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Gunnar Lindeberg

Observed names: G LINDEBERG, G Lindeberg, G. LINDEBERG, G. Lindeberg, GUNNAR LINDEBERG, Gunnar G. Lindeberg, Lindeberg, Gunnar
Institution: Uppsala University
Observed institutions: Leibniz University Hannover, Uppsala University, Uppsala University Hospital, Université de Sherbrooke, Universität Hamburg, Washington University in St. Louis, ETH Zurich, Allgemeine Gewerbeschule Basel, Max Planck Institute of Biochemistry, Institute of Molecular Biology and Biophysics
OpenAlex ID: A5110620719
The solution conformation of the antibacterial peptide cecropin A: a nuclear magnetic resonance and dynamical simulated annealing study
1988 · Tadeusz A. Holak, Aake Engstroem, et al. · Biochemistry · 283
Identification of functionally important amino acids in the cellulose‐binding domain of Trichoderma reesei cellobiohydrolase I
1995 · Markus Linder, Maija‐Liisa Mattinen, et al. · Protein Science · 218
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Rapid microwave-assisted Suzuki coupling on solid-phase
1996 · Mats Larhed, Gunnar Lindeberg, et al. · Tetrahedron Letters · 188
Vinyl Sulfide Cyclized Analogues of Angiotensin II with High Affinity and Full Agonist Activity at the AT1Receptor
2002 · Petra Johannesson, Gunnar Lindeberg, et al. · Journal of Medicinal Chemistry · 126
The difference in affinity between two fungal cellulose‐binding domains is dominated by a single amino acid substitution
1995 · Markus Linder, Gunnar Lindeberg, et al. · FEBS Letters · 125
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Acyl sulfonamides as potent protease inhibitors of the hepatitis C virus full-Length NS3 (Protease-Helicase/NTPase): A comparative study of different C-terminals
2003 · Anja Johansson, Anton Poliakov, et al. · Bioorganic & Medicinal Chemistry · 113
Three‐dimensional structures of three engineered cellulose‐binding domains of cellobiohydrolase I from Trichoderma reesei
1997 · Maija‐Liisa Mattinen, Maarit Kontteli, et al. · Protein Science · 88
Synthesis and Characterization of a High-Affinity NOTA-Conjugated Bombesin Antagonist for GRPR-Targeted Tumor Imaging
2013 · Zohreh Varasteh, Irina Velikyan, et al. · Bioconjugate Chemistry · 87
Selectivity of Cyclic [d-Nal7] and [d-Phe7] Substituted MSH Analogues for the Melanocortin Receptor Subtypes
1997 · Helgi B Schiöth, Ruta Muceniece, et al. · Peptides · 87
The Effect of Mini-PEG-Based Spacer Length on Binding and Pharmacokinetic Properties of a 68Ga-Labeled NOTA-Conjugated Antagonistic Analog of Bombesin
2014 · Zohreh Varasteh, Ulrika Rosenström, et al. · Molecules · 81
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Isolated fungal cellulose terminal domains and a synthetic minimum analogue bind to cellulose
1989 · Gunnar Johansson, Jerry Ståhlberg, et al. · FEBS Letters · 80
Design, Synthesis, and Biological Activities of Four Angiotensin II Receptor Ligands with γ-Turn Mimetics Replacing Amino Acid Residues 3−5
1997 · Boris Schmidt, Susanna Lindman, et al. · Journal of Medicinal Chemistry · 74
Opiate receptor affinity of peptides related to Leu-enkephalin
1976 · L. Terenius, A. Wahlström, et al. · Biochemical and Biophysical Research Communications · 71
Disulfide Cyclized Tripeptide Analogues of Angiotensin IV as Potent and Selective Inhibitors of Insulin-Regulated Aminopeptidase (IRAP)
2010 · Hanna Andersson, Heidi Demaegdt, et al. · Journal of Medicinal Chemistry · 69
The effect of macrocyclic chelators on the targeting properties of the 68Ga-labeled gastrin releasing peptide receptor antagonist PEG2-RM26
2014 · Zohreh Varasteh, Bogdan Mitran, et al. · Nuclear Medicine and Biology · 64
A Selective AT2 Receptor Ligand with a γ-Turn-Like Mimetic Replacing the Amino Acid Residues 4−5 of Angiotensin II
2004 · Ulrika Rosenström, Christian Sköld, et al. · Journal of Medicinal Chemistry · 60
Phenylglycine as a novel P2 scaffold in hepatitis C virus NS3 protease inhibitors
2006 · Pernilla Örtqvist, Shane D. Peterson, et al. · Bioorganic & Medicinal Chemistry · 53
Binding of cyclic and linear MSH core peptides to the melanocortin receptor subtypes
1997 · Helgi B Schiöth, Ruta Muceniece, et al. · European Journal of Pharmacology · 53
In Vitro and In Vivo Evaluation of a 18F-Labeled High Affinity NOTA Conjugated Bombesin Antagonist as a PET Ligand for GRPR-Targeted Tumor Imaging
2013 · Zohreh Varasteh, Ola Åberg, et al. · PLoS ONE · 51
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Potent Macrocyclic Inhibitors of Insulin-Regulated Aminopeptidase (IRAP) by Olefin Ring-Closing Metathesis
2011 · Hanna Andersson, Heidi Demaegdt, et al. · Journal of Medicinal Chemistry · 51
Structure-activity relationships of vasoactive peptides derived from fibrin or fibrinogen degraded by plasmin
1980 · Makonnen Belew, Bengt Gerdin, et al. · Biochimica et Biophysica Acta (BBA) - Protein Structure · 51
Selection of optimal chelator improves the contrast of GRPR imaging using bombesin analogue RM26
2016 · BOGDAN MITRAN, ZOHREH VARASTEH, et al. · International Journal of Oncology · 45
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New Selective AT2Receptor Ligands Encompassing a γ-Turn Mimetic Replacing the Amino Acid Residues 4−5 of Angiotensin II Act as Agonists
2005 · Ulrika Rosenström, Christian Sköld, et al. · Journal of Medicinal Chemistry · 42
Tetrapeptides as potent protease inhibitors of hepatitis C virus full-Length NS3 (Protease-Helicase/NTPase)
2002 · Anja Johansson, Anton Poliakov, et al. · Bioorganic & Medicinal Chemistry · 42
Immobilized metal ion affinity chromatography of synthetic peptides
1992 · Par Hansen, Gunnar Lindeberg, et al. · Journal of Chromatography A · 41
Works count: 124
Citation count: 3,407
H-index: 33
I10-index: 67
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