ReP USP - Resultado da busca

Artigo de periodico
NSC305787, a pharmacological ezrin inhibitor, exhibits antineoplastic activity in pancreatic cancer cells (2022)
Silva, Jean Carlos Lipreri da ; Carvalho, Maria Fernanda Lopes; Miranda, Lívia Bassani Lins De ; Almeida, Bruna Oliveira de ; Lima, Keli Cristina de; Machado Neto, João Agostinho
Fonte: Investigational New Drugs. Unidade: ICB
Assuntos: FARMACOLOGIA, ANTINEOPLÁSICOS, CÉLULAS CULTIVADAS DE TUMOR, NEOPLASIAS PANCREÁTICAS, COMPOSTOS AROMÁTICOS, CITOESQUELETO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Jean Carlos Lipreri da et al. NSC305787, a pharmacological ezrin inhibitor, exhibits antineoplastic activity in pancreatic cancer cells. Investigational New Drugs, p. 1-10, 2022Tradução . . Disponível em: https://doi.org/10.1007/s10637-022-01249-z. Acesso em: 31 ago. 2024.
APA
Silva, J. C. L. da, Carvalho, M. F. L., Miranda, L. B. L. D., Almeida, B. O. de, Lima, K. C. de, & Machado Neto, J. A. (2022). NSC305787, a pharmacological ezrin inhibitor, exhibits antineoplastic activity in pancreatic cancer cells. Investigational New Drugs, 1-10. doi:10.1007/s10637-022-01249-z
NLM
Silva JCL da, Carvalho MFL, Miranda LBLD, Almeida BO de, Lima KC de, Machado Neto JA. NSC305787, a pharmacological ezrin inhibitor, exhibits antineoplastic activity in pancreatic cancer cells [Internet]. Investigational New Drugs. 2022 ; 1-10.[citado 2024 ago. 31 ] Available from: https://doi.org/10.1007/s10637-022-01249-z
Vancouver
Silva JCL da, Carvalho MFL, Miranda LBLD, Almeida BO de, Lima KC de, Machado Neto JA. NSC305787, a pharmacological ezrin inhibitor, exhibits antineoplastic activity in pancreatic cancer cells [Internet]. Investigational New Drugs. 2022 ; 1-10.[citado 2024 ago. 31 ] Available from: https://doi.org/10.1007/s10637-022-01249-z
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
Fonte: Investigational New Drugs. Unidades: ICB, IQSC
Assuntos: FARMACOLOGIA, LEUCEMIA, ANTINEOPLÁSICOS, FOSFOPROTEÍNAS, MICROTÚBULOS, CÉLULAS CULTIVADAS DE TUMOR, PROLIFERAÇÃO CELULAR, CITOESQUELETO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 31 ago. 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 ago. 31 ] 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 ago. 31 ] 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
Fonte: Investigational New Drugs. Unidades: FM, ICB
Assuntos: ANATOMIA, FARMACOLOGIA, CÉLULAS CULTIVADAS DE TUMOR, CARCINOMA, NEOPLASIA ENDÓCRINA MÚLTIPLA, MICROTÚBULOS, FENÓTIPOS, CLONAGEM, ONCOPROTEÍNAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 31 ago. 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 ago. 31 ] 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 ago. 31 ] Available from: https://doi.org/10.1007/s10637-019-00846-9
Artigo de periodico
Xanthan gum-based hydrogel containing nanocapsules for cutaneous diphenyl diselenide delivery in melanoma therapy (2020)
Ferreira, Luana Mota; Sari, Marcel Henrique Marcondes; Azambuja, Juliana Hofstatter; Silveira, Elita Ferreira da; Cervi, Verônica Ferrari; Marchiori, Marila Crivellaro Lay; Maria-Engler, Silvya Stuchi ; Wink, Márcia Rosângela; Azevedo, Jéssica Gonçalves; Nogueira, Cristina Wayne; Braganhol, Elizandra; Cruz, Letícia
Fonte: Investigational New Drugs. Unidade: FCF
Assuntos: MELANOMA, NEOPLASIAS CUTÂNEAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA, Luana Mota et al. Xanthan gum-based hydrogel containing nanocapsules for cutaneous diphenyl diselenide delivery in melanoma therapy. Investigational New Drugs, v. 38, p. 662-674, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10637-019-00823-2. Acesso em: 31 ago. 2024.
