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Artigo de periodico
Integration of biophysical and biological approaches to validate fragment-like compounds targeting l,d-transpeptidases from Mycobacterium tuberculosis (2024)
Zúñiga, Gerardo Andrés Libreros ; Pavão, Danilo Pavão e ; Barroso, Vinícius de Morais ; Mesquita, Nathalya Cristina de Moraes Roso; Braga, Saulo Fehelberg Pinto; Oliva, Glaucius ; Ferreira, Rafaela Salgado ; Ishida, Kelly ; Dias, Marcio Vinicius Bertacine
Source: Bioorganic Chemistry. Unidades: IFSC, ICB
Subjects: QUÍMICA MÉDICA, TUBERCULOSE, PLANEJAMENTO DE FÁRMACOS, MYCOBACTERIUM TUBERCULOSIS
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ZÚÑIGA, Gerardo Andrés Libreros et al. Integration of biophysical and biological approaches to validate fragment-like compounds targeting l,d-transpeptidases from Mycobacterium tuberculosis. Bioorganic Chemistry, v. 142, n. Ja 2024, p. 106960-1-106960-11, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2023.106960. Acesso em: 27 abr. 2024.
APA
Zúñiga, G. A. L., Pavão, D. P. e, Barroso, V. de M., Mesquita, N. C. de M. R., Braga, S. F. P., Oliva, G., et al. (2024). Integration of biophysical and biological approaches to validate fragment-like compounds targeting l,d-transpeptidases from Mycobacterium tuberculosis. Bioorganic Chemistry, 142( Ja 2024), 106960-1-106960-11. doi:10.1016/j.bioorg.2023.106960
NLM
Zúñiga GAL, Pavão DP e, Barroso V de M, Mesquita NC de MR, Braga SFP, Oliva G, Ferreira RS, Ishida K, Dias MVB. Integration of biophysical and biological approaches to validate fragment-like compounds targeting l,d-transpeptidases from Mycobacterium tuberculosis [Internet]. Bioorganic Chemistry. 2024 ; 142( Ja 2024): 106960-1-106960-11.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.bioorg.2023.106960
Vancouver
Zúñiga GAL, Pavão DP e, Barroso V de M, Mesquita NC de MR, Braga SFP, Oliva G, Ferreira RS, Ishida K, Dias MVB. Integration of biophysical and biological approaches to validate fragment-like compounds targeting l,d-transpeptidases from Mycobacterium tuberculosis [Internet]. Bioorganic Chemistry. 2024 ; 142( Ja 2024): 106960-1-106960-11.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.bioorg.2023.106960
Trabalho de evento-resumo
Discovery of Plasmodium falciparum inhibitors as lead candidates for malaria (2023)
Guido, Rafael Victorio Carvalho ; Oliveira, Juliana Roberta Torini de Souza; Souza, Guilherme Eduardo de ; Zanini, Camila Lima; Paim, Juliana Calit ; Bargieri, Daniel Youssef ; Oliva, Glaucius ; Aguiar, Anna Caroline Campos ; Barbosa, Camila de Souza ; Ahmad, Anees ; Burtoloso, Antonio Carlos Bender ; Maluf, Sarah El Chamy; Moura, Igor Mota Rodrigues de
Source: Anais eletrônicos. Conference titles: Annual Meeting of the Brazilian Biophysical Society - SBBf. Unidades: IFSC, ICB, IQSC
Subjects: COVID-19, ANTIMALÁRICOS, MALÁRIA, PLANEJAMENTO DE FÁRMACOS, PLASMODIUM FALCIPARUM
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GUIDO, Rafael Victorio Carvalho et al. Discovery of Plasmodium falciparum inhibitors as lead candidates for malaria. 2023, Anais.. Campinas: Galoá, 2023. Disponível em: https://proceedings.science/sbbf-2023/papers/discovery-of-plasmodium-falciparum-inhibitors-as-lead-candidates-for-malaria?lang=en. Acesso em: 27 abr. 2024.
APA
Guido, R. V. C., Oliveira, J. R. T. de S., Souza, G. E. de, Zanini, C. L., Paim, J. C., Bargieri, D. Y., et al. (2023). Discovery of Plasmodium falciparum inhibitors as lead candidates for malaria. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/sbbf-2023/papers/discovery-of-plasmodium-falciparum-inhibitors-as-lead-candidates-for-malaria?lang=en
NLM
Guido RVC, Oliveira JRT de S, Souza GE de, Zanini CL, Paim JC, Bargieri DY, Oliva G, Aguiar ACC, Barbosa C de S, Ahmad A, Burtoloso ACB, Maluf SEC, Moura IMR de. Discovery of Plasmodium falciparum inhibitors as lead candidates for malaria [Internet]. Anais eletrônicos. 2023 ;[citado 2024 abr. 27 ] Available from: https://proceedings.science/sbbf-2023/papers/discovery-of-plasmodium-falciparum-inhibitors-as-lead-candidates-for-malaria?lang=en
Vancouver
Guido RVC, Oliveira JRT de S, Souza GE de, Zanini CL, Paim JC, Bargieri DY, Oliva G, Aguiar ACC, Barbosa C de S, Ahmad A, Burtoloso ACB, Maluf SEC, Moura IMR de. Discovery of Plasmodium falciparum inhibitors as lead candidates for malaria [Internet]. Anais eletrônicos. 2023 ;[citado 2024 abr. 27 ] Available from: https://proceedings.science/sbbf-2023/papers/discovery-of-plasmodium-falciparum-inhibitors-as-lead-candidates-for-malaria?lang=en
Artigo de periodico
A proteomic approach to identify digestive enzymes, their exocytic and microapocrine secretory routes and their compartmentalization in the midgut of Spodoptera frugiperda (2022)
Fuzita, Felipe Jun ; Palmisano, Giuseppe ; Pimenta, Daniel C. ; Terra, Walter Ribeiro ; Ferreira, Clélia
Source: Comparative Biochemistry and Physiology. Part B: Biochemistry & Molecular Biology. Unidades: ICB, IQ
Subjects: PARASITOLOGIA, PROTEÔMICA, INTESTINO DE ANIMAL, INSETOS, ENZIMAS, PROTEINASES
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FUZITA, Felipe Jun et al. A proteomic approach to identify digestive enzymes, their exocytic and microapocrine secretory routes and their compartmentalization in the midgut of Spodoptera frugiperda. Comparative Biochemistry and Physiology. Part B: Biochemistry & Molecular Biology, v. 257, p. 1-11, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.cbpb.2021.110670. Acesso em: 27 abr. 2024.
