Heterozygous deletion of AKT1 rescues cardiac contractility, but not hypertrophy, in a mouse model of Noonan Syndrome with Multiple Lentigines
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine,Molecular Biology
Reference43 articles.
1. Prevalence, clinical profile, and significance of left ventricular remodeling in the end-stage phase of hypertrophic cardiomyopathy;Harris;Circulation,2006
2. Genetic causes of human heart failure;Morita;J. Clin. Invest.,2005
3. Hypertrophic cardiomyopathy: present and future, with translation into contemporary cardiovascular medicine;Maron;J. Am. Coll. Cardiol.,2014
4. PTPN11 gene mutations: linking the Gln510Glu mutation to the “LEOPARD syndrome phenotype”;Digilio;Eur. J. Pediatr.,2006
5. PTPN11 gene mutation and severe neonatal hypertrophic cardiomyopathy: what is the link?;Faienza;Pediatr. Cardiol.,2009
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2. Low-dose Dasatinib Ameliorates Hypertrophic Cardiomyopathy in Noonan Syndrome with Multiple Lentigines;Cardiovascular Drugs and Therapy;2021-03-10
3. The RASopathy Family: Consequences of Germline Activation of the RAS/MAPK Pathway;Endocrine Reviews;2018-06-18
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