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PIVETTA, Thais P. et al. Nanoparticle systems for cancer phototherapy: an overview. Nanomaterials, v. 11, n. 11, p. 1-37, 2021Tradução . . Disponível em: https://doi.org/10.3390/nano11113132. Acesso em: 28 mar. 2024.
APA
Pivetta, T. P., Botteon, C. E. A., Ribeiro, P. A., Marcato, P. D., & Raposo, M. (2021). Nanoparticle systems for cancer phototherapy: an overview. Nanomaterials, 11( 11), 1-37. doi:10.3390/nano11113132
NLM
Pivetta TP, Botteon CEA, Ribeiro PA, Marcato PD, Raposo M. Nanoparticle systems for cancer phototherapy: an overview [Internet]. Nanomaterials. 2021 ; 11( 11): 1-37.[citado 2024 mar. 28 ] Available from: https://doi.org/10.3390/nano11113132
Vancouver
Pivetta TP, Botteon CEA, Ribeiro PA, Marcato PD, Raposo M. Nanoparticle systems for cancer phototherapy: an overview [Internet]. Nanomaterials. 2021 ; 11( 11): 1-37.[citado 2024 mar. 28 ] Available from: https://doi.org/10.3390/nano11113132
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Chimeric antigen receptor T Cells: development and production. . New York: Humana Press. Disponível em: https://doi.org/10.1007/978-1-0716-0146-4. Acesso em: 28 mar. 2024. , 2020
APA
Chimeric antigen receptor T Cells: development and production. (2020). Chimeric antigen receptor T Cells: development and production. New York: Humana Press. doi:10.1007/978-1-0716-0146-4
NLM
Chimeric antigen receptor T Cells: development and production [Internet]. 2020 ;[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
Vancouver
Chimeric antigen receptor T Cells: development and production [Internet]. 2020 ;[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
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Chimeric antigen receptor T Cell: development and production. . New York: Humana Press. Disponível em: https://doi.org/10.1007/978-1-0716-0146-4. Acesso em: 28 mar. 2024. , 2020
APA
Chimeric antigen receptor T Cell: development and production. (2020). Chimeric antigen receptor T Cell: development and production. New York: Humana Press. doi:10.1007/978-1-0716-0146-4
NLM
Chimeric antigen receptor T Cell: development and production [Internet]. 2020 ;[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
Vancouver
Chimeric antigen receptor T Cell: development and production [Internet]. 2020 ;[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
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SWIECH, Kamilla e MALMEGRIM, Kelen Cristina Ribeiro e PICANÇO-CASTRO, Virgínia. Immunotherapy is a treatment that boosts the body’s natural defenses to fight cancer. [Prefácio]. Chimeric antigen receptor T Cell: development and production. New York: Humana Press. Disponível em: https://doi.org/10.1007/978-1-0716-0146-4. Acesso em: 28 mar. 2024. , 2020
APA
Swiech, K., Malmegrim, K. C. R., & Picanço-Castro, V. (2020). Immunotherapy is a treatment that boosts the body’s natural defenses to fight cancer. [Prefácio]. Chimeric antigen receptor T Cell: development and production. New York: Humana Press. doi:10.1007/978-1-0716-0146-4
NLM
Swiech K, Malmegrim KCR, Picanço-Castro V. Immunotherapy is a treatment that boosts the body’s natural defenses to fight cancer. [Prefácio] [Internet]. Chimeric antigen receptor T Cell: development and production. 2020 ;274 .[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
Vancouver
Swiech K, Malmegrim KCR, Picanço-Castro V. Immunotherapy is a treatment that boosts the body’s natural defenses to fight cancer. [Prefácio] [Internet]. Chimeric antigen receptor T Cell: development and production. 2020 ;274 .[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
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MEHDIPOUR, Parinaz et al. Epigenetic therapy induces transcription of inverted SINEs and ADAR1 dependency. Nature, v. 588, n. 7836, p. 169-173, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41586-020-2844-1. Acesso em: 28 mar. 2024.
