Startseite UR
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, Wittmann, Hans-Joachim, Hübner, Harald, Gmeiner, Peter, Pockes, Steffen
und Strasser, Andrea
(2021)
Abolishing Dopamine D2long/D3 Receptor Affinity of Subtype-Selective Carbamoylguanidine-Type Histamine H2 Receptor Agonists.
Journal of Medicinal Chemistry 64 (12), S. 8684-8709.
Volltext nicht vorhanden.
, Honisch, Claudia
, Buschauer, Armin, Bernhardt, Günther und Pockes, Steffen
(2021)
Pharmacological characterization of a new series of carbamoylguanidines reveals potent agonism at the H2R and D3R.
European Journal of Medicinal Chemistry 214, S. 113190.
Volltext nicht vorhanden.
, Seibel, Ulla, Buschauer, Armin
und Bernhardt, Günther
(2020)
UR-DEBa242: A Py-5-Labeled Fluorescent Multipurpose Probe for Investigations on the Histamine H3 and H4 Receptors.
Journal of Medicinal Chemistry 63 (10), S. 5297-5311.
Volltext nicht vorhanden.
, Gomez-Lazaro, Maria, Tanaka, Miho, Ozawa, Takeaki, Keller, Max, Lamghari, Meriem, Buschauer, Armin und Bernhardt, Günther
(2020)
Fluorescent H2 Receptor Squaramide-Type Antagonists: Synthesis, Characterization, and Applications.
ACS Medicinal Chemistry Letters 11 (8), S. 1521-1528.
Volltext nicht vorhanden.
, Buschauer, Armin und Bernhardt, Günther
(2020)
Tariquidar-related triazoles as potent, selective and stable inhibitors of ABCG2 (BCRP).
European Journal of Medicinal Chemistry 191.
Volltext nicht vorhanden.
Pockes, Steffen, Wifling, David
, Buschauer, Armin
und Elz, Sigurd
(2019)
Structure‐Activity Relationship of Hetarylpropylguanidines Aiming at the Development of Selective Histamine Receptor Ligands †.
ChemistryOpen 8 (3), S. 285-297.
, Mogilski, Szczepan, Hagenow, Stefanie
, Kuder, Kamil, Głuch-Lutwin, Monika
, Siwek, Agata
, Więcek, Małgorzata, Kaleta, Maria, Seibel, Ulla, Buschauer, Armin, Filipek, Barbara, Stark, Holger
und Kieć-Kononowicz, Katarzyna
(2019)
Alkyl derivatives of 1,3,5-triazine as histamine H4 receptor ligands.
Bioorganic & Medicinal Chemistry 27 (7), S. 1254-1262.
Volltext nicht vorhanden.
, Pfleger, Christopher, Kaindl, Jonas, Ibrahim, Passainte, Kling, Ralf C., Buschauer, Armin, Gohlke, Holger und Clark, Timothy
(2019)
Basal Histamine H4Receptor Activation: Agonist Mimicry by the Diphenylalanine Motif.
Chemistry – A European Journal 25 (64), S. 14613-14624.
Volltext nicht vorhanden.
, Hübner, H., Gmeiner, P. und Wegener, Joachim
(2019)
Increasing the throughput of label-free cell assays to study the activation of G-protein-coupled receptors by using a serial agonist exposure protocol.
Integrative Biology 11 (3), S. 99-108.
Volltext nicht vorhanden.
und Bernhardt, Günther
(2019)
[3H]UR-DEBa176: A 2,4-Diaminopyrimidine-Type Radioligand Enabling Binding Studies at the Human, Mouse, and Rat Histamine H4 Receptors.
Journal of Medicinal Chemistry 62 (17), S. 8338-8356.
Volltext nicht vorhanden.
Littmann, Timo, Ozawa, Takeaki, Hoffmann, Carsten, Buschauer, Armin und Bernhardt, Günther
(2018)
A split luciferase-based probe for quantitative proximal determination of Gαq signalling in live cells.
