Aisha H Frazier

Molecular mechanisms of sarcomere dysfunction in dilated and hypertrophic cardiomyopathy.

Anne M Murphy, A. Murphy, Aisha H Frazier, 2011, Progress in pediatric cardiology.

A rasopathy phenotype with severe congenital hypertrophic obstructive cardiomyopathy associated with a PTPN11 mutation and a novel variant in SOS1

M. Halushka, M. Gunay‐Aygun, Carolyn D Applegate, 2012, American Journal of Medical Genetics. Part A.

Pediatric cardiac emergencies: Children are not small adults

K. Holmes, Aisha H Frazier, E. A. Hunt, 2011, Journal of emergencies, trauma, and shock.

Familial Hypertrophic Cardiomyopathy Associated with Cardiac β-Myosin Heavy Chain and Troponin I Mutations

Nicole M. Johnson, D. Judge, K. Holmes, 2008, Pediatric Cardiology.

Mothers and Fathers Experience Stress of Congenital Heart Disease Differently: Recommendations for Pediatric Critical Care*

Erica Sood, A. Kazak, Allison Karpyn, 2018, Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies.

Cardiac troponin I Pro82Ser variant induces diastolic dysfunction, blunts β-adrenergic response, and impairs myofilament cooperativity.

Pingbo Zhang, E. Takimoto, D. B. Foster, 2015, Journal of applied physiology.

Impact of site-specific phosphorylation of protein kinase A sites Ser23 and Ser24 of cardiac troponin I in human cardiomyocytes.

C. D. dos Remedios, J. van der Velden, P. Wijnker, 2013, American journal of physiology. Heart and circulatory physiology.

Repairing the myofilaments to heal the heart.

A. Murphy, Aisha H Frazier, 2007, American journal of physiology. Heart and circulatory physiology.

A rasopathy phenotype with severe congenital hypertrophic obstructive cardiomyopathy associated with a PTPN11 mutation and a novel variant in SOS1

M. Halushka, M. Gunay‐Aygun, R. Thompson, 2012, American journal of medical genetics. Part A.