-
1
-
-
20744456789
-
Solid phase peptide synthesis. I. The synthesis of a tetrapeptide
-
R.B. Merrifield (1963). Solid phase peptide synthesis. I. The synthesis of a tetrapeptide. J. Am. Chem. Soc. 85, 2149-2154.
-
(1963)
J. Am. Chem. Soc.
, vol.85
, pp. 2149-2154
-
-
Merrifield, R.B.1
-
2
-
-
0002210332
-
Solid-phase peptide synthesis
-
B. Gutte, Ed., Academic Press, San Diego
-
R.B. Merrifield. Solid-phase peptide synthesis, in: Peptides: Synthesis, Structures, and Applications, B. Gutte, Ed., p. 93-169, Academic Press, San Diego, 1995.
-
(1995)
Peptides: Synthesis, Structures, and Applications
, pp. 93-169
-
-
Merrifield, R.B.1
-
3
-
-
0025232814
-
Solid phase peptide synthesis utilizing 9-fluorenylmethoxycarbonyl amino acids
-
G.B. Fields and R.L. Noble (1990). Solid phase peptide synthesis utilizing 9-fluorenylmethoxycarbonyl amino acids. Int. J. Peptide Protein Res. 35, 161-214.
-
(1990)
Int. J. Peptide Protein Res.
, vol.35
, pp. 161-214
-
-
Fields, G.B.1
Noble, R.L.2
-
4
-
-
0029395709
-
Application of the multiple antigenic peptides (MAP) strategy to the production of prohormone convertases antibodies: Synthesis, characterization and use of 8-branched immunogenic peptides
-
A. Basak, A. Boudreault, A. Chen, M. Chretien, N.G. Seidah and C. Lazure (1995). Application of the multiple antigenic peptides (MAP) strategy to the production of prohormone convertases antibodies: synthesis, characterization and use of 8-branched immunogenic peptides. J. Peptide Sci. 1, 385-395.
-
(1995)
J. Peptide Sci.
, vol.1
, pp. 385-395
-
-
Basak, A.1
Boudreault, A.2
Chen, A.3
Chretien, M.4
Seidah, N.G.5
Lazure, C.6
-
5
-
-
0026567741
-
A chemically defined synthetic vaccine model for HIV-1
-
B. Nardelli, Y.-A. Lu, R.D. Shiu, C. Delpiere-Defoort, A.T. Profy and J.P. Tam (1992). A chemically defined synthetic vaccine model for HIV-1. J. Immunol. 148, 914-920.
-
(1992)
J. Immunol.
, vol.148
, pp. 914-920
-
-
Nardelli, B.1
Lu, Y.-A.2
Shiu, R.D.3
Delpiere-Defoort, C.4
Profy, A.T.5
Tam, J.P.6
-
6
-
-
0025099759
-
Incorporation of T and B epitopes of the circumsporozoite protein in a chemically defined synthetic vaccine against malaria
-
J.P. Tam, P. Clavijo, Y.-A. Lu, V. Nussenzweig, R. Nussenzweig and F. Zavala (1990). Incorporation of T and B epitopes of the circumsporozoite protein in a chemically defined synthetic vaccine against malaria. J. Exp. Med. 171, 299-306.
-
(1990)
J. Exp. Med.
, vol.171
, pp. 299-306
-
-
Tam, J.P.1
Clavijo, P.2
Lu, Y.-A.3
Nussenzweig, V.4
Nussenzweig, R.5
Zavala, F.6
-
7
-
-
0026673099
-
Immunogenic properties of multiple antigen peptide systems containing defined T and B epitopes
-
S.K. Chai, P. Clavijo, J.P. Tam and F. Zavala (1992). Immunogenic properties of multiple antigen peptide systems containing defined T and B epitopes. J. Immunol. 149, 2385-2390.
-
(1992)
J. Immunol.
, vol.149
, pp. 2385-2390
-
-
Chai, S.K.1
Clavijo, P.2
Tam, J.P.3
Zavala, F.4
-
8
-
-
0028928920
-
Synthesis of a diepitope multiple antigen peptide containing sequences from two malaria antigens using Fmoc chemistry
-
N. Ahlborg (1995). Synthesis of a diepitope multiple antigen peptide containing sequences from two malaria antigens using Fmoc chemistry. J. Immunol. Methods 179, 269-275.
-
(1995)
J. Immunol. Methods
, vol.179
, pp. 269-275
-
-
Ahlborg, N.1
-
9
-
-
0024310231
-
Vaccine engineering: Enhancement of immunogenicity of synthetic peptide vaccines related to hepatitis in chemically defined models consisting of T- and B-cell epitopes
-
J.P. Tam and Y.-A. Lu (1989). Vaccine engineering: enhancement of immunogenicity of synthetic peptide vaccines related to hepatitis in chemically defined models consisting of T- and B-cell epitopes. Proc. Natl. Acad. Sci. USA 86, 9084-9088.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 9084-9088
-
-
Tam, J.P.1
Lu, Y.-A.2
-
10
-
-
0024311629
-
High-density multiple antigen-peptide system for preparation of antipeptide antibodies
-
J.P. Tam (1989). High-density multiple antigen-peptide system for preparation of antipeptide antibodies. Methods Enzymol. 168, 7-15.
-
(1989)
Methods Enzymol.
, vol.168
, pp. 7-15
-
-
Tam, J.P.1
-
11
-
-
37049089078
-
A novel lysine-protecting procedure for continuous flow solid phase synthesis of branched peptides
-
B.W. Bycroft, W.C. Chan., S.R. Chhabra and N.D. Hove (1993). A novel lysine-protecting procedure for continuous flow solid phase synthesis of branched peptides. J. Chem. Soc., Chem. Commun., 778-779.
-
(1993)
J. Chem. Soc., Chem. Commun.
, pp. 778-779
-
-
Bycroft, B.W.1
Chan, W.C.2
Chhabra, S.R.3
Hove, N.D.4
-
12
-
-
0030979764
-
Solid-phase applications of Dde and the analogue Nde: Synthesis of trypanothlone disulphide
-
B. Kellam, B.W. Bycroft and S.R. Chhabra (1997). Solid-phase applications of Dde and the analogue Nde: synthesis of trypanothlone disulphide. Tetrahedron Lett. 38, 4849-4852.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 4849-4852
-
-
Kellam, B.1
Bycroft, B.W.2
Chhabra, S.R.3
-
13
-
-
0028957767
-
Preparation of the very acid-sensitive Fmoc-Lys(Mtt)-OH. Application in the synthesis of side-chain to side-chain cyclic peptides and oligolysine cores suitable for the solid-phase assembly of MAPs and TASPs
-
A. Aletras, K. Barlos, D. Gatos, S. Koutsogianni and P. Mamos (1995). Preparation of the very acid-sensitive Fmoc-Lys(Mtt)-OH. Application in the synthesis of side-chain to side-chain cyclic peptides and oligolysine cores suitable for the solid-phase assembly of MAPs and TASPs. Int. J. Peptide Protein Res. 45, 488-496.
-
(1995)
Int. J. Peptide Protein Res.
, vol.45
, pp. 488-496
-
-
Aletras, A.1
Barlos, K.2
Gatos, D.3
Koutsogianni, S.4
Mamos, P.5
-
14
-
-
2442755045
-
A side reaction of the Dde protecting group: Migration to an unprotected lysine
-
Abstract No. 399, Edinburgh, Scotland
-
K. Augustyns, W. Kraas and G. Jung. A side reaction of the Dde protecting group: migration to an unprotected lysine, in: Book of Abstracts, 24th Symposium of the EPS, Abstract No. 399, Edinburgh, Scotland, 1996.
-
(1996)
Book of Abstracts, 24th Symposium of the EPS
-
-
Augustyns, K.1
Kraas, W.2
Jung, G.3
-
15
-
-
0031916180
-
Investigation of the stability of the Dde protecting group used in peptide synthesis: Migration to an unprotected lysine
-
K. Augustyns, W. Kraas and G. Jung (1998). Investigation of the stability of the Dde protecting group used in peptide synthesis: migration to an unprotected lysine. J. Peptide Res. 51, 127-133.
-
(1998)
J. Peptide Res.
, vol.51
, pp. 127-133
-
-
Augustyns, K.1
Kraas, W.2
Jung, G.3
-
16
-
-
2442753467
-
Intramolecular migration of the β-Dde protecting group of diaminopropionyl to the α-position during Fmoc solid phase synthesis
-
Abstract No. 111, Nashville, Tennessee
-
A. Srinivasan, R.R. Wilhelm and M.A. Schmidt. Intramolecular migration of the β-Dde protecting group of diaminopropionyl to the α-position during Fmoc solid phase synthesis, in: Book of Abstracts, 15th APS, Abstract No. 111, Nashville, Tennessee, 1997.
-
(1997)
Book of Abstracts, 15th APS
-
-
Srinivasan, A.1
Wilhelm, R.R.2
Schmidt, M.A.3
-
17
-
-
0019086098
-
3-Nitro-2-pyridinesulfenyl (Npys) group. A novel selective protecting group which can be activated for peptide bond formation
-
R. Matsueda and R. Walter (1980). 3-Nitro-2-pyridinesulfenyl (Npys) group. A novel selective protecting group which can be activated for peptide bond formation. Int. J. Peptide Protein Res. 16, 392-401.
-
(1980)
Int. J. Peptide Protein Res.
, vol.16
, pp. 392-401
-
-
Matsueda, R.1
Walter, R.2
-
18
-
-
0025162612
-
Thiolysis of the 3-nitro-2-pyridinesulfenyl (Npys) protecting group
-
O. Rosen, S. Rubinraut and M. Fridkin (1990). Thiolysis of the 3-nitro-2-pyridinesulfenyl (Npys) protecting group. Int. J. Peptide Protein Res. 35, 545-549.
