Detalhe da pesquisa
1.
A tetrapeptide class of biased analgesics from an Australian fungus targets the µ-opioid receptor.
Proc Natl Acad Sci U S A
; 116(44): 22353-22358, 2019 10 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-31611414
2.
A first glimpse at the influence of body mass in the morphological integration of the limb long bones: an investigation in modern rhinoceroses.
J Anat
; 237(4): 704-726, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32519813
3.
FAAH inhibitors in the limelight, but regrettably.
Int J Clin Pharmacol Ther
; 54(7): 498-501, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27191771
4.
An Updated Review on the Metabolite (AM404)-Mediated Central Mechanism of Action of Paracetamol (Acetaminophen): Experimental Evidence and Potential Clinical Impact.
J Pain Res
; 16: 1081-1094, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37016715
5.
GPER involvement in inflammatory pain.
Steroids
; 200: 109311, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37734514
6.
Role of T CD4+ cells, macrophages, C-low threshold mechanoreceptors and spinal Cav 3.2 channels in inflammation and related pain-like symptoms in murine inflammatory models.
Br J Pharmacol
; 180(4): 385-400, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36131381
7.
Identification of a human estrogen receptor α tetrapeptidic fragment with dual antiproliferative and anti-nociceptive action.
Sci Rep
; 13(1): 1326, 2023 01 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-36693877
8.
[Paracetamol: a promising ancestor]. / Le paracétamol : un ancêtre plein d'avenir.
Therapie
; 67(4): 277-81, 2012.
Artigo
em Francês
| MEDLINE | ID: mdl-23110826
9.
Centrally expressed Cav3.2 T-type calcium channel is critical for the initiation and maintenance of neuropathic pain.
Elife
; 112022 11 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36416409
10.
Design, synthesis and biological evaluation of conformationnally-restricted analogues of E7010 as inhibitors of tubulin assembly (ITA) and vascular disrupting agents (VDA).
Eur J Med Chem
; 244: 114809, 2022 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36208509
11.
The Antitumor Peptide ERα17p Exerts Anti-Hyperalgesic and Anti-Inflammatory Actions Through GPER in Mice.
Front Endocrinol (Lausanne)
; 12: 578250, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33815268
12.
Paracetamol analogues conjugated by FAAH induce TRPV1-mediated antinociception without causing acute liver toxicity.
Eur J Med Chem
; 213: 113042, 2021 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33257173
13.
Paracetamol is a centrally acting analgesic using mechanisms located in the periaqueductal grey.
Br J Pharmacol
; 177(8): 1773-1792, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31734950
14.
Interspecific variation in the limb long bones among modern rhinoceroses-extent and drivers.
PeerJ
; 7: e7647, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31579585
15.
Commentary: harnessing the first peptidic modulator of the estrogen receptor GPER.
Front Pharmacol
; 15: 1413058, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38751778
16.
Ethosuximide improves chronic pain-induced anxiety- and depression-like behaviors.
Eur Neuropsychopharmacol
; 29(12): 1419-1432, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31767519
17.
Inhibition of Cav 3.2 calcium channels: A new target for colonic hypersensitivity associated with low-grade inflammation.
Br J Pharmacol
; 176(7): 950-963, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30714145
18.
The Peptide ERα17p Is a GPER Inverse Agonist that Exerts Antiproliferative Effects in Breast Cancer Cells.
Cells
; 8(6)2019 06 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-31207943
19.
Optimization of the synthesis of a key intermediate for the preparation of glucocorticoids.
Steroids
; 137: 14-21, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30017852
20.
Assessment of the effectiveness and safety of Ethosuximide in the Treatment of non-Diabetic Peripheral Neuropathic Pain: EDONOT-protocol of a randomised, parallel, controlled, double-blinded and multicentre clinical trial.
BMJ Open
; 6(12): e013530, 2016 12 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-27986742