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Artigo de periodico
Potential colchicine binding site inhibitors unraveled by virtual screening, molecular dynamics and MM/PBSA (2021)
Federico, Leonardo Bruno ; Silva, Guilherme Martins da ; Gomes, Suzane Quintana ; Francischini, Isaque Antônio Galindo ; Barcelos, Mariana Pegrucci ; Santos, Cleydson Breno Rodrigues dos; Costa, Luciano Tavares da; Rosa, Joaquín Maria Campos; Silva, Carlos Henrique Tomich de Paula da
Source: Computers in Biology and Medicine. Unidades: FCFRP, FFCLRP
Subjects: SÍTIOS DE LIGAÇÃO, ALCALOIDES, MICROTÚBULOS
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FEDERICO, Leonardo Bruno et al. Potential colchicine binding site inhibitors unraveled by virtual screening, molecular dynamics and MM/PBSA. Computers in Biology and Medicine, v. 137, p. 1-11, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.compbiomed.2021.104817. Acesso em: 20 out. 2024.
APA
Federico, L. B., Silva, G. M. da, Gomes, S. Q., Francischini, I. A. G., Barcelos, M. P., Santos, C. B. R. dos, et al. (2021). Potential colchicine binding site inhibitors unraveled by virtual screening, molecular dynamics and MM/PBSA. Computers in Biology and Medicine, 137, 1-11. doi:10.1016/j.compbiomed.2021.104817
NLM
Federico LB, Silva GM da, Gomes SQ, Francischini IAG, Barcelos MP, Santos CBR dos, Costa LT da, Rosa JMC, Silva CHT de P da. Potential colchicine binding site inhibitors unraveled by virtual screening, molecular dynamics and MM/PBSA [Internet]. Computers in Biology and Medicine. 2021 ; 137 1-11.[citado 2024 out. 20 ] Available from: https://doi.org/10.1016/j.compbiomed.2021.104817
Vancouver
Federico LB, Silva GM da, Gomes SQ, Francischini IAG, Barcelos MP, Santos CBR dos, Costa LT da, Rosa JMC, Silva CHT de P da. Potential colchicine binding site inhibitors unraveled by virtual screening, molecular dynamics and MM/PBSA [Internet]. Computers in Biology and Medicine. 2021 ; 137 1-11.[citado 2024 out. 20 ] Available from: https://doi.org/10.1016/j.compbiomed.2021.104817
Artigo de periodico
License to LAP (2021)
Cunha, Larissa Dias da
Source: Cell Host & Microbe. Unidade: FMRP
Subjects: DEGRANULAÇÃO CELULAR, IMUNIDADE, PROTEÍNAS, MICROTÚBULOS, FAGOCITOSE
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CUNHA, Larissa Dias da. License to LAP. Cell Host & Microbe, v. 29, n. 8, p. 1216-1217, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.chom.2021.07.010. Acesso em: 20 out. 2024.
APA
Cunha, L. D. da. (2021). License to LAP. Cell Host & Microbe, 29( 8), 1216-1217. doi:10.1016/j.chom.2021.07.010
NLM
Cunha LD da. License to LAP [Internet]. Cell Host & Microbe. 2021 ; 29( 8): 1216-1217.[citado 2024 out. 20 ] Available from: https://doi.org/10.1016/j.chom.2021.07.010
Vancouver
Cunha LD da. License to LAP [Internet]. Cell Host & Microbe. 2021 ; 29( 8): 1216-1217.[citado 2024 out. 20 ] Available from: https://doi.org/10.1016/j.chom.2021.07.010
Artigo de periodico
AD80, a multikinase inhibitor, exhibits antineoplastic effects in acute leukemia cellular models targeting the PI3K/STMN1 axis (2021)
Carlos, Jorge Antonio Elias Godoy; Lima, Kely; Costa-Lotufo, Letícia Veras ; Leitão, Andrei ; Machado Neto, João Agostinho
Source: Investigational New Drugs. Unidades: ICB, IQSC
Subjects: FARMACOLOGIA, LEUCEMIA, ANTINEOPLÁSICOS, FOSFOPROTEÍNAS, MICROTÚBULOS, CÉLULAS CULTIVADAS DE TUMOR, PROLIFERAÇÃO CELULAR, CITOESQUELETO
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CARLOS, Jorge Antonio Elias Godoy et al. AD80, a multikinase inhibitor, exhibits antineoplastic effects in acute leukemia cellular models targeting the PI3K/STMN1 axis. Investigational New Drugs, v. 39, n. 4, p. 1139-1149, 2021Tradução . . Disponível em: https://doi.org/10.1007/s10637-021-01066-w. Acesso em: 20 out. 2024.
