Michael Bressan

Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management

Vascular Development

A HCN4+ cardiomyogenic progenitor derived from the first heart field and human pluripotent stem cells

Pulmonary disease is a component of distal arthrogryposis type 5

Rapid adaptive optical recovery of optimal resolution over large volumes

Stem-cell therapy for cardiac disease

Hippo Pathway in Organ Size Control, Tissue Homeostasis, and Cancer

PDGF signalling controls age-dependent proliferation in pancreatic β-cells

Pericytes: Developmental, Physiological, and Pathological Perspectives, Problems, and Promises

Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1

Microfluidic organs-on-chips

Genetic Basis for Congenital Heart Defects: Current Knowledge

DNA methylation-based biomarkers and the epigenetic clock theory of ageing

Basic and Therapeutic Aspects of Angiogenesis

Light sheet microscopy for real-time developmental biology

Mutations in ECEL1 Cause Distal Arthrogryposis Type 5D

22q11.2 deletion syndrome

YAP1, the nuclear target of Hippo signaling, stimulates heart growth through cardiomyocyte proliferation but not hypertrophy

ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease: Executive Summary

Gain-of-function mutations in the mechanically activated ion channel PIEZO2 cause a subtype of Distal Arthrogryposis

Mesenchymal Stem Cells Derived from Dental Tissues vs. Those from Other Sources: Their Biology and Role in Regenerative Medicine

Bioengineered Myocardium Derived from Induced Pluripotent Stem Cells Improves Cardiac Function and Attenuates Cardiac Remodeling Following Chronic Myocardial Infarction in Rats

Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management

A dual role for ErbB2 signaling in cardiac trabeculation

Notochord-derived BMP antagonists inhibit endothelial cell generation and network formation

TBX5 Genetic Testing Validates Strict Clinical Criteria for Holt-Oram Syndrome

Mutation of Perinatal Myosin Heavy Chain Associated with a Carney Complex Variant

Early Mesodermal Cues Assign Avian Cardiac Pacemaker Fate Potential in a Tertiary Heart Field

Bone Marrow Oct3/4 ⁺ Cells Differentiate Into Cardiac Myocytes via Age-Dependent Paracrine Mechanisms