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Wayne N Frankel

Showing results (21-30 of 75) with videos related to

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Genomics|February 7, 2002
The muscular dystrophy with myositis (mdm) mouse mutation disrupts a skeletal muscle-specific domain of titinSean M Garvey, Chandrika Rajan, Allen P Lerner, et al.
Epilepsia|August 27, 2004
Mice carrying the szt1 mutation exhibit increased seizure susceptibility and altered sensitivity to compounds acting at the m-channelJames F Otto, Yan Yang, Wayne N Frankel, et al.
Brain Research|March 7, 2006
Auditory brainstem responses in 10 inbred strains of miceXiaoming Zhou, Philip H-S Jen, Kevin L Seburn, et al.
The Journal of Physiology|October 24, 2012
Aberrant sodium channel activity in the complex seizure disorder of Celf4 mutant miceWenzhi Sun, Jacy L Wagnon, Connie L Mahaffey, et al.
Plos Genetics|July 11, 2014
Unraveling genetic modifiers in the gria4 mouse model of absence epilepsyWayne N Frankel, Connie L Mahaffey, Tracy C McGarr, et al.
Stem Cells (Dayton, Ohio)|February 8, 2013
Elevated Id2 expression results in precocious neural stem cell depletion and abnormal brain developmentHee Jung Park, Mingi Hong, Roderick T Bronson, et al.
Plos Genetics|August 7, 2007
Complex seizure disorder caused by Brunol4 deficiency in miceYan Yang, Connie L Mahaffey, Nathalie Bérubé, et al.
Brain : a Journal of Neurology|February 17, 2026
Tiered modelling of a CACNA1A D1634N mutation linked to ataxia, epilepsy and cognitive deficitsJacqueline Niu, Chi-Kun Tong, Ekniel Francois, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 1, 2005
Development of a new genetic model for absence epilepsy: spike-wave seizures in C3H/He and backcross miceWayne N Frankel, Barbara Beyer, Christina R Maxwell, et al.
Human Molecular Genetics|February 9, 2006
Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2Jennifer A Kearney, Yan Yang, Barbara Beyer, et al.
Pageof 8

Showing results (21-30 of 75) with videos related to

Sort By:
Pageof 8
Genomics|February 7, 2002
The muscular dystrophy with myositis (mdm) mouse mutation disrupts a skeletal muscle-specific domain of titinSean M Garvey, Chandrika Rajan, Allen P Lerner, et al.
Epilepsia|August 27, 2004
Mice carrying the szt1 mutation exhibit increased seizure susceptibility and altered sensitivity to compounds acting at the m-channelJames F Otto, Yan Yang, Wayne N Frankel, et al.
Brain Research|March 7, 2006
Auditory brainstem responses in 10 inbred strains of miceXiaoming Zhou, Philip H-S Jen, Kevin L Seburn, et al.
The Journal of Physiology|October 24, 2012
Aberrant sodium channel activity in the complex seizure disorder of Celf4 mutant miceWenzhi Sun, Jacy L Wagnon, Connie L Mahaffey, et al.
Plos Genetics|July 11, 2014
Unraveling genetic modifiers in the gria4 mouse model of absence epilepsyWayne N Frankel, Connie L Mahaffey, Tracy C McGarr, et al.
Stem Cells (Dayton, Ohio)|February 8, 2013
Elevated Id2 expression results in precocious neural stem cell depletion and abnormal brain developmentHee Jung Park, Mingi Hong, Roderick T Bronson, et al.
Plos Genetics|August 7, 2007
Complex seizure disorder caused by Brunol4 deficiency in miceYan Yang, Connie L Mahaffey, Nathalie Bérubé, et al.
Brain : a Journal of Neurology|February 17, 2026
Tiered modelling of a CACNA1A D1634N mutation linked to ataxia, epilepsy and cognitive deficitsJacqueline Niu, Chi-Kun Tong, Ekniel Francois, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 1, 2005
Development of a new genetic model for absence epilepsy: spike-wave seizures in C3H/He and backcross miceWayne N Frankel, Barbara Beyer, Christina R Maxwell, et al.
Human Molecular Genetics|February 9, 2006
Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2Jennifer A Kearney, Yan Yang, Barbara Beyer, et al.
Pageof 8