(Pilot Program) The main goal of the proposed Center's Pilot Program is to foster the career development of junior investigators carrying out research in the field of cystic fibrosis (CF). A secondary goal is to attract more senior investigators from outside the field into areas of CF research. One mechanism that has been key to achieving these goals is our Pilot Program, which provides seed money for research that has not yet reached the stage of maturity necessary to garner funding through traditional NIH mechanisms. During the 21 years that the P30 Pilot Program has been running, it has funded 66 pilots in areas of CF research and other genetic diseases. Numerous junior investigators funded through this program have gone onto develop independent and well funded research programs. Prior to 2014, P30 Pilots included other genetic diseases and after that they were required to be focused on CF (including lung). In keeping with the overall shift of the Center's focus for this funding cycle, revisions to the Pilot Program include a requirement for the research to be focused on CF research related to the NIDDK mission (i.e., excluding lung). The Pilot Program is run through the Center's Administrative Core, with oversight from three committees: the Pilot and Feasibility Committee, the Executive Committee, and the External Advisory Committee. These groups take into account two external reviews per application in making decisions about funding. Progress of the pilot projects is monitored through numerous forums that are supported by the Center's Enrichment Program, and awardees are provided with extensive, constructive feedback that greatly facilitates the evolution of their research. In this section, we will summarize the progress made in past pilot projects and the success that many of the pilot holders have had to date. Notably, the 7 pilot grants that were funded during the last 5-year funding period resulted in 25 publications.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK054759-21
Application #
9983936
Study Section
Special Emphasis Panel (ZDK1)
Project Start
1998-09-30
Project End
2025-03-31
Budget Start
2020-06-01
Budget End
2021-05-31
Support Year
21
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Iowa
Department
Type
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Hammond, E; Chan, K S; Ames, J C et al. (2018) Impact of advanced detector technology and iterative reconstruction on low-dose quantitative assessment of lung computed tomography density in a biological lung model. Med Phys :
Bridges, Cory S; Miller, Pamela S; Lidbury, Jonathan A et al. (2018) Validation of a radioimmunoassay of serum trypsin-like immunoreactivity in ferrets. J Vet Diagn Invest 30:517-522
Labaki, Wassim W; Xia, Meng; Murray, Susan et al. (2018) NT-proBNP in stable COPD and future exacerbation risk: Analysis of the SPIROMICS cohort. Respir Med 140:87-93
Rotti, Pavana G; Xie, Weiliang; Poudel, Ananta et al. (2018) Pancreatic and Islet Remodeling in Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Knockout Ferrets. Am J Pathol 188:876-890
Norris, Andrew W; Uc, Aliye (2018) A Novel Stomach-Pancreas Connection: More than Physical. EBioMedicine 37:25-26
Lynch, Thomas J; Anderson, Preston J; Rotti, Pavana G et al. (2018) Submucosal Gland Myoepithelial Cells Are Reserve Stem Cells That Can Regenerate Mouse Tracheal Epithelium. Cell Stem Cell 22:779
Reed, Robert M; Cabral, Howard J; Dransfield, Mark T et al. (2018) Survival of Lung Transplant Candidates With COPD: BODE Score Reconsidered. Chest 153:697-701
Shim, Sung Shine; Schiebler, Mark L; Evans, Michael D et al. (2018) Lumen area change (Delta Lumen) between inspiratory and expiratory multidetector computed tomography as a measure of severe outcomes in asthmatic patients. J Allergy Clin Immunol 142:1773-1780.e9
Vargas Buonfiglio, Luis G; Borcherding, Jennifer A; Frommelt, Mark et al. (2018) Airway surface liquid from smokers promotes bacterial growth and biofilm formation via iron-lactoferrin imbalance. Respir Res 19:42
Fricke, Erin M; Elgin, Timothy G; Gong, Huiyu et al. (2018) Lipopolysaccharide-induced maternal inflammation induces direct placental injury without alteration in placental blood flow and induces a secondary fetal intestinal injury that persists into adulthood. Am J Reprod Immunol 79:e12816

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