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Full record GDS2248

Hereditary pulmonary arterial hypertension model: lung

Comparison of lungs of animals expressing a dominant negative type II bone morphogenic protein receptor (BMPRII) in smooth muscles to those with pulmonary arterial hypertension (PAH) induced by acute exposure to hypobaric hypoxia. BMPRII mutations are responsible for the majority of hereditary PAHs.
Organism:
Mus musculus
Type:
Expression profiling by array, count, 3 disease state, 3 protocol sets
Platform:
GPL339
Series:
GSE2773
5 Samples
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DataSet
Accession:
GDS2248
ID:
2248

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