APA
Fuzita, F. J., Palmisano, G., Pimenta, D. C., Terra, W. R., & Ferreira, C. (2022). A proteomic approach to identify digestive enzymes, their exocytic and microapocrine secretory routes and their compartmentalization in the midgut of Spodoptera frugiperda. Comparative Biochemistry and Physiology. Part B: Biochemistry & Molecular Biology, 257, 1-11. doi:10.1016/j.cbpb.2021.110670
NLM
Fuzita FJ, Palmisano G, Pimenta DC, Terra WR, Ferreira C. A proteomic approach to identify digestive enzymes, their exocytic and microapocrine secretory routes and their compartmentalization in the midgut of Spodoptera frugiperda [Internet]. Comparative Biochemistry and Physiology. Part B: Biochemistry & Molecular Biology. 2022 ; 257 1-11.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.cbpb.2021.110670
Vancouver
Fuzita FJ, Palmisano G, Pimenta DC, Terra WR, Ferreira C. A proteomic approach to identify digestive enzymes, their exocytic and microapocrine secretory routes and their compartmentalization in the midgut of Spodoptera frugiperda [Internet]. Comparative Biochemistry and Physiology. Part B: Biochemistry & Molecular Biology. 2022 ; 257 1-11.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.cbpb.2021.110670
Artigo de periodico
Autism spectrum disorder: signaling pathways and prospective therapeutic targets (2021)
Baranova, Juliana; Dragunas, Guilherme ; Botellho, Mayara C. S ; Ayub, Ana Luísa P ; Alves, Rebeca Bueno ; Alencar, Rebeca Rodrigues de ; Papaiz, Debora D; Sogayar, Mari Cleide ; Ulrich, Henning ; Correa, Ricardo G
Source: Cellular and Molecular Neurobiology. Unidades: IQ, ICB
Assunto: TRANSTORNO DO ESPECTRO AUTISTA
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BARANOVA, Juliana et al. Autism spectrum disorder: signaling pathways and prospective therapeutic targets. Cellular and Molecular Neurobiology, v. 41, p. 619–649, 2021Tradução . . Disponível em: https://doi.org/10.1007/s10571-020-00882-7. Acesso em: 27 abr. 2024.
APA
Baranova, J., Dragunas, G., Botellho, M. C. S., Ayub, A. L. P., Alves, R. B., Alencar, R. R. de, et al. (2021). Autism spectrum disorder: signaling pathways and prospective therapeutic targets. Cellular and Molecular Neurobiology, 41, 619–649. doi:10.1007/s10571-020-00882-7
NLM
Baranova J, Dragunas G, Botellho MCS, Ayub ALP, Alves RB, Alencar RR de, Papaiz DD, Sogayar MC, Ulrich H, Correa RG. Autism spectrum disorder: signaling pathways and prospective therapeutic targets [Internet]. Cellular and Molecular Neurobiology. 2021 ; 41 619–649.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1007/s10571-020-00882-7
Vancouver
Baranova J, Dragunas G, Botellho MCS, Ayub ALP, Alves RB, Alencar RR de, Papaiz DD, Sogayar MC, Ulrich H, Correa RG. Autism spectrum disorder: signaling pathways and prospective therapeutic targets [Internet]. Cellular and Molecular Neurobiology. 2021 ; 41 619–649.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1007/s10571-020-00882-7
Artigo de periodico
Non-Toxic dimeric peptides derived from the bothropstoxin-I are potent SARS-CoV-2 and papain-like protease inhibitors (2021)
Freire, Marjorie Caroline Liberato Cavalcanti ; Noske, Gabriela Dias; Bitencourt, Natália V.; Sanches, Paulo R. S.; Santos-Filho, Norival A.; Oliveira, Victor Gawriljuk Ferraro; Souza, Eduardo Pereira de ; Nogueira, Victor Henrique Rabesquine ; Godoy, Mariana Ortiz de; Nakamura, Aline Minali; Fernandes, Rafaela Sachetto ; Godoy, Andre Schutzer de ; Juliano, Maria A.; Peres, Bianca de Miranda ; Barbosa, Cecília G.; Moraes, Carolina B.; Freitas Junior, Lucio Holanda Gondim de ; Cilli, Eduardo Maffud ; Guido, Rafael Victorio Carvalho ; Oliva, Glaucius
Source: Molecules. Unidades: IFSC, ICB
Subjects: COVID-19, CORONAVIRUS, PLANEJAMENTO DE FÁRMACOS, PROTEÍNAS
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FREIRE, Marjorie Caroline Liberato Cavalcanti et al. Non-Toxic dimeric peptides derived from the bothropstoxin-I are potent SARS-CoV-2 and papain-like protease inhibitors. Molecules, v. 26, n. 16, p. 4896-1-4896-17, 2021Tradução . . Disponível em: https://doi.org/10.3390/molecules26164896. Acesso em: 27 abr. 2024.
