Familial dysautonomia model reveals Ikbkap deletion causes apoptosis of Pax3(+) progenitors and peripheral neurons

Por George, Lynn, Chaverra, Marta, Wolfe, Lindsey, Thorne, Julian, Close-Davis, Mattheson, Eibs, Amy, Riojas, Vickie, Grindeland, Andrea, Orr, Miranda, Carlson, George A., Lefcort, Frances
Publicado em 2013

The familial dysautonomia disease gene IKBKAP is required in the developing and adult mouse central nervous system

Por Chaverra, Marta, George, Lynn, Mergy, Marc, Waller, Hannah, Kujawa, Katharine, Murnion, Connor, Sharples, Ezekiel, Thorne, Julian, Podgajny, Nathaniel, Grindeland, Andrea, Ueki, Yumi, Eiger, Steven, Cusick, Cassie, Babcock, A. Michael, Carlson, George A., Lefcort, Frances
Publicado no Dis Model Mech (2017)

High resolution time-course mapping of early transcriptomic, molecular and cellular phenotypes in Huntington’s disease CAG knock-in mice across multiple genetic backgrounds

Por Ament, Seth A., Pearl, Jocelynn R., Grindeland, Andrea, St. Claire, Jason, Earls, John C., Kovalenko, Marina, Gillis, Tammy, Mysore, Jayalakshmi, Gusella, James F., Lee, Jong-Min, Kwak, Seung, Howland, David, Lee, Min Young, Baxter, David, Scherler, Kelsey, Wang, Kai, Geman, Donald, Carroll, Jeffrey B., MacDonald, Marcy E., Carlson, George, Wheeler, Vanessa C., Price, Nathan D., Hood, Leroy E.
Publicado no Hum Mol Genet (2017)