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1.
Dysregulated Smooth Muscle Cell BMPR2-ARRB2 Axis Causes Pulmonary Hypertension.
Circ Res
; 132(5): 545-564, 2023 03 03.
Article
in English
| MEDLINE | ID: mdl-36744494
2.
Codependence of Bone Morphogenetic Protein Receptor 2 and Transforming Growth Factor-ß in Elastic Fiber Assembly and Its Perturbation in Pulmonary Arterial Hypertension.
Arterioscler Thromb Vasc Biol
; 37(8): 1559-1569, 2017 08.
Article
in English
| MEDLINE | ID: mdl-28619995
3.
In Pulmonary Arterial Hypertension, Reduced BMPR2 Promotes Endothelial-to-Mesenchymal Transition via HMGA1 and Its Target Slug.
Circulation
; 133(18): 1783-94, 2016 May 03.
Article
in English
| MEDLINE | ID: mdl-27045138
4.
RNA Sequencing Analysis Detection of a Novel Pathway of Endothelial Dysfunction in Pulmonary Arterial Hypertension.
Am J Respir Crit Care Med
; 192(3): 356-66, 2015 Aug 01.
Article
in English
| MEDLINE | ID: mdl-26030479
5.
Loss of adenomatous poliposis coli-α3 integrin interaction promotes endothelial apoptosis in mice and humans.
Circ Res
; 111(12): 1551-64, 2012 Dec 07.
Article
in English
| MEDLINE | ID: mdl-23011394
6.
Hypoxia preconditioned mesenchymal stem cells improve vascular and skeletal muscle fiber regeneration after ischemia through a Wnt4-dependent pathway.
Mol Ther
; 18(8): 1545-52, 2010 Aug.
Article
in English
| MEDLINE | ID: mdl-20551912
7.
Amphetamines promote mitochondrial dysfunction and DNA damage in pulmonary hypertension.
JCI Insight
; 2(2): e90427, 2017 01 26.
Article
in English
| MEDLINE | ID: mdl-28138562
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