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Resultados de 1 a 10 de 21  para Produção Intelectual da USP

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1
A pluridimensional view of biased agonism
A pluridimensional view of biased agonism
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Artigo 		Adicionar ao Meu Espaço

A pluridimensional view of biased agonism

Cláudio Miguel Costa Neto Lucas T Parreiras-e-Silva; M Bouvier

Molecular Pharmacology Bethesda v. 90, n. 5, p. 587-595, 2016

Bethesda 2016

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2845506 Estantes Deslizantes )(Acessar)

2
Identifying Plasmodium falciparum receptor activation using bioluminescence resonance energy transfer (BRET)-based biosensors in HEK293 cells
Identifying Plasmodium falciparum receptor activation using bioluminescence resonance energy transfer (BRET)-based biosensors in HEK293 cells
Material Type:
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Identifying Plasmodium falciparum receptor activation using bioluminescence resonance energy transfer (BRET)-based biosensors in HEK293 cells

Pedro Henrique Scarpelli Pereira Célia Regina da Silva Garcia; Michel Bouvier

Shukla, Arun K., ed Methods in Cell Biology Amsterdam : Elsevier, 2021 348 p

Amsterdam Elsevier 2021

Item não circula. Consulte sua biblioteca.(Acessar)

3
Signal transduction profiling of angiotensin II type 1 receptor with mutations associated to atrial fibrillation in humans
Signal transduction profiling of angiotensin II type 1 receptor with mutations associated to atrial fibrillation in humans
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Signal transduction profiling of angiotensin II type 1 receptor with mutations associated to atrial fibrillation in humans

Sarah Capelupe Simões André L Balico-Silva; Lucas Tabajara Parreiras-e-Silva; André L. B Bitencourt; Michel Bouvier; Claudio Miguel Costa-Neto

Frontiers in Pharmacology Lausanne v. 11, on-line, 2020

Lausanne 2020

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 3192082 Acervo Digital )(Acessar)

4
Pharmacological characterization of 5-substituted 1-[(2,3-dihydro-1-benzofuran-2-yl)methyl]piperazines novel antagonists for the histamine H3 and H4 receptors with anti-inflammatory potential
Pharmacological characterization of 5-substituted 1-[(2,3-dihydro-1-benzofuran-2-yl)methyl]piperazines novel antagonists for the histamine H3 and H4 receptors with anti-inflammatory potential
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Pharmacological characterization of 5-substituted 1-[(2,3-dihydro-1-benzofuran-2-yl)methyl]piperazines novel antagonists for the histamine H3 and H4 receptors with anti-inflammatory potential

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; Cláudio Miguel Costa Neto; João P. S Fernandes

Frontiers in Pharmacology Lausanne v. 8, art. 825, 2017

Lausanne 2017

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2918308 Estantes Deslizantes )(Acessar)

5
Comparative analyses of downstream signal transduction targets modulated after activation of the AT1 receptor by two β-arrestin-biased agonists
Comparative analyses of downstream signal transduction targets modulated after activation of the AT1 receptor by two β-arrestin-biased agonists
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Comparative analyses of downstream signal transduction targets modulated after activation of the AT1 receptor by two β-arrestin-biased agonists

Geisa Aparecida dos Santos Diego A Duarte; Lucas T Parreiras-e-Silva; Felipe R Teixeira; Rafael Silva-Rocha; Eduardo Brandt de Oliveira; Michel Bouvier; Cláudio Miguel Costa Neto

Frontiers in Pharmacology Lausanne v. 6, art. 131, 2015

Lausanne 2015

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2726841 Estantes Deslizantes )(Acessar)

6
Novel potent (dihydro)benzofuranyl piperazines as human histamine receptor ligands functional characterization and modeling studies on H3 and H4 receptors
Novel potent (dihydro)benzofuranyl piperazines as human histamine receptor ligands functional characterization and modeling studies on H3 and H4 receptors
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Novel potent (dihydro)benzofuranyl piperazines as human histamine receptor ligands functional characterization and modeling studies on H3 and H4 receptors

Michelle F Corrêa André Luís Balico da Silva; Dóra J Kiss; Gustavo A. B Fernandes; Jhonatan Christian Maraschin; Lucas Tabajara Parreiras-e-Silva; Marina T Varela; Sarah Capelupe Simões; Michel Bouvier; György M Keserű; Claudio Miguel da Costa Neto; João Paulo S Fernandes

