Relatively frequent switching of transcription start sites during cerebellar development

por Zhang, Peter, Dimont, Emmanuel, Ha, Thomas, Swanson, Douglas J., Hide, Winston, Goldowitz, Dan
Publicado 2017

Nogo Receptor 1 (RTN4R) as a Candidate Gene for Schizophrenia: Analysis Using Human and Mouse Genetic Approaches

por Hsu, Ruby, Woodroffe, Abigail, Lai, Wen-Sung, Cook, Melloni N., Mukai, Jun, Dunning, Jonathan P., Swanson, Douglas J., Roos, J. Louw, Abecasis, Gonçalo R., Karayiorgou, Maria, Gogos, Joseph A.
Publicado 2007

Varied manifestations of persistent hyperplastic primary vitreous with graded somatic mosaic deletion of a single gene

por Mary-Sinclair, Michelle N., Wang, XiaoFei, Swanson, Douglas J., Sung, Caroline Y., Mendonca, Eneida A., Wroblewski, Kristen, Baumer, Shannon H., Goldowitz, Dan, Jablonski, Monica M., Skapek, Stephen X.
Publicado 2014

Correction to: Relatively frequent switching of transcription start sites during cerebellar development

por Zhang, Peter, Dimont, Emmanuel, Ha, Thomas, Swanson, Douglas J., Itoh, Masayoshi, Kawaji, Hideya, Lassmann, Timo, Daub, Carsten O., Arner, Erik, Carninci, Piero, Hayashizaki, Yoshihide, Forrest, Alistair R. R., Hide, Winston, Goldowitz, Dan
Publicado 2018

Identification of novel cerebellar developmental transcriptional regulators with motif activity analysis

por Ha, Thomas J., Zhang, Peter G. Y., Robert, Remi, Yeung, Joanna, Swanson, Douglas J., Mathelier, Anthony, Wasserman, Wyeth W., Im, Sujin, Itoh, Masayoshi, Kawaji, Hideya, Lassmann, Timo, Daub, Carsten O., Arner, Erik, Carninci, Piero, Hayashizaki, Yoshihide, Forrest, Alistair R. R., Goldowitz, Daniel
Publicado 2019