APA
Freire, M. C. L. C., Noske, G. D., Bitencourt, N. V., Sanches, P. R. S., Santos-Filho, N. A., Oliveira, V. G. F., et al. (2021). Non-Toxic dimeric peptides derived from the bothropstoxin-I are potent SARS-CoV-2 and papain-like protease inhibitors. Molecules, 26( 16), 4896-1-4896-17. doi:10.3390/molecules26164896
NLM
Freire MCLC, Noske GD, Bitencourt NV, Sanches PRS, Santos-Filho NA, Oliveira VGF, Souza EP de, Nogueira VHR, Godoy MO de, Nakamura AM, Fernandes RS, Godoy AS de, Juliano MA, Peres B de M, Barbosa CG, Moraes CB, Freitas Junior LHG de, Cilli EM, Guido RVC, Oliva G. Non-Toxic dimeric peptides derived from the bothropstoxin-I are potent SARS-CoV-2 and papain-like protease inhibitors [Internet]. Molecules. 2021 ; 26( 16): 4896-1-4896-17.[citado 2024 abr. 27 ] Available from: https://doi.org/10.3390/molecules26164896
Vancouver
Freire MCLC, Noske GD, Bitencourt NV, Sanches PRS, Santos-Filho NA, Oliveira VGF, Souza EP de, Nogueira VHR, Godoy MO de, Nakamura AM, Fernandes RS, Godoy AS de, Juliano MA, Peres B de M, Barbosa CG, Moraes CB, Freitas Junior LHG de, Cilli EM, Guido RVC, Oliva G. Non-Toxic dimeric peptides derived from the bothropstoxin-I are potent SARS-CoV-2 and papain-like protease inhibitors [Internet]. Molecules. 2021 ; 26( 16): 4896-1-4896-17.[citado 2024 abr. 27 ] Available from: https://doi.org/10.3390/molecules26164896
Artigo de periodico
Stimuli-responsive polymersomes of poly [2-(dimethylamino) ethyl methacrylate]-b-polystyrene (2021)
Souza, Valdomiro Vagner de ; Carretero, Gustavo Penteado Battesini ; Vitale, Phelipe Augusto Mariano ; Todeschini, Íris ; Kotani, Paloma Otsuke; Saraiva, Greice Kelle Viegas ; Carvalho, Cristiane Rodrigues Guzzo ; Chaimovich Guralnik, Hernan ; Florenzano, Fabio Herbst ; Cuccovia, Iolanda Midea
Source: Polymer Bulletin. Unidades: ICB, IQ, EEL
Subjects: MICROBIOLOGIA, POLÍMEROS (MATERIAIS), LIPOSSOMOS, MICROSCOPIA ELETRÔNICA
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SOUZA, Valdomiro Vagner de et al. Stimuli-responsive polymersomes of poly [2-(dimethylamino) ethyl methacrylate]-b-polystyrene. Polymer Bulletin, p. 21 , 2021Tradução . . Disponível em: https://doi.org/10.1007/s00289-020-03533-5. Acesso em: 27 abr. 2024.
APA
Souza, V. V. de, Carretero, G. P. B., Vitale, P. A. M., Todeschini, Í., Kotani, P. O., Saraiva, G. K. V., et al. (2021). Stimuli-responsive polymersomes of poly [2-(dimethylamino) ethyl methacrylate]-b-polystyrene. Polymer Bulletin, 21 . doi:10.1007/s00289-020-03533-5
NLM
Souza VV de, Carretero GPB, Vitale PAM, Todeschini Í, Kotani PO, Saraiva GKV, Carvalho CRG, Chaimovich Guralnik H, Florenzano FH, Cuccovia IM. Stimuli-responsive polymersomes of poly [2-(dimethylamino) ethyl methacrylate]-b-polystyrene [Internet]. Polymer Bulletin. 2021 ;21 .[citado 2024 abr. 27 ] Available from: https://doi.org/10.1007/s00289-020-03533-5
Vancouver
Souza VV de, Carretero GPB, Vitale PAM, Todeschini Í, Kotani PO, Saraiva GKV, Carvalho CRG, Chaimovich Guralnik H, Florenzano FH, Cuccovia IM. Stimuli-responsive polymersomes of poly [2-(dimethylamino) ethyl methacrylate]-b-polystyrene [Internet]. Polymer Bulletin. 2021 ;21 .[citado 2024 abr. 27 ] Available from: https://doi.org/10.1007/s00289-020-03533-5
Artigo de periodico
Histidine-based hydrogels via singlet-oxygen photooxidation (2021)
Liberato, Michelle da Silva; Cavalcante, Nayara G. S; Sindu, P. Abinaya; Jesus, Mônica Josiane Rodrigues ; Zelenovskii, Pavel; Carreira, Ana C. O; Baptista, Maurício da Silva ; Sogayar, Mari Cleide ; Ferreira, Luís Carlos de Souza ; Catalani, Luiz Henrique
Source: Soft Matter. Unidades: IQ, ICB
Subjects: OXIGÊNIO, PROTEÍNAS, DNA
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LIBERATO, Michelle da Silva et al. Histidine-based hydrogels via singlet-oxygen photooxidation. Soft Matter, v. 17, p. 10926-10934, 2021Tradução . . Disponível em: https://doi.org/10.1039/d1sm01023a. Acesso em: 27 abr. 2024.
APA
Liberato, M. da S., Cavalcante, N. G. S., Sindu, P. A., Jesus, M. J. R., Zelenovskii, P., Carreira, A. C. O., et al. (2021). Histidine-based hydrogels via singlet-oxygen photooxidation. Soft Matter, 17, 10926-10934. doi:10.1039/d1sm01023a
NLM
Liberato M da S, Cavalcante NGS, Sindu PA, Jesus MJR, Zelenovskii P, Carreira ACO, Baptista M da S, Sogayar MC, Ferreira LC de S, Catalani LH. Histidine-based hydrogels via singlet-oxygen photooxidation [Internet]. Soft Matter. 2021 ; 17 10926-10934.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1039/d1sm01023a
Vancouver
Liberato M da S, Cavalcante NGS, Sindu PA, Jesus MJR, Zelenovskii P, Carreira ACO, Baptista M da S, Sogayar MC, Ferreira LC de S, Catalani LH. Histidine-based hydrogels via singlet-oxygen photooxidation [Internet]. Soft Matter. 2021 ; 17 10926-10934.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1039/d1sm01023a
Artigo de periodico
Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria (2021)
Souza, Juliana Oliveira de; Almeida, Suzete M.; Souza, Guilherme Eduardo de ; Zanini, Camila Lima; Silva, Everton Machado da; Paim, Juliana Calit ; Bargieri, Daniel Youssef ; Amporndanai, Kangsa; Antonyuk, Svetlana V. ; Hasnain, S. Samar ; Cruz, Fabio C.; Pereira, Dhelio Batista ; Oliva, Glaucius ; Corrêa, Arlene G. ; Aguiar, Anna Caroline Campos ; Guido, Rafael Victorio Carvalho
Source: European Journal of Medicinal Chemistry Reports. Unidades: ICB, IFSC
Subjects: ANTIMALÁRICOS, ANTIPARASITÁRIOS, MALÁRIA, PLASMODIUM FALCIPARUM
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SOUZA, Juliana Oliveira de et al. Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria. European Journal of Medicinal Chemistry Reports, v. 3, p. 100012-1-100012-16 + supplementary data, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.ejmcr.2021.100012. Acesso em: 27 abr. 2024.
