-
1
-
-
57649155302
-
Proteases: multifunctional enzymes in life and disease
-
López-Otín C., Bond J.S. Proteases: multifunctional enzymes in life and disease. J. Biol. Chem. 2008, 283:30433-30437.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 30433-30437
-
-
López-Otín, C.1
Bond, J.S.2
-
3
-
-
70249099290
-
Cathepsin S regulates class II MHC processing in human CD4+ HLA-DR+ T cells
-
Costantino C.M., Ploegh H.L., Hafler D.A. Cathepsin S regulates class II MHC processing in human CD4+ HLA-DR+ T cells. J. Immunol. 2009, 183:945-952.
-
(2009)
J. Immunol.
, vol.183
, pp. 945-952
-
-
Costantino, C.M.1
Ploegh, H.L.2
Hafler, D.A.3
-
4
-
-
33847683870
-
Regulation of matrix metalloproteinase gene expression
-
Yan C., Boyd D.D. Regulation of matrix metalloproteinase gene expression. J. Cell Physiol. 2007, 211:19-26.
-
(2007)
J. Cell Physiol.
, vol.211
, pp. 19-26
-
-
Yan, C.1
Boyd, D.D.2
-
5
-
-
0031956497
-
Molecular mechanisms for the conversion of zymogens to active proteolytic enzymes
-
Khan A.R., James M.N. Molecular mechanisms for the conversion of zymogens to active proteolytic enzymes. Protein Sci. 1998, 7:815-836.
-
(1998)
Protein Sci.
, vol.7
, pp. 815-836
-
-
Khan, A.R.1
James, M.N.2
-
6
-
-
69249100500
-
Human caspases: activation, specificity, and regulation
-
Pop C., Salvesen G.S. Human caspases: activation, specificity, and regulation. J. Biol. Chem. 2009, 284:21777-21781.
-
(2009)
J. Biol. Chem.
, vol.284
, pp. 21777-21781
-
-
Pop, C.1
Salvesen, G.S.2
-
8
-
-
36549085160
-
Control of matrix metalloproteinase catalytic activity
-
Ra H.J., Parks W.C. Control of matrix metalloproteinase catalytic activity. Matrix Biol. 2007, 26:587-596.
-
(2007)
Matrix Biol.
, vol.26
, pp. 587-596
-
-
Ra, H.J.1
Parks, W.C.2
-
9
-
-
70349956567
-
Apoptosis and autophagy: regulation of caspase-9 by phosphorylation
-
Allan L.A., Clarke P.R. Apoptosis and autophagy: regulation of caspase-9 by phosphorylation. FEBS J. 2009, 276:6063-6073.
-
(2009)
FEBS J.
, vol.276
, pp. 6063-6073
-
-
Allan, L.A.1
Clarke, P.R.2
-
11
-
-
0036265909
-
Structure, function, and activation of coagulation factor VII
-
Eigenbrot C. Structure, function, and activation of coagulation factor VII. Curr. Protein Pept. Sci. 2002, 3:287-299.
-
(2002)
Curr. Protein Pept. Sci.
, vol.3
, pp. 287-299
-
-
Eigenbrot, C.1
-
12
-
-
0031883733
-
Lysosomes, a meeting point of proteins, chaperones, and proteases
-
Cuervo A.M., Dice J.F. Lysosomes, a meeting point of proteins, chaperones, and proteases. J. Mol. Med. 1998, 76:6-12.
-
(1998)
J. Mol. Med.
, vol.76
, pp. 6-12
-
-
Cuervo, A.M.1
Dice, J.F.2
-
13
-
-
38849143983
-
Neutrophil elastase, proteinase 3 and cathepsin G: physicochemical properties, activity and physiopathological functions
-
Korkmaz B., Moreau T., Gauthier F. Neutrophil elastase, proteinase 3 and cathepsin G: physicochemical properties, activity and physiopathological functions. Biochimie 2008, 90:227-242.
-
(2008)
Biochimie
, vol.90
, pp. 227-242
-
-
Korkmaz, B.1
Moreau, T.2
Gauthier, F.3
-
14
-
-
1642464622
-
Evolutionary families of peptidase inhibitors
-
Rawlings N.D., Tolle D.P., Barrett A.J. Evolutionary families of peptidase inhibitors. Biochem. J. 2004, 378:705-716.
-
(2004)
Biochem. J.
, vol.378
, pp. 705-716
-
-
Rawlings, N.D.1
Tolle, D.P.2
Barrett, A.J.3
-
15
-
-
0035986219
-
Regulating cysteine protease activity: essential role of protease inhibitors as guardians and regulators
-
Turk B., Turk D., Salvesen G.S. Regulating cysteine protease activity: essential role of protease inhibitors as guardians and regulators. Curr. Pharm Des. 2002, 8:1623-1637.
-
(2002)
Curr. Pharm Des.
, vol.8
, pp. 1623-1637
-
-
Turk, B.1
Turk, D.2
Salvesen, G.S.3
-
16
-
-
0034615550
-
Tissue inhibitors of metalloproteinases: evolution, structure and function
-
Brew K., Dinakarpandian D., Nagase H. Tissue inhibitors of metalloproteinases: evolution, structure and function. Biochim. Biophys. Acta 2000, 1477:267-283.
-
(2000)
Biochim. Biophys. Acta
, vol.1477
, pp. 267-283
-
-
Brew, K.1
Dinakarpandian, D.2
Nagase, H.3
-
17
-
-
43549111150
-
IAPs: more than just inhibitors of apoptosis proteins
-
Dubrez-Daloz L., Dupoux A., Cartier J. IAPs: more than just inhibitors of apoptosis proteins. Cell Cycle 2008, 7:1036-1046.
-
(2008)
Cell Cycle
, vol.7
, pp. 1036-1046
-
-
Dubrez-Daloz, L.1
Dupoux, A.2
Cartier, J.3
-
18
-
-
63849098507
-
Type 3 cystatins; fetuins, kininogen and histidine-rich glycoprotein
-
Lee C., Bongcam-Rudloff E., Sollner C., Jahnen-Dechent W., Claesson-Welsh L. Type 3 cystatins; fetuins, kininogen and histidine-rich glycoprotein. Front. Biosci. 2009, 14:2911-2922.
-
(2009)
Front. Biosci.
, vol.14
, pp. 2911-2922
-
-
Lee, C.1
Bongcam-Rudloff, E.2
Sollner, C.3
Jahnen-Dechent, W.4
Claesson-Welsh, L.5
-
19
-
-
38649083162
-
Multifaceted roles of human elafin and secretory leukocyte proteinase inhibitor (SLPI), two serine protease inhibitors of the chelonianin family
-
Moreau T., Baranger K., Dadé S., Dallet-Choisy S., Guyot N., Zani M.L. Multifaceted roles of human elafin and secretory leukocyte proteinase inhibitor (SLPI), two serine protease inhibitors of the chelonianin family. Biochimie 2008, 90:284-295.
-
(2008)
Biochimie
, vol.90
, pp. 284-295
-
-
Moreau, T.1
Baranger, K.2
Dadé, S.3
Dallet-Choisy, S.4
Guyot, N.5
Zani, M.L.6
-
20
-
-
0012813996
-
The bovine basic pancreatic trypsin inhibitor (Kunitz inhibitor): a milestone protein
-
Ascenzi P., Bocedi A., Bolognesi M., Spallarossa A., Coletta M., De Cristofaro R., Menegatti E. The bovine basic pancreatic trypsin inhibitor (Kunitz inhibitor): a milestone protein. Curr. Protein Pept. Sci. 2003, 4:231-251.
-
(2003)
Curr. Protein Pept. Sci.
, vol.4
, pp. 231-251
-
-
Ascenzi, P.1
Bocedi, A.2
Bolognesi, M.3
Spallarossa, A.4
Coletta, M.5
De Cristofaro, R.6
Menegatti, E.7
-
21
-
-
33748308883
-
Targeting proteases: successes, failures and future prospects
-
Turk B. Targeting proteases: successes, failures and future prospects. Nat. Rev. Drug Discov. 2006, 5:785-799.
-
(2006)
Nat. Rev. Drug Discov.
, vol.5
, pp. 785-799
-
-
Turk, B.1
-
22
-
-
56749133149
-
The ADAMs: signalling scissors in the tumour microenvironment
-
Murphy G. The ADAMs: signalling scissors in the tumour microenvironment. Nat. Rev. Cancer 2008, 8:929-941.
-
(2008)
Nat. Rev. Cancer
, vol.8
, pp. 929-941
-
-
Murphy, G.1
-
23
-
-
37549070672
-
Cysteine cathepsin proteases as pharmacological targets in cancer
-
Palermo C., Joyce J.A. Cysteine cathepsin proteases as pharmacological targets in cancer. Trends Pharmacol. Sci. 2008, 29:22-28.
-
(2008)
Trends Pharmacol. Sci.
