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J Ackerman

Showing results (771-780 of 1,140) with videos related to

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International Journal of Cardiology|July 9, 2016
Novel long QT syndrome-associated missense mutation, L762F, in CACNA1C-encoded L-type calcium channel imparts a slower inactivation tau and increased sustained and window currentAndrew P Landstrom, Nicole J Boczek, Dan Ye, et al.
Journal of Clinical Immunology|November 1, 1988
Induction of interleukin-4-dependent IgE synthesis and interleukin-5-dependent eosinophil differentiation by supernatants of a human helper T-cell cloneH H Jabara, S J Ackerman, D Vercelli, et al.
Heart Rhythm|March 16, 2010
Sudden infant death syndrome-associated mutations in the sodium channel beta subunitsBi-Hua Tan, Kavitha N Pundi, David W Van Norstrand, et al.
Circulation. Cardiovascular Genetics|December 15, 2017
Technical Advances for the Clinical Genomic Evaluation of Sudden Cardiac Death: Verification of Next-Generation Sequencing Panels for Hereditary Cardiovascular Conditions Using Formalin-Fixed Paraffin-Embedded Tissues and Dried Blood SpotsLinnea M Baudhuin, Charles Leduc, Laura J Train, et al.
Heart Rhythm|September 1, 2009
Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic testJamie D Kapplinger, David J Tester, Benjamin A Salisbury, et al.
The Journal of Biological Chemistry|June 15, 1992
Cell surface and intracellular functions for ricin galactose bindingD L Newton, R Wales, P T Richardson, et al.
Heart Rhythm|November 26, 2013
A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylationDaniel C Bartos, John R Giudicessi, David J Tester, et al.
Circulation. Arrhythmia and Electrophysiology|March 4, 2014
Pathogeneses of sudden cardiac death in national collegiate athletic association athletesKimberly G Harmon, Jonathan A Drezner, Joseph J Maleszewski, et al.
Optics Express|March 29, 2012
Optically generated reconfigurable photonic structures of elastic quasiparticles in frustrated cholesteric liquid crystalsIvan I Smalyukh, Daniel Kaputa, Aliaksandr V Kachynski, et al.
Journal of the American College of Cardiology|April 3, 2010
Clinical features and outcome of hypertrophic cardiomyopathy associated with triple sarcomere protein gene mutationsFrancesca Girolami, Carolyn Y Ho, Christopher Semsarian, et al.
Pageof 114

Showing results (771-780 of 1,140) with videos related to

Sort By:
Pageof 114
International Journal of Cardiology|July 9, 2016
Novel long QT syndrome-associated missense mutation, L762F, in CACNA1C-encoded L-type calcium channel imparts a slower inactivation tau and increased sustained and window currentAndrew P Landstrom, Nicole J Boczek, Dan Ye, et al.
Journal of Clinical Immunology|November 1, 1988
Induction of interleukin-4-dependent IgE synthesis and interleukin-5-dependent eosinophil differentiation by supernatants of a human helper T-cell cloneH H Jabara, S J Ackerman, D Vercelli, et al.
Heart Rhythm|March 16, 2010
Sudden infant death syndrome-associated mutations in the sodium channel beta subunitsBi-Hua Tan, Kavitha N Pundi, David W Van Norstrand, et al.
Circulation. Cardiovascular Genetics|December 15, 2017
Technical Advances for the Clinical Genomic Evaluation of Sudden Cardiac Death: Verification of Next-Generation Sequencing Panels for Hereditary Cardiovascular Conditions Using Formalin-Fixed Paraffin-Embedded Tissues and Dried Blood SpotsLinnea M Baudhuin, Charles Leduc, Laura J Train, et al.
Heart Rhythm|September 1, 2009
Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic testJamie D Kapplinger, David J Tester, Benjamin A Salisbury, et al.
The Journal of Biological Chemistry|June 15, 1992
Cell surface and intracellular functions for ricin galactose bindingD L Newton, R Wales, P T Richardson, et al.
Heart Rhythm|November 26, 2013
A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylationDaniel C Bartos, John R Giudicessi, David J Tester, et al.
Circulation. Arrhythmia and Electrophysiology|March 4, 2014
Pathogeneses of sudden cardiac death in national collegiate athletic association athletesKimberly G Harmon, Jonathan A Drezner, Joseph J Maleszewski, et al.
Optics Express|March 29, 2012
Optically generated reconfigurable photonic structures of elastic quasiparticles in frustrated cholesteric liquid crystalsIvan I Smalyukh, Daniel Kaputa, Aliaksandr V Kachynski, et al.
Journal of the American College of Cardiology|April 3, 2010
Clinical features and outcome of hypertrophic cardiomyopathy associated with triple sarcomere protein gene mutationsFrancesca Girolami, Carolyn Y Ho, Christopher Semsarian, et al.
Pageof 114