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N Frankel

Showing results (141-150 of 210) with videos related to

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Human Molecular Genetics|December 17, 2010
A novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in miceSatoko Tokuda, Connie L Mahaffey, Bobby Monks, et al.
The Journal of Biological Chemistry|July 7, 2001
Biochemical and biophysical evidence for gamma 2 subunit association with neuronal voltage-activated Ca2+ channelsM G Kang, C C Chen, R Felix, et al.
Human Molecular Genetics|April 18, 2003
Spontaneous deletion of epilepsy gene orthologs in a mutant mouse with a low electroconvulsive thresholdYan Yang, Barbara J Beyer, James F Otto, et al.
Nature Neuroscience|August 23, 2011
A new mode of corticothalamic transmission revealed in the Gria4(-/-) model of absence epilepsyJeanne T Paz, Astra S Bryant, Kathy Peng, et al.
Cell|November 2, 1990
Isotype switching of an immunoglobulin heavy chain transgene occurs by DNA recombination between different chromosomesR M Gerstein, W N Frankel, C L Hsieh, et al.
Genomics|June 15, 1997
Cloning, mRNA expression, and chromosomal mapping of mouse and human preprocortistatinL de Lecea, P Ruiz-Lozano, P E Danielson, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 7, 2024
Impaired axon initial segment structure and function in a model of <i>ARHGEF9</i> developmental and epileptic encephalopathyWanqi Wang, Damian J Williams, Jia Jie Teoh, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 11, 1999
Quantitative trait loci for bone density in C57BL/6J and CAST/EiJ inbred miceW G Beamer, K L Shultz, G A Churchill, et al.
Genomics|January 7, 1998
Neuropeptide Y receptor genes mapped in human and mouse: receptors with high affinity for pancreatic polypeptide are not clustered with receptors specific for neuropeptide Y and peptide YYC M Lutz, J E Richards, K L Scott, 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.
Pageof 21

Showing results (141-150 of 210) with videos related to

Sort By:
Pageof 21
Human Molecular Genetics|December 17, 2010
A novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in miceSatoko Tokuda, Connie L Mahaffey, Bobby Monks, et al.
The Journal of Biological Chemistry|July 7, 2001
Biochemical and biophysical evidence for gamma 2 subunit association with neuronal voltage-activated Ca2+ channelsM G Kang, C C Chen, R Felix, et al.
Human Molecular Genetics|April 18, 2003
Spontaneous deletion of epilepsy gene orthologs in a mutant mouse with a low electroconvulsive thresholdYan Yang, Barbara J Beyer, James F Otto, et al.
Nature Neuroscience|August 23, 2011
A new mode of corticothalamic transmission revealed in the Gria4(-/-) model of absence epilepsyJeanne T Paz, Astra S Bryant, Kathy Peng, et al.
Cell|November 2, 1990
Isotype switching of an immunoglobulin heavy chain transgene occurs by DNA recombination between different chromosomesR M Gerstein, W N Frankel, C L Hsieh, et al.
Genomics|June 15, 1997
Cloning, mRNA expression, and chromosomal mapping of mouse and human preprocortistatinL de Lecea, P Ruiz-Lozano, P E Danielson, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 7, 2024
Impaired axon initial segment structure and function in a model of <i>ARHGEF9</i> developmental and epileptic encephalopathyWanqi Wang, Damian J Williams, Jia Jie Teoh, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 11, 1999
Quantitative trait loci for bone density in C57BL/6J and CAST/EiJ inbred miceW G Beamer, K L Shultz, G A Churchill, et al.
Genomics|January 7, 1998
Neuropeptide Y receptor genes mapped in human and mouse: receptors with high affinity for pancreatic polypeptide are not clustered with receptors specific for neuropeptide Y and peptide YYC M Lutz, J E Richards, K L Scott, 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.
Pageof 21