Ankyrin-G isoform imbalance and interneuronopathy link epilepsy and bipolar disorder von Lopez, A Y, Wang, X, Xu, M, Maheshwari, A, Curry, D, Lam, S, Adesina, A M, Noebels, J L, Sun, Q-Q, Cooper, E C

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Abbreviated report of the NIH/NINDS workshop on sudden unexpected death in epilepsy von HIRSCH, L. J, DONNER, E. J, SO, E. L, JACOBS, M, NASHEF, L, NOEBELS, J. L, BUCHHALTER, J. R

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The biology of epilepsy genes von NOEBELS, Jeffrey L

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Mice with Truncated MeCP2 Recapitulate Many Rett Syndrome Features and Display Hyperacetylation of Histone H3 von Shahbazian, Mona D., Young, Juan I., Yuva-Paylor, Lisa A., Spencer, Corinne M., Antalffy, Barbara A., Noebels, Jeffrey L., Armstrong, Dawna L., Paylor, Richard, Zoghbi, Huda Y.

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MeCP2 is critical within HoxB1-derived tissues of mice for normal lifespan von Ward, Christopher S, Arvide, E Melissa, Huang, Teng-Wei, Yoo, Jong, Noebels, Jeffrey L, Neul, Jeffrey L

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Genetic Disruption of Cortical Interneuron Development Causes Region- and GABA Cell Type-Specific Deficits, Epilepsy, and Behavioral Dysfunction von Powell, Elizabeth M, Campbell, Daniel B, Stanwood, Gregg D, Davis, Caleb, Noebels, Jeffrey L, Levitt, Pat

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Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice von Pennacchio, Len A., Bouley, Donna M., Higgins, Kay M., Scott, Matthew P., Noebels, Jeffrey L., Myers, Richard M.

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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 von Jiang, Yong-hui, Armstrong, Dawna, Albrecht, Urs, Atkins, Coleen M, Noebels, Jeffrey L, Eichele, Gregor, Sweatt, J.David, Beaudet, Arthur L

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Mutations in High-Voltage-Activated Calcium Channel Genes Stimulate Low-Voltage-Activated Currents in Mouse Thalamic Relay Neurons von Zhang, Yi, Mori, Mayra, Burgess, Daniel L, Noebels, Jeffrey L

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Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10 von Matsuura, Tohru, Yamagata, Takanori, Burgess, Daniel L., Rasmussen, Astrid, Grewal, Raji P., Watase, Kei, Khajavi, Mehrdad, McCall, Alanna E., Davis, Caleb F., Zu, Lan, Achari, Madhureeta, Pulst, Stefan M., Alonso, Elisa, Noebels, Jeffrey L., Nelson, David L., Zoghbi, Huda Y., Ashizawa, Tetsuo

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Loss of BETA2/NeuroD Leads to Malformation of the Dentate Gyrus and Epilepsy von Liu, Min, Pleasure, Samuel J., Collins, Abigail E., Noebels, Jeffrey L., Naya, Francesco J., Tsai, Ming-Jer, Lowenstein, Daniel H.

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Future directions for epilepsy research von JACOBS, M. P, FISCHBACH, G. D, THEODORE, W. H, DAVIS, M. R, DICHTER, M. A, DINGLEDINE, R, LOWENSTEIN, D. H, MORRELL, M. J, NOEBELS, J. L, ROGAWSKI, M. A, SPENCER, S. S

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Elevated Thalamic Low-Voltage-Activated Currents Precede the Onset of Absence Epilepsy in the SNAP25-Deficient Mouse Mutant Coloboma von Zhang, Yi, Vilaythong, Alexander P, Yoshor, Daniel, Noebels, Jeffrey L

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Mice Lacking Sodium Channel beta 1 Subunits Display Defects in Neuronal Excitability, Sodium Channel Expression, and Nodal Architecture von Chen, C, Westenbroek, R E, Xu, X, Edwards, CA, Sorenson, DR, Chen, Y, McEwen, D P, O'Malley, HA, Bharucha, V, Meadows, L S, Knudsen, G A, Vilaythong, A, Noebels, J L, Saunders, T L

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Presynaptic Ca2+ Channels and Neurotransmitter Release at the Terminal of a Mouse Cortical Neuron von Qian, Jing, Noebels, Jeffrey L

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Apoptosis caused by cathepsins does not require Bid signaling in an in vivo model of progressive myoclonus epilepsy (EPM1) von Houseweart, M K, Vilaythong, A, Yin, X-M, Turk, B, Noebels, J L, Myers, R M

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Mutation in AP-3 δ in the mocha Mouse Links Endosomal Transport to Storage Deficiency in Platelets, Melanosomes, and Synaptic Vesicles von Kantheti, Prameela, Qiao, Xiaoxi, Diaz, Maria E, Peden, Andrew A, Meyer, Gary E, Carskadon, Shannon L, Kapfhamer, David, Sufalko, Damaris, Robinson, Margaret S, Noebels, Jeffrey L, Burmeister, Margit

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Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse von Burgess, D L, Jones, J M, Meisler, M H, Noebels, J L

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Epilepsy in Mice Deficient in the 65-kDa Isoform of Glutamic Acid Decarboxylase von Kash, Shera F., Johnson, Randall S., Tecott, Laurence H., Noebels, Jeffrey L., Mayfield, R. Dayne, Hanahan, Douglas, Baekkeskov, Steinunn

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Rocker Is a New Variant of the Voltage-Dependent Calcium Channel Gene Cacna1a von Zwingman, Theresa A, Neumann, Paul E, Noebels, Jeffrey L, Herrup, Karl

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