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Results 1 to 25 of 203252

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Selective isolation of tryptophan-containing peptides by hydrophobicity modulationSASAGAWA, T; TITANI, K; WALSH, K. A et al.Analytical biochemistry. 1983, Vol 134, Num 1, pp 224-229, issn 0003-2697Article

Modification of the disulphide bridge in cyclic melanotropinsLEBL, M; CODY, W. L; WILKES, B. C et al.Collection of Czechoslovak chemical communications. 1984, Vol 49, Num 11, pp 2680-2688, issn 0010-0765Article

Simple, rapid method for converting a peptide from one salt form to anotherGABRIEL, T. F.International journal of peptide & protein research. 1987, Vol 30, Num 1, pp 40-43, issn 0367-8377Article

Secretion of endothelin and related peptides from renal epithelial cell linesSHICHIRI, M; HIRATA, Y; EMORI, T et al.FEBS letters. 1989, Vol 253, Num 1-2, pp 203-206, issn 0014-5793, 4 p.Article

Peptide deformylase as biocatalyst for the synthesis of enantiomerically pure amino acid derivativesSONKE, Theo; KAPTEIN, Bernard; WAGNER, A. F et al.Journal of molecular catalysis. B, Enzymatic. 2004, Vol 29, Num 1-6, pp 265-277, issn 1381-1177, 13 p.Conference Paper

A novel strategy to mimic discontinuous protective epitopes using a synthetic scaffoldHIJNEN, Marcel; VAN ZOELEN, Dirk J; CHAMORRO, Cristina et al.Vaccine. 2007, Vol 25, Num 37-38, pp 6807-6817, issn 0264-410X, 11 p.Article

N-terminal pro-C-type natriuretic peptide, but not C-type natriuretic peptide, is greatly elevated in the fetal circulation. CommentaryPRICKETT, Timothy C. R; KAAJA, Risto J; NICHOLLS, M. Gary et al.Clinical science (1979). 2004, Vol 106, Num 5, pp 449-450, issn 0143-5221, 8 p.Article

Novel peptide fragments originating from PGLa and the caerulein and xenopsin precursors from Xenopus laevisGIBSON, B. W; POULTER, L; WILLIAMS, D. H et al.The Journal of biological chemistry (Print). 1986, Vol 261, Num 12, pp 5341-5349, issn 0021-9258Article

Will new generations of modified antimicrobial peptides improve their potential as pharmaceuticals?BROGDEN, Nicole K; BROGDEN, Kim A.International journal of antimicrobial agents (Print). 2011, Vol 38, Num 3, pp 217-225, issn 0924-8579, 9 p.Article

Nomenclature and symbolism for amino acids and peptidesPure and applied chemistry. 1984, Vol 56, Num 5, pp 595-623, issn 0033-4545Article

Infusion of a novel peptide, PHI, in man. Pharmacokinetics and effect on gastric secretionALLEN, J. M; CHRISTOFIDES, N. D; GORNACZ, G et al.Experientia. 1983, Vol 39, Num 10, pp 1129-1131, issn 0014-4754Article

GlutathioneMEISTER, A; ANDERSON, M. E.Annual review of biochemistry. 1983, Vol 52, pp 711-760, issn 0066-4154Article

Conotoxin MI: disulfide bonding and conformational statesGRAY, W. R; RIVIER, J. E; GALYEAN, R et al.The Journal of biological chemistry (Print). 1983, Vol 258, Num 20, pp 12247-12251, issn 0021-9258Article

The effect of some structural changes in the molecule of vasopressin on the duration of antidiuretic actionBARTH, T; HRBAS, P; SKOPKOVA, J et al.Collection of Czechoslovak chemical communications. 1984, Vol 49, Num 1, pp 137-140, issn 0010-0765Article

Synthese cyclischer und cyclisch verzweigter Tachykinin-Teilsequenzen. III: Darstellung von cyclo-[11-(S-carboxymethyl-L-homocystein)-Substanz P(6-11)-Hexapeptid] und zwei ringerweiterten Analoga = Synthèse de séquences cycliques et branchées cycliquement de la tachykinine. III: Synthèse de l'hexapeptide cyclo-[(S-carboxyméthyl-L-homocystéine)-11 substance P(6-11)] et de deux analogues au cycle élargi = Synthesis of cyclic and cyclically branched tachykinine partial sequences. III: Synthesis of the cyclo-[11-(S-carboxymethyl-L-homocystein)-substance P(6-11)-hexapeptide] and of two ring-expanded analoguesNEUBERT, K; HARTRODT, B; BERGER, E et al.Pharmazie. 1985, Vol 40, Num 9, pp 617-622, issn 0031-7144Article

Synthesis of cyclic and acyclic partial retro-inverso modified enkephalinsBERMAN, J. M; GOODMAN, M.International journal of peptide & protein research. 1984, Vol 23, Num 6, pp 610-620, issn 0367-8377Article

Synthese cyclischer und cyclisch-verzweigter Tachykinin-Teilsequenzen. I: Darstellung des homodet-cyclischen Eledoisin(6―11)-hexapeptides = Synthèse de séquences cycliques de la tachykinine. I: Préparation de l'hexapeptide cyclique homodet élédoisine (6-11) = Synthesis of cyclic and cyclically branched tachykinine partial sequences. I: Synthesis of the homodet-cyclic eledoisin (6-11) hexapeptideNEUBERT, K; BERGMANN, J; MANSFELD, J et al.Pharmazie. 1985, Vol 40, Num 7, pp 456-459, issn 0031-7144Article

High-molecular weight kininogen: a secreted platelet proteinSCHMAIER, A. H; ZUCKERBERG, A; SILVERMAN, C et al.The Journal of clinical investigation. 1983, Vol 71, Num 5, pp 1477-1489, issn 0021-9738Article

Les Dermaseptines : Pionniers pour de nouveaux agent anti-infectieuxZAIRI, Amira; HANI, Khaled.MHA (Sousse). 2007, Vol 19, Num 55, pp 10-18, issn 0330-8030, 9 p.Article

Proceedings/International symposium on opioid peptides in the periphery, Rome, Italy, May 23-25, 1984FRAIOLI, F; ISIDORI, A; MAZZETTI, M et al.Developments in neuroscience. 1984, Vol 18, issn 0165-7003, IX-298 pConference Proceedings

Dendroaspis natriuretic peptide is the most potent natriuretic peptide to cause relaxation of lower esophageal sphincterHUANG, Shih-Che.Regulatory peptides. 2011, Vol 167, Num 2-3, pp 246-249, issn 0167-0115, 4 p.Article

Polypeptide aptamer selection using a stabilized ribosome displayWEI WANG; SHUTA HART; MINGZHE LIU et al.Journal of bioscience and bioengineering. 2011, Vol 112, Num 5, pp 515-517, issn 1389-1723, 3 p.Article

Synthesis of cyclic peptides by solid phase methodologyLEBL, M; HRUBY, V. J.Tetrahedron letters. 1984, Vol 25, Num 20, pp 2067-2068, issn 0040-4039Article

Converting Peptides into Drug Leads by LipidationZHANG, L; BULAJ, G.Current medicinal chemistry. 2012, Vol 19, Num 11, pp 1602-1618, issn 0929-8673, 17 p.Article


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