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Artigo de periodico
The effect of MK-801 on stress-ethanol cross-sensitization is dissociable from its effects on nNOS activity (2023)
Santos, Jaqueline Rocha Borges dos ; Rae, Mariana Beu ; Szumlinski, Karen K. ; Teixeira, Simone Aparecida ; Muscará, Marcelo Nicolas ; Camarini, Rosana
Source: Alcohol. Unidade: ICB
Subjects: FARMACOLOGIA, ETANOL, GLUTAMATOS, AMINOÁCIDOS, ÓXIDO NÍTRICO, CÓRTEX PRÉ-FRONTAL, HIPOCAMPU DE ANIMAL, MODELOS ANIMAIS, CAMUNDONGOS, ESTRESSE
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SANTOS, Jaqueline Rocha Borges dos et al. The effect of MK-801 on stress-ethanol cross-sensitization is dissociable from its effects on nNOS activity. Alcohol, v. 112, p. 31-39, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.alcohol.2023.06.004. Acesso em: 06 nov. 2024.
APA
Santos, J. R. B. dos, Rae, M. B., Szumlinski, K. K., Teixeira, S. A., Muscará, M. N., & Camarini, R. (2023). The effect of MK-801 on stress-ethanol cross-sensitization is dissociable from its effects on nNOS activity. Alcohol, 112, 31-39. doi:10.1016/j.alcohol.2023.06.004
NLM
Santos JRB dos, Rae MB, Szumlinski KK, Teixeira SA, Muscará MN, Camarini R. The effect of MK-801 on stress-ethanol cross-sensitization is dissociable from its effects on nNOS activity [Internet]. Alcohol. 2023 ; 112 31-39.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.alcohol.2023.06.004
Vancouver
Santos JRB dos, Rae MB, Szumlinski KK, Teixeira SA, Muscará MN, Camarini R. The effect of MK-801 on stress-ethanol cross-sensitization is dissociable from its effects on nNOS activity [Internet]. Alcohol. 2023 ; 112 31-39.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.alcohol.2023.06.004
Artigo de periodico
Branched chain amino acids catabolism as a source of new drug targets in pathogenic protists (2023)
Souza, H. F. Santos ; Marsiccobetre, S. ; Souza, R. O. O. ; Martínez, L. A. Luévano ; Silber, Ariel Mariano
Source: Experimental Parasitology. Unidade: ICB
Subjects: PARASITOLOGIA, AMINOÁCIDOS, CÉLULAS EUCARIÓTICAS, CÉLULAS MUSCULARES, PROTEÍNAS
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SOUZA, H. F. Santos et al. Branched chain amino acids catabolism as a source of new drug targets in pathogenic protists. Experimental Parasitology, v. 249, p. 1-10, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.exppara.2023.108499. Acesso em: 06 nov. 2024.
APA
Souza, H. F. S., Marsiccobetre, S., Souza, R. O. O., Martínez, L. A. L., & Silber, A. M. (2023). Branched chain amino acids catabolism as a source of new drug targets in pathogenic protists. Experimental Parasitology, 249, 1-10. doi:10.1016/j.exppara.2023.108499
NLM
Souza HFS, Marsiccobetre S, Souza ROO, Martínez LAL, Silber AM. Branched chain amino acids catabolism as a source of new drug targets in pathogenic protists [Internet]. Experimental Parasitology. 2023 ; 249 1-10.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.exppara.2023.108499
Vancouver
Souza HFS, Marsiccobetre S, Souza ROO, Martínez LAL, Silber AM. Branched chain amino acids catabolism as a source of new drug targets in pathogenic protists [Internet]. Experimental Parasitology. 2023 ; 249 1-10.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.exppara.2023.108499
Artigo de periodico
Immune targets to stop future SARS-CoV-2 variants (2023)
Souza, Milena Silva; Farias, Jéssica Pires ; Luiz, Wilson Barros ; Birbrair, Alexander ; Durães-Carvalho, Ricardo ; Amorim, Jaime Henrique ; Ferreira, Luis Carlos de Souza
Source: Microbiology Spectrum. Unidade: ICB
Subjects: MICROBIOLOGIA, COVID-19, EPITOPOS, VARIAÇÃO GENÉTICA, VACINAS VIRAIS, MUTAÇÃO GENÉTICA, AMINOÁCIDOS
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SOUZA, Milena Silva et al. Immune targets to stop future SARS-CoV-2 variants. Microbiology Spectrum, v. 11, n. 6, p. 11 , 2023Tradução . . Disponível em: https://doi.org/10.1128/spectrum.02892-23. Acesso em: 06 nov. 2024.
