-
1
-
-
0023058313
-
Arg-Gly-Asp: A versatile cell recognition signal
-
Ruoslahti, E. and Piersbacher M. D., Arg-Gly-Asp: A versatile cell recognition signal, Cell, 44 (1986) 517-518.
-
(1986)
Cell
, vol.44
, pp. 517-518
-
-
Ruoslahti, E.1
Piersbacher, M.D.2
-
2
-
-
0022971171
-
Short synthetic peptide fragment of human interleukin 1 with immunostimulatory but not inflammatory activity
-
Antoni, G., Presentini, R., Perin, F., Tagliabue, A., Ghiara, P., Censin, S., Volpini, G., Villa, L. and Boraschi, D., Short synthetic peptide fragment of human interleukin 1 with immunostimulatory but not inflammatory activity, J. Immunlogy, 137 (1986) 3202-3204.
-
(1986)
J. Immunlogy
, vol.137
, pp. 3202-3204
-
-
Antoni, G.1
Presentini, R.2
Perin, F.3
Tagliabue, A.4
Ghiara, P.5
Censin, S.6
Volpini, G.7
Villa, L.8
Boraschi, D.9
-
3
-
-
0025260746
-
Peptide mimitics of an actin site on myosin span two functional domains on actin
-
Keane, A. M., Trayer, I. P., Levine, B. A., Zeugner, C. and Ruegg, J. C., Peptide mimitics of an actin site on myosin span two functional domains on actin, Nature, 344 (1990) 265-268.
-
(1990)
Nature
, vol.344
, pp. 265-268
-
-
Keane, A.M.1
Trayer, I.P.2
Levine, B.A.3
Zeugner, C.4
Ruegg, J.C.5
-
4
-
-
0032753729
-
The synthetic CD4 exocyclic CDR3.AME(82-89) inhibits NF-kappaB nuclear translocation, HIV-1 promoter activation, and viral gene expression
-
Roland, J., Berezov, A., Greene, M. I., Murali, R., Piatier-Tonneau, D., Devaux, C. and Briant, L., The synthetic CD4 exocyclic CDR3.AME(82-89) inhibits NF-kappaB nuclear translocation, HIV-1 promoter activation, and viral gene expression, DNA Cell Biol., 18 (1999) 819-828.
-
(1999)
DNA Cell Biol.
, vol.18
, pp. 819-828
-
-
Roland, J.1
Berezov, A.2
Greene, M.I.3
Murali, R.4
Piatier-Tonneau, D.5
Devaux, C.6
Briant, L.7
-
5
-
-
0035859911
-
Selection and characterization of a new class of peptide exosite inhibitors of coagulation factor VIIa
-
Dennis, M. S., Quan, C. R. M. and Lazarus, R. A., Selection and characterization of a new class of peptide exosite inhibitors of coagulation factor VIIa, Biochemistry, 40 (2001) 9513-9521.
-
(2001)
Biochemistry
, vol.40
, pp. 9513-9521
-
-
Dennis, M.S.1
Quan, C.R.M.2
Lazarus, R.A.3
-
6
-
-
0036144766
-
Inhibition of septic shock in mice by an oligopeptide from the beta-chain of human chorionic gonadotrophin hormone
-
Khan, N. A., Khan, A., Savelkoul, H. F and Benner, R., Inhibition of septic shock in mice by an oligopeptide from the beta-chain of human chorionic gonadotrophin hormone, Hum. Immunol., 63 (2001) 1-7.
-
(2001)
Hum. Immunol.
, vol.63
, pp. 1-7
-
-
Khan, N.A.1
Khan, A.2
Savelkoul, H.F.3
Benner, R.4
-
7
-
-
0036146048
-
A cyclic peptapeptide derived from the second EGF-like domain of Factor VII is an inhibitor of tissue factor dependent coagulation thrombus formation
-
Orning, L., Fischer, P. M., Hu, C. K., Agner, E., Engebretsen, M., Husbyn, M., Petersen, L. B., Orvim, U., Llinas, M. and Sakriassen, K. S., A cyclic peptapeptide derived from the second EGF-like domain of Factor VII is an inhibitor of tissue factor dependent coagulation thrombus formation, Thromb. Haemost., 87 (2002) 13-21.
