The mouse C9ORF72 ortholog is enriched in neurons known to degenerate in ALS and FTD

Por Suzuki, Naoki, Maroof, Asif, Merkle, Florian T, Koszka, Kathryn, Intoh, Atsushi, Armstrong, Ian, Moccia, Rob, Davis-Dusenbery, Brandi N, Eggan, Kevin
Publicado no Nat Neurosci (2013)

Loss-of-function mutations in the C9ORF72 mouse ortholog cause fatal autoimmune disease()

Por Burberry, Aaron, Suzuki, Naoki, Wang, Jin-Yuan, Moccia, Rob, Mordes, Daniel A., Stewart, Morag, Suzuki-Uematsu, Satomi, Ghosh, Sulagna, Singh, Ajay, Merkle, Florian T., Koszka, Kathryn, Li, Quan-Zhen, Zon, Leonard, Rossi, Derrick J., Trowbridge, Jennifer J., Notarangelo, Luigi D., Eggan, Kevin
Publicado no Sci Transl Med (2016)

Pathways Disrupted in Human ALS Motor Neurons Identified Through Genetic Correction of Mutant SOD1

Por Kiskinis, Evangelos, Sandoe, Jackson, Williams, Luis A., Boulting, Gabriella L., Moccia, Rob, Wainger, Brian J., Han, Steve, Peng, Theodore, Thams, Sebastian, Mikkilineni, Shravani, Mellin, Cassidy, Merkle, Florian T., Davis-Dusenbery, Brandi N., Ziller, Michael, Oakley, Derek, Ichida, Justin, Dicostanza, Stefania, Atwater, Nick, Maeder, Morgan L., Goodwin, Mathew J., Nemesh, James, Handsaker, Robert E., Paull, Daniel, Noggle, Scott, McCarroll, Steven A., Joung, J. Keith, Woolf, Clifford J., Brown, Robert H, Eggan, Kevin
Publicado no Cell Stem Cell (2014)