Диссертация (1145983), страница 41
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Kaur, V. Jain, M. Khuller [et al.] // Acta Obstet Gynecol Scand. 2005. - Vol. 84, № 10. - P. 929–933.41. Korobochka, R. Association between a functional dopamine D4 receptor promoter regionpolymorphism (-C521T) and pre-eclampsia: a family-based study / R. Korobochka, I.Gritsenko, R. Gonen [et al.] // Mol Hum Reprod. - 2006. - Vol. 12, № 2. - P. 85-88.42. Kvehaugen, A. S.
Single nucleotide polymorphisms in G protein signaling pathway genes inpreeclampsia / A. S. Kvehaugen, O. Melien, O. L. Holmen [et al.] // Hypertension. - 2013. Vol. 61, № 3. - P. 655-661.43. Lim, J. E. CD14 receptor gene promoter polymorphism: awakening maternal immunity duringpregnancy / J. E.
Lim, T. Kim, N. W. Lee [et al.] // J Int Med Res. - 2006. - Vol. 34, № 2. - P.176-182.44. Lim, J. H. Association between genetic polymorphisms in androgen receptor gene and the riskof preeclampsia in Korean women / J. H. Lim, S. Kim, S. W. Lee [et al.] // J Assist ReprodGenet. - 2011. - Vol. 28, № 1. - P. 85-90.45. Lim, P. O. Variation at the aldosterone synthase (CYP11B2) locus contributes to hypertensionin subjects with a raised aldosterone-to-renin ratio / P. O.
Lim, T. M. Macdonald, C. Holloway[et al.] // J Clin Endocrinol Metab. - 2002. - Vol. 87, № 9. - P. 4398-4402.46. Lin, J. Genetic thrombophilias and preeclampsia: a meta-analysis / J. Lin, P. August // ObstetGynecol. - 2005. - Vol. 105, № 1. - P. 182–192.47. Luizon, M. R. Tissue inhibitor of matrix metalloproteinase-1 polymorphism, plasma TIMP-1levels, and antihypertensive therapy responsiveness in hypertensive disorders of pregnancy //M. R. Luizon, A.
C. Palei, V. C. Sandrim [et al.] / Pharmacogenomics J. - 2014. - Vol. 14, № 6.- P. 535-541.16548. Luo, D. Prostasin gene polymorphism at rs12597511 is associated with severe preeclampsia inChinese Han women / D. Luo, Y. Zhang, Y. Bai [et al.] // Chin Med J (Engl). - 2014. - Vol.127, № 11. - P. 2048-2052.49. Moreau, P. HLA-G gene polymorphism in human placentas: possible association of G*0106allele with preeclampsia and miscarriage / P.
Moreau, L. Contu, F. Alba [et al.] // Biol Reprod.- 2008. - Vol. 79, № 3. - P. 459-467.50. Morrison, A. C. Genetic variation in solute carrier genes is associated with preeclampsia / A. C.Morrison, S. K. Srinivas, M. A. Elovitz, J. B. Puschett // Am J Obstet Gynecol. - 2010. - Vol.203, № 5. - P. 491.e1-491.e13.51. Moses, E. K. Genetic association of preeclampsia to the inflammatory response gene SEPS1 /E. K. Moses, M. P.
Johnson, L. Tømmerdal [et al.] // Am J Obstet Gynecol. - 2008. - Vol. 198,№ 3. - P. 336.e1-336.e5.52. Mouzat, K. A common polymorphism in NR1H2 (LXRbeta) is associated with preeclampsia /K. Mouzat, E. Mercier, A. Polge [et al.] // BMC Med Genet. - 2011. - Vol. 12: 145. - 9 p.53. Mtiraoui, N. Methylenetetrahydrofolate reductase C677T and A1298C polymorphism andchanges in homocysteine concentrations in women with idiopathic recurrent pregnancy losses /N. Mtiraoui, W.
