Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy
Cobos, Inma, Rubenstein, John L R, Calcagnotto, Maria Elisa, Vilaythong, Alex J, Thwin, Myo T, Noebels, Jeffrey L, Baraban, Scott C
Published in Nature neuroscience (01.08.2005)
Published in Nature neuroscience (01.08.2005)
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Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization
Singh, Nanda A., Otto, James F., Jill Dahle, E., Pappas, Chris, Leslie, Jonathan D., Vilaythong, Alex, Noebels, Jeffrey L., Steve White, H., Wilcox, Karen S., Leppert, Mark F.
Published in The Journal of physiology (15.07.2008)
Published in The Journal of physiology (15.07.2008)
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Mice lacking sodium channel beta1 subunits display defects in neuronal excitability, sodium channel expression, and nodal architecture
Chen, Chunling, Westenbroek, Ruth E, Xu, Xiaorong, Edwards, Chris A, Sorenson, Dorothy R, Chen, Yuan, McEwen, Dyke P, O'Malley, Heather A, Bharucha, Vandana, Meadows, Laurence S, Knudsen, Gabriel A, Vilaythong, Alex, Noebels, Jeffrey L, Saunders, Thomas L, Scheuer, Todd, Shrager, Peter, Catterall, William A, Isom, Lori L
Published in The Journal of neuroscience (21.04.2004)
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Published in The Journal of neuroscience (21.04.2004)
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Cathepsin B but not cathepsins L or S contributes to the pathogenesis of Unverricht-Lundborg progressive myoclonus epilepsy (EPM1)
Houseweart, Megan K, Pennacchio, Len A, Vilaythong, Alex, Peters, Christoph, Noebels, Jeffrey L, Myers, Richard M
Published in Journal of neurobiology (15.09.2003)
Published in Journal of neurobiology (15.09.2003)
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