Jeremy Tobias

Philip L Sannes1
Samuel H Jennings1
Maria Correa1
1Philip L Sannes
1Samuel H Jennings
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BACKGROUND Idiopathic pulmonary fibrosis (IPF) is a devastating interstitial pneumonia causing a loss of respiratory surface area due to a proliferative fibrotic response involving hyperplastic, hypertrophic, and metaplastic epithelium, cystic honeycomb change, septal expansion, and variable inflammation. Wnt (wingless) signaling glycoproteins are known to(More)
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