APA
Souza, M. S., Farias, J. P., Luiz, W. B., Birbrair, A., Durães-Carvalho, R., Amorim, J. H., & Ferreira, L. C. de S. (2023). Immune targets to stop future SARS-CoV-2 variants. Microbiology Spectrum, 11( 6), 11 . doi:10.1128/spectrum.02892-23
NLM
Souza MS, Farias JP, Luiz WB, Birbrair A, Durães-Carvalho R, Amorim JH, Ferreira LC de S. Immune targets to stop future SARS-CoV-2 variants [Internet]. Microbiology Spectrum. 2023 ; 11( 6): 11 .[citado 2024 nov. 06 ] Available from: https://doi.org/10.1128/spectrum.02892-23
Vancouver
Souza MS, Farias JP, Luiz WB, Birbrair A, Durães-Carvalho R, Amorim JH, Ferreira LC de S. Immune targets to stop future SARS-CoV-2 variants [Internet]. Microbiology Spectrum. 2023 ; 11( 6): 11 .[citado 2024 nov. 06 ] Available from: https://doi.org/10.1128/spectrum.02892-23
Artigo de periodico
Klotho increases antioxidant defenses in astrocytes and ubiquitin–proteasome activity in neurons (2023)
Orellana, Ana Maria ; Mazucanti, Caio Henrique ; Anjos, Leticia Pavan dos ; Lima, Larissa de Sá ; Kawamoto, Elisa Mitiko ; Scavone, Cristoforo
Source: Scientific Reports. Unidade: ICB
Subjects: FARMACOLOGIA, ENVELHECIMENTO CELULAR, ANTIOXIDANTES, ESTRESSE, INSULINA, ENZIMAS, AMINOÁCIDOS, ATIVAÇÃO ENZIMÁTICA, CAMUNDONGOS, NEURÔNIOS
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ORELLANA, Ana Maria et al. Klotho increases antioxidant defenses in astrocytes and ubiquitin–proteasome activity in neurons. Scientific Reports, 2023Tradução . . Disponível em: https://doi.org/10.1038/s41598-023-41166-6. Acesso em: 06 nov. 2024.
APA
Orellana, A. M., Mazucanti, C. H., Anjos, L. P. dos, Lima, L. de S., Kawamoto, E. M., & Scavone, C. (2023). Klotho increases antioxidant defenses in astrocytes and ubiquitin–proteasome activity in neurons. Scientific Reports. doi:10.1038/s41598-023-41166-6
NLM
Orellana AM, Mazucanti CH, Anjos LP dos, Lima L de S, Kawamoto EM, Scavone C. Klotho increases antioxidant defenses in astrocytes and ubiquitin–proteasome activity in neurons [Internet]. Scientific Reports. 2023 ;[citado 2024 nov. 06 ] Available from: https://doi.org/10.1038/s41598-023-41166-6
Vancouver
Orellana AM, Mazucanti CH, Anjos LP dos, Lima L de S, Kawamoto EM, Scavone C. Klotho increases antioxidant defenses in astrocytes and ubiquitin–proteasome activity in neurons [Internet]. Scientific Reports. 2023 ;[citado 2024 nov. 06 ] Available from: https://doi.org/10.1038/s41598-023-41166-6
Artigo de periodico
Genomes of Endotrypanum monterogeii from Panama and Zelonia costaricensis from Brazil: expansion of multigene families in Leishmaniinae parasites that are close relatives of Leishmania spp. (2023)
Tullume-Vergara, Percy Omar ; Caicedo, Kelly Yovani Olivos ; Calderon-Tantaleant, José Frankilin ; Serrano, Myrna Garcia ; Buck, Gregory A. ; Alves, João Marcelo Pereira ; Teixeira, Marta Maria Geraldes ; Shaw, Jeffrey Jon
Source: Pathogens. Unidades: ICB, BIOINFORMÁTICA
Subjects: PARASITOLOGIA, LEISHMANIA, GLICOPROTEÍNAS, FILOGENIA, ANIMAIS PARASITOS, CATALASE, ENZIMAS OXIRREDUTORAS, ATIVAÇÃO ENZIMÁTICA, AMINOÁCIDOS
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TULLUME-VERGARA, Percy Omar et al. Genomes of Endotrypanum monterogeii from Panama and Zelonia costaricensis from Brazil: expansion of multigene families in Leishmaniinae parasites that are close relatives of Leishmania spp. Pathogens, v. 12, n. 12, p. 21 , 2023Tradução . . Disponível em: https://doi.org/10.3390/pathogens12121409. Acesso em: 06 nov. 2024.