Scientific Reports 8 (17179), S. 1-10.
, Bernhardt, Günther, Plank, Nicole, Littmann, Timo, Schmidt, Peter, Yi, Cuiying, Li, Beibei, Ye, Sheng, Zhang, Rongguang, Xu, Bo, Larhammar, Dan, Stevens, Raymond C.
, Huster, Daniel, Meiler, Jens, Zhao, Qiang, Beck-Sickinger, Annette G., Buschauer, Armin und Wu, Beili
(2018)
Structural basis of ligand binding modes at the
Pockes, Steffen
, Wifling, David
, Keller, Max, Buschauer, Armin
und Elz, Sigurd
(2018)
Highly Potent, Stable, and Selective Dimeric Hetarylpropylguanidine-Type Histamine H2 Receptor Agonists.
ACS Omega 2018 (3), S. 2865-2882.
Littmann, Timo, Ozawa, Takeaki, Hoffmann, Carsten, Buschauer, Armin
und Bernhardt, Günther
(2018)
A split luciferase-based probe for quantitative proximal determination of Gαq signalling in live cells.
Scientific Reports 8 (1), S. 17179.
, Baumeister, Paul, Buschauer, Armin, Hofmann, Dagmar, Heinrich, Markus R., Clark, Timothy und Tschammer, Nuska
(2018)
Molecular Mechanisms of Biased and Probe-Dependent Signaling at CXC-Motif Chemokine Receptor CXCR3 Induced by Negative Allosteric Modulators.
Molecular Pharmacology 93 (4), S. 309-322.
Volltext nicht vorhanden.
, Zechner, Melanie, Taylor, Nicholas M. I.
, Bause, Manuel, Bauer, Stefanie, Bartholomaeus, Ruben, Bernhardt, Günther, König, Burkhard
, Buschauer, Armin, Stahlberg, Henning
, Altmann, Karl-Heinz und Locher, Kaspar P.
(2018)
Structural basis of small-molecule inhibition of human multidrug transporter ABCG2.
Nature Structural & Molecular Biology 25 (4), S. 333-340.
Volltext nicht vorhanden.
, König, Burkhard
und Ochoa-Puentes, Cristian
(2018)
Tariquidar-Related Chalcones and Ketones as ABCG2 Modulators.
ACS Medicinal Chemistry Letters 9, S. 854-859.
Volltext nicht vorhanden.
, Baumeister, Paul, Bernhardt, Günther und Buschauer, Armin
(2017)
Fluorescence- and radio-labeling of Lys4,Nle17,30hPP yields molecular tools for the NPY Y4 receptor.
Bioconjugate Chemistry.
Volltext nicht vorhanden.
, Maschauer, Simone, Brennauer, Albert, Tripal, Philipp, Koglin, Norman, Dittrich, Ralf, Bernhardt, Günther, Kuwert, Torsten, Wester, Hans-Jürgen, Buschauer, Armin
und Prante, Olaf
(2017)
Prototypic 18F-Labeled Argininamide-Type Neuropeptide Y Y1R Antagonists as Tracers for PET Imaging of Mammary Carcinoma.
ACS Medicinal Chemistry Letters 8, S. 304-309.
Volltext nicht vorhanden.
Kuhn, Kilian K., Littmann, Timo, Dukorn, Stefanie, Tanaka, Miho, Keller, Max, Ozawa, Takeaki, Bernhardt, Günther und Buschauer, Armin
(2017)
In Search of NPY Y4R Antagonists: Incorporation of Carbamoylated Arginine, Aza-Amino Acids, or d-Amino Acids into Oligopeptides Derived from the C-Termini of the Endogenous Agonists.
ACS Omega 2 (7), S. 3616-3631.
und Buschauer, Armin
(2016)
High affinity agonists of the neuropeptide Y (NPY) Y4 receptor derived from the C-terminal pentapeptide of human pancreatic polypeptide (hPP): synthesis, stereochemical discrimination and radiolabeling.
