Production and purification of L-asparaginase i small of Saccharomyces Cerevisiae (2018)
- Authors:
- Autor USP: MONTEIRO, GISELE - FCF
- Unidade: FCF
- Subjects: SACCHAROMYCES; ENZIMAS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Brazilian Journal of Pharmaceutical Sciences
- ISSN: 1984-8250
- Volume/Número/Paginação/Ano: v. 54, suppl. 1, p. 55 res. FCF105, 2018
- Conference titles: Pharmaceutical Science and Technology Meeting of the Faculty of Pharmaceutical Sciences, University of São Paulo
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ABNT
SILVA, Carolina e COSTA, Iris Munhoz e MONTEIRO, Gisele. Production and purification of L-asparaginase i small of Saccharomyces Cerevisiae. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. . Acesso em: 18 set. 2024. , 2018 -
APA
Silva, C., Costa, I. M., & Monteiro, G. (2018). Production and purification of L-asparaginase i small of Saccharomyces Cerevisiae. Brazilian Journal of Pharmaceutical Sciences. São Paulo: Faculdade de Ciências Farmacêuticas, Universidade de São Paulo. -
NLM
Silva C, Costa IM, Monteiro G. Production and purification of L-asparaginase i small of Saccharomyces Cerevisiae. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 55 res. FCF105.[citado 2024 set. 18 ] -
Vancouver
Silva C, Costa IM, Monteiro G. Production and purification of L-asparaginase i small of Saccharomyces Cerevisiae. Brazilian Journal of Pharmaceutical Sciences. 2018 ; 54 55 res. FCF105.[citado 2024 set. 18 ] - 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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