APA
Tullume-Vergara, P. O., Caicedo, K. Y. O., Calderon-Tantaleant, J. F., Serrano, M. G., Buck, G. A., Alves, J. M. P., et al. (2023). Genomes of Endotrypanum monterogeii from Panama and Zelonia costaricensis from Brazil: expansion of multigene families in Leishmaniinae parasites that are close relatives of Leishmania spp. Pathogens, 12( 12), 21 . doi:10.3390/pathogens12121409
NLM
Tullume-Vergara PO, Caicedo KYO, Calderon-Tantaleant JF, Serrano MG, Buck GA, Alves JMP, Teixeira MMG, Shaw JJ. Genomes of Endotrypanum monterogeii from Panama and Zelonia costaricensis from Brazil: expansion of multigene families in Leishmaniinae parasites that are close relatives of Leishmania spp. [Internet]. Pathogens. 2023 ; 12( 12): 21 .[citado 2024 nov. 06 ] Available from: https://doi.org/10.3390/pathogens12121409
Vancouver
Tullume-Vergara PO, Caicedo KYO, Calderon-Tantaleant JF, Serrano MG, Buck GA, Alves JMP, Teixeira MMG, Shaw JJ. Genomes of Endotrypanum monterogeii from Panama and Zelonia costaricensis from Brazil: expansion of multigene families in Leishmaniinae parasites that are close relatives of Leishmania spp. [Internet]. Pathogens. 2023 ; 12( 12): 21 .[citado 2024 nov. 06 ] Available from: https://doi.org/10.3390/pathogens12121409
Artigo de periodico
Urocortin expression in rat brain: evidence against a pervasive relationship of urocortin-containing projections with targets bearing type 2 CRF receptors (2023)
Vaugham, Joan; Arias, Carlos; Rissman, Robert A. ; Vale, Wylie W.; Sawchenko, Paul E. ; Bittencourt, Jackson Cioni
Source: The Journal of Comparative Neurology. Unidade: ICB
Subjects: ANATOMIA, HORMÔNIO LIBERADOR DE CORTICOTROFINA, RECEPTORES HORMONAIS, NEUROPEPTÍDEOS, VIAS NEURAIS, NEURÔNIOS, RNA MENSAGEIRO, AMINOÁCIDOS, EXPRESSÃO GÊNICA, MEDULA ESPINHAL, ESTRESSE, RATOS, CÉREBRO
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VAUGHAM, Joan et al. Urocortin expression in rat brain: evidence against a pervasive relationship of urocortin-containing projections with targets bearing type 2 CRF receptors. The Journal of Comparative Neurology, v. 415, n. 3, p. 285-312, 2023Tradução . . Disponível em: https://doi.org/10.1002/(SICI)1096-9861(19991220)415:3<285::AID-CNE1>3.0.CO;2-0. Acesso em: 06 nov. 2024.
APA
Vaugham, J., Arias, C., Rissman, R. A., Vale, W. W., Sawchenko, P. E., & Bittencourt, J. C. (2023). Urocortin expression in rat brain: evidence against a pervasive relationship of urocortin-containing projections with targets bearing type 2 CRF receptors. The Journal of Comparative Neurology, 415( 3), 285-312. doi:10.1002/(SICI)1096-9861(19991220)415:3<285::AID-CNE1>3.0.CO;2-0
NLM
Vaugham J, Arias C, Rissman RA, Vale WW, Sawchenko PE, Bittencourt JC. Urocortin expression in rat brain: evidence against a pervasive relationship of urocortin-containing projections with targets bearing type 2 CRF receptors [Internet]. The Journal of Comparative Neurology. 2023 ; 415( 3): 285-312.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/(SICI)1096-9861(19991220)415:3<285::AID-CNE1>3.0.CO;2-0
Vancouver
Vaugham J, Arias C, Rissman RA, Vale WW, Sawchenko PE, Bittencourt JC. Urocortin expression in rat brain: evidence against a pervasive relationship of urocortin-containing projections with targets bearing type 2 CRF receptors [Internet]. The Journal of Comparative Neurology. 2023 ; 415( 3): 285-312.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1002/(SICI)1096-9861(19991220)415:3<285::AID-CNE1>3.0.CO;2-0
Artigo de periodico
A selective inhibitor of Cardiac Troponin I Phosphorylation by Delta Protein Kinase C (δPKC) as a treatment for Ischemia-reperfusion injury (2022)
Qvit, Nir ; Lin, Amanda J. ; Elezaby, Aly ; Ostberg, Nicolai P. ; Campos, Juliane Cruz ; Ferreira, Julio Cesar Batista ; Rosen, Daria Mochly
Source: Pharmaceuticals. Unidade: ICB
Subjects: ANATOMIA, ISQUEMIA MIOCÁRDICA, TROPONINA I, PROTEÍNAS MUSCULARES, PEPTÍDEOS, INFARTO DO MIOCÁRDIO, CARDIOPATIAS, AMINOÁCIDOS
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QVIT, Nir et al. A selective inhibitor of Cardiac Troponin I Phosphorylation by Delta Protein Kinase C (δPKC) as a treatment for Ischemia-reperfusion injury. Pharmaceuticals, v. 15, n. 3, p. 1-11, 2022Tradução . . Disponível em: https://doi.org/10.3390/ph15030271. Acesso em: 06 nov. 2024.
