Chemical and genetic validation of thiamine utilization as an antimalarial drug target (2013)
- Authors:
- Autor USP: WRENGER, CARSTEN - ICB
- Unidade: ICB
- DOI: 10.1038/ncomms3060
- Subjects: PARASITOLOGIA; ANTIMALÁRICOS; ANIMAIS PARASITOS; ERITRÓCITOS; PLASMODIUM FALCIPARUM; RNA MENSAGEIRO; CROMATOGRAFIA LÍQUIDA DE ALTA PRESSÃO; EXPRESSÃO GÊNICA; REGULAÇÃO GÊNICA; PROTEÍNAS RECOMBINANTES
- Language: Inglês
- Imprenta:
- Source:
- Título: Nature Communications
- ISSN: 2041-1723
- Volume/Número/Paginação/Ano: v. 4, p. 1-11, 2013
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: hybrid
- Licença: cc-by-nc-nd
-
ABNT
CHAN, Xie Wah Audrey et al. Chemical and genetic validation of thiamine utilization as an antimalarial drug target. Nature Communications, v. 4, p. 1-11, 2013Tradução . . Disponível em: https://doi.org/10.1038/ncomms3060. Acesso em: 03 out. 2024. -
APA
Chan, X. W. A., Wrenger, C., Stahl, K., Bärbel Bergmann,, Winterberg, M., Müller, I. B., & Saliba, K. J. (2013). Chemical and genetic validation of thiamine utilization as an antimalarial drug target. Nature Communications, 4, 1-11. doi:10.1038/ncomms3060 -
NLM
Chan XWA, Wrenger C, Stahl K, Bärbel Bergmann, Winterberg M, Müller IB, Saliba KJ. Chemical and genetic validation of thiamine utilization as an antimalarial drug target [Internet]. Nature Communications. 2013 ; 4 1-11.[citado 2024 out. 03 ] Available from: https://doi.org/10.1038/ncomms3060 -
Vancouver
Chan XWA, Wrenger C, Stahl K, Bärbel Bergmann, Winterberg M, Müller IB, Saliba KJ. Chemical and genetic validation of thiamine utilization as an antimalarial drug target [Internet]. Nature Communications. 2013 ; 4 1-11.[citado 2024 out. 03 ] Available from: https://doi.org/10.1038/ncomms3060 - Staphylococcus aureus thiaminase II: oligomerization warrants proteolytic protection against serine proteases
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- Genome and secretome analysis of Staphylotrichum longicolleum DSM105789 cultured on agro-residual and chitinous biomass
- In vitro activity of extracts and isolated polyphenols from West African medicinal plants against Plasmodium falciparum
- Oxidative stress control by apicomplexan parasites
- Identification of a non-competitive inhibitor of Plasmodium falciparum aspartate transcarbamoylase
- Molecular modeling applied to nucleic acid-based molecule development
- Crystallization and preliminary X-ray diffraction of malate dehydrogenase from Plasmodium falciparum
Informações sobre o DOI: 10.1038/ncomms3060 (Fonte: oaDOI API)
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