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  • Source: Frontiers in Bioengineering and Biotechnology. Unidades: IQ, FM

    Subjects: ORGANELAS CELULARES, ENGENHARIA TECIDUAL, ORGANELAS CELULARES, INTESTINO DELGADO

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      LEVIN, Gabriel et al. R-Spondin 1 (RSPO1) increases mouse intestinal organoid unit size and survival in vitro and improves tissue-engineered small intestine formation in vivo. Frontiers in Bioengineering and Biotechnology, v. 8, p. 1-13 art. 476, 2020Tradução . . Disponível em: https://doi.org/10.3389/fbioe.2020.00476. Acesso em: 08 jun. 2024.
    • APA

      Levin, G., Zuber, S. M., Squillaro, A. I., Sogayar, M. C., Grikscheit, T. C., & Carreira, A. C. O. (2020). R-Spondin 1 (RSPO1) increases mouse intestinal organoid unit size and survival in vitro and improves tissue-engineered small intestine formation in vivo. Frontiers in Bioengineering and Biotechnology, 8, 1-13 art. 476. doi:10.3389/fbioe.2020.00476
    • NLM

      Levin G, Zuber SM, Squillaro AI, Sogayar MC, Grikscheit TC, Carreira ACO. R-Spondin 1 (RSPO1) increases mouse intestinal organoid unit size and survival in vitro and improves tissue-engineered small intestine formation in vivo [Internet]. Frontiers in Bioengineering and Biotechnology. 2020 ; 8 1-13 art. 476.[citado 2024 jun. 08 ] Available from: https://doi.org/10.3389/fbioe.2020.00476
    • Vancouver

      Levin G, Zuber SM, Squillaro AI, Sogayar MC, Grikscheit TC, Carreira ACO. R-Spondin 1 (RSPO1) increases mouse intestinal organoid unit size and survival in vitro and improves tissue-engineered small intestine formation in vivo [Internet]. Frontiers in Bioengineering and Biotechnology. 2020 ; 8 1-13 art. 476.[citado 2024 jun. 08 ] Available from: https://doi.org/10.3389/fbioe.2020.00476
  • Source: Abstracts. Conference titles: Congress of the Brazilian Society for Cell Biology. Unidade: IQ

    Subjects: NEOPLASIAS MAMÁRIAS, EXPRESSÃO GÊNICA

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      BATISTA, Marco Lázaro de Sousa et al. Investigating the role played by CD90/Thy-1 and EGFR in breast cancer by pathways and system biology approaches. 2018, Anais.. São Paulo: Sociedade Brasileira de Biologia Celular/SBBC, 2018. Disponível em: http://www.sbbc.org.br/wp-content/uploads/2014/08/Livro-ResumosSBBC2018.pdf. Acesso em: 08 jun. 2024.
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      Batista, M. L. de S., Lobba, A. R. M., Carreira, A. C. O., Sogayar, M. C., & Nishiyama Junior, M. Y. (2018). Investigating the role played by CD90/Thy-1 and EGFR in breast cancer by pathways and system biology approaches. In Abstracts. São Paulo: Sociedade Brasileira de Biologia Celular/SBBC. Recuperado de http://www.sbbc.org.br/wp-content/uploads/2014/08/Livro-ResumosSBBC2018.pdf
    • NLM

      Batista ML de S, Lobba ARM, Carreira ACO, Sogayar MC, Nishiyama Junior MY. Investigating the role played by CD90/Thy-1 and EGFR in breast cancer by pathways and system biology approaches [Internet]. Abstracts. 2018 ;[citado 2024 jun. 08 ] Available from: http://www.sbbc.org.br/wp-content/uploads/2014/08/Livro-ResumosSBBC2018.pdf
    • Vancouver

      Batista ML de S, Lobba ARM, Carreira ACO, Sogayar MC, Nishiyama Junior MY. Investigating the role played by CD90/Thy-1 and EGFR in breast cancer by pathways and system biology approaches [Internet]. Abstracts. 2018 ;[citado 2024 jun. 08 ] Available from: http://www.sbbc.org.br/wp-content/uploads/2014/08/Livro-ResumosSBBC2018.pdf
  • Source: Abstracts. Conference titles: Congress of the Brazilian Society for Cell Biology. Unidade: IQ

