検索結果 - Carleton P. Goold

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  1. 1
    The BMP Ligand Gbb Gates the Expression of Synaptic Homeostasis Independent of Synaptic Growth Control

    The BMP Ligand Gbb Gates the Expression of Synaptic Homeostasis Independent of Synaptic Growth Control 著者: Carleton P. Goold, Graeme W. Davis

    出版事項 2007
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  2. 2
    Single-Cell Optogenetic Excitation Drives Homeostatic Synaptic Depression

    Single-Cell Optogenetic Excitation Drives Homeostatic Synaptic Depression 著者: Carleton P. Goold, Roger A. Nicoll

    出版事項 2010
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  3. 3
    Mechanisms Underlying the Rapid Induction and Sustained Expression of Synaptic Homeostasis

    Mechanisms Underlying the Rapid Induction and Sustained Expression of Synaptic Homeostasis 著者: C. Andrew Frank, Matthew J. Kennedy, Carleton P. Goold, Kurt W. Marek, Graeme W. Davis

    出版事項 2006
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  4. 4
    Increased synapse elimination by microglia in schizophrenia patient-derived models of synaptic pruning

    Increased synapse elimination by microglia in schizophrenia patient-derived models of synaptic pruning 著者: Carl M. Sellgren, Jessica Gracias, Bradley Watmuff, Jonathan Biag, Jessica M. Thanos, Paul B. Whittredge, Ting Fu, Kathleen A. Worringer, Hannah E. Brown, Jennifer Wang, Ajamete Kaykas, Rakesh Karmacharya, Carleton P. Goold, Steven D. Sheridan, Roy H. Perlis

    出版事項 2019
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  5. 5
    A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients

    A deleterious Nav1.1 mutation selectively impairs telencephalic inhibitory neurons derived from Dravet Syndrome patients 著者: Yishan Sun, Sergiu P. Paşca, Thomas Portmann, Carleton P. Goold, Kathleen A. Worringer, Wendy Guan, Karen Cecilia Chan, Hui Gai, Daniel Vogt, Ying-Jiun J. Chen, Rong Mao, Karrie Chan, John L.R. Rubenstein, Daniel V. Madison, Joachim Hallmayer, Wendy Froehlich-Santino, Jonathan A. Bernstein, Ricardo E. Dolmetsch

    出版事項 2016
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  6. 6
    Behavioral Abnormalities and Circuit Defects in the Basal Ganglia of a Mouse Model of 16p11.2 Deletion Syndrome

    Behavioral Abnormalities and Circuit Defects in the Basal Ganglia of a Mouse Model of 16p11.2 Deletion Syndrome 著者: Thomas Portmann, Mu Yang, Rong Mao, Georgia Panagiotakos, Jacob Ellegood, Gül Dölen, Patrick L. Bader, Brad A. Grueter, Carleton P. Goold, Elaine Fisher, Katherine Clifford, Pavitra Rengarajan, David Kalikhman, Darren Loureiro, Nay L. Saw, Zhou Zhengqui, Michael A. Miller, Jason P. Lerch, R. Mark Henkelman, Mehrdad Shamloo, Robert C. Malenka, Jacqueline N. Crawley, Ricardo E. Dolmetsch

    出版事項 2014
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  7. 7
    Neuronal defects in a human cellular model of 22q11.2 deletion syndrome

    Neuronal defects in a human cellular model of 22q11.2 deletion syndrome 著者: Themasap A. Khan, Omer Revah, Aaron Gordon, Se‐Jin Yoon, Anna K. Krawisz, Carleton P. Goold, Yishan Sun, Chul Hoon Kim, Yuan Tian, Min-Yin Li, Julia M. Schaepe, Kazuya Ikeda, Neal D. Amin, Noriaki Sakai, Masayuki Yazawa, Leila Kushan, Seiji Nishino, Matthew H. Porteus, Judith L. Rapoport, Jonathan A. Bernstein, Ruth O’Hara, Carrie E. Bearden, Joachim Hallmayer, John R. Huguenard, Daniel H. Geschwind, Ricardo E. Dolmetsch, Sergiu P. Paşca

    出版事項 2020
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  8. 8
    Cerebrospinal fluid concentration of complement component 4A is increased in first episode schizophrenia

    Cerebrospinal fluid concentration of complement component 4A is increased in first episode schizophrenia 著者: Jessica Gracias, Funda Orhan, Elin Hörbeck, Jessica Holmén‐Larsson, Neda Khanlarkani, Susmita Malwade, Sravan K. Goparaju, Lilly Schwieler, Ilknur Safak Demirel, Ting Fu, Helena Fatouros‐Bergman, Aurimantas Pelanis, Carleton P. Goold, Anneli Goulding, Kristina Annerbrink, Anniella Isgren, Timea Sparding, Martin Schalling, Viviana A. Carcamo Yañez, Jens Göpfert, Johanna Nilsson, Ann Brinkmalm, Kaj Blennow, Henrik Zetterberg, Göran Engberg, Fredrik Piehl, Steven D. Sheridan, Roy H. Perlis, Simon Červenka, Sophie Erhardt, Mikael Landén, Carl M. Sellgren

    出版事項 2022
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  9. 9
    Association of<i>MTOR</i>Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism

    Association of<i>MTOR</i>Mutations With Developmental Brain Disorders, Including Megalencephaly, Focal Cortical Dysplasia, and Pigmentary Mosaicism 著者: Ghayda Mirzaa, Catarina D. Campbell, Nadia Solovieff, Carleton P. Goold, Laura A. Jansen, Suchithra Menon, Andrew E. Timms, Valerio Conti, Jonathan Biag, Carissa Olds, Evan A. Boyle, Sarah Collins, Gisele E. Ishak, Sandra L. Poliachik, Katta M. Girisha, Kit San Yeung, Brian Hon‐Yin Chung, Elisa Rahikkala, Sonya A. Gunter, Sharon S. McDaniel, Colleen Macmurdo, Jonathan A. Bernstein, Beth Martin, Rebecca Leary, Scott Mahan, Shanming Liu, Molly Weaver, Michael O. Dorschner, Shalini N. Jhangiani, Donna M. Muzny, Eric Boerwinkle, Richard A. Gibbs, James R. Lupski, Jay Shendure, Russell P. Saneto, Edward J. Novotny, Christopher J. Wilson, William R. Sellers, Michael Morrissey, Robert F. Hevner, Jeffrey G. Ojemann, Renzo Guerrini, Leon O. Murphy, Wendy Winckler, William B. Dobyns

    出版事項 2016
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