Zammiti, L. Ghazouani [et al.] // Reproduction. - 2006. - Vol. 131. - P. 395401.54. Muravská, A. Association of pregnancy-associated plasma protein A polymorphism withpreeclampsia - a pilot study / A. Muravská, A. Germanová, M. Jáchymová [et al.] // ClinBiochem. - 2011.
- Vol. 44, № 17-18. - P. 1380-1384.55. Nagy, B. Apolipoprotein E alleles in women with severe pre-eclampsia / B. Nagy, J. Jr. Rigo,L. Fintor [et al.] // Clin Pathol. - 1998. - Vol. 51, № 4. - P. 324-325.56. O’Shaughnessy, K. M. Thrombophilic polymorphisms in pre-eclampsia: altered frequency ofthe functional 98C>T polymorphism of glycoprotein IIIa / K. M.
O’Shaughnessy, B. Fu, S.Downing, N. H. Morris // J Med Genet. - 2001. - Vol.38, № 11. - P.775-777.57. Ota, S. Contribution of fetal ANXA5 gene promoter polymorphisms to the onset of preeclampsia / H. Miyamura, H. Nishizawa [et al.] // Placenta. - 2013. - Vol. 34, № 12. - P. 12021210.58. Ozturk, E. Genetic variation of myeloperoxidase gene contributes to preeclampsia: apreliminary association study in Turkish population / E. Ozturk, O. Balat, S. Pehlivan [et al.] //Hypertens Pregnancy. - 2011. - Vol. 30, № 4.
- P. 377-383.59. Pendeloski, K. P. Immunoregulatory gene polymorphisms in women with preeclampsia / K. P.Pendeloski, N. Sass, M. R. Torloni [et al.] // Hypertens Res. - 2011. - Vol. 34, № 3. - P. 384388.16660. Procopciuc, L. Angiotensinogen gene M235T variant and pre-eclampsia in Romanian pregnantwomen / L. Procopciuc, G. Jebeleanu, I. Surcel, M. Puscas // J Cell Mol Med. - 2002. - Vol.
6,№ 3. - P. 383-388.61. Procopciuc, L. M. Maternal/newborn genotype contribution of the renin-angiotensin system(Met235Thr, Thr174Met, I/D-ACE, A2350G-ACE, A1166C-AT2R1, C3123A- AT2R2, 83A/GREN) to the risk of pre-eclampsia: a Romanian study / L. M.
Procopciuc, G. Caracostea, G.Zaharie [et al.] // J Renin Angiotensin Aldosterone Syst. - 2011. - Vol. 12, № 4. - P. 539-548.62. Saadat, M. Genetic polymorphisms of glutathione S-transferase Z1 (GSTZ1) and susceptibilityto preeclampsia / M. Saadat, Z. Anvar, B. Namavar-Jahromi, I. Saadat // Mol Biol Rep. - 2012.- Vol. 39, № 9. - P. 8995-8998.63. Saarela, T. Tumour necrosis factor-alpha gene haplotype is associated with pre-eclampsia / T.Saarela, M. Hiltunen, S. Helisalmi [et al.] // Mol Hum Reprod.
- 2005. - Vol. 11, № 6. - P. 437440.64. Said, L. Maternal tumor necrosis factor receptor 2 gene variants associated with pre-eclampsiain Tunisian women / L. Said, R. Faleh, S. Smida [et al.] // J Obstet Gynaecol Res. - 2013. - Vol.39, № 8. - P. 1301-1307.65. Salimi, S. Possible association of IL-4 VNTR polymorphism with susceptibility topreeclampsia / S. Salimi, M. Mohammadoo-Khorasani, M. Yaghmaei [et al.] // Biomed Res Int.- 2014. - Vol. 2014, Article ID 497031.
- 5 p.66. Samsami, D. A. Heterozygosity in CTLA-4 gene and severe preeclampsia / D. A. Samsami, M.Doroudchi, T. Kalantari [et al.] // Int J Gynaecol Obstet. - 2005. - Vol. 88, № 1. - P. 19-24.67. Sandoval-Carrillo, A. Polymorphisms in the GSTT1 and GSTM1 genes are associated withincreased risk of preeclampsia in the Mexican mestizo population / A. Sandoval-Carrillo, M.Aguilar-Duran, F.
