[PDF][PDF] Angiotensin-converting enzyme and hypertension: a systemic analysis of various ACE inhibitors, their side effects, and bioactive peptides as a putative therapy …
Hypertension is a major risk factor for heart attack, produce atherosclerosis (hardening of the
arteries), congestive heart failure, stroke, kidney infection, blindness, end-stage renal …
arteries), congestive heart failure, stroke, kidney infection, blindness, end-stage renal …
Genetics of bicuspid aortic valve aortopathy
MG Andreassi, A Della Corte - Current opinion in cardiology, 2016 - journals.lww.com
The clinical variability seen in BAV aortopathy, in terms of phenotype and natural/clinical
history, suggests complex interactions between primary genetic defects, other modifier …
history, suggests complex interactions between primary genetic defects, other modifier …
[HTML][HTML] Genomic characterization of emergent pseudorabies virus in China reveals marked sequence divergence: evidence for the existence of two major genotypes
C Ye, QZ Zhang, ZJ Tian, H Zheng, K Zhao, F Liu… - Virology, 2015 - Elsevier
Recently pseudorabies outbreaks have occurred in many vaccinated farms in China. To
identify genetic characteristics of pseudorabies virus (PRV) strains, we obtained the …
identify genetic characteristics of pseudorabies virus (PRV) strains, we obtained the …
Involvement of the renin–angiotensin system in abdominal and thoracic aortic aneurysms
H Lu, DL Rateri, D Bruemmer, LA Cassis… - Clinical …, 2012 - portlandpress.com
Aortic aneurysms are relatively common maladies that may lead to the devastating
consequence of aortic rupture. AAAs (abdominal aortic aneurysms) and TAAs (thoracic …
consequence of aortic rupture. AAAs (abdominal aortic aneurysms) and TAAs (thoracic …
[HTML][HTML] The genetic and molecular basis of bicuspid aortic valve associated thoracic aortopathy: a link to phenotype heterogeneity
© AME Publishing Company. All rights reserved. Ann Cardiothorac Surg 2013; 2 (1): 83-91
www. annalscts. com an intrinsically 'weaker'aorta. In addition, the presence of valve …
www. annalscts. com an intrinsically 'weaker'aorta. In addition, the presence of valve …
[HTML][HTML] Thoracic aortic aneurysm development in patients with bicuspid aortic valve: what is the role of endothelial cells?
V Van de Pol, K Kurakula, MC DeRuiter… - Frontiers in …, 2017 - frontiersin.org
Bicuspid aortic valve (BAV) is the most common type of congenital cardiac malformation.
Patients with a BAV have a predisposition for the development of thoracic aortic aneurysm …
Patients with a BAV have a predisposition for the development of thoracic aortic aneurysm …
The revised role of TGF-β in aortic aneurysms in Marfan syndrome
R Franken, T Radonic, AW Den Hartog… - Netherlands Heart …, 2015 - Springer
Background Recently, we demonstrated that losartan reduced the aortic root dilatation rate
(AoDR) in adults with Marfan syndrome (MFS); however, responsiveness was diverse. The …
(AoDR) in adults with Marfan syndrome (MFS); however, responsiveness was diverse. The …
Genetic basis of familial valvular heart disease
570 Circ Cardiovasc Genet October 2012 semilunar (aortic and pulmonary) valve leaflets. 3,
8 The development of the outflow tract and semilunar valve is complex and involves …
8 The development of the outflow tract and semilunar valve is complex and involves …
[HTML][HTML] Bicuspid aortic valve-associated aortopathy: Where do we stand?
B Messner, D Bernhard - Journal of molecular and cellular cardiology, 2019 - Elsevier
Herein we summarize the current knowledge on the bicuspid aortic valve (BAV)-associated
aortopathy regarding clinical presentation and disease sub-classification, genetic …
aortopathy regarding clinical presentation and disease sub-classification, genetic …
[HTML][HTML] Angiotensin, transforming growth factor β and aortic dilatation in Marfan syndrome: of mice and humans
C Yu, RW Jeremy - IJC Heart & Vasculature, 2018 - Elsevier
Marfan syndrome is consequent upon mutations in FBN1, which encodes the extracellular
matrix microfibrillar protein fibrillin-1. The phenotype is characterised by development of …
matrix microfibrillar protein fibrillin-1. The phenotype is characterised by development of …