113.Blackwell J. M., Barton C. H., White J. K. et al. Genomic organisation and sequence of the human NRAMP gene: identification and mapping of a promoter region polymorphism // Mol. Med. - 1995. - Vol.1. - P. 194-205.

114.Blackwell M. J., Searle S. Genetic regulation of macrophage activation: understanding the function of Nramp1 (= Ity/Lsh/Bcg ) // Immunol. Lett. - 1999. - Vol. 65. - P. 73-80.

115.Bornman L., Campbell S. J., Fielding K. et al. Vitamin D receptor polymorphisms and susceptibility to tuberculosis in west Africa: a case-control and family study // J. Infect. Dis. - 2004. - Vol. 190(9). - P. 1631-1641.

116.Bradley D. J. Regulation of Leishmania populations within the host. II. Genetic control of acute susceptibility of mice to Leishimania donovani infection // Clin. Exp. Immunol. - 1977. - Vol. 30. - P. 130-140.

117.Brightbill H. D., Libraty D. H., Krutzik S. R. et al. Host defense mechanisms triggered by microbial lipoproteins through toll-like receptors // Science. - 1999. - Vol. 285. - P. 732-736.

118.Cadranel J., Hance A. J., Milleron B. et al. The production of 1,25(OH)2D3 by cells recovered by bronchoalveolar lavage and the role of this metabolite in calcium homeostasis // Am. Rev. Respir. Dis. - 1988. - Vol. 138. - P. 984-989.

119.Canonne-Hergaux F., Gruenheid S., Govoni G., Gros P. The Nramp1 protein and its role in resistance to infection and macrophage function // Proc. Assoc. Am. Physicians. - 1999. - Vol. 111(4). - P. 283-289.

120.Cellier M., Belouchi A., Gros P. Resistance to intracellular infections: comparative genome analysis of NRAMP // Trends Genet. - 1996. - Vol. 92. - P. 201-204.

121.Cellier M., Govoni G., Vidal S. et al. Human natural resistance-associated macrophage protein: cDNA cloning, chromosomal mapping, genomic organization, and tissue-specific expression // J. Exp. Med. - 1994. - Vol. 180. - P. 1741-1752.

122.Cellier M., Bergevin I., Boyer E. et al. Polyphyletic origins of bacterial Nramp transporters // Trends Genet. - 2001. - Vol. 17. - № 7. - P. 365-370.

123.Cervino A. C. L., Lakiss S., Sow O. et al. Fine mapping of a putative tuberculosis - susceptibility locus on chromosome -15q11-13 in African families // Hum. Mol. Genet. - 2002. - Vol. 11. - P. 1598-1603.

124.Cervino A. C. L., Lakiss S., Sow O., Hill A. V. S. Allelic association between the NRAMP1 gene and susceptibility to tuberculosis in Guinea - Conakry // Ann. Hum. Genet. - 2000. - Vol. 64. - P. 507-512.

125.Chan T. Y. Vitamin D deficiency and susceptibility to tuberculosis // Calcif. Tissue. Int. - 2000. - Vol. 66(6). - P. 476-478.

126.Chensue S. W., Davey V. P., Remick D. G., Kunkel S. L. Release of interleukin-1 by peripheral blood mononuclear cells in patiens with tuberculosis and active inflammation // Infect. Immun. - 1986. - Vol. 52, № 1. - P. 341-343.

127.Comstock G. W. Tuberculosis in twins: a reanalysis of the Prophit study // Am. Rew. Respir. Dis. - 1978. - Vol. 117. - P. 621-624.

128.Cooper A. M., Kipnis A., Turner J. et al. Mice lacking bioactive IL-12 can generate protective, antigen-specific cellular responses to mycobacterial infection only if the IL-12 p40 subunit is present // J. Immun. - 2002. - Vol. 168. - P. 1322-1327.

129.Cooper A. M., Magram J., Ferrante J., Orme I. M. Interleukin 12 (IL-12) Is crucial to the development of protective immunity in mice intravenously infected with Mycobacterium tuberculosis // J. Exp. Med. - 1997. - Vol. 186(1). - P. 39-45.

130.Davies P. D., Brown R. C., Woodhead J. S. Serum concentrations of vitamin D metabolites in untreated tuberculosis // Throax. - 1985. - Vol. 40. - P. 187-190.

131.Denis M. Killing of Mycobacterium tuberculosis within human monocytes: activation by cytokines and cacitriol // Clin. Exp. Immunol. - 1991. - Vol. 84. - P. 200-206.

