Identification of theMycobacterium tuberculosisprotein PE-PGRS62 as a novel effector that functions to block phagosome maturation and inhibit iNOS expression

The ESX-5 Secretion System of Mycobacterium marinum Modulates the Macrophage Response

(2014) A. M. Abdallah et al.   JOURNAL OF IMMUNOLOGY

Phagolysosome maturation of macrophages was reduced by PE_PGRS 62 protein expressing in Mycobacterium smegmatis and induced in IFN-γ priming

(2012) Ying Huang et al.   VETERINARY MICROBIOLOGY

PE_PGRS30 is required for the full virulence of Mycobacterium tuberculosis

(2011) Raffaella Iantomasi et al.   CELLULAR MICROBIOLOGY

SignalP 4.0: discriminating signal peptides from transmembrane regions

(2011) Thomas Nordahl Petersen et al.   NATURE METHODS

Identification of the Switch in Early-to-Late Endosome Transition

(2010) Dmitry Poteryaev et al.   CELL

The Multifunctional PE_PGRS11 Protein fromMycobacterium tuberculosisPlays a Role in Regulating Resistance to Oxidative Stress

(2010) Rashmi Chaturvedi et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Expression of PE_PGRS 62 protein in Mycobacterium smegmatis decrease mRNA expression of proinflammatory cytokines IL-1β, IL-6 in macrophages

(2010) Ying Huang et al.   MOLECULAR AND CELLULAR BIOCHEMISTRY

PPE and PE_PGRS proteins ofMycobacterium marinumare transported via the type VII secretion system ESX-5

(2009) Abdallah M. Abdallah et al.   MOLECULAR MICROBIOLOGY

A broad-range of recombination cloning vectors in mycobacteria

(2009) Jim Sun et al.   PLASMID

Mycolic Acid Modification by the mmaA4 Gene of M. tuberculosis Modulates IL-12 Production

(2008) Dee N. Dao et al.   PLoS Pathogens