Journal of Medicinal Chemistry 59 (13), S. 6045-6058.
Volltext nicht vorhanden.
und Buschauer, Armin
(2016)
Flavonoid derivatives as selective ABCC1 modulators: Synthesis and functional characterization.
European Journal of Medicinal Chemistry 109, S. 124-133.
Volltext nicht vorhanden.
, Wifling, David, Svobodova, Jaroslava, Bernhardt, Günther, Cabrele, Chiara
, Vanderheyden, Patrick, Gmeiner, Peter
und Buschauer, Armin
(2016)
Mimicking of arginine by functionalized Nω-carbamoylated arginine as a new broadly applicable approach to labeled bioactive peptides: high affinity angiotensin, neuropeptide Y, neuropeptide FF and neurotensin receptor ligands as examples.
Journal of Medicinal Chemistry 59 (5), S. 1925-1945.
Volltext nicht vorhanden.
, Buschauer, Armin, Neumann, Detlef
und Seifert, Roland
(2015)
Flow cytometric analysis with a fluorescent formyl peptide receptor ligand as a new method to study the pharmacological profile of the histamine H2-receptor.
Naunyn Schmiedebergs Archives of Pharmacology 388 (10), S. 1039-1052.
Volltext nicht vorhanden.
Wifling, David
, Bernhardt, Günther, Dove, Stefan und Buschauer, Armin
(2015)
The extracellular loop 2 (ECL2) of the human histamine H4 receptor substantially contributes to ligand binding and constitutive activity.
PLoS One 10 (1), S. 1-14.
Orlando, Zoya, Lengers, Isabelle, Melzig, Matthias F., Buschauer, Armin, Hensel, Andreas und Jose, Joachim
(2015)
Autodisplay of human hyaluronidase Hyal-1 on Escherichia coli and identification of plant-derived enzyme inhibitors.
Molecules 20 (9), S. 15449-15468.
Huber, Stefan, Huettner, Johannes Philip, Hacker, Kristina, Bernhardt, Günther, König, Jörg
und Buschauer, Armin
(2015)
Esters of bendamustine are by far more potent cytotoxic agents than the parent compound against human sarcoma and carcinoma cells.
PLoS One 10 (7), PLoSe0133743.
(2015)
Histamine H1- and H4-receptor signaling cooperatively regulate MAPK activation.
Biochemical Pharmacology 98 (3), S. 432-439.
Volltext nicht vorhanden.
, Bernhardt, Günther, Buschauer, Armin und Read, Roger W.
(2015)
M2 subtype preferring dibenzodiazepinone-type muscarinic receptor ligands: effect of chemical homo-dimerization on orthosteric (and allosteric?) binding.
Bioorganic & Medicinal Chemistry 23 (14), S. 3970-3990.
Volltext nicht vorhanden.
, Löffel, Karolin, Nordemann, Uwe, Strasser, Andrea, Bernhardt, Günther, Dove, Stefan, Seifert, Roland und Buschauer, Armin
(2015)
Molecular determinants for the high constitutive activity of the human histamine H4 receptor: Functional studies on orthologs and mutants.
British Journal of Pharmacology 172, S. 785-798.
Volltext nicht vorhanden.
, Kuhn, Kilian K., Mollereau, Catherine
, Dukorn, Stefanie, Schindler, Lisa, Bernhardt, Günther, König, Burkhard und Buschauer, Armin
(2015)
N(omega)-carbamoylation of the argininamide moiety: an avenue to insurmountable NPY Y1 receptor antagonists and a radiolabeled selective high affinity molecular tool ([3H]UR-MK299) with extended residence time.
Journal of Medicinal Chemistry 58 (22), S. 8834-8849.
Volltext nicht vorhanden.
, Buschauer, Armin, Holsboer, Florian und Hausch, Felix
(2014)
Loratadine and analogs: Discovery and preliminary SAR of inhibitors of the amino acid transporter B0AT2.
