Research Top

Saving tiny Hearts Research

Research

The primary purpose of the Saving tiny Hearts Society is to raise money to fund life saving research projects to improve, prolong and save the lives of those affected by Congenital Heart Defects.

We are honored to have a Medical Advisory Board (MAB) comprised of an elite group of world-renowned cardiothoracic surgeons, researchers and cardiologists. The MAB vets and determines which research projects the Saving tiny Hearts Society will fund. With the help of our MAB, money raised is allocated to fund the most promising research of number one birth defect worldwide.

2018 Grant Application

The Saving tiny Hearts Society awards research grants to early stage science with unique hypotheses
fostering the next generation of congenital heart defect research creating a strong foundation of
preliminary evidence to make scientific advancements.

As a private, not-for-profit source of funds for scientists studying congenital heart defects, the Saving
tiny Hearts Society focuses its funding on investigator-initiated, peer-reviewed proposals. This process
ensures that researchers propose projects they believe are ready to be tackled with the available
knowledge and techniques. This intellectual freedom encourages discovery in areas that scientists
believe are most likely to determine hidden causes and discover cures to prolong, improve and save the
lives of all children afflicted with congenital heart defects.

To streamline the grant application process, an electronic link has been provided below to download the
Saving tiny Hearts Society 2018 Grant Application. If you have additional questions regarding our
application process, please email, Larry Kluge, Medical Advisory Board Liaison at:
larryk@savingtinyhearts.org
2018 Grant Application PDF IconDownload the 2018 Grant Application

 

Projects Funded

2017
($370,000 total allocation)

Defining a Novel Pathway for Pediatric Sudden Cardiac Death
Investigation of Wntless in Heart Regeneration
Gene Editing Treatment of Catecholaminergic Polymorphic Ventricular Tachycardia
Mechanisms of Cardiomyocyte Renewal Regulated by Nkx2.5
Pedigree-Adapted Use of Genomic Sequencing for Deciphering Syndromic and Non Syndromic Congenital Heart Malformations
Design of Mechanical Circulatory Support for Failing Fontan Circulation
Creation of a Chronic Animal Model of Fontan Circulation Using Transcatheter Techniques
Stimulating Cardiomyocyte Proliferation as a Novel Therapy for CHD
Cardiac Energy Signature and Heart Failure in Congenital Heart Disease

2016
($328,000 total allocation)

Role of NOX-4 Dependent Notch1 Dysregulations on Cardiac Development in Fetal Alcohol Syndrome
Novel Arrhythmia Mechanisms in Long QT Syndrome
Feasibility of a Novel Fontan Right-Side Assist Device
Neuroprotective Strategies in Pediatric Surgery
Elucidating the Genetics and Epigenetics of Congenital Heart Defects Using Zebrafish Genome Engineering
The Effects of Pediatric-Specific HCM Mutations in B-Cardiac Myosin Power Generation

2014 – 2015
($200,000 total allocation)

Arrhythmogenic Substrate in Fontan Patients
Hypoplastic Left Heart Syndrome
Cardiac defects in LEOPARD Syndrome

2013 – 2014
($200,000 total allocation)

Long QT Vulnerability in SIDS
Notch Signaling & Ascending Aortic Aneurysm
Novel Mouse Model for CHD and Heterotaxy
Early Manifestation of AC in Children

2012 – 2013
($190,000 total allocation)

Early Manifestations of AC in Children
Improving Prenatal Screening for CHD
Augmenting O-GlcNAcylation
Myosin Heavy Chain 7 Mutation and HC
Arrhythmia & Sudden Cardiac Death in Children

2011 – 2012
($244,000 total allocation)

Arrhythmia and Sudden Cardiac Death in Children
Pulmonary Venous Obstruction in CHD
Brain MRI Atlas for Infants with CHD

2010 – 2011
($344,156 total allocation)

Mechanisms in the Pathogenesis of HLHS
Hypoxia on Neuro Outcome in CHD
Unbalanced Atrioventricular Septal Defect
3D Cardiac Tissue Engineering

2009 – 2010
($100,000 total allocation)

3D Tissue Engineering

2007 – 2009
($52,000 total allocation)

Myocardial Protection and Support in Cyanotic CHD