132.Dorman S. E., Holland S. M. Interferon-γ and interleukin-12 pathway defects and human disease // Cytokine Growth Factor Rev. - 2000. - Vol. 11. - P. 321-333.

133.Edwards J. H. Familial predisposition in man // Brit. Med. Bull. - 1969. - V. 25. - P. 58-64.

134.Falconer D. S. The inheritance of liability to certain diseases, estimated from the incidence among relatives // Ann. Hum. Genet. - 1965. - V. 29. - P. 51-76.

135.Fine P. E. M. Immunogenetics of susceptibility to leprosy, tuberculosis and leishmaniasis: An epidemiological perspective // Int. J. Leprosy. - 1981. - Vol. 49. - P. 437-454.

136.Flynn J. L., Goldstein M. M., Triebold K. J. et al. IL-12 increasis resistance of BALB/c mice to mucobacterium tuberculosis infection // J. Immunol. - 1995. - Vol. 155. - P. 2515-2524.

137.Flynn J. L., Chan J., Triebold K. J. et al. An essential role for interferon gamma in resistance to mucobacterium tuberculosis infection // J. Exp. Med. - 1993. - Vol. 178. - P. 2249-2254.

138.Forget A., Skamene B., Gros P. et al. Differences in response among inbred strains of mtce to infection with small doses of mycobacterium bovis (BCG) // Infect. Immun. - 1981. - Vol. 32. - P. 42-50.

139.Gao P. S., Fujishima S., Mao X.-Q. et al. Genetic variants of NRAMP1 and active tuberculosis in Japanese populations // Clin. Genet. - 2000. - Vol. 58. - P. 74-76.

140.Giovine F. S., Takhsh E., Blakemore A. I. F., Duff G. W. Single base polymorphism at-511 in the human interleykin-1β gene // Hum. Mol. Genet. - 1993. - Vol. 1. - P. 450.

141.Golli V., Ghitulescu I., Ionescu N. et al. Clinical and epidemiological significance of isolated culture Koch bacillus after conclusion of chemotherapy // Pneumoftiziol. - 1981. - Vol. 30, №1. - Р. 55-58.

142.Govoni G., Gros P. Macrophage NRAMP1 and its role in resistanse to microbial infections // Inflam. Res. - 1998. - Vol. 47, №7. - P. 277-284.

143.Govoni G., Vidal S., Gauthier S. et al. The Bcg/Ity/Lsh Locus: genetic transfer of resistance to infections in C57BL/6J mice transgenic for the Nramp1Gly169 allele // Infect. Immun. - 1996. - Vol. 64. - P. 2923-2929.

144.Greenwood C. M. T., Fujiwara T. M., Boothroyd L. J. et al. Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, large aboriginal canadian family // Am. J. Hum. Genet. - 2000. - Vol. 67. - P. 405-416.

145.Griffin M. D., Xing N., Kumar R. Vitamin D and its analogs as regulators of immune activation and antigen presentation // Annu. Rev. Nutr. - 2003. - Vol. 23. - P. 117-145.

146.Gros P., Skamene E., Forget A. Genetic control of natural resistance to Mycobacterium bovis (BCG) in mice // J. Immunol. - 1981. - Vol. 127, №6. - P. 2417-2421.

147.Gruenheid S., Gros P. Genetics susceptibility to intracellular infections: Nramp1, macrofage function and divalent cations transport // Curr. Opin. Microbiol. - 2000. - Vol. 3. - P. 43-48.

148.Gruenheid S., Pinner E., Desjardins M., Gros P. Natural resistance to infection with intracellular pathogens: the Nramp1 protein is recruited to the membrane of the phagosome // J. Exp. Med. - 1997. - Vol. 185. - P. 717-730.

149.Hall M. A., McGlinn E., Coakley G. et al. Genetic polymorphism of IL-12 p40 gene in immunemediated disease // Genes and Immunity. - 2000. - Vol. 1. - P. 219-224.

150.Hara H., Matsushima T., Soejima R. et al. A tuberculosis epidemic. An outbreak of cases in a furniture company // Kekkaku. - 1982. - Vol. 57, №9. - P. 491-496.

151.Hill A. V. S. Genetics and genomics of infectious disease susceptibility // Brit. Med. Bull. - 1999. - Vol. 55, №2. - P. 401-413.