APA
Mehdipour, P., Marhon, S. A., Ettayebi, I., Chakravarthy, A., Hosseini, A., Wang, Y., et al. (2020). Epigenetic therapy induces transcription of inverted SINEs and ADAR1 dependency. Nature, 588( 7836), 169-173. doi:10.1038/s41586-020-2844-1
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Mehdipour P, Marhon SA, Ettayebi I, Chakravarthy A, Hosseini A, Wang Y, Castro FA de, Loo Yau H, Ishak C, Abelson S, O’Brien CA, Carvalho DD de. Epigenetic therapy induces transcription of inverted SINEs and ADAR1 dependency [Internet]. Nature. 2020 ; 588( 7836): 169-173.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1038/s41586-020-2844-1
Vancouver
Mehdipour P, Marhon SA, Ettayebi I, Chakravarthy A, Hosseini A, Wang Y, Castro FA de, Loo Yau H, Ishak C, Abelson S, O’Brien CA, Carvalho DD de. Epigenetic therapy induces transcription of inverted SINEs and ADAR1 dependency [Internet]. Nature. 2020 ; 588( 7836): 169-173.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1038/s41586-020-2844-1
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SANTOS, Neife Aparecida Guinaim dos e FERREIRA, Rafaela Scalco e SANTOS, Antônio Cardozo dos. Overview of cisplatin-induced neurotoxicity and ototoxicity, and the protective agents. Food and Chemical Toxicology, v. 136, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2019.111079. Acesso em: 28 mar. 2024.
APA
Santos, N. A. G. dos, Ferreira, R. S., & Santos, A. C. dos. (2020). Overview of cisplatin-induced neurotoxicity and ototoxicity, and the protective agents. Food and Chemical Toxicology, 136. doi:10.1016/j.fct.2019.111079
NLM
Santos NAG dos, Ferreira RS, Santos AC dos. Overview of cisplatin-induced neurotoxicity and ototoxicity, and the protective agents [Internet]. Food and Chemical Toxicology. 2020 ; 136[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.fct.2019.111079
Vancouver
Santos NAG dos, Ferreira RS, Santos AC dos. Overview of cisplatin-induced neurotoxicity and ototoxicity, and the protective agents [Internet]. Food and Chemical Toxicology. 2020 ; 136[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.fct.2019.111079
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AZEVEDO, Júlia Teixeira Cottas de et al. Immunophenotypic analysis of CAR-T cells. Chimeric antigen receptor T Cell: development and production. Tradução . New York: Humana Press, 2020. p. 274 . Disponível em: https://doi.org/10.1007/978-1-0716-0146-4. Acesso em: 28 mar. 2024.
APA
Azevedo, J. T. C. de, Mizukami, A., Moço, P. D., & Malmegrim, K. C. R. (2020). Immunophenotypic analysis of CAR-T cells. In Chimeric antigen receptor T Cell: development and production (p. 274 ). New York: Humana Press. doi:10.1007/978-1-0716-0146-4
NLM
Azevedo JTC de, Mizukami A, Moço PD, Malmegrim KCR. Immunophenotypic analysis of CAR-T cells [Internet]. In: Chimeric antigen receptor T Cell: development and production. New York: Humana Press; 2020. p. 274 .[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
Vancouver
Azevedo JTC de, Mizukami A, Moço PD, Malmegrim KCR. Immunophenotypic analysis of CAR-T cells [Internet]. In: Chimeric antigen receptor T Cell: development and production. New York: Humana Press; 2020. p. 274 .[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
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OLIVEIRA, Herick Ulisses de et al. Investigation of the involvement of the endocannabinoid system in TENS-induced antinociception. The Journal of Pain, v. 21, n. 7/8, p. 820-835, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.jpain.2019.11.009. Acesso em: 28 mar. 2024.
APA
Oliveira, H. U. de, Santos, R. S. dos, Malta, I. H. S., Pinho, J. P., Almeida, A. F. S., Sorgi, C. A., et al. (2020). Investigation of the involvement of the endocannabinoid system in TENS-induced antinociception. The Journal of Pain, 21( 7/8), 820-835. doi:10.1016/j.jpain.2019.11.009
NLM
Oliveira HU de, Santos RS dos, Malta IHS, Pinho JP, Almeida AFS, Sorgi CA, Peti APF, Xavier GS, Reis LM dos, Faccioli LH, Cruz J dos S, Ferreira E, Galdino G. Investigation of the involvement of the endocannabinoid system in TENS-induced antinociception [Internet]. The Journal of Pain. 2020 ; 21( 7/8): 820-835.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.jpain.2019.11.009
Vancouver
Oliveira HU de, Santos RS dos, Malta IHS, Pinho JP, Almeida AFS, Sorgi CA, Peti APF, Xavier GS, Reis LM dos, Faccioli LH, Cruz J dos S, Ferreira E, Galdino G. Investigation of the involvement of the endocannabinoid system in TENS-induced antinociception [Internet]. The Journal of Pain. 2020 ; 21( 7/8): 820-835.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.jpain.2019.11.009
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CASTRO, Kelly Aparecida Dias de Freitas et al. Photodynamic treatment of melanoma cells using aza-dipyrromethenes as photosensitizers. Photochemical & Photobiological Sciences, v. 19, n. 7, p. 885-891, 2020Tradução . . Disponível em: https://doi.org/10.1039/d0pp00114g. Acesso em: 28 mar. 2024.
