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  • Source: Parasites & Vectros. Unidade: FM

    Subjects: LEISHMANIA (IMUNOLOGIA;PARASITOLOGIA), PROTEÍNAS, PROLIFERAÇÃO CELULAR, IMUNIZAÇÃO, INFLAMAÇÃO, LINFÓCITOS T

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      PASSERO, Luiz Felipe D. et al. Proteins of Leishmania (Viannia) shawi confer protection associated with Th1 immune response and memory generation. Parasites & Vectros, v. 5, n. 64, p. (on-line), 2012Tradução . . Disponível em: https://doi.org/10.1186/1756-3305-5-64. Acesso em: 17 jul. 2024.
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      Passero, L. F. D., Carvalho, A. K., Bordon, M. L. A. C., Bonfim-Melo, A., Carvalho, K., Kallás, E. G., et al. (2012). Proteins of Leishmania (Viannia) shawi confer protection associated with Th1 immune response and memory generation. Parasites & Vectros, 5( 64), (on-line). doi:10.1186/1756-3305-5-64
    • NLM

      Passero LFD, Carvalho AK, Bordon MLAC, Bonfim-Melo A, Carvalho K, Kallás EG, Santos BBA, Toyama MH, Paes-Leme A, Corbett CEP, Laurenti MD. Proteins of Leishmania (Viannia) shawi confer protection associated with Th1 immune response and memory generation [Internet]. Parasites & Vectros. 2012 ; 5( 64): (on-line).[citado 2024 jul. 17 ] Available from: https://doi.org/10.1186/1756-3305-5-64
    • Vancouver

      Passero LFD, Carvalho AK, Bordon MLAC, Bonfim-Melo A, Carvalho K, Kallás EG, Santos BBA, Toyama MH, Paes-Leme A, Corbett CEP, Laurenti MD. Proteins of Leishmania (Viannia) shawi confer protection associated with Th1 immune response and memory generation [Internet]. Parasites & Vectros. 2012 ; 5( 64): (on-line).[citado 2024 jul. 17 ] Available from: https://doi.org/10.1186/1756-3305-5-64
  • Source: Carcinogenesis. Unidade: IQ

    Subjects: DANO AO DNA, NEOPLASIAS, BIOQUÍMICA, CARCINOGÊNESE ANIMAL

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      MAYNARD, Scott et al. Base excision repair of oxidative DNA damage and association with cancer and aging. Carcinogenesis, v. 30, n. 1, p. 2-10, 2009Tradução . . Disponível em: https://doi.org/10.1093/carcin/bgn250. Acesso em: 17 jul. 2024.
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      Maynard, S., Harboe, C., Souza-Pinto, N. C. de, & Bohr, V. A. (2009). Base excision repair of oxidative DNA damage and association with cancer and aging. Carcinogenesis, 30( 1), 2-10. doi:10.1093/carcin/bgn250
    • NLM

      Maynard S, Harboe C, Souza-Pinto NC de, Bohr VA. Base excision repair of oxidative DNA damage and association with cancer and aging [Internet]. Carcinogenesis. 2009 ; 30( 1): 2-10.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/carcin/bgn250
    • Vancouver

      Maynard S, Harboe C, Souza-Pinto NC de, Bohr VA. Base excision repair of oxidative DNA damage and association with cancer and aging [Internet]. Carcinogenesis. 2009 ; 30( 1): 2-10.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/carcin/bgn250
  • Source: Journal of Nanobiotechnology. Unidade: IQ

    Subjects: NANOPARTÍCULAS, NANOTECNOLOGIA, CANDIDA ALBICANS

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      VIEIRA, Débora Braga e CARMONA-RIBEIRO, Ana Maria. Cationic nanoparticles for delivery of amphotericin B: preparation, characterization and activity in vitro. Journal of Nanobiotechnology, v. 6, n. 6, p. online, 2008Tradução . . Disponível em: https://doi.org/10.1186/1477-3155-6-6. Acesso em: 17 jul. 2024.
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      Vieira, D. B., & Carmona-Ribeiro, A. M. (2008). Cationic nanoparticles for delivery of amphotericin B: preparation, characterization and activity in vitro. Journal of Nanobiotechnology, 6( 6), online. doi:10.1186/1477-3155-6-6
    • NLM

