-
1
-
-
2542481724
-
Phase I study of bortezomib in refractory or relapsed acute leukemias
-
Cortes J., Thomas D., Koller C., Giles F., Estey E., Faderl S., Garcia-Manero G., McConkey D., Ruiz S.L., Guerciolini R., Wright J., and Kantarjian H. Phase I study of bortezomib in refractory or relapsed acute leukemias. Clin. Cancer Res. 10 (2004) 3371-3376
-
(2004)
Clin. Cancer Res.
, vol.10
, pp. 3371-3376
-
-
Cortes, J.1
Thomas, D.2
Koller, C.3
Giles, F.4
Estey, E.5
Faderl, S.6
Garcia-Manero, G.7
McConkey, D.8
Ruiz, S.L.9
Guerciolini, R.10
Wright, J.11
Kantarjian, H.12
-
2
-
-
46049107832
-
TROSY-based NMR evidence for a novel class of 20S proteasome inhibitors
-
Sprangers R., Li X.M., Mao X.L., Rubinstein J.L., Schimmer A.D., and Kay L.E. TROSY-based NMR evidence for a novel class of 20S proteasome inhibitors. Biochemistry 47 (2008) 6728-6734
-
(2008)
Biochemistry
, vol.47
, pp. 6728-6734
-
-
Sprangers, R.1
Li, X.M.2
Mao, X.L.3
Rubinstein, J.L.4
Schimmer, A.D.5
Kay, L.E.6
-
3
-
-
0035976835
-
α-Synuclein metabolism and aggregation is linked to ubiquitin-independent degradation by the proteasome
-
Tofaris G.K., Layfield R., and Spillantini M.G. α-Synuclein metabolism and aggregation is linked to ubiquitin-independent degradation by the proteasome. FEBS Lett. 509 (2001) 22-26
-
(2001)
FEBS Lett.
, vol.509
, pp. 22-26
-
-
Tofaris, G.K.1
Layfield, R.2
Spillantini, M.G.3
-
5
-
-
0030897031
-
Structure of 20S proteasome from yeast at 24 Å resolution
-
Groll M., Ditzel L., L€owe J., Stock D., Bochtler M., Bartunik H.D., and Huber R. Structure of 20S proteasome from yeast at 24 Å resolution. Nature 386 (1997) 463-471
-
(1997)
Nature
, vol.386
, pp. 463-471
-
-
Groll, M.1
Ditzel, L.2
Lowe, J.3
Stock, D.4
Bochtler, M.5
Bartunik, H.D.6
Huber, R.7
-
6
-
-
2342667387
-
The development of proteasome inhibitors as anticancer drugs
-
Adams J. The development of proteasome inhibitors as anticancer drugs. Cancer Cell 5 (2004) 417-421
-
(2004)
Cancer Cell
, vol.5
, pp. 417-421
-
-
Adams, J.1
-
7
-
-
0028150688
-
Inhibition of the proteolytic activity of the multicatalytic proteinase complex (proteasome) by substrate-related peptidyl aldehydes
-
Vinitsky A., Cardozo C., Sepp-Lorenzino L., Michaud C., and Orlowski M. Inhibition of the proteolytic activity of the multicatalytic proteinase complex (proteasome) by substrate-related peptidyl aldehydes. J. Biol. Chem. 269 (1994) 29860-29866
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 29860-29866
-
-
Vinitsky, A.1
Cardozo, C.2
Sepp-Lorenzino, L.3
Michaud, C.4
Orlowski, M.5
-
8
-
-
0032539571
-
Inhibitors of the chymotrypsin-like activity of proteasome based on di- and tri-peptidyl α-keto aldehydes (glyoxals)
-
Lynas J.F., Harriott P., Healy A., McKervey M.A., and Walker B. Inhibitors of the chymotrypsin-like activity of proteasome based on di- and tri-peptidyl α-keto aldehydes (glyoxals). Bioorg. Med. Chem. Lett. 8 (1998) 373-378
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 373-378
-
-
Lynas, J.F.1
Harriott, P.2
Healy, A.3
McKervey, M.A.4
Walker, B.5
-
10
-
-
0033817605
-
Degradation pathways of a peptide boronic acid derivative, 2-Pyz-(CO)-Phe-Leu-B(OH)2
-
Wu S., Waugh W., and Stella V.J. Degradation pathways of a peptide boronic acid derivative, 2-Pyz-(CO)-Phe-Leu-B(OH)2. J. Pharm. Sci. 89 (2000) 758-765
-
(2000)
