Cardiomyocyte proliferation and maturation: two sides of the same coin for heart regeneration

MT Zhao, S Ye, J Su, V Garg - Frontiers in cell and developmental …, 2020 - frontiersin.org
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 …

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 …

Impaired human cardiac cell development due to NOTCH1 deficiency

S Ye, C Wang, Z Xu, H Lin, X Wan, Y Yu… - Circulation …, 2023 - Am Heart Assoc
Background: NOTCH1 pathogenic variants are implicated in multiple types of congenital
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) …

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 …

Decoding genetics of congenital heart disease using patient-derived induced pluripotent stem cells (iPSCs)

H Lin, KL McBride, V Garg, MT Zhao - Frontiers in Cell and …, 2021 - frontiersin.org
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 …

Hypoplastic left heart syndrome: From bedside to bench and back

A Saraf, WM Book, TJ Nelson, C Xu - Journal of molecular and cellular …, 2019 - Elsevier
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 …

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 …

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 …

Single-cell reconstruction and mutation enrichment analysis identifies dysregulated cardiomyocyte and endothelial cells in congenital heart disease

R Tambi, B Zehra, S Nandkishore… - Physiological …, 2023 - journals.physiology.org
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 …