APA
Souza, J. O. de, Almeida, S. M., Souza, G. E. de, Zanini, C. L., Silva, E. M. da, Paim, J. C., et al. (2021). Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria. European Journal of Medicinal Chemistry Reports, 3, 100012-1-100012-16 + supplementary data. doi:10.1016/j.ejmcr.2021.100012
NLM
Souza JO de, Almeida SM, Souza GE de, Zanini CL, Silva EM da, Paim JC, Bargieri DY, Amporndanai K, Antonyuk SV, Hasnain SS, Cruz FC, Pereira DB, Oliva G, Corrêa AG, Aguiar ACC, Guido RVC. Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria [Internet]. European Journal of Medicinal Chemistry Reports. 2021 ; 3 100012-1-100012-16 + supplementary data.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.ejmcr.2021.100012
Vancouver
Souza JO de, Almeida SM, Souza GE de, Zanini CL, Silva EM da, Paim JC, Bargieri DY, Amporndanai K, Antonyuk SV, Hasnain SS, Cruz FC, Pereira DB, Oliva G, Corrêa AG, Aguiar ACC, Guido RVC. Parasitological profiling shows 4(1H)-quinolone derivatives as new lead candidates for malaria [Internet]. European Journal of Medicinal Chemistry Reports. 2021 ; 3 100012-1-100012-16 + supplementary data.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.ejmcr.2021.100012
Artigo de periodico
Heat shock protein B1 is a key mediator of prolactin-induced beta-cell cytoprotection against oxidative stress (2019)
Terra, Letícia F.; Wailemann, Rosângela A. M; Santos, Ancély Ferreira dos ; Gomes, Vinícius M.; Silva, Railmara Pereira da; Laporte, Anna; Meotti, Flavia Carla ; Terra, Walter Ribeiro ; Palmisano, Giuseppe ; Lortz, Stephan; Labriola, Leticia
Source: Free Radical Biology and Medicine. Unidades: IQ, ICB
Subjects: ESTRESSE OXIDATIVO, DIABETES MELLITUS, PARASITOLOGIA, PROLACTINA, ESTRESSE OXIDATIVO, PROTEÍNAS, ILHOTAS DE LANGERHANS, APOPTOSE, PROTEÍNAS DO CHOQUE TÉRMICO, CITOCINAS, ESPECTROMETRIA DE MASSAS, ANTIOXIDANTES
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TERRA, Letícia F. et al. Heat shock protein B1 is a key mediator of prolactin-induced beta-cell cytoprotection against oxidative stress. Free Radical Biology and Medicine, v. 134, p. 394-405, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.freeradbiomed.2019.01.023. Acesso em: 27 abr. 2024.
APA
Terra, L. F., Wailemann, R. A. M., Santos, A. F. dos, Gomes, V. M., Silva, R. P. da, Laporte, A., et al. (2019). Heat shock protein B1 is a key mediator of prolactin-induced beta-cell cytoprotection against oxidative stress. Free Radical Biology and Medicine, 134, 394-405. doi:10.1016/j.freeradbiomed.2019.01.023
NLM
Terra LF, Wailemann RAM, Santos AF dos, Gomes VM, Silva RP da, Laporte A, Meotti FC, Terra WR, Palmisano G, Lortz S, Labriola L. Heat shock protein B1 is a key mediator of prolactin-induced beta-cell cytoprotection against oxidative stress [Internet]. Free Radical Biology and Medicine. 2019 ; 134 394-405.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2019.01.023
Vancouver
Terra LF, Wailemann RAM, Santos AF dos, Gomes VM, Silva RP da, Laporte A, Meotti FC, Terra WR, Palmisano G, Lortz S, Labriola L. Heat shock protein B1 is a key mediator of prolactin-induced beta-cell cytoprotection against oxidative stress [Internet]. Free Radical Biology and Medicine. 2019 ; 134 394-405.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2019.01.023
Trabalho de evento-resumo
Biologia estrutural e busca por ligantes para a proteína NS5 do vírus da Zika (2019)
Oliveira, Ketllyn Irene Zagato; Mesquita, Nathalya Cristina de Moraes Roso; Zúñiga, Gerardo Andrés Libreros; Godoy, Andre Schutzer de; Dias, Marcio Vinicius Bertacine ; Oliva, Glaucius
Source: Book of abstracts. Conference titles: Semana Integrada do Instituto de Física de São Carlos - SIFSC. Unidades: ICB, IFSC
Subjects: FEBRE AMARELA, DOENÇAS TROPICAIS ANIMAL, ESTRUTURA MOLECULAR (QUÍMICA TEÓRICA), BIOFÍSICA
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OLIVEIRA, Ketllyn Irene Zagato et al. Biologia estrutural e busca por ligantes para a proteína NS5 do vírus da Zika. 2019, Anais.. São Carlos: Universidade de São Paulo - USP, Instituto de Física de São Carlos - IFSC, 2019. . Acesso em: 27 abr. 2024.
