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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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