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Kevin L Seburn

Showing results (1-10 of 33) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 12, 2006
Nmf11 is a novel ENU-induced mutation in the mouse glycine receptor alpha 1 subunitMaria Traka, Kevin L Seburn, Brian Popko
Methods in Molecular Biology (Clifton, N.J.)|December 17, 2009
Neuromuscular disease models and analysisRobert W Burgess, Gregory A Cox, Kevin L Seburn
Experimental Neurology|September 30, 2015
Altered terminal Schwann cell morphology precedes denervation in SOD1 miceDario I Carrasco, Kevin L Seburn, Martin J Pinter
Methods in Molecular Biology (Clifton, N.J.)|May 7, 2016
Neuromuscular Disease Models and AnalysisRobert W Burgess, Gregory A Cox, Kevin L Seburn
Genesis (New York, N.Y. : 2000)|August 29, 2012
Strain-specific hyperkyphosis and megaesophagus in Add1 null miceRaymond F Robledo, Kevin L Seburn, Anthony Nicholson, et al.
Journal of Neuropathology and Experimental Neurology|June 12, 2014
Lack of neuropathy-related phenotypes in hint1 knockout miceKevin L Seburn, Kathryn H Morelli, Albena Jordanova, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 2004
Three ENU-induced neurological mutations in the pore loop of sodium channel Scn8a (Na(v)1.6) and a genetically linked retinal mutation, rd13David A Buchner, Kevin L Seburn, Wayne N Frankel, et al.
Plos One|March 27, 2010
Nerve terminal degeneration is independent of muscle fiber genotype in SOD1 miceDario I Carrasco, Edyta K Bichler, Kevin L Seburn, et al.
Experimental Neurology|February 9, 2016
Abnormal response of distal Schwann cells to denervation in a mouse model of motor neuron diseaseDario I Carrasco, Ben A Bahr, Kevin L Seburn, et al.
Human Molecular Genetics|March 24, 2012
Severe disturbance in the Ca2+ signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla2g6Mikhail Strokin, Kevin L Seburn, Gregory A Cox, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 12, 2006
Nmf11 is a novel ENU-induced mutation in the mouse glycine receptor alpha 1 subunitMaria Traka, Kevin L Seburn, Brian Popko
Methods in Molecular Biology (Clifton, N.J.)|December 17, 2009
Neuromuscular disease models and analysisRobert W Burgess, Gregory A Cox, Kevin L Seburn
Experimental Neurology|September 30, 2015
Altered terminal Schwann cell morphology precedes denervation in SOD1 miceDario I Carrasco, Kevin L Seburn, Martin J Pinter
Methods in Molecular Biology (Clifton, N.J.)|May 7, 2016
Neuromuscular Disease Models and AnalysisRobert W Burgess, Gregory A Cox, Kevin L Seburn
Genesis (New York, N.Y. : 2000)|August 29, 2012
Strain-specific hyperkyphosis and megaesophagus in Add1 null miceRaymond F Robledo, Kevin L Seburn, Anthony Nicholson, et al.
Journal of Neuropathology and Experimental Neurology|June 12, 2014
Lack of neuropathy-related phenotypes in hint1 knockout miceKevin L Seburn, Kathryn H Morelli, Albena Jordanova, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 2004
Three ENU-induced neurological mutations in the pore loop of sodium channel Scn8a (Na(v)1.6) and a genetically linked retinal mutation, rd13David A Buchner, Kevin L Seburn, Wayne N Frankel, et al.
Plos One|March 27, 2010
Nerve terminal degeneration is independent of muscle fiber genotype in SOD1 miceDario I Carrasco, Edyta K Bichler, Kevin L Seburn, et al.
Experimental Neurology|February 9, 2016
Abnormal response of distal Schwann cells to denervation in a mouse model of motor neuron diseaseDario I Carrasco, Ben A Bahr, Kevin L Seburn, et al.
Human Molecular Genetics|March 24, 2012
Severe disturbance in the Ca2+ signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla2g6Mikhail Strokin, Kevin L Seburn, Gregory A Cox, et al.
Pageof 4