Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
23
pubmed:dateCreated
2007-6-12
pubmed:abstractText
Pulmonary arterial hypertension (PAH) is characterized by selective elevation of pulmonary arterial pressure. The pathological hallmark of PAH is the narrowing of pulmonary arterioles secondary to endothelial cell dysfunction and smooth muscle cell proliferation. Heterozygous mutations in BMPR2, encoding the type II bone morphogenetic protein receptor (BMPRII), were identified in PAH, suggesting that alterations to BMPRII function are involved in disease onset and/or progression.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1524-4539
pubmed:author
pubmed:issnType
Electronic
pubmed:day
12
pubmed:volume
115
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2957-68
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:17515463-Adult, pubmed-meshheading:17515463-Animals, pubmed-meshheading:17515463-Bone Morphogenetic Protein Receptors, Type II, pubmed-meshheading:17515463-Cell Proliferation, pubmed-meshheading:17515463-Down-Regulation, pubmed-meshheading:17515463-Female, pubmed-meshheading:17515463-GTP-Binding Proteins, pubmed-meshheading:17515463-Humans, pubmed-meshheading:17515463-Hypertension, Pulmonary, pubmed-meshheading:17515463-Male, pubmed-meshheading:17515463-Mice, pubmed-meshheading:17515463-Middle Aged, pubmed-meshheading:17515463-Muscle, Smooth, Vascular, pubmed-meshheading:17515463-Mutation, pubmed-meshheading:17515463-Myocytes, Smooth Muscle, pubmed-meshheading:17515463-Neoplasm Proteins, pubmed-meshheading:17515463-Protein Binding, pubmed-meshheading:17515463-Rats, pubmed-meshheading:17515463-Receptors, Cell Surface, pubmed-meshheading:17515463-Smad1 Protein, pubmed-meshheading:17515463-Two-Hybrid System Techniques
pubmed:year
2007
pubmed:articleTitle
Receptor for activated C-kinase 1, a novel interaction partner of type II bone morphogenetic protein receptor, regulates smooth muscle cell proliferation in pulmonary arterial hypertension.
pubmed:affiliation
University of Giessen Lung Center, Department of Medicine II, Justus Liebig University Giessen, D-35392 Giessen, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't