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Artigo de periodico
Protonation of two adjacent tyrosine residues influences the reduction of cytochrome 'c' by diphenylacetaldehyde: a possible mechanism to select the reducer agent of heme iron (2004)
Rinaldi, Tatiana Alvarez; Tersariol, Ivarne Luis dos Santos; Dyszy, Fabio Henrique; Prado, Fernanda Manso ; Nascimento, Otaciro Rangel ; Di Mascio, Paolo ; Nantes, Iseli Lourenço
Fonte: Free Radical Biology and Medicine. Unidades: IQ, IFSC
Assuntos: RADICAIS LIVRES, ESPECTROMETRIA DE MASSAS, RESSONÂNCIA PARAMAGNÉTICA DE SPIN, BIOQUÍMICA
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ABNT
RINALDI, Tatiana Alvarez et al. Protonation of two adjacent tyrosine residues influences the reduction of cytochrome 'c' by diphenylacetaldehyde: a possible mechanism to select the reducer agent of heme iron. Free Radical Biology and Medicine, v. 36, n. 6, p. 802-810, 2004Tradução . . Disponível em: https://doi.org/10.1016/j.freeradbiomed.2003.12.002. Acesso em: 19 out. 2024.
APA
Rinaldi, T. A., Tersariol, I. L. dos S., Dyszy, F. H., Prado, F. M., Nascimento, O. R., Di Mascio, P., & Nantes, I. L. (2004). Protonation of two adjacent tyrosine residues influences the reduction of cytochrome 'c' by diphenylacetaldehyde: a possible mechanism to select the reducer agent of heme iron. Free Radical Biology and Medicine, 36( 6), 802-810. doi:10.1016/j.freeradbiomed.2003.12.002
NLM
Rinaldi TA, Tersariol IL dos S, Dyszy FH, Prado FM, Nascimento OR, Di Mascio P, Nantes IL. Protonation of two adjacent tyrosine residues influences the reduction of cytochrome 'c' by diphenylacetaldehyde: a possible mechanism to select the reducer agent of heme iron [Internet]. Free Radical Biology and Medicine. 2004 ; 36( 6): 802-810.[citado 2024 out. 19 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2003.12.002
Vancouver
Rinaldi TA, Tersariol IL dos S, Dyszy FH, Prado FM, Nascimento OR, Di Mascio P, Nantes IL. Protonation of two adjacent tyrosine residues influences the reduction of cytochrome 'c' by diphenylacetaldehyde: a possible mechanism to select the reducer agent of heme iron [Internet]. Free Radical Biology and Medicine. 2004 ; 36( 6): 802-810.[citado 2024 out. 19 ] Available from: https://doi.org/10.1016/j.freeradbiomed.2003.12.002
Artigo de periodico
EPR studies of in vivo radical production by lipopolysaccharide: potential role of iron mobilized from iron-nitrosyl complexes (2003)
Linares, Edlaine ; Nakao, Lia Sumie; Augusto, Ohara ; Kadiiska, Maria B.
Fonte: Free Radical Biology and Medicine. Unidade: IQ
Assuntos: RADICAIS LIVRES, BIOQUÍMICA, RESSONÂNCIA PARAMAGNÉTICA DE SPIN
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LINARES, Edlaine et al. EPR studies of in vivo radical production by lipopolysaccharide: potential role of iron mobilized from iron-nitrosyl complexes. Free Radical Biology and Medicine, v. 34, n. 6, p. 766-773, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0891-5849(02)01424-7. Acesso em: 19 out. 2024.
APA
Linares, E., Nakao, L. S., Augusto, O., & Kadiiska, M. B. (2003). EPR studies of in vivo radical production by lipopolysaccharide: potential role of iron mobilized from iron-nitrosyl complexes. Free Radical Biology and Medicine, 34( 6), 766-773. doi:10.1016/s0891-5849(02)01424-7
NLM
Linares E, Nakao LS, Augusto O, Kadiiska MB. EPR studies of in vivo radical production by lipopolysaccharide: potential role of iron mobilized from iron-nitrosyl complexes [Internet]. Free Radical Biology and Medicine. 2003 ; 34( 6): 766-773.[citado 2024 out. 19 ] Available from: https://doi.org/10.1016/s0891-5849(02)01424-7
Vancouver
Linares E, Nakao LS, Augusto O, Kadiiska MB. EPR studies of in vivo radical production by lipopolysaccharide: potential role of iron mobilized from iron-nitrosyl complexes [Internet]. Free Radical Biology and Medicine. 2003 ; 34( 6): 766-773.[citado 2024 out. 19 ] Available from: https://doi.org/10.1016/s0891-5849(02)01424-7
Artigo de periodico
Synthesis and pharmacological properties of TOAC-labeled angiotensin and bradykinin analogs (2002)
Nakaie, C. R.; Silva, E. G.; Cilli, E. M.; Marchetto, R.; Schreier, Shirley ; Paiva, T. B.; Paiva, A. C. M.
Fonte: Peptides. Unidade: IQ
Assuntos: BIOQUÍMICA, PEPTÍDEOS (SÍNTESE), RESSONÂNCIA PARAMAGNÉTICA DE SPIN, FARMACOLOGIA (PROPRIEDADES)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NAKAIE, C. R. et al. Synthesis and pharmacological properties of TOAC-labeled angiotensin and bradykinin analogs. Peptides, v. 23, n. 1, p. 65-70, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0196-9781(01)00580-0. Acesso em: 19 out. 2024.
APA
Nakaie, C. R., Silva, E. G., Cilli, E. M., Marchetto, R., Schreier, S., Paiva, T. B., & Paiva, A. C. M. (2002). Synthesis and pharmacological properties of TOAC-labeled angiotensin and bradykinin analogs. Peptides, 23( 1), 65-70. doi:10.1016/s0196-9781(01)00580-0
NLM
Nakaie CR, Silva EG, Cilli EM, Marchetto R, Schreier S, Paiva TB, Paiva ACM. Synthesis and pharmacological properties of TOAC-labeled angiotensin and bradykinin analogs [Internet]. Peptides. 2002 ; 23( 1): 65-70.[citado 2024 out. 19 ] Available from: https://doi.org/10.1016/s0196-9781(01)00580-0
Vancouver
Nakaie CR, Silva EG, Cilli EM, Marchetto R, Schreier S, Paiva TB, Paiva ACM. Synthesis and pharmacological properties of TOAC-labeled angiotensin and bradykinin analogs [Internet]. Peptides. 2002 ; 23( 1): 65-70.[citado 2024 out. 19 ] Available from: https://doi.org/10.1016/s0196-9781(01)00580-0

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