1. Murray JF. A century of tuberculosis. Am J Respir Crit Care Med. 2004. 169:1181–1186.
2. Murray CJ, Styblo K, Rouillon A. Tuberculosis in developing countries: burden, intervention and cost. Bull Int Union Tuberc Lung Dis. 1990. 65:6–24.
3. Bellamy R. Genetic susceptibility to tuberculosis in human populations. Thorax. 1998. 53:588–593.
4. Marquet S, Schurr E. Genetics of susceptibility to infectious diseases: tuberculosis and leprosy as examples. Drug Metab Dispos. 2001. 29:479–483.
5. Schurr E, Buschman E, Malo D, Gros P, Skamene E. Immunogenetics of mycobacterial infections: mouse-human homologies. J Infect Dis. 1990. 161:634–639.
6. Plant J, Glynn AA. Genetics of resistance to infection with Salmonella typhimurium in mice. J Infect Dis. 1976. 133:72–78.
7. Blackwell JM, Roach TI, Atkinson SE, Ajioka JW, Barton CH, Shaw MA. Genetic regulation of macrophage priming/activation: the Lsh gene story. Immumol Lett. 1991. 30:241–248.
8. Vidal SM, Malo D, Vogan K, Skamene E, Gros P. Natural resistance to infection with intracellular parasites: isolation of a candidate for Bcg. Cell. 1993. 73:469–485.
9. Cellier M, Govoni G, Vidal S, Kwan T, Groulx N, Liu J, et al. Human natural resistance-associated macrophage protein: cDNA cloning, chromosomal mapping, genomic organization, and tissue-specific expression. J Exp Med. 1994. 180:1741–1752.
10. Liu J, Fujiwara TM, Buu NT, Sanchez FO, Cellier M, Paradis AJ, et al. Identification of polymorphism and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein gene. Am J Hum Genet. 1995. 56:845–853.
11. Bellamy R, Ruwende C, Corrah T, McAdam KP, Whittle HC, Hill AV. Variations in the NRAMP1 gene and susceptibility to tuberculosis in west africans. N Engl J Med. 1998. 338:640–644.
12. Kim HS, Park MH, Song EY, Park H, Kwon SY, Han SK, et al. Association of HLA-DR and HLA-DQ genes with susceptibility to pulmonary tuberculosis in Koreans: preliminary evidence of associations with drug resistance, disease severity, and disease recurrence. Hum Immunol. 2005. 66:1074–1081.
13. Rajalingam R, Mehra NK, Jain RC, Myneedu VP, Pande JN. Polymerase chain reaction-based sequence-specific oligonucleotide hybridization analysis of HLA class II antigens in pulmonary tuberculosis: relevance to chemotherapy and disease severity. J Infect Dis. 1996. 173:669–676.
14. Dubaniewicz A, Lewko B, Moszkowska G, Zamorska B, Stepinski J. Molecular subtypes of the HLA-DR antigens in pulmonary tuberculosis. Int J Infect Dis. 2000. 4:129–133.
15. Sharma SK, Turaga KK, Balamurugan A, Saha PK, Pandey RM, Jain NK, et al. Clinical and genetic risk factors for the development of multi-drug resistant tuberculosis in non-HIV infected patients at a tertiary care center in India: a case-control study. Infect Genet Evol. 2003. 3:183–188.
16. Comstock GW. Tuberculosis in twins: a re-analysis of the Prophit survey. Am Rev Respir Dis. 1978. 117:621–624.
17. Kallmann FJ, Reisner D. Twin studies on the significance of genetic factors in tuberculosis. Am Rev Tuberc. 1942. 47:549–574.
18. Stead WW, Senner JW, Reddick WT, Lofgren JP. Racial differences in susceptibility to infection by Mycobacterium tuberculosis. N Engl J Med. 1990. 322:422–427.
19. Rojas M, Barrera F, Puzo G, Garcia LF. Differential induction of apoptosis by virulent Mycobacterium Tuberculosis in resistant and susceptible murine macrophage. J Immunol. 1997. 159:1352–1361.
20. Xu DL, Goto Y, Endo F, Amoako KK, Shinjo T. The effect of Bcg gene on antigen presentation of spleen adherent cells and peritoneal macrophages from Mycobacterium bovis BCG-infected Bcgs and Bcgr mice. Vet Mocrobiol. 1997. 59:67–78.
21. Gruenheid S, Pinner E, Desjardins M, Gros P. Natural resistance to infection with intracellular parasites: The Nramp1 protein is recruited to the membrane of the phagosome. J Exp Med. 1997. 185:717–730.
22. Blackwell JM, Searle S. Genetic regulation of macrophage activation: understanding the function of NRAMP1(=Ity/Lsh/Bcg). Immun Letter. 1999. 65:73–80.
23. Govoni G, Gros P. Macrophage NRAMP1 and its role in resistance to microbial infections. Inflamm Res. 1998. 47:277–284.
24. Deretic V, Fratti RA. Mycobacterium tuberculosis phagosome. Mol Microbiol. 1999. 31:1603–1609.
25. Shaw MA, Collins A, Peacock CS, Miller EN, Black GF, Sibthorpe D, et al. Evidence that genetic susceptibility to Mycobacterium tuberculosis in an Brazilian population is under oligogenic control: linkage study of the candidate gene NRAMP1 and TNFA. Tuber Lung Dis. 1997. 78:35–45.
26. Blackwell JM. Genetics of host resistance and susceptibility to intramacrophage pathogens: a study of multicase families of tuberculosis, leprosy and leishmaniasis in north-eastern Brazil. Int J Parasitol. 1998. 28:21–28.
27. Huang JH, Oefner PJ, Adi V, Ratnam K, Ruoss SJ, Trako E, et al. Analyses of the NRAMP1 and IFN-γ R1 genes in women with Mycobacterium avium-intracellulare pulmonary disease. Am J Respir Crit Care Med. 1998. 157:377–381.