      Vieira DB, Carmona-Ribeiro AM. Cationic nanoparticles for delivery of amphotericin B: preparation, characterization and activity in vitro [Internet]. Journal of Nanobiotechnology. 2008 ; 6( 6): online.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1186/1477-3155-6-6
    • Vancouver

      Vieira DB, Carmona-Ribeiro AM. Cationic nanoparticles for delivery of amphotericin B: preparation, characterization and activity in vitro [Internet]. Journal of Nanobiotechnology. 2008 ; 6( 6): online.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1186/1477-3155-6-6
  • Source: Microbial Cell Factories. Unidade: IQ

    Subjects: SACCHAROMYCES, BIOQUÍMICA

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      BADOTTI, Fernanda et al. Switching the mode of sucrose utilization by Saccharomyces cerevisiae. Microbial Cell Factories, v. 7, n. 4, p. 1-11, 2008Tradução . . Disponível em: https://doi.org/10.1186/1475-2859-7-4. Acesso em: 17 jul. 2024.
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      Badotti, F., Dário, M. G., Alves Jr., S. L., Cordioli, M. L. A., Miletti, L. C., De Araujo, P. S., & Stambuk, B. J. C. U. (2008). Switching the mode of sucrose utilization by Saccharomyces cerevisiae. Microbial Cell Factories, 7( 4), 1-11. doi:10.1186/1475-2859-7-4
    • NLM

      Badotti F, Dário MG, Alves Jr. SL, Cordioli MLA, Miletti LC, De Araujo PS, Stambuk BJCU. Switching the mode of sucrose utilization by Saccharomyces cerevisiae [Internet]. Microbial Cell Factories. 2008 ; 7( 4): 1-11.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1186/1475-2859-7-4
    • Vancouver

      Badotti F, Dário MG, Alves Jr. SL, Cordioli MLA, Miletti LC, De Araujo PS, Stambuk BJCU. Switching the mode of sucrose utilization by Saccharomyces cerevisiae [Internet]. Microbial Cell Factories. 2008 ; 7( 4): 1-11.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1186/1475-2859-7-4
  • Source: Bioinformatics. Unidade: IQ

    Assunto: BIOINFORMÁTICA

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      SOUZA, Robson Francisco de et al. AMIN domains have a predicted role in localization of diverse periplasmic protein complexes. Bioinformatics, v. 24, n. 21 2008, p. 2423-2426, 2008Tradução . . Disponível em: https://doi.org/10.1093/bioinformatics/btn449. Acesso em: 17 jul. 2024.
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      Souza, R. F. de, Anantharaman, V., Souza, S. J. de, Aravind, L., & Gueiros Filho, F. J. (2008). AMIN domains have a predicted role in localization of diverse periplasmic protein complexes. Bioinformatics, 24( 21 2008), 2423-2426. doi:10.1093/bioinformatics/btn449
    • NLM

      Souza RF de, Anantharaman V, Souza SJ de, Aravind L, Gueiros Filho FJ. AMIN domains have a predicted role in localization of diverse periplasmic protein complexes [Internet]. Bioinformatics. 2008 ; 24( 21 2008): 2423-2426.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/bioinformatics/btn449
    • Vancouver

      Souza RF de, Anantharaman V, Souza SJ de, Aravind L, Gueiros Filho FJ. AMIN domains have a predicted role in localization of diverse periplasmic protein complexes [Internet]. Bioinformatics. 2008 ; 24( 21 2008): 2423-2426.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/bioinformatics/btn449
  • Source: Bioinformatics. Unidades: IME, IQ, BIOINFORMÁTICA