APA
Oliveira, K. I. Z., Mesquita, N. C. de M. R., Zúñiga, G. A. L., Godoy, A. S. de, Dias, M. V. B., & Oliva, G. (2019). Biologia estrutural e busca por ligantes para a proteína NS5 do vírus da Zika. In Book of abstracts. São Carlos: Universidade de São Paulo - USP, Instituto de Física de São Carlos - IFSC.
NLM
Oliveira KIZ, Mesquita NC de MR, Zúñiga GAL, Godoy AS de, Dias MVB, Oliva G. Biologia estrutural e busca por ligantes para a proteína NS5 do vírus da Zika. Book of abstracts. 2019 ;[citado 2024 abr. 27 ]
Vancouver
Oliveira KIZ, Mesquita NC de MR, Zúñiga GAL, Godoy AS de, Dias MVB, Oliva G. Biologia estrutural e busca por ligantes para a proteína NS5 do vírus da Zika. Book of abstracts. 2019 ;[citado 2024 abr. 27 ]
Trabalho de evento-resumo
Structural biology and ligand search for the NS5 protein of the Zika virus (2019)
Oliveira, Ketllyn Irene Zagato de; Mesquita, Nathalya Cristina de Moraes Roso; Zúñiga, Gerardo Andrés Libreros; Godoy, Andre Schutzer de Marcio Dias; Dias, Marcio Vinicius Bertacine ; Oliva, Glaucius
Source: Anais eletrônicos. Conference titles: Brazilian Symposium on Medicinal Chemistry - BrazMedChem. Unidades: ICB, IFSC
Subjects: ZIKA VÍRUS, PLANEJAMENTO DE FÁRMACOS, DOENÇAS TROPICAIS ANIMAL
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OLIVEIRA, Ketllyn Irene Zagato de et al. Structural biology and ligand search for the NS5 protein of the Zika virus. 2019, Anais.. Campinas: Galoá, 2019. Disponível em: https://proceedings.science/p/107126. Acesso em: 27 abr. 2024.
APA
Oliveira, K. I. Z. de, Mesquita, N. C. de M. R., Zúñiga, G. A. L., Godoy, A. S. de M. D., Dias, M. V. B., & Oliva, G. (2019). Structural biology and ligand search for the NS5 protein of the Zika virus. In Anais eletrônicos. Campinas: Galoá. Recuperado de https://proceedings.science/p/107126
NLM
Oliveira KIZ de, Mesquita NC de MR, Zúñiga GAL, Godoy AS de MD, Dias MVB, Oliva G. Structural biology and ligand search for the NS5 protein of the Zika virus [Internet]. Anais eletrônicos. 2019 ;[citado 2024 abr. 27 ] Available from: https://proceedings.science/p/107126
Vancouver
Oliveira KIZ de, Mesquita NC de MR, Zúñiga GAL, Godoy AS de MD, Dias MVB, Oliva G. Structural biology and ligand search for the NS5 protein of the Zika virus [Internet]. Anais eletrônicos. 2019 ;[citado 2024 abr. 27 ] Available from: https://proceedings.science/p/107126
Artigo de periodico
Inhibition of histone methyltransferase EZH2 in Schistosoma mansoni in vitro by GSK343 reduces egg laying and decreases the expression of genes implicated in DNA replication and noncoding RNA metabolism (2018)
Pereira, Adriana S. A; Amaral, Murilo S; Vasconcelos, Elton J. R; Pires, David S; Asif, Huma; dasilva, Lucas F; Vicente, David A. Morales; Carnairo, Vitor C; Angeli, Claudia Blanes; Palmisano, Giuseppe ; Fantappié, Marcelo Rosado; Pierce, Raymond J; Setubal, João Carlos ; Verjovski-Almeida, Sergio
Source: Plos Neglected Tropical Diseases. Unidades: ICB, IQ
Subjects: SCHISTOSOMA MANSONI, EXPRESSÃO GÊNICA, REPLICAÇÃO DO DNA
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ABNT
PEREIRA, Adriana S. A et al. Inhibition of histone methyltransferase EZH2 in Schistosoma mansoni in vitro by GSK343 reduces egg laying and decreases the expression of genes implicated in DNA replication and noncoding RNA metabolism. Plos Neglected Tropical Diseases, v. 12, n. 10, p. 1-38 art. e0006873, 2018Tradução . . Disponível em: https://doi.org/10.1371/journal.pntd.0006873. Acesso em: 27 abr. 2024.
