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W N Frankel

Showing results (71-80 of 82) with videos related to

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Cell|October 23, 1997
Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant miceG A Cox, C M Lutz, C L Yang, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 1, 1994
Maps from two interspecific backcross DNA panels available as a community genetic mapping resourceL B Rowe, J H Nadeau, R Turner, et al.
Nature Genetics|August 11, 1998
The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunitV A Letts, R Felix, G H Biddlecome, et al.
The Journal of Biological Chemistry|October 6, 1997
TRANCE is a novel ligand of the tumor necrosis factor receptor family that activates c-Jun N-terminal kinase in T cellsB R Wong, J Rho, J Arron, et al.
Neuroscience|July 4, 2008
Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologiesT Miki, T A Zwingman, M Wakamori, et al.
Nature Genetics|July 14, 1998
The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundariesK Kusumi, E S Sun, A W Kerrebrock, et al.
Human Molecular Genetics|January 12, 2001
Mouse models for the Wolf-Hirschhorn deletion syndromeD Näf, L A Wilson, R A Bergstrom, et al.
Neurobiology of Disease|March 25, 2014
Physiological and genetic analysis of multiple sodium channel variants in a model of genetic absence epilepsyM K Oliva, T C McGarr, B J Beyer, et al.
Nature|February 22, 1996
Disruption of the nuclear hormone receptor RORalpha in staggerer miceB A Hamilton, W N Frankel, A W Kerrebrock, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 7, 2001
Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cellsJ Barclay, N Balaguero, M Mione, et al.
Pageof 9

Showing results (71-80 of 82) with videos related to

Sort By:
Pageof 9
Cell|October 23, 1997
Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant miceG A Cox, C M Lutz, C L Yang, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 1, 1994
Maps from two interspecific backcross DNA panels available as a community genetic mapping resourceL B Rowe, J H Nadeau, R Turner, et al.
Nature Genetics|August 11, 1998
The mouse stargazer gene encodes a neuronal Ca2+-channel gamma subunitV A Letts, R Felix, G H Biddlecome, et al.
The Journal of Biological Chemistry|October 6, 1997
TRANCE is a novel ligand of the tumor necrosis factor receptor family that activates c-Jun N-terminal kinase in T cellsB R Wong, J Rho, J Arron, et al.
Neuroscience|July 4, 2008
Two novel alleles of tottering with distinct Ca(v)2.1 calcium channel neuropathologiesT Miki, T A Zwingman, M Wakamori, et al.
Nature Genetics|July 14, 1998
The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundariesK Kusumi, E S Sun, A W Kerrebrock, et al.
Human Molecular Genetics|January 12, 2001
Mouse models for the Wolf-Hirschhorn deletion syndromeD Näf, L A Wilson, R A Bergstrom, et al.
Neurobiology of Disease|March 25, 2014
Physiological and genetic analysis of multiple sodium channel variants in a model of genetic absence epilepsyM K Oliva, T C McGarr, B J Beyer, et al.
Nature|February 22, 1996
Disruption of the nuclear hormone receptor RORalpha in staggerer miceB A Hamilton, W N Frankel, A W Kerrebrock, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 7, 2001
Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cellsJ Barclay, N Balaguero, M Mione, et al.
Pageof 9