Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia

Por Chen, Dong-Hui, Brkanac, Zoran, Verlinde, Christophe L. M. J., Tan, Xiao-Jian, Bylenok, Laura, Nochlin, David, Matsushita, Mark, Lipe, Hillary, Wolff, John, Fernandez, Magali, Cimino, P. J., Bird, Thomas D., Raskind, Wendy H.
Publicado em 2003

Germline PTEN Promoter Mutations and Deletions in Cowden/Bannayan-Riley-Ruvalcaba Syndrome Result in Aberrant PTEN Protein and Dysregulation of the Phosphoinositol-3-Kinase/Akt Pat...

Por Zhou, Xiao-Ping, Waite, Kristin A., Pilarski, Robert, Hampel, Heather, Fernandez, Magali J., Bos, Cindy, Dasouki, Majed, Feldman, Gerald L., Greenberg, Lois A., Ivanovich, Jennifer, Matloff, Ellen, Patterson, Annette, Pierpont, Mary Ella, Russo, Donna, Nassif, Najah T., Eng, Charis
Publicado em 2003