APA
Qvit, N., Lin, A. J., Elezaby, A., Ostberg, N. P., Campos, J. C., Ferreira, J. C. B., & Rosen, D. M. (2022). A selective inhibitor of Cardiac Troponin I Phosphorylation by Delta Protein Kinase C (δPKC) as a treatment for Ischemia-reperfusion injury. Pharmaceuticals, 15( 3), 1-11. doi:10.3390/ph15030271
NLM
Qvit N, Lin AJ, Elezaby A, Ostberg NP, Campos JC, Ferreira JCB, Rosen DM. A selective inhibitor of Cardiac Troponin I Phosphorylation by Delta Protein Kinase C (δPKC) as a treatment for Ischemia-reperfusion injury [Internet]. Pharmaceuticals. 2022 ; 15( 3): 1-11.[citado 2024 nov. 06 ] Available from: https://doi.org/10.3390/ph15030271
Vancouver
Qvit N, Lin AJ, Elezaby A, Ostberg NP, Campos JC, Ferreira JCB, Rosen DM. A selective inhibitor of Cardiac Troponin I Phosphorylation by Delta Protein Kinase C (δPKC) as a treatment for Ischemia-reperfusion injury [Internet]. Pharmaceuticals. 2022 ; 15( 3): 1-11.[citado 2024 nov. 06 ] Available from: https://doi.org/10.3390/ph15030271
Artigo de periodico
BCR-ABL1 Tyrosine kinase complex signaling transduction: challenges to overcome resistance in chronic myeloid Leukemia (2022)
Amarante-Mendes, João Gustavo Pessini ; Rana, Aamir ; Datoguia, Tarcila Santos ; Hamerschlak, Nelson ; Brumatti, Gabriela
Source: Pharmaceutics. Unidade: ICB
Subjects: IMUNOLOGIA, TRANSDUÇÃO DE SINAL CELULAR, CROMOSSOMOS, MUTAÇÃO GENÉTICA, LEUCEMIA MIELOIDE, QUIMIOTERAPIA, AMINOÁCIDOS, PROTEÍNAS QUINASES
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AMARANTE-MENDES, João Gustavo Pessini et al. BCR-ABL1 Tyrosine kinase complex signaling transduction: challenges to overcome resistance in chronic myeloid Leukemia. Pharmaceutics, v. 14, n. 1, 2022Tradução . . Disponível em: https://doi.org/10.3390/pharmaceutics14010215. Acesso em: 06 nov. 2024.
APA
Amarante-Mendes, J. G. P., Rana, A., Datoguia, T. S., Hamerschlak, N., & Brumatti, G. (2022). BCR-ABL1 Tyrosine kinase complex signaling transduction: challenges to overcome resistance in chronic myeloid Leukemia. Pharmaceutics, 14( 1). doi:10.3390/pharmaceutics14010215
NLM
Amarante-Mendes JGP, Rana A, Datoguia TS, Hamerschlak N, Brumatti G. BCR-ABL1 Tyrosine kinase complex signaling transduction: challenges to overcome resistance in chronic myeloid Leukemia [Internet]. Pharmaceutics. 2022 ; 14( 1):[citado 2024 nov. 06 ] Available from: https://doi.org/10.3390/pharmaceutics14010215
Vancouver
Amarante-Mendes JGP, Rana A, Datoguia TS, Hamerschlak N, Brumatti G. BCR-ABL1 Tyrosine kinase complex signaling transduction: challenges to overcome resistance in chronic myeloid Leukemia [Internet]. Pharmaceutics. 2022 ; 14( 1):[citado 2024 nov. 06 ] Available from: https://doi.org/10.3390/pharmaceutics14010215
Artigo de periodico
Ru(II)/amino acid complexes inhibit the progression of breast cancer cells through multiple mechanism-induced apoptosis (2022)
Andrade, Francyelli Mello ; Guedes, Adriana P. M.; Pires, Wanessa C.; Sá, Vivianne de Souza Velozo ; Delmond, Kezia A.; Mendes, Davi ; Silva, Matheus Molina ; Matuda, Larissa ; Sousa, Maria Alice Montes de ; Reis, Paulo Melo ; Gomes, Clever C. ; Castro, Carlos Henrique; Almeida, Márcio Aurélio Pinheiro; Menck, Carlos Frederico Martins ; Batista, Alzir Azevedo ; Burikhanov, Ravshan ; Rangnekar, Vivek M. ; Lacerda, Elisângela Silveira
Source: Journal of Inorganic Biochemistry. Unidade: ICB
Subjects: MICROBIOLOGIA, APOPTOSE, CÉLULAS MORTAS, AMINOÁCIDOS, CÉLULAS CULTIVADAS DE TUMOR, NEOPLASIAS MAMÁRIAS, RUTÊNIO, METÁSTASE NEOPLÁSICA
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ANDRADE, Francyelli Mello et al. Ru(II)/amino acid complexes inhibit the progression of breast cancer cells through multiple mechanism-induced apoptosis. Journal of Inorganic Biochemistry, v. 226, p. 1-12, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.jinorgbio.2021.111625. Acesso em: 06 nov. 2024.
