2019
Dolack, ME, C Lee, Y Ru, A Marghoub, JT Richtsmeier, EW Jabs, M Moazen, DA Garzón-Alvarado, RH Kraft (2019) Computational morphogenesis of embryonic bone development: past, present, and future. In, GL Niebur, ed., Mechanobiology: from molecular sensing to disease. Elsevier. DOI: 10.1016/B978-0-12-817931-4.00011-X
Durham, E, Howie, NR, Larson, N, LaRue, A, Cray J(2019) Pharmacological exposures may precipitate craniosynostosis through targeted stem cell depletion, Stem Cell Research, https://doi.org/10.1016/j.scr.2019.101528.
Sewda, A, SR White, M Erazo, K Hao, G García-Fructuoso, I Fernández-Rodriguez, Y Heuzé, JT Richtsmeier, PA Romitti, B Reva, EW Jabs, I Peter 2019 Targeted next-generation sequencing identifies novel coding variants in patients with nonsyndromic craniosynostosis, Pediatric Research 6(85):463-468. PMC6398438
Motch Perrine, SM, Wu, M, Stephens, NB, Kriti, D, van Bakel, H, Wang Jabs, E, Richtsmeier, JT(2019) Mandibular dysmorphology due to abnormal embryonic osteogenesis in FGFR2-related craniosynostosis mice, Disease Models & Mechanisms, https://doi.org/10.1242/dmm.038513.
Lee, C, JT Richtsmeier, R Kraft (2019) A coupled reaction-diffusion-strain model predicts cranial vault formation in development and disease, Biomech model mechanobiol, https://doi.org/10.1007/s10237-019-01139-z. NIHMSID: 1019092. Abstract
Lesciotto, KM, Richtsmeier, JT (2019) Craniofacial skeletal response to encephalization: How do we know what we think we know? Amer J Phys Anthropol. 168(S67):27-46. https://onlinelibrary.wiley.com/doi/10.1002/ajpa.23766
Lesciotto KM, Motch Perrine SM, Kawasaki M, Stecko T, Ryan TM, Kawasaki K, Richtsmeier JT (2019) Phosphotungstic acid-enhanced microCT: Optimized protocols for embryonic and early postnatal mice. Developmental Dynamics 249(4): 573-585, https://doi.org/10.1002/dvdy.136. PMCID: PMC7125040 [with cover illustration]
Richtsmeier, JT and KM Lesciotto (2019) From phenotype to genotype and back again (Du génotype au phénotype et vice versa). BMSAP, https://doi.org/10.3166/bmsap-2019-0065.
Kim, J.-W., Zhang, H., Seymen, F., Koruyucu, M., Hu, Y., Kang, J., Kim, Y. J., Ikeda, A., Kasimoglu, Y., Bayram, M., Chuhua Zhang, C., Kawasaki, K., Bartlett, J. D., Saunders, T. L., Simmer, J. P., Hu, J. C.-C. (2019) Mutations in RELT cause autosomal recessive amelogenesis imperfecta.2019 Clin. Genet. 95: 375-383.https://onlinelibrary.wiley.com/doi/10.1111/cge.13487
Copyright Notice
The documents above are provided here as a means to ensure timely dissemination of scholarly and technical work on a noncommercial basis. Copyright and all rights therein are maintained by the authors or by other copyright holders, notwithstanding that they have offered their works here electronically. It is understood that all persons copying this information will adhere to the terms and constraints invoked by each author’s copyright. These works may not be re-posted without the explicit permission of the copyright holder.