Journal of Medicinal Chemistry 57 (22), S. 9473-9479.
Volltext nicht vorhanden.
, Buschauer, Armin, Witzgall, Ralph
und Göpferich, Achim
(2014)
Biodistribution of quantum dots in the kidney after intravenous injection.
Journal of Nanoscience and Nanotechnology 14 (5), S. 3313-3319.
Volltext nicht vorhanden.
, Buschauer, Armin und Seifert, Roland
(2014)
No evidence for histamine H4-receptor in human monocytes.
Journal of Pharmacology and Experimental Therapeutics 351 (3), S. 519-526.
Volltext nicht vorhanden.
Sadek, Bassem, Alisch, Rudi, Buschauer, Armin und Elz, Sigurd
(2013)
Synthesis and dual histamine H1 and H2 receptor antagonist activity of cyanoguanidine derivatives.
Molecules 18 (11), S. 14186-14202.
, Kaske, Melanie, Gutierrez-Abad, Raquel, Bernhardt, Günther, Illa, Ona
, Ortuño, Rosa, Cabrele, Chiara
, Buschauer, Armin und Reiser, Oliver
(2013)
Replacement of Thr32 and Gln34 in the C-terminal neuropeptide Y fragment 25-36 by cis-cyclobutane- and cis-cyclopentane β-amino acids shifts selectivity toward the Y4 receptor.
Journal of Medicinal Chemistry 56 (21), S. 8422-8431.
Volltext nicht vorhanden.
Nordemann, Uwe, Wifling, David
, Schnell, David, Bernhardt, Günther, Stark, Holger
, Seifert, Roland und Buschauer, Armin
(2013)
Luciferase reporter gene assay on human, murine and rat histamine H4 receptor orthologs: correlations and discrepancies between distal and proximal readouts.
PLoS One 8 (9), e73961.
und Buschauer, Armin
(2013)
Quinoline carboxamide-type ABCG2 modulators: Indole and quinoline moieties as anilide replacements.
ChemMedChem 8 (11), S. 1773-1778.
Volltext nicht vorhanden.
Brunskole Hummel, Irena, Kälble, Solveig, Burhenne, Heike, Reinartz, Michael T., Schwede, Frank, Buschauer, Armin und Seifert, Roland
(2013)
Dissociations in the effects of beta2-adrenergic receptor agonists on cAMP formation and superoxide production in human neutrophils: Support for the concept of functional selectivity.
PLoS One 8 (5), e64556.
(2013)
Benzanilide – Biphenyl Replacement: A Bioisosteric Approach to Quinoline Carboxamide-type ABCG2 Modulators.
ACS Medicinal Chemistry Letters 4 (4), S. 393-396.
Volltext nicht vorhanden.
, Baumeister, Paul, Keller, Max, Bernhardt, Günther und Buschauer, Armin
(2013)
[3H]UR-PLN196: A Selective Nonpeptide Radioligand and Insurmountable Antagonist for the Neuropeptide Y Y2 Receptor.
ChemMedChem 8 (4), S. 587-593.
Volltext nicht vorhanden.
Bodensteiner, Julian, Baumeister, Paul, Geyer, Roland, Buschauer, Armin und Reiser, Oliver
(2013)
Synthesis and pharmacological characterization of new tetrahydrofuran based compounds as conformationally constrained histamine receptor ligands.
Organic & biomolecular chemistry 11 (24), S. 4040-4055.
Memminger, Martin, Keller, Max, Lopuch, Miroslaw, Pop, Nathalie, Bernhardt, Günther, von Angerer, Erwin und Buschauer, Armin
(2012)
The Neuropeptide Y Y1 receptor: a diagnostic marker? Expression in MCF-7 breast cancer cells is down-regulated by antiestrogens in vitro and in xenografts.
PLoS ONE 7 (12), e51032.
, Argiolas, Antonio, Melis, Maria Rosaria und Gmeiner, Peter
(2012)
Novel azulene derivatives for the treatment of erectile dysfunction.
