Idiopathic and heritable PAH perturb common molecular pathways, correlated with increased MSX1 expression

The majority of pulmonary arterial hypertension (PAH) is not associated with BMPR2 mutation, and major risk factors for idiopathic PAH are not known. The objective of this study was to identify a gene expression signature for IPAH. To accomplish this, we used Affymetrix arrays to probe expression le...

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Detalles Bibliográficos
Autores principales: Austin, Eric D., Menon, Swapna, Hemnes, Anna R., Robinson, Linda R., Talati, Megha, Fox, Kelly L., Cogan, Joy D., Hamid, Rizwan, Hedges, Lora K., Robbins, Ivan, Lane, Kirk, Newman, John H., Loyd, James E., West, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224431/
https://www.ncbi.nlm.nih.gov/pubmed/22140629
http://dx.doi.org/10.4103/2045-8932.87308

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