152.Hill A. V. S. The immunogenetics of human infectious disease // Annu. Rev. Immunol. - 1998. - Vol. 16. - P. 593-617.

153.Hill W. G. Estimation of linkage disequilibrium in random mating populations // Hereditary. - 1974. - Vol. 33. - P. 229-479.

154.Jabado N., Jankowski A., Dougaparsad S. et al. Natural resistance to intracellular infections: natural resistance-associated macrophage protein 1 (NRAMP1) functions as a pH-dependent manganese transporter at the phagosomal membrane // J. Exp. Med. - 2000. - Vol. 192, № 9. - P. 1237-1247.

155.Jackett P. S., Aber V. R., Lowrie D. B. Virulence of Mycobacterium tuberculosis and susceptibility to peroxidative killing systems // J. Gen. Microbiol. - 1978. - Vol. 107(2). - P. 273-278.

156.Kallman F. J., Reisner D. Twin studies on the significance of genetic factors in tuberculosis // Am. Rev. Tuberc. - 1942. - Vol. 47. - P. 549-574.

157.Kameda K., Kuchii N., Horii F. et al. A study on the family contacts examination of tuberculosis patients // Kekkaku. - 1983. - Vol. 58, №1. - P. 33-37.

158.Kindler V., Sppino A. P., Grau G. E. et al. The inducing role of tumor necrosis factor in the daveloptment of bactericidal granulomas during BCG infection // Cell. - 1989. - Vol. 56. - P. 731-740.

159.Knight J. C., Kwiatkowski D. Inherited variability of tumor necrosis factor production and susceptibility to infectious disease // Proc. Assoc. Am. Physicians. - 1999. - Vol. 111. - № 4. - P. 290-298.

160.Kramnik I., Dietrich W. F., Demant P., Bloom B. R. Genetic control of resistance to experimental infection with virulent Mycobacterium tuberculosis // Proc. Natl. Acad. Sci. USA. - 2000. - Vol. 97(15). - P. 8560-8565.

161.Labuda M., Ross M. V., Fujiwara T. M. et al. Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q.II // Cytogenet. Cell Genet. - 1991. - Vol. 58. - P. 1978.

162.Lahiri D. K., Bye S., Nunberg J. I. et al. Anon-organic and non-enzymatic eztraction method gives higher yields of genomic DNA from whole-blood samples than do nine other methods used // J. Biochem. Biophys. Methods. - 1992. - Vol. 25. - P. 193-205.

163.Liu J., Fujiwara T. M., Buu N. T. et al. Identification of polymorphisms and sequence variants in the human homologue of the mouse natural resistance - associated macrophage protein gene // Am. J. Hum. Genet. - 1995. - Vol. 56. - P. 845-853.

164.Liu W., Cao W. C., Zhang C. Y. et al. VDR and NRAMP1 gene polymorphisms in susceptibility to pulmonary tuberculosis among the Chinese Han population: a case-control study // Int. J. Tuberc. Lung Dis. - 2004. - Vol. 8(4). - P. 428-434.

165.Lurie M. B., Zappasodi P., Dannenberg A. M., Weiss G. H. On the mechanism of genetic resistance to tuberculosis and its mode of inheritance // Am. J. Hum. Genet. - 1952. - Vol. 4. - P. 302-314.

166.Lynch C. J., Pierce-Chase C. H., Dubos R. A genetic study of susceptibility to experimental tuberculosis in mice infected with mammalian tubercle bacilli // J. Exp. Med. - 1965. - Vol. 121. - P. 1051-1070.

167.Malo D., Vogan K., Vidal S. et al. Haplotype mapping and sequence analysis of the mouse Nramp gene predict susceptibility to infection with intracellular parasites // Genomics. - 1994. - Vol. 23. - P. 51-61.

168.Marquet S., Lepage P., Hudson T. J. et al. Complete nucleotide sequence and genomic structure of the human NRAMP1 gene region on chromosome region 2q35 // Mamm. Genome. - 2000. - Vol. 11. - P. 755-762.

169.Mohan V. P., Scanga C. A., Yu K. Effects of Tumor Necrosis Factor alpha on host immune respons in chronic persistent tuberculosis: possible role for limiting Pathology // Infect. Immun. - 2001. - № 3. - P. 1847-1855.

170.Myrvik Q., Leake E. Wright M. Disruption of fhagosomal membranes of normal alveolar macrophages by the H37Rv strain of M. tuberculosis. A correlate of virulence // Am. Rev. Resp. Dis.- 1984. - Vol.129. - P.322-328.