, vol.29
, pp. 22-28
-
-
Palermo, C.1
Joyce, J.A.2
-
24
-
-
70349506754
-
Extracellular proteases as targets for drug development
-
Cudic M., Fields G.B. Extracellular proteases as targets for drug development. Curr. Protein Pept. Sci. 2009, 10:297-307.
-
(2009)
Curr. Protein Pept. Sci.
, vol.10
, pp. 297-307
-
-
Cudic, M.1
Fields, G.B.2
-
25
-
-
0017578611
-
Design of specific inhibitors of angiotensin converting enzyme: new class of orally acting active antihypertensive agents
-
Ondetti M.A., Rubin B., Cushman D.W. Design of specific inhibitors of angiotensin converting enzyme: new class of orally acting active antihypertensive agents. Science 1977, 196:441-444.
-
(1977)
Science
, vol.196
, pp. 441-444
-
-
Ondetti, M.A.1
Rubin, B.2
Cushman, D.W.3
-
26
-
-
33845339435
-
Protease inhibitors in the clinic
-
Abbenante G., Fairlie D.P. Protease inhibitors in the clinic. Med. Chem. 2005, 1:71-104.
-
(2005)
Med. Chem.
, vol.1
, pp. 71-104
-
-
Abbenante, G.1
Fairlie, D.P.2
-
27
-
-
2442723342
-
Treatment of human immunodeficiency virus infection with saquinavir, zidovudine, and zalcitabine. AIDS Clinical Trials Group
-
Collier A.C., Coombs R.W., Schoenfeld D.A., Bassett R.L., Timpone J., Baruch A., Jones M., Facey K., Whitacre C., McAuliffe V.J., Friedman H.M., Merigan T.C., Reichman R.C., Hooper C., Corey L. Treatment of human immunodeficiency virus infection with saquinavir, zidovudine, and zalcitabine. AIDS Clinical Trials Group. N. Engl. J. Med. 1996, 334:1011-1017.
-
(1996)
N. Engl. J. Med.
, vol.334
, pp. 1011-1017
-
-
Collier, A.C.1
Coombs, R.W.2
Schoenfeld, D.A.3
Bassett, R.L.4
Timpone, J.5
Baruch, A.6
Jones, M.7
Facey, K.8
Whitacre, C.9
McAuliffe, V.J.10
Friedman, H.M.11
Merigan, T.C.12
Reichman, R.C.13
Hooper, C.14
Corey, L.15
-
28
-
-
0030869269
-
Treatment with indinavir, zidovudine, and lamivudine in adults with human immunodeficiency virus infection and prior antiretroviral therapy
-
Gulick R.M., Mellors J.W., Havlir D., Eron J.J., Gonzalez C., McMahon D., Richman D.D., Valentine F.T., Jonas L., Meibohm A., Emini E.A., Chodakewitz J.A. Treatment with indinavir, zidovudine, and lamivudine in adults with human immunodeficiency virus infection and prior antiretroviral therapy. N. Engl. J. Med. 1997, 337:734-739.
-
(1997)
N. Engl. J. Med.
, vol.337
, pp. 734-739
-
-
Gulick, R.M.1
Mellors, J.W.2
Havlir, D.3
Eron, J.J.4
Gonzalez, C.5
McMahon, D.6
Richman, D.D.7
Valentine, F.T.8
Jonas, L.9
Meibohm, A.10
Emini, E.A.11
Chodakewitz, J.A.12
-
29
-
-
1842689611
-
Bortezomib and its role in the management of patients with multiple myeloma
-
Orlowski R.Z. Bortezomib and its role in the management of patients with multiple myeloma. Expert Rev. Anticancer Ther. 2004, 4:171-179.
-
(2004)
Expert Rev. Anticancer Ther.
, vol.4
, pp. 171-179
-
-
Orlowski, R.Z.1
-
30
-
-
0037192458
-
Matrix metalloproteinase inhibitors and cancer: trials and tribulations
-
Coussens L.M., Fingleton B., Matrisian L.M. Matrix metalloproteinase inhibitors and cancer: trials and tribulations. Science 2002, 295:2387-2392.
-
(2002)
Science
, vol.295
, pp. 2387-2392
-
-
Coussens, L.M.1
Fingleton, B.2
Matrisian, L.M.3
-
31
-
-
28144452675
-
Lysosomotropism of basic cathepsin K inhibitors contributes to increased cellular potencies against off-target cathepsins and reduced functional selectivity
-
Falgueyret J.P., Desmarais S., Oballa R., Black W.C., Cromlish W., Khougaz K., Lamontagne S., Massé F., Riendeau D., Toulmond S., Percival M.D. Lysosomotropism of basic cathepsin K inhibitors contributes to increased cellular potencies against off-target cathepsins and reduced functional selectivity. J. Med. Chem. 2005, 48:7535-7543.
-
(2005)
J. Med. Chem.
, vol.48
, pp. 7535-7543
-
-
Falgueyret, J.P.1
Desmarais, S.2
Oballa, R.3
Black, W.C.4
Cromlish, W.5
Khougaz, K.6
Lamontagne, S.7
Massé, F.8
Riendeau, D.9
Toulmond, S.10
Percival, M.D.11
-
32
-
-
34547838174
-
Insight into the structural determinants for selective inhibition of matrix metalloproteinases
-
Pirard B. Insight into the structural determinants for selective inhibition of matrix metalloproteinases. Drug Discov. Today 2007, 12:640-646.
-
(2007)
Drug Discov. Today
, vol.12
, pp. 640-646
-
-
Pirard, B.1
-
33
-
-
33749664751
-
The consequences of lysosomotropism on the design of selective cathepsin K inhibitors
-
Black W.C., Percival M.D. The consequences of lysosomotropism on the design of selective cathepsin K inhibitors. Chembiochem 2006, 7:1525-1534.
-
(2006)
Chembiochem
, vol.7
, pp. 1525-1534
-
-
Black, W.C.1
Percival, M.D.2
-
34
-
-
0022856832
-
The synthesis of peptidylfluoromethanes and their properties as inhibitors of serine proteinases and cysteine proteinases
-
Rauber P., Angliker H., Walker B., Shaw E. The synthesis of peptidylfluoromethanes and their properties as inhibitors of serine proteinases and cysteine proteinases. Biochem J. 1986, 239:633-640.
-
(1986)
Biochem J.
, vol.239
, pp. 633-640
-
-
Rauber, P.1
Angliker, H.2
Walker, B.3
Shaw, E.4
-
35
-
-
0036882396
-
Irreversible inhibitors of serine, cysteine, and threonine proteases
-
Powers J.C., Asgian J.L., Ekici O.D., James K.E. Irreversible inhibitors of serine, cysteine, and threonine proteases. Chem Rev. 2002, 102:4639-4750.
-
(2002)
Chem Rev.
, vol.102
, pp. 4639-4750
-
-
Powers, J.C.1
Asgian, J.L.2
Ekici, O.D.3
James, K.E.4
-
36
-
-
12444315984
-
Inhibition of papain-like cysteine proteases and legumain by caspase-specific inhibitors: when reaction mechanism is more important than specificity
-
Rozman-Pungercar J., Kopitar-Jerala N., Bogyo M., Turk D., Vasiljeva O., Stefe I., Vandenabeele P., Brömme D., Puizdar V., Fonović M., Trstenjak-Prebanda M., Dolenc I., Turk V., Turk B. Inhibition of papain-like cysteine proteases and legumain by caspase-specific inhibitors: when reaction mechanism is more important than specificity. Cell Death Differ. 2003, 10:881-888.
-
(2003)
Cell Death Differ.
, vol.10
, pp. 881-888
-
-
Rozman-Pungercar, J.1
Kopitar-Jerala, N.2
Bogyo, M.3
Turk, D.4
Vasiljeva, O.5
Stefe, I.6
Vandenabeele, P.7
Brömme, D.8
Puizdar, V.9
Fonović, M.10
Trstenjak-Prebanda, M.11
Dolenc, I.12
Turk, V.13
Turk, B.14
-
38
-
-
0037241478
-
Aprotinin: a serine protease inhibitor with therapeutic actions: its interaction with ACE inhibitors
-
Waxler B., Rabito S.F. Aprotinin: a serine protease inhibitor with therapeutic actions: its interaction with ACE inhibitors. Curr. Pharm. Des. 2003, 9:777-787.
-
(2003)
Curr. Pharm. Des.
, vol.9
, pp. 777-787
-
-
Waxler, B.1
Rabito, S.F.2
-
40
-
-
0025720555
-
Design, construction and function of a multicopy display vector using fusions to the major coat protein of bacteriophage M13
-
Markland W., Roberts B.L., Saxena M.J., Guterman S.K., Ladner R.C. Design, construction and function of a multicopy display vector using fusions to the major coat protein of bacteriophage M13. Gene 1991, 109:13-19.