-
(1990)
Int. J. Peptide Protein Res.
, vol.35
, pp. 545-549
-
-
Rosen, O.1
Rubinraut, S.2
Fridkin, M.3
-
19
-
-
0025335121
-
Design and synthesis of a peptide having chymotrypsin-like esterase activity
-
K.W. Hahn, W.A. Klis and J.M. Stewart (1990). Design and synthesis of a peptide having chymotrypsin-like esterase activity. Science 248, 1544-1547.
-
(1990)
Science
, vol.248
, pp. 1544-1547
-
-
Hahn, K.W.1
Klis, W.A.2
Stewart, J.M.3
-
20
-
-
0027240153
-
Synthesis and stability of 3-nitro-2-pyridinesulfenyl chloride (NpysCl)
-
K.C. Pugh, L. Cera and J.M. Stewart (1993). Synthesis and stability of 3-nitro-2-pyridinesulfenyl chloride (NpysCl). Int. J. Peptide Protein Res. 42, 159-164.
-
(1993)
Int. J. Peptide Protein Res.
, vol.42
, pp. 159-164
-
-
Pugh, K.C.1
Cera, L.2
Stewart, J.M.3
-
21
-
-
0028908881
-
ε-branching at lysine during solid-phase peptide synthesis. I. Application to the synthesis of a peptide template containing two addressable sites
-
ε-branching at lysine during solid-phase peptide synthesis. I. Application to the synthesis of a peptide template containing two addressable sites. Int. J. Peptide Protein Res. 45, 173-179.
-
(1995)
Int. J. Peptide Protein Res.
, vol.45
, pp. 173-179
-
-
Rajagopalan, S.1
Heck, T.J.2
Iwamoto, T.3
Tomich, J.M.4
-
22
-
-
0026707472
-
Novel version of multiple antigenic peptide allowing incorporation on a cysteine functionalized lysine tree
-
F. Baleux and P. Dubois (1992). Novel version of multiple antigenic peptide allowing incorporation on a cysteine functionalized lysine tree. Int. J. Peptide Protein Res. 40, 7-12.
-
(1992)
Int. J. Peptide Protein Res.
, vol.40
, pp. 7-12
-
-
Baleux, F.1
Dubois, P.2
-
23
-
-
0001155881
-
Use of an allylic anchor group and of its palladium catalyzed hydrostannolytic cleavage in the solid phase synthesis of protected peptide fragments
-
F. Guibé, O. Dangles, G. Balavoineand and A. Loffet (1989). Use of an allylic anchor group and of its palladium catalyzed hydrostannolytic cleavage in the solid phase synthesis of protected peptide fragments. Tetrahedron Lett. 30, 2641-2644.
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 2641-2644
-
-
Guibé, F.1
Dangles, O.2
Balavoineand, G.3
Loffet, A.4
-
24
-
-
0028142438
-
Mild and rapid azide-mediated, palladium catalyzed cleavage of allylester based protecting groups
-
G. Shapiro and D. Buechler (1994). Mild and rapid azide-mediated, palladium catalyzed cleavage of allylester based protecting groups. Tetrahedron Lett. 35, 5421-5424.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 5421-5424
-
-
Shapiro, G.1
Buechler, D.2
-
25
-
-
0027527619
-
Allyl-based groups for side-chain protection of amino-aclds
-
A. Loffet and H.X. Zhang (1993). Allyl-based groups for side-chain protection of amino-aclds. Int. J. Peptide Protein Res. 42, 346-351.
-
(1993)
Int. J. Peptide Protein Res.
, vol.42
, pp. 346-351
-
-
Loffet, A.1
Zhang, H.X.2
-
26
-
-
0011471348
-
Allyl based side-chain protection for SPPS
-
J.A. Smith and J.E. Rivier, Eds, ESCOM, Leiden
-
M.H. Lyttle and D. Hudson. Allyl based side-chain protection for SPPS, in: Peptides. Chemistry and Biology, J.A. Smith and J.E. Rivier, Eds, p. 583-584, ESCOM, Leiden, 1992.
-
(1992)
Peptides. Chemistry and Biology
, pp. 583-584
-
-
Lyttle, M.H.1
Hudson, D.2
-
27
-
-
0029115707
-
New allyl group for palladium catalyzed removal of allylic protections and transacylation of allyl carbamates
-
M. Dessolin, M.-G. Guillerez, N. Thieriet, F. Guibé and A. Loffet (1995). New allyl group for palladium catalyzed removal of allylic protections and transacylation of allyl carbamates. Tetrahedron Lett. 36, 5741-5744.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 5741-5744
-
-
Dessolin, M.1
Guillerez, M.-G.2
Thieriet, N.3
Guibé, F.4
Loffet, A.5
-
28
-
-
0028338351
-
-
P. Lloyd-Williams, A. Merzouk, F. Guibé, F. Albericio and E. Giralt (1994). Tetrahedron Lett. 35, 4437-4440.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 4437-4440
-
-
Lloyd-Williams, P.1
Merzouk, A.2
Guibé, F.3
Albericio, F.4
Giralt, E.5
-
29
-
-
0024834606
-
Multiple antigenic peptide method for producing antipeptide site-specific antibodies
-
D.N. Posnett and J.P. Tam (1989). Multiple antigenic peptide method for producing antipeptide site-specific antibodies. Methods Enzymol. 178, 739-746.
-
(1989)
Methods Enzymol.
, vol.178
, pp. 739-746
-
-
Posnett, D.N.1
Tam, J.P.2
-
30
-
-
0029572443
-
Coupling difficulty associated with interchain clustering and phase transition in solid phase peptide synthesis
-
J.P. Tam and Y.A. Lu (1995). Coupling difficulty associated with interchain clustering and phase transition in solid phase peptide synthesis. J. Am. Chem. Soc. 117, 12058-12063.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 12058-12063
-
-
Tam, J.P.1
Lu, Y.A.2
-
31
-
-
0019627519
-
Quantitative monitoring of solid-phase peptide synthesis by the ninhydrin reaction
-
V.K. Sarin, S.B.H. Kent, J.P. Tam and R.B. Merrifield (1981). Quantitative monitoring of solid-phase peptide synthesis by the ninhydrin reaction. Anal. Biochem. 117, 147-157.
-
(1981)
Anal. Biochem.
, vol.117
, pp. 147-157
-
-
Sarin, V.K.1
Kent, S.B.H.2
Tam, J.P.3
Merrifield, R.B.4
-
32
-
-
0017157455
-
A new microtest for the detection of incomplete coupling reactions in solid-phase peptide synthesis using 2,4,6,-trinitrobenzenesulphonic acid
-
W.S. Hancock and J.E. Battersby (1976). A new microtest for the detection of incomplete coupling reactions in solid-phase peptide synthesis using 2,4,6,-trinitrobenzenesulphonic acid. Anal. Biochem. 71, 260-264.
-
(1976)
Anal. Biochem.
, vol.71
, pp. 260-264
-
-
Hancock, W.S.1
Battersby, J.E.2
-
33
-
-
0001065043
-
'Magic Mixture', a powerful solvent system for solid-phase synthesis of 'difficult sequences'
-
R. Epton, Ed., Mayflower Worldwide Ltd., Birmingham
-
L. Zhang, C. Goldammer, B. Henkel., F. Zühl, G. Panhaus, G. Jung and E. Bayer. 'Magic Mixture', a powerful solvent system for solid-phase synthesis of 'difficult sequences', in: Innovation and Perspectives in Solid Phase Synthesis. Peptides, Proteins and Nucleic Acids, R. Epton, Ed., p. 711-716, Mayflower Worldwide Ltd., Birmingham, 1994.
-
(1994)
Innovation and Perspectives in Solid Phase Synthesis. Peptides, Proteins and Nucleic Acids
, pp. 711-716
-
-
Zhang, L.1
Goldammer, C.2
Henkel, B.3
Zühl, F.4
Panhaus, G.5
Jung, G.6
Bayer, E.7
-
34
-
-
0028450786
-
Accelerated protocols for solid-phase peptide synthesis at elevated temperature
-
A.K. Rabinovich and J.E. Rivier (1994). Accelerated protocols for solid-phase peptide synthesis at elevated temperature. Am. Biotechnol. Lab. 12, 48-51.
-
(1994)
Am. Biotechnol. Lab.
, vol.12
, pp. 48-51
-
-
Rabinovich, A.K.1
Rivier, J.E.2
-
35
-
-
0030743067
-
Solid-phase peptide synthesis at elevated temperatures: A search for and optimized synthesis condition of unsulfated cholecystokinin-12
-
L.M. Varanda and M.T. Miranda (1997). Solid-phase peptide synthesis at elevated temperatures: a search for and optimized synthesis condition of unsulfated cholecystokinin-12. J. Peptide Res. 50, 102-108.
-
(1997)
J. Peptide Res.
, vol.50
, pp. 102-108
-
-
Varanda, L.M.1
Miranda, M.T.2
-
36
-
-
0001079022
-
The studies of microwave effects on the chemical reactions
-
S.-T. Chen, P.-H. Tseng, H.-M. Yu, C.-Y. Wu, K.-F. Hsiao, S.-H. Wu and K.-T. Wang (1997). The studies of microwave effects on the chemical reactions. J. Chin. Chem. Soc. 44, 169-182.
-
(1997)
J. Chin. Chem. Soc.
, vol.44
, pp. 169-182
-
-
Chen, S.-T.1
Tseng, P.-H.2
Yu, H.-M.3
Wu, C.-Y.4
Hsiao, K.-F.5
Wu, S.-H.6
Wang, K.-T.7
-
37
-
-
0030738238
-
Preparation of a multiple antigen glycopeptide (MAG) carrying the Tn antigen
-
S. Bay, R. Lo-man, E. Osinaga, H. Nakada, C. Leclere and D. Cantacuzéne (1997). Preparation of a multiple antigen glycopeptide (MAG) carrying the Tn antigen. J. Peptide Res. 49, 620-625.