Bioorganic & medicinal chemistry letters 22 (23), S. 7151-7154.
Volltext nicht vorhanden.
, Buschauer, Armin und Seifert, Roland
(2012)
Incomplete activation of human eosinophils via the histamine H4-receptor: Evidence for ligand-specific receptor conformations.
Biochemical Pharmacology 84 (2), S. 192-203.
Volltext nicht vorhanden.
, Heinrich, Markus
, Baumeister, Paul, Buschauer, Armin und Tschammer, Nuska
(2012)
Synthesis and application of the first radioligand targeting the allosteric binding pocket of chemokine receptor CXCR3.
ChemMedChem 7 (8), S. 1481-1489.
Volltext nicht vorhanden.
, Salmen, Sunnhild, Textor, Christian, Bernhardt, Günther, Dove, Stefan und Buschauer, Armin
(2011)
Design of benzimidazole- and benzoxazole-2-thione derivatives as inhibitors of bacterial hyaluronan lyase.
European Journal of Medicinal Chemistry 46 (9), S. 4419-4429.
Volltext nicht vorhanden.
, Bernhardt, Günther, Seifert, Roland und Buschauer, Armin
(2011)
Functional reconstitution of human neuropeptide Y (NPY) Y2 and Y4 receptors in Sf9 insect cells.
Journal of Receptors and Signal Transduction 31 (4), S. 271-285.
Volltext nicht vorhanden.
, Pluym, Nikola, Bernhardt, Günther und Buschauer, Armin
(2011)
Red-fluorescent argininamide-type NPY Y(1) receptor antagonists as pharmacological tools.
Bioorganic & Medicinal Chemistry 19 (9), S. 2859-2878.
Volltext nicht vorhanden.
, Igel, Patrick, Dove, Stefan, Buschauer, Armin und Seifert, Roland
(2011)
Expression and functional properties of canine, rat and murine histamine H4-receptors in Sf9 insect cells.
Naunyn-Schmiedeberg's Archives of Pharmacology 383 (5), S. 457-470.
Volltext nicht vorhanden.
, Dove, Stefan, Brunskole, Irena, Neumann, Detlef
, Strasser, Andrea und Buschauer, Armin
(2011)
Paradoxical stimulatory effects of the “standard” histamine H4-receptor antagonist JNJ7777120: The H4-receptor joins the club of 7TM receptors exhibiting functional selectivity.
Molecular Pharmacology 79 (4), S. 631-638.
Volltext nicht vorhanden.
(2011)
Solid phase synthesis of tariquidar-related modulators of ABC transporters preferring breast cancer resistance protein (ABCG2).
Bioorganic & Medicinal Chemistry Letters 21 (12), S. 3654-3657.
Volltext nicht vorhanden.
(2011)
Synthesis and characterization of DMAP-Modified NPY Y1 receptor antagonists as acyl-transfer catalysts.
Collection of Czechoslovak chemical communications 76 (6), 763 -780.
Volltext nicht vorhanden.
, Cabrele, Chiara
, Keller, Max, Pluym, Nicola
, Buschauer, Armin, Rachel, Reinhard, Tessmar, Joerg
, Breunig, Miriam
und Goepferich, Achim
(2010)
G protein-coupled receptors function as logic gates for nanoparticle binding and cell uptake.
Proceedings of the National Academy of Sciences USA: PNAS 107 (23), S. 10667-10672.
Volltext nicht vorhanden.
(2010)
Conformations, Conformational Preferences, and Conformational Exchange of N'-Substituted N-Acylguanidines: Intermolecular Interactions Hold the Key.
J. Am. Chem. Soc. 132 (32), S. 11223-11233.
Volltext nicht vorhanden.
(2010)
N(G)-Acyl-argininamides as NPY Y (1) receptor antagonists: Influence of structurally diverse acyl substituents on stability and affinity.
Bioorganic & Medicinal Chemistry (18), S. 6292-6304.