APA
Castro, K. A. D. de F., Costa, L. D., Guieu, S., Biazzotto, J. C., Neves, M. G. P. M. S. da, Faustino, M. A. F., et al. (2020). Photodynamic treatment of melanoma cells using aza-dipyrromethenes as photosensitizers. Photochemical & Photobiological Sciences, 19( 7), 885-891. doi:10.1039/d0pp00114g
NLM
Castro KAD de F, Costa LD, Guieu S, Biazzotto JC, Neves MGPMS da, Faustino MAF, Silva RS da, Tomé AC. Photodynamic treatment of melanoma cells using aza-dipyrromethenes as photosensitizers [Internet]. Photochemical & Photobiological Sciences. 2020 ; 19( 7): 885-891.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1039/d0pp00114g
Vancouver
Castro KAD de F, Costa LD, Guieu S, Biazzotto JC, Neves MGPMS da, Faustino MAF, Silva RS da, Tomé AC. Photodynamic treatment of melanoma cells using aza-dipyrromethenes as photosensitizers [Internet]. Photochemical & Photobiological Sciences. 2020 ; 19( 7): 885-891.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1039/d0pp00114g
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SANTOS, Daiane Fernanda dos et al. Non-cytotoxic 1,2,3-triazole tethered fused heterocyclic ring derivatives display Tax protein inhibition and impair HTLV-1 infected cells. Bioorganic & Medicinal Chemistry, v. 28, n. 22, p. 1-9, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2020.115746. Acesso em: 28 mar. 2024.
APA
Santos, D. F. dos, Pilger, D. R. B. de, Vandermeulen, C., Khouri, R., Mantoani, S. P., Nunes, P. S. G., et al. (2020). Non-cytotoxic 1,2,3-triazole tethered fused heterocyclic ring derivatives display Tax protein inhibition and impair HTLV-1 infected cells. Bioorganic & Medicinal Chemistry, 28( 22), 1-9. doi:10.1016/j.bmc.2020.115746
NLM
Santos DF dos, Pilger DRB de, Vandermeulen C, Khouri R, Mantoani SP, Nunes PSG, Andrade P de, Carvalho I, Casseb JS do R, Twizere J-C, Willems L, Freitas Junior LHG de, Haddad SK. Non-cytotoxic 1,2,3-triazole tethered fused heterocyclic ring derivatives display Tax protein inhibition and impair HTLV-1 infected cells [Internet]. Bioorganic & Medicinal Chemistry. 2020 ; 28( 22): 1-9.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.bmc.2020.115746
Vancouver
Santos DF dos, Pilger DRB de, Vandermeulen C, Khouri R, Mantoani SP, Nunes PSG, Andrade P de, Carvalho I, Casseb JS do R, Twizere J-C, Willems L, Freitas Junior LHG de, Haddad SK. Non-cytotoxic 1,2,3-triazole tethered fused heterocyclic ring derivatives display Tax protein inhibition and impair HTLV-1 infected cells [Internet]. Bioorganic & Medicinal Chemistry. 2020 ; 28( 22): 1-9.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.bmc.2020.115746
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FUGIO, Lais Brigliadori e COELI-LACCHINI, Fernanda Borchers e LEOPOLDINO, Andréia Machado. Sphingolipids and mitochondrial dynamic. Cells, v. 9, n. 3, p. 1-14, 2020Tradução . . Disponível em: https://doi.org/10.3390/cells9030581. Acesso em: 28 mar. 2024.