APA
Andrade, F. M., Guedes, A. P. M., Pires, W. C., Sá, V. de S. V., Delmond, K. A., Mendes, D., et al. (2022). Ru(II)/amino acid complexes inhibit the progression of breast cancer cells through multiple mechanism-induced apoptosis. Journal of Inorganic Biochemistry, 226, 1-12. doi:10.1016/j.jinorgbio.2021.111625
NLM
Andrade FM, Guedes APM, Pires WC, Sá V de SV, Delmond KA, Mendes D, Silva MM, Matuda L, Sousa MAM de, Reis PM, Gomes CC, Castro CH, Almeida MAP, Menck CFM, Batista AA, Burikhanov R, Rangnekar VM, Lacerda ES. Ru(II)/amino acid complexes inhibit the progression of breast cancer cells through multiple mechanism-induced apoptosis [Internet]. Journal of Inorganic Biochemistry. 2022 ; 226 1-12.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.jinorgbio.2021.111625
Vancouver
Andrade FM, Guedes APM, Pires WC, Sá V de SV, Delmond KA, Mendes D, Silva MM, Matuda L, Sousa MAM de, Reis PM, Gomes CC, Castro CH, Almeida MAP, Menck CFM, Batista AA, Burikhanov R, Rangnekar VM, Lacerda ES. Ru(II)/amino acid complexes inhibit the progression of breast cancer cells through multiple mechanism-induced apoptosis [Internet]. Journal of Inorganic Biochemistry. 2022 ; 226 1-12.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.jinorgbio.2021.111625
Artigo de periodico
Completion of the gut microbial epi-bile acid pathway (2021)
Doden, Heidi L. ; Wolf, Patricia G. ; Gaskins, H. Rex ; Anantharaman, Karthik ; Alves, João Marcelo Pereira ; Ridlon, Jason M.
Source: Gut Microbes. Unidade: ICB
Subjects: PARASITOLOGIA, ÁCIDO GLUTÂMICO, AMINOÁCIDOS, CLOSTRIDIUM, ENZIMAS OXIRREDUTORAS, FILOGENIA, ESTUDOS DE COORTES, GENETICA MICROBIANA
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DODEN, Heidi L. et al. Completion of the gut microbial epi-bile acid pathway. Gut Microbes, v. 13, n. 1, p. 1-20, 2021Tradução . . Disponível em: https://doi.org/10.1080/19490976.2021.1907271. Acesso em: 06 nov. 2024.
APA
Doden, H. L., Wolf, P. G., Gaskins, H. R., Anantharaman, K., Alves, J. M. P., & Ridlon, J. M. (2021). Completion of the gut microbial epi-bile acid pathway. Gut Microbes, 13( 1), 1-20. doi:10.1080/19490976.2021.1907271
NLM
Doden HL, Wolf PG, Gaskins HR, Anantharaman K, Alves JMP, Ridlon JM. Completion of the gut microbial epi-bile acid pathway [Internet]. Gut Microbes. 2021 ; 13( 1): 1-20.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1080/19490976.2021.1907271
Vancouver
Doden HL, Wolf PG, Gaskins HR, Anantharaman K, Alves JMP, Ridlon JM. Completion of the gut microbial epi-bile acid pathway [Internet]. Gut Microbes. 2021 ; 13( 1): 1-20.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1080/19490976.2021.1907271
Artigo de periodico
Treatment strategies for glucose-6-phosphate dehydrogenase deficiency: past and future perspectives (2021)
Garcia, Adriana A. ; Koperniku, Ana ; Ferreira, Julio Cesar Batista ; Rosen, Daria Mochly
Source: Trends in Pharmacological Sciences. Unidade: ICB
Subjects: ANATOMIA, AMINOÁCIDOS, ATIVAÇÃO ENZIMÁTICA, GLICOSE, ERITRÓCITOS, ESTRESSE OXIDATIVO, MUTAÇÃO GENÉTICA
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GARCIA, Adriana A. et al. Treatment strategies for glucose-6-phosphate dehydrogenase deficiency: past and future perspectives. Trends in Pharmacological Sciences, v. 42, n. 10, p. 829-844, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.tips.2021.07.002. Acesso em: 06 nov. 2024.
