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Accession: PRJNA288713 ID: 288713

Homo sapiens (human)

Effects of BMPR2 Loss in Human Pulmonary Artery Endothelial Cells

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Pulmonary arterial hypertension (PAH) is a fatal disease characterized by a proliferative endothelial cell phenotype, inflammation and pulmonary vascular remodeling. More...
AccessionPRJNA288713; GEO: GSE70456
Data TypeTranscriptome or Gene expression
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
PublicationsAwad KS et al., "Raf/ERK drives the proliferative and invasive phenotype of BMPR2-silenced pulmonary artery endothelial cells.", Am J Physiol Lung Cell Mol Physiol, 2016 Jan 15;310(2):L187-201
SubmissionRegistration date: 1-Jul-2015
Functional Genomics and Proteomics Facility, Critical Care Medicine Department, NIH
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Publications
PubMed1
PMC1
Other datasets
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Spots788688
Data volume, Processed Mbytes17
Data volume, Supplementary Mbytes29

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