171.Nei M. Molecular population genetics and evolution. - New York, Amsterdam: North-Holland publishing companu, Oxford American Elsevier publishing company, 1975. - 288 p.р.

172.Nelson N. Metal ion transporters and homeostasis // EMBO J. - 1999. - Vol. 18. - P. 4361-4371.

173.Nicklin M. J. H., Weith A., Duff G. W. A physical map of the region encompassing the human interleykin-1-alpha, interleykin-1-beta, and interleykin-1 receptor antagonist genes // Genomics. - 1994. - Vol. 19. - P. 382-384.

174.Noben-Trauth N., Schweitzer P. A., Johnson K. R. et al. The interleukin-12 beta subunit (p40) maps to mouse chromosome 11 // Mamm. Genome. - 1996. - Vol. 7. - P 392.

175.North R. J., Medina E. How important is Nramp1 in tuberculosis? // Trends Microbiol. - 1998. - Vol. 6, №11. - P. 441-443.

176.Oppmann B., Lesley R., Blom B. et al. Novel p19 protein engages IL-12p40 to form a cytokine, IL-23, with biological activites similar as distinct from IL-12 // Immunity. - 2000. - Vol. 13. - P. 715-725.

177.Orme I. M., Cooper A. M. Cytokine / chemokine cascades in immunity to tuberculosis // Immunol. Today. - 1999. - Vol. 20. - P. 307-311.

178.Ottenhoff T. H. M., Verreck F. A. W., Lichtenauer-Kaligis E. G. R. et al. Genetics, cytokines and human infectious disease: lessons from weakly pathogenic mycobacteria and salmonellae // Nature Genetics. - 2002. - Vol. 32. - P. 97-104.

179.Patterson D., Jones C., Hart I. et al. The human interleukin-1 receptor antagonist (IL1RN) gene is located in the chromosome 2q14 region // Genomics. - 1993. - Vol. 15. - P. 173-176.

180.Pearce N. What does the odds ratio estimate in a case-control study? // Int. J. Epidemiol. - 1993. - Vol. 26 № 6. - P. 1189-1192.

181.Pоciot F., Molving J., Wogensen L. et al. A TaqI polymorphism in the human interleykin-1 beta (IL-1 beta) gene correlates with IL-1 beta sacretion in vitro // Eur. J. Clin. Invest. - 1992. - Vol. 22. - P. 396-402.

182.Rigby W. F. The immunobiology of vitamin D // Immunol. Today. - 1988. - Vol. 9. - P. 54-58.

183.Rook G. Role of activated macrophages in the immunopathology of tuberculosis // Brit. Med. Bull.- 1988.- Vol.44, №3.- P.611-623.

184.Rook G., Steele J., Fraher L. et al. Vitamin D3, gamma interferon, and control of mucobacterium tuberculosis by human monocytes // Immunology. - 1986. - Vol. 57. - P. 159-163.

185.Roth D. E., Soto G., Arenas F. et al. Association between vitamin D receptor gene polymorphisms and response to treatment of pulmonary tuberculosis // J. Infect. Dis. - 2004. - Vol. 190(5). - P.920-927.

186.Ryu S., Park Y. K., Bai G. H. et al. 3’UTR polymorphisms in the NRAMP1 gene are associated with susceptibility to tuberculosis in Koreans // Int. J. Tuberc. Lung Dis. - 2000. - Vol. 4, № 6. - P. 577-580.

187.Schlesinger L. S. Entry of Mycobacterium tuberculosis into mononuclear phagocytes // Curr. Top. Mycrobiol. Immunol. - 1996. - Vol. 215. - P. 71-96.

188.Schlesinger L. S. Role of mononuclear phagocytes in M. tuberculosis pathogenesis // J. Invest. Med. - 1996. - Vol. 44. - P. 312-323.

189.Selvaraj P., Kurian S. M., Uma H. et al. Influence of non-MHC genes on lymphocyte response to Mycobacterium tuberculosis antigens and tuberculin reactive status in pulmonary tuberculosis // Indian J. Med. Res. - 2000. - Vol. 112. - P. 86-92.

190.Servaraj P., Narayanan P. R., Reetha A. M. Association of vitamin D receptor genotypes with the susceptibility to pulmonary tuberculosis in femele patients and resistance contacts // Indian J. Med. Res. - 2000. - Vol. 111. - P. 172-179.

