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Biochemistry
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April 10, 2015
Personalized biochemistry and biophysics
Brett 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 epilepsy
Jeffrey D Calhoun, Carlos G Vanoye, Fernando Kok, et al.
Neuron
|
June 28, 2002
Molecular basis of an inherited epilepsy
Christoph Lossin, Dao W Wang, Thomas H Rhodes, et al.
Circulation
|
February 26, 2003
Factor V Leiden protects against blood loss and transfusion after cardiac surgery
Brian 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 spot
David A Buchner, Michelle Trudeau, Alfred L George, et al.
Channels (Austin, Tex.)
|
February 9, 2010
KCNQ1/KCNE1 assembly, co-translation not required
Carlos 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 expression
Christopher 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 block
Dao 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 site
Franklin 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 channels
Franklin M Mullins, Svetlana Z Stepanovic, Niloufar B Gillani, et al.
Page
of 30
Search research articles
Search
Showing results (81-90 of 296) with videos related to
Sort By:
Page
of 30
Biochemistry
|
April 10, 2015
Personalized biochemistry and biophysics
Brett 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 epilepsy
Jeffrey D Calhoun, Carlos G Vanoye, Fernando Kok, et al.
Neuron
|
June 28, 2002
Molecular basis of an inherited epilepsy
Christoph Lossin, Dao W Wang, Thomas H Rhodes, et al.
Circulation
|
February 26, 2003
Factor V Leiden protects against blood loss and transfusion after cardiac surgery
Brian 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 spot
David A Buchner, Michelle Trudeau, Alfred L George, et al.
Channels (Austin, Tex.)
|
February 9, 2010
KCNQ1/KCNE1 assembly, co-translation not required
Carlos 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 expression
Christopher 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 block
Dao 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 site
Franklin 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 channels
Franklin M Mullins, Svetlana Z Stepanovic, Niloufar B Gillani, et al.
Page
of 30