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GSE28043
Bmpr2 mutation in murine PMVEC
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Mus musculus
6 Downloadable Samples
Affymetrix Mouse Gene 1.0 ST Array (mogene10st)
Submitter Supplied Information
Description
Pulmonary arterial hypertension (PAH) is thought to be driven by dysfunction of pulmonary vascular microendothelial cells (PMVEC). Most hereditary PAH is associated with BMPR2 mutations.
PubMed ID
21696628
Publication Title
Physiologic and molecular consequences of endothelial Bmpr2 mutation.
Total Samples
6
Submitter’s Institution
Vanderbilt University
Authors
Majka S
,
Hagen M
,
Blackwell T
,
Harral J
,
Johnson JA
,
Gendron R
,
Paradis H
,
Crona D
,
Loyd JE
,
Nozik-Grayck E
,
Stenmark KR
,
West J
Source Repository
Gene Expression Omnibus (GEO)
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