Volltext nicht vorhanden.
, Schnell, David, Elz, Sigurd, Seifert, Roland und Buschauer, Armin
(2009)
N(G)-Acylated imidazolylpropylguanidines as potent histamine H4 receptor agonists: selectivity by variation of the N(G)-substituent.
Journal of Medicinal Chemistry 52 (8), S. 2623-2627.
Volltext nicht vorhanden.
, König, Burkhard
und Buschauer, Armin
(2009)
Potent and selective inhibitors of breast cancer resistance protein (ABCG2) derived from the p-glycoprotein (ABCB1) modulator tariquidar.
Journal of Medicinal Chemistry 52 (4), S. 1190-1197.
Volltext nicht vorhanden.
, Beck-Sickinger, Annette G., Bernhardt, Günther und Buschauer, Armin
(2008)
Guanidine - acylguanidine bioisosteric approach in the design of radioligands: Synthesis of a tritium-labeled N(G)-propionylargininamide ([3H]UR-MK114) as a highly potent and selective neuropeptide Y Y1 receptor antagonist.
Journal of Medicinal Chemistry 51 (24), S. 8168-8172.
Volltext nicht vorhanden.
, Schnell, David, Bernhardt, Günther, Dove, Stefan, Zabel, Manfred, Elz, Sigurd, Seifert, Roland und Buschauer, Armin
(2008)
Acylguanidines as bioisosteres of guanidines: N(G)-acylated imidazolylpropylguanidines, a new class of histamine H2 receptor agonists.
Journal of Medicinal Chemistry 51 (22), S. 7193-7204.
Volltext nicht vorhanden.
(2008)
Modular synthesis of non-peptidic bivalent NPY Y(1) receptor antagonists.
Bioorganic & Medicinal Chemistry 16 (22), S. 9858-9866.
Volltext nicht vorhanden.
Preuss, Hendrik, Ghorai, Prasanta, Kraus, Anja, Dove, Stefan, Buschauer, Armin und Seifert, Roland
(2007)
Constitutive Activity and Ligand Selectivity of Human,
Preuss, Hendrik, Ghorai, Prasanta, Kraus, Anja, Dove, Stefan, Buschauer, Armin und Seifert, Roland
(2007)
Mutations of Cys-17 and Ala-271 in the Human Histamine H₂
, Kraus, Anja, Cabrele, Chiara
, Beck-Sickinger, Annette G., Bernhardt, Günther und Buschauer, Armin
(2007)
Determination of affinity and activity of ligands at the human neuropeptide Y Y4 receptor by flow cytometry and aequorin luminescence.
Journal of Receptors and Signal Transduction 27 (4), S. 217-233.
Volltext nicht vorhanden.
Xie, Sheng-Xue, Schalkhausser, Fabian, Ye, Qi-Zhuang, Seifert, Roland und Buschauer, Armin
(2007)
Effects of Impromidine- and Arpromidine-Derived Guanidines on Recombinant Human and Guinea Pig Histamine H₁ and H₂ Receptors.
Archiv der Pharmazie 340 (1), S. 9-16.
, Keller, Max, Brennauer, Albert, Hoefelschweiger, Bianca K., Gross, Dietmar, Wolfbeis, Otto S.
, Bernhardt, Günther und Buschauer, Armin
(2007)
Synthesis and Characterization of the First Fluorescent Nonpeptide NPY Y1 Receptor Antagonist.
ChemBioChem 8 (16), S. 1981-1988.
Zugang zum Volltext eingeschränkt.
(2007)
Tariquidar analogues: synthesis by Cu(I)-catalysed N/O–aryl coupling and inhibitory activity against the ABCB1 transporter.
European Journal of Organic Chemistry 2007 (16), S. 2643-2649.
Volltext nicht vorhanden.
, Götte, Carsten, Buschauer, Armin, Benincori, Tiziana
und Reiser, Oliver
(2006)
Enantioselective hydrogenation of diaryl-substituted a,b-unsaturated nitriles.
