Search Results - Nathaniel P. Murphy
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1
Aberrant Expression of a Non-muscle RBFOX2 Isoform Triggers Cardiac Conduction Defects in Myotonic Dystrophy by Chaitali Misra, Sushant Bangru, Feikai Lin, Kin Lam, Sara N. Koenig, Ellen R. Lubbers, Jamila Hedhli, Nathaniel P. Murphy, Darren J. Parker, Lawrence W. Dobrucki, Thomas A. Cooper, Emad Tajkhorshid, Peter J. Mohler, Auinash Kalsotra
Published 2020Artigo -
2
Molecular Mechanisms Underlying Cardiac Protein Phosphatase 2A Regulation in Heart by Sean Thomas DeGrande, Sean C. Little, Derek J. Nixon, Patrick Wright, Jedidiah S. Snyder, Wen Dun, Nathaniel P. Murphy, Ahmet Kılıç, Robert Higgins, Philip F. Binkley, Penelope A. Boyden, Cynthia A. Carnes, Mark E. Anderson, Thomas J. Hund, Peter J. Mohler
Published 2012Artigo -
3
Novel Variant in the <i>ANK2</i> Membrane-Binding Domain Is Associated With Ankyrin-B Syndrome and Structural Heart Disease in a First Nations Population With a High Rate of Long Q... by Leigh Anne Swayne, Nathaniel P. Murphy, Sirisha Asuri, Lena W. Chen, Xiaoxue Xu, Sarah McIntosh, Chao Wang, Peter J. Lancione, Jason D. Roberts, Charles R. Kerr, Shubhayan Sanatani, Elizabeth D. Sherwin, Crystal F. Kline, Mingjie Zhang, Peter J. Mohler, Laura Arbour
Published 2017Artigo -
4
<i>SCN5A</i> variant that blocks fibroblast growth factor homologous factor regulation causes human arrhythmia by Hassan Musa, Crystal F. Kline, Amy C. Sturm, Nathaniel P. Murphy, Sara Adelman, Chaojian Wang, Hai Yan, B. Lamar Johnson, Thomas A. Csepe, Ahmet Kılıç, Robert Higgins, Paul M.L. Janssen, Vadim V. Fedorov, Raul Weiss, Christina Salazar, Thomas J. Hund, Geoffrey S. Pitt, Peter J. Mohler
Published 2015Artigo -
5
Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy by Jason D. Roberts, Nathaniel P. Murphy, Robert M. Hamilton, Ellen R. Lubbers, Cynthia A. James, Crystal F. Kline, Michael H. Gollob, Andrew D. Krahn, Amy C. Sturm, Hassan Musa, Mona El Refaey, Sara N. Koenig, Meriam Åström Aneq, Edgar T. Hoorntje, Sharon Graw, Robert Davies, Muhammad Rafiq, Tamara T. Koopmann, Shabana Aafaqi, Meena Fatah, David A. Chiasson, Matthew R.G. Taylor, Samantha L. Simmons, Mei Han, Chantal J.M. van Opbergen, Loren E. Wold, Gianfranco Sinagra, Kirti Mittal, Crystal Tichnell, Brittney Murray, Alberto Codima, Babak Nazer, Duy T. Nguyen, Gregory M. Marcus, Nara Sobriera, Elisabeth M. Lodder, Maarten P. van den Berg, Danna Spears, John F. Robinson, Philip C. Ursell, Anna K. Green, Allan C. Skanes, Anthony Tang, Martin J. Gardner, Robert A. Hegele, Toon A.B. van Veen, Arthur A.M. Wilde, Jeff S. Healey, Paul M.L. Janssen, Luisa Mestroni, J. Peter van Tintelen, Hugh Calkins, Daniel P. Judge, Thomas J. Hund, Melvin M. Scheinman, Peter J. Mohler
Published 2019Artigo
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Biology
Cell biology
Gene
Genetics
Internal medicine
Medicine
Ankyrin
Signal transduction
Sudden death
Alternative splicing
Ankyrin repeat
Biochemistry
Brugada syndrome
Cancer research
Cardiac muscle
Cardiomyopathy
Catenin
Channelopathy
Chemistry
Depolarization
Downregulation and upregulation
Endocrinology
Function (biology)
Gene expression
Gene isoform
Heart failure
Long QT syndrome
Messenger RNA
Molecular biology
Mutation