Смекни!
smekni.com

Аллельные варианты генов-кандидатов подверженности туберкулезу у русского населения Западной Сибири (стр. 20 из 20)

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.