Defining the extracellular matrix using proteomics

A Byron, JD Humphries… - International journal of …, 2013 - Wiley Online Library
The cell microenvironment has a profound influence on the behaviour, growth and survival
of cells. The extracellular matrix (ECM) provides not only mechanical and structural support …

Losartan reduces aortic dilatation rate in adults with Marfan syndrome: a randomized controlled trial

M Groenink, AW den Hartog, R Franken… - European heart …, 2013 - academic.oup.com
Abstract Aim Patients with Marfan syndrome have an increased risk of life-threatening aortic
complications, mostly preceded by aortic dilatation. Treatment with losartan, an angiotensin …

Aortopathy in Marfan syndrome: an update

F Romaniello, D Mazzaglia, A Pellegrino… - Cardiovascular …, 2014 - Elsevier
Marfan syndrome (MFS) is an inherited autosomal dominant multisystem disease caused by
mutations in the FBN1 gene encoding fibrillin-1, an extracellular matrix glycoprotein widely …

A deleterious gene-by-environment interaction imposed by calcium channel blockers in Marfan syndrome

JJ Doyle, AJ Doyle, NK Wilson, JP Habashi, D Bedja… - Elife, 2015 - elifesciences.org
Calcium channel blockers (CCBs) are prescribed to patients with Marfan syndrome for
prophylaxis against aortic aneurysm progression, despite limited evidence for their efficacy …

Genetic dissection of Marfan syndrome and related connective tissue disorders: an update 2012

S Hoffjan - Molecular Syndromology, 2012 - karger.com
Marfan syndrome (MFS) is an autosomal dominant disorder of the connective tissue
characterized by early development of thoracic aortic aneurysms/dissections together with …

The potential beneficial effects of resveratrol on cardiovascular complications in Marfan syndrome patients–insights from rodent-based animal studies

MM van Andel, M Groenink, AH Zwinderman… - International journal of …, 2019 - mdpi.com
Marfan syndrome (MFS) patients are at risk for cardiovascular disease. In particular, for
aortic aneurysm formation, which ultimately can result in a life-threatening aortic dissection …

Diagnosis and genetics of Marfan syndrome

R Franken, TJ Heesterbeek, V de Waard… - Expert opinion on …, 2014 - Taylor & Francis
Introduction: Marfan syndrome (MFS) is a connective tissue disorder with highly variable
features in cardiovascular, ocular and skeletal systems. MFS is generally caused by one of …

Aortic dilatation and dissection in Turner syndrome: what we know, what we are unclear about and what we should do in clinical practice?

SC Wong, M Cheung, M Zacharin - International journal of …, 2014 - degruyter.com
Aortic dilatation and aortic dissection are increasingly recognised in patients with Turner
syndrome (TS). Risk factors for aortic dissection include aortic dilatation, bicuspid aortic …

Aortic root disease in athletes: aortic root dilation, anomalous coronary artery, bicuspid aortic valve, and Marfan's syndrome

ES Yim - Sports Medicine, 2013 - Springer
Two professional athletes in the US National Basketball Association required surgery for
aortic root dilation in 2012. These cases have attracted attention in sports medicine to the …

No beneficial effect of general and specific anti-inflammatory therapies on aortic dilatation in Marfan mice

R Franken, S Hibender, AW den Hartog, T Radonic… - PLoS …, 2014 - journals.plos.org
Aims Patients with Marfan syndrome have an increased risk of life-threatening aortic
complications, mostly preceded by aortic dilatation. In the FBN1 C1039G/+ Marfan mouse …