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Parte de monografia/livro
Structure-based drug design (2021)
Ferreira, Leonardo Luiz Gomes ; Andricopulo, Adriano Defini
Source: Burger's medicinal chemistry, drug discovery and development. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, MACROMOLÉCULA, MODELAGEM MOLECULAR
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ABNT
FERREIRA, Leonardo Luiz Gomes e ANDRICOPULO, Adriano Defini. Structure-based drug design. Burger's medicinal chemistry, drug discovery and development. Tradução . Hoboken: Wiley, 2021. p. 6032 . Disponível em: https://doi.org/10.1002/0471266949.bmc141.pub2. Acesso em: 17 nov. 2024.
APA
Ferreira, L. L. G., & Andricopulo, A. D. (2021). Structure-based drug design. In Burger's medicinal chemistry, drug discovery and development (p. 6032 ). Hoboken: Wiley. doi:10.1002/0471266949.bmc141.pub2
NLM
Ferreira LLG, Andricopulo AD. Structure-based drug design [Internet]. In: Burger's medicinal chemistry, drug discovery and development. Hoboken: Wiley; 2021. p. 6032 .[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/0471266949.bmc141.pub2
Vancouver
Ferreira LLG, Andricopulo AD. Structure-based drug design [Internet]. In: Burger's medicinal chemistry, drug discovery and development. Hoboken: Wiley; 2021. p. 6032 .[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/0471266949.bmc141.pub2
Trabalho de evento-resumo
Activity of fractions obtained from extract of Fusarium oxysporum isolated from Senna spectabilis against Staphylococcus epidermidis in biofilm and planktonic forms (2019)
Righetto, Gabriela Marinho; Selegato, D. M.; Gamboa, I. C.; Camargo, Ilana Lopes Baratella da Cunha
Source: Abstracts. Conference titles: ASM/ESCMID Conference on Drug Development to Meet the Challenge of Antimicrobial Resistance. Unidade: IFSC
Subjects: BIOFILMES, STAPHYLOCOCCUS, FUSARIUM
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ABNT
RIGHETTO, Gabriela Marinho et al. Activity of fractions obtained from extract of Fusarium oxysporum isolated from Senna spectabilis against Staphylococcus epidermidis in biofilm and planktonic forms. 2019, Anais.. Washington, DC: American Society for Microbiology - ASM, 2019. Disponível em: https://www.asm.org/ASM/media/Events-PDFs/2019ASMESCMID-Final-Abstracts.pdf. Acesso em: 17 nov. 2024.
APA
Righetto, G. M., Selegato, D. M., Gamboa, I. C., & Camargo, I. L. B. da C. (2019). Activity of fractions obtained from extract of Fusarium oxysporum isolated from Senna spectabilis against Staphylococcus epidermidis in biofilm and planktonic forms. In Abstracts. Washington, DC: American Society for Microbiology - ASM. Recuperado de https://www.asm.org/ASM/media/Events-PDFs/2019ASMESCMID-Final-Abstracts.pdf
NLM
Righetto GM, Selegato DM, Gamboa IC, Camargo ILB da C. Activity of fractions obtained from extract of Fusarium oxysporum isolated from Senna spectabilis against Staphylococcus epidermidis in biofilm and planktonic forms [Internet]. Abstracts. 2019 ;[citado 2024 nov. 17 ] Available from: https://www.asm.org/ASM/media/Events-PDFs/2019ASMESCMID-Final-Abstracts.pdf
Vancouver
Righetto GM, Selegato DM, Gamboa IC, Camargo ILB da C. Activity of fractions obtained from extract of Fusarium oxysporum isolated from Senna spectabilis against Staphylococcus epidermidis in biofilm and planktonic forms [Internet]. Abstracts. 2019 ;[citado 2024 nov. 17 ] Available from: https://www.asm.org/ASM/media/Events-PDFs/2019ASMESCMID-Final-Abstracts.pdf
Trabalho de evento-resumo
Novel brominated vinylic fatty acids effectively inhibit the leishmania topoisomerase IB enzyme mediated by halogen bond formation (2019)
Carballeira, Néstor M.; Alequín, Denisse; Lotti, Leilani M.; Matos, Victorio Jauregui; Ferreira, Leonardo Luiz Gomes ; Andricopulo, Adriano Defini ; Reguera, Rosa M.; Pérez-Pertejo, Yolanda; Balaña-Fouce, Rafael
Source: Abstracts. Conference titles: Annual Meeting of the American Society of Pharmacognosy - ASP. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, LEISHMANIA
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CARBALLEIRA, Néstor M. et al. Novel brominated vinylic fatty acids effectively inhibit the leishmania topoisomerase IB enzyme mediated by halogen bond formation. 2019, Anais.. Northbrook: American Society of Pharmacognosy - ASP, 2019. Disponível em: http://aspmeetings.pharmacognosy.us/wp-content/uploads/2019/07/ASP2019-Electronic-Program-and-Abstract-Book-Final.pdf. Acesso em: 17 nov. 2024.