APA
Carlos, J. A. E. G., Lima, K., Costa-Lotufo, L. V., Leitão, A., & Machado Neto, J. A. (2021). AD80, a multikinase inhibitor, exhibits antineoplastic effects in acute leukemia cellular models targeting the PI3K/STMN1 axis. Investigational New Drugs, 39( 4), 1139-1149. doi:10.1007/s10637-021-01066-w
NLM
Carlos JAEG, Lima K, Costa-Lotufo LV, Leitão A, Machado Neto JA. AD80, a multikinase inhibitor, exhibits antineoplastic effects in acute leukemia cellular models targeting the PI3K/STMN1 axis [Internet]. Investigational New Drugs. 2021 ; 39( 4): 1139-1149.[citado 2024 out. 20 ] Available from: https://doi.org/10.1007/s10637-021-01066-w
Vancouver
Carlos JAEG, Lima K, Costa-Lotufo LV, Leitão A, Machado Neto JA. AD80, a multikinase inhibitor, exhibits antineoplastic effects in acute leukemia cellular models targeting the PI3K/STMN1 axis [Internet]. Investigational New Drugs. 2021 ; 39( 4): 1139-1149.[citado 2024 out. 20 ] Available from: https://doi.org/10.1007/s10637-021-01066-w
Artigo de periodico
Stathmin 1 is highly expressed and associated with survival outcome in malignant adrenocortical tumours (2020)
Passaia, Bárbara dos Santos; Lima, Keli ; Kremer, Jean Lucas ; Conceição, Barbara Brito da ; Mariani, Beatriz Marinho de Paula ; Silva, Jean Carlos Lipreri da ; Zerbini, Maria Claudia Nogueira ; Fragoso, Maria Candida Barisson Villares ; Machado Neto, João Agostinho ; Lotfi, Claudimara Ferini Pacicco
Source: Investigational New Drugs. Unidades: FM, ICB
Subjects: ANATOMIA, FARMACOLOGIA, CÉLULAS CULTIVADAS DE TUMOR, CARCINOMA, NEOPLASIA ENDÓCRINA MÚLTIPLA, MICROTÚBULOS, FENÓTIPOS, CLONAGEM, ONCOPROTEÍNAS
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PASSAIA, Bárbara dos Santos et al. Stathmin 1 is highly expressed and associated with survival outcome in malignant adrenocortical tumours. Investigational New Drugs, v. 38, p. 899–908, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10637-019-00846-9. Acesso em: 20 out. 2024.