APA
Ferreira, L. M., Sari, M. H. M., Azambuja, J. H., Silveira, E. F. da, Cervi, V. F., Marchiori, M. C. L., et al. (2020). Xanthan gum-based hydrogel containing nanocapsules for cutaneous diphenyl diselenide delivery in melanoma therapy. Investigational New Drugs, 38, 662-674. doi:10.1007/s10637-019-00823-2
NLM
Ferreira LM, Sari MHM, Azambuja JH, Silveira EF da, Cervi VF, Marchiori MCL, Maria-Engler SS, Wink MR, Azevedo JG, Nogueira CW, Braganhol E, Cruz L. Xanthan gum-based hydrogel containing nanocapsules for cutaneous diphenyl diselenide delivery in melanoma therapy [Internet]. Investigational New Drugs. 2020 ; 38 662-674.[citado 2024 ago. 31 ] Available from: https://doi.org/10.1007/s10637-019-00823-2
Vancouver
Ferreira LM, Sari MHM, Azambuja JH, Silveira EF da, Cervi VF, Marchiori MCL, Maria-Engler SS, Wink MR, Azevedo JG, Nogueira CW, Braganhol E, Cruz L. Xanthan gum-based hydrogel containing nanocapsules for cutaneous diphenyl diselenide delivery in melanoma therapy [Internet]. Investigational New Drugs. 2020 ; 38 662-674.[citado 2024 ago. 31 ] Available from: https://doi.org/10.1007/s10637-019-00823-2
Artigo de periodico
Design, synthesis and cytotoxicity of the antitumor agent 1-azabicycles for chemoresistant glioblastoma cells (2020)
Oliveira, Mona; Santana, Lourenço Luis Botelho de; Serafim, José Claudio; Santos, Airam Oliveira; Quintino, Michelle Pereira; Correia, José Tiago Menezes; Damasceno, Fábio; Sabino, José Ricardo; Pires, Thiago Rubens Cardim; Coelho, Paulo Lucas Cerqueira; Lopes, Giselle Pinto de Faria; Ulrich, Henning ; Costa, Silvia Lima; Cunha, Silvio
Fonte: Investigational New Drugs. Unidade: IQ
Assuntos: CÉLULAS, GLIOMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Mona et al. Design, synthesis and cytotoxicity of the antitumor agent 1-azabicycles for chemoresistant glioblastoma cells. Investigational New Drugs, v. 38, p. 1257–1271, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10637-019-00877-2. Acesso em: 31 ago. 2024.
APA
Oliveira, M., Santana, L. L. B. de, Serafim, J. C., Santos, A. O., Quintino, M. P., Correia, J. T. M., et al. (2020). Design, synthesis and cytotoxicity of the antitumor agent 1-azabicycles for chemoresistant glioblastoma cells. Investigational New Drugs, 38, 1257–1271. doi:10.1007/s10637-019-00877-2
NLM
Oliveira M, Santana LLB de, Serafim JC, Santos AO, Quintino MP, Correia JTM, Damasceno F, Sabino JR, Pires TRC, Coelho PLC, Lopes GP de F, Ulrich H, Costa SL, Cunha S. Design, synthesis and cytotoxicity of the antitumor agent 1-azabicycles for chemoresistant glioblastoma cells [Internet]. Investigational New Drugs. 2020 ; 38 1257–1271.[citado 2024 ago. 31 ] Available from: https://doi.org/10.1007/s10637-019-00877-2
Vancouver
Oliveira M, Santana LLB de, Serafim JC, Santos AO, Quintino MP, Correia JTM, Damasceno F, Sabino JR, Pires TRC, Coelho PLC, Lopes GP de F, Ulrich H, Costa SL, Cunha S. Design, synthesis and cytotoxicity of the antitumor agent 1-azabicycles for chemoresistant glioblastoma cells [Internet]. Investigational New Drugs. 2020 ; 38 1257–1271.[citado 2024 ago. 31 ] Available from: https://doi.org/10.1007/s10637-019-00877-2
Artigo de periodico
The DNA methyltransferase inhibitor zebularine exerts antitumor effects and reveal BATF2 as a poor prognostic marker for childhood medulloblastoma (2017)
Andrade, Augusto Faria; Borges, Kleiton Silva; Suazo, Veridiana Kill; Geron, Lenisa; Corrêa, Carolina Alves Pereira; Castro-Gamero, Angel Mauricio; Vasconcelos, Elton José Rosas de; Oliveira, Ricardo Santos de; Neder, Luciano; Yunes, José Andres; Aguiar, Simone dos Santos; Scrideli, Carlos Alberto; Tone, Luiz Gonzaga