J. Pharm. Sci.
, vol.89
, pp. 758-765
-
-
Wu, S.1
Waugh, W.2
Stella, V.J.3
-
11
-
-
4143146428
-
Dipeptide boronic acid, a novel proteasome inhibitor, prevents islet-allograft rejection
-
Wu Y.L., Han B., Luo H.Y., Shi G.X., and Wu J.P. Dipeptide boronic acid, a novel proteasome inhibitor, prevents islet-allograft rejection. Transplantation 78 (2004) 360-366
-
(2004)
Transplantation
, vol.78
, pp. 360-366
-
-
Wu, Y.L.1
Han, B.2
Luo, H.Y.3
Shi, G.X.4
Wu, J.P.5
-
12
-
-
0033230405
-
Towards subunit-specific proteasome inhibitors: synthesis and evaluation of peptide α′,β′-epoxyketones
-
Elfsson M., Splittgerber U., Myung J., Mohan R., and Crews C.M. Towards subunit-specific proteasome inhibitors: synthesis and evaluation of peptide α′,β′-epoxyketones. Chem. Biol. 6 (1999) 811-822
-
(1999)
Chem. Biol.
, vol.6
, pp. 811-822
-
-
Elfsson, M.1
Splittgerber, U.2
Myung, J.3
Mohan, R.4
Crews, C.M.5
-
13
-
-
0035927193
-
A new structural class of selective and non-covalent inhibitors of the chymotrypsin-like activity of the 20S proteasome
-
García-Echeverría C., Imbach P., France D., Fu{combining double acute accent}rst P., Lang M., Noorani M., Scholz D., Zimmermanna J., and Fureta P. A new structural class of selective and non-covalent inhibitors of the chymotrypsin-like activity of the 20S proteasome. Bioorg. Med. Chem. Lett. 11 (2001) 1317-1319
-
(2001)
Bioorg. Med. Chem. Lett.
, vol.11
, pp. 1317-1319
-
-
García-Echeverría, C.1
Imbach, P.2
France, D.3
Furst, P.4
Lang, M.5
Noorani, M.6
Scholz, D.7
Zimmermanna, J.8
Fureta, P.9
-
14
-
-
0030595329
-
Autocatalytic subunit processing couples active site formation in the 20S proteasome to completion of assembly
-
Chen P., and Hochstrasser M. Autocatalytic subunit processing couples active site formation in the 20S proteasome to completion of assembly. Cell 86 (1996) 961-972
-
(1996)
Cell
, vol.86
, pp. 961-972
-
-
Chen, P.1
Hochstrasser, M.2
-
15
-
-
0027980319
-
Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules
-
Rock K.L., Gramm C., Rothstein L., Clark K., Stein R., Dick L., Hwang D., and Goldberg A.L. Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules. Cell 78 (1994) 761-771
-
(1994)
Cell
, vol.78
, pp. 761-771
-
-
Rock, K.L.1
Gramm, C.2
Rothstein, L.3
Clark, K.4
Stein, R.5
Dick, L.6
Hwang, D.7
Goldberg, A.L.8
-
16
-
-
0030774890
-
The active sites of the eukaryotic 20S proteasome and their involvement in subunit precursor processing
-
Heinemeyer W., Fischer M., Krimmer T., Stachon U., and Wolf D.H. The active sites of the eukaryotic 20S proteasome and their involvement in subunit precursor processing. J. Biol. Chem. 272 (1997) 25200-25209
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 25200-25209
-
-
Heinemeyer, W.1
Fischer, M.2
Krimmer, T.3
Stachon, U.4
Wolf, D.H.5
-
17
-
-
0032539702
-
Potent and selective inhibitors of the proteasome: dipeptidyl boronic acids
-
Adams J., Behnke M., Chen S., Cruickshank A.A., Dick L.R., Grenier L., Klunder J.M., Ma Y.T., Plamonda L., and Stein R.L. Potent and selective inhibitors of the proteasome: dipeptidyl boronic acids. Bioorg. Med. Chem. Lett. 8 (1998) 333-338
-
(1998)
Bioorg. Med. Chem. Lett.
, vol.8
, pp. 333-338
-
-
Adams, J.1
Behnke, M.2
Chen, S.3
Cruickshank, A.A.4
Dick, L.R.5
Grenier, L.6
Klunder, J.M.7
Ma, Y.T.8
Plamonda, L.9
Stein, R.L.10
-
18
-
-
33644886305
-
Vertebrate freezing survival: regulation of the multicatalytic proteinase complex and controls on protein degradation
-
Woods A.K., and Storey K.B. Vertebrate freezing survival: regulation of the multicatalytic proteinase complex and controls on protein degradation. Biochim. Biophys. Acta 1760 (2006) 395-403
-
(2006)
Biochim. Biophys. Acta
, vol.1760
, pp. 395-403
-
-
Woods, A.K.1
Storey, K.B.2
-
19
-
-
0017226658
-
A new fluorogenic substrate for chymotrypsin
-
Zimmerman M., Yurewicz E., and Patel G. A new fluorogenic substrate for chymotrypsin. Anal. Biochem. 70 (1976) 258-262
-
(1976)
Anal. Biochem.