APA
Passaia, B. dos S., Lima, K., Kremer, J. L., Conceição, B. B. da, Mariani, B. M. de P., Silva, J. C. L. da, et al. (2020). Stathmin 1 is highly expressed and associated with survival outcome in malignant adrenocortical tumours. Investigational New Drugs, 38, 899–908. doi:10.1007/s10637-019-00846-9
NLM
Passaia B dos S, Lima K, Kremer JL, Conceição BB da, Mariani BM de P, Silva JCL da, Zerbini MCN, Fragoso MCBV, Machado Neto JA, Lotfi CFP. Stathmin 1 is highly expressed and associated with survival outcome in malignant adrenocortical tumours [Internet]. Investigational New Drugs. 2020 ; 38 899–908.[citado 2024 out. 20 ] Available from: https://doi.org/10.1007/s10637-019-00846-9
Vancouver
Passaia B dos S, Lima K, Kremer JL, Conceição BB da, Mariani BM de P, Silva JCL da, Zerbini MCN, Fragoso MCBV, Machado Neto JA, Lotfi CFP. Stathmin 1 is highly expressed and associated with survival outcome in malignant adrenocortical tumours [Internet]. Investigational New Drugs. 2020 ; 38 899–908.[citado 2024 out. 20 ] Available from: https://doi.org/10.1007/s10637-019-00846-9
Artigo de periodico
Biological effects of an oxyphytosterol generated by β-Sitosterol ozonization (2020)
Takayasu, Bianca Sayuri ; Martins, Igor R. ; Garnique, Anali Del Milagro Bernabe ; Miyamoto, Sayuri ; Santelli, Glaucia Maria Machado ; Uemi, Miriam ; Onuki, Janina
Source: Archives of Biochemistry and Biophysics. Unidades: IQ, ICB
Subjects: ÓLEOS VEGETAIS, BIOQUÍMICA, BIOFÍSICA, BIOLOGIA CELULAR, CITOMETRIA DE FLUXO, MICROSCOPIA CONFOCAL, MICROSCOPIA DE FLUORESCÊNCIA, MICROTÚBULOS, ESTRESSE OXIDATIVO
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TAKAYASU, Bianca Sayuri et al. Biological effects of an oxyphytosterol generated by β-Sitosterol ozonization. Archives of Biochemistry and Biophysics, v. 695, p. 1-10 art. 108654, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.abb.2020.108654. Acesso em: 20 out. 2024.
APA
Takayasu, B. S., Martins, I. R., Garnique, A. D. M. B., Miyamoto, S., Santelli, G. M. M., Uemi, M., & Onuki, J. (2020). Biological effects of an oxyphytosterol generated by β-Sitosterol ozonization. Archives of Biochemistry and Biophysics, 695, 1-10 art. 108654. doi:10.1016/j.abb.2020.108654
NLM
Takayasu BS, Martins IR, Garnique ADMB, Miyamoto S, Santelli GMM, Uemi M, Onuki J. Biological effects of an oxyphytosterol generated by β-Sitosterol ozonization [Internet]. Archives of Biochemistry and Biophysics. 2020 ; 695 1-10 art. 108654.[citado 2024 out. 20 ] Available from: https://doi.org/10.1016/j.abb.2020.108654
Vancouver
Takayasu BS, Martins IR, Garnique ADMB, Miyamoto S, Santelli GMM, Uemi M, Onuki J. Biological effects of an oxyphytosterol generated by β-Sitosterol ozonization [Internet]. Archives of Biochemistry and Biophysics. 2020 ; 695 1-10 art. 108654.[citado 2024 out. 20 ] Available from: https://doi.org/10.1016/j.abb.2020.108654
Artigo de periodico
Genetic risk for Alzheimer's disease and functional brain connectivity in children and adolescents (2019)
Axelrud, Luiza Kvitko; Sato, Joao Ricardo; Santoro, Marcos Leite; Talarico, Fernanda; Pine, Daniel Samuel; Rohde, Luis Augusto; Zugman, Andre; Amaro Junior, Edson ; Bressan, Rodrigo Affonseca; Miguel Filho, Eurípedes Constantino
Source: Neurobiology of aging. Unidade: FM
Subjects: DOENÇA DE ALZHEIMER, MICROTÚBULOS, RISCO, GENÓTIPOS, NEUROIMAGEM, COGNIÇÃO, FUNÇÃO EXECUTIVA, ADEREÇOS, CRIANÇAS
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AXELRUD, Luiza Kvitko et al. Genetic risk for Alzheimer's disease and functional brain connectivity in children and adolescents. Neurobiology of aging, v. 82, p. 10-17, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.neurobiolaging.2019.06.011. Acesso em: 20 out. 2024.
