D S Krafte - JoVE Visualize

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 1, 1988

Evidence for the involvement of more than one mRNA species in controlling the inactivation process of rat and rabbit brain Na channels expressed in Xenopus oocytesD S Krafte, T P Snutch, J P Leonard, et al.

Journal of Molecular and Cellular Cardiology|February 1, 1995

Stable expression and functional characterization of a human cardiac Na+ channel gene in mammalian cellsD S Krafte, W A Volberg, L Rapp, et al.

The Journal of General Physiology|October 1, 1990

Inactivation of cloned Na channels expressed in Xenopus oocytesD S Krafte, A L Goldin, V J Auld, et al.

Proceedings of the National Academy of Sciences of the United States of America|January 1, 1990

A neutral amino acid change in segment IIS4 dramatically alters the gating properties of the voltage-dependent sodium channelV J Auld, A L Goldin, D S Krafte, et al.

Biochemical and Biophysical Research Communications|February 27, 1996

Identification of three separate binding sites on SHK toxin, a potent inhibitor of voltage-dependent potassium channels in human T-lymphocytes and rat brainM W Pennington, V M Mahnir, D S Krafte, et al.

Molecular Pharmacology|April 18, 2001

Direct activation of an inwardly rectifying potassium channel by arachidonic acidY Liu, D Liu, L Heath, et al.

European Journal of Pharmacology|February 15, 1994

Pharmacological modulation of human cardiac Na+ channelsD S Krafte, K Davison, N Dugrenier, et al.

Neuron|August 1, 1988

A rat brain Na+ channel alpha subunit with novel gating propertiesV J Auld, A L Goldin, D S Krafte, et al.

International Journal of Peptide and Protein Research|November 1, 1995

Chemical synthesis and characterization of ShK toxin: a potent potassium channel inhibitor from a sea anemoneM W Pennington, M E Byrnes, I Zaydenberg, et al.

Journal of Medicinal Chemistry|July 7, 1995

Synthesis and structure-activity relationships of 6-heterocyclic-substituted purines as inactivation modifiers of cardiac sodium channelsK G Estep, K A Josef, E R Bacon, et al.

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Showing results (11-20 of 21) with videos related to

Sort By:

Pageof 3

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 1, 1988

Evidence for the involvement of more than one mRNA species in controlling the inactivation process of rat and rabbit brain Na channels expressed in Xenopus oocytesD S Krafte, T P Snutch, J P Leonard, et al.

Journal of Molecular and Cellular Cardiology|February 1, 1995

Stable expression and functional characterization of a human cardiac Na+ channel gene in mammalian cellsD S Krafte, W A Volberg, L Rapp, et al.

The Journal of General Physiology|October 1, 1990

Inactivation of cloned Na channels expressed in Xenopus oocytesD S Krafte, A L Goldin, V J Auld, et al.

Proceedings of the National Academy of Sciences of the United States of America|January 1, 1990

A neutral amino acid change in segment IIS4 dramatically alters the gating properties of the voltage-dependent sodium channelV J Auld, A L Goldin, D S Krafte, et al.

Biochemical and Biophysical Research Communications|February 27, 1996

Identification of three separate binding sites on SHK toxin, a potent inhibitor of voltage-dependent potassium channels in human T-lymphocytes and rat brainM W Pennington, V M Mahnir, D S Krafte, et al.

Molecular Pharmacology|April 18, 2001

Direct activation of an inwardly rectifying potassium channel by arachidonic acidY Liu, D Liu, L Heath, et al.

European Journal of Pharmacology|February 15, 1994

Pharmacological modulation of human cardiac Na+ channelsD S Krafte, K Davison, N Dugrenier, et al.

Neuron|August 1, 1988

A rat brain Na+ channel alpha subunit with novel gating propertiesV J Auld, A L Goldin, D S Krafte, et al.

International Journal of Peptide and Protein Research|November 1, 1995

Chemical synthesis and characterization of ShK toxin: a potent potassium channel inhibitor from a sea anemoneM W Pennington, M E Byrnes, I Zaydenberg, et al.

Journal of Medicinal Chemistry|July 7, 1995

Synthesis and structure-activity relationships of 6-heterocyclic-substituted purines as inactivation modifiers of cardiac sodium channelsK G Estep, K A Josef, E R Bacon, et al.

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