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    Publisher: Academic Journals Inc., USA
   
  Current Research in Tuberculosis is dedicated to publish high quality research work from all over the world on clinical and epidemiological aspects of tuberculosis. Scope of the journal includes: respiratory diseases and therapeutic interventions, adult and pediatric medicine, epidemiology, immunology and cell biology, physiology, pharmacology, occupational disorders, and the role of allergens and pollutants.

Current Research in Tuberculosis now accepting new submissions. Submit your best paper via online submission system.
  Editor-in-Chief:  Apply for Editor-in-Chief
 
 
Am Ende, C.W., S.E. Knudson, N. Liu, J. Childs and T.J. Sullivan et al., 2008. Synthesis and in vitro antimycobacterial activity of b-ring modified diaryl ether inha inhibitors. Bioorg. Med. Chem. Lett., 18: 3029-3033.
CrossRef  |  
Bonnac, L., G. Gao, L. Chen, K. Felczak and E.M. Bennett et al., 2007. Synthesis of 4-phenoxybenzamide adenine dinucleotide as NAD analogue with inhibitory activity against Enoyl-ACP Reductase (InhA) of Mycobacterium tuberculosis. Bioorg. Med. Chem. Lett., 17: 4588-4591.
Direct Link  |  
Kruh, N.A., J.G. Borgaro, B.P. Ruzsicska, H. Xu and P.J. Tonge, 2008. A novel interaction linking the FAS-II and PDIM biosynthetic pathways. J. Biol. Chem., 283: 31719-31725.
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Li, J., H. Xu and Y. Zhang, 2005. Metallic samarium and iodine promoted facile and efficient syntheses of trisubstituted alkenes from the acetates of baylisľhillman adducts. Tetrahedron Lett., 46: 1931-1934.
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Ni, S., Y. Pan, P. Wu, Y. Chen, C. Fu and H. Xu, 2004. Analysis of volatile oil from Lygodium japonicum by GC-MS. Chinese Pharmaceutical J., 39: 99-100.
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Tremblay, L.W., H. Xu and J.S. Blanchard, 2010. Structures of the Michaelis complex (1.2 ┼) and the covalent acyl intermediate (2.0 ┼) of cefamandole bound in the active sites of the Mycobacterium tuberculosis β-lactamase K73A and E166A mutants. Biochemistry, 49: 9685-9687.
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Xu, H., S.S. Hegde and J.S. Blanchard, 2011. Reversible Acetylation and Inactivation of Mycobacterium tuberculosis acetyl-CoA synthetase is dependent on cAMP. Biochemistry, 50: 5883-5892.
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Xu, H., T.J. Sullivan, J. Sekiguchi, T. Kirikae and I. Ojima et al., 2008. Mechanism and inhibition of saFabI, the enoyl reductase from Staphylococcus aureus. Biochemistry, 47: 4228-4236.
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