-
(1991)
Gene
, vol.109
, pp. 13-19
-
-
Markland, W.1
Roberts, B.L.2
Saxena, M.J.3
Guterman, S.K.4
Ladner, R.C.5
-
41
-
-
0026471308
-
Protease inhibitor display M13 phage: selection of high-affinity neutrophil elastase inhibitors
-
Roberts B.L., Markland W., Siranosian K., Saxena M.J., Guterman S.K., Ladner R.C. Protease inhibitor display M13 phage: selection of high-affinity neutrophil elastase inhibitors. Gene 1992, 121:9-15.
-
(1992)
Gene
, vol.121
, pp. 9-15
-
-
Roberts, B.L.1
Markland, W.2
Siranosian, K.3
Saxena, M.J.4
Guterman, S.K.5
Ladner, R.C.6
-
42
-
-
0026568164
-
Directed evolution of a protein: selection of potent neutrophil elastase inhibitors displayed on M13 fusion phage
-
Roberts B.L., Markland W., Ley A.C., Kent R.B., White D.W., Guterman S.K., Ladner R.C. Directed evolution of a protein: selection of potent neutrophil elastase inhibitors displayed on M13 fusion phage. Proc. Natl. Acad. Sci. U.S.A. 1992, 89:2429-2433.
-
(1992)
Proc. Natl. Acad. Sci. U.S.A.
, vol.89
, pp. 2429-2433
-
-
Roberts, B.L.1
Markland, W.2
Ley, A.C.3
Kent, R.B.4
White, D.W.5
Guterman, S.K.6
Ladner, R.C.7
-
43
-
-
0029953760
-
Iterative optimization of high-affinity proteases inhibitors using phage display. 1. Plasmin
-
Markland W., Ley A.C., Lee S.W., Ladner R.C. Iterative optimization of high-affinity proteases inhibitors using phage display. 1. Plasmin. Biochemistry 1994, 35:8045-8057.
-
(1994)
Biochemistry
, vol.35
, pp. 8045-8057
-
-
Markland, W.1
Ley, A.C.2
Lee, S.W.3
Ladner, R.C.4
-
44
-
-
0028085530
-
Kunitz domain inhibitors of tissue factor - factor VIIa. I. Potent inhibitors selected from libraries by phage display
-
Dennis M.S., Lazarus R.A. Kunitz domain inhibitors of tissue factor - factor VIIa. I. Potent inhibitors selected from libraries by phage display. J. Biol. Chem. 1994, 269:22129-22136.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 22129-22136
-
-
Dennis, M.S.1
Lazarus, R.A.2
-
45
-
-
0028100458
-
Kunitz domain inhibitors of tissue factor - factor VIIa. II. Potent and specific inhibitors by competitive phage selection
-
Dennis M.S., Lazarus R.A. Kunitz domain inhibitors of tissue factor - factor VIIa. II. Potent and specific inhibitors by competitive phage selection. J. Biol. Chem. 1994, 269:22137-22144.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 22137-22144
-
-
Dennis, M.S.1
Lazarus, R.A.2
-
46
-
-
0029894775
-
Iterative optimization of high-affinity protease inhibitors using phage display. 2. Plasma kallikrein and thrombin
-
Markland W., Ley A.C., Ladner R.C. Iterative optimization of high-affinity protease inhibitors using phage display. 2. Plasma kallikrein and thrombin. Biochemistry 1996, 35:8058-8067.
-
(1996)
Biochemistry
, vol.35
, pp. 8058-8067
-
-
Markland, W.1
Ley, A.C.2
Ladner, R.C.3
-
47
-
-
0031712910
-
Molecular genetics of C1 inhibitor
-
Tosi M. Molecular genetics of C1 inhibitor. Immunobiology 1998, 199:358-365.
-
(1998)
Immunobiology
, vol.199
, pp. 358-365
-
-
Tosi, M.1
-
48
-
-
10644286657
-
The pathophysiology of hereditary angioedema
-
Davis A.E. The pathophysiology of hereditary angioedema. Clin. Immunol. 2005, 114:3-9.
-
(2005)
Clin. Immunol.
, vol.114
, pp. 3-9
-
-
Davis, A.E.1
-
49
-
-
0141527407
-
Approaches toward reversal of increased vascular permeability in C1 inhibitor deficient mice
-
Han Lee E.D., Pappalardo E., Scafidi J., Davis A.E. Approaches toward reversal of increased vascular permeability in C1 inhibitor deficient mice. Immunol. Lett. 2003, 89:155-160.
-
(2003)
Immunol. Lett.
, vol.89
, pp. 155-160
-
-
Han Lee, E.D.1
Pappalardo, E.2
Scafidi, J.3
Davis, A.E.4
-
50
-
-
34547127401
-
Critical role of kallikrein in hereditary angioedema pathogenesis: a clinical trial of ecallantide, a novel kallikrein inhibitor
-
Schneider L., Lumry W., Vegh A., Williams A.H., Schmalbach T. Critical role of kallikrein in hereditary angioedema pathogenesis: a clinical trial of ecallantide, a novel kallikrein inhibitor. J. Allergy Clin. Immunol. 2007, 120:416-422.
-
(2007)
J. Allergy Clin. Immunol.
, vol.120
, pp. 416-422
-
-
Schneider, L.1
Lumry, W.2
Vegh, A.3
Williams, A.H.4
Schmalbach, T.5
-
51
-
-
0033428850
-
Evidence for excessive bronchial inflammation during an acute exacerbation of chronic obstructive pulmonary disease in patients with alpha(1)-antitrypsin deficiency (PiZ)
-
Hill A.T., Campbell E.J., Bayley D.L., Hill S.L., Stockley R.A. Evidence for excessive bronchial inflammation during an acute exacerbation of chronic obstructive pulmonary disease in patients with alpha(1)-antitrypsin deficiency (PiZ). Am. J. Respir. Crit. Care Med. 1999, 160:1968-1975.
-
(1999)
Am. J. Respir. Crit. Care Med.
, vol.160
, pp. 1968-1975
-
-
Hill, A.T.1
Campbell, E.J.2
Bayley, D.L.3
Hill, S.L.4
Stockley, R.A.5
-
52
-
-
0026451068
-
Proteinase/proteinase inhibitor imbalance in sputum sol phases from patients with chronic obstructive pulmonary disease. Suggestions for a key role played by antileukoprotease
-
Piccioni P.D., Kramps J.A., Rudolphus A., Bulgheroni A., Luisetti M. Proteinase/proteinase inhibitor imbalance in sputum sol phases from patients with chronic obstructive pulmonary disease. Suggestions for a key role played by antileukoprotease. Chest 1992, 102:1470-1476.
-
(1992)
Chest
, vol.102
, pp. 1470-1476
-
-
Piccioni, P.D.1
Kramps, J.A.2
Rudolphus, A.3
Bulgheroni, A.4
Luisetti, M.5
-
53
-
-
76249114693
-
Decreased levels of secretory leucoprotease inhibitor in the pseudomonas-infected cystic fibrosis lung are due to neutrophil elastase degradation
-
Weldon S., McNally P., McElvaney N.G., Elborn J.S., McAuley D.F., Wartelle J., Belaaouaj A., Levine R.L., Taggart C.C. Decreased levels of secretory leucoprotease inhibitor in the pseudomonas-infected cystic fibrosis lung are due to neutrophil elastase degradation. J. Immunol. 2009, 183:8148-8156.
-
(2009)
J. Immunol.
, vol.183
, pp. 8148-8156
-
-
Weldon, S.1
McNally, P.2
McElvaney, N.G.3
Elborn, J.S.4
McAuley, D.F.5
Wartelle, J.6
Belaaouaj, A.7
Levine, R.L.8
Taggart, C.C.9
-
54
-
-
34247588138
-
Neutrophil elastase up-regulates cathepsin B and matrix metalloprotease-2 expression
-
Geraghty P., Rogan M.P., Greene C.M., Boxio R.M., Poiriert T., O'Mahony M., Belaaouaj A., O'Neill S.J., Taggart C.C., McElvaney N.G. Neutrophil elastase up-regulates cathepsin B and matrix metalloprotease-2 expression. J. Immunol. 2007, 178:5871-5878.