Bioorganic & Medicinal Chemistry Oxford v. 30, art. 115924, [10] p, 2021

Oxford 2021

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 3197489 Acervo Digital )(Acessar)

7
Ang-(1-7) is an endogenous β-arrestin-biased agonist of the AT1 receptor with protective action in cardiac hypertrophy
Ang-(1-7) is an endogenous β-arrestin-biased agonist of the AT1 receptor with protective action in cardiac hypertrophy
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Ang-(1-7) is an endogenous β-arrestin-biased agonist of the AT1 receptor with protective action in cardiac hypertrophy

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 Alberto Aguiar da Silva; Emiliana P Abrao; Eduardo Brandt de Oliveira; Michel Bouvier; Rita de Cássia Aleixo Tostes; Cláudio Miguel Costa Neto

Scientific Reports London v. 7, n.1, art. 11903, 2017

London 2017

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2916108 Estantes Deslizantes )(Acessar)

8
Functional selectivity profiling of the angiotensin II type 1 receptor using pathway-wide BRET signaling sensors
Functional selectivity profiling of the angiotensin II type 1 receptor using pathway-wide BRET signaling sensors
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Functional selectivity profiling of the angiotensin II type 1 receptor using pathway-wide BRET signaling sensors

Yoon Namkung Christian LeGouill; Sahil Kumar; Yubo Cao; Larissa B Teixeira; Viktoriya Lukasheva; Jenna Giubilaro; Sarah Capelupe Simões; Jean-Michel Longpré; Dominic Devost; Terence E Hébert; Graciela Piñeyro; Richard Leduc; Claudio Miguel da Costa Neto; Michel Bouvier; Stéphane A Laporte

Science Signaling Washington v. 11, n. 559,art. eaat 1631, 2018

Washington 2018

Acesso online. A biblioteca também possui exemplares impressos.

9
Functional New World monkey oxytocin forms elicit an altered signaling profile and promotes parental care in rats
Functional New World monkey oxytocin forms elicit an altered signaling profile and promotes parental care in rats
Material Type:
Artigo 		Adicionar ao Meu Espaço

Functional New World monkey oxytocin forms elicit an altered signaling profile and promotes parental care in rats

Lucas T. Parreiras e Silva Pedro Vargas Pinilla; Diego A Duarte; Dânae Longo; Grace Violeta Espinoza Pardo; Andrea Dulor Finkler; Vanessa Rodrigues Paixão Côrtes; Pâmela Paré; Diego Luiz Rovaris; Eduardo Brandt de Oliveira; Rafael Andrade Caceres; Gislene L Gonçalves; Michel Bouvier; Francisco M Salzano; Aldo B Lucion; Cláudio Miguel Costa Neto; Maria Cátira Bortolini

Proceedings of the National Academy of Sciences Washington v. 114, n. 34, p. 9044-9049, 2017

Washington 2017

Localização: FMRP - Fac. Medicina de Ribeirão Preto    (pcd 2921046 Estantes Deslizantes )(Acessar)

10
Arginine kinase overexpression improves Trypanosoma cruzi survival capability
Arginine kinase overexpression improves Trypanosoma cruzi survival capability
Material Type:
Artigo de Congresso 		Adicionar ao Meu Espaço

Arginine kinase overexpression improves Trypanosoma cruzi survival capability

Guillermo D. Alonso Soledad Ivaldi; Ariel Mariano Silber; Léon Bouvier; Maria Júlia Manso Alves; Héctor N Torres; Mirtha M Flawiá; Claudio A Pereira; Annual Meeting on Basic Research in Chagas Disease (30. 2003 Caxambu); Meeting of the Brazilian Society of Protozoology (19. 2003 Caxambu)

Revista do Instituto de Medicina Tropical de São Paulo, São Paulo, v. 45, supl. 13, res. BQ10, 2003.

São Paulo 2003

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Bouvier, L
  2. Alves, M
  3. Pereira, C
  4. Bouvier, M
  5. Costa-Neto, C

Neste Assunto:

  1. Trypanosoma Cruzi
  2. Bioquímica
  3. Doença De Chagas
  4. Receptores
  5. Transdução De Sinal Celular

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.