Familial Atypical Hemolytic Uremic Syndrome: A Review of Its Genetic and Clinical Aspects

Por Bu, Fengxiao, Borsa, Nicolo, Gianluigi, Ardissino, Smith, Richard J. H.
Publicado em 2012

Comprehensive Genetic Analysis of Complement and Coagulation Genes in Atypical Hemolytic Uremic Syndrome

Por Bu, Fengxiao, Maga, Tara, Meyer, Nicole C., Wang, Kai, Thomas, Christie P., Nester, Carla M., Smith, Richard J. H.
Publicado em 2014

TBC1D24 Mutation Causes Autosomal Dominant Non-Syndromic Hearing Loss

Por Azaiez, Hela, Booth, Kevin T., Bu, Fengxiao, Huygen, Patrick, Shibata, Seiji, Shearer, A. Eliot, Kolbe, Diana, Meyer, Nicole, Black-Ziegelbein, E. Ann, Smith, Richard J.H.
Publicado no Hum Mutat (2014)

Factors Predicting Vitamin D Response Variation in Non-Hispanic White Postmenopausal Women

Por Zhao, Lan-Juan, Zhou, Yu, Bu, Fengxiao, Travers-Gustafson, Dianne, Ye, An, Xu, Xiaojing, Hamm, Lee, Gorsage, Daniel Michael, Fang, Xiang, Deng, Hong-Wen, Recker, Robert R., Lappe, Joan M.
Publicado em 2012

HOMER2, a Stereociliary Scaffolding Protein, Is Essential for Normal Hearing in Humans and Mice

Por Azaiez, Hela, Decker, Amanda R., Booth, Kevin T., Simpson, Allen C., Shearer, A. Eliot, Huygen, Patrick L. M., Bu, Fengxiao, Hildebrand, Michael S., Ranum, Paul T., Shibata, Seiji B., Turner, Ann, Zhang, Yuzhou, Kimberling, William J., Cornell, Robert A., Smith, Richard J. H.
Publicado no PLoS Genet (2015)

High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies

Por Bu, Fengxiao, Borsa, Nicolo Ghiringhelli, Jones, Michael B., Takanami, Erika, Nishimura, Carla, Hauer, Jill J., Azaiez, Hela, Black-Ziegelbein, Elizabeth A., Meyer, Nicole C., Kolbe, Diana L., Li, Yingyue, Frees, Kathy, Schnieders, Michael J., Thomas, Christie, Nester, Carla, Smith, Richard J.H.
Publicado no J Am Soc Nephrol (2016)