Use of pex and pgex bacterial heterologous protein expression systems for recombinant oncoprotein production and antisera generation (1997)
- Autores:
- Autor USP: SOGAYAR, MARI CLEIDE - IQ
- Unidade: IQ
- Assuntos: BIOQUÍMICA; ESCHERICHIA
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: Biotechnology and Applied Biochemistry
- Volume/Número/Paginação/Ano: v. 25, pt.3, p. 207-15, 1997
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ABNT
POMPEIA, C e ORTIS, Fernanda e ARMELIN, M C S. Use of pex and pgex bacterial heterologous protein expression systems for recombinant oncoprotein production and antisera generation. Biotechnology and Applied Biochemistry, v. 25, p. 207-15, 1997Tradução . . Acesso em: 24 abr. 2024. -
APA
Pompeia, C., Ortis, F., & Armelin, M. C. S. (1997). Use of pex and pgex bacterial heterologous protein expression systems for recombinant oncoprotein production and antisera generation. Biotechnology and Applied Biochemistry, 25, 207-15. -
NLM
Pompeia C, Ortis F, Armelin MCS. Use of pex and pgex bacterial heterologous protein expression systems for recombinant oncoprotein production and antisera generation. Biotechnology and Applied Biochemistry. 1997 ; 25 207-15.[citado 2024 abr. 24 ] -
Vancouver
Pompeia C, Ortis F, Armelin MCS. Use of pex and pgex bacterial heterologous protein expression systems for recombinant oncoprotein production and antisera generation. Biotechnology and Applied Biochemistry. 1997 ; 25 207-15.[citado 2024 abr. 24 ] - Role of polyoma t antigens in balb-c/3t3 cells growth control deregulation
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- T antigens role in polyomavirus transformation: c-myc but not c-fos or c-jun expression is a target for middle t
- Cdna cloning and expression of growth control genes
- Fibroblast growth factor and camp induce the expression of fos and jun proto-oncogenes in pc12 cells
- Molecular bases for the transformed to normal phenotypic reversion induced by glucocorticoid hormoners in rat glioma
- Cloning of differentially expressed genes involved glucocorticoid-induced phenotypic reversion of c6 glioma cells
- Hydrazine derivative - induced proliferation superimposed on citotoxity in cultured moused fibroblasts
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