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Alfred L George

Showing results (81-90 of 296) with videos related to

Pageof 30
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Biochemistry|April 10, 2015
Personalized biochemistry and biophysicsBrett M Kroncke, Carlos G Vanoye, Jens Meiler, et al.
Neurology. Genetics|December 22, 2017
Characterization of a <i>KCNB1</i> variant associated with autism, intellectual disability, and epilepsyJeffrey D Calhoun, Carlos G Vanoye, Fernando Kok, et al.
Neuron|June 28, 2002
Molecular basis of an inherited epilepsyChristoph Lossin, Dao W Wang, Thomas H Rhodes, et al.
Circulation|February 26, 2003
Factor V Leiden protects against blood loss and transfusion after cardiac surgeryBrian S Donahue, David Gailani, Michael S Higgins, et al.
Genomics|September 19, 2003
High-resolution mapping of the sodium channel modifier Scnm1 on mouse chromosome 3 and identification of a 1.3-kb recombination hot spotDavid A Buchner, Michelle Trudeau, Alfred L George, et al.
Channels (Austin, Tex.)|February 9, 2010
KCNQ1/KCNE1 assembly, co-translation not requiredCarlos G Vanoye, Richard C Welch, Changlin Tian, et al.
The Journal of Biological Chemistry|October 23, 2012
Nontruncating SCN1A mutations associated with severe myoclonic epilepsy of infancy impair cell surface expressionChristopher H Thompson, J Christopher Porter, Kristopher M Kahlig, et al.
Circulation|January 24, 2002
Clinical, genetic, and biophysical characterization of SCN5A mutations associated with atrioventricular conduction blockDao W Wang, Prakash C Viswanathan, Jeffrey R Balser, et al.
The Journal of General Physiology|October 3, 2002
Extracellular sodium interacts with the HERG channel at an outer pore siteFranklin M Mullins, Svetlana Z Stepanovic, Reshma R Desai, et al.
The Journal of Physiology|June 1, 2004
Functional interaction between extracellular sodium, potassium and inactivation gating in HERG channelsFranklin M Mullins, Svetlana Z Stepanovic, Niloufar B Gillani, et al.
Pageof 30

Showing results (81-90 of 296) with videos related to

Sort By:
Pageof 30
Biochemistry|April 10, 2015
Personalized biochemistry and biophysicsBrett M Kroncke, Carlos G Vanoye, Jens Meiler, et al.
Neurology. Genetics|December 22, 2017
Characterization of a <i>KCNB1</i> variant associated with autism, intellectual disability, and epilepsyJeffrey D Calhoun, Carlos G Vanoye, Fernando Kok, et al.
Neuron|June 28, 2002
Molecular basis of an inherited epilepsyChristoph Lossin, Dao W Wang, Thomas H Rhodes, et al.
Circulation|February 26, 2003
Factor V Leiden protects against blood loss and transfusion after cardiac surgeryBrian S Donahue, David Gailani, Michael S Higgins, et al.
Genomics|September 19, 2003
High-resolution mapping of the sodium channel modifier Scnm1 on mouse chromosome 3 and identification of a 1.3-kb recombination hot spotDavid A Buchner, Michelle Trudeau, Alfred L George, et al.
Channels (Austin, Tex.)|February 9, 2010
KCNQ1/KCNE1 assembly, co-translation not requiredCarlos G Vanoye, Richard C Welch, Changlin Tian, et al.
The Journal of Biological Chemistry|October 23, 2012
Nontruncating SCN1A mutations associated with severe myoclonic epilepsy of infancy impair cell surface expressionChristopher H Thompson, J Christopher Porter, Kristopher M Kahlig, et al.
Circulation|January 24, 2002
Clinical, genetic, and biophysical characterization of SCN5A mutations associated with atrioventricular conduction blockDao W Wang, Prakash C Viswanathan, Jeffrey R Balser, et al.
The Journal of General Physiology|October 3, 2002
Extracellular sodium interacts with the HERG channel at an outer pore siteFranklin M Mullins, Svetlana Z Stepanovic, Reshma R Desai, et al.
The Journal of Physiology|June 1, 2004
Functional interaction between extracellular sodium, potassium and inactivation gating in HERG channelsFranklin M Mullins, Svetlana Z Stepanovic, Niloufar B Gillani, et al.
Pageof 30