H. Rink

发表

Pulse Fourier transform water suppression and underwater decoupling in aqueous solutions

G. Matson, J. D. Cutnell, G. N. Mar, 1980 .

Radiolabeled Bicyclic Somatostatin-Based Analogs: A Novel Class of Potential Radiotracers for SPECT/PET of Neuroendocrine Tumors

J. Reubi, G. Nicolas, H. Maecke, 2010, The Journal of Nuclear Medicine.

Changes in interactions in complexes of hirudin derivatives and human α‐thrombin due to different crystal forms

M. Grütter, J. Priestle, J. Rahuel, 1993, Protein science : a publication of the Protein Society.

A new peptidic somatostatin agonist with high affinity to all five somatostatin receptors.

J. Reubi, B. Waser, H. Mäcke, 2002, European journal of pharmacology.

‘Antiflammins’: Two nonapeptide fragments of uteroglobin and lipocortin I have no phospholipase A2 ‐inhibitory and anti‐inflammatory activity

J. Pfeilschifter, H. Rink, I. Wiesenberg, 1990, FEBS letters.

High-field 1H NMR studies of synthetic analogs of somatostatin. Structural features involving aromatic residues in an active eight-membered ring analog.

J. D. Cutnell, P. Hug, G. L. La Mar, 1982, Biochimica et biophysica acta.

Glycopeptide solid-phase synthesis with an acetic acid-labile trialkoxy-benzhydryl linker

B. Ernst, H. Rink, 1991 .

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.

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

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

Solid-phase synthesis of protected peptide fragments using a trialkoxy-diphenyl-methylester resin.

H. Rink, 1987 .

Synthesis of 3-Adenyl- and 3-Thyminylcyclobutane-1,1-dimethanols and Their Homo-octameric Phosphodiesters

J. Henlin, H. Rink, G. Baschang, 1992 .

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

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

Synthesis of 3-Adenyl- and 3-Thyminylcyclobutane-1,1-dimethanols and Their Homo-Octameric Phosphodiesters.

J. Henlin, H. Rink, G. Baschang, 1992 .

A new combination of protecting groups and links for encoded synthetic libraries suited for consecutive tests on the solid phase and in solution

E. Felder, G. Heizmann, H. Rink, 1996, Molecular Diversity.

New Pansomatostatin Ligands and Their Chelated Versions: Affinity Profile, Agonist Activity, Internalization, and Tumor Targeting

S. Schulz, J. Reubi, Hanwen Zhang, 2008, Clinical Cancer Research.

The structural elements of hirudin which bind to the fibrinogen recognition site of thrombin are exclusively located within its acidic C‐terminal tail

Jui-Yoa Chang, H. Rink, J. Schlaeppi, 1990, FEBS letters.

Preparation of monoclonal antibodies to hirudin and hirudin peptides

Jui-Yoa Chang, S. Vekemans, H. Rink, 1990 .

Central actions of somatostatin.

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

New Pansomatostatin Ligands and Their Chelated Versions: Affinity Profile, Agonist Activity, Internalization, and Tumor Targeting

S. Schulz, J. Reubi, Hanwen Zhang, 2008, Clinical Cancer Research.

Procalcitonin NH2‐terminal cleavage peptide has no mitogenic effect on normal human osteoblast‐like cells

B. Riggs, C. Hassager, T. Spelsberg, 1991, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Analysis of synthetic peptides using matrix-assisted laser desorption ionization mass spectrometry.

M. Mutter, K. O. Börnsen, H. Rink, 1992, Peptide research.

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

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

Contributions from hydration of carboxylate groups to the spectrum of water-polypeptide proton-proton Overhauser effects in aqueous solution

K. Wüthrich, G. Otting, E. Liepinsh, 1993, Journal of biomolecular NMR.