The BMP Ligand Gbb Gates the Expression of Synaptic Homeostasis Independent of Synaptic Growth Control

Por Goold, Carleton P., Davis, Graeme W.
Publicado em 2007

Single-Cell Optogenetic Excitation Drives Homeostatic Synaptic Depression

Por Goold, Carleton P., Nicoll, Roger A.
Publicado em 2010

Mechanisms Underlying the Rapid Induction and Sustained Expression of Synaptic Homeostasis

Por Frank, C. Andrew, Kennedy, Matthew J., Goold, Carleton P., Marek, Kurt W., Davis, Graeme W.
Publicado em 2006

Increased synapse elimination by microglia in schizophrenia patient-derived models of synaptic pruning

Por Sellgren, Carl M., Gracias, Jessica, Watmuff, Bradley, Biag, Jonathan D., Thanos, Jessica M., Whittredge, Paul B., Fu, Ting, Worringer, Kathleen, Brown, Hannah E., Wang, Jennifer, Kaykas, Ajamete, Karmacharya, Rakesh, Goold, Carleton P., Sheridan, Steven D., Perlis, Roy H.
Publicado no Nat Neurosci (2019)

A deleterious Na(v)1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients

Por Sun, Yishan, Paşca, Sergiu P, Portmann, Thomas, Goold, Carleton, Worringer, Kathleen A, Guan, Wendy, Chan, Karen C, Gai, Hui, Vogt, Daniel, Chen, Ying-Jiun J, Mao, Rong, Chan, Karrie, Rubenstein, John LR, Madison, Daniel V, Hallmayer, Joachim, Froehlich-Santino, Wendy M, Bernstein, Jonathan A, Dolmetsch, Ricardo E
Publicado no eLife (2016)

Behavioral Abnormalities and Circuit Defects in the Basal Ganglia of a Mouse Model of 16p11.2 Deletion Syndrome

Por Portmann, Thomas, Yang, Mu, Mao, Rong, Panagiotakos, Georgia, Ellegood, Jacob, Dolen, Gul, Bader, Patrick L., Grueter, Brad A., Goold, Carleton, Fisher, Elaine, Clifford, Katherine, Rengarajan, Pavitra, Kalikhman, David, Loureiro, Darren, Saw, Nay L., Zhengqui, Zhou, Miller, Michael A., Lerch, Jason P., Henkelman, Mark, Shamloo, Mehrdad, Malenka, Robert C., Crawley, Jacqueline N., Dolmetsch, Ricardo E.
Publicado no Cell Rep (2014)

Wide spectrum of developmental brain disorders from megalencephaly to focal cortical dysplasia and pigmentary mosaicism caused by mutations of MTOR

Por Mirzaa, Ghayda M., Campbell, Catarina D., Solovieff, Nadia, Goold, Carleton, Jansen, Laura A., Menon, Suchithra, Timms, Andrew E., Conti, Valerio, Biag, Jonathan D., Adams, Carissa, Boyle, Evan August, Collins, Sarah, Ishak, Gisele, Poliachik, Sandra, Girisha, Katta M., Yeung, Kit San, Chung, Brian Hon Yin, Rahikkala, Elisa, Gunter, Sonya A., McDaniel, Sharon S., Macmurdo, Colleen Forsyth, Bernstein, Jonathan A., Martin, Beth, Leary, Rebecca, Mahan, Scott, Liu, Shanming, Weaver, Molly, Doerschner, Michael, Jhangiani, Shalini, Muzny, Donna M., Boerwinkle, Eric, Gibbs, Richard A., Lupski, James R., Shendure, Jay, Saneto, Russell P., Novotny, Edward J., Wilson, Christopher J., Sellers, William R., Morrissey, Michael, Hevner, Robert F., Ojemann, Jeffrey G., Guerrini, Renzo, Murphy, Leon O., Winckler, Wendy, Dobyns, William B.
Publicado no JAMA Neurol (2016)