    Subjects: NEOPLASIAS MAMÁRIAS, EXPRESSÃO GÊNICA

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      FERREIRA, Henrique César de Jesus et al. Identification and functional characterization of lncRNA LINC01133 by CRISPR/CAS9 editing system in human breast cancer cell lines. 2018, Anais.. São Paulo: Sociedade Brasileira de Biologia Celular/SBBC, 2018. Disponível em: http://www.sbbc.org.br/wp-content/uploads/2014/08/Livro-ResumosSBBC2018.pdf. Acesso em: 08 jun. 2024.
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      Ferreira, H. C. de J., Machado, R. A. C., Carreira, A. C. O., & Sogayar, M. C. (2018). Identification and functional characterization of lncRNA LINC01133 by CRISPR/CAS9 editing system in human breast cancer cell lines. In Abstracts. São Paulo: Sociedade Brasileira de Biologia Celular/SBBC. Recuperado de http://www.sbbc.org.br/wp-content/uploads/2014/08/Livro-ResumosSBBC2018.pdf
    • NLM

      Ferreira HC de J, Machado RAC, Carreira ACO, Sogayar MC. Identification and functional characterization of lncRNA LINC01133 by CRISPR/CAS9 editing system in human breast cancer cell lines [Internet]. Abstracts. 2018 ;[citado 2024 jun. 08 ] Available from: http://www.sbbc.org.br/wp-content/uploads/2014/08/Livro-ResumosSBBC2018.pdf
    • Vancouver

      Ferreira HC de J, Machado RAC, Carreira ACO, Sogayar MC. Identification and functional characterization of lncRNA LINC01133 by CRISPR/CAS9 editing system in human breast cancer cell lines [Internet]. Abstracts. 2018 ;[citado 2024 jun. 08 ] Available from: http://www.sbbc.org.br/wp-content/uploads/2014/08/Livro-ResumosSBBC2018.pdf
  • Source: Haemophilia. Unidades: IME, IQ, BIOTECNOLOGIA

    Subjects: BIOINFORMÁTICA, HEMOFILIA

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      MOLINA, Erika de Simone et al. A quantitative and humane tail bleeding assay for efficacy evaluation of antihaemophilic factors in haemophilia A mice. Haemophilia, v. 20, p. e392-e398, 2014Tradução . . Disponível em: https://doi.org/10.1111/hae.12484. Acesso em: 08 jun. 2024.
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      Molina, E. de S., Fujita, A., Sogayar, M. C., & Demasi, M. A. A. (2014). A quantitative and humane tail bleeding assay for efficacy evaluation of antihaemophilic factors in haemophilia A mice. Haemophilia, 20, e392-e398. doi:10.1111/hae.12484
    • NLM

      Molina E de S, Fujita A, Sogayar MC, Demasi MAA. A quantitative and humane tail bleeding assay for efficacy evaluation of antihaemophilic factors in haemophilia A mice [Internet]. Haemophilia. 2014 ; 20 e392-e398.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1111/hae.12484
    • Vancouver

      Molina E de S, Fujita A, Sogayar MC, Demasi MAA. A quantitative and humane tail bleeding assay for efficacy evaluation of antihaemophilic factors in haemophilia A mice [Internet]. Haemophilia. 2014 ; 20 e392-e398.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1111/hae.12484
  • Source: BMC Cell Biology. Unidades: IME, IQ

    Assunto: BIOLOGIA CELULAR

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      HALCSIK, Erik et al. New insights in osteogenic differentiation revealed by mass spectrometric assessment of phosphorylated substrates in murine skin mesenchymal cells. BMC Cell Biology, v. 14, p. 1-19, 2013Tradução . . Disponível em: https://doi.org/10.1186/1471-2121-14-47. Acesso em: 08 jun. 2024.
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      Halcsik, E., Forni, M. F., Fujita, A., Verano-Braga, T., Jensen, O. N., & Sogayar, M. C. (2013). New insights in osteogenic differentiation revealed by mass spectrometric assessment of phosphorylated substrates in murine skin mesenchymal cells. BMC Cell Biology, 14, 1-19. doi:10.1186/1471-2121-14-47
    • NLM

      Halcsik E, Forni MF, Fujita A, Verano-Braga T, Jensen ON, Sogayar MC. New insights in osteogenic differentiation revealed by mass spectrometric assessment of phosphorylated substrates in murine skin mesenchymal cells [Internet]. BMC Cell Biology. 2013 ; 14 1-19.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1186/1471-2121-14-47
    • Vancouver

      Halcsik E, Forni MF, Fujita A, Verano-Braga T, Jensen ON, Sogayar MC. New insights in osteogenic differentiation revealed by mass spectrometric assessment of phosphorylated substrates in murine skin mesenchymal cells [Internet]. BMC Cell Biology. 2013 ; 14 1-19.[citado 2024 jun. 08 ] Available from: https://doi.org/10.1186/1471-2121-14-47

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