Fonte: Investigational New Drugs. Unidade: FMRP
Assuntos: EPIGÊNESE GENÉTICA, MEDULOBLASTOMA, ANTINEOPLÁSICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANDRADE, Augusto Faria et al. The DNA methyltransferase inhibitor zebularine exerts antitumor effects and reveal BATF2 as a poor prognostic marker for childhood medulloblastoma. Investigational New Drugs, v. 35, n. 1, p. 26-36, 2017Tradução . . Disponível em: https://doi.org/10.1007/s10637-016-0401-4. Acesso em: 31 ago. 2024.
APA
Andrade, A. F., Borges, K. S., Suazo, V. K., Geron, L., Corrêa, C. A. P., Castro-Gamero, A. M., et al. (2017). The DNA methyltransferase inhibitor zebularine exerts antitumor effects and reveal BATF2 as a poor prognostic marker for childhood medulloblastoma. Investigational New Drugs, 35( 1), 26-36. doi:10.1007/s10637-016-0401-4
NLM
Andrade AF, Borges KS, Suazo VK, Geron L, Corrêa CAP, Castro-Gamero AM, Vasconcelos EJR de, Oliveira RS de, Neder L, Yunes JA, Aguiar S dos S, Scrideli CA, Tone LG. The DNA methyltransferase inhibitor zebularine exerts antitumor effects and reveal BATF2 as a poor prognostic marker for childhood medulloblastoma [Internet]. Investigational New Drugs. 2017 ; 35( 1): 26-36.[citado 2024 ago. 31 ] Available from: https://doi.org/10.1007/s10637-016-0401-4
Vancouver
Andrade AF, Borges KS, Suazo VK, Geron L, Corrêa CAP, Castro-Gamero AM, Vasconcelos EJR de, Oliveira RS de, Neder L, Yunes JA, Aguiar S dos S, Scrideli CA, Tone LG. The DNA methyltransferase inhibitor zebularine exerts antitumor effects and reveal BATF2 as a poor prognostic marker for childhood medulloblastoma [Internet]. Investigational New Drugs. 2017 ; 35( 1): 26-36.[citado 2024 ago. 31 ] Available from: https://doi.org/10.1007/s10637-016-0401-4
Artigo de periodico
Erratum to: The DNA methyltransferase inhibitor zebularine exerts antitumor effects and reveals BATF2 as a poor prognostic marker for childhood medulloblastoma (2017)
Andrade, Augusto Faria; Borges, Kleiton Silva; Suazo, Veridiana Kiill; Geron, Lenisa; Corrêa, Carolina Alves Pereira; Castro-Gamero, Angel Mauricio; de Vasconcelos, Elton José Rosas; Oliveira, Ricardo Santos de; Neder, Luciano; Yunes, José Andres; Aguiar, Simone dos Santos; Scrideli, Carlos Alberto; Tone, Luiz Gonzaga
Fonte: Investigational New Drugs. Unidade: FMRP
Assuntos: EPIGÊNESE GENÉTICA, MEDULOBLASTOMA, ANTINEOPLÁSICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANDRADE, Augusto Faria et al. Erratum to: The DNA methyltransferase inhibitor zebularine exerts antitumor effects and reveals BATF2 as a poor prognostic marker for childhood medulloblastoma. Investigational New Drugs, v. 35, n. 1, 2017Tradução . . Disponível em: https://doi.org/10.1007/s10637-016-0412-1. Acesso em: 31 ago. 2024.
APA
Andrade, A. F., Borges, K. S., Suazo, V. K., Geron, L., Corrêa, C. A. P., Castro-Gamero, A. M., et al. (2017). Erratum to: The DNA methyltransferase inhibitor zebularine exerts antitumor effects and reveals BATF2 as a poor prognostic marker for childhood medulloblastoma. Investigational New Drugs, 35( 1). doi:10.1007/s10637-016-0412-1
NLM
Andrade AF, Borges KS, Suazo VK, Geron L, Corrêa CAP, Castro-Gamero AM, de Vasconcelos EJR, Oliveira RS de, Neder L, Yunes JA, Aguiar S dos S, Scrideli CA, Tone LG. Erratum to: The DNA methyltransferase inhibitor zebularine exerts antitumor effects and reveals BATF2 as a poor prognostic marker for childhood medulloblastoma [Internet]. Investigational New Drugs. 2017 ; 35( 1):[citado 2024 ago. 31 ] Available from: https://doi.org/10.1007/s10637-016-0412-1
