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Functional characterization of two novel mammalian electrogenic proton-dependent amino acid cotransportersA cluster of proton/amino acid transporter genes in the human and mouse genomesSubstrate recognition by the mammalian proton-dependent amino acid transporter PAT1.The proton/amino acid cotransporter PAT2 is expressed in neurons with a different subcellular localization than its paralog PAT1.Analysis of the transport properties of side chain modified dipeptides at the mammalian peptide transporter PEPT1.A rapid in vitro screening for delivery of peptide-derived peptidase inhibitors as potential drug candidates via epithelial peptide transporters.Substrate specificity and transport mode of the proton-dependent amino acid transporter mPAT2.A novel bifunctionality: PAT1 and PAT2 mediate electrogenic proton/amino acid and electroneutral proton/fatty acid symport.Kinetics of bidirectional H+ and substrate transport by the proton-dependent amino acid symporter PAT1H+/amino acid transporter 1 (PAT1) is the imino acid carrier: An intestinal nutrient/drug transporter in human and rat.Modeling of the relationship between dipeptide structure and dipeptide stability, permeability, and ACE inhibitory activity.The steroid glycoside H.g.-12 from Hoodia gordonii activates the human bitter receptor TAS2R14 and induces CCK release from HuTu-80 cells.Angiotensin converting enzyme inhibitory peptides from a lactotripeptide-enriched milk beverage are absorbed intact into the circulation.Rapid and sustained systemic circulation of conjugated gut microbial catabolites after single-dose black tea extract consumption.Current in vitro testing of bioactive peptides is not valuable.Protein hydrolysates induce CCK release from enteroendocrine cells and act as partial agonists of the CCK1 receptor.Intragastric layering of lipids delays lipid absorption and increases plasma CCK but has minor effects on gastric emptying and appetite.The angiotensin converting enzyme inhibitory tripeptides Ile-Pro-Pro and Val-Pro-Pro show increasing permeabilities with increasing physiological relevance of absorption models.Intragastric infusion of pea-protein hydrolysate reduces test-meal size in rats more than pea protein.
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name
Martin Foltz
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type
label
Martin Foltz
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prefLabel
Martin Foltz
@en