, vol.70
, pp. 258-262
-
-
Zimmerman, M.1
Yurewicz, E.2
Patel, G.3
-
20
-
-
0036882396
-
Irreversible inhibitors of serine, cysteine, and threonine proteases
-
Powers J.C., Asgian J.L., Ekici O.D., and James K.E. Irreversible inhibitors of serine, cysteine, and threonine proteases. Chem. Rev. 102 (2002) 4639-4750
-
(2002)
Chem. Rev.
, vol.102
, pp. 4639-4750
-
-
Powers, J.C.1
Asgian, J.L.2
Ekici, O.D.3
James, K.E.4
-
21
-
-
40749103758
-
Novel CADD-based peptidyl vinyl ester derivatives as potential proteasome inhibitors
-
Mou K., Xu B., Ma C., Yang X.M., Zou X.M., Lü Y., and Xu P. Novel CADD-based peptidyl vinyl ester derivatives as potential proteasome inhibitors. Bioorg. Med. Chem. Lett. 18 (2008) 2198-2202
-
(2008)
Bioorg. Med. Chem. Lett.
, vol.18
, pp. 2198-2202
-
-
Mou, K.1
Xu, B.2
Ma, C.3
Yang, X.M.4
Zou, X.M.5
Lü, Y.6
Xu, P.7
-
22
-
-
0347089217
-
Recent progress in high-performance capillary bioseparations
-
Huck C.W., Stecher G., Bakry R., and Bonn G.K. Recent progress in high-performance capillary bioseparations. Electrophoresis 24 (2003) 3977-3997
-
(2003)
Electrophoresis
, vol.24
, pp. 3977-3997
-
-
Huck, C.W.1
Stecher, G.2
Bakry, R.3
Bonn, G.K.4
-
23
-
-
20544470071
-
Kinetic study of cytochrome P450 3A4 activity on warfarin by capillary electrophoresis with fluorescence detection
-
Zhang J., Thanh-Ha P.T., Lou Y.J., Hoogmartens J., and Schepdael A.V. Kinetic study of cytochrome P450 3A4 activity on warfarin by capillary electrophoresis with fluorescence detection. J. Chromatogr. A 1082 (2005) 235-239
-
(2005)
J. Chromatogr. A
, vol.1082
, pp. 235-239
-
-
Zhang, J.1
Thanh-Ha, P.T.2
Lou, Y.J.3
Hoogmartens, J.4
Schepdael, A.V.5
-
24
-
-
23944441167
-
Kinetic study of CYP3A4 activity on verapamil by capillary electrophoresis
-
Zhang J., Thanh-Ha P.T., Lou Y.J., Hoogmartens J., and Schepdael A.V. Kinetic study of CYP3A4 activity on verapamil by capillary electrophoresis. J. Pharm. Biomed. Anal. 39 (2005) 612-617
-
(2005)
J. Pharm. Biomed. Anal.
, vol.39
, pp. 612-617
-
-
Zhang, J.1
Thanh-Ha, P.T.2
Lou, Y.J.3
Hoogmartens, J.4
Schepdael, A.V.5
-
25
-
-
34249655690
-
Characterization of procaine metabolism as probe for the butyrylcholinesterase enzyme investigation by simultaneous determination of procaine and its metabolite using capillary electrophoresis with electrochemiluminescence detection
-
Yuan J.P., Yin J.Y., and Wang E.K. Characterization of procaine metabolism as probe for the butyrylcholinesterase enzyme investigation by simultaneous determination of procaine and its metabolite using capillary electrophoresis with electrochemiluminescence detection. J. Chromatogr. A 1154 (2007) 368-372
-
(2007)
J. Chromatogr. A
, vol.1154
, pp. 368-372
-
-
Yuan, J.P.1
Yin, J.Y.2
Wang, E.K.3
-
26
-
-
34548859817
-
Inhibition of choline transport by redox-active cholinomimetic bis-catechol reagents
-
Cai S., Mukherjee J., Tillekeratne L.M.V., Hudson R.A., and Kirchhoff J.R. Inhibition of choline transport by redox-active cholinomimetic bis-catechol reagents. Bioorg. Med. Chem. 15 (2007) 7042-7047
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 7042-7047
-
-
Cai, S.1
Mukherjee, J.2
Tillekeratne, L.M.V.3
Hudson, R.A.4
Kirchhoff, J.R.5
-
27
-
-
56849110845
-
Enzymatic assay of marine bacterial phosphatases by capillary electrophoresis with laser-induced fluorescence detection
-
Chichester K.D., Sebastian M., Ammerman J.W., and Colyer C.L. Enzymatic assay of marine bacterial phosphatases by capillary electrophoresis with laser-induced fluorescence detection. Electrophoresis 29 (2008) 3810-3816
-
(2008)
Electrophoresis
, vol.29
, pp. 3810-3816
-
-
Chichester, K.D.1
Sebastian, M.2
Ammerman, J.W.3
Colyer, C.L.4
-
28
-
-
54249114843
-
A capillary electrophoresis assay for recombinant Bacillus subtilis protoporphyrinogen oxidase
-
Tan Y., Sun L., Xi Z., Yang G.F., Jiang D.Q., Yan X.P., Yang X., and Li H.Y. A capillary electrophoresis assay for recombinant Bacillus subtilis protoporphyrinogen oxidase. Anal. Biochem. 383 (2008) 200-204
-
(2008)
Anal. Biochem.