    Subjects: EXPRESSÃO GÊNICA, BIOQUÍMICA

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      FUJITA, André et al. Time-varying modeling of gene expression regulatory networks using the wavelet dynamic vector autoregressive method. Bioinformatics, v. 23, n. 13, p. 1623-1630, 2007Tradução . . Disponível em: https://doi.org/10.1093/bioinformatics/btm151. Acesso em: 17 jul. 2024.
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      Fujita, A., Sato, J. R., Garay-Malpartida, H. M., Morettin, P. A., Sogayar, M. C., & Ferreira, C. E. (2007). Time-varying modeling of gene expression regulatory networks using the wavelet dynamic vector autoregressive method. Bioinformatics, 23( 13), 1623-1630. doi:10.1093/bioinformatics/btm151
    • NLM

      Fujita A, Sato JR, Garay-Malpartida HM, Morettin PA, Sogayar MC, Ferreira CE. Time-varying modeling of gene expression regulatory networks using the wavelet dynamic vector autoregressive method [Internet]. Bioinformatics. 2007 ; 23( 13): 1623-1630.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/bioinformatics/btm151
    • Vancouver

      Fujita A, Sato JR, Garay-Malpartida HM, Morettin PA, Sogayar MC, Ferreira CE. Time-varying modeling of gene expression regulatory networks using the wavelet dynamic vector autoregressive method [Internet]. Bioinformatics. 2007 ; 23( 13): 1623-1630.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/bioinformatics/btm151
  • Source: Journal of Antimicrobial Chemotherapy. Unidade: IQ

    Subjects: SINERGISMO DE DROGAS, BIOQUÍMICA

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      LINCOPAN, Nilton e CARMONA-RIBEIRO, Ana Maria. Lipid-covered drug particles: combined action of dioctadecyldimethylammonium bromide and amphotericin B or miconazole. Journal of Antimicrobial Chemotherapy, v. 58, n. 1, p. 66-75, 2006Tradução . . Disponível em: https://doi.org/10.1093/jac/dkl153. Acesso em: 17 jul. 2024.
    • APA

      Lincopan, N., & Carmona-Ribeiro, A. M. (2006). Lipid-covered drug particles: combined action of dioctadecyldimethylammonium bromide and amphotericin B or miconazole. Journal of Antimicrobial Chemotherapy, 58( 1), 66-75. doi:10.1093/jac/dkl153
    • NLM

      Lincopan N, Carmona-Ribeiro AM. Lipid-covered drug particles: combined action of dioctadecyldimethylammonium bromide and amphotericin B or miconazole [Internet]. Journal of Antimicrobial Chemotherapy. 2006 ; 58( 1): 66-75.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/jac/dkl153
    • Vancouver

      Lincopan N, Carmona-Ribeiro AM. Lipid-covered drug particles: combined action of dioctadecyldimethylammonium bromide and amphotericin B or miconazole [Internet]. Journal of Antimicrobial Chemotherapy. 2006 ; 58( 1): 66-75.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/jac/dkl153
  • Source: Journal of Antimicrobial Chemotherapy. Unidade: IQ

    Subjects: CANDIDA ALBICANS, ADSORÇÃO, ANTIFÚNGICOS (ATIVIDADE)

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      VIEIRA, Débora Braga e CARMONA-RIBEIRO, Ana Maria. Cationic lipids and surfactants as antifungal agents: mode of action. Journal of Antimicrobial Chemotherapy, v. 58, n. 4, p. 760-767, 2006Tradução . . Disponível em: https://doi.org/10.1093/jac/dkl312. Acesso em: 17 jul. 2024.
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      Vieira, D. B., & Carmona-Ribeiro, A. M. (2006). Cationic lipids and surfactants as antifungal agents: mode of action. Journal of Antimicrobial Chemotherapy, 58( 4), 760-767. doi:10.1093/jac/dkl312
    • NLM

