P. Sieber

发表

A New Acid-Labile Anchor Group for the Solid-Phase Synthesis of C-Terminal Peptide Amides by the Fmoc Method.

P. Sieber, 1987 .

Synthesis and biological activity of seventeen analogues of human insulin.

M. de Gasparo, P. Sieber, B. Riniker, 1979, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

Revised amino-acid sequences for porcine and human adrenocorticotrophic hormone.

H. Zuber, P. Sieber, B. Riniker, 1972, Nature: New biology.

Synthesis and Biological Activity of Two Disulphide Bond Isomers of Human Insulin: [A7-A11 ,A6-B7-Cystine]- and [A6-A7,A11-B7-Cystine]insulin (Human)

M. de Gasparo, P. Sieber, B. Riniker, 1978, Hoppe-Seyler's Zeitschrift fur physiologische Chemie.

[Structure-activity relationship of human calcitonin. III. Biological activity of synthetic analogues with shortened or terminally modified peptide chains (author's transl)].

P. Sieber, B. Riniker, B. Kamber, 1976, Experientia.

A large fragment approach to DNA synthesis: total synthesis of a gene for the protease inhibitor eglin c from the leech Hirudo medicinalis and its expression in E. coli.

P. Sieber, H. Rink, M. Liersch, 1984, Nucleic acids research.

A new acid-labile anchor group for the solid-phase synthesis of C-terminal peptide amides by the Fmoc method.

P. Sieber, 1987 .

Conversion of NGurethane protected arginine to ornithine in peptide solid phase synthesis

P. Sieber, H. Rink, F. Raschdorf, 1984 .

[Human calcitonin. VI. Synthesis of calcitonin M].

P. Sieber, B. Riniker, W. Rittel, 1970, Helvetica chimica acta.

A General Strategy for the Synthesis of Large Peptides: r1~he Combined Solid-Phase and Solution Approach.

H. Fretz, A. Flörsheimer, P. Sieber, 1993 .

An improved method for anchoring of 9-fluorenylmethoxycarbonyl-amino acids to 4-alkoxybenzyl alcohol resins.

P. Sieber, 1987 .

Total Synthesis of Adrenocorticotrophic Hormone

R. Schwyzer, P. Sieber, 1963, Nature.

The synthesis of cystine peptides by iodine oxidation of s trityl cysteine and s acetamidomethyl cysteine peptides

P. Sieber, B. Riniker, B. Kamber, 1980 .

PROTECTION OF CARBOXAMIDE FUNCTIONS BY THE TRITYL RESIDUE. APPLICATION TO PEPTIDE SYNTHESIS

P. Sieber, B. Riniker, 1991 .

Protection of histidine in peptide synthesis: A Reassessment of the trityl group

P. Sieber, B. Riniker, 1987 .

[Thyrocalcitonin. IV. The total synthesis of alpha-thyrocalcitonin].

P. Sieber, B. Riniker, W. Rittel, 1969, Helvetica chimica acta.

Differences between in-vitro and in-vivo potencies of corticotrophins: an interpretation in terms of metabolic stability.

C. McMartin, P. Sieber, W. Rittel, 1977, The Journal of endocrinology.

Overexpression and Structural Characterization of the Phage T4 Protein DsbA

R. Müller, R. Jaenicke, M. Boehm, 1998, Biological chemistry.

Modification of tryptophan residues during acidolysis of 4-methoxy-2,3,6-trimethylbenzenesulfonyl groups. Effects of scavengers

P. Sieber, 1987 .

Biological activity of synthetic human corticotropin with revised amino acid sequence.

P. Sieber, B. Riniker, W. Rittel, 1974, Acta endocrinologica.

The Scientific Foundations of Consumer Advice : Some Comments

J. Morgan, P. Sieber, 2022 .

Iodine Oxidation of S‐Trityl‐ and S‐Acetamidomethyl‐cysteine‐peptides Containing Tryptophan: Conditions Leading to the Formation of Tryptophan‐2‐thioethers

P. Sieber, B. Riniker, B. Kamber, 1980 .

IODINE OXIDATION OF S‐TRITYL‐ AND S‐ACETAMIDOMETHYLCYSTEINEPEPTIDES CONTAINING TRYPTOPHAN: CONDITIONS LEADING TO THE FORMATION OF TRYPTOPHAN‐2‐THIOETHERS

P. Sieber, B. Riniker, B. Kamber, 1981 .

Central actions of somatostatin.

H. Bittiger, H. Olpe, P. Sieber, 1980, European journal of pharmacology.

Synthesis and biological activity of five d-Cys analogs of human insulin

M. Gasparo, P. Sieber, B. Riniker, 1979 .

CONVERSION OF NG-URETHANE PROTECTED ARGININE TO ORNITHINE IN PEPTIDE SOLID-PHASE SYNTHESIS

P. Sieber, H. Rink, F. Raschdorf, 1984 .