Tetrahedron Letters 47 (22), S. 3733-3736.
Volltext nicht vorhanden.
, Mayer, Matthias, Ziemek, Ralf, Li, Liantao, Hutzler, Christoph
, Bernhardt, Günther und Buschauer, Armin
(2006)
A Simple and Powerful Flow Cytometric Method for the Simultaneous Determination of Multiple Parameters at G-Protein-coupled Receptor Subtypes.
ChemBioChem 7 (9), S. 1400-1409.
Volltext nicht vorhanden.
, Botzki, Alexander
, Nukui, Masatoshi, Mewbourne, R. Brandon, Lamani, Ejvis, Braun, Stephan, von Angerer, Erwin, Bernhardt, Günther, Dove, Stefan, Buschauer, Armin und Jedrzejas, Mark J.
(2006)
Design of new benzoxazole-2-thione derived inhibitors of Streptococcus pneumoniae hyaluronan lyase: structure of a complex with a 2-phenylindole.
Glycobiology 16 (8), S. 757-765.
Volltext nicht vorhanden.
, Ye, Qi-Zhuang, Bernhardt, Günther, Seifert, Roland und Buschauer, Armin
(2006)
Synthesis and pharmacological characterization of novel fluorescent histamine H2-receptor ligands derived from aminopotentidine.
Bioorganic & Medicinal Chemistry Letters 16 (15), S. 3886-3890.
Volltext nicht vorhanden.
(2004)
Functional Expression of the Interleukin-11 Receptor α-Chain and Evidence of Antiapoptotic Effects in Human Colonic Epithelial Cells.
The Journal of Biological Chemistry 279 (11), S. 10304-10315.
Volltext nicht vorhanden.
, Rigden, Daniel J.
, Braun, Stephan, Nukui, Masatoshi, Salmen, Sunnhild, Hoechstetter, Julia, Bernhardt, Günther, Dove, Stefan, Jedrzejas, Mark J. und Buschauer, Armin
(2004)
l-Ascorbic Acid 6-Hexadecanoate, a Potent Hyaluronidase Inhibitor.
Journal of Biological Chemistry 279 (44), S. 45990-45997.
Volltext nicht vorhanden.
, Schreiber, Elvira, Bernhardt, Günther, Peng, Shiqi und Buschauer, Armin
(2003)
Preparation of fluorescent nonpeptidic neuropeptide Y receptor ligands: analogues of the quinazoline-type anti-obesity Y5 antagonist CGP 71683A.
Arch Pharm (Weinheim) 336 (12), S. 585-590.
Volltext nicht vorhanden.
, Bernhardt, Günther
, Buschauer, Armin
, Jauch, Karl-Walter und Zirngibl, Hubert
(2002)
Erratum to “High-Resolution Reversed-Phase High-Performance Liquid Chromatography Analysis of Polyamines and Their Monoacetyl Conjugates by Fluorescence Detection after Derivatization with N-Hydroxysuccinimidyl 6-Quinolinyl Carbamate” [Anal. Biochem. 247 (1997) 294–304].
Analytical Biochemistry 311 (1), S. 100.
Volltext nicht vorhanden.
, Bernhardt, Günther
, Buschauer, Armin
, Jauch, Karl-Walter und Zirngibl, Hubert
(2002)
High-Resolution Reversed-Phase High-Performance Liquid Chromatography Analysis of Polyamines and Their Monoacetyl Conjugates by Fluorescence Detection after Derivatization withN-Hydroxysuccinimidyl 6-Quinolinyl Carbamate.
Analytical Biochemistry 247 (2), S. 294-304.
Volltext nicht vorhanden.
, Bernhardt, Günther, Buschauer, Armin, Thasler, Wolfgang E., Dolgner, Doris, Zirngibl, Hubert und Jauch, Karl-Walter
(2002)
Polyamine levels of human colorectal adenocarcinomas are correlate with tumor stage and grade,.
