Detalhe da pesquisa
1.
How Instructions, Learning, and Expectations Shape Pain and Neurobiological Responses.
Annu Rev Neurosci
; 46: 167-189, 2023 07 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36917820
2.
Nav1.7 as a chondrocyte regulator and therapeutic target for osteoarthritis.
Nature
; 625(7995): 557-565, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-38172636
3.
A monoclonal antibody that targets a NaV1.7 channel voltage sensor for pain and itch relief.
Cell
; 157(6): 1393-1404, 2014 06 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-24856969
4.
Specialized Pro-Resolving Mediators as Resolution Pharmacology for the Control of Pain and Itch.
Annu Rev Pharmacol Toxicol
; 63: 273-293, 2023 Jan 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36100219
5.
Biased Agonism: Lessons from Studies of Opioid Receptor Agonists.
Annu Rev Pharmacol Toxicol
; 63: 491-515, 2023 01 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36170657
6.
Endogenous and Exogenous Opioids in Pain.
Annu Rev Neurosci
; 41: 453-473, 2018 07 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29852083
7.
Unidirectional cross-activation of GRPR by MOR1D uncouples itch and analgesia induced by opioids.
Cell
; 147(2): 447-58, 2011 Oct 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-22000021
8.
Therapeutic antagonism of the neurokinin 1 receptor in endosomes provides sustained pain relief.
Proc Natl Acad Sci U S A
; 120(22): e2220979120, 2023 05 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37216510
9.
A randomized clinical trial of the efficacy and safety of rivipansel for sickle cell vaso-occlusive crisis.
Blood
; 141(2): 168-179, 2023 01 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35981565
10.
Physicians prescribe fewer analgesics during night shifts than day shifts.
Proc Natl Acad Sci U S A
; 119(27): e2200047119, 2022 07 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35759656
11.
Serodolin, a ß-arrestin-biased ligand of 5-HT7 receptor, attenuates pain-related behaviors.
Proc Natl Acad Sci U S A
; 119(21): e2118847119, 2022 05 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-35594393
12.
Multitarget nociceptor sensitization by a promiscuous peptide from the venom of the King Baboon spider.
Proc Natl Acad Sci U S A
; 119(5)2022 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35074873
13.
Dehydroepiandrosterone Sulfate (DHEAS) Is an Endogenous Kv7 Channel Modulator That Reduces Kv7/M-Current Suppression and Inflammatory Pain.
J Neurosci
; 43(43): 7073-7083, 2023 10 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37648450
14.
Pharmacologic Characterization of LTGO-33, a Selective Small Molecule Inhibitor of the Voltage-Gated Sodium Channel NaV1.8 with a Unique Mechanism of Action.
Mol Pharmacol
; 105(3): 233-249, 2024 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-38195157
15.
Design, synthesis, and mechanism of action of novel µ-conotoxin KIIIA analogues for inhibition of the voltage-gated sodium channel Nav1.7.
J Biol Chem
; 299(4): 103068, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36842500
16.
AMPAkines have site-specific analgesic effects in the cortex.
Mol Pain
; 20: 17448069231214677, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-37921508
17.
Toward reducing racialized pain care disparities: Approaching cannabis research and access through the lens of equity and inclusion.
Cancer
; 130(4): 497-504, 2024 02 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37941524
18.
Revisiting prostaglandin E2: A promising therapeutic target for osteoarthritis.
Clin Immunol
; 260: 109904, 2024 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38262526
19.
Polymyalgia rheumatica.
Lancet
; 402(10411): 1459-1472, 2023 10 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37832573
20.
Neutrophil extracellular traps as a unique target in the treatment of inflammatory pain.
Biochem Biophys Res Commun
; 710: 149896, 2024 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38604072