APA
Carballeira, N. M., Alequín, D., Lotti, L. M., Matos, V. J., Ferreira, L. L. G., Andricopulo, A. D., et al. (2019). Novel brominated vinylic fatty acids effectively inhibit the leishmania topoisomerase IB enzyme mediated by halogen bond formation. In Abstracts. Northbrook: American Society of Pharmacognosy - ASP. Recuperado de http://aspmeetings.pharmacognosy.us/wp-content/uploads/2019/07/ASP2019-Electronic-Program-and-Abstract-Book-Final.pdf
NLM
Carballeira NM, Alequín D, Lotti LM, Matos VJ, Ferreira LLG, Andricopulo AD, Reguera RM, Pérez-Pertejo Y, Balaña-Fouce R. Novel brominated vinylic fatty acids effectively inhibit the leishmania topoisomerase IB enzyme mediated by halogen bond formation [Internet]. Abstracts. 2019 ;[citado 2024 nov. 17 ] Available from: http://aspmeetings.pharmacognosy.us/wp-content/uploads/2019/07/ASP2019-Electronic-Program-and-Abstract-Book-Final.pdf
Vancouver
Carballeira NM, Alequín D, Lotti LM, Matos VJ, Ferreira LLG, Andricopulo AD, Reguera RM, Pérez-Pertejo Y, Balaña-Fouce R. Novel brominated vinylic fatty acids effectively inhibit the leishmania topoisomerase IB enzyme mediated by halogen bond formation [Internet]. Abstracts. 2019 ;[citado 2024 nov. 17 ] Available from: http://aspmeetings.pharmacognosy.us/wp-content/uploads/2019/07/ASP2019-Electronic-Program-and-Abstract-Book-Final.pdf
Trabalho de evento-resumo
Orbitides: a quite unusual class of biologically active small peptides in some plant species from brazilian biodiversity (2017)
Pinto, Meri Emili F.; Ramalho, Suelem D.; Nascimento, Marlon de O.; Sanches, Paulo R. S.; Silveira, Edilberto R.; Krogh, Renata; Cilli, Eduardo M.; Andricopulo, Adriano Defini ; Lopes, Norberto Peporine; Bolzani, Vanderlan S.
Source: Proceedings. Conference titles: IUPAC World Chemistry Congress. Unidade: IFSC
Subjects: QUÍMICA MÉDICA, BIODIVERSIDADE
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ABNT
PINTO, Meri Emili F. et al. Orbitides: a quite unusual class of biologically active small peptides in some plant species from brazilian biodiversity. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry - IUPAC, 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 17 nov. 2024.
APA
Pinto, M. E. F., Ramalho, S. D., Nascimento, M. de O., Sanches, P. R. S., Silveira, E. R., Krogh, R., et al. (2017). Orbitides: a quite unusual class of biologically active small peptides in some plant species from brazilian biodiversity. In Proceedings. Durham: International Union of Pure and Applied Chemistry - IUPAC. Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Pinto MEF, Ramalho SD, Nascimento M de O, Sanches PRS, Silveira ER, Krogh R, Cilli EM, Andricopulo AD, Lopes NP, Bolzani VS. Orbitides: a quite unusual class of biologically active small peptides in some plant species from brazilian biodiversity [Internet]. Proceedings. 2017 ;[citado 2024 nov. 17 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Pinto MEF, Ramalho SD, Nascimento M de O, Sanches PRS, Silveira ER, Krogh R, Cilli EM, Andricopulo AD, Lopes NP, Bolzani VS. Orbitides: a quite unusual class of biologically active small peptides in some plant species from brazilian biodiversity [Internet]. Proceedings. 2017 ;[citado 2024 nov. 17 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
Multi parametric optimization of a series of potent cruzain inhibitors as drug candidates for chagas disease (2017)
Pauli, Ivani; R. Junior, Celso; Slafer, Brian; Dessoy, Marco A.; Souza, Mariana L.; Ferreira, Rafaela S.; Magalhães, Luma G.; Krogh, Renata; Dias, Luiz C.; Andricopulo, Adriano Defini
Source: Proceedings. Conference titles: IUPAC World Chemistry Congress. Unidade: IFSC
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, MODELAGEM MOLECULAR
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PAULI, Ivani et al. Multi parametric optimization of a series of potent cruzain inhibitors as drug candidates for chagas disease. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry - IUPAC, 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 17 nov. 2024.
APA
Pauli, I., R. Junior, C., Slafer, B., Dessoy, M. A., Souza, M. L., Ferreira, R. S., et al. (2017). Multi parametric optimization of a series of potent cruzain inhibitors as drug candidates for chagas disease. In Proceedings. Durham: International Union of Pure and Applied Chemistry - IUPAC. Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Pauli I, R. Junior C, Slafer B, Dessoy MA, Souza ML, Ferreira RS, Magalhães LG, Krogh R, Dias LC, Andricopulo AD. Multi parametric optimization of a series of potent cruzain inhibitors as drug candidates for chagas disease [Internet]. Proceedings. 2017 ;[citado 2024 nov. 17 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Pauli I, R. Junior C, Slafer B, Dessoy MA, Souza ML, Ferreira RS, Magalhães LG, Krogh R, Dias LC, Andricopulo AD. Multi parametric optimization of a series of potent cruzain inhibitors as drug candidates for chagas disease [Internet]. Proceedings. 2017 ;[citado 2024 nov. 17 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
Identification of carbamoylimidazoles as novel cruzain inhibitors with in vitro and in vivo trypanocidal activity (2017)
Souza, Mariana L.; Ferreira, Rafaela S.; Magalhães, Luma Godoy; Rezende Jr, Celso; Slafer, Brian; Chavez, Rocio; Krogh, Renata; Cruz, Fábio C.; Oliva, Glaucius ; Dias, Luiz C.; Andricopulo, Adriano Defini
Source: Proceedings. Conference titles: IUPAC World Chemistry Congress. Unidade: IFSC
Subjects: DOENÇA DE CHAGAS, TRYPANOSOMA CRUZI, MODELAGEM MOLECULAR
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ABNT
SOUZA, Mariana L. et al. Identification of carbamoylimidazoles as novel cruzain inhibitors with in vitro and in vivo trypanocidal activity. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry - IUPAC, 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 17 nov. 2024.
