H+-coupled nutrient, micronutrient and drug transporters in the mammalian small intestine
Author:
Publisher
Wiley
Subject
Physiology,Physiology (medical),Nutrition and Dietetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1113/expphysiol.2005.029959/fullpdf
Reference201 articles.
1. Vigabatrin transport across the human intestinal epithelial (Caco-2) brush-border membrane is via the H+-coupled amino acid transporter hPAT1;Abbot;Br J Pharmacol,2006
2. H+/amino acid transporter 1 (PAT1) is the imino acid carrier: an intestinal nutrient/drug transporter in human and rat;Anderson;Gastroenterology,2004
3. Inhibition of intestinal dipeptide transport by the neuropeptide VIP is an anti-absorptive effect via the VPAC1 receptor in a human enterocyte-like cell line (Caco-2);Anderson;Br J Pharmacol,2003
4. Indirect regulation of the intestinal H+-coupled amino acid transporter hPAT1 (SLC36A1);Anderson;J Cell Physiol,2005
5. Regulation of intestinal hPepT1 (SLC15A1) activity by phosphodiesterase inhibitors is via inhibition of NHE3 (SLC9A3);Anderson;Biochim Biophys Acta,2007
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