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N Frankel

Showing results (121-130 of 210) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 26, 2000
A new spontaneous mouse mutation in the Kcne1 geneV A Letts, A Valenzuela, C Dunbar, et al.
Genes, Brain, and Behavior|July 13, 2011
Etiology of a genetically complex seizure disorder in Celf4 mutant miceJ L Wagnon, C L Mahaffey, W Sun, 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.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
The AXB and BXA set of recombinant inbred mouse strainsJ D Marshall, J L Mu, Y C Cheah, et al.
Muscle & Nerve|May 10, 2005
Gait analysis detects early changes in transgenic SOD1(G93A) miceChristine M Wooley, Roger B Sher, Ajit Kale, et al.
Genomics|July 1, 1997
Genetic and physical maps of the stargazer locus on mouse chromosome 15V A Letts, A Valenzuela, J P Kirley, et al.
Mutation Research|April 1, 1993
Molecular analysis of viable spontaneous and radiation-induced albino (c)-locus mutations in the mouseE M Rinchik, J P Stoye, W N Frankel, et al.
Lipids|April 1, 1994
Effect of n-3 fatty acid-rich fish oil supplementation on the oxidation of low density lipoproteinsE N Frankel, E J Parks, R Xu, et al.
Plos One|February 8, 2022
Sequencing SARS-CoV-2 from antigen testsAshley Nazario-Toole, Holly M Nguyen, Hui Xia, et al.
Neurobiology of Disease|January 25, 2020
Altered excitatory transmission onto hippocampal interneurons in the IQSEC2 mouse model of X-linked neurodevelopmental diseaseMegha Sah, Amy N Shore, Sabrina Petri, et al.
Pageof 21

Showing results (121-130 of 210) with videos related to

Sort By:
Pageof 21
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 26, 2000
A new spontaneous mouse mutation in the Kcne1 geneV A Letts, A Valenzuela, C Dunbar, et al.
Genes, Brain, and Behavior|July 13, 2011
Etiology of a genetically complex seizure disorder in Celf4 mutant miceJ L Wagnon, C L Mahaffey, W Sun, 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.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
The AXB and BXA set of recombinant inbred mouse strainsJ D Marshall, J L Mu, Y C Cheah, et al.
Muscle & Nerve|May 10, 2005
Gait analysis detects early changes in transgenic SOD1(G93A) miceChristine M Wooley, Roger B Sher, Ajit Kale, et al.
Genomics|July 1, 1997
Genetic and physical maps of the stargazer locus on mouse chromosome 15V A Letts, A Valenzuela, J P Kirley, et al.
Mutation Research|April 1, 1993
Molecular analysis of viable spontaneous and radiation-induced albino (c)-locus mutations in the mouseE M Rinchik, J P Stoye, W N Frankel, et al.
Lipids|April 1, 1994
Effect of n-3 fatty acid-rich fish oil supplementation on the oxidation of low density lipoproteinsE N Frankel, E J Parks, R Xu, et al.
Plos One|February 8, 2022
Sequencing SARS-CoV-2 from antigen testsAshley Nazario-Toole, Holly M Nguyen, Hui Xia, et al.
Neurobiology of Disease|January 25, 2020
Altered excitatory transmission onto hippocampal interneurons in the IQSEC2 mouse model of X-linked neurodevelopmental diseaseMegha Sah, Amy N Shore, Sabrina Petri, et al.
Pageof 21