Postdoctoral, Craniofacial Development, University of Colorado Denver Anschutz Medical Campus
Ph.D., Biochemistry and Molecular Biology, Hunan Normal University
B.S, Biology, Hunan Normal University
Alternative Splicing Program during Craniofacial Development
Craniofacial Development and Orofacial Clefting at Single Cell Resolution
Dr. Li’s complete list of published work can be found on her My NCBI page.
Lee S, Sears MJ, Zhang Z, Li H, Salhab I, Krebs P, Xing Y, Nah HD, Williams T, Carstens RP. Cleft lip and cleft palate (CL/P) in Esrp1 KO mice is associated with alterations in epithelial-mesenchymal crosstalk. Development (2020), doi: 10.1242/dev.187369.
Li H, Jones KL, Hooper JE, Williams T. The molecular anatomy of mammalian upper lip and primary palate fusion at single cell resolution. Development (2019), 146(12), dev174888.
Van Otterloo E, Li H, Jones K, Williams T. AP-2α and AP-2β cooperatively orchestrate homeobox gene expression during branchial arch patterning. Development (2018), 145 (2), dev157438.
Hooper J, Feng W, Li H, Leach S, Phang T, Siska C, Jones K, Spritz R, Hunter L, Williams T. Systems biology of facial development: contributions of ectoderm and mesenchyme. Developmental Biology (2017), 426 (1): 97-114.
Green R, Feng W, Phang T, Fish J, Li H, Spritz R, Marcucio R, Hooper J, Jamniczky H, Hallgrímsson B, and Williams T. Tfap2a-dependent changes in mouse facial morphology result in clefting that can be ameliorated by a reduction in Fgf8 gene dosage. Disease Models & Mechanisms (2015), 7: 31-43.
Li H, Sheridan R, Williams T. Analysis of TFAP2A mutations in Branchio-Oculo-Facial Syndrome indicates functional complexity within the AP-2α DNA-binding domain. Human Molecular Genetics (2013), 22(16), 3195-3206.
Li H, & Williams T. Separation of mouse embryonic facial ectoderm and mesenchyme. Journal of Visualized Experiments (2013), (74). doi:10.3791/50248.