-
(2007)
J. Immunol.
, vol.178
, pp. 5871-5878
-
-
Geraghty, P.1
Rogan, M.P.2
Greene, C.M.3
Boxio, R.M.4
Poiriert, T.5
O'Mahony, M.6
Belaaouaj, A.7
O'Neill, S.J.8
Taggart, C.C.9
McElvaney, N.G.10
-
55
-
-
0035929634
-
Interleukin-8 up-regulation by neutrophil elastase is mediated by MyD88/IRAK/TRAF-6 in human bronchial epithelium
-
Walsh D.E., Greene C.M., Carroll T.P., Taggart C.C., Gallagher P.M., O'Neill S.J., McElvaney N.G. Interleukin-8 up-regulation by neutrophil elastase is mediated by MyD88/IRAK/TRAF-6 in human bronchial epithelium. J. Biol. Chem. 2001, 276:35494-35499.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 35494-35499
-
-
Walsh, D.E.1
Greene, C.M.2
Carroll, T.P.3
Taggart, C.C.4
Gallagher, P.M.5
O'Neill, S.J.6
McElvaney, N.G.7
-
56
-
-
0036008396
-
Protection against acute lung injury by intravenous or intratracheal pretreatment with EPI-HNE-4, a new potent neutrophil elastase inhibitor
-
Delacourt C., Hérigault S., Delclaux C., Poncin A., Levame M., Harf A., Saudubray F., Lafuma C. Protection against acute lung injury by intravenous or intratracheal pretreatment with EPI-HNE-4, a new potent neutrophil elastase inhibitor. Am. J. Respir. Cell Mol. Biol. 2003, 26:290-297.
-
(2003)
Am. J. Respir. Cell Mol. Biol.
, vol.26
, pp. 290-297
-
-
Delacourt, C.1
Hérigault, S.2
Delclaux, C.3
Poncin, A.4
Levame, M.5
Harf, A.6
Saudubray, F.7
Lafuma, C.8
-
57
-
-
33645037291
-
Phase IIa clinical study of a new human neutrophil elastase inhibitor (hNE), EPI-hNE4 (DX-890), with repeated administration by inhalation in adult cystic fibrosis patients
-
Saudubray F., Labbe A., Durieu I., Wallaert B., Sayah H., Assael B., Cazzola G., Dubray C., Poncin A., Lafuma C., Williams T., Bokman A., Clavien H. Phase IIa clinical study of a new human neutrophil elastase inhibitor (hNE), EPI-hNE4 (DX-890), with repeated administration by inhalation in adult cystic fibrosis patients. J. Cystic Fibrosis 2003, 2(Suppl. 1):A85.
-
(2003)
J. Cystic Fibrosis
, vol.2
, Issue.SUPPL. 1
-
-
Saudubray, F.1
Labbe, A.2
Durieu, I.3
Wallaert, B.4
Sayah, H.5
Assael, B.6
Cazzola, G.7
Dubray, C.8
Poncin, A.9
Lafuma, C.10
Williams, T.11
Bokman, A.12
Clavien, H.13
-
58
-
-
36049003663
-
PEGylated DX-1000: pharmacokinetics and antineoplastic activity of a specific plasmin inhibitor
-
Devy L., Rabbani S.A., Stochl M., Ruskowski M., Mackie I., Naa L., Toews M., van Gool R., Chen J., Ley A., Ladner R.C., Dransfield D.T., Henderikx P. PEGylated DX-1000: pharmacokinetics and antineoplastic activity of a specific plasmin inhibitor. Neoplasia 2007, 9:927-937.
-
(2007)
Neoplasia
, vol.9
, pp. 927-937
-
-
Devy, L.1
Rabbani, S.A.2
Stochl, M.3
Ruskowski, M.4
Mackie, I.5
Naa, L.6
Toews, M.7
van Gool, R.8
Chen, J.9
Ley, A.10
Ladner, R.C.11
Dransfield, D.T.12
Henderikx, P.13
-
59
-
-
33845993299
-
Isolation of intracellular proteinase inhibitors derived from designed ankyrin repeat proteins by genetic screening
-
Kawe M., Forrer P., Amstutz P., Plückthun A. Isolation of intracellular proteinase inhibitors derived from designed ankyrin repeat proteins by genetic screening. J. Biol. Chem. 2006, 281:40252-40263.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 40252-40263
-
-
Kawe, M.1
Forrer, P.2
Amstutz, P.3
Plückthun, A.4
-
60
-
-
34247853389
-
Inhibition of caspase-2 by a designed ankyrin repeat protein: specificity, structure, and inhibition mechanism
-
Schweizer A., Roschitzki-Voser H., Amstutz P., Briand C., Gulotti-Georgieva M., Prenosil E., Binz H.K., Capitani G., Baici A., Plückthun A., Grütter M.G. Inhibition of caspase-2 by a designed ankyrin repeat protein: specificity, structure, and inhibition mechanism. Structure 2007, 15:625-636.
-
(2007)
Structure
, vol.15
, pp. 625-636
-
-
Schweizer, A.1
Roschitzki-Voser, H.2
Amstutz, P.3
Briand, C.4
Gulotti-Georgieva, M.5
Prenosil, E.6
Binz, H.K.7
Capitani, G.8
Baici, A.9
Plückthun, A.10
Grütter, M.G.11
-
61
-
-
0032546736
-
Engineering bidentate macromolecular inhibitors for trypsin and urokinase-type plasminogen activator
-
Yang S.Q., Craik C.S. Engineering bidentate macromolecular inhibitors for trypsin and urokinase-type plasminogen activator. J. Mol. Biol. 1998, 279:1001-1011.
-
(1998)
J. Mol. Biol.
, vol.279
, pp. 1001-1011
-
-
Yang, S.Q.1
Craik, C.S.2
-
62
-
-
0042861481
-
Engineering of a macromolecular scaffold to develop specific protease inhibitors
-
Stoop A.A., Craik C.S. Engineering of a macromolecular scaffold to develop specific protease inhibitors. Nat. Biotechnol. 2003, 21:1063-1068.
-
(2003)
Nat. Biotechnol.
, vol.21
, pp. 1063-1068
-
-
Stoop, A.A.1
Craik, C.S.2
-
63
-
-
0030796292
-
Characterization of engineered hepatitis C virus NS3 protease inhibitors affinity selected from human pancreatic secretory trypsin inhibitor and minibody repertoires
-
Dimasi N., Martin F., Volpari C., Brunetti M., Biasiol G., Altamura S., Cortese R., De Francesco R., Steinkühler C., Sollazzo M. Characterization of engineered hepatitis C virus NS3 protease inhibitors affinity selected from human pancreatic secretory trypsin inhibitor and minibody repertoires. J. Virol. 1997, 71:7461-7469.
-
(1997)
J. Virol.
, vol.71
, pp. 7461-7469
-
-
Dimasi, N.1
Martin, F.2
Volpari, C.3
Brunetti, M.4
Biasiol, G.5
Altamura, S.6
Cortese, R.7
De Francesco, R.8
Steinkühler, C.9
Sollazzo, M.10
-
64
-
-
0032544214
-
Design of selective eglin inhibitors of HCV NS3 proteinase
-
Martin F., Dimasi N., Volpari C., Perrera C., Di Marco S., Brunetti M., Steinkühler C., De Francesco R., Sollazzo M. Design of selective eglin inhibitors of HCV NS3 proteinase. Biochemistry 1998, 37:11459-11468.
-
(1998)
Biochemistry
, vol.37
, pp. 11459-11468
-
-
Martin, F.1
Dimasi, N.2
Volpari, C.3
Perrera, C.4
Di Marco, S.5
Brunetti, M.6
Steinkühler, C.7
De Francesco, R.8
Sollazzo, M.9
-
65
-
-
70350130097
-
Proteases and antiproteases in chronic neutrophilic lung disease - relevance to drug discovery
-
Greene C.M., McElvaney N.G. Proteases and antiproteases in chronic neutrophilic lung disease - relevance to drug discovery. Br. J. Pharmacol. 2009, 158:1048-1058.
-
(2009)
Br. J. Pharmacol.
, vol.158
, pp. 1048-1058
-
-
Greene, C.M.1
McElvaney, N.G.2
-
66
-
-
0033571453
-
Activation of caspases in lethal experimental hepatitis and prevention by acute phase proteins
-
Van Molle W., Denecker G., Rodriguez I., Brouckaert P., Vandenabeele P., Libert C. Activation of caspases in lethal experimental hepatitis and prevention by acute phase proteins. J. Immunol. 1999, 163:5235-5241.
-
(1999)
J. Immunol.
, vol.163
, pp. 5235-5241
-
-
Van Molle, W.1
Denecker, G.2
Rodriguez, I.3
Brouckaert, P.4
Vandenabeele, P.5
Libert, C.6
-
67
-
-
55849136929
-
Curative and beta cell regenerative effects of alpha1-antitrypsin treatment in autoimmune diabetic NOD mice
-
Koulmanda M., Bhasin M., Hoffman L., Fan Z., Qipo A., Shi H., Bonner-Weir S., Putheti P., Degauque N., Libermann T.A., Auchincloss H., Flier J.S., Strom T.B. Curative and beta cell regenerative effects of alpha1-antitrypsin treatment in autoimmune diabetic NOD mice. Proc. Natl. Acad. Sci. U.S.A. 2008, 105:16242-16247.
-
(2008)
Proc. Natl. Acad. Sci. U.S.A.