Vázquez-Alaniz [et al.] // Genet Mol Res. - 2014. - Vol. 13, № 1. - P. 21602165.68. Sato, I. Study of association between hypertensive disorders of pregnancy and the humancoagulation factor XI gene / T. Nakayama, A. Maruyama [et al.] // Hypertens Pregnancy. 2006. - Vol. 25, № 1. - P. 21-31.69. Seremak-Mrozikiewicz, A. A1166C mutation of angiotensin II type 1 receptor gene iscorrelated with umbilical blood flow velocimetry in women with preeclampsia / A.
SeremakMrozikiewicz, M. Dubiel, K. Drews [et al.] // J Matern Fetal Neonatal Med. - 2005. - Vol. 17,№ 2. - P. 117-121.70. Seremak-Mrozikiewicz, A. Genetic variability of endothelin-1 system in gestationalhypertension and preeclampsia [Abstract] / A. Seremak-Mrozikiewicz, M. Barlik, M. Perlik [etal.] // Ginekol Pol. - 2011b. - Vol. 82, № 5. - P. 363-370.16771.
Seremak-Mrozikiewicz, A. The significance of −786T > C polymorphism of endothelial NOsynthase (eNOS) gene in severe preeclampsia / A. Seremak-Mrozikiewicz, K. Drews, M. Barlik[et al.] // J Matern Fetal Neonatal Med. - 2011a. - Vol. 24, № 3. - P. 432-436.72. Seremak-Mrozikiewicz, A. The significance of genetic polymorphisms of factor v leiden andprothrombin in the preeclamptic polish women / A. Seremak-Mrozikiewicz, K. Drews, E.Wender-Ozegowska, P. M. Mrozikiewicz // J Thromb Thrombolysis. - 2010. - Vol.
30, № 1. P. 97-104.73. Sharma, P. Mining literature for a comprehensive pathway analysis: a case study for retrievalof homocysteine related genes for genetic and epigenetic studies / P. Sharma, R. D.Senthilkumar, V. Brahmachari [et al.] // Lipids Health Dis. -2006. - Vol. 5: 1. - 19 p.74. Shim, J. Y. Vascular endothelial growth factor gene +936 C/T polymorphism is associated withpreeclampsia in Korean women / J. Y.
Shim, J. K. Jun, B. K. Jung [et al.] // Am J ObstetGynecol. - 2007. - Vol. 197, № 3. - P. 271.e1-271.e4.75. Shimodaira, M. Estrogen synthesis genes CYP19A1, HSD3B1, and HSD3B2 in hypertensivedisorders of pregnancy / M. Shimodaira, T. Nakayama, I. Sato [et al.] // Endocrine. - 2012. Vol. 42, № 3. - P. 700-707.76.
Shimodaira, M. Glucocorticoid synthesis-related genes: HSD11B1 and HSD11B2 inhypertensive disorders in pregnancy / M. Shimodaira, T. Nakayama, I. Sato [et al.] // GynecolEndocrinol. - 2013. - Vol. 29, № 7. - P. 657-661.77. Sowmya, S. Interleukin 10 Gene Promoter Polymorphisms in Women with early onsetPreeclampsia / S. Sowmya, K. S. Manjari, A. Ramaiah [et al.] // Clin Exp Immunol.
- 2014. Vol. 178, № 2. - P. 334-341.78. Srinivas, S. K. Allelic variations in angiogenic pathway genes are associated with preeclampsia/ S. K. Srinivas, A. C. Morrison, C. M. Andrela, M. A. Elovitz // Am J Obstet Gynecol. - 2010.- Vol. 202, № 5. - P. 445.e1-445.e11.79. Stiefel, P. Genotype of the CYBA promoter -930A/G, polymorphism C677T of the MTHFR andAPOE genotype in patients with hypertensive disorders of pregnancy: an observational study /P.
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