DNMT3A Haploinsufficiency Results in Behavioral Deficits and Global Epigenomic Dysregulation Shared across Neurodevelopmental Disorders

por Christian, Diana L., Wu, Dennis Y., Martin, Jenna R., Moore, J. Russell, Liu, Yiran R., Clemens, Adam W., Nettles, Sabin A., Kirkland, Nicole M., Papouin, Thomas, Hill, Cheryl A., Wozniak, David F., Dougherty, Joseph D., Gabel, Harrison W.
Publicado 2020

Functional and epigenetic phenotypes of humans and mice with DNMT3A Overgrowth Syndrome

por Smith, Amanda M., LaValle, Taylor A., Shinawi, Marwan, Ramakrishnan, Sai M., Abel, Haley J., Hill, Cheryl A., Kirkland, Nicole M., Rettig, Michael P., Helton, Nichole M., Heath, Sharon E., Ferraro, Francesca, Chen, David Y., Adak, Sangeeta, Semenkovich, Clay F., Christian, Diana L., Martin, Jenna R., Gabel, Harrison W., Miller, Christopher A., Ley, Timothy J.
Publicado 2021

Preclinical research in Rett syndrome: setting the foundation for translational success

por Katz, David M., Berger-Sweeney, Joanne E., Eubanks, James H., Justice, Monica J., Neul, Jeffrey L., Pozzo-Miller, Lucas, Blue, Mary E., Christian, Diana, Crawley, Jacqueline N., Giustetto, Maurizio, Guy, Jacky, Howell, C. James, Kron, Miriam, Nelson, Sacha B., Samaco, Rodney C., Schaevitz, Laura R., St. Hillaire-Clarke, Coryse, Young, Juan L., Zoghbi, Huda Y., Mamounas, Laura A.
Publicado 2012