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UBE3A Regulates Synaptic Plasticity and Learning and Memory by Controlling SK2 Channel Endocytosis por Jiandong Sun, Guoqi Zhu, Yan Liu, Steve Standley, Angela Ji, Rashmi Tunuguntla, Yubin Wang, Chad F. Claus, Yun Luo, Michel Baudry, Xiaoning Bi

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Variable epilepsy phenotypes associated with a familial intragenic deletion of the <i>SCN1A</i> gene por Renzo Guerrini, Elena Cellini, Davide Mei, Tiziana Metitieri, Cristina Petrelli, Daniela Pucatti, Carla Marini, Nelia Zamponi

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From UBE3A to Angelman syndrome: a substrate perspective por Gabrielle L. Sell, Seth S. Margolis

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Allelic specificity of Ube3a Expression In The Mouse Brain During Postnatal Development por Matthew C. Judson, Jason O. Sosa‐Pagan, Wilmer A. Del Cid, Ji Eun Han, Benjamin D. Philpot

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Derangements of Hippocampal Calcium/Calmodulin-Dependent Protein Kinase II in a Mouse Model for Angelman Mental Retardation Syndrome por Edwin J. Weeber, Yong‐hui Jiang, Ype Elgersma, Andrew W. Varga, Yarimar Carrasquillo, Sarah E. Brown, Jill M. Christian, Banefsheh Mirnikjoo, Alcino J. Silva, Arthur L. Beaudet, J. David Sweatt

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Role of ubiquitin and the HPV E6 oncoprotein in E6AP-mediated ubiquitination por Franziska Mortensen, Daniel Schneider, Tanja Barbic, Anna Sladewska-Marquardt, Simone Kühnle, Andreas Marx, Martin Scheffner

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Genetics of Angelman Syndrome por Yong-hui Jiang, Efrat Lev-Lehman, Jan Bressler, Ting‐Fen Tsai, Arthur L. Beaudet

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A therapeutic trial of pro‐methylation dietary supplements in Angelman syndrome por Lynne M. Bird, Wen‐Hann Tan, Carlos A. Bacino, Sarika U. Peters, Steven A. Skinner, Irina Anselm, Rene Barbieri‐Welge, Astrid Bauer‐Carlin, Jennifer Gentile, Daniel G. Glaze, Lucia T. Horowitz, Kriti Mohan, Mark Nespeca, Trilochan Sahoo, Dean Sarco, Susan E. Waisbren, Arthur L. Beaudet

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Ube3a mRNA and protein expression are not decreased in Mecp2 mutant mice por Amy Lawson‐Yuen, Daniel Liu, Liqun Han, Zhichun Jiang, Guochuan Tsai, Alo C. Basu, Jonathan Picker, Jiamin Feng, Joseph T. Coyle

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Epilepsy in patients with Angelman syndrome por Agata Fiumara, Annarita Pittalà, Mariadonatella Cocuzza, Giovanni Sorge

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Angelman syndrome: insights into genomic imprinting and neurodevelopmental phenotypes por Angela M. Mabb, Matthew C. Judson, Mark J. Zylka, Benjamin D. Philpot

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Angelman syndrome-associated ubiquitin ligase UBE3A/E6AP mutants interfere with the proteolytic activity of the proteasome por Vjekoslav Tomaić, Lawrence Banks

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Mutation of HERC2 causes developmental delay with Angelman-like features por Gaurav V. Harlalka, Emma L. Baple, Harold E. Cross, Simone Kühnle, Monica Cubillos‐Rojas, Konstantin Matentzoglu, Michael A. Patton, Karin Wagner, Roselyn Coblentz, Debra L Ford, Deborah Mackay, Barry A. Chioza, Martin Scheffner, José Luís Rosa, Andrew H. Crosby

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The Human Aminophospholipid-Transporting ATPase Gene ATP10C Maps Adjacent to UBE3A and Exhibits Similar Imprinted Expression por Laura B. K. Herzing, Soo‐Jeong Kim, Edwin H. Cook, David H. Ledbetter

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Mutation of the Angelman Ubiquitin Ligase in Mice Causes Increased Cytoplasmic p53 and Deficits of Contextual Learning and Long-Term Potentiation por Yong‐hui Jiang, Dawna Armstrong, Urs Albrecht, Coleen M. Atkins, Jeffrey L. Noebels, Gregor Eichele, J. David Sweatt, Arthur L. Beaudet

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Towards a therapy for Angelman syndrome by targeting a long non-coding RNA por Linyan Meng, Amanda J. Ward, Seung Chun, C. Frank Bennett, Arthur L. Beaudet, Frank Rigo

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Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype-phenotype correlations por Trilochan Sahoo

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Altered Ultrasonic Vocalization and Impaired Learning and Memory in Angelman Syndrome Mouse Model with a Large Maternal Deletion from Ube3a to Gabrb3 por Yong‐hui Jiang, Yanzhen Pan, Li Zhu, Luis Landa, Jong W. Yoo, Corinne M. Spencer, Isabel Lorenzo, Murray H. Brilliant, Jeffrey L. Noebels, Arthur L. Beaudet

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Biochemical Analysis of Angelman Syndrome-associated Mutations in the E3 Ubiquitin Ligase E6-associated Protein por Eric M. Cooper, Amy W. Hudson, Joseph Amos, Joseph Wagstaff, Peter M. Howley

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Molecular and Clinical Aspects of Angelman Syndrome por Aditi I Dagli, Karin Buiting, Charles A. Williams

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