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Cyclic biphenyl ether tripeptides as proteasom inhibitors.

MPS-Authors
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Kaiser,  M.
Moroder, Luis / Bioorganic Chemistry, Max Planck Institute of Biochemistry, Max Planck Society;

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Milbradt,  A. G.
Moroder, Luis / Bioorganic Chemistry, Max Planck Institute of Biochemistry, Max Planck Society;

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Renner,  C.
Moroder, Luis / Bioorganic Chemistry, Max Planck Institute of Biochemistry, Max Planck Society;

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Assfalg-Machleidt,  I.
Moroder, Luis / Bioorganic Chemistry, Max Planck Institute of Biochemistry, Max Planck Society;

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Groll,  M.
Huber, Robert / Structure Research, Max Planck Institute of Biochemistry, Max Planck Society;

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Huber,  R.
Huber, Robert / Structure Research, Max Planck Institute of Biochemistry, Max Planck Society;

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Moroder,  L.
Moroder, Luis / Bioorganic Chemistry, Max Planck Institute of Biochemistry, Max Planck Society;

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Citation

Kaiser, M., Milbradt, A. G., Renner, C., Assfalg-Machleidt, I., Groll, M., Huber, R., et al. (2004). Cyclic biphenyl ether tripeptides as proteasom inhibitors. In M. Chorev, & T. K. Sawyer (Eds.), Peptide Revolution: Genomics, Proteomics & Therapeutics (pp. 348-349). Cardiff, Ca.: American Peptide Society.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-6A50-B
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