International Journal of Colorectal Disease 17 (6), S. 381-387.
Volltext nicht vorhanden.
Fellner, Stephan, Bauer, Björn, Miller, David S., Schaffrick, Martina, Fankhänel, Martina, Spruß, Thilo, Bernhardt, Günther, Graeff, Claudia, Färber, Lothar, Gschaidmeier, Harald, Buschauer, Armin und Fricker, Gert
(2002)
Transport of paclitaxel (Taxol) across the blood-brain barrier in vitro and in vivo.
The Journal of Clinical Investigation 110 (9), S. 1309-1318.
(2002)
Transport of paclitaxel (Taxol) across the blood-brain barrier in vitro and in vivo.
Journal of Clinical Investigation 110 (9), S. 1309-1318.
Volltext nicht vorhanden.
, Spruss, Thilo, Bernhardt, Günther, Buschauer, Armin und Goepferich, Achim
(2001)
Programmable biodegradable implants.
Journal of Controlled Release 73 (1), S. 75-88.
Volltext nicht vorhanden.
, Rau, Franz, Range, Klaus-Jürgen, Krey, Volker, Uffrecht, Anka und Buschauer, Armin
(2000)
Absolute configuration of (-)-4-(3,4-dichlorophenyl)-4-(2-pyridyl)butanoic acid: essential information to determine crucial steric feature of arpromidine-type histamine H_2 receptor agonists.
Acta Crystallographica Section C 56, S. 250-251.
Volltext nicht vorhanden.
, Bernhardt, G., Buschauer, Armin
, Spruss, Thilo, Dolgner, Doris, Jauch, K. W. und Zirngibl, H.
(1997)
An in vitro / in vivo model for studying the role of polyamines in human pancreatic carcinoma.
Gastroenterology 112 (4), A1485.
Volltext nicht vorhanden.
, Bernhardt, Günther, Buschauer, Armin, Jauch, Karl-Walter und Zirngibl, Hubert
(1997)
High-resolution RP HPLC analysis of polyamines and their monoacetyl conjugates by fluorescence detection after derivatization with N-hydroxy-succinimidyl 6-quinolinyl carbamate.
Anal. Biochem 247, S. 294-304.
Volltext nicht vorhanden.
, Heinmoeller, E., Buschauer, Armin
, Bernhardt, Günther
, Gruber, R., Rueschoff, J. und Zirngibl, H.
(1996)
A new HPLC-method for the determination of polyamines (PA) in the subpicomolar range: PA and ornithine-decarboxylase (ODC) in human pancreatic carcinoma cell lines.
European Journal of Cell Biology 69 (42), S. 157.
Volltext nicht vorhanden.
Seifert, Roland, Höer, Ariane, Offermann, Stefan, Buschauer, Armin und Schunack, Walter
(1992)
Histamine increases Ca^2+ in dibutyryl cyclic AMP-differentiated HL-60 cells via H_1-receptors and is an incomplete secretagogue.
Mol. Pharmacol. 42, S. 227-234.
Seifert, Roland, Höer, Ariane, Schwaner, Ingo und Buschauer, Armin
(1992)
Histamine increases cytosolic Ca^2+ in HL-60 promyelocytes predominantly via H_2-receptors with an unique agonist/antagonist profile and induces functional differentiation.
Molecular Pharmacology 42, S. 235-241.
Burde, Rahel, Buschauer, Armin und Seifert, Roland
(1990)
Characterization of histamine H_2-receptors in human neutrophils with a series of guanidine analogues of impromidine: Are cell type-specific H_2-receptors involved in the regulation of NADPH oxidase?
Naunyn-Schmiedeberg's Archives of Pharmacology 341, S. 455-461.
Burde, Rahel, Seifert, Roland, Buschauer, Armin und Schultz, Günther
(1989)
Histamine inhibits activation of human neutrophils and HL-60 leukemic cells via H_2-receptors.
Naunyn-Schmiedeberg's archives of pharmacology 340, S. 671-678.
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