Normal and abnormal development of the aortic wall and valve: correlation with clinical entities
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M. Goumans | M. Jongbloed | M. DeRuiter | A. G. Gittenberger-de Groot | R. Poelmann | R. Klautz | A. G. Groot | N. Grewal | Nimrat Grewal
[1] M. Goumans,et al. Bicuspid aortic valve: phosphorylation of c-Kit and downstream targets are prognostic for future aortopathy. , 2014, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.
[2] M. Goumans,et al. Ascending aorta dilation in association with bicuspid aortic valve: a maturation defect of the aortic wall. , 2014, The Journal of thoracic and cardiovascular surgery.
[3] A. Nakano,et al. Nkx2‐5 lineage tracing visualizes the distribution of second heart field‐derived aortic smooth muscle , 2013, Genesis.
[4] Robert H. Anderson,et al. Neural crest cells are required for correct positioning of the developing outflow cushions and pattern the arterial valve leaflets , 2013, Cardiovascular research.
[5] Paul Coucke,et al. Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD. , 2013, International journal of cardiology.
[6] A. Franco‐Cereceda,et al. Impaired Collagen Biosynthesis and Cross‐linking in Aorta of Patients With Bicuspid Aortic Valve , 2013, Journal of the American Heart Association.
[7] R. Jeremy,et al. The genetic and molecular basis of bicuspid aortic valve associated thoracic aortopathy: a link to phenotype heterogeneity. , 2013, Annals of cardiothoracic surgery.
[8] T. Kuntze,et al. Relation of Bicuspid Aortic Valve Morphology to the Dilatation Pattern of the Proximal Aorta: Focus on the Transvalvular Flow , 2012, Cardiology research and practice.
[9] M. Goumans,et al. The arterial and cardiac epicardium in development, disease and repair. , 2012, Differentiation; research in biological diversity.
[10] V. Kaartinen,et al. Deficient Signaling via Alk2 (Acvr1) Leads to Bicuspid Aortic Valve Development , 2012, PloS one.
[11] G. Andelfinger,et al. Loss of Gata5 in mice leads to bicuspid aortic valve. , 2011, The Journal of clinical investigation.
[12] R. Hinton,et al. Heart valve structure and function in development and disease. , 2011, Annual review of physiology.
[13] G. Vriend,et al. Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritis , 2011, Nature Genetics.
[14] J. Epstein,et al. Cardiac neural crest orchestrates remodeling and functional maturation of mouse semilunar valves. , 2011, The Journal of clinical investigation.
[15] S. Kurtovic,et al. Diverging Alternative Splicing Fingerprints in the Transforming Growth Factor-β Signaling Pathway Identified in Thoracic Aortic Aneurysms , 2011, Molecular medicine.
[16] A. Goette,et al. Atrial expression of endothelial nitric oxide synthase in patients with and without atrial fibrillation. , 2010, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.
[17] K. Teo,et al. Association of Bicuspid Aortic Valve Morphology and Aortic Root Dimensions: A Substudy of the Aortic Stenosis Progression Observation Measuring Effects of Rosuvastatin (ASTRONOMER) Study , 2010, Echocardiography.
[18] Santanu Chakraborty,et al. Transcriptional Regulation of Heart Valve Progenitor Cells , 2010, Pediatric Cardiology.
[19] A. C. Durán,et al. Bicuspid aortic valves with different spatial orientations of the leaflets are distinct etiological entities. , 2009, Journal of the American College of Cardiology.
[20] K. Yutzey,et al. Heart Valve Development: Regulatory Networks in Development and Disease , 2009, Circulation research.
[21] A. Al Haj Zen,et al. Syndromic and non‐syndromic aneurysms of the human ascending aorta share activation of the Smad2 pathway , 2009, The Journal of pathology.
[22] D. Benson. Thar's tendons in them thar valves! , 2008, Circulation Research.
[23] S. Siu,et al. Outcomes in adults with bicuspid aortic valves. , 2008, JAMA.
[24] D. Milewicz,et al. Genetic basis of thoracic aortic aneurysms and dissections: focus on smooth muscle cell contractile dysfunction. , 2008, Annual review of genomics and human genetics.
[25] A. Karsan,et al. Notch Signaling in Cardiac Development , 2008, Circulation research.
[26] B. Conley,et al. Endoglin is required for myogenic differentiation potential of neural crest stem cells. , 2007, Developmental biology.
