Study of the production conditions of bacterial l-asparaginase in pichia pastoris (2018)
- Autores:
- Autor USP: MONTEIRO, GISELE - FCF
- Unidade: FCF
- Assunto: ENZIMAS
- Agências de fomento:
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: Brazilian Journal of Pharmaceutical Sciences
- ISSN: 1984-8250
- Volume/Número/Paginação/Ano: v. 54, suppl. 1, p. 51 res.FCF097, 2018
- Nome do evento: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo
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ABNT
HO, Daniele Chun e MONTEIRO, Gisele. Study of the production conditions of bacterial l-asparaginase in pichia pastoris. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 28 mar. 2024. , 2018 -
APA
Ho, D. C., & Monteiro, G. (2018). Study of the production conditions of bacterial l-asparaginase in pichia pastoris. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. -
NLM
Ho DC, Monteiro G. Study of the production conditions of bacterial l-asparaginase in pichia pastoris. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 51 res.FCF097.[citado 2024 mar. 28 ] -
Vancouver
Ho DC, Monteiro G. Study of the production conditions of bacterial l-asparaginase in pichia pastoris. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 51 res.FCF097.[citado 2024 mar. 28 ] - Cloning and expression of L-asparaginase from Escherichia coli in a Pichia pastoris strain with humanized glycosylation
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- Characterization of a type II L-Asparaginase from the halotolerant bacillus subtilis CH11
- Study of the Saccharomyces cerevisiae L-asparaginase 1 expression in Pichia pastoris glycoswitch strain): potential use in the treatment of acute lymphoblastic leukemia (LLA)
- Cloning and expression of L-asparaginase from Escherichia coli in a pichia pastoris strain with humanized glycosylation
- Identification of molecular targets associated with resistance or sensibility to analogs of rebeccamycin using saccharomyces cerevisiae as a model cell
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