-
(1997)
J. Peptide Res.
, vol.49
, pp. 620-625
-
-
Bay, S.1
Lo-man, R.2
Osinaga, E.3
Nakada, H.4
Leclere, C.5
Cantacuzéne, D.6
-
38
-
-
0028947942
-
Unprotected peptides as building blocks for branched peptides and peptide dendrimers
-
J.C. Spetzler, J.P. Tam (1995). Unprotected peptides as building blocks for branched peptides and peptide dendrimers. Int. J. Peptide Protein Res. 45, 78-85.
-
(1995)
Int. J. Peptide Protein Res.
, vol.45
, pp. 78-85
-
-
Spetzler, J.C.1
Tam, J.P.2
-
39
-
-
0028960723
-
Unprotected peptides as building blocks for the synthesis of peptide dendrimers with oxime, hydrazone, and thiazolidine linkages
-
J. Shao and J.P. Tam (1995) Unprotected peptides as building blocks for the synthesis of peptide dendrimers with oxime, hydrazone, and thiazolidine linkages. J. Am. Chem. Soc. 117, 3893-3899.
-
(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 3893-3899
-
-
Shao, J.1
Tam, J.P.2
-
40
-
-
0003014488
-
Direct synthesis and characterization of multi-dendritic peptides for use as immunogens
-
H.H. Keah, E. Kecorius and M.T.W. Hearn (1998). Direct synthesis and characterization of multi-dendritic peptides for use as immunogens. J. Peptide Res. 51, 2-8.
-
(1998)
J. Peptide Res.
, vol.51
, pp. 2-8
-
-
Keah, H.H.1
Kecorius, E.2
Hearn, M.T.W.3
-
41
-
-
0028220676
-
The role of solid-phase fragment condensation (SPFC) in peptide synthesis
-
H. Benz (1994). The role of solid-phase fragment condensation (SPFC) in peptide synthesis. Synthesis, 337-358.
-
(1994)
Synthesis
, pp. 337-358
-
-
Benz, H.1
-
42
-
-
0024530927
-
Peptide and protein synthesis by segment synthesis-condensation
-
E.T. Kaiser, H. Nihara, G.A. Laforet, J.W. Kelly, L. Walters, M.A. Findeis and T. Sasaki (1989). Peptide and protein synthesis by segment synthesis-condensation. Science 243, 187-192.
-
(1989)
Science
, vol.243
, pp. 187-192
-
-
Kaiser, E.T.1
Nihara, H.2
Laforet, G.A.3
Kelly, J.W.4
Walters, L.5
Findeis, M.A.6
Sasaki, T.7
-
43
-
-
0002522544
-
Synthesis and applications of branched peptides in immunological methods and vaccines
-
B. Gutte, Ed., Academic Press, San Diego
-
J.P. Tam. Synthesis and applications of branched peptides in immunological methods and vaccines, in: Peptides: Synthesis, Structures, and Applications, B. Gutte, Ed., p. 455-500, Academic Press, San Diego, 1995.
-
(1995)
Peptides: Synthesis, Structures, and Applications
, pp. 455-500
-
-
Tam, J.P.1
-
44
-
-
0029420802
-
Chemoselective approaches to the preparation of peptide dendrimers and branched artificial proteins using unprotected peptides as building blocks
-
J.P. Tam and J.C. Spetzler (1995). Chemoselective approaches to the preparation of peptide dendrimers and branched artificial proteins using unprotected peptides as building blocks. Biomed. Peptide Protein Nucl. Acids 1, 123-132.
-
(1995)
Biomed. Peptide Protein Nucl. Acids
, vol.1
, pp. 123-132
-
-
Tam, J.P.1
Spetzler, J.C.2
-
45
-
-
0025235971
-
Chemical modifications of proteins: History and applications
-
G.E. Means and R.E. Feney (1990). Chemical modifications of proteins: history and applications. Bioconjug. Chem. 2, 2-12.
-
(1990)
Bioconjug. Chem.
, vol.2
, pp. 2-12
-
-
Means, G.E.1
Feney, R.E.2
-
46
-
-
0026951113
-
Radiohalogenation of proteins: An overview of radionuclides, labeling methods, and reagents for conjugate labeling
-
D.S. Wilbur (1992). Radiohalogenation of proteins: an overview of radionuclides, labeling methods, and reagents for conjugate labeling. Bioconjug. Chem. 3, 433-470.
-
(1992)
Bioconjug. Chem.
, vol.3
, pp. 433-470
-
-
Wilbur, D.S.1
-
47
-
-
0029917571
-
Comparison of antibodies raised against the peptide 10-24 of chicken riboflavin carrier protein (cRCP) by classical and multiple antigen peptide (MAP) approaches
-
S.D. Mahale, J. Pereira, U. Natraj and K.S. Iyer (1996). Comparison of antibodies raised against the peptide 10-24 of chicken riboflavin carrier protein (cRCP) by classical and multiple antigen peptide (MAP) approaches. J. Immunol. Methods 190, 215-219.
-
(1996)
J. Immunol. Methods
, vol.190
, pp. 215-219
-
-
Mahale, S.D.1
Pereira, J.2
Natraj, U.3
Iyer, K.S.4
-
48
-
-
0025771238
-
Chemically unambiguous peptide immunogen: Preparation, orientation and antigenicity of purified peptide conjugated to the multiple antigen peptide system
-
Y.A. Lu, P. Clavijo, M. Galantino, Z.Y. Shen, W. Liu, J.P. Tam (1991). Chemically unambiguous peptide immunogen: preparation, orientation and antigenicity of purified peptide conjugated to the multiple antigen peptide system. Mol. Immunol 28, 623-630.
-
(1991)
Mol. Immunol
, vol.28
, pp. 623-630
-
-
Lu, Y.A.1
Clavijo, P.2
Galantino, M.3
Shen, Z.Y.4
Liu, W.5
Tam, J.P.6
-
50
-
-
0002282429
-
The periodate oxidation of amino acids with reference to studies on glycoproteins
-
J.R. Clam and L. Hough (1965). The periodate oxidation of amino acids with reference to studies on glycoproteins. Biochem. J. 94, 17-24.
-
(1965)
Biochem. J.
, vol.94
, pp. 17-24
-
-
Clam, J.R.1
Hough, L.2
-
51
-
-
2442737957
-
The synthesis of peptide secondary structure mimetics with covalent hydrogen bond mimics on the solid support
-
R.S. Hodges and J.A. Smith, Eds., ESCOM, Leiden
-
L.-C. Chiang, E. Cabezas, J.C. Calvo and A.C. Satterthwait. The synthesis of peptide secondary structure mimetics with covalent hydrogen bond mimics on the solid support, in: Peptides. Chemistry, Structure and Biology, R.S. Hodges and J.A. Smith, Eds., p. 278-280, ESCOM, Leiden, 1994.
-
(1994)
Peptides. Chemistry, Structure and Biology
, pp. 278-280
-
-
Chiang, L.-C.1
Cabezas, E.2
Calvo, J.C.3
Satterthwait, A.C.4
-
52
-
-
0028223433
-
Peptide segment ligation strategy without use of protecting groups
-
C.F. Liu and J.P. Tam (1994). Peptide segment ligation strategy without use of protecting groups. Proc. Natl. Acad. Sci. USA 91, 6584-6588.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 6584-6588
-
-
Liu, C.F.1
Tam, J.P.2
-
53
-
-
0009976942
-
Steroid-protein conjugates. I. Preparation and characterization of conjugates of bovine serum albumin with testosterone and with cortisone
-
B.F. Erlanger, F. Borek, S.M. Beiser and S. Lieberman (1957). Steroid-protein conjugates. I. Preparation and characterization of conjugates of bovine serum albumin with testosterone and with cortisone. J. Biol. Chem. 228, 713-727.
-
(1957)
J. Biol. Chem.
, vol.228
, pp. 713-727
-
-
Erlanger, B.F.1
Borek, F.2
Beiser, S.M.3
Lieberman, S.4
-
54
-
-
0017863234
-
Preparation of protein conjugates via intermolecular disulfide bond formation
-
T.P. King, Y. Li and L. Kochoumian (1978). Preparation of protein conjugates via intermolecular disulfide bond formation. Biochemistry 17, 1499-1506.
-
(1978)
Biochemistry
, vol.17
, pp. 1499-1506
-
-
King, T.P.1
Li, Y.2
Kochoumian, L.3
-
55
-
-
0000113093
-
Compounds of thiol acids with aldehydes
-
M.P. Schubert (1936). Compounds of thiol acids with aldehydes. J. Biol. Chem. 114, 341-350.
-
(1936)
J. Biol. Chem.
, vol.114
, pp. 341-350
-
-
Schubert, M.P.1
-
56
-
-
0028231302
-
Facile synthesis of homogenous artificial proteins
-
K. Rose (1994). Facile synthesis of homogenous artificial proteins. J. Am. Chem. Soc. 116, 30-33.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 30-33
-
-
Rose, K.1
-
57
-
-
0026857064
-
Construction of protein analogues by site-specific condensation of unprotected fragments
-
H.F. Gaertner, K. Rose, R. Cotton, D. Timms, R. Camble and R.E. Offord (1992). Construction of protein analogues by site-specific condensation of unprotected fragments. Bioconjug. Chem. 3, 262-268.
-
(1992)
Bioconjug. Chem.