APA
Pereira, A. S. A., Amaral, M. S., Vasconcelos, E. J. R., Pires, D. S., Asif, H., dasilva, L. F., et al. (2018). Inhibition of histone methyltransferase EZH2 in Schistosoma mansoni in vitro by GSK343 reduces egg laying and decreases the expression of genes implicated in DNA replication and noncoding RNA metabolism. Plos Neglected Tropical Diseases, 12( 10), 1-38 art. e0006873. doi:10.1371/journal.pntd.0006873
NLM
Pereira ASA, Amaral MS, Vasconcelos EJR, Pires DS, Asif H, dasilva LF, Vicente DAM, Carnairo VC, Angeli CB, Palmisano G, Fantappié MR, Pierce RJ, Setubal JC, Verjovski-Almeida S. Inhibition of histone methyltransferase EZH2 in Schistosoma mansoni in vitro by GSK343 reduces egg laying and decreases the expression of genes implicated in DNA replication and noncoding RNA metabolism [Internet]. Plos Neglected Tropical Diseases. 2018 ; 12( 10): 1-38 art. e0006873.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1371/journal.pntd.0006873
Vancouver
Pereira ASA, Amaral MS, Vasconcelos EJR, Pires DS, Asif H, dasilva LF, Vicente DAM, Carnairo VC, Angeli CB, Palmisano G, Fantappié MR, Pierce RJ, Setubal JC, Verjovski-Almeida S. Inhibition of histone methyltransferase EZH2 in Schistosoma mansoni in vitro by GSK343 reduces egg laying and decreases the expression of genes implicated in DNA replication and noncoding RNA metabolism [Internet]. Plos Neglected Tropical Diseases. 2018 ; 12( 10): 1-38 art. e0006873.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1371/journal.pntd.0006873
Artigo de periodico
Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells (2018)
Caires-Júnior, Luiz Carlos; Goulart, Ernesto ; Melo, Uirá Souto; Araujo, Bruno Silva Henrique ; Alvizi, Lucas; Schanoski, Alessandra Soares; Oliveira, Danyllo Felipe de; Kobayashi, Gerson Shigeru; Griesi-Oliveira, Karina; Musso, Camila Manso; Amaral, Murilo Sena; Silva, Lucas Ferreira da; Astray, Renato Mancini ; Suárez-Patiño, Sandra Fernanda; Monteiro, Daniella Cristina Ventini; Silva, Sérgio Gomes da; Yamamoto, Guilherme Lopes; Ezquina, Suzana; Naslavsky, Michel ; Silva, Kayque Telles Alves; Weinmann, Karina; Linden, Vanessa van der; Linden, Helio Van der; Oliveira, João Mendes Ricardo de; Arrais, Nivia Rodrigues Maria; Melo, Adriana; Figueiredo, Thalita; Santos, Silvana; Meira, Joanna Goes Castro; Passos, Saulo Duarte; Almeida, Roque Pacheco de; Bispo, Ana Jovina Barreto; Cavalheiro, Esper Abrão; Kalil, Jorge; Cunha-Neto, Edécio; Nakaya, Helder Takashi Imoto ; Santos, Robert Andreata; Ferreira, Luís Carlos de Souza ; Verjovski-Almeida, Sergio ; Ho, Paulo Lee; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Nature Communications. Unidades: FM, FCF, ICB, IQ, IB
Subjects: ZIKA VÍRUS, GÊMEOS, MALFORMAÇÕES, EXPRESSÃO GÊNICA, TRANSMISSÃO DE DOENÇAS, MICROCEFALIA, BIOLOGIA CELULAR, MICROBIOLOGIA
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ABNT
CAIRES-JÚNIOR, Luiz Carlos et al. Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells. Nature Communications, v. 9, p. 1-11, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41467-017-02790-9. Acesso em: 27 abr. 2024.
APA
Caires-Júnior, L. C., Goulart, E., Melo, U. S., Araujo, B. S. H., Alvizi, L., Schanoski, A. S., et al. (2018). Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells. Nature Communications, 9, 1-11. doi:10.1038/s41467-017-02790-9
NLM
Caires-Júnior LC, Goulart E, Melo US, Araujo BSH, Alvizi L, Schanoski AS, Oliveira DF de, Kobayashi GS, Griesi-Oliveira K, Musso CM, Amaral MS, Silva LF da, Astray RM, Suárez-Patiño SF, Monteiro DCV, Silva SG da, Yamamoto GL, Ezquina S, Naslavsky M, Silva KTA, Weinmann K, Linden V van der, Linden HV der, Oliveira JMR de, Arrais NRM, Melo A, Figueiredo T, Santos S, Meira JGC, Passos SD, Almeida RP de, Bispo AJB, Cavalheiro EA, Kalil J, Cunha-Neto E, Nakaya HTI, Santos RA, Ferreira LC de S, Verjovski-Almeida S, Ho PL, Passos-Bueno MR, Zatz M. Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells [Internet]. Nature Communications. 2018 ; 9 1-11.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1038/s41467-017-02790-9
Vancouver
Caires-Júnior LC, Goulart E, Melo US, Araujo BSH, Alvizi L, Schanoski AS, Oliveira DF de, Kobayashi GS, Griesi-Oliveira K, Musso CM, Amaral MS, Silva LF da, Astray RM, Suárez-Patiño SF, Monteiro DCV, Silva SG da, Yamamoto GL, Ezquina S, Naslavsky M, Silva KTA, Weinmann K, Linden V van der, Linden HV der, Oliveira JMR de, Arrais NRM, Melo A, Figueiredo T, Santos S, Meira JGC, Passos SD, Almeida RP de, Bispo AJB, Cavalheiro EA, Kalil J, Cunha-Neto E, Nakaya HTI, Santos RA, Ferreira LC de S, Verjovski-Almeida S, Ho PL, Passos-Bueno MR, Zatz M. Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells [Internet]. Nature Communications. 2018 ; 9 1-11.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1038/s41467-017-02790-9
Artigo de periodico
Comprehensive glycoprofiling of the epimastigote and trypomastigote stages of Trypanosoma cruzi (2017)
Alves, Maria Júlia Manso ; Kawahara, Rebeca; Viner, Rosa; Colli, Walter ; Mattos, Eliciane Cevolani; Thaysen Andersen, Morten; Larsen, Martin Rossel; Palmisano, Giuseppe
Source: Journal of Proteomics. Unidades: IQ, ICB
Subjects: TRYPANOSOMA CRUZI, GLICOPROTEÍNAS, ESPECTROMETRIA DE MASSAS
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ABNT
ALVES, Maria Júlia Manso et al. Comprehensive glycoprofiling of the epimastigote and trypomastigote stages of Trypanosoma cruzi. Journal of Proteomics, v. 151, p. 182-192, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.jprot.2016.05.034. Acesso em: 27 abr. 2024.