, vol.105
, pp. 16242-16247
-
-
Koulmanda, M.1
Bhasin, M.2
Hoffman, L.3
Fan, Z.4
Qipo, A.5
Shi, H.6
Bonner-Weir, S.7
Putheti, P.8
Degauque, N.9
Libermann, T.A.10
Auchincloss, H.11
Flier, J.S.12
Strom, T.B.13
-
69
-
-
74449091958
-
Safety and efficacy of alpha-1-antitrypsin augmentation therapy in the treatment of patients with alpha-1-antitrypsin deficiency
-
Petrache I., Hajjar J., Campos M. Safety and efficacy of alpha-1-antitrypsin augmentation therapy in the treatment of patients with alpha-1-antitrypsin deficiency. Biologics 2009, 3:193-204.
-
(2009)
Biologics
, vol.3
, pp. 193-204
-
-
Petrache, I.1
Hajjar, J.2
Campos, M.3
-
70
-
-
31544470902
-
Safety and efficacy of recombinant alpha(1)-antitrypsin therapy in cystic fibrosis
-
Martin S.L., Downey D., Bilton D., Keogan M.T., Edgar J., Elborn J.S. Safety and efficacy of recombinant alpha(1)-antitrypsin therapy in cystic fibrosis. Pediatr. Pulmonol. 2006, 41:177-183.
-
(2006)
Pediatr. Pulmonol.
, vol.41
, pp. 177-183
-
-
Martin, S.L.1
Downey, D.2
Bilton, D.3
Keogan, M.T.4
Edgar, J.5
Elborn, J.S.6
-
71
-
-
0021956126
-
Isolation and properties of recombinant DNA produced variants of human alpha 1-proteinase inhibitor
-
Travis J., Owen M., George P., Carrell R., Rosenberg S., Hallewell R.A., Barr P.J. Isolation and properties of recombinant DNA produced variants of human alpha 1-proteinase inhibitor. J. Biol. Chem. 1985, 260:4384-4389.
-
(1985)
J. Biol. Chem.
, vol.260
, pp. 4384-4389
-
-
Travis, J.1
Owen, M.2
George, P.3
Carrell, R.4
Rosenberg, S.5
Hallewell, R.A.6
Barr, P.J.7
-
72
-
-
0034282683
-
Oxidation of either methionine 351 or methionine 358 in alpha 1-antitrypsin causes loss of anti-neutrophil elastase activity
-
Taggart C., Cervantes-Laurean D., Kim G., McElvaney N.G., Wehr N., Moss J., Levine R.L. Oxidation of either methionine 351 or methionine 358 in alpha 1-antitrypsin causes loss of anti-neutrophil elastase activity. J. Biol. Chem. 2000, 275:27258-27265.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 27258-27265
-
-
Taggart, C.1
Cervantes-Laurean, D.2
Kim, G.3
McElvaney, N.G.4
Wehr, N.5
Moss, J.6
Levine, R.L.7
-
73
-
-
0026474443
-
Modulation of airway inflammation in cystic fibrosis. In vivo suppression of interleukin-8 levels on the respiratory epithelial surface by aerosolization of recombinant secretory leukoprotease inhibitor
-
McElvaney N.G., Nakamura H., Birrer P., Hébert C.A., Wong W.L., Alphonso M., Baker J.B., Catalano M.A., Crystal R.G. Modulation of airway inflammation in cystic fibrosis. In vivo suppression of interleukin-8 levels on the respiratory epithelial surface by aerosolization of recombinant secretory leukoprotease inhibitor. J. Clin. Invest. 1992, 90:1296-1301.
-
(1992)
J. Clin. Invest.
, vol.90
, pp. 1296-1301
-
-
McElvaney, N.G.1
Nakamura, H.2
Birrer, P.3
Hébert, C.A.4
Wong, W.L.5
Alphonso, M.6
Baker, J.B.7
Catalano, M.A.8
Crystal, R.G.9
-
74
-
-
0026041548
-
Oxidation-resistant variants of recombinant antileucoprotease are better inhibitors of human-neutrophil-elastase-induced emphysema in hamsters than natural recombinant antileucoprotease
-
Rudolphus A., Heinzel-Wieland R., Vincent V.A., Saunders D., Steffens G.J., Dijkman J.H., Kramps J.A. Oxidation-resistant variants of recombinant antileucoprotease are better inhibitors of human-neutrophil-elastase-induced emphysema in hamsters than natural recombinant antileucoprotease. Clin. Sci. (Lond). 1991, 81:777-784.
-
(1991)
Clin. Sci. (Lond).
, vol.81
, pp. 777-784
-
-
Rudolphus, A.1
Heinzel-Wieland, R.2
Vincent, V.A.3
Saunders, D.4
Steffens, G.J.5
Dijkman, J.H.6
Kramps, J.A.7
-
75
-
-
78149359926
-
-
http://www.proteo.de.
-
-
-
-
76
-
-
61449195271
-
Protease inhibitors derived from elafin and SLPI and engineered to have enhanced specificity towards neutrophil serine proteases
-
Zani M.L., Baranger K., Guyot N., Dallet-Choisy S., Moreau T. Protease inhibitors derived from elafin and SLPI and engineered to have enhanced specificity towards neutrophil serine proteases. Protein Sci. 2009, 18:579-594.
-
(2009)
Protein Sci.
, vol.18
, pp. 579-594
-
-
Zani, M.L.1
Baranger, K.2
Guyot, N.3
Dallet-Choisy, S.4
Moreau, T.5
-
77
-
-
0035823570
-
Cathepsin B, L, and S cleave and inactivate secretory leucoprotease inhibitor
-
Taggart C.C., Lowe G.J., Greene C.M., Mulgrew A.T., O'Neill S.J., Levine R.L., McElvaney N.G. Cathepsin B, L, and S cleave and inactivate secretory leucoprotease inhibitor. J. Biol. Chem. 2001, 276:33345-33352.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 33345-33352
-
-
Taggart, C.C.1
Lowe, G.J.2
Greene, C.M.3
Mulgrew, A.T.4
O'Neill, S.J.5
Levine, R.L.6
McElvaney, N.G.7
-
78
-
-
57749104104
-
Elafin, an elastase-specific inhibitor, is cleaved by its cognate enzyme neutrophil elastase in sputum from individuals with cystic fibrosis
-
Guyot N., Butler M.W., McNally P., Weldon S., Greene C.M., Levine R.L., O'Neill S.J., Taggart C.C., McElvaney N.G. Elafin, an elastase-specific inhibitor, is cleaved by its cognate enzyme neutrophil elastase in sputum from individuals with cystic fibrosis. J. Biol. Chem. 2008, 283:32377-32385.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 32377-32385
-
-
Guyot, N.1
Butler, M.W.2
McNally, P.3
Weldon, S.4
Greene, C.M.5
Levine, R.L.6
O'Neill, S.J.7
Taggart, C.C.8
McElvaney, N.G.9
-
79
-
-
0028237920
-
Maturation of human procathepsin B. Proenzyme activation and proteolytic processing of the precursor to the mature proteinase, in vitro, are primarily unimolecular processes
-
Mach L., Mort J.S., Glössl J. Maturation of human procathepsin B. Proenzyme activation and proteolytic processing of the precursor to the mature proteinase, in vitro, are primarily unimolecular processes. J. Biol. Chem. 1994, 269:13030-13035.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 13030-13035
-
-
Mach, L.1
Mort, J.S.2
Glössl, J.3
-
80
-
-
2442610018
-
Structure-function relationships in class CA1 cysteine peptidase propeptides
-
Wiederanders B. Structure-function relationships in class CA1 cysteine peptidase propeptides. Acta. Biochim. Pol. 2003, 50:691-713.
-
(2003)
Acta. Biochim. Pol.
, vol.50
, pp. 691-713
-
-
Wiederanders, B.1
-
81
-
-
0030038759
-
Potency and selectivity of the cathepsin L propeptide as an inhibitor of cysteine proteases
-
Carmona E., Dufour E., Plouffe C., Takebe S., Mason P., Mort J.S., Ménard R. Potency and selectivity of the cathepsin L propeptide as an inhibitor of cysteine proteases. Biochemistry 1996, 35:8149-8157.
-
(1996)
Biochemistry
, vol.35
, pp. 8149-8157
-
-
Carmona, E.1
Dufour, E.2
Plouffe, C.3
Takebe, S.4
Mason, P.5
Mort, J.S.6
Ménard, R.7
-
82
-
-
0033776087
-
Potency and selectivity of inhibition of cathepsin K, L and S by their respective propeptides
-
Guay J., Falgueyret J.P., Ducret A., Percival M.D., Mancini J.A. Potency and selectivity of inhibition of cathepsin K, L and S by their respective propeptides. Eur. J. Biochem. 2000, 267:6311-6318.
-
(2000)
Eur. J. Biochem.
