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Research Articles

STOX1 promotor region -922 T > C polymorphism is associated with Early-Onset preeclampsia

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References

  • Abel, D., et al., 2012. Transcription factor STOX1A promotes mitotic entry by binding to the CCNB1 promotor. PLoS One, 7 (1), e29769.
  • American College of Obstetricians and Gynecologists (ACOG). 2013. Task Force on Hypertension in Pregnancy. Hypertension in Pregnancy. Report of the American College of Obstetricians and Gynecologists’ Task Force on Htypertension in Pregnancy. ObstetGynecol, 122 (5), 1122–1131.
  • Bellamy, L., et al., 2007. Pre-eclampsia and risk of cardiovascular disease and cancer in later life: Systematic review and meta-analysis. BMJ, 335 (7627), 974.
  • Berends, A.L., et al., 2007. STOX1 gene in pre-eclampsia and intrauterine growth restriction. An İnternational Journal of Obstetrics and Gynaecology, 114 (9), 1163–1167.
  • Espinoza, J., et al., 2019. ACOG Practice Bulletin No. 202: gestational hypertension and preeclampsia. Obstet Gynecol, 133 (1), e1–25.
  • Doridot, L., et al., 2014. Nitroso-redox balance and mitochondrial homeostasis are regulated by STOX1, a pre-eclampsia-associated gene. Antioxidants & Redox Signaling, 21 (6), 819–834.
  • Ducat, A., et al., 2016. Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia. Scientific Reports, 6, 19196.
  • Ducat, A., et al., 2020. Molecular mechanisms of trophoblast dysfunction mediated by ımbalance between STOX1 ısoforms. iScience, 23 (5), 101086.
  • England, L. and Zhang, J., 2007. Smoking and risk of preeclampsia: a systematic review. Frontiers in Bioscience, 12, 2471–2483.
  • Hansen, A.T., et al., 2018. The genetic component of preeclampsia: a whole-exome sequencing study. PloS One, 13 (5), e0197217.
  • Haram, K., Mortensen, J.H. and Nagy, B., 2014. Genetic aspects of preeclampsia and the HELLP syndrome. Journal of Pregnancy, 2014, 910751.
  • Iglesias-Platas, I., et al., 2007. STOX1 is not imprinted and is not likely to be involved in preeclampsia. Nature Genetics, 39 (3), 279–280.
  • Jakovljevic, T.S., et al., 2021. Association between endothelial nitric oxide synthase (eNOS)-786 T/C and 27-bp VNTR 4b/a polymorphisms and preeclampsia development. Reprod. Science, 28 (12), 3529–3539.
  • Jim, B. and Karumanchi, S.A., 2017. Preeclampsia: pathogenesis, prevention, and long-term complications. Seminars in Nephrology, 37 (4), 386–397.
  • Jimenez, K.M., et al., 2020. Identifying new potential genetic biomarkers for HELLP syndrome using massive parallel sequencing. Pregnancy Hypertension, 22, 181–190.
  • Johnson, M.P., et al., 2007. Identification of two novel quantitative trait loci for pre-eclampsia susceptibility on chromosomes 5q and 13q using a variance components-based linkage approach. Molecular Human Reproduction, 13 (1), 61–67.
  • LaMarca, B., et al., 2016. Identifying immune mechanisms mediating the hypertension during preeclampsia. American Journal of Physiology, 311 (1), R1–9.
  • Lain, K.Y., et al., 2003. Smoking during pregnancy is associated with alterations in markers of endothelial function. American Journal of Obstetrics and Gynecology, 189 (4), 1196–1201.
  • Laivuori, H., et al., 2003. Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families. American Journal of Human Genetics, 72 (1), 168–177.
  • Ma’ayeh, M. and Costantine, M.M., 2020. Prevention of preeclampsia. Seminars in Fetal & Neonatal Medicine, 25 (5), 101123.
  • McGinnis, R., et al., 2017. Variants in the fetal genome near FTL1 are associated with risk of preeclampsia. Nature Genetics, 49 (8), 1255–1260.
  • Mijal, R.S., et al., 2011. Midpregnancy levels of angiogenic markers in relation to maternal characteristics. American Journal of Obstetrics and Gynecology, 204 (3), 244.e1-12–244.12.
  • Mirkovic, L., Nejkovic, L. and Micic, J., 2018. A new pathophysiological concept and new classification of pre-eclampsia. Vojnosanitetski Pregled, 75 (1), 83–94.
  • Moses, E.K., et al., 2006. Objective prioritization of positional candidate genes at a quantitative trait locus for pre-eclampsia on 2q22. Molecular Human Reproduction, 12 (8), 505–512.
  • Oudejans, C.B., et al., 2004. The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas. Molecular Human Reproduction, 10 (8), 589–598.
  • Pinarbasi, E., et al., 2020. STOX1 gene Y153H polymorphism is associated with early-onset preeclampsia in Turkish population. Gene, 754, 144894.
  • Rigourd, V., et al., 2008. STOX1 overexpression in choriocarcinoma cells mimics transcriptional alterations observed in preeclamptic placentas. PLoS One, 3 (12), e3905.
  • Salonen Ros, H., et al., 2000. Genetic effects on the liability of developing preeclampsia and gestational hypertension. American Journal of Medical Genetics, 91 (4), 256–260.
  • Ullrich, A., et al., 1977. Rat insülin genes: construction of plasmids containing the coding sequences. Science, 196 (4296), 1313–1319.
  • Than, N.G., et al., 2018. Integrated systems biology approach ıdentifies Novel maternal and placental pathways of preeclampsia. Frontiers in İmmunology, 9, 1661.
  • Vaiman, D. and Miralles, F., 2016. Targeting STOX1 in the therapy of preeclampsia. Expert Opinion on Therapeutic Targets, 20 (12), 1433–1443.
  • van Dijk, M., et al., 2005. Maternal segregation of the Dutch preeclampsia locus at 10q22 with a new member of the winged helix gene family. Nature Genetics, 37 (5), 514–519.
  • van Dijk, M., et al., 2010. Differential methylation of STOX1 in human placenta. Epigenetics, 5 (8), 736–742.

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