APA
Alves, M. J. M., Kawahara, R., Viner, R., Colli, W., Mattos, E. C., Thaysen Andersen, M., et al. (2017). Comprehensive glycoprofiling of the epimastigote and trypomastigote stages of Trypanosoma cruzi. Journal of Proteomics, 151, 182-192. doi:10.1016/j.jprot.2016.05.034
NLM
Alves MJM, Kawahara R, Viner R, Colli W, Mattos EC, Thaysen Andersen M, Larsen MR, Palmisano G. Comprehensive glycoprofiling of the epimastigote and trypomastigote stages of Trypanosoma cruzi [Internet]. Journal of Proteomics. 2017 ; 151 182-192.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.jprot.2016.05.034
Vancouver
Alves MJM, Kawahara R, Viner R, Colli W, Mattos EC, Thaysen Andersen M, Larsen MR, Palmisano G. Comprehensive glycoprofiling of the epimastigote and trypomastigote stages of Trypanosoma cruzi [Internet]. Journal of Proteomics. 2017 ; 151 182-192.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.jprot.2016.05.034
Artigo de periodico
Role of cathepsins D in the midgut of Dysdercus peruvianus (2017)
Pimentel, André Coppe; Fuzita, Felipe J; Palmisano, Giuseppe ; Ferreira, Clélia ; Terra, Walter Ribeiro
Source: Comparative Biochemistry and Physiology B. Unidades: ICB, IQ
Subjects: HEMIPTERA, DIGESTÃO ANIMAL, ENZIMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PIMENTEL, André Coppe et al. Role of cathepsins D in the midgut of Dysdercus peruvianus. Comparative Biochemistry and Physiology B, v. 204, p. 45-52, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.cbpb.2016.11.004. Acesso em: 27 abr. 2024.
APA
Pimentel, A. C., Fuzita, F. J., Palmisano, G., Ferreira, C., & Terra, W. R. (2017). Role of cathepsins D in the midgut of Dysdercus peruvianus. Comparative Biochemistry and Physiology B, 204, 45-52. doi:10.1016/j.cbpb.2016.11.004
NLM
Pimentel AC, Fuzita FJ, Palmisano G, Ferreira C, Terra WR. Role of cathepsins D in the midgut of Dysdercus peruvianus [Internet]. Comparative Biochemistry and Physiology B. 2017 ; 204 45-52.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.cbpb.2016.11.004
Vancouver
Pimentel AC, Fuzita FJ, Palmisano G, Ferreira C, Terra WR. Role of cathepsins D in the midgut of Dysdercus peruvianus [Internet]. Comparative Biochemistry and Physiology B. 2017 ; 204 45-52.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.cbpb.2016.11.004
Artigo de periodico
Membrane damage by betulinic acid provides insights into cellular aging (2017)
Martins, Waleska K; Gomide, Andreza B; Costa, Érico T; Junqueira, Helena Couto; Stolf, Beatriz Simonsen ; Itri, Rosangela; Baptista, Maurício da Silva
Source: Biochimica Biophysica Acta A. Unidades: IQ, IF, ICB
Subjects: LIPOSSOMOS, MITOCÔNDRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARTINS, Waleska K et al. Membrane damage by betulinic acid provides insights into cellular aging. Biochimica Biophysica Acta A, v. 1861, n. 1, p. 3129-3143, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.bbagen.2016.10.018. Acesso em: 27 abr. 2024.
APA
Martins, W. K., Gomide, A. B., Costa, É. T., Junqueira, H. C., Stolf, B. S., Itri, R., & Baptista, M. da S. (2017). Membrane damage by betulinic acid provides insights into cellular aging. Biochimica Biophysica Acta A, 1861( 1), 3129-3143. doi:10.1016/j.bbagen.2016.10.018
NLM
Martins WK, Gomide AB, Costa ÉT, Junqueira HC, Stolf BS, Itri R, Baptista M da S. Membrane damage by betulinic acid provides insights into cellular aging [Internet]. Biochimica Biophysica Acta A. 2017 ; 1861( 1): 3129-3143.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.bbagen.2016.10.018
Vancouver
Martins WK, Gomide AB, Costa ÉT, Junqueira HC, Stolf BS, Itri R, Baptista M da S. Membrane damage by betulinic acid provides insights into cellular aging [Internet]. Biochimica Biophysica Acta A. 2017 ; 1861( 1): 3129-3143.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.bbagen.2016.10.018
Trabalho de evento-resumo
Detergent resistant domains in the midgut microvillar membrane of Spodoptera Frugiperda larvae (2016)
Fuzita, Felipe Jun; Palmisano, Giuseppe ; Pimenta, Daniel Carvalho; Terra, Walter Ribeiro ; Ferreira, Clélia
Source: Abstracts. Conference titles: Annual Meeting of the Brazilian Society for Biochemistry and Molecular Biology (SBBq). Unidades: ICB, IQ
Subjects: LIPÍDEOS, BIOQUÍMICA, PROTEÍNAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FUZITA, Felipe Jun et al. Detergent resistant domains in the midgut microvillar membrane of Spodoptera Frugiperda larvae. 2016, Anais.. Natal: Sociedade Brasileira de Bioquímica e Biologia Molecular (SBBq), 2016. . Acesso em: 27 abr. 2024.
APA
Fuzita, F. J., Palmisano, G., Pimenta, D. C., Terra, W. R., & Ferreira, C. (2016). Detergent resistant domains in the midgut microvillar membrane of Spodoptera Frugiperda larvae. In Abstracts. Natal: Sociedade Brasileira de Bioquímica e Biologia Molecular (SBBq).
NLM
Fuzita FJ, Palmisano G, Pimenta DC, Terra WR, Ferreira C. Detergent resistant domains in the midgut microvillar membrane of Spodoptera Frugiperda larvae. Abstracts. 2016 ;[citado 2024 abr. 27 ]
Vancouver
Fuzita FJ, Palmisano G, Pimenta DC, Terra WR, Ferreira C. Detergent resistant domains in the midgut microvillar membrane of Spodoptera Frugiperda larvae. Abstracts. 2016 ;[citado 2024 abr. 27 ]
Artigo de periodico
Glycated reconstructed human skin as a platform to study the pathogenesis of skin aging (2015)
Pennacchi, Paula Comune; Almeida, Maíra Estanislau Soares de; Gomes, Octavio Luis Alves; Flores, Fernanda Faião; Crepaldi, Maria Clara de Araújo; Santos, Marinilce Fagundes dos ; Barros, Silvia Berlanga de Moraes ; Maria-Engler, Silvya Stuchi
Source: Tissue Engineering A. Unidades: ICB, FCF
Subjects: ENVELHECIMENTO, PELES
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ABNT
PENNACCHI, Paula Comune et al. Glycated reconstructed human skin as a platform to study the pathogenesis of skin aging. Tissue Engineering A, v. 21, n. 17-18, p. 2417-2425, 2015Tradução . . Disponível em: https://doi.org/10.1089/ten.tea.2015.0009. Acesso em: 27 abr. 2024.