, vol.267
, pp. 6311-6318
-
-
Guay, J.1
Falgueyret, J.P.2
Ducret, A.3
Percival, M.D.4
Mancini, J.A.5
-
83
-
-
34249106050
-
Inhibition of cathepsin L-like proteases by cathepsin V propeptide
-
Burden R.E., Snoddy P., Jefferies C.A., Walker B., Scott C.J. Inhibition of cathepsin L-like proteases by cathepsin V propeptide. Biol. Chem. 2007, 388:541-545.
-
(2007)
Biol. Chem.
, vol.388
, pp. 541-545
-
-
Burden, R.E.1
Snoddy, P.2
Jefferies, C.A.3
Walker, B.4
Scott, C.J.5
-
84
-
-
0027068057
-
Potent slow-binding inhibition of cathepsin B by its propeptide
-
Fox T., de Miguel E., Mort J.S., Storer A.C. Potent slow-binding inhibition of cathepsin B by its propeptide. Biochemistry 1992, 31:12571-12576.
-
(1992)
Biochemistry
, vol.31
, pp. 12571-12576
-
-
Fox, T.1
de Miguel, E.2
Mort, J.S.3
Storer, A.C.4
-
85
-
-
0030565487
-
Inhibition of cathepsin B by its propeptide: use of overlapping peptides to identify a critical segment
-
Chagas J.R., Ferrer-Di Martino M., Gauthier F., Lalmanach G. Inhibition of cathepsin B by its propeptide: use of overlapping peptides to identify a critical segment. FEBS Lett. 1996, 392:233-236.
-
(1996)
FEBS Lett.
, vol.392
, pp. 233-236
-
-
Chagas, J.R.1
Ferrer-Di Martino, M.2
Gauthier, F.3
Lalmanach, G.4
-
86
-
-
0037153194
-
Design of noncovalent inhibitors of human cathepsin L. From the 96-residue proregion to optimized tripeptides
-
Chowdhury S.F., Sivaraman J., Wang J., Devanathan G., Lachance P., Qi H., Ménard R., Lefebvre J., Konishi Y., Cygler M., Sulea T., Purisima E.O. Design of noncovalent inhibitors of human cathepsin L. From the 96-residue proregion to optimized tripeptides. J. Med. Chem. 2002, 45:5321-5329.
-
(2002)
J. Med. Chem.
, vol.45
, pp. 5321-5329
-
-
Chowdhury, S.F.1
Sivaraman, J.2
Wang, J.3
Devanathan, G.4
Lachance, P.5
Qi, H.6
Ménard, R.7
Lefebvre, J.8
Konishi, Y.9
Cygler, M.10
Sulea, T.11
Purisima, E.O.12
-
87
-
-
41649103656
-
Recombinant cathepsin S propeptide attenuates cell invasion by inhibition of cathepsin L-like proteases in tumor microenvironment
-
Burden R.E., Snoddy P., Buick R.J., Johnston J.A., Walker B., Scott C.J. Recombinant cathepsin S propeptide attenuates cell invasion by inhibition of cathepsin L-like proteases in tumor microenvironment. Mol. Cancer Ther. 2008, 7:538-547.
-
(2008)
Mol. Cancer Ther.
, vol.7
, pp. 538-547
-
-
Burden, R.E.1
Snoddy, P.2
Buick, R.J.3
Johnston, J.A.4
Walker, B.5
Scott, C.J.6
-
89
-
-
0642311142
-
Use of phage display to select novel cystatins specific for Acanthoscelides obtectus cysteine proteinases
-
Melo F.R., Mello M.O., Franco O.L., Rigden D.J., Mello L.V., Genú A.M., Silva-Filho M.C., Gleddie S., Grossi-de-Sá M.F. Use of phage display to select novel cystatins specific for Acanthoscelides obtectus cysteine proteinases. Biochim. Biophys. Acta 2003, 1651:146-152.
-
(2003)
Biochim. Biophys. Acta
, vol.1651
, pp. 146-152
-
-
Melo, F.R.1
Mello, M.O.2
Franco, O.L.3
Rigden, D.J.4
Mello, L.V.5
Genú, A.M.6
Silva-Filho, M.C.7
Gleddie, S.8
Grossi-de-Sá, M.F.9
-
90
-
-
77951573241
-
Antibodies to watch in 2010
-
[Epub ahead of print]
-
Reichert J.M. Antibodies to watch in 2010. MAbs 2010, 2. [Epub ahead of print].
-
(2010)
MAbs
, vol.2
-
-
Reichert, J.M.1
-
91
-
-
0016756272
-
Continuous cultures of fused cells secreting antibody of predefined specificity
-
Köhler G., Milstein C. Continuous cultures of fused cells secreting antibody of predefined specificity. Nature 1975, 256:495-497.
-
(1975)
Nature
, vol.256
, pp. 495-497
-
-
Köhler, G.1
Milstein, C.2
-
92
-
-
0022355587
-
Human immune response to multiple injections of murine monoclonal IgG
-
Shawler D.L., Bartholomew R.M., Smith L.M., Dillman R.O. Human immune response to multiple injections of murine monoclonal IgG. J. Immunol. 1985, 135:1530-1535.
-
(1985)
J. Immunol.
, vol.135
, pp. 1530-1535
-
-
Shawler, D.L.1
Bartholomew, R.M.2
Smith, L.M.3
Dillman, R.O.4
-
94
-
-
52649109068
-
The TRAIL apoptotic pathway in cancer onset, progression and therapy
-
Johnstone R.W., Frew A.J., Smyth M.J. The TRAIL apoptotic pathway in cancer onset, progression and therapy. Nat. Rev. Cancer 2008, 8:782-798.
-
(2008)
Nat. Rev. Cancer
, vol.8
, pp. 782-798
-
-
Johnstone, R.W.1
Frew, A.J.2
Smyth, M.J.3
-
95
-
-
56949108012
-
Her2-positive breast cancer: Herceptin and beyond
-
Dean-Colomb W., Esteva F.J. Her2-positive breast cancer: Herceptin and beyond. Eur. J. Cancer 2008, 44:2806-2812.
-
(2008)
Eur. J. Cancer
, vol.44
, pp. 2806-2812
-
-
Dean-Colomb, W.1
Esteva, F.J.2
-
96
-
-
0035253586
-
Phase Ib trial of intravenous recombinant humanized monoclonal antibody to vascular endothelial growth factor in combination with chemotherapy in patients with advanced cancer: pharmacologic and long-term safety data
-
Margolin K., Gordon M.S., Holmgren E., Gaudreault J., Novotny W., Fyfe G., Adelman D., Stalter S., Breed J. Phase Ib trial of intravenous recombinant humanized monoclonal antibody to vascular endothelial growth factor in combination with chemotherapy in patients with advanced cancer: pharmacologic and long-term safety data. J. Clin. Oncol. 2001, 19:851-856.
-
(2001)
J. Clin. Oncol.
, vol.19
, pp. 851-856
-
-
Margolin, K.1
Gordon, M.S.2
Holmgren, E.3
Gaudreault, J.4
Novotny, W.5
Fyfe, G.6
Adelman, D.7
Stalter, S.8
Breed, J.9
-
97
-
-
70349967965
-
Anti-TNF biologic agents: still the therapy of choice for rheumatoid arthritis
-
Taylor P.C., Feldmann M. Anti-TNF biologic agents: still the therapy of choice for rheumatoid arthritis. Nat. Rev. Rheumatol. 2009, 5:578-582.
-
(2009)
Nat. Rev. Rheumatol.
, vol.5
, pp. 578-582
-
-
Taylor, P.C.1
Feldmann, M.2
-
98
-
-
0028066935
-
Hybridoma cells producing antibodies to cathepsin L have greatly reduced potential for tumour growth
-
Weber E., Günther D., Laube F., Wiederanders B., Kirschke H. Hybridoma cells producing antibodies to cathepsin L have greatly reduced potential for tumour growth. J. Cancer Res. Clin. Oncol. 1994, 120:564-567.
-
(1994)
J. Cancer Res. Clin. Oncol.
, vol.120
, pp. 564-567
-
-
Weber, E.1
Günther, D.2
Laube, F.3
Wiederanders, B.4
Kirschke, H.5
-
99
-
-
71049189254
-
Unraveling the allosteric mechanism of serine protease inhibition by an antibody
-
Ganesan R., Eigenbrot C., Wu Y., Liang W.C., Shia S., Lipari M.T., Kirchhofer D. Unraveling the allosteric mechanism of serine protease inhibition by an antibody. Structure 2009, 17:1614-1624.
-
(2009)
Structure
, vol.17
, pp. 1614-1624
-
-
Ganesan, R.1
Eigenbrot, C.2
Wu, Y.3
Liang, W.C.4
Shia, S.5
Lipari, M.T.6
Kirchhofer, D.7
-
100
-
-
38049174343
-
Structural insight into distinct mechanisms of protease inhibition by antibodies
-
Wu Y., Eigenbrot C., Liang W.C., Stawicki S., Shia S., Fan B., Ganesan R., Lipari M.T., Kirchhofer D. Structural insight into distinct mechanisms of protease inhibition by antibodies. Proc. Natl. Acad. Sci. U.S.A. 2007, 104:19784-19789.
