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Liping Feng, MD

Property title
Assistant Professor of Obstetrics and Gynecology
Campus Mail: 303 Research Drive, 246 Sands, Durham, NC 27710
Phone: (919) 613-1459
Email: feng0007@mc.duke.edu

My research has focused on understanding the mechanisms of pregnancy complications associated with infection and maternal chemical exposures. These works are translated then to the clinical care of women through studies dedicated to identify risk factors and novel biomarkers for early prediction and prevention of adverse birth outcomes.

Liping Feng, MD, devotes her entire career to improving pregnancy outcomes through innovative research. Dr. Feng conducts both basic science/laboratory research, as well as participates in clinical studies. Her laboratory has focused on understanding the mechanisms of preterm birth, which is an important cause of perinatal and neonates’ mortality and morbidity. Currently, she has three lines of investigation focused on the roles of inflammation/infection, genetic variation, and environmental exposure in pregnancy complications, such as preterm birth and preeclampsia. This work is translated then to the clinical care of women through studies dedicated to identify risk factors and novel biomarkers for early prediction and prevention of pregnancy complications.

In addition, Dr. Feng has established an international collaboration in Global Women’s Health. She has recently affiliated with the Duke Global Health Institute (DGHI) and participates in a DGHI research. She has an interest in DGHI education, and service or policy initiatives, including mentoring and teaching graduate and professional students on fieldwork and research.

Education and Training

  • M.D., Harbin Medical University (China), 1997

Research

My research has focused on understanding the mechanisms of pregnancy complications associated with infection and maternal chemical exposures. These works are translated then to the clinical care of women through studies dedicated to identify risk factors and novel biomarkers for early prediction and prevention of adverse birth outcomes.

Liping Feng, MD, devotes her entire career to improving pregnancy outcomes through innovative research. Dr. Feng conducts both basic science/laboratory research, as well as participates in clinical studies. Her laboratory has focused on understanding the mechanisms of preterm birth, which is an important cause of perinatal and neonates’ mortality and morbidity. Currently, she has three lines of investigation focused on the roles of inflammation/infection, genetic variation, and environmental exposure in pregnancy complications, such as preterm birth and preeclampsia. This work is translated then to the clinical care of women through studies dedicated to identify risk factors and novel biomarkers for early prediction and prevention of pregnancy complications.

In addition, Dr. Feng has established an international collaboration in Global Women’s Health. She has recently affiliated with the Duke Global Health Institute (DGHI) and participates in a DGHI research. She has an interest in DGHI education, and service or policy initiatives, including mentoring and teaching graduate and professional students on fieldwork and research.

Projects

  • Understanding chemical exposure of PFBS during pregnancy and birth outcomes using in vitro and in vivo models. Using these models established in my lab, we could also test other environmental exposures

  • Investigating the impact of E-waste recycling and birth outcomes in China (Global health)

  • Building a novel in vitro placental model (collaboration with BME) to explore the mechanisms of ZIKA virus in utero transmission

  • Determine the roles of an understudied bacteria, Ureaplasma, in pregnancy

Publications

Murtha, A, Feng, L, Yonish, B, and Schomberg, D. "Progesterone protects chorion and decidua cells from calcium induced cell death in primary cell culture." December 2006.

Full Text

Mills, AA, Yonish, B, Feng, L, Schomberg, DW, Heine, RP, and Murtha, AP. "Characterization of progesterone receptor isoform expression in fetal membranes." Am J Obstet Gynecol 195, no. 4 (October 2006): 998-1003.

Full Text

Mills, A, Yonish, B, Feng, L, and Murtha (F), A. "Characterization of progesterone receptor isoform expression in fetal membranes." December 2005.

Full Text

Yan, H, Yin, P, Park, SH, Li, HY, Feng, LP, Guan, XJ, Liu, DG, Reif, JH, and LaBean, TH. "Self-assembled DNA structures for nanoconstruction." 2004.

Scholars@Duke

Yan, H, Feng, L, LaBean, TH, and Reif, JH. "Parallel molecular computations of pairwise exclusive-or (XOR) using DNA "string tile" self-assembly." J Am Chem Soc 125, no. 47 (November 26, 2003): 14246-14247.

Full Text

Feng, L, Park, SH, Reif, JH, and Yan, H. "A two-state DNA lattice switched by DNA nanoactuator." Angew Chem Int Ed Engl 42, no. 36 (September 22, 2003): 4342-4346.

Full Text

Yan, H, LaBean, TH, Feng, L, and Reif, JH. "Directed nucleation assembly of DNA tile complexes for barcode-patterned lattices." Proc Natl Acad Sci U S A 100, no. 14 (July 8, 2003): 8103-8108.

Full Text

LaBean, TH, Yan, H, Park, SH, Feng, LP, Yin, P, Li, HY, Ahn, SJ, Liu, D, Guan, XJ, and Reif, JH. "Overview of new structures for DNA-Based nanofabrication and computation." 2003.

Scholars@Duke

Pages