APA
Fugio, L. B., Coeli-Lacchini, F. B., & Leopoldino, A. M. (2020). Sphingolipids and mitochondrial dynamic. Cells, 9( 3), 1-14. doi:10.3390/cells9030581
NLM
Fugio LB, Coeli-Lacchini FB, Leopoldino AM. Sphingolipids and mitochondrial dynamic [Internet]. Cells. 2020 ; 9( 3): 1-14.[citado 2024 mar. 28 ] Available from: https://doi.org/10.3390/cells9030581
Vancouver
Fugio LB, Coeli-Lacchini FB, Leopoldino AM. Sphingolipids and mitochondrial dynamic [Internet]. Cells. 2020 ; 9( 3): 1-14.[citado 2024 mar. 28 ] Available from: https://doi.org/10.3390/cells9030581
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RODRIGUES, Fernando Postalli et al. Real-time redox monitoring of a nitrosyl ruthenium complex acting as NO-donor agent in a single A549 cancer cell with multiplex Fourier-transform infrared microscopy. Nitric Oxide: Biology and Chemistry, v. 96, p. 29-34, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.niox.2020.01.005. Acesso em: 28 mar. 2024.
APA
Rodrigues, F. P., Macedo, L. J. A. de, Máximo, L. N. C., Sales, F. C. P. F., Silva, R. S. da, & Crespilho, F. N. (2020). Real-time redox monitoring of a nitrosyl ruthenium complex acting as NO-donor agent in a single A549 cancer cell with multiplex Fourier-transform infrared microscopy. Nitric Oxide: Biology and Chemistry, 96, 29-34. doi:10.1016/j.niox.2020.01.005
NLM
Rodrigues FP, Macedo LJA de, Máximo LNC, Sales FCPF, Silva RS da, Crespilho FN. Real-time redox monitoring of a nitrosyl ruthenium complex acting as NO-donor agent in a single A549 cancer cell with multiplex Fourier-transform infrared microscopy [Internet]. Nitric Oxide: Biology and Chemistry. 2020 ; 96 29-34.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.niox.2020.01.005
Vancouver
Rodrigues FP, Macedo LJA de, Máximo LNC, Sales FCPF, Silva RS da, Crespilho FN. Real-time redox monitoring of a nitrosyl ruthenium complex acting as NO-donor agent in a single A549 cancer cell with multiplex Fourier-transform infrared microscopy [Internet]. Nitric Oxide: Biology and Chemistry. 2020 ; 96 29-34.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.niox.2020.01.005
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MARTINS-TEIXEIRA, Maristela B. e CARVALHO, Ivone. Antitumour anthracyclines: progress and perspectives. ChemMedChem, v. 15, n. 11, p. 933-948, 2020Tradução . . Disponível em: https://doi.org/10.1002/cmdc.202000131. Acesso em: 28 mar. 2024.
APA
Martins-Teixeira, M. B., & Carvalho, I. (2020). Antitumour anthracyclines: progress and perspectives. ChemMedChem, 15( 11), 933-948. doi:10.1002/cmdc.202000131
NLM
Martins-Teixeira MB, Carvalho I. Antitumour anthracyclines: progress and perspectives [Internet]. ChemMedChem. 2020 ; 15( 11): 933-948.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/cmdc.202000131
Vancouver
Martins-Teixeira MB, Carvalho I. Antitumour anthracyclines: progress and perspectives [Internet]. ChemMedChem. 2020 ; 15( 11): 933-948.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1002/cmdc.202000131
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FEDERICO, Leonardo Bruno et al. Identification of novel αβ-tubulin modulators with antiproliferative activity directed to cancer therapy using ligand and structure-based virtual screening. International Journal of Biological Macromolecules, v. 165, p. 3040-3050, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2020.10.136. Acesso em: 28 mar. 2024.
