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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 3
2003 1
2004 3
2005 3
2006 4
2007 4
2008 7
2009 15
2010 16
2011 16
2012 11
2013 18
2014 21
2015 14
2016 16
2017 24
2018 19
2019 23
2020 19
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208 results
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Page 1
In Vitro Analyses of Novel HCN4 Gene Mutations.
Möller M, Silbernagel N, Wrobel E, Stallmayer B, Amedonu E, Rinné S, Peischard S, Meuth SG, Wünsch B, Strutz-Seebohm N, Decher N, Schulze-Bahr E, Seebohm G. Möller M, et al. Among authors: wunsch b. Cell Physiol Biochem. 2018;49(3):1197-1207. doi: 10.1159/000493301. Epub 2018 Sep 7. Cell Physiol Biochem. 2018. PMID: 30196304 Free article.
A common mechanism allows selective targeting of GluN2B subunit-containing N-methyl-D-aspartate receptors.
Schreiber JA, Schepmann D, Frehland B, Thum S, Datunashvili M, Budde T, Hollmann M, Strutz-Seebohm N, Wünsch B, Seebohm G. Schreiber JA, et al. Among authors: wunsch b. Commun Biol. 2019 Nov 15;2:420. doi: 10.1038/s42003-019-0645-6. eCollection 2019. Commun Biol. 2019. PMID: 31754650 Free PMC article.
Synthesis of 3-aza[4.4.3]propellanes with high σ1 receptor affinity.
Torres-Gómez H, Daniliuc C, Schepmann D, Wünsch B. Torres-Gómez H, et al. Among authors: wunsch b. Bioorg Med Chem. 2018 May 1;26(8):1705-1712. doi: 10.1016/j.bmc.2018.02.019. Epub 2018 Feb 15. Bioorg Med Chem. 2018. PMID: 29482951
Structure of the σ1 receptor and its ligand binding site.
Brune S, Pricl S, Wünsch B. Brune S, et al. Among authors: wunsch b. J Med Chem. 2013 Dec 27;56(24):9809-19. doi: 10.1021/jm400660u. Epub 2013 Sep 10. J Med Chem. 2013. PMID: 23964901 Review.
Synthesis and evaluation of a [18F]BODIPY-labeled caspase-inhibitor.
Ortmeyer CP, Haufe G, Schwegmann K, Hermann S, Schäfers M, Börgel F, Wünsch B, Wagner S, Hugenberg V. Ortmeyer CP, et al. Among authors: wunsch b. Bioorg Med Chem. 2017 Apr 1;25(7):2167-2176. doi: 10.1016/j.bmc.2017.02.033. Epub 2017 Feb 16. Bioorg Med Chem. 2017. PMID: 28284866
Fluorinated GluN2B Receptor Antagonists with a 3-Benzazepine Scaffold Designed for PET Studies.
Szermerski M, Börgel F, Schepmann D, Haider A, Betzel T, Ametamey SM, Wünsch B. Szermerski M, et al. Among authors: wunsch b. ChemMedChem. 2018 May 23;13(10):1058-1068. doi: 10.1002/cmdc.201700819. Epub 2018 Apr 17. ChemMedChem. 2018. PMID: 29522653
Fluorinated PET Tracers for Molecular Imaging of σ1 Receptors in the Central Nervous System.
Weber F, Brust P, Laurini E, Pricl S, Wünsch B. Weber F, et al. Among authors: wunsch b. Adv Exp Med Biol. 2017;964:31-48. doi: 10.1007/978-3-319-50174-1_4. Adv Exp Med Biol. 2017. PMID: 28315263 Review.
Pyridine bioisosteres of potent GluN2B subunit containing NMDA receptor antagonists with benzo[7]annulene scaffold.
Zscherp R, Baumeister S, Schepmann D, Wünsch B. Zscherp R, et al. Among authors: wunsch b. Eur J Med Chem. 2018 Sep 5;157:397-404. doi: 10.1016/j.ejmech.2018.08.003. Epub 2018 Aug 4. Eur J Med Chem. 2018. PMID: 30103189
Synthesis and Pharmacological Evaluation of Enantiomerically Pure GluN2B Selective NMDA Receptor Antagonists.
Börgel F, Szermerski M, Schreiber JA, Temme L, Strutz-Seebohm N, Lehmkuhl K, Schepmann D, Ametamey SM, Seebohm G, Schmidt TJ, Wünsch B. Börgel F, et al. Among authors: wunsch b. ChemMedChem. 2018 Aug 10;13(15):1580-1587. doi: 10.1002/cmdc.201800214. Epub 2018 Jul 4. ChemMedChem. 2018. PMID: 29806151
Structure-Activity Relationships of Cinnamate Ester Analogues as Potent Antiprotozoal Agents.
Bernal FA, Kaiser M, Wünsch B, Schmidt TJ. Bernal FA, et al. Among authors: wunsch b. ChemMedChem. 2020 Jan 7;15(1):68-78. doi: 10.1002/cmdc.201900544. Epub 2019 Nov 12. ChemMedChem. 2020. PMID: 31697437 Free PMC article.
208 results
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