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Immunotherapeutical potential of Mycobacterium vaccae on M. tuberculosis infection in mice.
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Syntheses and studies of quinolone-cephalosporins as potential anti-tuberculosis agents.
Bioorg Med Chem Lett. 2006 Nov 1;16(21):5534-7. doi: 10.1016/j.bmcl.2006.08.045. Epub 2006 Aug 30.
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Immunotherapy with Mycobacterium vaccae in the treatment of tuberculosis.
Front Biosci. 2004 May 1;9:1701-19. doi: 10.2741/1292.
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An alternative procedure for preparation of cefdinir.
Farmaco. 2003 Jun;58(6):409-18. doi: 10.1016/S0014-827X(03)00063-6.
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Oxazolidinone structure-activity relationships leading to linezolid.
Angew Chem Int Ed Engl. 2003 May 9;42(18):2010-23. doi: 10.1002/anie.200200528.
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Design, synthesis, and biological evaluation of a series of beta-lactam-based prodrugs.
Bioorg Med Chem. 2002 Nov;10(11):3489-98. doi: 10.1016/s0968-0896(02)00256-0.
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Synthesis and antibacterial activity of [6,5,5] and [6,6,5] tricyclic fused oxazolidinones.
Bioorg Med Chem Lett. 1998 May 19;8(10):1231-6. doi: 10.1016/s0960-894x(98)00194-2.

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