Structure-based drug design for new therapies for Leishmaniasis and Chagas disease (2025)
- Authors:
- Autor USP: SILBER, ARIEL MARIANO - ICB
- Unidade: ICB
- DOI: 10.1107/S2053273324099194
- Subjects: PARASITOLOGIA; PROTOZOA; ANTIPARASITÁRIOS; LEISHMANIA; AMINOÁCIDOS; DOENÇA DE CHAGAS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Acta Crystallographica. Section A: Foundations and Advances
- ISSN: 2053-2733
- Volume/Número/Paginação/Ano: v. 80, res. e80, 2024
- Conference titles: European Crystallography Meeting
- Este artigo possui versão em acesso aberto
- URL de acesso aberto
- PDF de acesso aberto
- Versão do Documento: Versão publicada (Published version)
-
Status: Artigo possui acesso gratuito no site do editor (Bronze Open Access) -
ABNT
POHL, Ehmke et al. Structure-based drug design for new therapies for Leishmaniasis and Chagas disease. Acta Crystallographica. Section A: Foundations and Advances. Hoboken: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://doi.org/10.1107/S2053273324099194. Acesso em: 15 mar. 2026. , 2025 -
APA
Pohl, E., Silber, A. M., Pohl, S. F., & Sowerby, K. (2025). Structure-based drug design for new therapies for Leishmaniasis and Chagas disease. Acta Crystallographica. Section A: Foundations and Advances. Hoboken: Instituto de Ciências Biomédicas, Universidade de São Paulo. doi:10.1107/S2053273324099194 -
NLM
Pohl E, Silber AM, Pohl SF, Sowerby K. Structure-based drug design for new therapies for Leishmaniasis and Chagas disease [Internet]. Acta Crystallographica. Section A: Foundations and Advances. 2025 ; 80[citado 2026 mar. 15 ] Available from: https://doi.org/10.1107/S2053273324099194 -
Vancouver
Pohl E, Silber AM, Pohl SF, Sowerby K. Structure-based drug design for new therapies for Leishmaniasis and Chagas disease [Internet]. Acta Crystallographica. Section A: Foundations and Advances. 2025 ; 80[citado 2026 mar. 15 ] Available from: https://doi.org/10.1107/S2053273324099194 - Higher expression of proline dehydrogenase altered mitochondrial function and increased Trypanosoma cruzi differentiation in vitro and in the insect vector
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