Hereditary & Pediatric Disorders of the Pancreas
Research on hereditary and pediatric disorders of the pancreas.
The Hereditary and Pediatric Disorders of the Pancreas program supports research on the genetic factors contributing to the etiology of pancreatic diseases and on childhood disorders of the pancreas. Particular areas of interest include understanding genetic factors and their interactions with exogenous insults, with respect to pathogenesis, complications, and natural history of pancreatitis and other pancreatic disorders. Studies involve genetic screenings that identify gene mutations in candidate genes or their regulatory elements that are associated with pancreatic structural or functional abnormalities. Researchers are focused on the identification of biologic or molecular mechanisms of pancreatic injury associated with the identification of mutant alleles; the generation of novel animal models of pancreatitis or abnormal pancreatic function by expression of mutant genes associated with pancreatic disease; and the identification of other genetic and environmental factors that influence the development and course of pancreatitis in genetically susceptible individuals.
NIDDK Program Staff
Recent Funding OpportunitiesView More Recent Funding Opportunities
NIDDK Central Repository Non-renewable Sample Access (X01 Clinical Trial Not Allowed)
PHS 2022-2 Omnibus Solicitation of the NIH, CDC and FDA for Small Business Innovation Research Grant Applications (Parent SBIR [R43/R44] Clinical Trial Not Allowed)
PHS 2022-2 Omnibus Solicitation of the NIH and CDC for Small Business Innovation Research Grant Applications (Parent SBIR [R43/R44] Clinical Trial Required)
PHS 2022-2 Omnibus Solicitation of the NIH for Small Business Technology Transfer Grant Applications (Parent STTR [R41/R42] Clinical Trial Not Allowed)
Promoting Organ and Tissue Donation Among Health Disparity Populations (R01 - Clinical Trial Optional)
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