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Science Signaling
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May 14, 2009
TRPM1 forms ion channels associated with melanin content in melanocytes
Elena Oancea, Joris Vriens, Sebastian Brauchi, et al.
Circulation
|
March 31, 2004
Compound mutations: a common cause of severe long-QT syndrome
Peter Westenskow, Igor Splawski, Katherine W Timothy, et al.
The Journal of Biological Chemistry
|
June 7, 2006
CACNA1H mutations in autism spectrum disorders
Igor Splawski, Dana S Yoo, Stephanie C Stotz, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 3, 2005
Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations
Igor Splawski, Katherine W Timothy, Niels Decher, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 5, 2004
A cardiac arrhythmia syndrome caused by loss of ankyrin-B function
Peter J Mohler, Igor Splawski, Carlo Napolitano, et al.
Cardiovascular Research
|
June 15, 2007
Impaired interaction between the slide helix and the C-terminus of Kir2.1: a novel mechanism of Andersen syndrome
Niels Decher, Vijay Renigunta, Marylou Zuzarte, et al.
Science (New York, N.Y.)
|
August 24, 2002
Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia
Igor Splawski, Katherine W Timothy, Michihiro Tateyama, et al.
Journal of the American College of Cardiology
|
September 15, 2004
An intronic mutation causes long QT syndrome
Li Zhang, G Michael Vincent, Marco Baralle, et al.
Cell
|
September 30, 2004
Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism
Igor Splawski, Katherine W Timothy, Leah M Sharpe, et al.
Heart Rhythm
|
April 27, 2005
Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing
Michael J Ackerman, Igor Splawski, Jonathan C Makielski, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Science Signaling
|
May 14, 2009
TRPM1 forms ion channels associated with melanin content in melanocytes
Elena Oancea, Joris Vriens, Sebastian Brauchi, et al.
Circulation
|
March 31, 2004
Compound mutations: a common cause of severe long-QT syndrome
Peter Westenskow, Igor Splawski, Katherine W Timothy, et al.
The Journal of Biological Chemistry
|
June 7, 2006
CACNA1H mutations in autism spectrum disorders
Igor Splawski, Dana S Yoo, Stephanie C Stotz, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
May 3, 2005
Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations
Igor Splawski, Katherine W Timothy, Niels Decher, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 5, 2004
A cardiac arrhythmia syndrome caused by loss of ankyrin-B function
Peter J Mohler, Igor Splawski, Carlo Napolitano, et al.
Cardiovascular Research
|
June 15, 2007
Impaired interaction between the slide helix and the C-terminus of Kir2.1: a novel mechanism of Andersen syndrome
Niels Decher, Vijay Renigunta, Marylou Zuzarte, et al.
Science (New York, N.Y.)
|
August 24, 2002
Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia
Igor Splawski, Katherine W Timothy, Michihiro Tateyama, et al.
Journal of the American College of Cardiology
|
September 15, 2004
An intronic mutation causes long QT syndrome
Li Zhang, G Michael Vincent, Marco Baralle, et al.
Cell
|
September 30, 2004
Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism
Igor Splawski, Katherine W Timothy, Leah M Sharpe, et al.
Heart Rhythm
|
April 27, 2005
Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing
Michael J Ackerman, Igor Splawski, Jonathan C Makielski, et al.
Page
of 2