APA
Garcia, A. A., Koperniku, A., Ferreira, J. C. B., & Rosen, D. M. (2021). Treatment strategies for glucose-6-phosphate dehydrogenase deficiency: past and future perspectives. Trends in Pharmacological Sciences, 42( 10), 829-844. doi:10.1016/j.tips.2021.07.002
NLM
Garcia AA, Koperniku A, Ferreira JCB, Rosen DM. Treatment strategies for glucose-6-phosphate dehydrogenase deficiency: past and future perspectives [Internet]. Trends in Pharmacological Sciences. 2021 ; 42( 10): 829-844.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tips.2021.07.002
Vancouver
Garcia AA, Koperniku A, Ferreira JCB, Rosen DM. Treatment strategies for glucose-6-phosphate dehydrogenase deficiency: past and future perspectives [Internet]. Trends in Pharmacological Sciences. 2021 ; 42( 10): 829-844.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1016/j.tips.2021.07.002
Artigo de periodico
Seriniquinones as therapeutic leads for treatment of BRAF and NRAS mutant melanomas (2021)
Hirata, Amanda Soares ; Teixeira, Paula Rezende ; Machado Neto, João Agostinho ; Jimenez, Paula C. ; Clair, James J. La ; Fenical, William ; Costa-Lotufo, Letícia Veras
Source: Molecules. Unidade: ICB
Subjects: FARMACOLOGIA, APOPTOSE, PRODUTOS NATURAIS, PEPTÍDEOS, AMINOÁCIDOS, CÉLULAS CULTIVADAS DE TUMOR, MELANOMA, MOLÉCULA, BACTÉRIAS AERÓBICAS
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HIRATA, Amanda Soares et al. Seriniquinones as therapeutic leads for treatment of BRAF and NRAS mutant melanomas. Molecules, v. 26, n. 23, p. 1-15, 2021Tradução . . Disponível em: https://doi.org/10.3390/molecules26237362. Acesso em: 06 nov. 2024.
APA
Hirata, A. S., Teixeira, P. R., Machado Neto, J. A., Jimenez, P. C., Clair, J. J. L., Fenical, W., & Costa-Lotufo, L. V. (2021). Seriniquinones as therapeutic leads for treatment of BRAF and NRAS mutant melanomas. Molecules, 26( 23), 1-15. doi:10.3390/molecules26237362
NLM
Hirata AS, Teixeira PR, Machado Neto JA, Jimenez PC, Clair JJL, Fenical W, Costa-Lotufo LV. Seriniquinones as therapeutic leads for treatment of BRAF and NRAS mutant melanomas [Internet]. Molecules. 2021 ; 26( 23): 1-15.[citado 2024 nov. 06 ] Available from: https://doi.org/10.3390/molecules26237362
Vancouver
Hirata AS, Teixeira PR, Machado Neto JA, Jimenez PC, Clair JJL, Fenical W, Costa-Lotufo LV. Seriniquinones as therapeutic leads for treatment of BRAF and NRAS mutant melanomas [Internet]. Molecules. 2021 ; 26( 23): 1-15.[citado 2024 nov. 06 ] Available from: https://doi.org/10.3390/molecules26237362
Artigo de periodico
The ‘in vivo lifestyle’ of bile acid 7α-dehydroxylating bacteria: comparative genomics, metatranscriptomic, and bile acid metabolomics analysis of a defined microbial community in gnotobiotic mice (2020)
Ridlon, Jason M. ; Devendram, Saravanan; Alves, João Marcelo Pereira ; Doden, Heidi ; Wolf, Patricia G. ; Pereira, Gabriel V. ; Ly, Lindsey; Volland, Alyssa; Takei, Hajime ; Nittono, Hiroshi; Murai, Tsuyoshi; Kurosawa, Takao ; Chlipala, George E. ; Green, Stefan J. ; Hernandez, Alvaro G. Hernandez ; Fields, Christopher J. ; Wright, Christy L. ; Kakiyama, Genta; Cann, Isaac ; Kashyap, Purna ; McCracken, Vance ; Gaskins, H. Rex
Source: Gut Microbes. Unidade: ICB
Subjects: PARASITOLOGIA, RNA, SEQUENCIAMENTO GENÉTICO, CLOSTRIDIUM, GENÔMICA, AMINOÁCIDOS, EXPRESSÃO GÊNICA
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ABNT
RIDLON, Jason M. et al. The ‘in vivo lifestyle’ of bile acid 7α-dehydroxylating bacteria: comparative genomics, metatranscriptomic, and bile acid metabolomics analysis of a defined microbial community in gnotobiotic mice. Gut Microbes, v. 11, n. 3, p. 381-404, 2020Tradução . . Disponível em: https://doi.org/10.1080/19490976.2019.1618173. Acesso em: 06 nov. 2024.