      Vieira DB, Carmona-Ribeiro AM. Cationic lipids and surfactants as antifungal agents: mode of action [Internet]. Journal of Antimicrobial Chemotherapy. 2006 ; 58( 4): 760-767.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/jac/dkl312
    • Vancouver

      Vieira DB, Carmona-Ribeiro AM. Cationic lipids and surfactants as antifungal agents: mode of action [Internet]. Journal of Antimicrobial Chemotherapy. 2006 ; 58( 4): 760-767.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/jac/dkl312
  • Source: Malaria Journal. Unidades: ICB, FCF

    Subjects: PLASMODIUM, IMUNOLOGIA, PLASMODIUM, ANTÍGENOS

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      OLIVEIRA, Tatiane Rodrigues de et al. Evaluation of the acquired immune responses to Plasmodium vivax VIR variant antigens in individuals living in malaria-endemic areas of Brazil. Malaria Journal, v. 5, p. 1-10, 2006Tradução . . Acesso em: 17 jul. 2024.
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      Oliveira, T. R. de, Fernandez-Becerra, C., Jimenez, M. C. S., Del Portillo, H. A., & Soares, I. da S. (2006). Evaluation of the acquired immune responses to Plasmodium vivax VIR variant antigens in individuals living in malaria-endemic areas of Brazil. Malaria Journal, 5, 1-10.
    • NLM

      Oliveira TR de, Fernandez-Becerra C, Jimenez MCS, Del Portillo HA, Soares I da S. Evaluation of the acquired immune responses to Plasmodium vivax VIR variant antigens in individuals living in malaria-endemic areas of Brazil. Malaria Journal. 2006 ; 5 1-10.[citado 2024 jul. 17 ]
    • Vancouver

      Oliveira TR de, Fernandez-Becerra C, Jimenez MCS, Del Portillo HA, Soares I da S. Evaluation of the acquired immune responses to Plasmodium vivax VIR variant antigens in individuals living in malaria-endemic areas of Brazil. Malaria Journal. 2006 ; 5 1-10.[citado 2024 jul. 17 ]
  • Source: Journal of Antimicrobial Chemotherapy. Unidade: FCF

    Subjects: MYCOBACTERIUM TUBERCULOSIS, RESISTÊNCIA MICROBIANA ÀS DROGAS

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      BARCO, Patrícia et al. pncA mutations in pyrazinamide-resistant Mycobacterium tuberculosis clinical isolates from the southeast region of Brazil. Journal of Antimicrobial Chemotherapy, v. 58, n. 5, p. 930-935, 2006Tradução . . Disponível em: https://doi.org/10.1093/jac/dkl363. Acesso em: 17 jul. 2024.
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      Barco, P., Cardoso, R. F., Hirata, R. D. C., Leite, C. Q. F., Pandolfi, J. R. C., Sato, D. N., et al. (2006). pncA mutations in pyrazinamide-resistant Mycobacterium tuberculosis clinical isolates from the southeast region of Brazil. Journal of Antimicrobial Chemotherapy, 58( 5), 930-935. doi:10.1093/jac/dkl363
    • NLM

      Barco P, Cardoso RF, Hirata RDC, Leite CQF, Pandolfi JRC, Sato DN, Shikama M de L, Melo FAF de, Mamizuka EM, Campanerut PAZ, Hirata MH. pncA mutations in pyrazinamide-resistant Mycobacterium tuberculosis clinical isolates from the southeast region of Brazil [Internet]. Journal of Antimicrobial Chemotherapy. 2006 ; 58( 5): 930-935.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/jac/dkl363
    • Vancouver

      Barco P, Cardoso RF, Hirata RDC, Leite CQF, Pandolfi JRC, Sato DN, Shikama M de L, Melo FAF de, Mamizuka EM, Campanerut PAZ, Hirata MH. pncA mutations in pyrazinamide-resistant Mycobacterium tuberculosis clinical isolates from the southeast region of Brazil [Internet]. Journal of Antimicrobial Chemotherapy. 2006 ; 58( 5): 930-935.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/jac/dkl363
  • Source: Carcinogenesis. Unidade: FCF

