Impaired intestinal free fatty acid transport followed by chylomicron malformation, not pancreatic insufficiency, cause metabolic defects in cystic fibrosis

Author:

Teng Lihong,Dedousis NikolaosORCID,Adeshirlarijaney Aneseh,Kanshana Jitendra S.,Liu Min,Hodges Craig A.,Kohan Alison B.ORCID

Publisher

Elsevier BV

Reference103 articles.

1. Cellular localization of the cystic fibrosis transmembrane conductance regulator in mouse intestinal tract;Ameen;Histochem. Cell Biol.,2000

2. CFTR High Expresser Cells in cystic fibrosis and intestinal diseases;Reis;Heliyon,2023

3. Characterization of CFTR high expresser cells in the intestine;Jakab;Am. J. Physiol. Gastrointest. Liver Physiol.,2013

4. Chloride conductance of CFTR facilitates basal Cl -/HCO 3- exchange in the villous epithelium of intact murine duodenum;Simpson;Am. J. Physiol. Gastrointest. Liver Physiol.,2005

5. Growth deficits in cystic fibrosis mice begin in utero prior to IGF-1 reduction;Darrah;PLoS One,2017

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