APA
Ridlon, J. M., Devendram, S., Alves, J. M. P., Doden, H., Wolf, P. G., Pereira, G. V., et al. (2020). The ‘in vivo lifestyle’ of bile acid 7α-dehydroxylating bacteria: comparative genomics, metatranscriptomic, and bile acid metabolomics analysis of a defined microbial community in gnotobiotic mice. Gut Microbes, 11( 3), 381-404. doi:10.1080/19490976.2019.1618173
NLM
Ridlon JM, Devendram S, Alves JMP, Doden H, Wolf PG, Pereira GV, Ly L, Volland A, Takei H, Nittono H, Murai T, Kurosawa T, Chlipala GE, Green SJ, Hernandez AGH, Fields CJ, Wright CL, Kakiyama G, Cann I, Kashyap P, McCracken V, Gaskins HR. The ‘in vivo lifestyle’ of bile acid 7α-dehydroxylating bacteria: comparative genomics, metatranscriptomic, and bile acid metabolomics analysis of a defined microbial community in gnotobiotic mice [Internet]. Gut Microbes. 2020 ; 11( 3): 381-404.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1080/19490976.2019.1618173
Vancouver
Ridlon JM, Devendram S, Alves JMP, Doden H, Wolf PG, Pereira GV, Ly L, Volland A, Takei H, Nittono H, Murai T, Kurosawa T, Chlipala GE, Green SJ, Hernandez AGH, Fields CJ, Wright CL, Kakiyama G, Cann I, Kashyap P, McCracken V, Gaskins HR. The ‘in vivo lifestyle’ of bile acid 7α-dehydroxylating bacteria: comparative genomics, metatranscriptomic, and bile acid metabolomics analysis of a defined microbial community in gnotobiotic mice [Internet]. Gut Microbes. 2020 ; 11( 3): 381-404.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1080/19490976.2019.1618173
Artigo de periodico
Tyrosine hydroxylase neurons regulate growth hormone secretion via short-loop negative feedback (2020)
Wasinski, Frederick ; Pedroso, João Alfredo Bolivar ; Santos, Willian Oliveira dos; Furigo, Isadora Clivatti ; Galiano, David Garcia ; Elias, Carol F. ; List, Edward O. ; Kopchick, John J.; Szawka, Raphael E. ; Donato Junior, José
Source: Journal of Neuroscience. Unidade: ICB
Subjects: FISIOLOGIA, CATECOLAMINAS, RECEPTORES DE DOPAMINA, RECEPTORES DE CATECOLAMINA, HIPOTÁLAMO, NEUROPEPTÍDEOS, AMINOÁCIDOS, CAMUNDONGOS, HORMÔNIO DO CRESCIMENTO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
WASINSKI, Frederick et al. Tyrosine hydroxylase neurons regulate growth hormone secretion via short-loop negative feedback. Journal of Neuroscience, v. 40, n. 22, p. 4309-4322, 2020Tradução . . Disponível em: https://doi.org/10.1523/JNEUROSCI.2531-19.2020. Acesso em: 06 nov. 2024.
APA
Wasinski, F., Pedroso, J. A. B., Santos, W. O. dos, Furigo, I. C., Galiano, D. G., Elias, C. F., et al. (2020). Tyrosine hydroxylase neurons regulate growth hormone secretion via short-loop negative feedback. Journal of Neuroscience, 40( 22), 4309-4322. doi:10.1523/JNEUROSCI.2531-19.2020
NLM
Wasinski F, Pedroso JAB, Santos WO dos, Furigo IC, Galiano DG, Elias CF, List EO, Kopchick JJ, Szawka RE, Donato Junior J. Tyrosine hydroxylase neurons regulate growth hormone secretion via short-loop negative feedback [Internet]. Journal of Neuroscience. 2020 ; 40( 22): 4309-4322.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1523/JNEUROSCI.2531-19.2020
Vancouver
Wasinski F, Pedroso JAB, Santos WO dos, Furigo IC, Galiano DG, Elias CF, List EO, Kopchick JJ, Szawka RE, Donato Junior J. Tyrosine hydroxylase neurons regulate growth hormone secretion via short-loop negative feedback [Internet]. Journal of Neuroscience. 2020 ; 40( 22): 4309-4322.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1523/JNEUROSCI.2531-19.2020
Artigo de periodico
Effect of protein denaturation and enzyme inhibitors on proteasomal-mediated production of peptides in human embryonic kidney cells (2019)
Dasgupta, Sayani ; Fishman, Michael A. ; Castro, Leandro M. ; Tashima, Alexandre Keiji ; Ferro, Emer Suavinho ; Fricker, Lloyd D.
Source: Biomolecules. Unidade: ICB
Subjects: FARMACOLOGIA, INIBIDORES DE ENZIMAS, PEPTÍDEOS, AMINOÁCIDOS, ESPECTROMETRIA DE MASSAS, RIM, EMBRIÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DASGUPTA, Sayani et al. Effect of protein denaturation and enzyme inhibitors on proteasomal-mediated production of peptides in human embryonic kidney cells. Biomolecules, v. 9, n. 6, p. 18, 2019Tradução . . Disponível em: https://doi.org/10.3390/biom9060207. Acesso em: 06 nov. 2024.
