Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency von Dugger, Sarah A, Dhindsa, Ryan S, Sampaio, Gabriela De Almeida, Ressler, Andrew K, Rafikian, Elizabeth E, Petri, Sabrina, Letts, Verity A, Teoh, JiaJie, Ye, Junqiang, Colombo, Sophie, Peng, Yueqing, Yang, Mu, Boland, Michael J, Frankel, Wayne N, Goldstein, David B

Volltext

A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice von Boumil, Rebecca M, Letts, Verity A, Roberts, Monica C, Lenz, Christine, Mahaffey, Connie L, Zhang, Zhong-Wei, Moser, Tobias, Frankel, Wayne N

Volltext

Unraveling genetic modifiers in the gria4 mouse model of absence epilepsy von Frankel, Wayne N, Mahaffey, Connie L, McGarr, Tracy C, Beyer, Barbara J, Letts, Verity A

Volltext

Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy von Asinof, Samuel K, Sukoff Rizzo, Stacey J, Buckley, Alexandra R, Beyer, Barbara J, Letts, Verity A, Frankel, Wayne N, Boumil, Rebecca M

Volltext

Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice von Papale, Ligia A., Beyer, Barbara, Jones, Julie M., Sharkey, Lisa M., Tufik, Sergio, Epstein, Michael, Letts, Verity A., Meisler, Miriam H., Frankel, Wayne N., Escayg, Andrew

Volltext

A Targeted Mutation in Cacng4 Exacerbates Spike-Wave Seizures in Stargazer (Cacng2) Mice von Letts, Verity A., Mahaffey, Connie L., Beyer, Barbara, Frankel, Wayne N., Takahashi, Joseph S.

Volltext

Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4 von Beyer, Barbara, Deleuze, Charlotte, Letts, Verity A., Mahaffey, Connie L., Boumil, Rebecca M., Lew, Timothy A., Huguenard, John R., Frankel, Wayne N.

Volltext

Ducky Mouse Phenotype of Epilepsy and Ataxia Is Associated with Mutations in the Cacna2d2 Gene and Decreased Calcium Channel Current in Cerebellar Purkinje Cells von Barclay, Jane, Balaguero, Nuria, Mione, Marina, Ackerman, Susan L, Letts, Verity A, Brodbeck, Jens, Canti, Carles, Meir, Alon, Page, Karen M, Kusumi, Kenro, Perez-Reyes, Edward, Lander, Eric S, Frankel, Wayne N, Gardiner, R. Mark, Dolphin, Annette C, Rees, Michele

Volltext

The mouse fidgetin gene defines a new role for AAA family proteins in mammalian development von Frankel, Wayne N, Cox, Gregory A, Mahaffey, Connie L, Nystuen, Arne, Letts, Verity A

Volltext

Development of a New Genetic Model for Absence Epilepsy: Spike-Wave Seizures in C3H/He and Backcross Mice von Frankel, Wayne N, Beyer, Barbara, Maxwell, Christina R, Pretel, Stephanie, Letts, Verity A, Siegel, Steven J

Volltext

Spontaneous deletion of epilepsy gene orthologs in a mutant mouse with a low electroconvulsive threshold von Yang, Yan, Beyer, Barbara J., Otto, James F., O'Brien, Timothy P., Letts, Verity A., White, H. Steve, Frankel, Wayne N.

Volltext

Stargazer—A Mouse to Seize von Letts, Verity A.

Volltext

Phenotypic heterogeneity in the stargazin allelic series von Letts, Verity A, Kang, Myoung-Goo, Mahaffey, Connie L, Beyer, Barbara, Tenbrink, Heather, Campbell, Kevin P, Frankel, Wayne N

Volltext

Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant mice von Neumann, Paul E, Frankel, Wayne N, Letts, Verity A, Coffin, John M, Copp, Andrew J, Bernfield, Merton

Volltext

Unraveling Genetic Modifiers in the Gria4 Mouse Model of Absence Epilepsy: e1004454 von Frankel, Wayne N, Mahaffey, Connie L, McGarr, Tracy C, Beyer, Barbara J, Letts, Verity A

Volltext

Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic Encephalopathy: e1005347 von Asinof, Samuel K, Rizzo, Stacey JSukoff, Buckley, Alexandra R, Beyer, Barbara J, Letts, Verity A, Frankel, Wayne N, Boumil, Rebecca M

Volltext

A Curly-Tail Modifier Locus,mct1,on Mouse Chromosome 17 von LETTS, VERITY A., SCHORK, NICHOLAS J., COPP, ANDREW J., BERNFIELD, MERTON, FRANKEL, WAYNE N.

Volltext

The mouse stargazer gene encodes a neuronal Ca2+-channel γ subunit von Letts, Verity A., Felix, Ricardo, Biddlecome, Gloria H., Arikkath, Jyothi, Mahaffey, Connie L., Valenzuela, Alicia, Bartlett, Frederick S., Mori, Yasuo, Campbell, Kevin P., Frankel, Wayne N.

Volltext

Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologies von Miki, T, Zwingman, T.A, Wakamori, M, Lutz, C.M, Cook, S.A, Hosford, D.A, Herrup, K, Fletcher, C.F, Mori, Y, Frankel, W.N, Letts, V.A

Volltext

A Missense Mutation in a Highly Conserved Alternate Exon of Dynamin-1 Causes Epilepsy in Fitful Mice: e1001046 von Boumil, Rebecca M, Letts, Verity A, Roberts, Monica C, Lenz, Christine, Mahaffey, Connie L, Zhang, Zhong-wei, Moser, Tobias, Frankel, Wayne N

Volltext