, vol.383
, pp. 200-204
-
-
Tan, Y.1
Sun, L.2
Xi, Z.3
Yang, G.F.4
Jiang, D.Q.5
Yan, X.P.6
Yang, X.7
Li, H.Y.8
-
29
-
-
59249100307
-
A capillary electrophoresis method for evaluation of Aβ proteolysis in vitro
-
Alper B.J., and Schmidt W.K. A capillary electrophoresis method for evaluation of Aβ proteolysis in vitro. J. Neurosci. Methods 178 (2009) 40-45
-
(2009)
J. Neurosci. Methods
, vol.178
, pp. 40-45
-
-
Alper, B.J.1
Schmidt, W.K.2
-
30
-
-
61849120768
-
9-Fluorenylmethoxycarbonyl-labeled peptides as substrates in a capillary electrophoresis-based assay for sirtuin enzymes
-
Fan Y., Ludewig R., and Scriba G.K.E. 9-Fluorenylmethoxycarbonyl-labeled peptides as substrates in a capillary electrophoresis-based assay for sirtuin enzymes. Anal. Biochem. 387 (2009) 243-248
-
(2009)
Anal. Biochem.
, vol.387
, pp. 243-248
-
-
Fan, Y.1
Ludewig, R.2
Scriba, G.K.E.3
-
31
-
-
0037102093
-
Studies of reversible inhibition, irreversible inhibition, and activation of alkaline phosphatase by capillary electrophoresis
-
Whisnan A.R., and Gilman S.D. Studies of reversible inhibition, irreversible inhibition, and activation of alkaline phosphatase by capillary electrophoresis. Anal. Biochem. 307 (2002) 226-234
-
(2002)
Anal. Biochem.
, vol.307
, pp. 226-234
-
-
Whisnan, A.R.1
Gilman, S.D.2
-
32
-
-
5644277656
-
Capillary electrophoretic approach to screen for enzyme inhibitors in natural extracts
-
Belenky A., Hughes D., Korneev A., and Dunayevskiy Y. Capillary electrophoretic approach to screen for enzyme inhibitors in natural extracts. J. Chromatogr. A 1053 (2004) 247-251
-
(2004)
J. Chromatogr. A
, vol.1053
, pp. 247-251
-
-
Belenky, A.1
Hughes, D.2
Korneev, A.3
Dunayevskiy, Y.4
-
33
-
-
0037401443
-
Assessment of proteasome activity in cell lysates and tissue homogenates using peptide substrates
-
Rodgers K.J., and Dean R.T. Assessment of proteasome activity in cell lysates and tissue homogenates using peptide substrates. Intl. J. Biochem. Cell Biol. 35 (2003) 716-727
-
(2003)
Intl. J. Biochem. Cell Biol.
, vol.35
, pp. 716-727
-
-
Rodgers, K.J.1
Dean, R.T.2
-
34
-
-
0030726132
-
Specificities of cell permeant peptidyl inhibitors for the proteinase activities of μ-calpain and the 20S proteasome
-
Mellgren R.L. Specificities of cell permeant peptidyl inhibitors for the proteinase activities of μ-calpain and the 20S proteasome. J. Biol. Chem. 272 (1997) 29899-29903
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 29899-29903
-
-
Mellgren, R.L.1
-
35
-
-
23344435097
-
Tripeptide mimetics inhibit the 20S proteasome by covalent bonding to the active threonines
-
Braun H.A., Umbreen S., Groll M., Kuckelkorn U., Mlynarczuk I., Wigand M.E., Drung I., Kloetzel P.M., and Schmidt B. Tripeptide mimetics inhibit the 20S proteasome by covalent bonding to the active threonines. J. Biol. Chem. 280 (2005) 28394-28411
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 28394-28411
-
-
Braun, H.A.1
Umbreen, S.2
Groll, M.3
Kuckelkorn, U.4
Mlynarczuk, I.5
Wigand, M.E.6
Drung, I.7
Kloetzel, P.M.8
Schmidt, B.9
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