APA
Dasgupta, S., Fishman, M. A., Castro, L. M., Tashima, A. K., Ferro, E. S., & Fricker, L. D. (2019). Effect of protein denaturation and enzyme inhibitors on proteasomal-mediated production of peptides in human embryonic kidney cells. Biomolecules, 9( 6), 18. doi:10.3390/biom9060207
NLM
Dasgupta S, Fishman MA, Castro LM, Tashima AK, Ferro ES, Fricker LD. Effect of protein denaturation and enzyme inhibitors on proteasomal-mediated production of peptides in human embryonic kidney cells [Internet]. Biomolecules. 2019 ; 9( 6): 18.[citado 2024 nov. 06 ] Available from: https://doi.org/10.3390/biom9060207
Vancouver
Dasgupta S, Fishman MA, Castro LM, Tashima AK, Ferro ES, Fricker LD. Effect of protein denaturation and enzyme inhibitors on proteasomal-mediated production of peptides in human embryonic kidney cells [Internet]. Biomolecules. 2019 ; 9( 6): 18.[citado 2024 nov. 06 ] Available from: https://doi.org/10.3390/biom9060207
Artigo de periodico
Novel avian paramyxovirus (APMV-15) isolated from a migratory bird in South America (2017)
Thomazelli, Luciano Matsumiya ; Araujo, Jansen de ; Fabrizio, Thomas ; Walker, David; Reischak, Dilmara ; Ometto, Tatiana ; Barbosa, Carla Meneguin ; Petry, Maria Virginia ; Webby, Richard J. ; Durigon, Edison Luiz
Source: PL o S One. Unidades: ICB, BIOTECNOLOGIA
Subjects: MICROBIOLOGIA, AVES, PARAMYXOVIRUS, GENÉTICA ANIMAL, NUCLEOTÍDEOS, GENOMAS, SEQUENCIAMENTO GENÉTICO, AMINOÁCIDOS, FILOGENIA, GENÉTICA ANIMAL, GENES VIRAIS, VÍRUS DE RNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
THOMAZELLI, Luciano Matsumiya et al. Novel avian paramyxovirus (APMV-15) isolated from a migratory bird in South America. PL o S One, v. 12, n. 5, p. 7 , 2017Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0177214. Acesso em: 06 nov. 2024.
APA
Thomazelli, L. M., Araujo, J. de, Fabrizio, T., Walker, D., Reischak, D., Ometto, T., et al. (2017). Novel avian paramyxovirus (APMV-15) isolated from a migratory bird in South America. PL o S One, 12( 5), 7 . doi:10.1371/journal.pone.0177214
NLM
Thomazelli LM, Araujo J de, Fabrizio T, Walker D, Reischak D, Ometto T, Barbosa CM, Petry MV, Webby RJ, Durigon EL. Novel avian paramyxovirus (APMV-15) isolated from a migratory bird in South America [Internet]. PL o S One. 2017 ; 12( 5): 7 .[citado 2024 nov. 06 ] Available from: https://doi.org/10.1371/journal.pone.0177214
Vancouver
Thomazelli LM, Araujo J de, Fabrizio T, Walker D, Reischak D, Ometto T, Barbosa CM, Petry MV, Webby RJ, Durigon EL. Novel avian paramyxovirus (APMV-15) isolated from a migratory bird in South America [Internet]. PL o S One. 2017 ; 12( 5): 7 .[citado 2024 nov. 06 ] Available from: https://doi.org/10.1371/journal.pone.0177214
Artigo de periodico
Alterations of the intracellular peptidome in response to the proteasome inhibitor bortezomib (2013)
Gelman, Julia S.; Sironi, Juan ; Berezniuk, Iryna; Dasgupta, Sayani ; Castro, Leandro Mantovani de ; Gozzo, Fabio Cesar ; Ferro, Emer Suavinho ; Fricker, Lloyd D.
Source: Plos One. Unidade: ICB
Subjects: HISTOLOGIA, PEPTÍDEOS, NEUROBLASTOMA, ANTINEOPLÁSICOS, AMINOÁCIDOS, CÉLULAS CULTIVADAS DE TUMOR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GELMAN, Julia S. et al. Alterations of the intracellular peptidome in response to the proteasome inhibitor bortezomib. Plos One, v. 8, n. 1, p. 1-13, 2013Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0053263. Acesso em: 06 nov. 2024.
APA
Gelman, J. S., Sironi, J., Berezniuk, I., Dasgupta, S., Castro, L. M. de, Gozzo, F. C., et al. (2013). Alterations of the intracellular peptidome in response to the proteasome inhibitor bortezomib. Plos One, 8( 1), 1-13. doi:10.1371/journal.pone.0053263
NLM
Gelman JS, Sironi J, Berezniuk I, Dasgupta S, Castro LM de, Gozzo FC, Ferro ES, Fricker LD. Alterations of the intracellular peptidome in response to the proteasome inhibitor bortezomib [Internet]. Plos One. 2013 ; 8( 1): 1-13.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1371/journal.pone.0053263
Vancouver
Gelman JS, Sironi J, Berezniuk I, Dasgupta S, Castro LM de, Gozzo FC, Ferro ES, Fricker LD. Alterations of the intracellular peptidome in response to the proteasome inhibitor bortezomib [Internet]. Plos One. 2013 ; 8( 1): 1-13.[citado 2024 nov. 06 ] Available from: https://doi.org/10.1371/journal.pone.0053263

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