APA
Souza, M. L., Ferreira, R. S., Magalhães, L. G., Rezende Jr, C., Slafer, B., Chavez, R., et al. (2017). Identification of carbamoylimidazoles as novel cruzain inhibitors with in vitro and in vivo trypanocidal activity. In Proceedings. Durham: International Union of Pure and Applied Chemistry - IUPAC. Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Souza ML, Ferreira RS, Magalhães LG, Rezende Jr C, Slafer B, Chavez R, Krogh R, Cruz FC, Oliva G, Dias LC, Andricopulo AD. Identification of carbamoylimidazoles as novel cruzain inhibitors with in vitro and in vivo trypanocidal activity [Internet]. Proceedings. 2017 ;[citado 2024 nov. 17 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Souza ML, Ferreira RS, Magalhães LG, Rezende Jr C, Slafer B, Chavez R, Krogh R, Cruz FC, Oliva G, Dias LC, Andricopulo AD. Identification of carbamoylimidazoles as novel cruzain inhibitors with in vitro and in vivo trypanocidal activity [Internet]. Proceedings. 2017 ;[citado 2024 nov. 17 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Artigo de periodico
Formation of a ternary complex for selenocysteine biosynthesis in bacteria (2015)
Silva, Ivan R.; Serrão, Vitor H. B.; Manzine, Lívia Regina; Faim, Lívia M.; Silva, Marco T. A.; Makki, Raphaela; Saidemberg, Daniel Menezes; Cornélio, Marinônio L.; Palma, Mário S.; Thiemann, Otávio Henrique
Source: Journal of Biological Chemistry. Unidade: IFSC
Subjects: SELÊNIO, RNA DE TRANSFERÊNCIA, BACTÉRIAS
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ABNT
SILVA, Ivan R. et al. Formation of a ternary complex for selenocysteine biosynthesis in bacteria. Journal of Biological Chemistry, v. 290, n. 49, p. 29178-29188 + Supplemental data, 2015Tradução . . Disponível em: https://doi.org/10.1074/jbc.M114.613406. Acesso em: 17 nov. 2024.
APA
Silva, I. R., Serrão, V. H. B., Manzine, L. R., Faim, L. M., Silva, M. T. A., Makki, R., et al. (2015). Formation of a ternary complex for selenocysteine biosynthesis in bacteria. Journal of Biological Chemistry, 290( 49), 29178-29188 + Supplemental data. doi:10.1074/jbc.M114.613406
NLM
Silva IR, Serrão VHB, Manzine LR, Faim LM, Silva MTA, Makki R, Saidemberg DM, Cornélio ML, Palma MS, Thiemann OH. Formation of a ternary complex for selenocysteine biosynthesis in bacteria [Internet]. Journal of Biological Chemistry. 2015 ; 290( 49): 29178-29188 + Supplemental data.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1074/jbc.M114.613406
Vancouver
Silva IR, Serrão VHB, Manzine LR, Faim LM, Silva MTA, Makki R, Saidemberg DM, Cornélio ML, Palma MS, Thiemann OH. Formation of a ternary complex for selenocysteine biosynthesis in bacteria [Internet]. Journal of Biological Chemistry. 2015 ; 290( 49): 29178-29188 + Supplemental data.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1074/jbc.M114.613406
Artigo de periodico
Crystal structure of a Schistosoma mansoni septin reveals the phenomenon of strand slippage in septins dependent on the nature of the bound nucleotide (2014)
Zeraik, Ana E.; Pereira, Humberto d'Muniz; Santos, Yuri V.; Brandão Neto, José; Spoerner, Michael; Santos, Maiara S.; Colnago, Luiz A.; Garratt, Richard Charles ; Araújo, Ana Paula Ulian de ; De Marco, Ricardo
Source: Journal of Biological Chemistry. Unidade: IFSC
Subjects: ENZIMAS (ESTUDO), SCHISTOSOMA MANSONI
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ABNT
ZERAIK, Ana E. et al. Crystal structure of a Schistosoma mansoni septin reveals the phenomenon of strand slippage in septins dependent on the nature of the bound nucleotide. Journal of Biological Chemistry, v. 289, n. 11, p. 7799-7811, 2014Tradução . . Disponível em: https://doi.org/10.1074/jbc.M113.525352. Acesso em: 17 nov. 2024.
