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Expert Review of Molecular Diagnostics Volume 14, 2014 - Issue 5
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Editorial

Measuring hypoxia-induced RNA in maternal blood: a new way to identify critically hypoxic fetuses in utero?

Clare L WhiteheadTranslational Obstetrics Group, Department of Obstetrics and Gynaecology, University of Melbourne, Mercy Hospital for Women, 163 Studley Rd., Heidelberg 3084, Victoria, Australia
&
Stephen TongTranslational Obstetrics Group, Department of Obstetrics and Gynaecology, University of Melbourne, Mercy Hospital for Women, 163 Studley Rd., Heidelberg 3084, Victoria, AustraliaCorrespondence[email protected]
Pages 509-511 | Published online: 30 Apr 2014

References

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  • Poon LL, Leung TN, Lau TK, Lo YM. Presence of fetal RNA in maternal plasma. Clin Chem 2000;46:1832-4
  • Lawn JE, Blencowe H, Pattinson R, et al. Stillbirths: where? When? Why? How to make the data count? Lancet 2011;377:1448-63
  • Lawn JE, Lee AC, Kinney M, et al. Two million intrapartum-related stillbirths and neonatal deaths: where, why, and what can be done? Int J Gynaecol Obstet 2009;107(Suppl 1):S5-18. S19
  • Ross MG. Labor and fetal heart rate decelerations: relation to fetal metabolic acidosis. Clin Obstet Gynecol 2011;54:74-82
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  • Whitehead C, Teh WT, Walker SP, et al. Quantifying circulating hypoxia-induced RNA transcripts in maternal blood to determine in utero fetal hypoxic status. BMC Med 2013;11:256
  • Whitehead CL, Teh WT, Walker SP, et al. Circulating MicroRNAs in maternal blood as potential biomarkers for fetal hypoxia in-utero. PLoS One 2013;8:e78487

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