Jonathan C Makielski

发表

Blockade of HERG cardiac K+ current by antifungal drug miconazole

Haruhiko Abe, Kazunobu Kawakami, Toshihisa Nagatomo, 2005, British journal of pharmacology.

SCN5A Rare Variants in Familial Dilated Cardiomyopathy Decrease Peak Sodium Current Depending on the Common Polymorphism H558R and Common Splice Variant Q1077del

Ana Morales, Nadine Norton, N. Norton, 2010, Clinical and translational science.

SCN4B-Encoded Sodium Channel &bgr;4 Subunit in Congenital Long-QT Syndrome

Michael J Ackerman, Samuel Canizales-Quinteros, M. Tusié-Luna, 2007, Circulation.

Late sodium current: A mechanism for angina, heart failure, and arrhythmia.

J. Makielski, Jonathan C Makielski, 2016, Trends in cardiovascular medicine.

SIDS: genetic and environmental influences may cause arrhythmia in this silent killer.

J. Makielski, Jonathan C Makielski, 2006, The Journal of clinical investigation.

KCNJ2 mutations in arrhythmia patients referred for LQT testing: a mutation T305A with novel effect on rectification properties.

Michael J Ackerman, D. Tester, M. Ackerman, 2007, Heart rhythm.

Mutant Caveolin-3 Induces Persistent Late Sodium Current and Is Associated With Long-QT Syndrome

Michael J Ackerman, Zhaohui Li, J. Towbin, 2006, Circulation.

A Ubiquitous Splice Variant and a Common Polymorphism Affect Heterologous Expression of Recombinant Human SCN5A Heart Sodium Channels

Michael J Ackerman, Matthew D. Pagel, D. Tester, 2003, Circulation research.

A common human SCN5A polymorphism modifies expression of an arrhythmia causing mutation.

Michael J Ackerman, M. Ackerman, C. Valdivia, 2003, Physiological genomics.

Specific serine proteases selectively damage KCNH2 (hERG1) potassium channels and I(Kr).

C. January, C. Valdivia, J. Foell, 2006, American journal of physiology. Heart and circulatory physiology.

Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3.

Michael J Ackerman, D. Tester, M. Ackerman, 2007, Heart rhythm.

Temperature dependence of early and late currents in human cardiac wild-type and long Q-T ΔKPQ Na+ channels.

Toshihisa Nagatomo, C. January, J. Makielski, 1998, American journal of physiology. Heart and circulatory physiology.

Inherited Arrhythmias: A National Heart, Lung, and Blood Institute and Office of Rare Diseases Workshop Consensus Report About the Diagnosis, Phenotyping, Molecular Mechanisms, and Therapeutic Approaches for Primary Cardiomyopathies of Gene Mutations Affecting Ion Channel Function

Michael J Ackerman, Colleen E Clancy, Stephan E Lehnart, 2007, Circulation.

IK1-enhanced human-induced pluripotent stem cell-derived cardiomyocytes: an improved cardiomyocyte model to investigate inherited arrhythmia syndromes.

C. January, T. Kamp, J. Makielski, 2016, American journal of physiology. Heart and circulatory physiology.