APA
Zeraik, A. E., Pereira, H. d'M., Santos, Y. V., Brandão Neto, J., Spoerner, M., Santos, M. S., et al. (2014). Crystal structure of a Schistosoma mansoni septin reveals the phenomenon of strand slippage in septins dependent on the nature of the bound nucleotide. Journal of Biological Chemistry, 289( 11), 7799-7811. doi:10.1074/jbc.M113.525352
NLM
Zeraik AE, Pereira H d'M, Santos YV, Brandão Neto J, Spoerner M, Santos MS, Colnago LA, Garratt RC, Araújo APU de, De Marco R. Crystal structure of a Schistosoma mansoni septin reveals the phenomenon of strand slippage in septins dependent on the nature of the bound nucleotide [Internet]. Journal of Biological Chemistry. 2014 ; 289( 11): 7799-7811.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1074/jbc.M113.525352
Vancouver
Zeraik AE, Pereira H d'M, Santos YV, Brandão Neto J, Spoerner M, Santos MS, Colnago LA, Garratt RC, Araújo APU de, De Marco R. Crystal structure of a Schistosoma mansoni septin reveals the phenomenon of strand slippage in septins dependent on the nature of the bound nucleotide [Internet]. Journal of Biological Chemistry. 2014 ; 289( 11): 7799-7811.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1074/jbc.M113.525352
Trabalho de evento-resumo
Virtual screening strategies for the discovery of new inhibitors of cruzain from Trypanosoma cruzi (2014)
Souza, Mariana Laureano de; Ferreira, Rafaela S.; Krogh, Renata; Oliva, Glaucius ; Dias, Luiz C.; Andricopulo, Adriano Defini
Source: Abstracts. Conference titles: ACS National Meeting and Exposition. Unidade: IFSC
Subjects: TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS, PLANEJAMENTO DE FÁRMACOS
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ABNT
SOUZA, Mariana Laureano de et al. Virtual screening strategies for the discovery of new inhibitors of cruzain from Trypanosoma cruzi. 2014, Anais.. Washington, DC: American Chemical Society - ACS, 2014. . Acesso em: 17 nov. 2024.
APA
Souza, M. L. de, Ferreira, R. S., Krogh, R., Oliva, G., Dias, L. C., & Andricopulo, A. D. (2014). Virtual screening strategies for the discovery of new inhibitors of cruzain from Trypanosoma cruzi. In Abstracts. Washington, DC: American Chemical Society - ACS.
NLM
Souza ML de, Ferreira RS, Krogh R, Oliva G, Dias LC, Andricopulo AD. Virtual screening strategies for the discovery of new inhibitors of cruzain from Trypanosoma cruzi. Abstracts. 2014 ;[citado 2024 nov. 17 ]
Vancouver
Souza ML de, Ferreira RS, Krogh R, Oliva G, Dias LC, Andricopulo AD. Virtual screening strategies for the discovery of new inhibitors of cruzain from Trypanosoma cruzi. Abstracts. 2014 ;[citado 2024 nov. 17 ]
Artigo de periodico
Synthesis, biological evaluation, and structure-activity relationships of potent noncovalent and nonpeptidic cruzain inhibitors as anti-Trypanosoma cruzi agents (2014)
Ferreira, Rafaela S.; Dessoy, Marco A.; Pauli, Ivani; Souza, Mariana L.; Krogh, Renata; Sales, Ana I. L.; Oliva, Glaucius ; Dias, Luiz C.; Andricopulo, Adriano Defini
Source: Journal of Medicinal Chemistry. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS (TRATAMENTO)
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ABNT
FERREIRA, Rafaela S. et al. Synthesis, biological evaluation, and structure-activity relationships of potent noncovalent and nonpeptidic cruzain inhibitors as anti-Trypanosoma cruzi agents. Journal of Medicinal Chemistry, v. 57, n. 6, p. 2380-2392, 2014Tradução . . Disponível em: https://doi.org/10.1021/jm401709b. Acesso em: 17 nov. 2024.
APA
Ferreira, R. S., Dessoy, M. A., Pauli, I., Souza, M. L., Krogh, R., Sales, A. I. L., et al. (2014). Synthesis, biological evaluation, and structure-activity relationships of potent noncovalent and nonpeptidic cruzain inhibitors as anti-Trypanosoma cruzi agents. Journal of Medicinal Chemistry, 57( 6), 2380-2392. doi:10.1021/jm401709b
NLM
Ferreira RS, Dessoy MA, Pauli I, Souza ML, Krogh R, Sales AIL, Oliva G, Dias LC, Andricopulo AD. Synthesis, biological evaluation, and structure-activity relationships of potent noncovalent and nonpeptidic cruzain inhibitors as anti-Trypanosoma cruzi agents [Internet]. Journal of Medicinal Chemistry. 2014 ; 57( 6): 2380-2392.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1021/jm401709b
Vancouver
Ferreira RS, Dessoy MA, Pauli I, Souza ML, Krogh R, Sales AIL, Oliva G, Dias LC, Andricopulo AD. Synthesis, biological evaluation, and structure-activity relationships of potent noncovalent and nonpeptidic cruzain inhibitors as anti-Trypanosoma cruzi agents [Internet]. Journal of Medicinal Chemistry. 2014 ; 57( 6): 2380-2392.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1021/jm401709b
Artigo de periodico
A ribokinase family conserved monovalent cation binding site enhances the MgATP-induced inhibition in E. coli phosphofructokinase-2 (2013)
Baez, Mauricio; Cabrera, Ricardo; Pereira, Humberto d'Muniz; Blanco, Alejandro; Villalobos, Pablo; Ramírez-Sarmiento, César A.; Caniuguir, Andrés; Guixé, Victoria; Garratt, Richard Charles ; Babul, Jorge
Source: Biophysical Journal. Unidade: IFSC
Subjects: ENZIMAS, ESCHERICHIA COLI, PROTEÍNAS
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ABNT
BAEZ, Mauricio et al. A ribokinase family conserved monovalent cation binding site enhances the MgATP-induced inhibition in E. coli phosphofructokinase-2. Biophysical Journal, v. 105, n. 1, p. 185-193, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.bpj.2013.05.028. Acesso em: 17 nov. 2024.
