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Rab7: crystallization of intact and C-terminal truncated constructs complexed with GDP and GppNHp.
Proteins. 1997 Feb;27(2):210-2. doi: 10.1002/(sici)1097-0134(199702)27:2<210::aid-prot7>3.0.co;2-j.
Proteins. 1997.
PMID: 9061785
Rab7: NMR and kinetics analysis of intact and C-terminal truncated constructs.
Neu M, Brachvogel V, Oschkinat H, Zerial M, Metcalf P.
Neu M, et al. Among authors: brachvogel v.
Proteins. 1997 Feb;27(2):204-9. doi: 10.1002/(sici)1097-0134(199702)27:2<204::aid-prot6>3.0.co;2-f.
Proteins. 1997.
PMID: 9061784
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Crystallization and initial crystallographic results for pepstatin A inhibited bovine cathepsin D.
Bieber F, Brachvogel V, Arni R, Fusek M, Metcalf P.
Bieber F, et al. Among authors: brachvogel v.
J Mol Biol. 1992 Oct 20;227(4):1265-8. doi: 10.1016/0022-2836(92)90539-v.
J Mol Biol. 1992.
PMID: 1433300
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Insights into the bile acid transportation system: the human ileal lipid-binding protein-cholyltaurine complex and its comparison with homologous structures.
Kurz M, Brachvogel V, Matter H, Stengelin S, Thüring H, Kramer W.
Kurz M, et al. Among authors: brachvogel v.
Proteins. 2003 Feb 1;50(2):312-28. doi: 10.1002/prot.10289.
Proteins. 2003.
PMID: 12486725
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Design and quantitative structure-activity relationship of 3-amidinobenzyl-1H-indole-2-carboxamides as potent, nonchiral, and selective inhibitors of blood coagulation factor Xa.
Matter H, Defossa E, Heinelt U, Blohm PM, Schneider D, Müller A, Herok S, Schreuder H, Liesum A, Brachvogel V, Lönze P, Walser A, Al-Obeidi F, Wildgoose P.
Matter H, et al. Among authors: brachvogel v.
J Med Chem. 2002 Jun 20;45(13):2749-69. doi: 10.1021/jm0111346.
J Med Chem. 2002.
PMID: 12061878
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Quantitative structure-activity relationship of human neutrophil collagenase (MMP-8) inhibitors using comparative molecular field analysis and X-ray structure analysis.
Matter H, Schwab W, Barbier D, Billen G, Haase B, Neises B, Schudok M, Thorwart W, Schreuder H, Brachvogel V, Lönze P, Weithmann KU.
Matter H, et al. Among authors: brachvogel v.
J Med Chem. 1999 Jun 3;42(11):1908-20. doi: 10.1021/jm980631s.
J Med Chem. 1999.
PMID: 10354399
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Acyl ureas as human liver glycogen phosphorylase inhibitors for the treatment of type 2 diabetes.
Klabunde T, Wendt KU, Kadereit D, Brachvogel V, Burger HJ, Herling AW, Oikonomakos NG, Kosmopoulou MN, Schmoll D, Sarubbi E, von Roedern E, Schönafinger K, Defossa E.
Klabunde T, et al. Among authors: brachvogel v.
J Med Chem. 2005 Oct 6;48(20):6178-93. doi: 10.1021/jm049034y.
J Med Chem. 2005.
PMID: 16190745
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