-
(2007)
Proc. Natl. Acad. Sci. U.S.A.
, vol.104
, pp. 19784-19789
-
-
Wu, Y.1
Eigenbrot, C.2
Liang, W.C.3
Stawicki, S.4
Shia, S.5
Fan, B.6
Ganesan, R.7
Lipari, M.T.8
Kirchhofer, D.9
-
101
-
-
0031576997
-
Three-dimensional structure of an Fab-peptide complex: structural basis of HIV-1 protease inhibition by a monoclonal antibody
-
Lescar J., Stouracova R., Riottot M.M., Chitarra V., Brynda J., Fabry M., Horejsi M., Sedlacek J., Bentley G.A. Three-dimensional structure of an Fab-peptide complex: structural basis of HIV-1 protease inhibition by a monoclonal antibody. J. Mol. Biol. 1997, 267:1207-1222.
-
(1997)
J. Mol. Biol.
, vol.267
, pp. 1207-1222
-
-
Lescar, J.1
Stouracova, R.2
Riottot, M.M.3
Chitarra, V.4
Brynda, J.5
Fabry, M.6
Horejsi, M.7
Sedlacek, J.8
Bentley, G.A.9
-
102
-
-
0034793819
-
Structural basis of HIV-1 and HIV-2 protease inhibition by a monoclonal antibody
-
Rezacova P., Lescar J., Brynda J., Fabry M., Horejsi M., Sedlacek J., Bentley G.A. Structural basis of HIV-1 and HIV-2 protease inhibition by a monoclonal antibody. Structure 2001, 9:887-895.
-
(2001)
Structure
, vol.9
, pp. 887-895
-
-
Rezacova, P.1
Lescar, J.2
Brynda, J.3
Fabry, M.4
Horejsi, M.5
Sedlacek, J.6
Bentley, G.A.7
-
103
-
-
13844250583
-
Crystal structure of a cross-reaction complex between an anti-HIV-1 protease antibody and an HIV-2 protease peptide
-
Rezacova P., Brynda J., Lescar J., Fabry M., Horejsi M., Sieglova I., Sedlacek J., Bentley G.A. Crystal structure of a cross-reaction complex between an anti-HIV-1 protease antibody and an HIV-2 protease peptide. J. Struct. Biol. 2005, 149:332-337.
-
(2005)
J. Struct. Biol.
, vol.149
, pp. 332-337
-
-
Rezacova, P.1
Brynda, J.2
Lescar, J.3
Fabry, M.4
Horejsi, M.5
Sieglova, I.6
Sedlacek, J.7
Bentley, G.A.8
-
104
-
-
0030818332
-
Intracellular antibodies (intrabodies) for gene therapy of infectious diseases
-
Rondon I.J., Marasco W.A. Intracellular antibodies (intrabodies) for gene therapy of infectious diseases. Annu. Rev. Microbiol. 1997, 51:257-283.
-
(1997)
Annu. Rev. Microbiol.
, vol.51
, pp. 257-283
-
-
Rondon, I.J.1
Marasco, W.A.2
-
105
-
-
1642535587
-
Inhibition of tumorigenicity and metastasis of human melanoma cells by anti-cathepsin L single chain variable fragment
-
Rousselet N., Mills L., Jean D., Tellez C., Bar-Eli M., Frade R. Inhibition of tumorigenicity and metastasis of human melanoma cells by anti-cathepsin L single chain variable fragment. Cancer Res. 2004, 64:146-151.
-
(2004)
Cancer Res.
, vol.64
, pp. 146-151
-
-
Rousselet, N.1
Mills, L.2
Jean, D.3
Tellez, C.4
Bar-Eli, M.5
Frade, R.6
-
106
-
-
49549114453
-
Intratumoral gene delivery of anti-cathepsin L single-chain variable fragment by lentiviral vector inhibits tumor progression induced by human melanoma cells
-
Frade R., Rousselet N., Jean D. Intratumoral gene delivery of anti-cathepsin L single-chain variable fragment by lentiviral vector inhibits tumor progression induced by human melanoma cells. Cancer Gene Ther 2008, 15:591-604.
-
(2008)
Cancer Gene Ther
, vol.15
, pp. 591-604
-
-
Frade, R.1
Rousselet, N.2
Jean, D.3
-
107
-
-
33645748575
-
Antibodies neutralizing hepsin protease activity do not impact cell growth but inhibit invasion of prostate and ovarian tumor cells in culture
-
Xuan J.A., Schneider D., Toy P., Lin R., Newton A., Zhu Y., Finster S., Vogel D., Mintzer B., Dinter H., Light D., Parry R., Polokoff M., Whitlow M., Wu Q., Parry G. Antibodies neutralizing hepsin protease activity do not impact cell growth but inhibit invasion of prostate and ovarian tumor cells in culture. Cancer Res. 2006, 66:3611-3619.
-
(2006)
Cancer Res.
, vol.66
, pp. 3611-3619
-
-
Xuan, J.A.1
Schneider, D.2
Toy, P.3
Lin, R.4
Newton, A.5
Zhu, Y.6
Finster, S.7
Vogel, D.8
Mintzer, B.9
Dinter, H.10
Light, D.11
Parry, R.12
Polokoff, M.13
Whitlow, M.14
Wu, Q.15
Parry, G.16
-
108
-
-
23944489424
-
Deregulated matriptase causes ras-independent multistage carcinogenesis and promotes ras-mediated malignant transformation
-
List K., Szabo R., Molinolo A., Sriuranpong V., Redeye V., Murdock T., Burke B., Nielsen B.S., Gutkind J.S., Bugge T.H. Deregulated matriptase causes ras-independent multistage carcinogenesis and promotes ras-mediated malignant transformation. Genes Dev. 2005, 19:1934-1950.
-
(2005)
Genes Dev.
, vol.19
, pp. 1934-1950
-
-
List, K.1
Szabo, R.2
Molinolo, A.3
Sriuranpong, V.4
Redeye, V.5
Murdock, T.6
Burke, B.7
Nielsen, B.S.8
Gutkind, J.S.9
Bugge, T.H.10
-
109
-
-
0037417780
-
Potent and selective inhibition of membrane-type serine protease 1 by human single-chain antibodies
-
Sun J., Pons J., Craik C.S. Potent and selective inhibition of membrane-type serine protease 1 by human single-chain antibodies. Biochemistry 2003, 42:892-900.
-
(2003)
Biochemistry
, vol.42
, pp. 892-900
-
-
Sun, J.1
Pons, J.2
Craik, C.S.3
-
110
-
-
34248583079
-
The mechanism of inhibition of antibody-based inhibitors of membrane-type serine protease 1 (MT-SP1)
-
Farady C.J., Sun J., Darragh M.R., Miller S.M., Craik C.S. The mechanism of inhibition of antibody-based inhibitors of membrane-type serine protease 1 (MT-SP1). J. Mol. Biol. 2007, 369:1041-1051.
-
(2007)
J. Mol. Biol.
, vol.369
, pp. 1041-1051
-
-
Farady, C.J.1
Sun, J.2
Darragh, M.R.3
Miller, S.M.4
Craik, C.S.5
-
111
-
-
44949119318
-
Structure of an Fab-protease complex reveals a highly specific non-canonical mechanism of inhibition
-
Farady C.J., Egea P.F., Schneider E.L., Darragh M.R., Craik C.S. Structure of an Fab-protease complex reveals a highly specific non-canonical mechanism of inhibition. J. Mol. Biol. 2008, 380:351-360.
-
(2008)
J. Mol. Biol.
, vol.380
, pp. 351-360
-
-
Farady, C.J.1
Egea, P.F.2
Schneider, E.L.3
Darragh, M.R.4
Craik, C.S.5
-
112
-
-
0034832988
-
Localization of epitopes for monoclonal antibodies to urokinase-type plasminogen activator: relationship between epitope localization and effects of antibodies on molecular interactions of the enzyme
-
Petersen H.H., Hansen M., Schousboe S.L., Andreasen P.A. Localization of epitopes for monoclonal antibodies to urokinase-type plasminogen activator: relationship between epitope localization and effects of antibodies on molecular interactions of the enzyme. Eur. J. Biochem. 2001, 268:4430-4439.
-
(2001)
Eur. J. Biochem.
, vol.268
, pp. 4430-4439
-
-
Petersen, H.H.1
Hansen, M.2
Schousboe, S.L.3
Andreasen, P.A.4
-
113
-
-
33749017931
-
Cysteine cathepsins: multifunctional enzymes in cancer
-
Mohamed M.M., Sloane B.F. Cysteine cathepsins: multifunctional enzymes in cancer. Nat. Rev. Cancer 2006, 6:764-775.
