[HTML][HTML] Animal Models, Pathogenesis, and Potential Treatment of Thoracic Aortic Aneurysm
Y Wang, IS Panicker, J Anesi, O Sargisson… - International Journal of …, 2024 - mdpi.com
Thoracic aortic aneurysm (TAA) has a prevalence of 0.16–0.34% and an incidence of 7.6
per 100,000 person-years, accounting for 1–2% of all deaths in Western countries …
per 100,000 person-years, accounting for 1–2% of all deaths in Western countries …
Participation of oleic acid in the formation of the aortic aneurysm in Marfan syndrome patients
ME Soto, AVI Hernández, VG Lans… - Prostaglandins & other …, 2016 - Elsevier
Marfan syndrome (MFS) is associated with progressive aortic dilatation and endothelial
dysfunction that lead to early acute dissection and rupture of the aorta and sudden death …
dysfunction that lead to early acute dissection and rupture of the aorta and sudden death …
Imbalanced synthesis of cyclooxygenase‐derived thromboxane A2 and prostacyclin compromises vasomotor function of the thoracic aorta in Marfan syndrome
AWY Chung, HHC Yang… - British journal of …, 2007 - Wiley Online Library
Background and purpose: Thoracic aortic dissection is a life‐threatening complication of
Marfan syndrome, a connective tissue disorder caused by mutations in the gene encoding …
Marfan syndrome, a connective tissue disorder caused by mutations in the gene encoding …
Selective loss of basal but not receptor-stimulated relaxation by endothelial nitric oxide synthase after isolation of the mouse aorta
J Van Langen, P Fransen, CE Van Hove… - European journal of …, 2012 - Elsevier
Bioavailability of nitric oxide (NO) is mostly studied in isolated blood vessels. We
investigated changes in basal and receptor-stimulated endothelial NO synthase (eNOS) …
investigated changes in basal and receptor-stimulated endothelial NO synthase (eNOS) …
Recent molecular biological progress in Marfan syndrome and Marfan-associated disorders
LG Gao, F Luo, RT Hui, XL Zhou - Ageing research reviews, 2010 - Elsevier
Marfan syndrome (MFS) is a connective tissue disorder with autosomal dominant
inheritance. Advances in medicine and surgery have increased the average lifespan of …
inheritance. Advances in medicine and surgery have increased the average lifespan of …
[HTML][HTML] Pleiotropic activation of endothelial function by angiotensin II receptor blockers is crucial to their protective anti-vascular remodeling effects
AY Tehrani, Z White, LW Tung, RRY Zhao, N Milad… - Scientific Reports, 2022 - nature.com
There are no therapeutics that directly enhance chronic endothelial nitric oxide (NO)
release, which is typically associated with vascular homeostasis. In contrast, angiotensin II …
release, which is typically associated with vascular homeostasis. In contrast, angiotensin II …
Understanding genomic medicine for thoracic aortic disease through the lens of induced pluripotent stem cells
AA Singh, DK Shetty, AG Jacob, S Bayraktar… - Frontiers in …, 2024 - frontiersin.org
Thoracic aortic disease (TAD) is often silent until a life-threatening complication occurs.
However, genetic information can inform both identification and treatment at an early stage …
However, genetic information can inform both identification and treatment at an early stage …
[HTML][HTML] Immunohistochemistry comparing endoscopic vein harvesting vs. open vein harvesting on saphenous vein endothelium
MH Nezafati, P Nezafati, S Amoueian… - Journal of …, 2014 - Springer
Objective The present study attempts to compare the immunohistochemistry (IHC) of von
Willebrand factor (vWf), endothelial cadherin, Caveolin and endothelial Nitric Oxide …
Willebrand factor (vWf), endothelial cadherin, Caveolin and endothelial Nitric Oxide …
Reversible cerebral vasoconstriction syndrome and posterior reversible encephalopathy syndrome in a boy with Loeys‐Dietz syndrome
Y Akazawa, Y Inaba, A Hachiya… - American Journal of …, 2015 - Wiley Online Library
Loeys‐Dietz syndrome (LDS) is an autosomal dominant connective tissue disorder, caused
by heterozygous mutations in TGFBR1 or TGFBR2 and characterized by vascular …
by heterozygous mutations in TGFBR1 or TGFBR2 and characterized by vascular …
NADPH oxidase 4 attenuates cerebral artery changes during the progression of Marfan syndrome
Y Onetti, T Meirelles, AP Dantas… - American Journal …, 2016 - journals.physiology.org
Marfan syndrome (MFS) is a connective tissue disorder that is often associated with the
fibrillin-1 (Fbn1) gene mutation and characterized by cardiovascular alterations …
fibrillin-1 (Fbn1) gene mutation and characterized by cardiovascular alterations …