, vol.3
, pp. 262-268
-
-
Gaertner, H.F.1
Rose, K.2
Cotton, R.3
Timms, D.4
Camble, R.5
Offord, R.E.6
-
58
-
-
0023055743
-
Preparation of protein conjugates via intermolecular hydrazone linkage
-
T.P King, S.W. Zhao and T. Lam (1986). Preparation of protein conjugates via intermolecular hydrazone linkage. Biochemistry 25, 5774-5779.
-
(1986)
Biochemistry
, vol.25
, pp. 5774-5779
-
-
King, T.P.1
Zhao, S.W.2
Lam, T.3
-
59
-
-
0026826660
-
Site-directed conjugation of nonpeptide groups to peptides and proteins via periodate oxidation of a 2-amino alcohol. Application to modification at N-terminal serine
-
K.F. Geoghegan and J.G. Stroh (1992). Site-directed conjugation of nonpeptide groups to peptides and proteins via periodate oxidation of a 2-amino alcohol. Application to modification at N-terminal serine. Bioconjug. Chem. 3, 138-146.
-
(1992)
Bioconjug. Chem.
, vol.3
, pp. 138-146
-
-
Geoghegan, K.F.1
Stroh, J.G.2
-
60
-
-
0019529504
-
Peptide segment coupling in aqueous medium: Silver ion activation of the thiolcarboxyl group
-
J. Blake (1981). Peptide segment coupling in aqueous medium: silver ion activation of the thiolcarboxyl group. Int. J. Peptide Protein Res. 17, 273-274.
-
(1981)
Int. J. Peptide Protein Res.
, vol.17
, pp. 273-274
-
-
Blake, J.1
-
61
-
-
84985687610
-
The amine capture strategy for peptide bond formation-an outline of progress
-
D.S. Kemp (1981). The amine capture strategy for peptide bond formation-an outline of progress. Biopolymers 20, 1793-1804.
-
(1981)
Biopolymers
, vol.20
, pp. 1793-1804
-
-
Kemp, D.S.1
-
62
-
-
0024413577
-
Peptide synthesis by prior thiol capture. 6. Rates of the disulfide bond forming capture reaction and demonstration of the overall strategy by synthesis of the C-terminal 29-peptide sequence of BPTI
-
N. Fotouhi, N.G. Galakatos and D.S. Kemp (1989). Peptide synthesis by prior thiol capture. 6. Rates of the disulfide bond forming capture reaction and demonstration of the overall strategy by synthesis of the C-terminal 29-peptide sequence of BPTI. J. Org. Chem. 54, 2803-2817.
-
(1989)
J. Org. Chem.
, vol.54
, pp. 2803-2817
-
-
Fotouhi, N.1
Galakatos, N.G.2
Kemp, D.S.3
-
63
-
-
0343110277
-
Peptide synthesis by prior thiol capture. 4. Amide bond formation: The effect of a side-chain substituent on the rates of intramolecular O,N-acyl transfer
-
D.S. Kemp, N.G. Galakatos, D. Dranginis, C. Ashton, N. Fotouhi and T.P. Curran (1986). Peptide synthesis by prior thiol capture. 4. Amide bond formation: the effect of a side-chain substituent on the rates of intramolecular O,N-acyl transfer. J. Org. Chem. 51, 3320-3324.
-
(1986)
J. Org. Chem.
, vol.51
, pp. 3320-3324
-
-
Kemp, D.S.1
Galakatos, N.G.2
Dranginis, D.3
Ashton, C.4
Fotouhi, N.5
Curran, T.P.6
-
64
-
-
0025802610
-
Resolution of the histidine problem for thiol capture-synthesis of a 39-peptide
-
D.S. Kemp and R.I. Carey (1991). Resolution of the histidine problem for thiol capture-synthesis of a 39-peptide. Tetrahedron Lett. 32, 2845-2848.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 2845-2848
-
-
Kemp, D.S.1
Carey, R.I.2
-
65
-
-
0031013619
-
Orthogonal coupling of unprotected peptide segments through histidyl amino terminus
-
L. Zhang and J.P. Tam (1997). Orthogonal coupling of unprotected peptide segments through histidyl amino terminus. Tetrahedron Lett. 38, 3-6.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 3-6
-
-
Zhang, L.1
Tam, J.P.2
-
66
-
-
0029559773
-
Peptide synthesis using unprotected peptides through orthogonal coupling methods
-
J.P. Tam, Y.A. Lu, C.F. Liu and J. Shao (1995). Peptide synthesis using unprotected peptides through orthogonal coupling methods. Proc. Natl. Acad. Sci. USA 92, 12485-12489.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 12485-12489
-
-
Tam, J.P.1
Lu, Y.A.2
Liu, C.F.3
Shao, J.4
-
67
-
-
0002632421
-
Assembly of cyclic peptide dendrimers from unprotected linear building blocks in aqueous solution
-
T.D. Pallin and J.P. Tam (1996). Assembly of cyclic peptide dendrimers from unprotected linear building blocks in aqueous solution. J. Chem. Soc., Chem. Commun., 1345-1346.
-
(1996)
J. Chem. Soc., Chem. Commun.
, pp. 1345-1346
-
-
Pallin, T.D.1
Tam, J.P.2
-
68
-
-
0030897311
-
Synthesis and application of unprotected cyclic peptides as building blocks for peptide dendrimers
-
L. Zhang and J.P. Tam (1997). Synthesis and application of unprotected cyclic peptides as building blocks for peptide dendrimers. J. Am. Chem. Soc. 119, 2363-2370.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 2363-2370
-
-
Zhang, L.1
Tam, J.P.2
-
69
-
-
0030292260
-
Self-assembly of cyclic peptides on a dendrimer: Multiple cyclic antigen peptides
-
J.C. Spetzler and J.P. Tam (1996). Self-assembly of cyclic peptides on a dendrimer: multiple cyclic antigen peptides. Peptide Res. 9, 290-296.
-
(1996)
Peptide Res.
, vol.9
, pp. 290-296
-
-
Spetzler, J.C.1
Tam, J.P.2
-
70
-
-
2442750504
-
Vaccine design: The orthogonal incorporation of cyclic peptides as multiple antigens attached to dendrimeric cores
-
P.T.P. Kaumaya and R.S. Hodges, Eds, Mayflower Scientific Ltd., Kingswinford
-
T.D. Pallin and J.P. Tam. Vaccine design: the orthogonal incorporation of cyclic peptides as multiple antigens attached to dendrimeric cores, in: Peptides: Chemistry, Structure and Biology, P.T.P. Kaumaya and R.S. Hodges, Eds, p. 853-854, Mayflower Scientific Ltd., Kingswinford, 1996.
-
(1996)
Peptides: Chemistry, Structure and Biology
, pp. 853-854
-
-
Pallin, T.D.1
Tam, J.P.2
-
71
-
-
0028886196
-
Cyclisation of totally unprotected peptides in aqueous solution by oxime formation
-
T.D. Pallin and J.P. Tam (1995). Cyclisation of totally unprotected peptides in aqueous solution by oxime formation. J. Chem. Soc., Chem. Commun., 2021-2022.
-
(1995)
J. Chem. Soc., Chem. Commun.
, pp. 2021-2022
-
-
Pallin, T.D.1
Tam, J.P.2
-
72
-
-
0031894588
-
Chemical ligation of unprotected peptides directly from a solid support
-
J.A. Camarero, G.J. Cotton. A. Adeva and T.W. Muir (1998). Chemical ligation of unprotected peptides directly from a solid support. J. Peptide Res. 51, 303-316.
-
(1998)
J. Peptide Res.
, vol.51
, pp. 303-316
-
-
Camarero, J.A.1
Cotton, G.J.2
Adeva, A.3
Muir, T.W.4
-
73
-
-
0030070347
-
Concept and design of a new class of sequential oligopeptide carriers (SOC) for covalent attachment of multiple antigenic peptides
-
V. Tsikaris, C. Sakarellos, M.T. Cung, M. Marraud and M. Sakarellos-Daitsiotis (1996). Concept and design of a new class of sequential oligopeptide carriers (SOC) for covalent attachment of multiple antigenic peptides. Biopolymers 38, 291-293.
-
(1996)
Biopolymers
, vol.38
, pp. 291-293
-
-
Tsikaris, V.1
Sakarellos, C.2
Cung, M.T.3
Marraud, M.4
Sakarellos-Daitsiotis, M.5
-
74
-
-
0030271708
-
Construction and application of a new class of sequential oligopeptide carriers (SOCn) for multiple anchoring of antigenic peptides - Application to the acetylcholine receptor (AChR) main immunogenic region
-
V. Tsikaris, C. Sakarellos, M. Sakarellos-Daitsiotis, P. Orlewski, M. Marraud, M.T. Cung, E. Vatzaki and S. Tzartos (1996). Construction and application of a new class of sequential oligopeptide carriers (SOCn) for multiple anchoring of antigenic peptides - application to the acetylcholine receptor (AChR) main immunogenic region. Int. J. Biol. Macromol. 19, 195-205.
-
(1996)
Int. J. Biol. Macromol.
, vol.19
, pp. 195-205
-
-
Tsikaris, V.1
Sakarellos, C.2
Sakarellos-Daitsiotis, M.3
Orlewski, P.4
Marraud, M.5
Cung, M.T.6
Vatzaki, E.7
Tzartos, S.8
-
75
-
-
0027960890
-
Conformatlonal preferences of oligopeptides rich in alpha-aminoisobutyric acid. III. Design, synthesis and hydrogen bonding in 3(10)-hellces
-
V.A. Bindra and A. Kuki (1994). Conformatlonal preferences of oligopeptides rich in alpha-aminoisobutyric acid. III. Design, synthesis and hydrogen bonding in 3(10)-hellces. Int. J. Peptide Protein Res. 44, 539-548.
-
(1994)
Int. J. Peptide Protein Res.
