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Idiopathic pulmonary fibrosis (IPF) is a progressive and fatal lung disease that causes scarring of the lungs and an inability to breathe. IPF affects individuals 65 years of age and older with the number of cases at approximately 200,000 and on the rise.
The CIRM hPSC Repository contains hPSCs representing IPF as well as controls without diagnosed lung disorders. All samples are tied to corresponding demographic and clinical information.
Or use our Advanced Clinical Data Search to narrow your results.*Lines are grown feeder free on E8/vitronectin and are frozen in colony form.
CIRM Repository samples are accompanied by standardized sets of clinical data (Clinical Data Questionnaires).
Use the Advanced Clinical Data Search to locate samples based on clinical data in the above questionnaires.