Regulation of glutamate receptor internalization by the spine cytoskeleton is mediated by its PKA-dependent association with CPG2

by Loebrich, Sven, Djukic, Biljana, Tong, Zachary J., Cottrell, Jeffrey R., Turrigiano, Gina G., Nedivi, Elly
Published 2014

Molecular diversity of glutamatergic and GABAergic synapses from multiplexed fluorescence imaging

by Danielson, Eric, Perez de Arce, Karen, Cimini, Beth, Wamhoff, Eike-Christian, Singh, Shantanu, Cottrell, Jeffrey R, Carpenter, Anne E, Bathe, Mark
Published 2021

Molecular diversity of glutamatergic and GABAergic synapses from multiplexed fluorescence imaging

by Danielson, Eric, Perez de Arce, Karen, Cimini, Beth, Wamhoff, Eike-Christian, Singh, Shantanu, Cottrell, Jeffrey R, Carpenter, Anne E, Bathe, Mark
Published 2022

Multiplexed and high-throughput neuronal fluorescence imaging with diffusible probes

by Guo, Syuan-Ming, Veneziano, Remi, Gordonov, Simon, Li, Li, Danielson, Eric W, Perez de Arce, Karen, Park, Demian, Kulesa, Anthony Benjamin, Wamhoff, Eike-Christian, Blainey, Paul C., Blainey, Paul C, Boyden, Edward, Cottrell, Jeffrey R., Bathe, Mark
Published 2020

Selective inhibition of glycogen synthase kinase 3α corrects pathophysiology in a mouse model of fragile X syndrome

by McCamphill, Patrick K., Stoppel, Laura J., Senter, Rebecca K., Lewis, Michael C., Heynen, Arnold J., Stoppel, David C., Sridhar, Vinay, Collins, Katie A., Shi, Xi, Pan, Jen Q., Madison, Jon, Cottrell, Jeffrey R., Huber, Kimberly M., Scolnick, Edward M., Holson, Edward B., Wagner, Florence F., Bear, Mark F.
Published 2022

Selective inhibition of glycogen synthase kinase 3α corrects pathophysiology in a mouse model of fragile X syndrome

by McCamphill, Patrick K, Stoppel, Laura J, Senter, Rebecca K, Lewis, Michael C, Heynen, Arnold J, Stoppel, David C, Sridhar, Vinay, Collins, Katie A, Shi, Xi, Pan, Jen Q, Madison, Jon, Cottrell, Jeffrey R, Huber, Kimberly M, Scolnick, Edward M, Holson, Edward B, Wagner, Florence F, Bear, Mark F
Published 2021

Regulation of purine metabolism connects KCTD13 to a metabolic disorder with autistic features

by Madison, Jon M, Duong, Karen, Vieux, Ellen F, Udeshi, Namrata D, Iqbal, Sumaiya, Requadt, Elise, Fereshetian, Shaunt, Lewis, Michael C, Gomes, Antonio S, Pierce, Kerry A, Platt, Randall J, Zhang, Feng, Campbell, Arthur J, Lal, Dennis, Wagner, Florence F, Clish, Clary B, Carr, Steven A, Sheng, Morgan, Scolnick, Edward M, Cottrell, Jeffrey R
Published 2021