-
(2002)
Thromb. Haemost.
, vol.87
, pp. 13-21
-
-
Orning, L.1
Fischer, P.M.2
Hu, C.K.3
Agner, E.4
Engebretsen, M.5
Husbyn, M.6
Petersen, L.B.7
Orvim, U.8
Llinas, M.9
Sakriassen, K.S.10
-
8
-
-
0038529679
-
Pharmacological profiles of peptide drug candidates for the treatment of Alzheimer's disease
-
Adessi, C., Frossard, M. J., Boissard, C., Fraga, S., Bieler, S., Ruckle, T., Vilbois, F., Robinson, S. M., Mutter, M., Banks, W. A. and Soto, C., Pharmacological profiles of peptide drug candidates for the treatment of Alzheimer's disease, J. Biol. Chem., 278 (2003) 13905-13911.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 13905-13911
-
-
Adessi, C.1
Frossard, M.J.2
Boissard, C.3
Fraga, S.4
Bieler, S.5
Ruckle, T.6
Vilbois, F.7
Robinson, S.M.8
Mutter, M.9
Banks, W.A.10
Soto, C.11
-
9
-
-
0037424522
-
Structural determinants of the calpain inhibitory activity of calpastatin peptide B27-WT
-
Betts, R., Weinsheimer, S., Blouse, G. E. and Anagli J., Structural determinants of the calpain inhibitory activity of calpastatin peptide B27-WT, J. Biol. Chem., 278 (2003) 7800-7809.
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 7800-7809
-
-
Betts, R.1
Weinsheimer, S.2
Blouse, G.E.3
Anagli, J.4
-
10
-
-
0037119455
-
Hydropathic complementarity determines interaction of epitope (869)HITDTNNK(876) in Manduca sexta Bt-R(1) receptor with loop 2 of domain II of Bacillus thuringiensis Cry1A toxins
-
Gomez, I., Miranda-Rios, J., Rudino-Pinera, E., Oltean, D. I., Gill, S. S., Bravo, A. and Soberon, M., Hydropathic complementarity determines interaction of epitope (869)HITDTNNK(876) in Manduca sexta Bt-R(1) receptor with loop 2 of domain II of Bacillus thuringiensis Cry1A toxins, J. Biol. Chem., 277 (2002) 30137-30143.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 30137-30143
-
-
Gomez, I.1
Miranda-Rios, J.2
Rudino-Pinera, E.3
Oltean, D.I.4
Gill, S.S.5
Bravo, A.6
Soberon, M.7
-
11
-
-
0037077727
-
Inhibition of hepatitis C virus NS3 protease by peptides derived from complementarity-determining regions (CDRs) of the monoclonal antibody 8D4: Tolerance of a CDR peptide to conformational changes of a target
-
Tsumoto, K., Misawa, S., Ohba, Y., Ueno, T., Hayashi, H., Kasai, N., Watanabe, H., Asano, R. and Kumagai, I., Inhibition of hepatitis C virus NS3 protease by peptides derived from complementarity-determining regions (CDRs) of the monoclonal antibody 8D4: Tolerance of a CDR peptide to conformational changes of a target, FEBS Lett., 525 (2002) 77-82.
-
(2002)
FEBS Lett.
, vol.525
, pp. 77-82
-
-
Tsumoto, K.1
Misawa, S.2
Ohba, Y.3
Ueno, T.4
Hayashi, H.5
Kasai, N.6
Watanabe, H.7
Asano, R.8
Kumagai, I.9
-
12
-
-
0036402032
-
Structure-based design of mimetics for granulocyte-macrophage colony stimulating factor (GM-CSF)
-
Monfardini, C., Canziani, G., Plugariu, C., Kieber Emmons, T., Godillot, A. P., Kwah, J., Bajgier, J., Chaiken, I. and Williams, W. V., Structure-based design of mimetics for granulocyte-macrophage colony stimulating factor (GM-CSF), Curr. Pharm. Des., 8 (2002) 2185-2199.