APA
Axelrud, L. K., Sato, J. R., Santoro, M. L., Talarico, F., Pine, D. S., Rohde, L. A., et al. (2019). Genetic risk for Alzheimer's disease and functional brain connectivity in children and adolescents. Neurobiology of aging, 82, 10-17. doi:10.1016/j.neurobiolaging.2019.06.011
NLM
Axelrud LK, Sato JR, Santoro ML, Talarico F, Pine DS, Rohde LA, Zugman A, Amaro Junior E, Bressan RA, Miguel Filho EC. Genetic risk for Alzheimer's disease and functional brain connectivity in children and adolescents [Internet]. Neurobiology of aging. 2019 ; 82 10-17.[citado 2024 out. 20 ] Available from: https://doi.org/10.1016/j.neurobiolaging.2019.06.011
Vancouver
Axelrud LK, Sato JR, Santoro ML, Talarico F, Pine DS, Rohde LA, Zugman A, Amaro Junior E, Bressan RA, Miguel Filho EC. Genetic risk for Alzheimer's disease and functional brain connectivity in children and adolescents [Internet]. Neurobiology of aging. 2019 ; 82 10-17.[citado 2024 out. 20 ] Available from: https://doi.org/10.1016/j.neurobiolaging.2019.06.011
Artigo de periodico
Graphene oxide-based nanomaterial interaction with human breast cancer cells (2019)
Ribeiro, Beatriz Fumelli Monti ; Souza, Marcelo Medina de; Fernandes, Daniela Silvestrini ; Carmo, Devaney Ribeiro do ; Santelli, Glaucia Maria Machado
Source: Journal of Biomedical Materials Research. Part A (Online). Unidade: ICB
Subjects: BIOLOGIA CELULAR, CÉLULAS CULTIVADAS DE TUMOR, NEOPLASIAS MAMÁRIAS, CARBONO, PROLIFERAÇÃO CELULAR, INTERAÇÃO CELULAR, NANOPARTÍCULAS, MICROTÚBULOS
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RIBEIRO, Beatriz Fumelli Monti et al. Graphene oxide-based nanomaterial interaction with human breast cancer cells. Journal of Biomedical Materials Research. Part A (Online), p. 8 , 2019Tradução . . Disponível em: https://doi.org/10.1002/jbm.a.36864. Acesso em: 20 out. 2024.
APA
Ribeiro, B. F. M., Souza, M. M. de, Fernandes, D. S., Carmo, D. R. do, & Santelli, G. M. M. (2019). Graphene oxide-based nanomaterial interaction with human breast cancer cells. Journal of Biomedical Materials Research. Part A (Online), 8 . doi:10.1002/jbm.a.36864
NLM
Ribeiro BFM, Souza MM de, Fernandes DS, Carmo DR do, Santelli GMM. Graphene oxide-based nanomaterial interaction with human breast cancer cells [Internet]. Journal of Biomedical Materials Research. Part A (Online). 2019 ;8 .[citado 2024 out. 20 ] Available from: https://doi.org/10.1002/jbm.a.36864
Vancouver
Ribeiro BFM, Souza MM de, Fernandes DS, Carmo DR do, Santelli GMM. Graphene oxide-based nanomaterial interaction with human breast cancer cells [Internet]. Journal of Biomedical Materials Research. Part A (Online). 2019 ;8 .[citado 2024 out. 20 ] Available from: https://doi.org/10.1002/jbm.a.36864
Artigo de periodico
A molecular modeling study of combretastatin-like chalcones as anticancer agents using PLS, ANN and consensus models (2018)
Lipinski, Célio Fernando; Oliveira, Aline Alves; Honorio, Kathia Maria; Oliveira, Patrícia Rufino; Silva, Alberico Borges Ferreira da
Source: Structural Chemistry: computational and experimental studies of chemical and biological systems. Unidades: EACH, IQSC
Subjects: MICROTÚBULOS, NEOPLASIAS, BIOLOGIA MOLECULAR
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LIPINSKI, Célio Fernando et al. A molecular modeling study of combretastatin-like chalcones as anticancer agents using PLS, ANN and consensus models. Structural Chemistry: computational and experimental studies of chemical and biological systems, v. 29, p. 01-09, 2018Tradução . . Disponível em: https://doi.org/10.1007/s11224-017-1072-2. Acesso em: 20 out. 2024.
