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1.
NMR Structural Analysis of Isolated Shaker Voltage-Sensing Domain in LPPG Micelles.
Biophys J
; 117(2): 388-398, 2019 07 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-31301804
2.
The parmodulin NRD-21 is an allosteric inhibitor of PAR1 Gq signaling with improved anti-inflammatory activity and stability.
Bioorg Med Chem
; 27(17): 3788-3796, 2019 09 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-31320211
3.
Monitoring Replication Protein A (RPA) dynamics in homologous recombination through site-specific incorporation of non-canonical amino acids.
Nucleic Acids Res
; 45(16): 9413-9426, 2017 Sep 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-28934470
4.
Synthetic Analogues of the Snail Toxin 6-Bromo-2-mercaptotryptamine Dimer (BrMT) Reveal That Lipid Bilayer Perturbation Does Not Underlie Its Modulation of Voltage-Gated Potassium Channels.
Biochemistry
; 57(18): 2733-2743, 2018 05 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-29616558
5.
Characterization of Protease-Activated Receptor (PAR) ligands: Parmodulins are reversible allosteric inhibitors of PAR1-driven calcium mobilization in endothelial cells.
Bioorg Med Chem
; 26(9): 2514-2529, 2018 05 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-29685684
6.
Synthesis and initial pharmacology of dual-targeting ligands for putative complexes of integrin αVß3 and PAR2.
RSC Med Chem
; 11(8): 940-949, 2020 Aug 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33479689
7.
Discovery, Optimization, and Characterization of ML417: A Novel and Highly Selective D3 Dopamine Receptor Agonist.
J Med Chem
; 63(10): 5526-5567, 2020 05 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-32342685
8.
Design and Evaluation of Heterobivalent PAR1-PAR2 Ligands as Antagonists of Calcium Mobilization.
ACS Med Chem Lett
; 10(1): 121-126, 2019 Jan 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-30655958
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