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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Medknow Publications & Media Pvt Ltd 2011
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3224431/
https://ncbi.nlm.nih.gov/pubmed/22140629
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2045-8932.87308
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