Showing 1 - 9 results of 9 for search 'Madison, Jon', query time: 0.03s
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Epigenetic Characterization of the FMR1 Gene and Aberrant Neurodevelopment in Human Induced Pluripotent Stem Cell Models of Fragile X Syndrome by Theriault, Kraig M., Daheron, Laurence, Loring, Jeanne F., Sheridan, Steven, Reis, Surya A., Zhou, Fen, Madison, Jon M., Haggarty, Stephen J.
Published 2012
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Functional implications of a psychiatric risk variant within CACNA1C in induced human neurons by Yoshimizu, Takao, Pan, Jen Q., Mungenast, Alison, Madison, Jon Morrow, Su, S., Ketterman, Joshua, Ongur, Dost, McPhie, D., Cohen, B., Perlis, Roy H., Tsai, Li-Huei
Published 2016
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Common DISC1 Polymorphisms Disrupt Wnt/GSK3β Signaling and Brain Development by Singh, Karun K., De Rienzo, Gianluca, Drane, Laurel, Mao, Yingwei, Flood, Zachary, Madison, Jon M., Ferreira, Manuel, Bergen, Sarah, King, Cillian, Sklar, Pamela, Sive, Hazel, Tsai, Li-Huei, Singh, Karun K.
Published 2014
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Disrupted in Schizophrenia 1 Regulates Neuronal Progenitor Proliferation via Modulation of GSK3β/β-Catenin Signaling by Mao, Yingwei, Ge, Xuecai, Frank, Christopher Lee, Madison, Jon M., Koehler, Angela Nicole, Doud, Mary Kathryn, Tassa, Carlos, Berry, Erin M., Soda, Takahiro, Singh, Karun K., Biechele, Travis, Petryshen, Tracey L., Moon, Randall T., Haggarty, Stephen J., Tsai, Li-Huei
Published 2015
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Combining NGN2 Programming with Developmental Patterning Generates Human Excitatory Neurons with NMDAR-Mediated Synaptic Transmission by Nehme, Ralda, Zuccaro, Emanuela, Ghosh, Sulagna Dia, Li, Chenchen, Sherwood, John L., Pietilainen, Olli, Barrett, Lindy E., Limone, Francesco, Worringer, Kathleen A., Kommineni, Sravya, Zang, Ying, Cacchiarelli, Davide, Meissner, Alex, Adolfsson, Rolf, Haggarty, Stephen, Madison, Jon, Muller, Matthias, Arlotta, Paola, Fu, Zhanyan, Feng, Guoping, Eggan, Kevin
Published 2018
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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
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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
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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
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