2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM guidelines for the diagnosis and management of patients with thoracic aortic disease: a report of the …

Writing Group Members, LF Hiratzka, GL Bakris… - Circulation, 2010 - ahajournals.org
2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM Guidelines for the Diagnosis and
Management of Patients With Thoracic Aortic Disease | Circulation Science Volunteer Warning …

The role matrix metalloproteinases in the production of aortic aneurysm

SW Rabkin - Progress in molecular biology and translational …, 2017 - Elsevier
Matrix metalloproteinases (MMPs) have been implicated in the pathogenesis of aortic
aneurysm because the histology of thoracic aortic aneurysm (TAA) and abdominal aortic …

Vascular smooth muscle cell plasticity and autophagy in dissecting aortic aneurysms

M Clément, J Chappell, J Raffort, F Lareyre… - … , and vascular biology, 2019 - ahajournals.org
Objective—Recent studies suggested the occurrence of phenotypic switching of vascular
smooth muscle cells (VSMCs) during the development of aortic aneurysm (AA). However …

Tgfbr2 disruption in postnatal smooth muscle impairs aortic wall homeostasis

W Li, Q Li, Y Jiao, L Qin, R Ali, J Zhou, J Ferruzzi… - The Journal of clinical …, 2014 - jci.org
TGF-β is essential for vascular development; however, excess TGF-β signaling promotes
thoracic aortic aneurysm and dissection in multiple disorders, including Marfan syndrome …

MicroRNA-29 in aortic dilation: implications for aneurysm formation

RA Boon, T Seeger, S Heydt, A Fischer… - Circulation …, 2011 - ahajournals.org
Rationale: Aging represents a major risk factor for coronary artery disease and aortic
aneurysm formation. MicroRNAs (miRs) have emerged as key regulators of biological …

Ascending aortic dilatation associated with bicuspid aortic valve: pathophysiology, molecular biology, and clinical implications

TM Tadros, MD Klein, OM Shapira - Circulation, 2009 - ahajournals.org
BAV aortas have histopathological findings similar to those of Marfan syndrome aortas, the
underlying genetic abnormality of Marfan syndrome—mutation in the FBN1 gene that …

Genetic basis of thoracic aortic aneurysms and dissections: focus on smooth muscle cell contractile dysfunction

DM Milewicz, DC Guo, V Tran-Fadulu… - … Rev. Genomics Hum …, 2008 - annualreviews.org
Thoracic aortic aneurysms leading to type A dissections (TAAD) can be inherited in isolation
or in association with genetic syndromes, such as Marfan syndrome and Loeys-Dietz …

Neutrophil-derived matrix metalloproteinase 9 triggers acute aortic dissection

T Kurihara, R Shimizu-Hirota, M Shimoda, T Adachi… - Circulation, 2012 - ahajournals.org
Background—Acute aortic dissection (AAD) is a life-threatening vascular disease without
effective pharmaceutical therapy. Matrix metalloproteinases (MMPs) are implicated in the …

AGGF1 therapy inhibits thoracic aortic aneurysms by enhancing integrin α7-mediated inhibition of TGF-β1 maturation and ERK1/2 signaling

X Da, Z Li, X Huang, Z He, Y Yu, T Tian, C Xu… - Nature …, 2023 - nature.com
Thoracic aortic aneurysm (TAA) is a localized or diffuse dilatation of the thoracic aortas, and
causes many sudden deaths each year worldwide. However, there is no effective …

Massive aggrecan and versican accumulation in thoracic aortic aneurysm and dissection

FS Cikach, CD Koch, TJ Mead, J Galatioto… - JCI …, 2018 - pmc.ncbi.nlm.nih.gov
Proteoglycan accumulation is a hallmark of medial degeneration in thoracic aortic aneurysm
and dissection (TAAD). Here, we defined the aortic proteoglycanome using mass …