
GENETIC PREDISPOSITION TO PRE-ECLAMPSIA:
POLYMORPHISM OF GENES INVOLVED IN
REGULATION OF ENDOTHELIAL FUNCTIONS
Mozgovaia EV, Malysheva OV, Ivashchenko TE, Baranov VS* *Corresponding Author: Professor Dr. Vladislav S. Baranov, Laboratory of Prenatal Diagnosis of Inherited Disorders, D.O. Ott Research Institute of Obstetrics and Gynecology, Russian Academy of Medical Sciences, Mendeleevskaya line 3, St. Petersburg 199034, Russia; Tel/Fax: +07-812-328-0487; E-mail: baranov@vb2475. spb.edu page: 19
|
REFERENCES
1. Ness RB, Roberts JM. Heterogeneous causes constituting the single syndrome of pre-eclampsia: a hypothesis and its implications. Am J Obstet Gynecol 1996; 175: 1365-1370.
2. Spiridonova MG, Stepanov _A, Pousirev VP, Karpoy YS. Analysis of gene complex predisposing to coronary atherosclerosis. Genetics 2002; 38(3): 383-392.
3. Tuddenham EGD, Cooper DN. The Molecular Genetics of Haemostasis and its Inherited Disorders. Oxford Monographs on Medical Genetics 25, Oxford University Press, Oxford, UK, 1994; 585.
4. Folio M, Ginsburg D. Structure and expression of the human gene encoding plasminogen activator inhibitor, PAI-1. Gene 1989; 84: 447-453.
5. Yamada N, Arinami T, Yamakawa-Kobayashi K. The 4G/5G polymorphism of the plasminogen activator inhibitor-1 gene is assotiated with severe pre-eclampsia. J Hum Genet 2000; 45(3): 138-141.
6. Zhou N, Yu P, Chen J, Huang H, Jiang S. Detection of insertion/deletion polymorphism of angiotensin converting enzymegene in pre-eclampsia. (Chinese.) Zhonghua Yi Xue Yi Chuan Xue Za Zhi 1999; 16(1): 29-31.
7. Heiskanen JTM, Pirskanen MM, Hiltunen MJ, Mannermaa AJ, Punnonen KRA, Heinonen ST. Insertion-deletion polymorphism in the gene for angiotensin-converting enzyme is associated with obstetric cholestasis but not with pre-eclampsia. Am J Obstet Gynecol 2001; 185: 600-603.
8. Knowles RG, Moncada S. Nitric oxide synthases in mammals. Biochem J 1994; 298: 249-258.
9. Tempfer C, Soebbing D, Dorman K, Gregg AR. A NOS3 polymorphism is associated with pre-eclampsia. Am J Obstet Gynecol 1999; 180(1 Pt 2): S18.
10. Buttke TM, Sandstrom PA. Oxidative stress as a mediator of apoptosis. Immunol Today 1994; 15: 7–10.
11. Bashford MT, Michael T, Hefler L, Vertrees TW, Roa BB, Gregg A. Angiotensinogen and endothelial nitric oxide synthase gene polymorphisms among Hispanic patients with pre-eclampsia. Am J Obstet Gynecol 2001; 184: 1345-1351.
12. Livingston JC, Park V, Barton JR, Elfering S, Haddad B, Mabie WC. Lack of association of severe pre-eclampsia with maternal and fetal mutant alleles for tumor necrosis factor a and lymphotoxin a genes and plasma tumor necrosis factor a levels. Am J Obstet Gynecol 2001; 184: 1273-1277.
13. Wilson AG, Symons JA. Effects of a polymorphism in the human TNF-a promoter on transcriptional activation. Proc Natl Acad Sci USA 1997; 94: 3195-3199.
14. Watson MA, Steward RK, Smith GB, Massey TE, Bell DA. Human glutathione S-transferase P1 polymorphisms: relationship to lung tissue enzyme activity and population frequency distribution. Carcinogenesis 1998; 9: 275-280.
15. Zusterzeel PL, Visser W, Peters WH, Merkus HW, Nelen WL, Steegers EA. Polymorphism in the glutathione S-transferase PI gene and risk for pre-eclampsia. Obstet Gynecol 2000; 96(l): 50-54.
16. Kingdom J, Huppertz B, Seaward G, Kaufman P. Development of the placental villous tree and its consequences for fetal growth. J Obstet Gynecol 2000; 92: 35-43.
|
|
|
|



 |
Number 27 VOL. 27 (2), 2024 |
Number 27 VOL. 27 (1), 2024 |
Number 26 Number 26 VOL. 26(2), 2023 All in one |
Number 26 VOL. 26(2), 2023 |
Number 26 VOL. 26, 2023 Supplement |
Number 26 VOL. 26(1), 2023 |
Number 25 VOL. 25(2), 2022 |
Number 25 VOL. 25 (1), 2022 |
Number 24 VOL. 24(2), 2021 |
Number 24 VOL. 24(1), 2021 |
Number 23 VOL. 23(2), 2020 |
Number 22 VOL. 22(2), 2019 |
Number 22 VOL. 22(1), 2019 |
Number 22 VOL. 22, 2019 Supplement |
Number 21 VOL. 21(2), 2018 |
Number 21 VOL. 21 (1), 2018 |
Number 21 VOL. 21, 2018 Supplement |
Number 20 VOL. 20 (2), 2017 |
Number 20 VOL. 20 (1), 2017 |
Number 19 VOL. 19 (2), 2016 |
Number 19 VOL. 19 (1), 2016 |
Number 18 VOL. 18 (2), 2015 |
Number 18 VOL. 18 (1), 2015 |
Number 17 VOL. 17 (2), 2014 |
Number 17 VOL. 17 (1), 2014 |
Number 16 VOL. 16 (2), 2013 |
Number 16 VOL. 16 (1), 2013 |
Number 15 VOL. 15 (2), 2012 |
Number 15 VOL. 15, 2012 Supplement |
Number 15 Vol. 15 (1), 2012 |
Number 14 14 - Vol. 14 (2), 2011 |
Number 14 The 9th Balkan Congress of Medical Genetics |
Number 14 14 - Vol. 14 (1), 2011 |
Number 13 Vol. 13 (2), 2010 |
Number 13 Vol.13 (1), 2010 |
Number 12 Vol.12 (2), 2009 |
Number 12 Vol.12 (1), 2009 |
Number 11 Vol.11 (2),2008 |
Number 11 Vol.11 (1),2008 |
Number 10 Vol.10 (2), 2007 |
Number 10 10 (1),2007 |
Number 9 1&2, 2006 |
Number 9 3&4, 2006 |
Number 8 1&2, 2005 |
Number 8 3&4, 2004 |
Number 7 1&2, 2004 |
Number 6 3&4, 2003 |
Number 6 1&2, 2003 |
Number 5 3&4, 2002 |
Number 5 1&2, 2002 |
Number 4 Vol.3 (4), 2000 |
Number 4 Vol.2 (4), 1999 |
Number 4 Vol.1 (4), 1998 |
Number 4 3&4, 2001 |
Number 4 1&2, 2001 |
Number 3 Vol.3 (3), 2000 |
Number 3 Vol.2 (3), 1999 |
Number 3 Vol.1 (3), 1998 |
Number 2 Vol.3(2), 2000 |
Number 2 Vol.1 (2), 1998 |
Number 2 Vol.2 (2), 1999 |
Number 1 Vol.3 (1), 2000 |
Number 1 Vol.2 (1), 1999 |
Number 1 Vol.1 (1), 1998 |
|
|