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Wayne N Frankel

Showing results (41-50 of 75) with videos related to

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Human Molecular Genetics|March 5, 2008
Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4Barbara Beyer, Charlotte Deleuze, Verity A Letts, et al.
Plos Genetics|August 12, 2010
A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful miceRebecca M Boumil, Verity A Letts, Monica C Roberts, et al.
Plos Genetics|July 1, 2015
Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic EncephalopathySamuel K Asinof, Stacey J Sukoff Rizzo, Alexandra R Buckley, et al.
Genetics|September 16, 2008
A targeted deleterious allele of the splicing factor SCNM1 in the mouseViive M Howell, Georgius de Haan, Sarah Bergren, et al.
Genome Biology|June 19, 2012
The genomic landscape shaped by selection on transposable elements across 18 mouse strainsChristoffer Nellåker, Thomas M Keane, Binnaz Yalcin, et al.
Nature|September 28, 2002
The harlequin mouse mutation downregulates apoptosis-inducing factorJeffrey A Klein, Chantal M Longo-Guess, Marlies P Rossmann, et al.
Biorxiv : the Preprint Server for Biology|October 24, 2023
Heterozygous expression of a <i>Kcnt1</i> gain-of-function variant has differential effects on SST- and PV-expressing cortical GABAergic neuronsAmy N Shore, Keyong Li, Mona Safari, et al.
Human Molecular Genetics|March 4, 2009
Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in miceLigia A Papale, Barbara Beyer, Julie M Jones, et al.
Plos One|May 2, 2015
DBA/2J genetic background exacerbates spontaneous lethal seizures but lessens amyloid deposition in a mouse model of Alzheimer's diseaseHarriet M Jackson, Kristen D Onos, Keating W Pepper, et al.
Genome Research|August 13, 2016
Inhibition of microRNA 128 promotes excitability of cultured cortical neuronal networksK Melodi McSweeney, Ayal B Gussow, Shelton S Bradrick, et al.
Pageof 8

Showing results (41-50 of 75) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|March 5, 2008
Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4Barbara Beyer, Charlotte Deleuze, Verity A Letts, et al.
Plos Genetics|August 12, 2010
A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful miceRebecca M Boumil, Verity A Letts, Monica C Roberts, et al.
Plos Genetics|July 1, 2015
Independent Neuronal Origin of Seizures and Behavioral Comorbidities in an Animal Model of a Severe Childhood Genetic Epileptic EncephalopathySamuel K Asinof, Stacey J Sukoff Rizzo, Alexandra R Buckley, et al.
Genetics|September 16, 2008
A targeted deleterious allele of the splicing factor SCNM1 in the mouseViive M Howell, Georgius de Haan, Sarah Bergren, et al.
Genome Biology|June 19, 2012
The genomic landscape shaped by selection on transposable elements across 18 mouse strainsChristoffer Nellåker, Thomas M Keane, Binnaz Yalcin, et al.
Nature|September 28, 2002
The harlequin mouse mutation downregulates apoptosis-inducing factorJeffrey A Klein, Chantal M Longo-Guess, Marlies P Rossmann, et al.
Biorxiv : the Preprint Server for Biology|October 24, 2023
Heterozygous expression of a <i>Kcnt1</i> gain-of-function variant has differential effects on SST- and PV-expressing cortical GABAergic neuronsAmy N Shore, Keyong Li, Mona Safari, et al.
Human Molecular Genetics|March 4, 2009
Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in miceLigia A Papale, Barbara Beyer, Julie M Jones, et al.
Plos One|May 2, 2015
DBA/2J genetic background exacerbates spontaneous lethal seizures but lessens amyloid deposition in a mouse model of Alzheimer's diseaseHarriet M Jackson, Kristen D Onos, Keating W Pepper, et al.
Genome Research|August 13, 2016
Inhibition of microRNA 128 promotes excitability of cultured cortical neuronal networksK Melodi McSweeney, Ayal B Gussow, Shelton S Bradrick, et al.
Pageof 8