191.Sevaraj P., Narayanan P. R., Reetha A. M. Association of functional mutant homozygotes of the mannose binding protein gene with susceptibility to pulmonary tuberculosis in India // Tuberc. Lung. Dis. - 1999. - Vol. 79. - P. 221-227.

192.Sieburth D., Fabs E. W., Warrington J. A. et al. Assignment of NKSF/IL-12, a unique cytokine composed of two unrelated subunits, to chromosomes 3 and 5 // Genomics. - 1992. - Vol. 14. - P. 59-62.

193.Skamene E., Kongshavn P. A. L., Landy M. Genetic control of natural resistance to infection and malignancy - New York: Academic Press.,1980. - 280 p.р.

194.Skamene E. The Bcg gene story // Immunobiology. - 1994. - Vol. 191. - P. 451-460.

195.Soborg C., Andersen A. B., Madsen H. O. et al. Natural resistance-associated macrophage protein 1 are associated with microscopy-positive tuberculosis // J. Infect. Dis. - 2002. - Vol. 186 - № 4. - P. 517-521.

196.Spielman R. S., McGinnis R. E., Ewens W. J. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM) // Am. J. Hum. Genet. - 1993. - Vol. 52. - P. 506-516.

197.Spielman R. S., Ewens W. J. The TDT and other family-based tests for linkage disequilibrium and association // Am. J. Hum. Genet. - 1996. - V. 59. - P. 983-989.

198.Stead W. W. Genetics and resistance to tuberculosis: could resistance be enhanced by genetics engineering? // Ann. Int. Med. - 1992. - Vol. 116. - P. 937-941.

199.Stead W. W., Senner J. W., Reddick W. T., Lofgren J. P. Racial differences in susceptibility to infection by Mycobacterium tuberculosis // N. Engl. J. Med. - 1990. - Vol. 322. - P.422-427.

200.Tarlow J. K., Blakemore I. F., Lennard A. et al. Polymorphism in human IL-1 receptor antagonist gene intron 2 is caused by variable numer of an 860-bp tandem repeat // Hum. Genet. - 1993. - Vol. 91. - P. 403-404.

201.Uitterlinden A. G., Fang Y., Meurs J. B. et al. Genetics and biology of vitamin D receptor polymorphisms // Gene. - 2004. - Vol. 338(2). - P. 143-156.

202.Vidal S. M., Malo D., Vogan K. et al. Natural resistance to infection with intracellular parasites: isolation of a candidate for Bcg // Cell. - 1993. - Vol. 73, №3. - P. 469-485.

203.Walker L., Lowrie D. B. Killing of Mycobacterium microti by immunologically activated macrophages // Nature. - 1981. - Vol. 293. - P. 69-71.

204.Warrington J. A., Bailey S. K., Armstrong E. et al. A radiation hybrid map of 18 growth factor, growth factor receptor, hormone receptor, or neurotransmitter receptor genes on the distal region of the long arm of chromosome 5 // Genomics. - 1992. - Vol. 13. - P. 803-808.

205.Warrington J. A., Bengtsson U. High-resolution physical mapping of human 5q31-q33 using three methods: radiation hybrid mapping, interphase fiuorescence in situ hybridization, and pulsed-field gel electrophoresis // Genomics. - 1994. - Vol. 24. - P. 395-398.

206.Wilkinson R. J., Lieweiyn M., Toossi Z. et al. Influence of vitamin D deficiency and vitamin D receptor polymorphisms on tuberculosis among Gujarati Asians in west London: a case-control study // Lancet. - 2000. - Vol. 355. - P. 618-621.

207.Wilkinson R. J., Patel P., Llewelyn M. et al. Influence of Polymorphism in the Genes for the Interleukin (IL)-1 Receptor Antagonist and IL-1β on Tuberculosis // J. Exp. Med. - 1999. - Vol. 189 (12). - P. 1863-1873.

208.Yang Y. S., Kim S. J., Kim J. W., Koh E. M. NRAMP1 gene polymorphisms in patients with rheumatoid arthritis in Koreans // J. Korean Med. Sci. - 2000. - № 15. - P. 83-87.

209.Zaahl M. G., Robson K. J. H., Warnich L. et al. Expression of SLC11A1 (NRAMP1) 5’-(GT)n repeat: Opposite effect in the presence of - 237C → T // Blood Cells, Molecules, and Diseases. - 2004. - Vol. 33. - P. 45-50.

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