Feng Wang

发表

Altered NADH/NAD+ Ratio Mediates Coresistance to Isoniazid and Ethionamide in Mycobacteria

C. Vilchèze, T. Weisbrod, Bing Chen, 2005, Antimicrobial Agents and Chemotherapy.

Transfer of a point mutation in Mycobacterium tuberculosis inhA resolves the target of isoniazid

C. Vilchèze, T. Weisbrod, L. Kremer, 2006, Nature Medicine.

Mycobacterium tuberculosis Dihydrofolate Reductase Is Not a Target Relevant to the Antitubercular Activity of Isoniazid

C. Vilchèze, Feng Wang, D. Alland, 2010, Antimicrobial Agents and Chemotherapy.

Identification of a type III thioesterase reveals the function of an operon crucial for Mtb virulence.

Feng Wang, J. Sacchettini, R. Langley, 2007, Chemistry & biology.

Natural product inhibitors of fatty acid biosynthesis: synthesis of the marine microbial metabolites pseudopyronines A and B and evaluation of their anti-infective activities

Feng Wang, J. Sacchettini, R. Perozzo, 2008 .

Microsoft Word-JBC_final_revision1.docx

Feng Wang, J. Sacchettini, T. Ioerger, 2013 .

Hydrogen peroxide-mediated isoniazid activation catalyzed by Mycobacterium tuberculosis catalase-peroxidase (KatG) and its S315T mutant.

Feng Wang, J. Sacchettini, Hong-Xiu Yu, 2006, Biochemistry.

Altered NADH/NAD (cid:1) Ratio Mediates Coresistance to Isoniazid and Ethionamide in Mycobacteria

C. Vilchèze, T. Weisbrod, L. Kremer, 2005 .

Mechanism of thioamide drug action against tuberculosis and leprosy

James C. Sacchettini, William R. Jacobs, Gulcin Gulten, 2007, The Journal of experimental medicine.

Triclosan Derivatives: Towards Potent Inhibitors of Drug‐Sensitive and Drug‐Resistant Mycobacterium tuberculosis

Joel S. Freundlich, James C Sacchettini, Joel S Freundlich, 2009, ChemMedChem.

Structures of Mycobacterium tuberculosis FadD10 protein reveal a new type of adenylate-forming enzyme.

Feng Wang, J. Sacchettini, T. Ioerger, 2013, The Journal of Biological Chemistry.

Structures of Mycobacterium tuberculosis FadD10 Protein Reveal a New Type of Adenylate-forming Enzyme*

Feng Wang, J. Sacchettini, T. Ioerger, 2013, The Journal of Biological Chemistry.

Crystal Structure and Activity Studies of the Mycobacterium tuberculosis β-Lactamase Reveal Its Critical Role in Resistance to β-Lactam Antibiotics

Feng Wang, J. Sacchettini, C. Cassidy, 2006, Antimicrobial Agents and Chemotherapy.

[Detection of pncA mutation associated with pyrazinamide resistance in Mycobacterium tuberculosis by high-resolution melting cure analysis].

Feng Wang, Xiao-li Liu, C. Hong, 2013, Zhonghua jie he he hu xi za zhi = Zhonghua jiehe he huxi zazhi = Chinese journal of tuberculosis and respiratory diseases.

Crystal structure and activity studies of the Mycobacterium tuberculosis beta-lactamase reveal its critical role in resistance to beta-lactam antibiotics.

Feng Wang, J. Sacchettini, C. Cassidy, 2006, Antimicrobial agents and chemotherapy.

Biochemical characterization of enoyl reductase involved in Type II fatty acid synthesis in the intestinal coccidium Eimeria tenella (Phylum Apicomplexa).

Feng Wang, J. Sacchettini, Xiangshi Tan, 2007, FEMS microbiology letters.