, vol.44
, pp. 539-548
-
-
Bindra, V.A.1
Kuki, A.2
-
76
-
-
2442765512
-
A conformationally based rational design of multiple antigenic peptide carriers: The potential for disease treatment
-
P.T.P. Kaumaya and R.S. Hodges, Eds, Mayflower Scientific Ltd., Kingswinford
-
C. Sakarellos, V. Tsikaris, S. Kosma, M. Sakarellos-Daitsiotis, E. Vatzaki, S.J. Tzaros, M.T. Cung and M. Marraud. A conformationally based rational design of multiple antigenic peptide carriers: the potential for disease treatment, in: Peptides: Chemistry, Structure and Biology, P.T.P. Kaumaya and R.S. Hodges, Eds, p. 816-817, Mayflower Scientific Ltd., Kingswinford, 1996.
-
(1996)
Peptides: Chemistry, Structure and Biology
, pp. 816-817
-
-
Sakarellos, C.1
Tsikaris, V.2
Kosma, S.3
Sakarellos-Daitsiotis, M.4
Vatzaki, E.5
Tzaros, S.J.6
Cung, M.T.7
Marraud, M.8
-
77
-
-
0030239337
-
Use of sequential oligopeptide carriers (SOCn) in the design of potent Leishmania gp63 immunogenic peptides
-
V. Tsikaris, C. Sakarellos, M. Sakarellos-Daitsiotis, M.T. Cung, M. Marraud, G. Konidou, A. Tzinia and K.P. Soteriadou (1996). Use of sequential oligopeptide carriers (SOCn) in the design of potent Leishmania gp63 immunogenic peptides. Peptide Res. 9, 240-247.
-
(1996)
Peptide Res.
, vol.9
, pp. 240-247
-
-
Tsikaris, V.1
Sakarellos, C.2
Sakarellos-Daitsiotis, M.3
Cung, M.T.4
Marraud, M.5
Konidou, G.6
Tzinia, A.7
Soteriadou, K.P.8
-
78
-
-
0001094662
-
Glycobiology: Toward understanding the function of sugars
-
R.A. Dwek (1996). Glycobiology: toward understanding the function of sugars. Chem. Rev. 96, 683-720.
-
(1996)
Chem. Rev.
, vol.96
, pp. 683-720
-
-
Dwek, R.A.1
-
79
-
-
0027318961
-
Biological roles of ollgosaccharides: All of the theories are correct
-
A. Varki (1993). Biological roles of ollgosaccharides: all of the theories are correct. Glycobiology 3, 97-130.
-
(1993)
Glycobiology
, vol.3
, pp. 97-130
-
-
Varki, A.1
-
81
-
-
0021999503
-
Demonstration by monoclonal antibodies that carbohydrate structures of glycoproteins and glycolipids are onco-developmental antigens
-
T. Feizi (1985). Demonstration by monoclonal antibodies that carbohydrate structures of glycoproteins and glycolipids are onco-developmental antigens. Nature 314, 53-57.
-
(1985)
Nature
, vol.314
, pp. 53-57
-
-
Feizi, T.1
-
82
-
-
0024585483
-
Aberrant glycosylation in tumors and tumor-associated carbohydrate antigens
-
S. Hakomori (1989). Aberrant glycosylation in tumors and tumor-associated carbohydrate antigens. Adv. Cancer Res. 52, 257-331.
-
(1989)
Adv. Cancer Res.
, vol.52
, pp. 257-331
-
-
Hakomori, S.1
-
83
-
-
0021601136
-
Cell surface glycoconjugates as onco-differentiation markers in hematopoietic cells
-
M. Fukuda (1985). Cell surface glycoconjugates as onco-differentiation markers in hematopoietic cells. Biochim. Biophys. Acta 780, 119-150.
-
(1985)
Biochim. Biophys. Acta
, vol.780
, pp. 119-150
-
-
Fukuda, M.1
-
85
-
-
0023488843
-
Identification of an inducible endothelial-leukocyte adhesion molecule
-
M.P. Bevilacqua, J.S. Pober, D.L. Mendrick, R.S. Cotran and M.A. Gimbrone (1987). Identification of an inducible endothelial-leukocyte adhesion molecule. Proc. Natl. Acad. Sci. USA 84, 9238-9242.
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, pp. 9238-9242
-
-
Bevilacqua, M.P.1
Pober, J.S.2
Mendrick, D.L.3
Cotran, R.S.4
Gimbrone, M.A.5
-
86
-
-
0021141716
-
T and Tn, general carcinoma autoantigens
-
G.F. Springer (1984). T and Tn, general carcinoma autoantigens. Science 224, 1198-1206.
-
(1984)
Science
, vol.224
, pp. 1198-1206
-
-
Springer, G.F.1
-
87
-
-
0025992169
-
Possible functions of tumor-associated carbohydrate antigens
-
S.I. Hakomori (1991). Possible functions of tumor-associated carbohydrate antigens. Curr. Opin. Immunol. 3, 646-653.
-
(1991)
Curr. Opin. Immunol.
, vol.3
, pp. 646-653
-
-
Hakomori, S.I.1
-
88
-
-
0018853556
-
Primary structure of glycoprotein glycans: Basis for the molecular biology of glycoproteins
-
J. Montreuil (1980). Primary structure of glycoprotein glycans: basis for the molecular biology of glycoproteins. Adv. Carbohydr. Chem. Biochem. 37, 157-223.
-
(1980)
Adv. Carbohydr. Chem. Biochem.
, vol.37
, pp. 157-223
-
-
Montreuil, J.1
-
90
-
-
0027519943
-
Protein glycosylation. Structural and functional aspects
-
H. Lis and N. Sharon (1993). Protein glycosylation. Structural and functional aspects. Eur. J. Biochem. 218, 1-27.
-
(1993)
Eur. J. Biochem.
, vol.218
, pp. 1-27
-
-
Lis, H.1
Sharon, N.2
-
91
-
-
0025102915
-
Syntheses, conformations and X-ray structure analyses of the saccharide chains from the core regions of glycoproteins
-
H. Paulsen (1990). Syntheses, conformations and X-ray structure analyses of the saccharide chains from the core regions of glycoproteins. Angew. Chem. Int. Ed. Engl. 29, 823-839.
-
(1990)
Angew. Chem. Int. Ed. Engl.
, vol.29
, pp. 823-839
-
-
Paulsen, H.1
-
92
-
-
0026655074
-
Enzyme-catalyzed oligosaccharide synthesis
-
Y. Ichikawa, G.C. Look and C.H. Wong (1992). Enzyme-catalyzed oligosaccharide synthesis. Anal. Biochem. 202, 215-238.
-
(1992)
Anal. Biochem.
, vol.202
, pp. 215-238
-
-
Ichikawa, Y.1
Look, G.C.2
Wong, C.H.3
-
93
-
-
84985598642
-
Synthesis of glycopeptides, partial structures of biological recognition components
-
H. Kunz (1987). Synthesis of glycopeptides, partial structures of biological recognition components. Angew. Chem. Int. Ed. Engl. 26, 294-308.
-
(1987)
Angew. Chem. Int. Ed. Engl.
, vol.26
, pp. 294-308
-
-
Kunz, H.1
-
94
-
-
0343052906
-
Mucin type glycopeptides: Synthesis of Core 2, Core 6, and F1-α building blocks and some unexpected reactions
-
D. Qiu and R.R. Koganty (1997). Mucin type glycopeptides: synthesis of Core 2, Core 6, and F1-α building blocks and some unexpected reactions. Tetrahedron Lett. 38, 45-48.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 45-48
-
-
Qiu, D.1
Koganty, R.R.2
-
95
-
-
0031552087
-
Chemoenzymatic synthesis of Galαl-3Gal, Galαl-3Galβ 1-4GlcNAc, and their PEG-conjugates
-
I. Matsuo, H. Fujimoto, M. Isomura and K. Ajisaka (1997). Chemoenzymatic synthesis of Galαl-3Gal, Galαl-3Galβ 1-4GlcNAc, and their PEG-conjugates. Bioorg. Med. Chem. Lett. 7, 255-258.
-
(1997)
Bioorg. Med. Chem. Lett.
, vol.7
, pp. 255-258
-
-
Matsuo, I.1
Fujimoto, H.2
Isomura, M.3
Ajisaka, K.4
-
96
-
-
0002107732
-
The chemistry of neoglycoconjugates
-
R. Roy (1998). The chemistry of neoglycoconjugates. Carbohydr. Chem., 243-321.
-
(1998)
Carbohydr. Chem.
, pp. 243-321
-
-
Roy, R.1
-
97
-
-
0000250138
-
Carbohydrate-protein interactions in antibodies and lectins
-
D.R. Bundle and N.M. Young (1992). Carbohydrate-protein interactions in antibodies and lectins. Curr. Opin. Struct. Biol. 2, 666-673.
-
(1992)
Curr. Opin. Struct. Biol.
, vol.2
, pp. 666-673
-
-
Bundle, D.R.1
Young, N.M.2
-
98
-
-
0029069994
-
The differences in structural specificity for recognition and binding between asialoglycoprotein receptors of liver and macrophages
-
K. Ozaki, R.T. Lee, Y.C. Lee and T. Kawasaki (1995). The differences in structural specificity for recognition and binding between asialoglycoprotein receptors of liver and macrophages. Glycoconj. J. 12, 268-274.
-
(1995)
Glycoconj. J.
, vol.12
, pp. 268-274
-
-
Ozaki, K.1
Lee, R.T.2
Lee, Y.C.3
Kawasaki, T.4
-
99
-
-
0027944416
-
Single step syntheses of lactosylated clusters by telomerizatlons
-
S. Aravind, W.K.C. Park, S. Brochu and R. Roy (1994). Single step syntheses of lactosylated clusters by telomerizatlons. Tetrahedron Lett. 35, 7739-7742.
