The list of publications supported by the National Institutes of Health (NIH) common fund glycoscience program, grant number 1R21AI129873.
- Ferreira, C. R., Xia, Z. J., Clement, A., Parry, D. A., Davids, M., Taylan, F., Sharma, P., Turgeon, C. T., Blanco-Sanchez, B., Ng, B. G., Logan, C. V., Wolfe, L. A., Solomon, B. D., Cho, M. T., Douglas, G., Carvalho, D. R., Bratke, H., Haug, M. G., Phillips, J. B., Wegner, J., Tiemeyer, M., Aoki, K., Undiagnosed Diseases, N., Scottish Genome, P., Nordgren, A., Hammarsjo, A., Duker, A. L., Rohena, L., Hove, H. B., Ek, J., Adams, D., Tifft, C. J., Onyekweli, T., Weixel, T., Macnamara, E., Radtke, K., Powis, Z., Earl, D., Gabriel, M., Russi, A. H. S., Brick, L., Kozenko, M., Tham, E., Raymond, K. M., Phillips, J. A., 3rd, Tiller, G. E., Wilson, W. G., Hamid, R., Malicdan, M. C. V., Nishimura, G., Grigelioniene, G., Jackson, A., Westerfield, M., Bober, M. B., Gahl, W. A., and Freeze, H. H. (2018) A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation. Am J Hum Genet 103, 553-567
- Miller, J. J., Aoki, K., Mascari, C. A., Beltrame, A. K., Sokumbi, O., North, P. E., Tiemeyer, M., Kriegel, A. J., and Dahms, N. M. (2018) alpha-Galactosidase A-deficient rats accumulate glycosphingolipids and develop cardiorenal phenotypes of Fabry disease. FASEB J, fj201800771R
- Miller, J. J., Aoki, K., Moehring, F., Murphy, C. A., O’Hara, C. L., Tiemeyer, M., Stucky, C. L., and Dahms, N. M. (2018) Neuropathic pain in a Fabry disease rat model. JCI Insight 3