Delzer J[au] - Search Results

Year	Number of Results
1984	1
1985	1
2002	2
2003	2
2005	2
2006	3
2007	1
2008	2
2009	1
2011	1
2014	1
2015	2
2016	1
2024	0

1

New nikkomycins by mutasynthesis and directed fermentation.

Delzer J, Fiedler HP, Müller H, Zähner H, Rathmann R, Ernst K, König WA. Delzer J, et al. J Antibiot (Tokyo). 1984 Jan;37(1):80-2. doi: 10.7164/antibiotics.37.80. J Antibiot (Tokyo). 1984. PMID: 6698891 Free article. No abstract available.

2

Disposition and drug-drug interaction potential of veliparib (ABT-888), a novel and potent inhibitor of poly(ADP-ribose) polymerase.

Li X, Delzer J, Voorman R, de Morais SM, Lao Y. Li X, et al. Among authors: delzer j. Drug Metab Dispos. 2011 Jul;39(7):1161-9. doi: 10.1124/dmd.110.037820. Epub 2011 Mar 24. Drug Metab Dispos. 2011. PMID: 21436403

3

A fluorescence-based in vitro assay for drug interactions with breast cancer resistance protein (BCRP, ABCG2).

Mahringer A, Delzer J, Fricker G. Mahringer A, et al. Among authors: delzer j. Eur J Pharm Biopharm. 2009 Aug;72(3):605-13. doi: 10.1016/j.ejpb.2009.01.010. Eur J Pharm Biopharm. 2009. PMID: 19572416

4

Long-term fade study of the DT-702 LiF: Mg,Cu,P TLD.

Delzer JA, Hawley JR, Romanyukha A, Nemmers S, Selwyn R, Benevides LA. Delzer JA, et al. Radiat Prot Dosimetry. 2008;131(3):279-86. doi: 10.1093/rpd/ncn182. Epub 2008 Jul 11. Radiat Prot Dosimetry. 2008. PMID: 18621919

5

Genomic Knockout of Endogenous Canine P-Glycoprotein in Wild-Type, Human P-Glycoprotein and Human BCRP Transfected MDCKII Cell Lines by Zinc Finger Nucleases.

Gartzke D, Delzer J, Laplanche L, Uchida Y, Hoshi Y, Tachikawa M, Terasaki T, Sydor J, Fricker G. Gartzke D, et al. Among authors: delzer j. Pharm Res. 2015 Jun;32(6):2060-71. doi: 10.1007/s11095-014-1599-5. Epub 2014 Dec 19. Pharm Res. 2015. PMID: 25522789

6

Synthesis and SAR of N-substituted dibenzazepinone derivatives as novel potent and selective alpha(V)beta(3) antagonists.

Kling A, Backfisch G, Delzer J, Geneste H, Graef C, Holzenkamp U, Hornberger W, Lange UE, Lauterbach A, Mack H, Seitz W, Subkowski T. Kling A, et al. Among authors: delzer j. Bioorg Med Chem Lett. 2002 Feb 11;12(3):441-6. doi: 10.1016/s0960-894x(01)00773-9. Bioorg Med Chem Lett. 2002. PMID: 11814816

7

Synthesis and SAR of highly potent and selective dopamine D(3)-receptor antagonists: 1H-pyrimidin-2-one derivatives.

Geneste H, Backfisch G, Braje W, Delzer J, Haupt A, Hutchins CW, King LL, Kling A, Teschendorf HJ, Unger L, Wernet W. Geneste H, et al. Among authors: delzer j. Bioorg Med Chem Lett. 2006 Feb;16(3):490-4. doi: 10.1016/j.bmcl.2005.10.068. Epub 2005 Nov 11. Bioorg Med Chem Lett. 2006. PMID: 16290141

8

Synthesis and SAR of highly potent and selective dopamine D3-receptor antagonists: variations on the 1H-pyrimidin-2-one theme.

Geneste H, Amberg W, Backfisch G, Beyerbach A, Braje WM, Delzer J, Haupt A, Hutchins CW, King LL, Sauer DR, Unger L, Wernet W. Geneste H, et al. Among authors: delzer j. Bioorg Med Chem Lett. 2006 Apr 1;16(7):1934-7. doi: 10.1016/j.bmcl.2005.12.079. Epub 2006 Jan 24. Bioorg Med Chem Lett. 2006. PMID: 16439127

9

Synthesis and SAR of highly potent and selective dopamine D(3)-receptor antagonists: Quinolin(di)one and benzazepin(di)one derivatives. herve.geneste@abbott.com.

Geneste H, Backfisch G, Braje W, Delzer J, Haupt A, Hutchins CW, King LL, Lubisch W, Steiner G, Teschendorf HJ, Unger L, Wernet W. Geneste H, et al. Among authors: delzer j. Bioorg Med Chem Lett. 2006 Feb;16(3):658-62. doi: 10.1016/j.bmcl.2005.10.035. Epub 2005 Nov 2. Bioorg Med Chem Lett. 2006. PMID: 16271293

10

Design and synthesis of 1,5- and 2,5-substituted tetrahydrobenzazepinones as novel potent and selective integrin alphaVbeta3 antagonists.

Kling A, Backfisch G, Delzer J, Geneste H, Graef C, Hornberger W, Lange UE, Lauterbach A, Seitz W, Subkowski T. Kling A, et al. Among authors: delzer j. Bioorg Med Chem. 2003 Apr 3;11(7):1319-41. doi: 10.1016/s0968-0896(02)00616-8. Bioorg Med Chem. 2003. PMID: 12628659

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