-
(1994)
Tetrahedron Lett.
, vol.35
, pp. 7739-7742
-
-
Aravind, S.1
Park, W.K.C.2
Brochu, S.3
Roy, R.4
-
100
-
-
0002773690
-
Enhanced biochemical affinities of multivalent neoglycoconjugates
-
Y.C. Lee and R.T. Lee, Eds, Academic Press, San Diego
-
R.T. Lee and Y.C. Lee. Enhanced biochemical affinities of multivalent neoglycoconjugates, in: Neoglycoconjugates: Preparation and Applications, Y.C. Lee and R.T. Lee, Eds, p. 23-57, Academic Press, San Diego, 1994.
-
(1994)
Neoglycoconjugates: Preparation and Applications
, pp. 23-57
-
-
Lee, R.T.1
Lee, Y.C.2
-
101
-
-
0002450287
-
Design and Syntheses of Glycoconjugates
-
S.-H. Khan and R.O. Neil, Eds, Harwood Academic, Amsterdam, Netherlands
-
R. Roy. Design and Syntheses of Glycoconjugates, in: Modern Methods in Carbohydrate Synthesis, S.-H. Khan and R.O. Neil, Eds, p. 378-415, Harwood Academic, Amsterdam, Netherlands, 1995.
-
(1995)
Modern Methods in Carbohydrate Synthesis
, pp. 378-415
-
-
Roy, R.1
-
102
-
-
0001420002
-
Glycodendrimers: A new class of biopolymers
-
R. Roy (1996). Glycodendrimers: a new class of biopolymers. Polymer News 21, 226-232.
-
(1996)
Polymer News
, vol.21
, pp. 226-232
-
-
Roy, R.1
-
103
-
-
0027740240
-
Solid-phase synthesis of dendritic sialoside inhibitors of influenza A virus haemagglutinin
-
R. Roy, D. Zanini, S.J. Meunier and A. Romanowska (1993). Solid-phase synthesis of dendritic sialoside inhibitors of influenza A virus haemagglutinin. J. Chem. Soc., Chem. Commun., 1869-1872.
-
(1993)
J. Chem. Soc., Chem. Commun.
, pp. 1869-1872
-
-
Roy, R.1
Zanini, D.2
Meunier, S.J.3
Romanowska, A.4
-
104
-
-
0000439588
-
Novel dendritic α-sialosides: Synthesis of glycodendrimers based on a 3,3′-iminobis(propylamine) core
-
D. Zanini and R. Roy (1996). Novel dendritic α-sialosides: synthesis of glycodendrimers based on a 3,3′-iminobis(propylamine) core. J. Org. Chem. 61, 7348-7354.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 7348-7354
-
-
Zanini, D.1
Roy, R.2
-
105
-
-
0030915343
-
Glycodendrimer synthesis without using protecting groups
-
C. Kieburg and T.K. Lindhorst (1997). Glycodendrimer synthesis without using protecting groups. Tetrahedron Lett. 38, 3885-3888.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 3885-3888
-
-
Kieburg, C.1
Lindhorst, T.K.2
-
106
-
-
0030803087
-
A convergent synthesis of a carbohydrate containing dendrimer
-
P.R. Ashton, S.E. Boyd, C.L. Brown. N. Jayaraman and J.F. Stoddart (1997). A convergent synthesis of a carbohydrate containing dendrimer. Angew. Chem. Int. Ed. Engl. 36, 732-735.
-
(1997)
Angew. Chem. Int. Ed. Engl.
, vol.36
, pp. 732-735
-
-
Ashton, P.R.1
Boyd, S.E.2
Brown, C.L.3
Jayaraman, N.4
Stoddart, J.F.5
-
107
-
-
0029911174
-
Glycocoating of oligovalent amines: Synthesis of thiourea-bridged cluster glycosides from glycosyl isothiocyanates
-
T.K. Lindhorst and C. Kieburg (1996). Glycocoating of oligovalent amines: synthesis of thiourea-bridged cluster glycosides from glycosyl isothiocyanates. Angew. Chem. Int. Ed. Engl. 35, 1953-1956.
-
(1996)
Angew. Chem. Int. Ed. Engl.
, vol.35
, pp. 1953-1956
-
-
Lindhorst, T.K.1
Kieburg, C.2
-
108
-
-
0029098813
-
Synthesis of novel dendritic glycosides
-
D. Zanini, W.K.C. Park and R. Roy (1995). Synthesis of novel dendritic glycosides. Tetrahedron Lett. 36, 7383-7386.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 7383-7386
-
-
Zanini, D.1
Park, W.K.C.2
Roy, R.3
-
109
-
-
0027052956
-
Synthesis of esterase-resistant 9-O-acetylated polysialoside as inhibitor of influenza C virus hemagglutinin
-
R. Roy, F.O. Andersson, G. Harms, S. Klem and R. Schauer (1992). Synthesis of esterase-resistant 9-O-acetylated polysialoside as inhibitor of influenza C virus hemagglutinin. Angew. Chem. Int. Ed. Eng. 31, 1478-1481.
-
(1992)
Angew. Chem. Int. Ed. Eng.
, vol.31
, pp. 1478-1481
-
-
Roy, R.1
Andersson, F.O.2
Harms, G.3
Klem, S.4
Schauer, R.5
-
110
-
-
0030294757
-
Macromolecular recognition: Effect of multivalency in the inhibition of binding of yeast mannan to concanavalin A and pea lectins by mannosylated dendrimers
-
D. Pagé, D. Zanini and R. Roy (1996). Macromolecular recognition: effect of multivalency in the inhibition of binding of yeast mannan to concanavalin A and pea lectins by mannosylated dendrimers. Bioorg. Med. Chem. 4, 1949-1961.
-
(1996)
Bioorg. Med. Chem.
, vol.4
, pp. 1949-1961
-
-
Pagé, D.1
Zanini, D.2
Roy, R.3
-
111
-
-
0030971899
-
Synthesis of new α-thiosialodendrimers and their binding properties to the sialic acid specific lectin from Limax flavus
-
D. Zanini and R. Roy (1997). Synthesis of new α-thiosialodendrimers and their binding properties to the sialic acid specific lectin from Limax flavus. J. Am. Chem. Soc. 119, 2088-2095.
-
(1997)
J. Am. Chem. Soc.
, vol.119
, pp. 2088-2095
-
-
Zanini, D.1
Roy, R.2
-
112
-
-
0030230298
-
Synthesis of clustered D-GalNAc (Tn) and D-Glaβ(1 → 3)GalNAc (T) antigenic motifs using a pentaerythritol scaffold
-
S. Hanessian, D. Qiu, H. Prabhanjan, G.V. Reddy and B. Lou (1996). Synthesis of clustered D-GalNAc (Tn) and D-Glaβ(1 → 3)GalNAc (T) antigenic motifs using a pentaerythritol scaffold. Can. J. Chem. 74, 1738-1747.
-
(1996)
Can. J. Chem.
, vol.74
, pp. 1738-1747
-
-
Hanessian, S.1
Qiu, D.2
Prabhanjan, H.3
Reddy, G.V.4
Lou, B.5
-
113
-
-
0028535167
-
Synthetic peptides as binding-step based catalytic mimics
-
E. Perez-Paya, R.A. Houghten and S.E. Blondelle (1994). Synthetic peptides as binding-step based catalytic mimics. Peptide Res. 7, 286-288.
-
(1994)
Peptide Res.
, vol.7
, pp. 286-288
-
-
Perez-Paya, E.1
Houghten, R.A.2
Blondelle, S.E.3
-
114
-
-
0024040279
-
Toward a better understanding of protein folding pathways
-
T.E. Creihton (1988). Toward a better understanding of protein folding pathways. Proc. Natl. Acad. Aci. USA 85, 5082-5086.
-
(1988)
Proc. Natl. Acad. Aci. USA
, vol.85
, pp. 5082-5086
-
-
Creihton, T.E.1
-
115
-
-
0024391879
-
How does protein folding get started?
-
R.L. Baldwin (1989). How does protein folding get started? Trends Biochem. Sci. 14, 291-294.
-
(1989)
Trends Biochem. Sci.
, vol.14
, pp. 291-294
-
-
Baldwin, R.L.1
-
116
-
-
0024665396
-
A chemical approach to protein design - Template-assembled synthetic proteins (TASP)
-
M. Mutter and S. Vuilleumier (1989). A chemical approach to protein design - template-assembled synthetic proteins (TASP). Angew. Chem. Int. Ed. Engl. 28, 535-554.
-
(1989)
Angew. Chem. Int. Ed. Engl.
, vol.28
, pp. 535-554
-
-
Mutter, M.1
Vuilleumier, S.2
-
117
-
-
0027453389
-
Synthesis, structure and activity of artificial, rationally designed catalytic polypeptides
-
K. Johnsson, R.K. Allemann, H. Widmer and S.A. Benner (1993). Synthesis, structure and activity of artificial, rationally designed catalytic polypeptides. Nature 365, 530-532.
-
(1993)
Nature
, vol.365
, pp. 530-532
-
-
Johnsson, K.1
Allemann, R.K.2
Widmer, H.3
Benner, S.A.4
-
119
-
-
84985719600
-
Relationship between conformation and physicochemical properties of polypeptides. I. Synthesis of homo- and co-oligopeptides by the liquid phase method
-
S. Abd El Rahman, H. Anzinger and M. Mutter (1980). Relationship between conformation and physicochemical properties of polypeptides. I. Synthesis of homo- and co-oligopeptides by the liquid phase method. Biopolymers 19, 173-187.
