Background: Marfan syndrome (MFS) is associated with TGF (transforming growth factor) β–
stimulated ERK (extracellular signal-regulated kinase) activity in vascular smooth muscle …

Marfan syndrome (MFS) is one of the most common inherited disorders of connective tissue
caused by mutations of the fibrillin-1 gene (FBN1). Vascular abnormalities, such as the …

Marfan syndrome (MFS) is an inherited disorder that affects the connective tissues and
mainly presents in the bones, eyes, and cardiovascular system, etc. Aortic pathology is the …

Marfan syndrome (MFS) is an autosomal dominant disorder caused by a heterozygous
mutation of the FBN1 gene. MFS patients present oxidative stress that disturbs redox …

Emerging role of radiogenomics in genetically triggered thoracic aortic aneurysm and dissection:
a narrative review - PMC Back to Top Skip to main content NIH NLM Logo Access keys NCBI …

Editorial: Aortic diseases involving visceral artery: clinical therapeutic management and
related basic research Aortic diseases involving visceral arteries mainly include true and …

Background D-dimer (DD) is a vital biomarker to rule out the diagnosis of aortic dissection
(AD). However, the DD level in some patients with AD is not high in clinical practice, which …

Marfan syndrome (MFS) is a multisystem conncctivc tissue disease with autosomal dominant
inheritance. It is mainly caused by FBN1 gene mutation and often has different clinical …

Over the last decade with the advent of new genetic technologies such as CRISPR and
more recently described, seekRNA, we now have the ability to transfer genetic materials …

We present a case report of a 30-year-old Marfan syndrome patient who underwent a David
procedure for severe aortic valve insufficiency and Valsalva aneurysm. Harvested aortic …