-
1
-
-
0024509701
-
Isolation of a cDNA clone derived from blood-borne non-A, non-B viral hepatitis
-
Choo QL, Kuo G, Weiner AJ, Overby LR, Bradley DW, Houghton M. Isolation of a cDNA clone derived from blood-borne non-A, non-B viral hepatitis. Science 1989; 244: 359-362.
-
(1989)
Science
, vol.244
, pp. 359-362
-
-
Choo, Q.L.1
Kuo, G.2
Weiner, A.J.3
Overby, L.R.4
Bradley, D.W.5
Houghton, M.6
-
2
-
-
0024511734
-
An assay for circulating antibodies to a major etiologicvirus of human non-A, non-B hepatitis
-
Kuo G, Choo QL, Alter HJ, Gitnick GL, Redecker AG, Purcell RH, Myamura T, Dienstag JL, Alter MJ, Syevens CE, Tagtmeyer GE, Bonino F, Colombo M, Lee WS, Kuo C, Berger K, Shister JR, Overby LR, Bradley DW, Houghton M. An assay for circulating antibodies to a major etiologicvirus of human non-A, non-B hepatitis. Science 1989; 244: 362-364.
-
(1989)
Science
, vol.244
, pp. 362-364
-
-
Kuo, G.1
Choo, Q.L.2
Alter, H.J.3
Gitnick, G.L.4
Redecker, A.G.5
Purcell, R.H.6
Myamura, T.7
Dienstag, J.L.8
Alter, M.J.9
Syevens, C.E.10
Tagtmeyer, G.E.11
Bonino, F.12
Colombo, M.13
Lee, W.S.14
Kuo, C.15
Berger, K.16
Shister, J.R.17
Overby, L.R.18
Bradley, D.W.19
Houghton, M.20
more..
-
3
-
-
0000361013
-
Hepatitis C viruses
-
Fields BN, Knipe DM, Howley PM (eds), 3rd edn. Raven Press: New York
-
Houghton M. Hepatitis C viruses. In Fields Virology, Fields BN, Knipe DM, Howley PM (eds), 3rd edn. Raven Press: New York, 1996; 1035-1058.
-
(1996)
Fields Virology
, pp. 1035-1058
-
-
Houghton, M.1
-
4
-
-
0030733423
-
Hepatitis C virus NS3/4A protease
-
Kwong AD. Hepatitis C virus NS3/4A protease. Curr. Op. Infect. Dis. 1997; 10: 485-490.
-
(1997)
Curr. Op. Infect. Dis.
, vol.10
, pp. 485-490
-
-
Kwong, A.D.1
-
5
-
-
0343433408
-
Cysteine proteases and their inhibitors
-
Otto H-H, Schirmeister T. Cysteine proteases and their inhibitors. Chem. Rev. 1997; 97: 133-171.
-
(1997)
Chem. Rev.
, vol.97
, pp. 133-171
-
-
Otto, H.-H.1
Schirmeister, T.2
-
6
-
-
0030777280
-
A simple linker for the attachment of aldehydes to the solid phase. Application to solid phase synthesis by the Multipin™ method
-
Ede NJ, Bray AM. A simple linker for the attachment of aldehydes to the solid phase. Application to solid phase synthesis by the Multipin™ method. Tetrahedron Lett. 1997; 38: 7119-7122.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 7119-7122
-
-
Ede, N.J.1
Bray, A.M.2
-
7
-
-
0001122247
-
Automated synthesis of peptyde C-terminal aldehydes
-
Murphy AM, Dagnino R Jr., Vallar PL, Trippe AJ, Sherman SL, Lumpkln RH, Tamura SY, Webb TR. Automated synthesis of peptyde C-terminal aldehydes. J. Am. Chem. Soc. 1992; 114: 3156-3157.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 3156-3157
-
-
Murphy, A.M.1
Dagnino Jr., R.2
Vallar, P.L.3
Trippe, A.J.4
Sherman, S.L.5
Lumpkln, R.H.6
Tamura, S.Y.7
Webb, T.R.8
-
8
-
-
0000883039
-
Solid phase synthesis of C-terminal peptide aldehydes
-
Fehrentz J-A, Paris M, Heitz A, Velek J, Winternitz F, Martinez J. Solid phase synthesis of C-terminal peptide aldehydes. J. Org. Chem. 1997; 62: 6792-6796.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 6792-6796
-
-
Fehrentz, J.-A.1
Paris, M.2
Heitz, A.3
Velek, J.4
Winternitz, F.5
Martinez, J.6
-
9
-
-
0030696606
-
Use of ozonolysis in the synthesis of C-termlnal peptide aldehydes on solid support
-
Pothion C, Paris M, Heitz A, Rocheblave L, Rouch F, Fehrentz J-A, Martinez J. Use of ozonolysis in the synthesis of C-termlnal peptide aldehydes on solid support. Tetrahedron Lett. 1997; 44: 7749-7752.
-
(1997)
Tetrahedron Lett.
, vol.44
, pp. 7749-7752
-
-
Pothion, C.1
Paris, M.2
Heitz, A.3
Rocheblave, L.4
Rouch, F.5
Fehrentz, J.-A.6
Martinez, J.7
-
10
-
-
0032171322
-
A practical method for the combinatorial synthesis of peptide aldehydes
-
Hall BJ, Sutherland JD. A practical method for the combinatorial synthesis of peptide aldehydes. Tetrahedron Letts. 1998; 39: 6593-6596.
