Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Sarah C. Simões"'
Autor:
Sarah C. Simões, André L. Balico-Silva, Lucas T. Parreiras-e-Silva, André L. B. Bitencourt, Michel Bouvier, Claudio M. Costa-Neto
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2020)
The AT1 receptor (AT1R) has a major role in the Renin-Angiotensin System, being involved in several physiological events including blood pressure control and electrolyte balance. The AT1R is a member of the G protein coupled receptors (GPCR) family,
Externí odkaz:
https://doaj.org/article/31ce0111fb9b419d9d7001acd6fe7d18
Autor:
Larissa B. Teixeira, Lucas T. Parreiras-e-Silva, Thiago Bruder-Nascimento, Diego A. Duarte, Sarah C. Simões, Rafael M. Costa, Deisy Y. Rodríguez, Pedro A. B. Ferreira, Carlos A. A. Silva, Emiliana P. Abrao, Eduardo B. Oliveira, Michel Bouvier, Rita C. Tostes, Claudio M. Costa-Neto
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-10 (2017)
Abstract The renin-angiotensin system (RAS) plays a key role in the control of vasoconstriction as well as sodium and fluid retention mediated mainly by angiotensin (Ang) II acting at the AT1 receptor (AT1R). Ang-(1-7) is another RAS peptide, identif
Externí odkaz:
https://doaj.org/article/2fef525bd7c04daf974776365ec10caf
Autor:
Michelle F. Corrêa, Álefe J. R. Barbosa, Larissa B. Teixeira, Diego A. Duarte, Sarah C. Simões, Lucas T. Parreiras-e-Silva, Aleksandro M. Balbino, Richardt G. Landgraf, Michel Bouvier, Claudio M. Costa-Neto, João P. S. Fernandes
Publikováno v:
Frontiers in Pharmacology, Vol 8 (2017)
The histamine receptors (HRs) are traditional G protein-coupled receptors of extensive therapeutic interest. Recently, H3R and H4R subtypes have been targeted in drug discovery projects for inflammation, asthma, pain, cancer, Parkinson’s, and Alzhe
Externí odkaz:
https://doaj.org/article/510424b0114e473eb461e2f50e3faac8
Autor:
José A. F. P. Villar, Gustavo H. R. Viana, Leandro A. Barbosa, Fernando P. Varotti, Sarah C. Simões, Andersson Barison, Estrela M. P. V. E. Souza, Marina G. da Silva, Graziele D. da Silva
Publikováno v:
Molecules, Vol 17, Iss 9, Pp 10331-10343 (2012)
A series of new chalcones substituted with azide/triazole groups were designed and synthesized, and their cytotoxic activity was evaluated in vitro against the HeLa cell line. O-Alkylation, Claisen-Schmidt condensation and Cu(I)-catalyzed cycloadditi
Externí odkaz:
https://doaj.org/article/712b200d3ff84d7a9597cda58f3e5de1
Autor:
Cibele Cardoso, Josane de Freitas Sousa, Felipe Freitas-Castro, Graziela de Moura Aguiar, Natália Volgarine Scaraboto, Sarah C. Simões, Anelisa Ramão, Jessica Rodrigues Plaça, Wilson A. Silva
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
BACKGROUND: Expression dysregulation of HOX homeobox genes has been observed in several cancers, including head and neck squamous cell carcinoma (HNSC). Although characterization of HOX gene roles in HNSC development has been reported, there is still
Autor:
Michelle F, Corrêa, André L, Balico-Silva, Dóra J, Kiss, Gustavo A B, Fernandes, Jhonatan C, Maraschin, Lucas T, Parreiras-E-Silva, Marina T, Varela, Sarah C, Simões, Michel, Bouvier, György M, Keserű, Claudio M, Costa-Neto, João Paulo S, Fernandes
Publikováno v:
Bioorganicmedicinal chemistry. 30
Histamine acts through four different receptors (H
Autor:
Larissa de Bortoli Teixeira, Maria Luiza Morais Barreto-Chaves, Claudio M. Costa-Neto, Sarah C. Simões, Caroline Antunes Lino, Tábatha de Oliveira Silva, Gabriela Placoná Diniz
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
We have previously reported that angiotensin II receptor type 1 (AT1R) contributes to the hypertrophic effects of thyroid hormones (TH) in cardiac cells. Even though evidence indicates crosstalks between TH and AT1R, the underlying mechanisms are poo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::458bf626096041ed0f0ac6d96fa80cca
Autor:
Michel Bouvier, Viktoriya Lukasheva, Sarah C. Simões, Yubo Cao, Larissa B. Teixeira, Christian LeGouill, Dominic Devost, Jean-Michel Longpré, Graciela Piñeyro, Richard Leduc, Sahil Kumar, Yoon Namkung, Stéphane A. Laporte, Terence E. Hébert, Jenna Giubilaro, Claudio M. Costa-Neto
Publikováno v:
Science signaling. 11(559)
G protein-coupled receptors (GPCRs) are important therapeutic targets that exhibit functional selectivity (biased signaling), in which different ligands or receptor variants elicit distinct downstream signaling. Understanding all the signaling events
Autor:
João Paulo S. Fernandes, György M. Keserű, Michel Bouvier, Dóra J. Kiss, Marina T. Varela, Claudio M. Costa-Neto, Sarah C. Simões, Jhonatan Christian Maraschin, André L. Balico-Silva, Michelle Fidelis Corrêa, Lucas T. Parreiras-e-Silva, Gustavo A.B. Fernandes
Publikováno v:
Bioorganic & Medicinal Chemistry. 30:115924
Histamine acts through four different receptors (H1R-H4R), the H3R and H4R being the most explored in the last years as drug targets. The H3R is a potential target to treat narcolepsy, Parkinson’s disease, epilepsy, schizophrenia and several other
Autor:
Diego A. Duarte, Michel Bouvier, Claudio M. Costa-Neto, Richardt G. Landgraf, Larissa B. Teixeira, Aleksandro Martins Balbino, João Paulo S. Fernandes, Álefe Jhonatas Ramos Barbosa, Sarah C. Simões, Michelle Fidelis Corrêa, Lucas T. Parreiras-e-Silva
Publikováno v:
Frontiers in Pharmacology, Vol 8 (2017)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
The histamine receptors (HRs) are traditional G protein-coupled receptors of extensive therapeutic interest. Recently, H3R and H4R subtypes have been targeted in drug discovery projects for inflammation, asthma, pain, cancer, Parkinson's, and Alzheim