Exocrine Pancreatic Alterations in Long-Lived Surviving Cystic Fibrosis Mice
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Reference40 articles.
1. Identification of the Cystic Fibrosis Gene: Genetic Analysis
2. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA
3. Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping
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1. Small adipose stores in cystic fibrosis mice are characterized by reduced cell volume, not cell number;American Journal of Physiology-Gastrointestinal and Liver Physiology;2018-12-01
2. Pancreatic pathophysiology in cystic fibrosis;The Journal of Pathology;2015-10-01
3. Animal models of gastrointestinal and liver diseases. Animal models of cystic fibrosis: gastrointestinal, pancreatic, and hepatobiliary disease and pathophysiology;American Journal of Physiology-Gastrointestinal and Liver Physiology;2015-03-15
4. The Cystic Fibrosis of Exocrine Pancreas;Cold Spring Harbor Perspectives in Medicine;2013-05-01
5. Altered de novo lipogenesis contributes to low adipose stores in cystic fibrosis mice;American Journal of Physiology-Gastrointestinal and Liver Physiology;2012-08-15
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