-
(1980)
Biopolymers
, vol.19
, pp. 173-187
-
-
Abd El Rahman, S.1
Anzinger, H.2
Mutter, M.3
-
120
-
-
0005946926
-
Linear oligopeptides. 78. Effect of the insertion of a proline residue on the conformation of host peptides
-
C. Toniolo, G.M. Bonora M. Mutter and V.N.R. Pialli (1981). Linear oligopeptides. 78. Effect of the insertion of a proline residue on the conformation of host peptides. Makromol. Chem. 182, 2007-2014.
-
(1981)
Makromol. Chem.
, vol.182
, pp. 2007-2014
-
-
Toniolo, C.1
Bonora, G.M.2
Mutter, M.3
Pialli, V.N.R.4
-
121
-
-
84987592601
-
Conformational studies on pepUdes containing enantiomeric α-methyl α-amino acids. Part I. Differential conformational properties of (R) and (S)-2-methyl aspartic acid
-
93
-
K-.H. Altmann, E. Altmann and M. Mutter (1992). 93. Conformational studies on pepUdes containing enantiomeric α-methyl α-amino acids. Part I. Differential conformational properties of (R) and (S)-2-methyl aspartic acid. Helv. Chim. Acta 75, 1198-1210.
-
(1992)
Helv. Chim. Acta
, vol.75
, pp. 1198-1210
-
-
Altmann, K.-H.1
Altmann, E.2
Mutter, M.3
-
123
-
-
11944257538
-
Secondary structure nucleation in peptides. Transition metal ion stabilized α-helices
-
M.R. Ghadiri and C. Choi (1990). Secondary structure nucleation in peptides. Transition metal ion stabilized α-helices. J. Am. Chem. Soc. 112, 1630-1632.
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 1630-1632
-
-
Ghadiri, M.R.1
Choi, C.2
-
124
-
-
0020462668
-
Structure of thermolysin refined at 1.6 Ȧ resolution
-
M.A. Holmes and B.W. Matthews (1980). Structure of thermolysin refined at 1.6 Ȧ resolution. J. Mol. Biol 160, 623-639.
-
(1980)
J. Mol. Biol
, vol.160
, pp. 623-639
-
-
Holmes, M.A.1
Matthews, B.W.2
-
125
-
-
0023053018
-
Structure determination of Panulirus interruptus haemocyanin at 3.2 Ȧ resolution. Successful phase extension by six-fold density averaging
-
W.P. Gaykema, A. Volbeda and W.G. Hol (1986). Structure determination of Panulirus interruptus haemocyanin at 3.2 Ȧ resolution. Successful phase extension by six-fold density averaging. J. Mol. Biol 187, 255-275.
-
(1986)
J. Mol. Biol
, vol.187
, pp. 255-275
-
-
Gaykema, W.P.1
Volbeda, A.2
Hol, W.G.3
-
126
-
-
0025484611
-
Peptidomimetics and the template approach to nucleation of β-sheets and α-helices in peptides
-
D.S. Kemp (1990). Peptidomimetics and the template approach to nucleation of β-sheets and α-helices in peptides. Trends Biotechnol. 8, 249-255.
-
(1990)
Trends Biotechnol.
, vol.8
, pp. 249-255
-
-
Kemp, D.S.1
-
127
-
-
0001141181
-
A convergent approach to protein design. Metal ion-assisted spontaneous self-assembly of a polypeptide into a triple-helix bundle protein
-
M.R. Ghadiri, C. Soares and C. Choi (1992). A convergent approach to protein design. Metal ion-assisted spontaneous self-assembly of a polypeptide into a triple-helix bundle protein. J. Am. Chem. Soc. 114, 825-831.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 825-831
-
-
Ghadiri, M.R.1
Soares, C.2
Choi, C.3
-
128
-
-
85022457076
-
Tetraphilin: A four-helix proton channel built on a tetraphenylporphyrin framework
-
K.S. Ackerfeldt, R.M. Kim, D. Camac, J.T. Groves, J.D. Lear and W.F. DeGrado (1992). Tetraphilin: a four-helix proton channel built on a tetraphenylporphyrin framework. J. Am. Chem. Soc. 114, 9656-9657.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 9656-9657
-
-
Ackerfeldt, K.S.1
Kim, R.M.2
Camac, D.3
Groves, J.T.4
Lear, J.D.5
DeGrado, W.F.6
-
129
-
-
85007885646
-
Iron(II) organizes a synthetic peptide into three-helix bundles
-
M. Lieberman and T. Sasaki (1991). Iron(II) organizes a synthetic peptide into three-helix bundles. J. Am. Chem. Soc. 113, 1470-1471.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 1470-1471
-
-
Lieberman, M.1
Sasaki, T.2
-
130
-
-
84989506919
-
Design of an artificial four-helix bundle metalloprotein via a novel ruthenium(II)-assisted self-assembly process
-
M.R. Ghadiri, C. Soares and C. Choi (1992). Design of an artificial four-helix bundle metalloprotein via a novel ruthenium(II)-assisted self-assembly process. J. Am. Chem. Soc. 114, 4000-4002.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 4000-4002
-
-
Ghadiri, M.R.1
Soares, C.2
Choi, C.3
-
131
-
-
0028154527
-
Design of a heme-binding four-helix bundle
-
C.T. Choma, J.D. Lear, M.J. Nelson, P.L. Dutton, D.E. Robertson and W.F. DeGrado (1994). Design of a heme-binding four-helix bundle. J. Am. Chem. Soc. 116, 856-865.
-
(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 856-865
-
-
Choma, C.T.1
Lear, J.D.2
Nelson, M.J.3
Dutton, P.L.4
Robertson, D.E.5
DeGrado, W.F.6
-
132
-
-
0028281579
-
Design and synthesis of multi-haem proteins
-
D.E. Robertson, R.S. Farid, C.C. Moser, J.L. Urbauer, S.E. Mulholland, R. Pidikiti, J.D. Lear, A.J. Wand, W.F. DeGrado and P.D. Dutton (1994). Design and synthesis of multi-haem proteins. Nature 368, 425-432.
-
(1994)
Nature
, vol.368
, pp. 425-432
-
-
Robertson, D.E.1
Farid, R.S.2
Moser, C.C.3
Urbauer, J.L.4
Mulholland, S.E.5
Pidikiti, R.6
Lear, J.D.7
Wand, A.J.8
DeGrado, W.F.9
Dutton, P.D.10
-
133
-
-
84936887577
-
A dibenzofuran-based amino acid designed to nuleate antiparallel β-sheet structure: Evidence for intramolecular hydrogen-bond formation
-
H. Diaz, J.R. Espina and J.W. Kelly (1992). A dibenzofuran-based amino acid designed to nuleate antiparallel β-sheet structure: evidence for intramolecular hydrogen-bond formation. J. Am. Chem. Soc. 114, 8316-8318.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 8316-8318
-
-
Diaz, H.1
Espina, J.R.2
Kelly, J.W.3
-
134
-
-
0024574972
-
Helichrome: Synthesis and enzymatic activity of a designed hemeprotein
-
T. Sasaki and E.T Kaiser (1989). Helichrome: synthesis and enzymatic activity of a designed hemeprotein. J. Am. Chem. Soc. 111, 380-381.
-
(1989)
J. Am. Chem. Soc.
, vol.111
, pp. 380-381
-
-
Sasaki, T.1
Kaiser, E.T.2
-
135
-
-
84986364653
-
The construction of new proteins. Part III. Artificial folding units by assembly of amphiphilic secondary structures on a template
-
94
-
M. Mutter, E. Altmann, K.-H. Altmann, R. Hersperger, P. Koziej, K. Nebel, G. Tuchscherer and S. Vuilleumier (1988). 94. The construction of new proteins. Part III. Artificial folding units by assembly of amphiphilic secondary structures on a template. Helv. Chim. Acta 71, 835-847.
-
(1988)
Helv. Chim. Acta
, vol.71
, pp. 835-847
-
-
Mutter, M.1
Altmann, E.2
Altmann, K.-H.3
Hersperger, R.4
Koziej, P.5
Nebel, K.6
Tuchscherer, G.7
Vuilleumier, S.8
-
136
-
-
0009673779
-
Synthetic protein with a new three-dimensional architecture
-
G.R. Marshall, Ed., ESCOM, Leiden
-
M. Mutter. Synthetic protein with a new three-dimensional architecture, in: Peptides. Chemistry and Biology, G.R. Marshall, Ed., p. 349-353, ESCOM, Leiden, 1988.
-
(1988)
Peptides. Chemistry and Biology
, pp. 349-353
-
-
Mutter, M.1
-
138
-
-
0026942147
-
Molecular dynamics conformational search of six cyclic peptides used in the template assembled synthetic protein approach for protein de novo design
-
R. Floegel and M. Mutter (1992). Molecular dynamics conformational search of six cyclic peptides used in the template assembled synthetic protein approach for protein de novo design. Biopolymers 32, 1283-1310.
-
(1992)
Biopolymers
, vol.32
, pp. 1283-1310
-
-
Floegel, R.1
Mutter, M.2
-
139
-
-
0000439676
-
Convenient total synthesis of a 4-helix TASP molecule by the chemoselective ligation
-
P.E. Dawson and S.B.H. Kent (1993). Convenient total synthesis of a 4-helix TASP molecule by the chemoselective ligation. J. Am. Chem. Soc. 115, 7263-7266.
-
(1993)
J. Am. Chem. Soc.
, vol.115
, pp. 7263-7266
-
-
Dawson, P.E.1
Kent, S.B.H.2
-
140
-
-
0027195926
-
The TASP concept: Mimetics of peptide ligands, protein surfaces and folding units
-
G. Tuchscherer, B. Dorner, U. Sila, B. Kamber and M. Mutter (1993). The TASP concept: mimetics of peptide ligands, protein surfaces and folding units. Tetrahedron 49, 3559-3575.