APA
Baez, M., Cabrera, R., Pereira, H. d'M., Blanco, A., Villalobos, P., Ramírez-Sarmiento, C. A., et al. (2013). A ribokinase family conserved monovalent cation binding site enhances the MgATP-induced inhibition in E. coli phosphofructokinase-2. Biophysical Journal, 105( 1), 185-193. doi:10.1016/j.bpj.2013.05.028
NLM
Baez M, Cabrera R, Pereira H d'M, Blanco A, Villalobos P, Ramírez-Sarmiento CA, Caniuguir A, Guixé V, Garratt RC, Babul J. A ribokinase family conserved monovalent cation binding site enhances the MgATP-induced inhibition in E. coli phosphofructokinase-2 [Internet]. Biophysical Journal. 2013 ; 105( 1): 185-193.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.bpj.2013.05.028
Vancouver
Baez M, Cabrera R, Pereira H d'M, Blanco A, Villalobos P, Ramírez-Sarmiento CA, Caniuguir A, Guixé V, Garratt RC, Babul J. A ribokinase family conserved monovalent cation binding site enhances the MgATP-induced inhibition in E. coli phosphofructokinase-2 [Internet]. Biophysical Journal. 2013 ; 105( 1): 185-193.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.bpj.2013.05.028
Artigo de periodico
Immunization with purine salvation pathway recombinant enzymes induces the production of anti- Schistosoma mansoni immunoglobulines (2013)
Neris, Débora Meira; Pereira, Humberto d'Muniz; Souza, Laís Cristina de; Correia, Ricardo de Oliveira; Rodolpho, Joice Margareth de Almeida; Oliveira, Sandra Regina Pereira de; Dejani, Naiara Naiana; Adachi, Felipe de Pontes; Rodrigues, Vanderlei; Garratt, Richard Charles ; Anibal, Fernanda de Freitas
Source: International Trends in Immunity. Unidades: IFSC, FMRP
Subjects: SCHISTOSOMA MANSONI, IMUNOLOGIA, ENZIMAS
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ABNT
NERIS, Débora Meira et al. Immunization with purine salvation pathway recombinant enzymes induces the production of anti- Schistosoma mansoni immunoglobulines. International Trends in Immunity, v. 1, n. 3, p. 49-56, 2013Tradução . . Disponível em: http://researchpub.org/journal/iti/number/vol1-no3/vol1-no3-6.pdf. Acesso em: 17 nov. 2024.
APA
Neris, D. M., Pereira, H. d'M., Souza, L. C. de, Correia, R. de O., Rodolpho, J. M. de A., Oliveira, S. R. P. de, et al. (2013). Immunization with purine salvation pathway recombinant enzymes induces the production of anti- Schistosoma mansoni immunoglobulines. International Trends in Immunity, 1( 3), 49-56. Recuperado de http://researchpub.org/journal/iti/number/vol1-no3/vol1-no3-6.pdf
NLM
Neris DM, Pereira H d'M, Souza LC de, Correia R de O, Rodolpho JM de A, Oliveira SRP de, Dejani NN, Adachi F de P, Rodrigues V, Garratt RC, Anibal F de F. Immunization with purine salvation pathway recombinant enzymes induces the production of anti- Schistosoma mansoni immunoglobulines [Internet]. International Trends in Immunity. 2013 ; 1( 3): 49-56.[citado 2024 nov. 17 ] Available from: http://researchpub.org/journal/iti/number/vol1-no3/vol1-no3-6.pdf
Vancouver
Neris DM, Pereira H d'M, Souza LC de, Correia R de O, Rodolpho JM de A, Oliveira SRP de, Dejani NN, Adachi F de P, Rodrigues V, Garratt RC, Anibal F de F. Immunization with purine salvation pathway recombinant enzymes induces the production of anti- Schistosoma mansoni immunoglobulines [Internet]. International Trends in Immunity. 2013 ; 1( 3): 49-56.[citado 2024 nov. 17 ] Available from: http://researchpub.org/journal/iti/number/vol1-no3/vol1-no3-6.pdf
Trabalho de evento-resumo periodico
On the structural and biochemical properties of the human septins: SEPT3 (2013)
Macedo, Joci N. A.; Valadares, Napoleão F.; Marques, Ivo A.; Ferreira, Frederico M.; Damalio, Julio C. P.; Pereira, Humberto d'Muniz; Garratt, Richard Charles ; Araújo, Ana Paula Ulian de
Source: Biophysical Journal. Conference titles: Annual Meeting of the Biophysical Society. Unidade: IFSC
Subjects: PROTEÍNAS (HUMANO;ESTUDO), PROTEÍNAS RECOMBINANTES
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ABNT
MACEDO, Joci N. A. et al. On the structural and biochemical properties of the human septins: SEPT3. Biophysical Journal. Saint Louis: Cell Press. Disponível em: https://doi.org/10.1016/j.bpj.2012.11.3144. Acesso em: 17 nov. 2024. , 2013
APA
Macedo, J. N. A., Valadares, N. F., Marques, I. A., Ferreira, F. M., Damalio, J. C. P., Pereira, H. d'M., et al. (2013). On the structural and biochemical properties of the human septins: SEPT3. Biophysical Journal. Saint Louis: Cell Press. doi:10.1016/j.bpj.2012.11.3144
NLM
Macedo JNA, Valadares NF, Marques IA, Ferreira FM, Damalio JCP, Pereira H d'M, Garratt RC, Araújo APU de. On the structural and biochemical properties of the human septins: SEPT3 [Internet]. Biophysical Journal. 2013 ; 104( Ja 2013): 567a.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.bpj.2012.11.3144
