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Artigo de periodico
Proteomic profiling of the proteolytic events in the secretome of the transformed phenotype of melanocyte-derived cells using Terminal Amine Isotopic Labeling of Substrates (2019)
Liberato, Tarcisio; Fukushima, Isabella; Kitano, Eduardo S; Serrano, Solange M. T; Chammas, Roger; Zelanis, Andre
Source: Journal of proteomics. Unidade: FM
Subjects: PROTEÔMICA, MELANOMA, FENÓTIPOS, ONCOGENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIBERATO, Tarcisio et al. Proteomic profiling of the proteolytic events in the secretome of the transformed phenotype of melanocyte-derived cells using Terminal Amine Isotopic Labeling of Substrates. Journal of proteomics, v. 192, p. 291-298, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.jprot.2018.09.010. Acesso em: 10 maio 2024.
APA
Liberato, T., Fukushima, I., Kitano, E. S., Serrano, S. M. T., Chammas, R., & Zelanis, A. (2019). Proteomic profiling of the proteolytic events in the secretome of the transformed phenotype of melanocyte-derived cells using Terminal Amine Isotopic Labeling of Substrates. Journal of proteomics, 192, 291-298. doi:10.1016/j.jprot.2018.09.010
NLM
Liberato T, Fukushima I, Kitano ES, Serrano SMT, Chammas R, Zelanis A. Proteomic profiling of the proteolytic events in the secretome of the transformed phenotype of melanocyte-derived cells using Terminal Amine Isotopic Labeling of Substrates [Internet]. Journal of proteomics. 2019 ; 192 291-298.[citado 2024 maio 10 ] Available from: https://doi.org/10.1016/j.jprot.2018.09.010
Vancouver
Liberato T, Fukushima I, Kitano ES, Serrano SMT, Chammas R, Zelanis A. Proteomic profiling of the proteolytic events in the secretome of the transformed phenotype of melanocyte-derived cells using Terminal Amine Isotopic Labeling of Substrates [Internet]. Journal of proteomics. 2019 ; 192 291-298.[citado 2024 maio 10 ] Available from: https://doi.org/10.1016/j.jprot.2018.09.010
Artigo de periodico
A first step towards building spectral libraries as complementary tools for snake venom proteome/peptidome studies (2019)
Zelanis, Andre; Silva, Debora A; Kitano, Eduardo S ; Liberato, Tarcisio; Fukushima, Isabella; Serrano, Solange M. T; Tashima, Alexandre K
Source: Comparative biochemistry and physiology d-genomics & proteomics. Unidade: FM
Subjects: VENENOS DE ORIGEM ANIMAL, SERPENTES, PEPTÍDEOS, PROTEÍNAS, PROTEÔMICA, BANCO DE DADOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZELANIS, Andre et al. A first step towards building spectral libraries as complementary tools for snake venom proteome/peptidome studies. Comparative biochemistry and physiology d-genomics & proteomics, v. 31, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.cbd.2019.100599. Acesso em: 10 maio 2024.
APA
Zelanis, A., Silva, D. A., Kitano, E. S., Liberato, T., Fukushima, I., Serrano, S. M. T., & Tashima, A. K. (2019). A first step towards building spectral libraries as complementary tools for snake venom proteome/peptidome studies. Comparative biochemistry and physiology d-genomics & proteomics, 31. doi:10.1016/j.cbd.2019.100599
NLM
Zelanis A, Silva DA, Kitano ES, Liberato T, Fukushima I, Serrano SMT, Tashima AK. A first step towards building spectral libraries as complementary tools for snake venom proteome/peptidome studies [Internet]. Comparative biochemistry and physiology d-genomics & proteomics. 2019 ; 31[citado 2024 maio 10 ] Available from: https://doi.org/10.1016/j.cbd.2019.100599
Vancouver
Zelanis A, Silva DA, Kitano ES, Liberato T, Fukushima I, Serrano SMT, Tashima AK. A first step towards building spectral libraries as complementary tools for snake venom proteome/peptidome studies [Internet]. Comparative biochemistry and physiology d-genomics & proteomics. 2019 ; 31[citado 2024 maio 10 ] Available from: https://doi.org/10.1016/j.cbd.2019.100599
Artigo de periodico
Proteomic and interactome approaches reveal PAK4, PHB-2, and 14-3-3 eta as targets of overactivated Cdc42 in cellular responses to Genomic instability (2019)
Silva, Luiz E; Souza, Renan C; Kitano, Eduardo S; Monteiro, Lucas F; Iwai, Leo Kei ; Forti, Fábio Luís
Source: Journal of Proteome Research. Unidade: IQ
Subjects: RADIAÇÃO ULTRAVIOLETA, GENÔMICA, ESPECTROMETRIA DE MASSAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Luiz E et al. Proteomic and interactome approaches reveal PAK4, PHB-2, and 14-3-3 eta as targets of overactivated Cdc42 in cellular responses to Genomic instability. Journal of Proteome Research, v. 18, n. 10, p. 3597-3614, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.jproteome.9b00260. Acesso em: 10 maio 2024.
APA
Silva, L. E., Souza, R. C., Kitano, E. S., Monteiro, L. F., Iwai, L. K., & Forti, F. L. (2019). Proteomic and interactome approaches reveal PAK4, PHB-2, and 14-3-3 eta as targets of overactivated Cdc42 in cellular responses to Genomic instability. Journal of Proteome Research, 18( 10), 3597-3614. doi:10.1021/acs.jproteome.9b00260
NLM
Silva LE, Souza RC, Kitano ES, Monteiro LF, Iwai LK, Forti FL. Proteomic and interactome approaches reveal PAK4, PHB-2, and 14-3-3 eta as targets of overactivated Cdc42 in cellular responses to Genomic instability [Internet]. Journal of Proteome Research. 2019 ; 18( 10): 3597-3614.[citado 2024 maio 10 ] Available from: https://doi.org/10.1021/acs.jproteome.9b00260
Vancouver
Silva LE, Souza RC, Kitano ES, Monteiro LF, Iwai LK, Forti FL. Proteomic and interactome approaches reveal PAK4, PHB-2, and 14-3-3 eta as targets of overactivated Cdc42 in cellular responses to Genomic instability [Internet]. Journal of Proteome Research. 2019 ; 18( 10): 3597-3614.[citado 2024 maio 10 ] Available from: https://doi.org/10.1021/acs.jproteome.9b00260

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