Cardiomyocyte proliferation and maturation: two sides of the same coin for heart regeneration
In the past few decades, cardiac regeneration has been the central target for restoring the
injured heart. In mammals, cardiomyocytes are terminally differentiated and rarely divide …
injured heart. In mammals, cardiomyocytes are terminally differentiated and rarely divide …
Heart failure in single right ventricle congenital heart disease: physiological and molecular considerations
AM Garcia, JT Beatty… - American Journal of …, 2020 - journals.physiology.org
Because of remarkable surgical and medical advances over the past several decades, there
are growing numbers of infants and children living with single ventricle congenital heart …
are growing numbers of infants and children living with single ventricle congenital heart …
Impaired human cardiac cell development due to NOTCH1 deficiency
Background: NOTCH1 pathogenic variants are implicated in multiple types of congenital
heart defects including hypoplastic left heart syndrome, where the left ventricle is …
heart defects including hypoplastic left heart syndrome, where the left ventricle is …
Genetic etiology of left‐sided obstructive heart lesions: a story in development
LE Parker, AP Landstrom - Journal of the American Heart …, 2021 - Am Heart Assoc
Congenital heart disease is the most common congenital defect observed in newborns.
Within the spectrum of congenital heart disease are left‐sided obstructive lesions (LSOLs) …
Within the spectrum of congenital heart disease are left‐sided obstructive lesions (LSOLs) …
Hand factors in cardiac development
RM George, AB Firulli - The Anatomical Record, 2019 - Wiley Online Library
Congenital heart defects account for 1% of infant mortality and 10% of in utero deaths. As
the vertebrate embryo develops, multiple tissue types develop in tandem to morphologically …
the vertebrate embryo develops, multiple tissue types develop in tandem to morphologically …
Decoding genetics of congenital heart disease using patient-derived induced pluripotent stem cells (iPSCs)
Congenital heart disease (CHD) is the most common cause of infant death associated with
birth defects. Recent next-generation genome sequencing has uncovered novel genetic …
birth defects. Recent next-generation genome sequencing has uncovered novel genetic …
Hypoplastic left heart syndrome: From bedside to bench and back
Abstract Hypoplastic Left Heart Syndrome (HLHS) is a complex Congenital Heart Disease
(CHD) that was almost universally fatal until the advent of the Norwood operation in 1981 …
(CHD) that was almost universally fatal until the advent of the Norwood operation in 1981 …
Overlapping but distinct roles for NOTCH receptors in human cardiovascular disease
JAN Meester, A Verstraeten, M Alaerts… - Clinical …, 2019 - Wiley Online Library
The NOTCH signalling pathway is an essential pathway, involved in many cellular
processes, including cell fate decision, cell proliferation, and cell death and important in the …
processes, including cell fate decision, cell proliferation, and cell death and important in the …
Exploring the mutational landscape of isolated congenital heart defects: an exome sequencing study using cardiac DNA
I Meerschaut, W Steyaert, T Bové, K François… - Genes, 2022 - mdpi.com
Congenital heart defects (CHD) are the most common congenital anomalies in liveborn
children. In contrast to syndromic CHD (SCHD), the genetic basis of isolated CHD (ICHD) is …
children. In contrast to syndromic CHD (SCHD), the genetic basis of isolated CHD (ICHD) is …
Single-cell reconstruction and mutation enrichment analysis identifies dysregulated cardiomyocyte and endothelial cells in congenital heart disease
Congenital heart disease (CHD) is one of the most prevalent neonatal congenital
anomalies. To catalog the putative candidate CHD risk genes, we collected 16,349 variants …
anomalies. To catalog the putative candidate CHD risk genes, we collected 16,349 variants …