Vancouver
Macedo JNA, Valadares NF, Marques IA, Ferreira FM, Damalio JCP, Pereira H d'M, Garratt RC, Araújo APU de. On the structural and biochemical properties of the human septins: SEPT3 [Internet]. Biophysical Journal. 2013 ; 104( Ja 2013): 567a.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1016/j.bpj.2012.11.3144
Trabalho de evento-resumo
Application of bioisosterism approach in the design, synthesis, and biological evaluation of nitrofurazone derivatives as antichagasic candidates (2013)
Trossini, Gustavo Henrique Goulart ; Arribas, Marco; Nishikawa, Michele; Gonçalves, José Eduardo; Oliveira, Tiago Franco de; Loureiro, Ana Paula de Melo ; Storpirtis, Silvia ; Krogh, Renata; Andricopulo, Adriano Defini ; Ferreira, Elizabeth Igne
Source: Abstracts. Conference titles: Spring National Meeting and Exposition. Unidades: FCF, IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS (ESTUDO;TRATAMENTO)
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ABNT
TROSSINI, Gustavo Henrique Goulart et al. Application of bioisosterism approach in the design, synthesis, and biological evaluation of nitrofurazone derivatives as antichagasic candidates. 2013, Anais.. Washington, DC: American Chemical Society - ACS, 2013. . Acesso em: 17 nov. 2024.
APA
Trossini, G. H. G., Arribas, M., Nishikawa, M., Gonçalves, J. E., Oliveira, T. F. de, Loureiro, A. P. de M., et al. (2013). Application of bioisosterism approach in the design, synthesis, and biological evaluation of nitrofurazone derivatives as antichagasic candidates. In Abstracts. Washington, DC: American Chemical Society - ACS.
NLM
Trossini GHG, Arribas M, Nishikawa M, Gonçalves JE, Oliveira TF de, Loureiro AP de M, Storpirtis S, Krogh R, Andricopulo AD, Ferreira EI. Application of bioisosterism approach in the design, synthesis, and biological evaluation of nitrofurazone derivatives as antichagasic candidates. Abstracts. 2013 ;[citado 2024 nov. 17 ]
Vancouver
Trossini GHG, Arribas M, Nishikawa M, Gonçalves JE, Oliveira TF de, Loureiro AP de M, Storpirtis S, Krogh R, Andricopulo AD, Ferreira EI. Application of bioisosterism approach in the design, synthesis, and biological evaluation of nitrofurazone derivatives as antichagasic candidates. Abstracts. 2013 ;[citado 2024 nov. 17 ]
Trabalho de evento-resumo
SAR studies on a series of reversible competitive inhibitors of cruzain from Trypanosoma cruzi (2013)
Pauli, Ivani; Souza, Mariana L. de Souza; Ferreira, Rafaela S.; Krogh, Renata; Duarte, Simone Michelan; Dessoy, Marco Aurélio; Dias, Luiz Carlos; Andricopulo, Adriano Defini
Source: Abstracts. Conference titles: Spring National Meeting and Exposition. Unidade: IFSC
Subjects: PLANEJAMENTO DE FÁRMACOS, TRYPANOSOMA CRUZI, DOENÇA DE CHAGAS (ESTUDO;TRATAMENTO), ENZIMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAULI, Ivani et al. SAR studies on a series of reversible competitive inhibitors of cruzain from Trypanosoma cruzi. 2013, Anais.. Washington, DC: American Chemical Society - ACS, 2013. . Acesso em: 17 nov. 2024.
APA
Pauli, I., Souza, M. L. de S., Ferreira, R. S., Krogh, R., Duarte, S. M., Dessoy, M. A., et al. (2013). SAR studies on a series of reversible competitive inhibitors of cruzain from Trypanosoma cruzi. In Abstracts. Washington, DC: American Chemical Society - ACS.
NLM
Pauli I, Souza ML de S, Ferreira RS, Krogh R, Duarte SM, Dessoy MA, Dias LC, Andricopulo AD. SAR studies on a series of reversible competitive inhibitors of cruzain from Trypanosoma cruzi. Abstracts. 2013 ;[citado 2024 nov. 17 ]
Vancouver
Pauli I, Souza ML de S, Ferreira RS, Krogh R, Duarte SM, Dessoy MA, Dias LC, Andricopulo AD. SAR studies on a series of reversible competitive inhibitors of cruzain from Trypanosoma cruzi. Abstracts. 2013 ;[citado 2024 nov. 17 ]
Trabalho de evento-resumo
Structural and chemical basis for the antimetastatic properties of a series of migrastatin analogs (2012)
Santos, Ricardo N.; Duarte, Simone Michelan; Guido, Rafael Victorio Carvalho ; Dias, Lucas C.; Oliva, Glaucius ; Andricopulo, Adriano Defini
Source: Abstracts. Conference titles: Spring National Meeting and Exposition. Unidade: IFSC
Subjects: FÁRMACOS (ESTUDO;DESENVOLVIMENTO), NEOPLASIAS (ESTUDO;TRATAMENTO), METÁSTASE NEOPLÁSICA (CONTROLE)
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ABNT
SANTOS, Ricardo N. et al. Structural and chemical basis for the antimetastatic properties of a series of migrastatin analogs. 2012, Anais.. Washington, DC: American Chemical Society - ACS, 2012. . Acesso em: 17 nov. 2024.
