Detalhe da pesquisa
1.
Precision-engineered Peptide and Protein Analogs: Establishing a New Discovery Platform for Potent GPCR Modulators.
Chimia (Aarau)
; 75(6): 489-494, 2021 Jun 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-34233810
2.
Rapid and low-cost multiplex synthesis of chemokine analogs.
J Biol Chem
; 293(49): 19092-19100, 2018 12 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30305389
3.
δ-Conotoxins synthesized using an acid-cleavable solubility tag approach reveal key structural determinants for NaV subtype selectivity.
J Biol Chem
; 289(51): 35341-50, 2014 Dec 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25352593
4.
Arylsulfatases and neuraminidases modulate engagement of CCR5 by chemokines by removing key electrostatic interactions.
Sci Rep
; 14(1): 292, 2024 01 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38167636
5.
Structural basis of the activation of the CC chemokine receptor 5 by a chemokine agonist.
Sci Adv
; 7(25)2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34134983
6.
Author Correction: Arylsulfatases and neuraminidases modulate engagement of CCR5 by chemokines by removing key electrostatic interactions.
Sci Rep
; 14(1): 7399, 2024 Mar 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38548801
7.
Mechanism and molecular basis for the sodium channel subtype specificity of µ-conopeptide CnIIIC.
Br J Pharmacol
; 167(3): 576-86, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22537004
8.
A novel µ-conopeptide, CnIIIC, exerts potent and preferential inhibition of NaV1.2/1.4 channels and blocks neuronal nicotinic acetylcholine receptors.
Br J Pharmacol
; 166(5): 1654-68, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22229737