APA
Lipinski, C. F., Oliveira, A. A., Honorio, K. M., Oliveira, P. R., & Silva, A. B. F. da. (2018). A molecular modeling study of combretastatin-like chalcones as anticancer agents using PLS, ANN and consensus models. Structural Chemistry: computational and experimental studies of chemical and biological systems, 29, 01-09. doi:10.1007/s11224-017-1072-2
NLM
Lipinski CF, Oliveira AA, Honorio KM, Oliveira PR, Silva ABF da. A molecular modeling study of combretastatin-like chalcones as anticancer agents using PLS, ANN and consensus models [Internet]. Structural Chemistry: computational and experimental studies of chemical and biological systems. 2018 ; 29 01-09.[citado 2024 out. 20 ] Available from: https://doi.org/10.1007/s11224-017-1072-2
Vancouver
Lipinski CF, Oliveira AA, Honorio KM, Oliveira PR, Silva ABF da. A molecular modeling study of combretastatin-like chalcones as anticancer agents using PLS, ANN and consensus models [Internet]. Structural Chemistry: computational and experimental studies of chemical and biological systems. 2018 ; 29 01-09.[citado 2024 out. 20 ] Available from: https://doi.org/10.1007/s11224-017-1072-2
Artigo de periodico
Discovery of a series of acridinones as mechanism-based tubulin assembly inhibitors with anticancer activity (2016)
Magalhães, Luma G.; Marques, Fernando B.; Fonseca, Marina B.; Rogério, Kamilla R.; Graebin, Cedric S.; Andricopulo, Adriano Defini
Source: PLOS One. Unidade: IFSC
Subjects: NEOPLASIAS, MICROTÚBULOS, PRODUTOS NATURAIS
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ABNT
MAGALHÃES, Luma G. et al. Discovery of a series of acridinones as mechanism-based tubulin assembly inhibitors with anticancer activity. PLOS One, v. 11, n. 8, p. e0160842-1-e0160842-17, 2016Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0160842. Acesso em: 20 out. 2024.
APA
Magalhães, L. G., Marques, F. B., Fonseca, M. B., Rogério, K. R., Graebin, C. S., & Andricopulo, A. D. (2016). Discovery of a series of acridinones as mechanism-based tubulin assembly inhibitors with anticancer activity. PLOS One, 11( 8), e0160842-1-e0160842-17. doi:10.1371/journal.pone.0160842
NLM
Magalhães LG, Marques FB, Fonseca MB, Rogério KR, Graebin CS, Andricopulo AD. Discovery of a series of acridinones as mechanism-based tubulin assembly inhibitors with anticancer activity [Internet]. PLOS One. 2016 ; 11( 8): e0160842-1-e0160842-17.[citado 2024 out. 20 ] Available from: https://doi.org/10.1371/journal.pone.0160842
Vancouver
Magalhães LG, Marques FB, Fonseca MB, Rogério KR, Graebin CS, Andricopulo AD. Discovery of a series of acridinones as mechanism-based tubulin assembly inhibitors with anticancer activity [Internet]. PLOS One. 2016 ; 11( 8): e0160842-1-e0160842-17.[citado 2024 out. 20 ] Available from: https://doi.org/10.1371/journal.pone.0160842
Trabalho de evento-resumo
Identification of a new class of microtubule polymerization inhibitors for the treatment of cancer (2013)
Santos, Ricardo N.; Fernandes, Daniara C.; Altei, Wanessa F.; Santos, Marilia S.; Rodrigues Junior, Manoel Trindade; Coelho, Fernando; Andricopulo, Adriano Defini
Source: Abstracts. Conference titles: Spring National Meeting and Exposition. Unidade: IFSC
Subjects: MICROTÚBULOS, NEOPLASIAS (TRATAMENTO), POLIMERIZAÇÃO
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ABNT
SANTOS, Ricardo N. et al. Identification of a new class of microtubule polymerization inhibitors for the treatment of cancer. 2013, Anais.. Washington, DC: American Chemical Society - ACS, 2013. . Acesso em: 20 out. 2024.