APA
Santos, R. N., Duarte, S. M., Guido, R. V. C., Dias, L. C., Oliva, G., & Andricopulo, A. D. (2012). Structural and chemical basis for the antimetastatic properties of a series of migrastatin analogs. In Abstracts. Washington, DC: American Chemical Society - ACS.
NLM
Santos RN, Duarte SM, Guido RVC, Dias LC, Oliva G, Andricopulo AD. Structural and chemical basis for the antimetastatic properties of a series of migrastatin analogs. Abstracts. 2012 ;[citado 2024 nov. 17 ]
Vancouver
Santos RN, Duarte SM, Guido RVC, Dias LC, Oliva G, Andricopulo AD. Structural and chemical basis for the antimetastatic properties of a series of migrastatin analogs. Abstracts. 2012 ;[citado 2024 nov. 17 ]
Artigo de periodico
Mitochondrial localization and structure-based phosphate activation mechanism of glutaminase C with implications for cancer metabolism (2012)
Cassago, Alexandre; Ferreira, Amanda P. S.; Ferreira, Igor M.; Fornezari, Camila; Gomes, Emerson R. M.; Greene, Kai Su; Pereira, Humberto d'Muniz; Garratt, Richard Charles ; Dias, Sandra M. G.; Ambrosio, Andre Luis Berteli
Source: Proceedings of the National Academy of Sciences - PNAS. Unidade: IFSC
Subjects: METABOLISMO DE PROTEÍNA, GLUTAMINA, ENZIMAS, RNA MENSAGEIRO, NEOPLASIAS (METABOLISMO)
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ABNT
CASSAGO, Alexandre et al. Mitochondrial localization and structure-based phosphate activation mechanism of glutaminase C with implications for cancer metabolism. Proceedings of the National Academy of Sciences - PNAS, v. 109, n. Ja 2012, p. 1092-1097, 2012Tradução . . Disponível em: https://doi.org/10.1073/pnas.1112495109. Acesso em: 17 nov. 2024.
APA
Cassago, A., Ferreira, A. P. S., Ferreira, I. M., Fornezari, C., Gomes, E. R. M., Greene, K. S., et al. (2012). Mitochondrial localization and structure-based phosphate activation mechanism of glutaminase C with implications for cancer metabolism. Proceedings of the National Academy of Sciences - PNAS, 109( Ja 2012), 1092-1097. doi:10.1073/pnas.1112495109
NLM
Cassago A, Ferreira APS, Ferreira IM, Fornezari C, Gomes ERM, Greene KS, Pereira H d'M, Garratt RC, Dias SMG, Ambrosio ALB. Mitochondrial localization and structure-based phosphate activation mechanism of glutaminase C with implications for cancer metabolism [Internet]. Proceedings of the National Academy of Sciences - PNAS. 2012 ; 109( Ja 2012): 1092-1097.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1073/pnas.1112495109
Vancouver
Cassago A, Ferreira APS, Ferreira IM, Fornezari C, Gomes ERM, Greene KS, Pereira H d'M, Garratt RC, Dias SMG, Ambrosio ALB. Mitochondrial localization and structure-based phosphate activation mechanism of glutaminase C with implications for cancer metabolism [Internet]. Proceedings of the National Academy of Sciences - PNAS. 2012 ; 109( Ja 2012): 1092-1097.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1073/pnas.1112495109
Artigo de periodico
Dissecting the structure, thermodynamic stability, and aggregation properties of the A25T transthyretin (A25T-TTR) variant involved in leptomeningeal amyloidosis: identifying protein partners that co-aggregate during A25T-TTR fibrillogenesis in cerebrospinal fluid (2011)
Azevedo, Estefania P. C.; Pereira, Humberto D'Muniz; Garratt, Richard Charles ; Kelly, Jeffery W.; Foguel, Debora; Palhano, Fernando L.
Source: Biochemistry. Unidade: IFSC
Subjects: PROTEÍNAS (ESTUDO), CRISTALOGRAFIA ESTRUTURAL, MODELOS (ESTRUTURA)
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ABNT
AZEVEDO, Estefania P. C. et al. Dissecting the structure, thermodynamic stability, and aggregation properties of the A25T transthyretin (A25T-TTR) variant involved in leptomeningeal amyloidosis: identifying protein partners that co-aggregate during A25T-TTR fibrillogenesis in cerebrospinal fluid. Biochemistry, v. 50, n. 51, p. 11070-11083, 2011Tradução . . Disponível em: https://doi.org/10.1021/bi201365r. Acesso em: 17 nov. 2024.
