Vitamin B6-dependent enzymes in the human malaria parasite Plasmodium falciparum: a druggable target? (2014)
- Authors:
- Kronenberger, Thales - Universidade de São Paulo (USP)
- Lindner, Jasmin - Universidade de São Paulo (USP)
- Meissner, Kamila Anna - Universidade de São Paulo (USP)
- Zimbres, Flávia Menezes - Universidade de São Paulo (USP)
- Coronado, Monika A.
- Sauer, Frank Martin - Universidade de São Paulo (USP)
- Schettert, Isolmar
- Wrenger, Carsten

- Autor USP: WRENGER, CARSTEN - ICB
- Unidade: ICB
- DOI: 10.1155/2014/108516
- Assunto: PARASITOLOGIA
- Language: Inglês
- Imprenta:
- Source:
- Título: Biomed Research International
- ISSN: 2314-6141
- Volume/Número/Paginação/Ano: v. 2014, ID 108516, p. 1-11, 2014
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
KRONENBERGER, Thales et al. Vitamin B6-dependent enzymes in the human malaria parasite Plasmodium falciparum: a druggable target?. Biomed Research International, v. 2014, p. 1-11, 2014Tradução . . Disponível em: https://doi.org/10.1155/2014/108516. Acesso em: 28 dez. 2025. -
APA
Kronenberger, T., Lindner, J., Meissner, K. A., Zimbres, F. M., Coronado, M. A., Sauer, F. M., et al. (2014). Vitamin B6-dependent enzymes in the human malaria parasite Plasmodium falciparum: a druggable target? Biomed Research International, 2014, 1-11. doi:10.1155/2014/108516 -
NLM
Kronenberger T, Lindner J, Meissner KA, Zimbres FM, Coronado MA, Sauer FM, Schettert I, Wrenger C. Vitamin B6-dependent enzymes in the human malaria parasite Plasmodium falciparum: a druggable target? [Internet]. Biomed Research International. 2014 ; 2014 1-11.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1155/2014/108516 -
Vancouver
Kronenberger T, Lindner J, Meissner KA, Zimbres FM, Coronado MA, Sauer FM, Schettert I, Wrenger C. Vitamin B6-dependent enzymes in the human malaria parasite Plasmodium falciparum: a druggable target? [Internet]. Biomed Research International. 2014 ; 2014 1-11.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1155/2014/108516 - Cytometric quantification of singlet oxygen in the human malaria parasite Plasmodium falciparum
- Exploring aspartate transcarbamoylase: a promising broad-spectrum target for drug development
- The crystal structure of the Plasmodium falciparum PdxK provides an experimental model for pro-drug activation
- Staphylococcus aureus thiaminase II: oligomerization warrants proteolytic protection against serine proteases
- Insights into the genome and secretome of Fusarium metavorans DSM105788 by cultivation on agro-residual biomass and synthetic nutrient sources
- Targeting the vitamin biosynthesis pathways for the treatment of malaria
- Plasmodium falciparum GFP-E-NTPDase expression at the intraerythrocytic stages and its inhibition blocks the development of the human malaria parasite
- 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
Informações sobre o DOI: 10.1155/2014/108516 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas