valine and sincalide

valine has been researched along with sincalide in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Knapp, RJ; Malatynska, E; Stropova, D; Varga, E; Yamamura, HI	1
Adachi, Y; Hirouchi, M; Hu, Z; Maeda, K; Sugiyama, Y; Yamashiro, W	1

Other Studies

2 other study(ies) available for valine and sincalide

Article	Year
The role of the Val353 residue in antagonist binding to rat CCK-B receptors. Neuroreport, 1995, Jun-19, Volume: 6, Issue:9 Topics: Amino Acids; Animals; Binding, Competitive; Dose-Response Relationship, Drug; Mutation; Peptide Fragments; Peptoids; Rats; Rats, Inbred Strains; Receptors, Cholecystokinin; Sincalide; Valine	1995
Involvement of transporters in the hepatic uptake and biliary excretion of valsartan, a selective antagonist of the angiotensin II AT1-receptor, in humans. Drug metabolism and disposition: the biological fate of chemicals, 2006, Volume: 34, Issue:7 Topics: Adenosine Triphosphate; Angiotensin II Type 1 Receptor Blockers; Animals; Bile; Cell Line; Cell Membrane; Disease Models, Animal; Estrone; Hepatocytes; Humans; Hyperbilirubinemia; Liver-Specific Organic Anion Transporter 1; Male; Membrane Transport Proteins; Multidrug Resistance-Associated Protein 2; Multidrug Resistance-Associated Proteins; Organic Anion Transporters; Organic Anion Transporters, Sodium-Independent; Rats; Rats, Sprague-Dawley; Sincalide; Solute Carrier Organic Anion Transporter Family Member 1B3; Tetrazoles; Transfection; Valine; Valsartan	2006

Article

Year

The role of the Val353 residue in antagonist binding to rat CCK-B receptors.

Neuroreport, 1995, Jun-19, Volume: 6, Issue:9

Topics: Amino Acids; Animals; Binding, Competitive; Dose-Response Relationship, Drug; Mutation; Peptide Fragments; Peptoids; Rats; Rats, Inbred Strains; Receptors, Cholecystokinin; Sincalide; Valine

1995

Involvement of transporters in the hepatic uptake and biliary excretion of valsartan, a selective antagonist of the angiotensin II AT1-receptor, in humans.

Drug metabolism and disposition: the biological fate of chemicals, 2006, Volume: 34, Issue:7

Topics: Adenosine Triphosphate; Angiotensin II Type 1 Receptor Blockers; Animals; Bile; Cell Line; Cell Membrane; Disease Models, Animal; Estrone; Hepatocytes; Humans; Hyperbilirubinemia; Liver-Specific Organic Anion Transporter 1; Male; Membrane Transport Proteins; Multidrug Resistance-Associated Protein 2; Multidrug Resistance-Associated Proteins; Organic Anion Transporters; Organic Anion Transporters, Sodium-Independent; Rats; Rats, Sprague-Dawley; Sincalide; Solute Carrier Organic Anion Transporter Family Member 1B3; Tetrazoles; Transfection; Valine; Valsartan

2006