APA
Federico, L. B., Silva, G. M. da, Dias, A. de F., Figueiró, F., Battastini, A. M. O., Santos, C. B. R. dos, et al. (2020). Identification of novel αβ-tubulin modulators with antiproliferative activity directed to cancer therapy using ligand and structure-based virtual screening. International Journal of Biological Macromolecules, 165, 3040-3050. doi:10.1016/j.ijbiomac.2020.10.136
NLM
Federico LB, Silva GM da, Dias A de F, Figueiró F, Battastini AMO, Santos CBR dos, Costa LT, Campos Rosa JM, Silva CHT de P da. Identification of novel αβ-tubulin modulators with antiproliferative activity directed to cancer therapy using ligand and structure-based virtual screening [Internet]. International Journal of Biological Macromolecules. 2020 ; 165 3040-3050.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.ijbiomac.2020.10.136
Vancouver
Federico LB, Silva GM da, Dias A de F, Figueiró F, Battastini AMO, Santos CBR dos, Costa LT, Campos Rosa JM, Silva CHT de P da. Identification of novel αβ-tubulin modulators with antiproliferative activity directed to cancer therapy using ligand and structure-based virtual screening [Internet]. International Journal of Biological Macromolecules. 2020 ; 165 3040-3050.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.ijbiomac.2020.10.136
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MIZUKAMI, Amanda e SWIECH, Kamilla. Platforms for clinical-grade CAR-T cell expansion. Chimeric antigen receptor T Cell: development and production. Tradução . New York: Humana Press, 2020. p. 274 . Disponível em: https://doi.org/10.1007/978-1-0716-0146-4. Acesso em: 28 mar. 2024.
APA
Mizukami, A., & Swiech, K. (2020). Platforms for clinical-grade CAR-T cell expansion. In Chimeric antigen receptor T Cell: development and production (p. 274 ). New York: Humana Press. doi:10.1007/978-1-0716-0146-4
NLM
Mizukami A, Swiech K. Platforms for clinical-grade CAR-T cell expansion [Internet]. In: Chimeric antigen receptor T Cell: development and production. New York: Humana Press; 2020. p. 274 .[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
Vancouver
Mizukami A, Swiech K. Platforms for clinical-grade CAR-T cell expansion [Internet]. In: Chimeric antigen receptor T Cell: development and production. New York: Humana Press; 2020. p. 274 .[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/978-1-0716-0146-4
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AZEVEDO, Júlia Teixeira Cottas de et al. Optimizing intracellular signaling domains for CAR-NK cells. Hematology, Transfusion and Cell Therapy. São Paulo: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.htct.2020.10.710. Acesso em: 28 mar. 2024. , 2020
APA
Azevedo, J. T. C. de, Silvestre, R. N., Pessoni, A. M., Farias, K. C. R. M. de, Covas, D. T., & Picanço-Castro, V. (2020). Optimizing intracellular signaling domains for CAR-NK cells. Hematology, Transfusion and Cell Therapy. São Paulo: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. doi:10.1016/j.htct.2020.10.710
NLM
Azevedo JTC de, Silvestre RN, Pessoni AM, Farias KCRM de, Covas DT, Picanço-Castro V. Optimizing intracellular signaling domains for CAR-NK cells [Internet]. Hematology, Transfusion and Cell Therapy. 2020 ; 42 S422-S423.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.htct.2020.10.710
Vancouver
Azevedo JTC de, Silvestre RN, Pessoni AM, Farias KCRM de, Covas DT, Picanço-Castro V. Optimizing intracellular signaling domains for CAR-NK cells [Internet]. Hematology, Transfusion and Cell Therapy. 2020 ; 42 S422-S423.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.htct.2020.10.710
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GOMES, Kauan Ribeiro de Sena et al. Non-viral engineering of CAR-NK cells for cancer immunotherapy. Hematology, Transfusion and Cell Therapy. São Paulo: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.htct.2020.10.706. Acesso em: 28 mar. 2024. , 2020
APA
Gomes, K. R. de S., Silvestre, R. N., Azevedo, J. T. C. de, Swiech, K., Farias, K. C. R. M. de, Covas, D. T., & Picanço-Castro, V. (2020). Non-viral engineering of CAR-NK cells for cancer immunotherapy. Hematology, Transfusion and Cell Therapy. São Paulo: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. doi:10.1016/j.htct.2020.10.706
NLM
Gomes KR de S, Silvestre RN, Azevedo JTC de, Swiech K, Farias KCRM de, Covas DT, Picanço-Castro V. Non-viral engineering of CAR-NK cells for cancer immunotherapy [Internet]. Hematology, Transfusion and Cell Therapy. 2020 ; 42 S420.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.htct.2020.10.706