APA
Pennacchi, P. C., Almeida, M. E. S. de, Gomes, O. L. A., Flores, F. F., Crepaldi, M. C. de A., Santos, M. F. dos, et al. (2015). Glycated reconstructed human skin as a platform to study the pathogenesis of skin aging. Tissue Engineering A, 21( 17-18), 2417-2425. doi:10.1089/ten.tea.2015.0009
NLM
Pennacchi PC, Almeida MES de, Gomes OLA, Flores FF, Crepaldi MC de A, Santos MF dos, Barros SB de M, Maria-Engler SS. Glycated reconstructed human skin as a platform to study the pathogenesis of skin aging [Internet]. Tissue Engineering A. 2015 ; 21( 17-18): 2417-2425.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1089/ten.tea.2015.0009
Vancouver
Pennacchi PC, Almeida MES de, Gomes OLA, Flores FF, Crepaldi MC de A, Santos MF dos, Barros SB de M, Maria-Engler SS. Glycated reconstructed human skin as a platform to study the pathogenesis of skin aging [Internet]. Tissue Engineering A. 2015 ; 21( 17-18): 2417-2425.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1089/ten.tea.2015.0009
Artigo de periodico
Production of vegetable oil blends and structured lipids and their effect on wound healing (2015)
Ract, Juliana Neves Rodrigues ; Soares, Fabiana Andréia Schafer de Martini; Rodrigues, Hosana Gomes; Bortolon, José Ricardo; Murata, Gilson Masahiro; Gonçalves, Maria Inês de Almeida; Hatanaka, Elaine; Curi, Rui; Gioielli, Luiz Antonio
Source: Brazilian Journal of Pharmaceutical Sciences. Unidades: FCF, ICB
Subjects: LIPÍDEOS, CICATRIZAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RACT, Juliana Neves Rodrigues et al. Production of vegetable oil blends and structured lipids and their effect on wound healing. Brazilian Journal of Pharmaceutical Sciences, v. 51, n. 2, p. 415-427, 2015Tradução . . Disponível em: https://doi.org/10.1590/s1984-82502015000200019. Acesso em: 27 abr. 2024.
APA
Ract, J. N. R., Soares, F. A. S. de M., Rodrigues, H. G., Bortolon, J. R., Murata, G. M., Gonçalves, M. I. de A., et al. (2015). Production of vegetable oil blends and structured lipids and their effect on wound healing. Brazilian Journal of Pharmaceutical Sciences, 51( 2), 415-427. doi:10.1590/s1984-82502015000200019
NLM
Ract JNR, Soares FAS de M, Rodrigues HG, Bortolon JR, Murata GM, Gonçalves MI de A, Hatanaka E, Curi R, Gioielli LA. Production of vegetable oil blends and structured lipids and their effect on wound healing [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2015 ; 51( 2): 415-427.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1590/s1984-82502015000200019
Vancouver
Ract JNR, Soares FAS de M, Rodrigues HG, Bortolon JR, Murata GM, Gonçalves MI de A, Hatanaka E, Curi R, Gioielli LA. Production of vegetable oil blends and structured lipids and their effect on wound healing [Internet]. Brazilian Journal of Pharmaceutical Sciences. 2015 ; 51( 2): 415-427.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1590/s1984-82502015000200019
Artigo de periodico
Proteins differentially expressed in human beta-cells-enriched pancreatic islet cultures and human insulinomas (2013)
Terra, Letícia F.; Teixeira, Priscila C.; Wailemann, Rosangela A. M.; Zelanis, André; Palmisano, Giuseppe ; Cunha-Neto, Edecio; Kalil, Jorge; Larsen, Martin R.; Labriola, Leticia ; Sogayar, Mari Cleide
Source: Molecular and Cellular Endocrinology. Unidades: ICB, FM, IQ
Subjects: PANCREATITE, ESPECTROMETRIA DE MASSAS, BIOLOGIA MOLECULAR, FENÓTIPOS, PARASITOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TERRA, Letícia F. et al. Proteins differentially expressed in human beta-cells-enriched pancreatic islet cultures and human insulinomas. Molecular and Cellular Endocrinology, v. 381, n. 1-2, p. 16-25, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2013.07.004. Acesso em: 27 abr. 2024.
APA
Terra, L. F., Teixeira, P. C., Wailemann, R. A. M., Zelanis, A., Palmisano, G., Cunha-Neto, E., et al. (2013). Proteins differentially expressed in human beta-cells-enriched pancreatic islet cultures and human insulinomas. Molecular and Cellular Endocrinology, 381( 1-2), 16-25. doi:10.1016/j.mce.2013.07.004
NLM
Terra LF, Teixeira PC, Wailemann RAM, Zelanis A, Palmisano G, Cunha-Neto E, Kalil J, Larsen MR, Labriola L, Sogayar MC. Proteins differentially expressed in human beta-cells-enriched pancreatic islet cultures and human insulinomas [Internet]. Molecular and Cellular Endocrinology. 2013 ; 381( 1-2): 16-25.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.mce.2013.07.004
Vancouver
Terra LF, Teixeira PC, Wailemann RAM, Zelanis A, Palmisano G, Cunha-Neto E, Kalil J, Larsen MR, Labriola L, Sogayar MC. Proteins differentially expressed in human beta-cells-enriched pancreatic islet cultures and human insulinomas [Internet]. Molecular and Cellular Endocrinology. 2013 ; 381( 1-2): 16-25.[citado 2024 abr. 27 ] Available from: https://doi.org/10.1016/j.mce.2013.07.004

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