-
(1993)
Tetrahedron
, vol.49
, pp. 3559-3575
-
-
Tuchscherer, G.1
Dorner, B.2
Sila, U.3
Kamber, B.4
Mutter, M.5
-
141
-
-
0001334464
-
Template-assembled synthetic proteins with four-helix-bundle topology. Total chemical synthesis and conformational studies
-
M. Mutter, G. Tuchscherer, C. Miller, K.-H. Altmann, R.I. Carey, D.F. Wyss, A.M. Labhardt and J.E. Rivier (1992). Template-assembled synthetic proteins with four-helix-bundle topology. Total chemical synthesis and conformational studies. J. Am. Chem. Soc. 114, 1463-1470.
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 1463-1470
-
-
Mutter, M.1
Tuchscherer, G.2
Miller, C.3
Altmann, K.-H.4
Carey, R.I.5
Wyss, D.F.6
Labhardt, A.M.7
Rivier, J.E.8
-
142
-
-
0029762859
-
Template assembled synthetic proteins (TASP) as functional mimetics of proteins
-
M. Mutter, P. Dumy, P. Garrouste, C. Lehmann, M. Mathieu, C. Peggion, S. Peluso, A. Razaname and G. Tuchscherer (1996). Template assembled synthetic proteins (TASP) as functional mimetics of proteins. Angew. Chem. Int. Ed. Engl. 35, 1482-1485.
-
(1996)
Angew. Chem. Int. Ed. Engl.
, vol.35
, pp. 1482-1485
-
-
Mutter, M.1
Dumy, P.2
Garrouste, P.3
Lehmann, C.4
Mathieu, M.5
Peggion, C.6
Peluso, S.7
Razaname, A.8
Tuchscherer, G.9
-
143
-
-
0025329415
-
Synthesis of a 4-helix bundle-like template-assembled synthetic protein (TASP) by condensation of a protected peptide on a conformationally constrained cyclic carrier
-
I. Ernest, S. Vuilleumier, H. Fritz and M. Mutter (1990). Synthesis of a 4-helix bundle-like template-assembled synthetic protein (TASP) by condensation of a protected peptide on a conformationally constrained cyclic carrier. Tetrahedron Lett. 31, 4015-4018.
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 4015-4018
-
-
Ernest, I.1
Vuilleumier, S.2
Fritz, H.3
Mutter, M.4
-
144
-
-
84987482281
-
Template-assembled synthetic proteins (TASP). Cyclic templates with incorporated turn-inducing mimics
-
I. Ernest, J. Kalvoda, C. Sigel, G. Rihs, H. Fritz, M.J.J. Blommers, F. Raschdorf, E. Francotte and M. Mutter (1993). Template-assembled synthetic proteins (TASP). Cyclic templates with incorporated turn-inducing mimics. Helv. Chim. Acta 76, 1539-1563.
-
(1993)
Helv. Chim. Acta
, vol.76
, pp. 1539-1563
-
-
Ernest, I.1
Kalvoda, J.2
Sigel, C.3
Rihs, G.4
Fritz, H.5
Blommers, M.J.J.6
Raschdorf, F.7
Francotte, E.8
Mutter, M.9
-
145
-
-
0027756777
-
Template assembled synthetic proteins: Condensation of a multifunctional peptide to a topological template via chemoselective ligation
-
G. Tuchscherer (1993). Template assembled synthetic proteins: condensation of a multifunctional peptide to a topological template via chemoselective ligation. Tetrahedron Lett. 34, 8419-8422.
-
(1993)
Tetrahedron Lett.
, vol.34
, pp. 8419-8422
-
-
Tuchscherer, G.1
-
146
-
-
0000021544
-
A chemical method for new proteins. Template associated synthetic proteins (TASP)
-
M. Mutter and S. Vuilleumier (1989). A chemical method for new proteins. Template associated synthetic proteins (TASP). Angew. Chem. 101, 551-592.
-
(1989)
Angew. Chem.
, vol.101
, pp. 551-592
-
-
Mutter, M.1
Vuilleumier, S.2
-
147
-
-
0024560724
-
The construction of new proteins: V. A template-assembled synthetic protein (TASP) containing both a 4-helix bundle and beta-barrel-like structure
-
M. Mutter, R. Hersperger, K. Gubernator and K. Muller (1989). The construction of new proteins: V. A template-assembled synthetic protein (TASP) containing both a 4-helix bundle and beta-barrel-like structure. Proteins 5, 13-21.
-
(1989)
Proteins
, vol.5
, pp. 13-21
-
-
Mutter, M.1
Hersperger, R.2
Gubernator, K.3
Muller, K.4
-
148
-
-
0026723158
-
Design and immunological properties of topographic immunogenic determinants of a protein antigen (LDH-C4) as vaccines
-
P.T. Kaumaya, A.M. VanBuskirk, E. Goldberg and S.K. Pierce (1992). Design and immunological properties of topographic immunogenic determinants of a protein antigen (LDH-C4) as vaccines. J. Biol. Chem. 267, 6338-6346.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 6338-6346
-
-
Kaumaya, P.T.1
Vanbuskirk, A.M.2
Goldberg, E.3
Pierce, S.K.4
-
149
-
-
0028878086
-
A convenient synthesis of cyclic peptides as regioselectively addressable functionalized templates (RAFT)
-
P. Dumy, I.M. Eggleston, S. Cervigni, U. Sila, X. Sun and M. Mutter (1995). A convenient synthesis of cyclic peptides as regioselectively addressable functionalized templates (RAFT). Tetrahedron Lett. 36, 1255-1258.
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 1255-1258
-
-
Dumy, P.1
Eggleston, I.M.2
Cervigni, S.3
Sila, U.4
Sun, X.5
Mutter, M.6
-
150
-
-
17944394280
-
Inhibition of HIV infection by pseudopeptides blocking viral envelope glycoprotein-mediated membrane fusion and cell death
-
C. Callebaut, E. Jacotot, G. Guichard, B. Krust, M. Rey-Cuille, D. Cointe, N. Benkirane, J. Blanco, S. Muller, J. Briand and A.G. Hovanessian (1996). Inhibition of HIV infection by pseudopeptides blocking viral envelope glycoprotein-mediated membrane fusion and cell death. Virology 218, 181-192.
-
(1996)
Virology
, vol.218
, pp. 181-192
-
-
Callebaut, C.1
Jacotot, E.2
Guichard, G.3
Krust, B.4
Rey-Cuille, M.5
Cointe, D.6
Benkirane, N.7
Blanco, J.8
Muller, S.9
Briand, J.10
Hovanessian, A.G.11
-
151
-
-
15144351708
-
Pseudopeptide TASP inhibitors of HIV entry bind specifically to a 95-kDa cell surface protein
-
C. Callebaut, E. Jacotot, B. Krust, G. Guichard, J. Blanco, A. Valenzuela, J. Svab, S. Muller, J.P. Briand and A.G. Hovanessian (1997). Pseudopeptide TASP inhibitors of HIV entry bind specifically to a 95-kDa cell surface protein. J. Biol. Chem. 272, 7159-7166.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 7159-7166
-
-
Callebaut, C.1
Jacotot, E.2
Krust, B.3
Guichard, G.4
Blanco, J.5
Valenzuela, A.6
Svab, J.7
Muller, S.8
Briand, J.P.9
Hovanessian, A.G.10
-
152
-
-
2442749031
-
Template-assisted protein design: Chimeric TASP by chemoselective ligation
-
P.T.P. Kaumaya and R.S. Hodges, Eds, Mayflower Scientific Ltd., Kingswinford
-
S.E. Cervigni, P. Dumy. P.T.P. Kaumaya, M. Mathieu, O. Nyanguile, C. Peggion, A. Razaname, G. Tuchscherer and M. Mutter. Template-assisted protein design: chimeric TASP by chemoselective ligation, in: Peptides, Chemistry, Structure and Biology, P.T.P. Kaumaya and R.S. Hodges, Eds, p. 555-557, Mayflower Scientific Ltd., Kingswinford, 1996.
-
(1996)
Peptides, Chemistry, Structure and Biology
, pp. 555-557
-
-
Cervigni, S.E.1
Dumy, P.2
Kaumaya, P.T.P.3
Mathieu, M.4
Nyanguile, O.5
Peggion, C.6
Razaname, A.7
Tuchscherer, G.8
Mutter, M.9
-
153
-
-
2442727610
-
Conformational studies of RAFT molecules for protein design
-
P.T.P. Kaumaya and R.S. Hodges, Eds, Mayflower Scientific Ltd., Kingswinford
-
P. Dumy, I.M. Eggleston, G. Esposito, S. Nicula and M. Mutter. Conformational studies of RAFT molecules for protein design, in: Peptides: Chemistry, Structure and Biology, P.T.P. Kaumaya and R.S. Hodges, Eds, p. 605-606, Mayflower Scientific Ltd., Kingswinford, 1996.
-
(1996)
Peptides: Chemistry, Structure and Biology
, pp. 605-606
-
-
Dumy, P.1
Eggleston, I.M.2
Esposito, G.3
Nicula, S.4
Mutter, M.5
-
154
-
-
0030249565
-
Solution structure of regioselectively addressable functionalized templates: An NMR and restrained molecular dynamics investigation
-
P. Dumy, I.M. Eggleston, G. Esposito, S. Nicula and M. Mutter (1996). Solution structure of regioselectively addressable functionalized templates: an NMR and restrained molecular dynamics investigation. Biopolymers 39, 297-308.
-
(1996)
Biopolymers
, vol.39
, pp. 297-308
-
-
Dumy, P.1
Eggleston, I.M.2
Esposito, G.3
Nicula, S.4
Mutter, M.5
|