Pulmonary endothelial cell DNA methylation signature in pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is a severe and incurable pulmonary vascular disease. One of the primary origins of PAH is pulmonary endothelial dysfunction leading to vasoconstriction, aberrant angiogenesis and smooth muscle cell proliferation, endothelial-to-mesenchymal transition, thrombosi...

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Detalles Bibliográficos
Publicado en:Oncotarget
Main Authors: Hautefort, Aurélie, Chesné, Julie, Preussner, Jens, Pullamsetti, Soni S, Tost, Jorg, Looso, Mario, Antigny, Fabrice, Girerd, Barbara, Riou, Marianne, Eddahibi, Saadia, Deleuze, Jean-François, Seeger, Werner, Fadel, Elie, Simonneau, Gerald, Montani, David, Humbert, Marc, Perros, Frédéric
Formato: Artigo
Idioma:Inglês
Publicado: Impact Journals LLC 2017
Assuntos:
Research Paper
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5581088/
https://ncbi.nlm.nih.gov/pubmed/28881789
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.18031
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