Vancouver
Gomes KR de S, Silvestre RN, Azevedo JTC de, Swiech K, Farias KCRM de, Covas DT, Picanço-Castro V. Non-viral engineering of CAR-NK cells for cancer immunotherapy [Internet]. Hematology, Transfusion and Cell Therapy. 2020 ; 42 S420.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.htct.2020.10.706
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CACEMIRO, Maira da Costa et al. Arachidonic acid (aa)-derived lipid mediators are increased in the bone marrow plasma from polycythemia vera and essential thrombocythemia patients. Hematology, Transfusion and Cell Therapy. São José do Rio Preto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.htct.2020.10.197. Acesso em: 28 mar. 2024. , 2020
APA
Cacemiro, M. da C., Cominal, J. G., Pontes, L. L. de F., Sorgi, C. A., Faccioli, L. H., & Castro, F. A. de. (2020). Arachidonic acid (aa)-derived lipid mediators are increased in the bone marrow plasma from polycythemia vera and essential thrombocythemia patients. Hematology, Transfusion and Cell Therapy. São José do Rio Preto: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1016/j.htct.2020.10.197
NLM
Cacemiro M da C, Cominal JG, Pontes LL de F, Sorgi CA, Faccioli LH, Castro FA de. Arachidonic acid (aa)-derived lipid mediators are increased in the bone marrow plasma from polycythemia vera and essential thrombocythemia patients [Internet]. Hematology, Transfusion and Cell Therapy. 2020 ; 42 S117.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.htct.2020.10.197
Vancouver
Cacemiro M da C, Cominal JG, Pontes LL de F, Sorgi CA, Faccioli LH, Castro FA de. Arachidonic acid (aa)-derived lipid mediators are increased in the bone marrow plasma from polycythemia vera and essential thrombocythemia patients [Internet]. Hematology, Transfusion and Cell Therapy. 2020 ; 42 S117.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.htct.2020.10.197
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VIEGAS, Juliana Santos Rosa et al. Therapeutic applications and delivery systems for triptolide. Drug Delivery and Translational Research, v. 10, n. 6, p. 1584-1600, 2020Tradução . . Disponível em: https://doi.org/10.1007/s13346-020-00827-z. Acesso em: 28 mar. 2024.
APA
Viegas, J. S. R., Praça, F. S. G., Kravicz, M. H., & Bentley, M. V. L. B. (2020). Therapeutic applications and delivery systems for triptolide. Drug Delivery and Translational Research, 10( 6), 1584-1600. doi:10.1007/s13346-020-00827-z
NLM
Viegas JSR, Praça FSG, Kravicz MH, Bentley MVLB. Therapeutic applications and delivery systems for triptolide [Internet]. Drug Delivery and Translational Research. 2020 ; 10( 6): 1584-1600.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/s13346-020-00827-z
Vancouver
Viegas JSR, Praça FSG, Kravicz MH, Bentley MVLB. Therapeutic applications and delivery systems for triptolide [Internet]. Drug Delivery and Translational Research. 2020 ; 10( 6): 1584-1600.[citado 2024 mar. 28 ] Available from: https://doi.org/10.1007/s13346-020-00827-z
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERBEL, Giovana Michelassi et al. A inibição farmacológica de JAK e expressão elevada de LATS2 induz apoptose e reduz proliferação de linhagem celular JAK2V617F. Hematology, Transfusion and Cell Therapy. São José do Rio Preto: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.htct.2020.10.195. Acesso em: 28 mar. 2024. , 2020
APA
Berbel, G. M., Cominal, J. G., Pereira, L. M., Natsui, A. P. Y., Castro, F. A. de, & Cacemiro, M. da C. (2020). A inibição farmacológica de JAK e expressão elevada de LATS2 induz apoptose e reduz proliferação de linhagem celular JAK2V617F. Hematology, Transfusion and Cell Therapy. São José do Rio Preto: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. doi:10.1016/j.htct.2020.10.195
NLM
Berbel GM, Cominal JG, Pereira LM, Natsui APY, Castro FA de, Cacemiro M da C. A inibição farmacológica de JAK e expressão elevada de LATS2 induz apoptose e reduz proliferação de linhagem celular JAK2V617F [Internet]. Hematology, Transfusion and Cell Therapy. 2020 ; 42[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.htct.2020.10.195
Vancouver
Berbel GM, Cominal JG, Pereira LM, Natsui APY, Castro FA de, Cacemiro M da C. A inibição farmacológica de JAK e expressão elevada de LATS2 induz apoptose e reduz proliferação de linhagem celular JAK2V617F [Internet]. Hematology, Transfusion and Cell Therapy. 2020 ; 42[citado 2024 mar. 28 ] Available from: https://doi.org/10.1016/j.htct.2020.10.195