Bmpr2 mutation in murine PMVEC

ABSTRACT: 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. However, the physiologic and molecular consequences of expression of BMPR2 mutations in PMVEC are unknown. PMVEC were isolated from triple transgenic mice carrying the immortomouse gene, a transactivator, and either control, Bmpr2delx4+ or Bmpr2R899X mutation

ORGANISM(S): Mus musculus

SUBMITTER: James West 

PROVIDER: E-GEOD-28043 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress