Vascular smooth muscle cells and arterial stiffening: relevance in development, aging, and disease

P Lacolley, V Regnault, P Segers… - Physiological …, 2017 - journals.physiology.org
The cushioning function of large arteries encompasses distension during systole and recoil
during diastole which transforms pulsatile flow into a steady flow in the microcirculation …

Vascular extracellular matrix and arterial mechanics

JE Wagenseil, RP Mecham - Physiological reviews, 2009 - journals.physiology.org
An important factor in the transition from an open to a closed circulatory system was a
change in vessel wall structure and composition that enabled the large arteries to store and …

The Ehlers–Danlos syndrome, a disorder with many faces

A De Paepe, F Malfait - Clinical genetics, 2012 - Wiley Online Library
The Ehlers–Danlos syndromes (EDSs) comprise a heterogeneous group of diseases,
characterized by fragility of the soft connective tissues and widespread manifestations in …

Anatomy and organization of human skin

JA McGrath, RAJ Eady, FM Pope - Rook's textbook of …, 2004 - books.google.com
Human skin consists of a stratified, cellular epidermis and an underlying dermis of
connective tissue [1–5]. The dermal–epidermal junction is undulating in section; ridges of …

Effect of celiprolol on prevention of cardiovascular events in vascular Ehlers-Danlos syndrome: a prospective randomised, open, blinded-endpoints trial

KT Ong, J Perdu, J De Backer, E Bozec, P Collignon… - The Lancet, 2010 - thelancet.com
Summary Background Vascular Ehlers-Danlos syndrome is a rare severe disease that
causes arterial dissections and ruptures that can lead to early death. No preventive …

The type of variants at the COL3A1 gene associates with the phenotype and severity of vascular Ehlers–Danlos syndrome

M Frank, J Albuisson, B Ranque, L Golmard… - European Journal of …, 2015 - nature.com
Abstract Vascular Ehlers–Danlos syndrome (vEDS) is a rare and severe autosomal
dominant disorder caused by variants at the COL3A1 gene. Clinical characteristics and …

G protein-coupled receptor 56 and collagen III, a receptor-ligand pair, regulates cortical development and lamination

R Luo, SJ Jeong, Z Jin, N Strokes… - Proceedings of the …, 2011 - National Acad Sciences
GPR56, an orphan G protein-coupled receptor (GPCR) from the family of adhesion GPCRs,
plays an indispensable role in cortical development and lamination. Mutations in the GPR56 …

The Ehlers‐Danlos syndrome

B Steinmann, PM Royce… - Connective tissue and …, 2002 - Wiley Online Library
Summary The Ehlers‐Danlos syndrome (EDS) is a heterogeneous group of heritable
disorders of connective tissue characterized by articular hypermobility, skin …

The genetics of thoracic aortic aneurysms and dissection: a clinical perspective

NP Ostberg, MA Zafar, BA Ziganshin, JA Elefteriades - Biomolecules, 2020 - mdpi.com
Thoracic aortic aneurysm and dissection (TAAD) affects many patients globally and has high
mortality rates if undetected. Once thought to be solely a degenerative disease that afflicted …

Ehlers-Danlos syndrome type IV

DP Germain - Orphanet Journal of Rare Diseases, 2007 - Springer
Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS), is an
inherited connective tissue disorder defined by characteristic facial features (acrogeria) in …