APA
Azevedo, E. P. C., Pereira, H. D. 'M., Garratt, R. C., Kelly, J. W., Foguel, D., & Palhano, F. L. (2011). Dissecting the structure, thermodynamic stability, and aggregation properties of the A25T transthyretin (A25T-TTR) variant involved in leptomeningeal amyloidosis: identifying protein partners that co-aggregate during A25T-TTR fibrillogenesis in cerebrospinal fluid. Biochemistry, 50( 51), 11070-11083. doi:10.1021/bi201365r
NLM
Azevedo EPC, Pereira HD'M, Garratt RC, Kelly JW, Foguel D, Palhano FL. Dissecting the structure, thermodynamic stability, and aggregation properties of the A25T transthyretin (A25T-TTR) variant involved in leptomeningeal amyloidosis: identifying protein partners that co-aggregate during A25T-TTR fibrillogenesis in cerebrospinal fluid [Internet]. Biochemistry. 2011 ; 50( 51): 11070-11083.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1021/bi201365r
Vancouver
Azevedo EPC, Pereira HD'M, Garratt RC, Kelly JW, Foguel D, Palhano FL. Dissecting the structure, thermodynamic stability, and aggregation properties of the A25T transthyretin (A25T-TTR) variant involved in leptomeningeal amyloidosis: identifying protein partners that co-aggregate during A25T-TTR fibrillogenesis in cerebrospinal fluid [Internet]. Biochemistry. 2011 ; 50( 51): 11070-11083.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1021/bi201365r
Artigo de periodico
Purine nucleoside phosphorylase from Schistosoma mansoni in complex with ribose-1-phosphate (2011)
Pereira, Humberto D'Muniz; Oliva, Glaucius ; Garratt, Richard Charles
Source: Journal of Synchrotron Radiation. Unidade: IFSC
Subjects: DOENÇAS PARASITÁRIAS (ESTUDO;TRATAMENTO), FÁRMACOS (DESENVOLVIMENTO), SCHISTOSOMA MANSONI, ENZIMAS, LIGANTES
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ABNT
PEREIRA, Humberto D'Muniz e OLIVA, Glaucius e GARRATT, Richard Charles. Purine nucleoside phosphorylase from Schistosoma mansoni in complex with ribose-1-phosphate. Journal of Synchrotron Radiation, v. 18, n. Ja 2011, p. 62-65, 2011Tradução . . Disponível em: https://doi.org/10.1107/S0909049510027718. Acesso em: 17 nov. 2024.
APA
Pereira, H. D. 'M., Oliva, G., & Garratt, R. C. (2011). Purine nucleoside phosphorylase from Schistosoma mansoni in complex with ribose-1-phosphate. Journal of Synchrotron Radiation, 18( Ja 2011), 62-65. doi:10.1107/S0909049510027718
NLM
Pereira HD'M, Oliva G, Garratt RC. Purine nucleoside phosphorylase from Schistosoma mansoni in complex with ribose-1-phosphate [Internet]. Journal of Synchrotron Radiation. 2011 ; 18( Ja 2011): 62-65.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1107/S0909049510027718
Vancouver
Pereira HD'M, Oliva G, Garratt RC. Purine nucleoside phosphorylase from Schistosoma mansoni in complex with ribose-1-phosphate [Internet]. Journal of Synchrotron Radiation. 2011 ; 18( Ja 2011): 62-65.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1107/S0909049510027718
Artigo de periodico
The crystal complex of phosphofructokinase-2 of Escherichia coli with fructose-6-phosphate: kinetic and structural analysis of the allosteric ATP inhibition (2011)
Cabrera, Ricardo; Baez, Mauricio; Pereira, Humberto D'Muniz; Caniuguir, Andrés; Garratt, Richard Charles ; Babul, Jorge
Source: Journal of Biological Chemistry. Unidade: IFSC
Subjects: ESCHERICHIA COLI, ENZIMAS, INIBIDORES DE ENZIMAS, CRISTALOGRAFIA ESTRUTURAL
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ABNT
CABRERA, Ricardo et al. The crystal complex of phosphofructokinase-2 of Escherichia coli with fructose-6-phosphate: kinetic and structural analysis of the allosteric ATP inhibition. Journal of Biological Chemistry, v. 286, n. 7, p. 5774-5783, 2011Tradução . . Disponível em: https://doi.org/10.1074/jbc.M110.163162. Acesso em: 17 nov. 2024.
APA
Cabrera, R., Baez, M., Pereira, H. D. 'M., Caniuguir, A., Garratt, R. C., & Babul, J. (2011). The crystal complex of phosphofructokinase-2 of Escherichia coli with fructose-6-phosphate: kinetic and structural analysis of the allosteric ATP inhibition. Journal of Biological Chemistry, 286( 7), 5774-5783. doi:10.1074/jbc.M110.163162
NLM
Cabrera R, Baez M, Pereira HD'M, Caniuguir A, Garratt RC, Babul J. The crystal complex of phosphofructokinase-2 of Escherichia coli with fructose-6-phosphate: kinetic and structural analysis of the allosteric ATP inhibition [Internet]. Journal of Biological Chemistry. 2011 ; 286( 7): 5774-5783.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1074/jbc.M110.163162
Vancouver
Cabrera R, Baez M, Pereira HD'M, Caniuguir A, Garratt RC, Babul J. The crystal complex of phosphofructokinase-2 of Escherichia coli with fructose-6-phosphate: kinetic and structural analysis of the allosteric ATP inhibition [Internet]. Journal of Biological Chemistry. 2011 ; 286( 7): 5774-5783.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1074/jbc.M110.163162

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