Making needles less prickly

Por Lardner, David R.R., Spencer, Adam O.
Publicado no CMAJ (2015)

Open source and DIY hardware for DNA nanotechnology labs

Por Damase, Tulsi R., Stephens, Daniel, Spencer, Adam, Allen, Peter B.
Publicado no J Biol Methods (2015)

PRK1 Distribution in Normal Tissues and Carcinomas: Overexpression and Activation in Ovarian Serous Carcinoma

Por Galgano, Mary T., Conaway, Mark, Spencer, Adam M., Paschal, Bryce M., Frierson, Henry F.
Publicado em 2009

Karyopherin α7 (KPNA7), a divergent member of the importin α family of nuclear import receptors

Por Kelley, Joshua B, Talley, Ashley M, Spencer, Adam, Gioeli, Daniel, Paschal, Bryce M
Publicado em 2010

Ligand Binding to the Androgen Receptor Induces Conformational Changes That Regulate Phosphatase Interactions

Por Yang, Chun-Song, Xin, Hong-Wu, Kelley, Joshua B., Spencer, Adam, Brautigan, David L., Paschal, Bryce M.
Publicado em 2007

Androgen Induces a Switch from Cytoplasmic Retention to Nuclear Import of the Androgen Receptor

Por Ni, Li, Llewellyn, Ryan, Kesler, Cristina T., Kelley, Joshua B., Spencer, Adam, Snow, Chelsi J., Shank, Leonard, Paschal, Bryce M.
Publicado em 2013

The Defective Nuclear Lamina in Hutchinson-Gilford Progeria Syndrome Disrupts the Nucleocytoplasmic Ran Gradient and Inhibits Nuclear Localization of Ubc9

Por Kelley, Joshua B., Datta, Sutirtha, Snow, Chelsi J., Chatterjee, Mandovi, Ni, Li, Spencer, Adam, Yang, Chun-Song, Cubeñas-Potts, Caelin, Matunis, Michael J., Paschal, Bryce M.
Publicado em 2011

Autosomal recessive mutations in nuclear transport factor KPNA7 are associated with infantile spasms and cerebellar malformation

Por Paciorkowski, Alex R, Weisenberg, Judy, Kelley, Joshua B, Spencer, Adam, Tuttle, Emily, Ghoneim, Dalia, Thio, Liu Lin, Christian, Susan L, Dobyns, William B, Paschal, Bryce M
Publicado em 2014

De Novo Mutations in SIK1 Cause a Spectrum of Developmental Epilepsies

Por Hansen, Jeanne, Snow, Chelsi, Tuttle, Emily, Ghoneim, Dalia H., Yang, Chun-Song, Spencer, Adam, Gunter, Sonya A., Smyser, Christopher D., Gurnett, Christina A., Shinawi, Marwan, Dobyns, William B., Wheless, James, Halterman, Marc W., Jansen, Laura A., Paschal, Bryce M., Paciorkowski, Alex R.
Publicado no Am J Hum Genet (2015)

De Novo Mutations in SIK1 Cause a Spectrum of Developmental Epilepsies

Por Hansen, Jeanne, Snow, Chelsi, Tuttle, Emily, Ghoneim, Dalia H., Yang, Chun-Song, Spencer, Adam, Gunter, Sonya A., Smyser, Christopher D., Gurnett, Christina A., Shinawi, Marwan, Dobyns, William B., Wheless, James, Halterman, Marc W., Jansen, Laura A., Paschal, Bryce M., Paciorkowski, Alex R.
Publicado no Am J Hum Genet (2015)