-
(2006)
Nat. Rev. Cancer
, vol.6
, pp. 764-775
-
-
Mohamed, M.M.1
Sloane, B.F.2
-
114
-
-
0034725119
-
Human procathepsin B interacts with the annexin II tetramer on the surface of tumor cells
-
Mai J., Finley R.L., Waisman D.M., Sloane B.F. Human procathepsin B interacts with the annexin II tetramer on the surface of tumor cells. J. Biol. Chem. 2000, 275:12806-12812.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 12806-12812
-
-
Mai, J.1
Finley, R.L.2
Waisman, D.M.3
Sloane, B.F.4
-
115
-
-
33745824230
-
Carboxypeptidase cathepsin X mediates beta2-integrin-dependent adhesion of differentiated U-937 cells
-
Obermajer N., Premzl A., Zavasnik Bergant T., Turk B., Kos J. Carboxypeptidase cathepsin X mediates beta2-integrin-dependent adhesion of differentiated U-937 cells. Exp. Cell Res. 2006, 312:2515-2527.
-
(2006)
Exp. Cell Res.
, vol.312
, pp. 2515-2527
-
-
Obermajer, N.1
Premzl, A.2
Zavasnik Bergant, T.3
Turk, B.4
Kos, J.5
-
116
-
-
0037442576
-
Intracellular and extracellular cathepsin B facilitate invasion of MCF-10A neoT cells through reconstituted extracellular matrix in vitro
-
Premzl A., Zavasnik-Bergant V., Turk V., Kos J. Intracellular and extracellular cathepsin B facilitate invasion of MCF-10A neoT cells through reconstituted extracellular matrix in vitro. Exp. Cell Res. 2003, 283:206-214.
-
(2003)
Exp. Cell Res.
, vol.283
, pp. 206-214
-
-
Premzl, A.1
Zavasnik-Bergant, V.2
Turk, V.3
Kos, J.4
-
117
-
-
33646827205
-
Cathepsin S controls angiogenesis and tumor growth via matrix-derived angiogenic factors
-
Wang B., Sun J., Kitamoto S., Yang M., Grubb A., Chapman H.A., Kalluri R., Shi G.P. Cathepsin S controls angiogenesis and tumor growth via matrix-derived angiogenic factors. J. Biol. Chem. 2006, 281:6020-6029.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 6020-6029
-
-
Wang, B.1
Sun, J.2
Kitamoto, S.3
Yang, M.4
Grubb, A.5
Chapman, H.A.6
Kalluri, R.7
Shi, G.P.8
-
118
-
-
33644784910
-
Distinct roles for cysteine cathepsin genes in multistage tumorigenesis
-
Gocheva V., Zeng W., Ke D., Klimstra D., Reinheckel T., Peters C., Hanahan D., Joyce J.A. Distinct roles for cysteine cathepsin genes in multistage tumorigenesis. Genes Dev. 2006, 20:543-556.
-
(2006)
Genes Dev.
, vol.20
, pp. 543-556
-
-
Gocheva, V.1
Zeng, W.2
Ke, D.3
Klimstra, D.4
Reinheckel, T.5
Peters, C.6
Hanahan, D.7
Joyce, J.A.8
-
119
-
-
31544467539
-
Molecular fingerprinting and autocrine growth regulation of endothelial cells in a murine model of hepatocellular carcinoma
-
Ryschich E., Lizdenis P., Ittrich C., Benner A., Stahl S., Hamann A., Schmidt J., Knolle P., Arnold B., Hämmerling G.J., Ganss R. Molecular fingerprinting and autocrine growth regulation of endothelial cells in a murine model of hepatocellular carcinoma. Cancer Res. 2006, 66:198-211.
-
(2006)
Cancer Res.
, vol.66
, pp. 198-211
-
-
Ryschich, E.1
Lizdenis, P.2
Ittrich, C.3
Benner, A.4
Stahl, S.5
Hamann, A.6
Schmidt, J.7
Knolle, P.8
Arnold, B.9
Hämmerling, G.J.10
Ganss, R.11
-
120
-
-
70349665206
-
Antibody-mediated inhibition of cathepsin S blocks colorectal tumor invasion and angiogenesis
-
Burden R.E., Gormley J.A., Jaquin T.J., Small D.M., Quinn D.J., Hegarty S.M., Ward C., Walker B., Johnston J.A., Olwill S.A., Scott C.J. Antibody-mediated inhibition of cathepsin S blocks colorectal tumor invasion and angiogenesis. Clin. Cancer Res. 2009, 15:6042-6051.
-
(2009)
Clin. Cancer Res.
, vol.15
, pp. 6042-6051
-
-
Burden, R.E.1
Gormley, J.A.2
Jaquin, T.J.3
Small, D.M.4
Quinn, D.J.5
Hegarty, S.M.6
Ward, C.7
Walker, B.8
Johnston, J.A.9
Olwill, S.A.10
Scott, C.J.11
-
121
-
-
0030922759
-
Affinity selection of a camelized V(H) domain antibody inhibitor of hepatitis C virus NS3 protease
-
Martin F., Volpari C., Steinkuhler C., Dimasi N., Brunetti M., Biasiol G., Altamura S., Cortese R., De Francesco R., Sollazzo M. Affinity selection of a camelized V(H) domain antibody inhibitor of hepatitis C virus NS3 protease. Protein Eng. 1997, 10:607-614.
-
(1997)
Protein Eng.
, vol.10
, pp. 607-614
-
-
Martin, F.1
Volpari, C.2
Steinkuhler, C.3
Dimasi, N.4
Brunetti, M.5
Biasiol, G.6
Altamura, S.7
Cortese, R.8
De Francesco, R.9
Sollazzo, M.10
-
122
-
-
33645305964
-
High-throughput affinity ranking of antibodies using surface plasmon resonance microarrays
-
Wassaf D., Kuang G., Kopacz K., Wu Q.L., Nguyen Q., Toews M., Cosic J., Jacques J., Wiltshire S., Lambert J., Pazmany C.C., Hogan S., Ladner R.C., Nixon A.E., Sexton D.J. High-throughput affinity ranking of antibodies using surface plasmon resonance microarrays. Anal. Biochem. 2006, 351:241-253.
-
(2006)
Anal. Biochem.
, vol.351
, pp. 241-253
-
-
Wassaf, D.1
Kuang, G.2
Kopacz, K.3
Wu, Q.L.4
Nguyen, Q.5
Toews, M.6
Cosic, J.7
Jacques, J.8
Wiltshire, S.9
Lambert, J.10
Pazmany, C.C.11
Hogan, S.12
Ladner, R.C.13
Nixon, A.E.14
Sexton, D.J.15
-
123
-
-
70149116329
-
Specific inhibition of tissue kallikrein 1 with a human monoclonal antibody reveals a potential role in airway diseases
-
Sexton D.J., Chen T., Martik D., Kuzmic P., Kuang G., Chen J., Nixon A.E., Zuraw B.L., Forteza R.M., Abraham W.M., Wood C.R. Specific inhibition of tissue kallikrein 1 with a human monoclonal antibody reveals a potential role in airway diseases. Biochem. J. 2009, 422:383-392.
-
(2009)
Biochem. J.
, vol.422
, pp. 383-392
-
-
Sexton, D.J.1
Chen, T.2
Martik, D.3
Kuzmic, P.4
Kuang, G.5
Chen, J.6
Nixon, A.E.7
Zuraw, B.L.8
Forteza, R.M.9
Abraham, W.M.10
Wood, C.R.11
-
124
-
-
60649108677
-
Selective inhibition of matrix metalloproteinase-14 blocks tumor growth, invasion, and angiogenesis
-
Devy L., Huang L., Naa L., Yanamandra N., Pieters H., Frans N., Chang E., Tao Q., Vanhove M., Lejeune A., van Gool R., Sexton D.J., Kuang G., Rank D., Hogan S., Pazmany C., Ma Y.L., Schoonbroodt S., Nixon A.E., Ladner R.C., Hoet R., Henderikx P., Tenhoor C., Rabbani S.A., Valentino M.L., Wood C.R., Dransfield D.T. Selective inhibition of matrix metalloproteinase-14 blocks tumor growth, invasion, and angiogenesis. Cancer Res. 2009, 69:1517-1526.
-
(2009)
Cancer Res.
, vol.69
, pp. 1517-1526
-
-
Devy, L.1
Huang, L.2
Naa, L.3
Yanamandra, N.4
Pieters, H.5
Frans, N.6
Chang, E.7
Tao, Q.8
Vanhove, M.9
Lejeune, A.10
van Gool, R.11
Sexton, D.J.12
Kuang, G.13
Rank, D.14
Hogan, S.15
Pazmany, C.16
Ma, Y.L.17
Schoonbroodt, S.18
Nixon, A.E.19
Ladner, R.C.20
Hoet, R.21
Henderikx, P.22
Tenhoor, C.23
Rabbani, S.A.24
Valentino, M.L.25
Wood, C.R.26
Dransfield, D.T.27
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