[27] Paul Khairy,et al. Bicuspid aortic valve morphology and interventions in the young. , 2007, Journal of the American College of Cardiology.
[28] H. Sievers,et al. A classification system for the bicuspid aortic valve from 304 surgical specimens. , 2007, The Journal of thoracic and cardiovascular surgery.
[29] Jeffery A. Jones,et al. xpression of matrix metalloproteinases and endogenous nhibitors within ascending aortic aneurysms of patients ith bicuspid or tricuspid aortic valves , 2007 .
[30] H. Schäfers,et al. Endothelial nitric oxide synthase in bicuspid aortic valve disease. , 2007, The Annals of thoracic surgery.
[31] J. Epstein,et al. An essential role for Notch in neural crest during cardiovascular development and smooth muscle differentiation. , 2007, The Journal of clinical investigation.
[32] Robert K. Yu,et al. Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections (vol 39, pg 1488, 2007) , 2008 .
[33] V. Garg,et al. Molecular genetics of aortic valve disease , 2006, Current opinion in cardiology.
[34] D. Milewicz,et al. Genetic basis of thoracic aortic aneurysms and aortic dissections , 2005, American journal of medical genetics. Part C, Seminars in medical genetics.
[35] M. Moon,et al. The bicuspid aortic valve. , 2005, Current problems in cardiology.
[36] M. DeRuiter,et al. Basics of Cardiac Development for the Understanding of Congenital Heart Malformations , 2005, Pediatric Research.
[37] Joyce Bischoff,et al. Heart valve development: endothelial cell signaling and differentiation. , 2004, Circulation research.
[38] Yusuke Nakamura,et al. Heterozygous TGFBR2 mutations in Marfan syndrome , 2004, Nature Genetics.
[39] Benjamin R. Arenkiel,et al. Ablation of specific expression domains reveals discrete functions of ectoderm- and endoderm-derived FGF8 during cardiovascular and pharyngeal development , 2003, Development.
[40] S. Nakatani,et al. Failure to Prevent Progressive Dilation of Ascending Aorta by Aortic Valve Replacement in Patients With Bicuspid Aortic Valve: Comparison With Tricuspid Aortic Valve , 2003, Circulation.
[41] A. Tajik,et al. Is aortic dilatation an atherosclerosis-related process? Clinical, laboratory, and transesophageal echocardiographic correlates of thoracic aortic dimensions in the population with implications for thoracic aortic aneurysm formation. , 2003, Journal of the American College of Cardiology.
[42] Frank Noack,et al. Histopathological grading of ascending aortic aneurysm: comparison of patients with bicuspid versus tricuspid aortic valve. , 2003, The Journal of heart valve disease.
[43] T. Doetschman,et al. Double-Outlet Right Ventricle and Overriding Tricuspid Valve Reflect Disturbances of Looping, Myocardialization, Endocardial Cushion Differentiation, and Apoptosis in TGF-β2–Knockout Mice , 2001 .
[44] Takayuki Asahara,et al. The morphogen Sonic hedgehog is an indirect angiogenic agent upregulating two families of angiogenic growth factors , 2001, Nature Medicine.
[45] E. Boerwinkle,et al. Familial Thoracic Aortic Aneurysms and Dissections: Genetic Heterogeneity With a Major Locus Mapping to 5q13-14 , 2001, Circulation.
[46] T. Doetschman,et al. Double-outlet right ventricle and overriding tricuspid valve reflect disturbances of looping, myocardialization, endocardial cushion differentiation, and apoptosis in TGF-beta(2)-knockout mice. , 2001, Circulation.
[47] D. Schuppan,et al. Collagens Serve as an Extracellular Store of Bioactive Interleukin 2* , 2000, The Journal of Biological Chemistry.
[48] T. Mikawa,et al. Neural crest cells in outflow tract septation of the embryonic chicken heart: Differentiation and apoptosis , 1998, Developmental dynamics : an official publication of the American Association of Anatomists.
[49] A. Hunter,et al. A prospective study to assess the frequency of familial clustering of congenital bicuspid aortic valve. , 1997, Journal of the American College of Cardiology.
[50] D. Bergqvist. Ehlers-Danlos type IV syndrome. A review from a vascular surgical point of view. , 1996, The European journal of surgery = Acta chirurgica.
[51] Ada Hamosh,et al. Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene , 1991, Nature.
[52] R. Emanuel,et al. Congenitally bicuspid aortic valves. Clinicogenetic study of 41 families. , 1978, British heart journal.