APA
Santos, R. N., Fernandes, D. C., Altei, W. F., Santos, M. S., Rodrigues Junior, M. T., Coelho, F., & Andricopulo, A. D. (2013). Identification of a new class of microtubule polymerization inhibitors for the treatment of cancer. In Abstracts. Washington, DC: American Chemical Society - ACS.
NLM
Santos RN, Fernandes DC, Altei WF, Santos MS, Rodrigues Junior MT, Coelho F, Andricopulo AD. Identification of a new class of microtubule polymerization inhibitors for the treatment of cancer. Abstracts. 2013 ;[citado 2024 out. 20 ]
Vancouver
Santos RN, Fernandes DC, Altei WF, Santos MS, Rodrigues Junior MT, Coelho F, Andricopulo AD. Identification of a new class of microtubule polymerization inhibitors for the treatment of cancer. Abstracts. 2013 ;[citado 2024 out. 20 ]
Artigo de periodico
Parthenogenetic activation of bovine oocytes using single and combined strontium, ionomycin and 6-dimethylaminopurine treatments (2007)
Méo, Simone Cristina; Yamazaki, W.; Ferreira, C. R.; Perecin, F.; Saraiva, N. Z.; Leal, Cláudia Lima Verde; Garcia, J. M.
Source: Zygote. Unidade: FZEA
Subjects: BOVINOS, CROMATINA, EMBRIÃO DE ANIMAL (DESENVOLVIMENTO), MICROTÚBULOS, OÓCITOS
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MÉO, Simone Cristina et al. Parthenogenetic activation of bovine oocytes using single and combined strontium, ionomycin and 6-dimethylaminopurine treatments. Zygote, v. No 2007, n. 4, p. 295-306, 2007Tradução . . Disponível em: https://doi.org/10.1017/s0967199407004285. Acesso em: 20 out. 2024.
APA
Méo, S. C., Yamazaki, W., Ferreira, C. R., Perecin, F., Saraiva, N. Z., Leal, C. L. V., & Garcia, J. M. (2007). Parthenogenetic activation of bovine oocytes using single and combined strontium, ionomycin and 6-dimethylaminopurine treatments. Zygote, No 2007( 4), 295-306. doi:10.1017/s0967199407004285
NLM
Méo SC, Yamazaki W, Ferreira CR, Perecin F, Saraiva NZ, Leal CLV, Garcia JM. Parthenogenetic activation of bovine oocytes using single and combined strontium, ionomycin and 6-dimethylaminopurine treatments [Internet]. Zygote. 2007 ; No 2007( 4): 295-306.[citado 2024 out. 20 ] Available from: https://doi.org/10.1017/s0967199407004285
Vancouver
Méo SC, Yamazaki W, Ferreira CR, Perecin F, Saraiva NZ, Leal CLV, Garcia JM. Parthenogenetic activation of bovine oocytes using single and combined strontium, ionomycin and 6-dimethylaminopurine treatments [Internet]. Zygote. 2007 ; No 2007( 4): 295-306.[citado 2024 out. 20 ] Available from: https://doi.org/10.1017/s0967199407004285

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