Cancer estimates in Brazil reveal progress for the most lethal malignancies [Editorial] (2020)
- Authors:
- USP affiliated authors: ANDRICOPULO, ADRIANO DEFINI - IFSC ; FERREIRA, LEONARDO LUIZ GOMES - IFSC
- Unidade: IFSC
- DOI: 10.2174/156802662022200917110555
- Subjects: PLANEJAMENTO DE FÁRMACOS; NEOPLASIAS; QUÍMICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Current Topics in Medicinal Chemistry
- ISSN: 1568-0266
- Volume/Número/Paginação/Ano: v. 20, n. 22, p. 1962-1966, 2020
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
FERREIRA, Leonardo Luiz Gomes e ANDRICOPULO, Adriano Defini. Cancer estimates in Brazil reveal progress for the most lethal malignancies [Editorial]. Current Topics in Medicinal Chemistry. Sharjah: Instituto de Física de São Carlos, Universidade de São Paulo. Disponível em: https://doi.org/10.2174/156802662022200917110555. Acesso em: 23 abr. 2024. , 2020 -
APA
Ferreira, L. L. G., & Andricopulo, A. D. (2020). Cancer estimates in Brazil reveal progress for the most lethal malignancies [Editorial]. Current Topics in Medicinal Chemistry. Sharjah: Instituto de Física de São Carlos, Universidade de São Paulo. doi:10.2174/156802662022200917110555 -
NLM
Ferreira LLG, Andricopulo AD. Cancer estimates in Brazil reveal progress for the most lethal malignancies [Editorial] [Internet]. Current Topics in Medicinal Chemistry. 2020 ; 20( 22): 1962-1966.[citado 2024 abr. 23 ] Available from: https://doi.org/10.2174/156802662022200917110555 -
Vancouver
Ferreira LLG, Andricopulo AD. Cancer estimates in Brazil reveal progress for the most lethal malignancies [Editorial] [Internet]. Current Topics in Medicinal Chemistry. 2020 ; 20( 22): 1962-1966.[citado 2024 abr. 23 ] Available from: https://doi.org/10.2174/156802662022200917110555 - Novel brominated vinylic fatty acids effectively inhibit the leishmania topoisomerase IB enzyme mediated by halogen bond formation
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Informações sobre o DOI: 10.2174/156802662022200917110555 (Fonte: oaDOI API)
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