-
(2002)
Curr. Pharm. Des.
, vol.8
, pp. 2185-2199
-
-
Monfardini, C.1
Canziani, G.2
Plugariu, C.3
Kieber Emmons, T.4
Godillot, A.P.5
Kwah, J.6
Bajgier, J.7
Chaiken, I.8
Williams, W.V.9
-
13
-
-
0029826905
-
Hormone mimicry
-
Wells, J. A., Hormone mimicry, Science, 273 (1996) 449-450.
-
(1996)
Science
, vol.273
, pp. 449-450
-
-
Wells, J.A.1
-
14
-
-
0030773876
-
Peptide agonist of the thrombopoietin receptor as potent as the natural cytokine
-
Cwirla, S. E., Balasubramanian, P., Duffin, D. J., Wagstrom, C. R., Gates, C. M., Singer, S. C., Davis, A. M., Tansik, R. L., Mattheakis, L. C., Boytos, C. M., Schatz, P. J., Baccanari, D. P., Wrighton, N. C., Barrett, R. W. and Dower, W. J., Peptide agonist of the thrombopoietin receptor as potent as the natural cytokine, Science, 276 (1997) 1696-91997.
-
(1997)
Science
, vol.276
, pp. 1696-91997
-
-
Cwirla, S.E.1
Balasubramanian, P.2
Duffin, D.J.3
Wagstrom, C.R.4
Gates, C.M.5
Singer, S.C.6
Davis, A.M.7
Tansik, R.L.8
Mattheakis, L.C.9
Boytos, C.M.10
Schatz, P.J.11
Baccanari, D.P.12
Wrighton, N.C.13
Barrett, R.W.14
Dower, W.J.15
-
15
-
-
0030687562
-
Structure-based design and characterization of exocyclic peptidomimetics that inhibit TNF alpha binding to its receptor
-
Takasaki, W., Kajino, Y., Kajino, K., Murali, R. and Greene, M. I., Structure-based design and characterization of exocyclic peptidomimetics that inhibit TNF alpha binding to its receptor, Nat. Biotechnol., 15 (1997) 1266-1270.
-
(1997)
Nat. Biotechnol.
, vol.15
, pp. 1266-1270
-
-
Takasaki, W.1
Kajino, Y.2
Kajino, K.3
Murali, R.4
Greene, M.I.5
-
16
-
-
0035822269
-
Modified peptide antagonists of interleukin 5 exhibit extended in vivo persistence but restricted species specificity
-
Uings, I. J., Balasubramanian, P., McLoughlin, P. G., Yin, Q., Dash, L., Beresford, A., Kearney, S., Barrett, R. W., McKinnon, M. and England, B. P., Modified peptide antagonists of interleukin 5 exhibit extended in vivo persistence but restricted species specificity, Cytokine, 7 (2001) 10-9.
-
(2001)
Cytokine
, vol.7
, pp. 10-19
-
-
Uings, I.J.1
Balasubramanian, P.2
McLoughlin, P.G.3
Yin, Q.4
Dash, L.5
Beresford, A.6
Kearney, S.7
Barrett, R.W.8
McKinnon, M.9
England, B.P.10
-
17
-
-
0037022298
-
Stable 'zeta' peptides that act as potent antagonists of the high-affinity IgE receptor
-
Nakamura, G. R., Reynolds, M. E., Chen, Y. M., Starovasnik, M. A. and Lowman, H. B., Stable 'zeta' peptides that act as potent antagonists of the high-affinity IgE receptor, PNAS, 99 (2002) 1303-1308.
-
(2002)
PNAS
, vol.99
, pp. 1303-1308
-
-
Nakamura, G.R.1
Reynolds, M.E.2
Chen, Y.M.3
Starovasnik, M.A.4
Lowman, H.B.5
-
18
-
-
0032540032
-
T-20 and Trimiris
-
James, T-20 and Trimiris, AIDS Treat News, 293 (1998) 1-6.
-
(1998)
AIDS Treat News
, vol.293
, pp. 1-6
-
-
James1
|