Vancouver
Andrade AF, Borges KS, Suazo VK, Geron L, Corrêa CAP, Castro-Gamero AM, de Vasconcelos EJR, Oliveira RS de, Neder L, Yunes JA, Aguiar S dos S, Scrideli CA, Tone LG. Erratum to: The DNA methyltransferase inhibitor zebularine exerts antitumor effects and reveals BATF2 as a poor prognostic marker for childhood medulloblastoma [Internet]. Investigational New Drugs. 2017 ; 35( 1):[citado 2024 ago. 31 ] Available from: https://doi.org/10.1007/s10637-016-0412-1
Artigo de periodico
Tetra-O-methyl nordihydroguaiaretic acid, an inhibitor of Sp1-mediated survivin transcription, induces apoptosis and acts synergistically with chemo-radiotherapy in glioblastoma cells (2013)
Castro-Gamero, Angel Mauricio; Borges, Kleiton Silva; Moreno, Daniel Antunes; Suazo, Veridiana Kill; Fujinami, Mayara Missono; Queiroz, Rosane Gomes de Paula; Oliveira, Harley Francisco de; Carlotti Júnior, Carlos Gilberto; Scrideli, Carlos Alberto; Tone, Luiz Gonzaga
Fonte: Investigational New Drugs. Unidade: FMRP
Assuntos: GENES, FÁRMACOS (COMBINAÇÃO), RADIOTERAPIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO-GAMERO, Angel Mauricio et al. Tetra-O-methyl nordihydroguaiaretic acid, an inhibitor of Sp1-mediated survivin transcription, induces apoptosis and acts synergistically with chemo-radiotherapy in glioblastoma cells. Investigational New Drugs, v. 31, n. 4, p. 858-870, 2013Tradução . . Disponível em: https://doi.org/10.1007/s10637-012-9917-4. Acesso em: 31 ago. 2024.
APA
Castro-Gamero, A. M., Borges, K. S., Moreno, D. A., Suazo, V. K., Fujinami, M. M., Queiroz, R. G. de P., et al. (2013). Tetra-O-methyl nordihydroguaiaretic acid, an inhibitor of Sp1-mediated survivin transcription, induces apoptosis and acts synergistically with chemo-radiotherapy in glioblastoma cells. Investigational New Drugs, 31( 4), 858-870. doi:10.1007/s10637-012-9917-4
NLM
Castro-Gamero AM, Borges KS, Moreno DA, Suazo VK, Fujinami MM, Queiroz RG de P, Oliveira HF de, Carlotti Júnior CG, Scrideli CA, Tone LG. Tetra-O-methyl nordihydroguaiaretic acid, an inhibitor of Sp1-mediated survivin transcription, induces apoptosis and acts synergistically with chemo-radiotherapy in glioblastoma cells [Internet]. Investigational New Drugs. 2013 ; 31( 4): 858-870.[citado 2024 ago. 31 ] Available from: https://doi.org/10.1007/s10637-012-9917-4
Vancouver
Castro-Gamero AM, Borges KS, Moreno DA, Suazo VK, Fujinami MM, Queiroz RG de P, Oliveira HF de, Carlotti Júnior CG, Scrideli CA, Tone LG. Tetra-O-methyl nordihydroguaiaretic acid, an inhibitor of Sp1-mediated survivin transcription, induces apoptosis and acts synergistically with chemo-radiotherapy in glioblastoma cells [Internet]. Investigational New Drugs. 2013 ; 31( 4): 858-870.[citado 2024 ago. 31 ] Available from: https://doi.org/10.1007/s10637-012-9917-4
Artigo de periodico
A novel proteasome inhibitor acting in mitochondrial dysfunction, ER stress and ROS production (2013)
Maria, Durvanei Augusto; Souza, Jean Gabriel de; Morais, Katia L. P.; Berra, Carolina Maria; Zampolli, Hamilton de Campos; Demasi, Marilene; Simons, Simone Michaela; Saito, Renata de Freitas; Chammas, Roger; Chudzinski-Tavassi, Ana Marisa
Fonte: Investigational New Drugs. Unidade: FM
Assuntos: ESTRESSE, NEOPLASIAS (TERAPIA), MECANISMOS DE CONTROLE CELULAR, ADENOCARCINOMA, APOPTOSE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARIA, Durvanei Augusto et al. A novel proteasome inhibitor acting in mitochondrial dysfunction, ER stress and ROS production. Investigational New Drugs, v. 31, n. 3, p. 493-505, 2013Tradução . . Disponível em: http://link.springer.com/article/10.1007/s10637-012-9871-1. Acesso em: 31 ago. 2024.