-
(1998)
Tetrahedron Letts.
, vol.39
, pp. 6593-6596
-
-
Hall, B.J.1
Sutherland, J.D.2
-
11
-
-
0001550377
-
Solid phase synthesis of peptidyl aldehydes from C-terminal thiazolidinyl peptides
-
Galcotti N, Giraud M, Jouin P. Solid phase synthesis of peptidyl aldehydes from C-terminal thiazolidinyl peptides. Letts. Pept. Sci. 1997; 4: 437-440.
-
(1997)
Letts. Pept. Sci.
, vol.4
, pp. 437-440
-
-
Galcotti, N.1
Giraud, M.2
Jouin, P.3
-
12
-
-
0032503569
-
Backbone amide linker (BAL) strategy for solid-phase synthesis of C-terminal-modified and cyclic peptides
-
Jensen KJ, Alsina J, Songster MF, Vagner J, Albericio F, Barany G. Backbone amide linker (BAL) strategy for solid-phase synthesis of C-terminal-modified and cyclic peptides. J. Am. Chem. Soc. 1998; 120: 5441-5452.
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 5441-5452
-
-
Jensen, K.J.1
Alsina, J.2
Songster, M.F.3
Vagner, J.4
Albericio, F.5
Barany, G.6
-
13
-
-
0033524892
-
Solid phase synthesis of tyrosine peptide aldehydes. Analogues of (S)-MAPI
-
Page P, Bradley M, Walters I, Teague S. Solid phase synthesis of tyrosine peptide aldehydes. Analogues of (S)-MAPI. J. Org. Chem. 1999; 64: 794-799.
-
(1999)
J. Org. Chem.
, vol.64
, pp. 794-799
-
-
Page, P.1
Bradley, M.2
Walters, I.3
Teague, S.4
-
14
-
-
85004872164
-
An efficient synthesis of optically active α-(t-butoxycarbonylamino)-aldehydes from α-amino acids
-
Fehrentz J-A, Castro B. An efficient synthesis of optically active α-(t-butoxycarbonylamino)-aldehydes from α-amino acids. Synthesis 1983; 676-678.
-
(1983)
Synthesis
, pp. 676-678
-
-
Fehrentz, J.-A.1
Castro, B.2
-
15
-
-
0029952823
-
Pseudo-prolines as a solubilizing, structure-disrupting protection technique in peptide synthesis
-
Wöhr T, Wahl F, Nefzi A, Rohwedder B, Sato T, Sun X, Mutter M. Pseudo-prolines as a solubilizing, structure-disrupting protection technique in peptide synthesis. J. Am. Chem. Soc. 1996; 116: 9218-9227.
-
(1996)
J. Am. Chem. Soc.
, vol.116
, pp. 9218-9227
-
-
Wöhr, T.1
Wahl, F.2
Nefzi, A.3
Rohwedder, B.4
Sato, T.5
Sun, X.6
Mutter, M.7
-
16
-
-
0032560602
-
Potent peptide inhibitors of human hepatitis C virus NS3 protease are obtained by optimising the cleavage products
-
Ingallinella P, Altamura S, Blanchi E, Taliani M. Ingenito R, Cortese R, De Francesco R, Steinkühler C, Pessi A. Potent peptide inhibitors of human hepatitis C virus NS3 protease are obtained by optimising the cleavage products. Biochemistry 1998; 37: 8906-8914.
-
(1998)
Biochemistry
, vol.37
, pp. 8906-8914
-
-
Ingallinella, P.1
Altamura, S.2
Blanchi, E.3
Taliani, M.4
Ingenito, R.5
Cortese, R.6
De Francesco, R.7
Steinkühler, C.8
Pessi, A.9
-
17
-
-
0030871616
-
Mechanistic role of an NS4A peptide cofactor with the truncated NS3 protease of hepatitis C virus: Elucidation of the NS4A stimulatory effect via kinectic analysis and inhibitor mapping
-
Landro JA, Raybuck SA, Luong YPC, O'Malley ET, Harbeson SL, Morgenstern KA, Rao G, Livingston DJ. Mechanistic role of an NS4A peptide cofactor with the truncated NS3 protease of hepatitis C virus: Elucidation of the NS4A stimulatory effect via kinectic analysis and inhibitor mapping. Biochemistry 1997; 36: 9340-9348.
-
(1997)
Biochemistry
, vol.36
, pp. 9340-9348
-
-
Landro, J.A.1
Raybuck, S.A.2
Luong, Y.P.C.3
O'Malley, E.T.4
Harbeson, S.L.5
Morgenstern, K.A.6
Rao, G.7
Livingston, D.J.8
-
18
-
-
0032493405
-
Peptide-based inhibitors of the hepatitis C virus serine protease
-
Llinàs-Brunet M, Bailey M, Fazal G, Goulet S, Halmos T, Laplante S, Maurice R, Poirier M, Poupart M-A, Thibeault D, Wernic D, Lamarre D. Peptide-based inhibitors of the hepatitis C virus serine protease. Bioorg. Med. Chem. Letts. 1998; 8: 1713-1718.
-
(1998)
Bioorg. Med. Chem. Letts.
, vol.8
, pp. 1713-1718
-
-
Llinàs-Brunet, M.1
Bailey, M.2
Fazal, G.3
Goulet, S.4
Halmos, T.5
Laplante, S.6
Maurice, R.7
Poirier, M.8
Poupart, M.-A.9
Thibeault, D.10
Wernic, D.11
Lamarre, D.12
|