B. Peschke

发表

2-(4-alkylpiperazin-1-yl)quinolines as a new class of imidazole-free histamine H3 receptor antagonists.

K. Rimvall, F. Zaragoza, H. Stephensen, 2005, Journal of medicinal chemistry.

Hypertension is associated with hyperlipidemia, coronary heart disease and chronic graft failure in kidney transplant recipients.

H. Geiger, B. Peschke, H. Kachel, 1999, Clinical nephrology.

Lipoproteins and apolipoproteins during the progression of chronic renal disease.

W. März, P. Grützmacher, W. Schoeppe, 1988, Nephron.

Preliminary Evaluation of the Effects of Cold Atmospheric PlasmaApplication Rate on the Proliferation Behavior of Keratinocytes In VitroMeasured Using CK-5, CK-10, CK-14, Ki-67 and p53 Expression

A. Kramer, J. Lademann, B. Hartmann, 2016 .

A novel B-domain O-glycoPEGylated FVIII (N8-GP) demonstrates full efficacy and prolonged effect in hemophilic mice models.

L. Thim, H. Rahbek-Nielsen, E. Persson, 2013, Blood.

THROMBOSIS AND HEMOSTASIS A novel B-domain O-glycoPEGylated FVIII ( N 8-GP ) demonstrates full ef fi cacy and prolonged effect in hemophilic mice models

L. Thim, H. Rahbek-Nielsen, E. Persson, 2013 .

The Pinene Path to Taxanes. 4. Approaches to Taxol and Taxol Analogs through Elaboration of Aromatic C-Ring Precursors.

D. B. Rawlins, P. Wender, T. Glass, 1996, The Journal of organic chemistry.

Early changes of plasma lipid status and glucose tolerance during the course of chronic renal failure.

P. Grützmacher, W. Schoeppe, B. Peschke, 1984, Contributions to nephrology.

Increase of Neuronal Histamine in Obese Rats Is Associated with Decreases in Body Weight and Plasma Triglycerides

H. H. Refsgaard, K. Rimvall, V. Golozoubova, 2006, Obesity.

efficacy and prolonged effect in hemophilic mice models A novel B-domain O-glycoPEGylated FVIII (N8-GP) demonstrates full

H. Rahbek-Nielsen, P. Johansen, F. Rode, 2013 .

TYPE III HYPERLIPOPROTEINEMIA ACQUIRED BY LIVER TRANSPLANTATION

E. Scheuermann, W. Schoeppe, W. Gross, 1993, Transplantation.

Pharmacological characterisation of a new oral GH secretagogue, NN703.

K. Raun, T. Hansen, M. Ankersen, 1999, European journal of endocrinology.

The influence of conformational restriction in the C-terminus of growth hormone secretagogues on their potency.

K. Raun, T. Hansen, M. Ankersen, 2002, European journal of medicinal chemistry.

New highly potent dipeptidic growth hormone secretagogues with low molecular weight.

K. Raun, T. Hansen, M. Ankersen, 2000, European journal of medicinal chemistry.

New growth hormone secretagogues: C-terminal modified sulfonamide-analogues of NN703.

B. S. Hansen, B. Peschke, 1999, Bioorganic & medicinal chemistry letters.

A new series of highly potent growth hormone-releasing peptides derived from ipamorelin.

K. Raun, K. Madsen, H. Thøgersen, 1998, Journal of medicinal chemistry.

Aminomethylthiophene‐2‐carboxylic Acids as Dipeptide Mimetic in New Growth Hormone Secretagogues.

K. Madsen, N. L. Johansen, B. S. Hansen, 1997 .

Investigation of Bioisosteres of the Growth Hormone Secretagogue L‐692, 429.

T. Hansen, M. Ankersen, B. S. Hansen, 1997 .

INVESTIGATION OF BIOISOSTERS OF THE GROWTH HORMONE SECRETAGOGUE L-692,429.

T. Hansen, M. Ankersen, B. S. Hansen, 1997 .

Synthesis of amino alcohols on solid support via sulfonium-ion mediated Darzens reaction

J. Breinholt, B. Peschke, Joan Gredal Bundgaard, 2001 .

Antagonistic targeting of the histamine H3 receptor decreases caloric intake in higher mammalian species.

S. Hastrup, B. Hansen, K. Rimvall, 2007, Biochemical pharmacology.

Design, synthesis and biological activity of novel peptidyl benzyl ketone FVIIa inhibitors.

D. Tanner, M. Storgaard, F. Zaragoza, 2011, Bioorganic & medicinal chemistry letters.

A vinyl sulfone/vinyl sulfoxide based route to C(6)–;C(7) methylene-bridged derivatives of estradiol

M. Thiel, H. Künzer, B. Peschke, 1996 .

The pinene path to taxol: Readily accessible a-ring building blocks based on novel alkyl- and alkenyllithium reagents with internal carbonyl groups

D. B. Rawlins, L. Wessjohann, P. Wender, 1995 .

Cinnamic amides of (S)-2-(aminomethyl)pyrrolidines are potent H3 antagonists.

H. H. Refsgaard, D. Viuff, I. Pettersson, 2004, Bioorganic & medicinal chemistry.

Diastereo‐ and enantioselective synthesis of 1,2:5,6‐diepoxy‐4‐hydroxyalkyl carbamates. – regioselective ring opening and their transformation into doubly C‐branched deoxy sugar analogues

B. Peschke, D. Hoppe, J. Lüßmann, 1992 .

Microbial metabolism of quinoline and related compounds. X. The molybdopterin cofactors of quinoline oxidoreductases from Pseudomonas putida 86 and Rhodococcus spec. B1 and of xanthine dehydrogenase from Pseudomonas putida 86.

F. Lingens, B. Peschke, B. Tshisuaka, 1991, Biological Chemistry Hoppe-Seyler.

Microbial metabolism of quinoline and related compounds. XII. Isolation and characterization of the quinoline oxidoreductase from Rhodococcus spec. B1 compared with the quinoline oxidoreductase from Pseudomonas putida 86.

F. Lingens, B. Peschke, 1991, Biological chemistry Hoppe-Seyler.

Benzo[b]thiophene-2-carboxamides and benzo[b]furan-2-carboxamides are potent antagonists of the human H3-receptor.

D. Viuff, K. Rimvall, R. Hohlweg, 2006, Bioorganic & medicinal chemistry letters.

Aminomethylthiophene-2-carboxylic acids as dipeptide mimetic in new growth hormone secretagogues

K. Madsen, N. L. Johansen, B. S. Hansen, 1997 .

Antituberculous drugs in kidney transplant recipients treated with cyclosporine.

E. Scheuermann, W. Schoeppe, B. Peschke, 1993, Transplantation.

C-Terminally PEGylated hGH-derivatives.

M. Zundel, K. Madsen, Anja K Pedersen, 2007, Bioorganic & medicinal chemistry.

Second generation anti-HCV test: seroprevalence in hemodialysis patients and blood donors.

E. Scheuermann, W. Schoeppe, S. Seidl, 1992, Transplantation Proceedings.