steverding, D.7
-
10
-
-
0018927978
-
In vitro cloning of animal-infective bloodstream forms of Trypanosoma brucei
-
Hirumi H, Hirumi K, Doyle JJ, Cross GAM (1980) In vitro cloning of animal-infective bloodstream forms of Trypanosoma brucei. Parasitology 80:371-382
-
(1980)
Parasitology
, vol.80
, pp. 371-382
-
-
Hirumi, H.1
Hirumi, K.2
Doyle, J.J.3
Cross, G.A.M.4
-
11
-
-
0343431431
-
Purification and characterization of proteasomes from Trypanosoma brucei
-
Hua S-B, To W-Y, Nguyen TT, Wong M-L, Wang CC (1996) Purification and characterization of proteasomes from Trypanosoma brucei. Mol Biochem Parasitol 78:33-46
-
(1996)
Mol Biochem Parasitol
, vol.78
, pp. 33-46
-
-
Hua, S.-B.1
To, W.-Y.2
Nguyen, T.T.3
Wong, M.-L.4
Wang, C.C.5
-
12
-
-
0027753162
-
50 in studies of drug resistance of malaria parasites
-
50 in studies of drug resistance of malaria parasites. Acta Trop 55:257-261
-
(1993)
Acta Trop
, vol.55
, pp. 257-261
-
-
Huber, W.1
Koella, J.C.2
-
13
-
-
0034819479
-
Extended peptide-based inhibitors efficiently target the proteasome and reveal overlapping specificities of the catalytic β-subunits
-
Kessler BM, Tortorella D, Altun M, Kisselev AF, Fiebiger E, Hekking BG, Ploegh HL, Overkleeft HS (2001) Extended peptide-based inhibitors efficiently target the proteasome and reveal overlapping specificities of the catalytic β-subunits. Chem Biol 8:913-929
-
(2001)
Chem Biol
, vol.8
, pp. 913-929
-
-
Kessler, B.M.1
Tortorella, D.2
Altun, M.3
Kisselev, A.F.4
Fiebiger, E.5
Hekking, B.G.6
Ploegh, H.L.7
Overkleeft, H.S.8
-
14
-
-
0034864799
-
Proteasome inhibitors: From research tools to drug candidates
-
Kisselev AF, Goldberg AL (2001) Proteasome inhibitors: from research tools to drug candidates. Chem Biol 8:739-758
-
(2001)
Chem Biol
, vol.8
, pp. 739-758
-
-
Kisselev, A.F.1
Goldberg, A.L.2
-
15
-
-
0034904388
-
Drug resistance in Trypanosoma brucei spp., the causative agents of sleeping sickness in man and nagana in cattle
-
Matovu E, Seebeck T, Enyaru JCK, Kaminsky R (2001) Drug resistance in Trypanosoma brucei spp., the causative agents of sleeping sickness in man and nagana in cattle. Microbes Infect 3:763-770
-
(2001)
Microbes Infect
, vol.3
, pp. 763-770
-
-
Matovu, E.1
Seebeck, T.2
Enyaru, J.C.K.3
Kaminsky, R.4
-
16
-
-
0034815454
-
In vitro effect of alkaloids on bloodstream forms of Trypanosoma brucei and T. congolense
-
Merschjohann K, Sporer F, Steverding D, Wink M (2001) In vitro effect of alkaloids on bloodstream forms of Trypanosoma brucei and T. congolense. Planta Med 67:623-627
-
(2001)
Planta Med
, vol.67
, pp. 623-627
-
-
Merschjohann, K.1
Sporer, F.2
Steverding, D.3
Wink, M.4
-
17
-
-
0023728105
-
The behavior and significance of slow-binding enzyme inhibitors
-
Morrison JF, Walsh CT (1988) The behavior and significance of slow-binding enzyme inhibitors. Adv Enzymol Relat Areas Mol Biol 61:201-301
-
(1988)
Adv Enzymol Relat Areas Mol Biol
, vol.61
, pp. 201-301
-
-
Morrison, J.F.1
Walsh, C.T.2
-
18
-
-
0035853116
-
Global analysis of proteasomal substrate specificity using positional-scanning libraries of covalent inhibitors
-
Nazif T, Bogyo M (2001) Global analysis of proteasomal substrate specificity using positional-scanning libraries of covalent inhibitors. Proc Natl Acad Sci U S A 98:2967-2972
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 2967-2972
-
-
Nazif, T.1
Bogyo, M.2
-
20
-
-
0029099619
-
Vinyl sulfones as mechanism-based cysteine protease inhibitors
-
Palmer JT, Rasnick D, Klaus JL, Brömme D (1995) Vinyl sulfones as mechanism-based cysteine protease inhibitors. J Med Chem 38:3193-196
-
(1995)
J Med Chem
, vol.38
, pp. 3193-3196
-
-
Palmer, J.T.1
Rasnick, D.2
Klaus, J.L.3
Brömme, D.4
-
21
-
-
0031438791
-
Differential toxicity of ricin and diphtheria toxin for bloodstream forms of Trypanosoma brucei
-
Scory S, Steverding D (1997) Differential toxicity of ricin and diphtheria toxin for bloodstream forms of Trypanosoma brucei. Mol Biochem Parasitol 90:289-295
-
(1997)
Mol Biochem Parasitol
, vol.90
, pp. 289-295
-
-
Scory, S.1
Steverding, D.2
-
22
-
-
0038521266
-
Biochemical analysis of the 20S proteasome of Trypanosoma brucei
-
Wang CC, Bozdech Z, Liu CL, Shipway A, Backes BJ, Harris JL, Bogyo M (2002) Biochemical analysis of the 20S proteasome of Trypanosoma brucei. J Biol Chem 278:15800-15808
-
(2002)
J Biol Chem
, vol.278
, pp. 15800-15808
-
-
Wang, C.C.1
Bozdech, Z.2
Liu, C.L.3
Shipway, A.4
Backes, B.J.5
Harris, J.L.6
Bogyo, M.7
-
23
-
-
4344709649
-
African trypanosomiasis or sleeping sickness
-
World Health Organisation (2001) African trypanosomiasis or sleeping sickness. World Health Organ Fact Sheet 259:http://www.who.int/mediacentre/ factsheets/fs259/en
-
(2001)
World Health Organ Fact Sheet
, vol.259
-
-
|