APA
Maria, D. A., Souza, J. G. de, Morais, K. L. P., Berra, C. M., Zampolli, H. de C., Demasi, M., et al. (2013). A novel proteasome inhibitor acting in mitochondrial dysfunction, ER stress and ROS production. Investigational New Drugs, 31( 3), 493-505. doi:10.1007/s10637-012-9871-1
NLM
Maria DA, Souza JG de, Morais KLP, Berra CM, Zampolli H de C, Demasi M, Simons SM, Saito R de F, Chammas R, Chudzinski-Tavassi AM. A novel proteasome inhibitor acting in mitochondrial dysfunction, ER stress and ROS production [Internet]. Investigational New Drugs. 2013 ; 31( 3): 493-505.[citado 2024 ago. 31 ] Available from: http://link.springer.com/article/10.1007/s10637-012-9871-1
Vancouver
Maria DA, Souza JG de, Morais KLP, Berra CM, Zampolli H de C, Demasi M, Simons SM, Saito R de F, Chammas R, Chudzinski-Tavassi AM. A novel proteasome inhibitor acting in mitochondrial dysfunction, ER stress and ROS production [Internet]. Investigational New Drugs. 2013 ; 31( 3): 493-505.[citado 2024 ago. 31 ] Available from: http://link.springer.com/article/10.1007/s10637-012-9871-1
Artigo de periodico
Phase I and pharmacokinetic study of 3'-C-ethynylcytidine (TAS-106), an inhibitor of RNA polymerase I, II and III, in patients with advanced solid malignancies (2012)
Hammond-Thelin, Lisa A.; Thomas, Melanie B.; Iwasaki, Michiko; Abbruzzese, James L.; Lassere, Yvonne; Meyers, Christina A.; Hoff, Paulo; Bono, Johann de; Norris, Jody; Matsushita, Hitoshi; Mita, Akira; Rowinsky, Eric K.
Fonte: Investigational New Drugs. Unidade: FM
Assuntos: REAÇÃO EM CADEIA POR POLIMERASE, ANTINEOPLÁSICOS (APLICAÇÕES TERAPÊUTICAS), PROLIFERAÇÃO CELULAR, FARMACODINÂMICA, ESTADIAMENTO DE NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HAMMOND-THELIN, Lisa A. et al. Phase I and pharmacokinetic study of 3'-C-ethynylcytidine (TAS-106), an inhibitor of RNA polymerase I, II and III, in patients with advanced solid malignancies. Investigational New Drugs, v. 30, n. 1, p. 316-326, 2012Tradução . . Disponível em: http://link.springer.com/article/10.1007/s10637-010-9535-y?null. Acesso em: 31 ago. 2024.
APA
Hammond-Thelin, L. A., Thomas, M. B., Iwasaki, M., Abbruzzese, J. L., Lassere, Y., Meyers, C. A., et al. (2012). Phase I and pharmacokinetic study of 3'-C-ethynylcytidine (TAS-106), an inhibitor of RNA polymerase I, II and III, in patients with advanced solid malignancies. Investigational New Drugs, 30( 1), 316-326. doi:10.1007/s10637-010-9535-y
NLM
Hammond-Thelin LA, Thomas MB, Iwasaki M, Abbruzzese JL, Lassere Y, Meyers CA, Hoff P, Bono J de, Norris J, Matsushita H, Mita A, Rowinsky EK. Phase I and pharmacokinetic study of 3'-C-ethynylcytidine (TAS-106), an inhibitor of RNA polymerase I, II and III, in patients with advanced solid malignancies [Internet]. Investigational New Drugs. 2012 ; 30( 1): 316-326.[citado 2024 ago. 31 ] Available from: http://link.springer.com/article/10.1007/s10637-010-9535-y?null
Vancouver
Hammond-Thelin LA, Thomas MB, Iwasaki M, Abbruzzese JL, Lassere Y, Meyers CA, Hoff P, Bono J de, Norris J, Matsushita H, Mita A, Rowinsky EK. Phase I and pharmacokinetic study of 3'-C-ethynylcytidine (TAS-106), an inhibitor of RNA polymerase I, II and III, in patients with advanced solid malignancies [Internet]. Investigational New Drugs. 2012 ; 30( 1): 316-326.[citado 2024 ago. 31 ] Available from: http://link.springer.com/article/10.1007/s10637-010-9535-y?null

Unidades USP

ReP

Filtros

Unidades USP

Departamento

Autores

Autores USP

Ano de publicação

Assuntos

Agência de fomento

Indexado em

Afiliação dos autores externos não normalizada