    Subjects: MELANOMA ANIMAL, CARCINOGÊNESE ANIMAL

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      ESPÍNDOLA, Roseli de Moura et al. Geranylgeraniol and beta-ionone inhibit hepatic preneoplastic lesions, cell proliferation, total plasma cholesterol and DNA damage during the initial phases of hepatocarcinogenesis, but only the former inhibits NF-'kappa'B activation. Carcinogenesis, v. 26, n. 6, p. 1091-1099, 2005Tradução . . Disponível em: https://doi.org/10.1093/carcin/bgi047. Acesso em: 17 jul. 2024.
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      Espíndola, R. de M., Mazzantini, R. P., Ong, T. P., Conti, A. de, Heidor, R., & Moreno, F. S. (2005). Geranylgeraniol and beta-ionone inhibit hepatic preneoplastic lesions, cell proliferation, total plasma cholesterol and DNA damage during the initial phases of hepatocarcinogenesis, but only the former inhibits NF-'kappa'B activation. Carcinogenesis, 26( 6), 1091-1099. doi:10.1093/carcin/bgi047
    • NLM

      Espíndola R de M, Mazzantini RP, Ong TP, Conti A de, Heidor R, Moreno FS. Geranylgeraniol and beta-ionone inhibit hepatic preneoplastic lesions, cell proliferation, total plasma cholesterol and DNA damage during the initial phases of hepatocarcinogenesis, but only the former inhibits NF-'kappa'B activation [Internet]. Carcinogenesis. 2005 ; 26( 6): 1091-1099.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/carcin/bgi047
    • Vancouver

      Espíndola R de M, Mazzantini RP, Ong TP, Conti A de, Heidor R, Moreno FS. Geranylgeraniol and beta-ionone inhibit hepatic preneoplastic lesions, cell proliferation, total plasma cholesterol and DNA damage during the initial phases of hepatocarcinogenesis, but only the former inhibits NF-'kappa'B activation [Internet]. Carcinogenesis. 2005 ; 26( 6): 1091-1099.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/carcin/bgi047
  • Source: Carcinogenesis. Unidade: FCF

    Subjects: NUTRIÇÃO, NEOPLASIAS HEPÁTICAS (PREVENÇÃO E CONTROLE), VITAMINA A, CARCINÓGENOS QUÍMICOS

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      FONSSECA, Elaine Maria de Almeida et al. All-trans and 9-cis retinoic acids, retinol and 'beta'-carotene chemopreventive activities during the initial phases of hepatocarcinogenesis involve distinct actions on glutathione S-transferase positive preneoplastic lesions remodeling and DNA damage. Carcinogenesis, v. 26, n. 11, p. 1940-1946, 2005Tradução . . Acesso em: 17 jul. 2024.
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      Fonsseca, E. M. de A., Chagas, C. E. A., Mazzantini, R. P., Heidor, R., Ong, T. P., & Moreno, F. S. (2005). All-trans and 9-cis retinoic acids, retinol and 'beta'-carotene chemopreventive activities during the initial phases of hepatocarcinogenesis involve distinct actions on glutathione S-transferase positive preneoplastic lesions remodeling and DNA damage. Carcinogenesis, 26( 11), 1940-1946.
    • NLM

      Fonsseca EM de A, Chagas CEA, Mazzantini RP, Heidor R, Ong TP, Moreno FS. All-trans and 9-cis retinoic acids, retinol and 'beta'-carotene chemopreventive activities during the initial phases of hepatocarcinogenesis involve distinct actions on glutathione S-transferase positive preneoplastic lesions remodeling and DNA damage. Carcinogenesis. 2005 ; 26( 11): 1940-1946.[citado 2024 jul. 17 ]
    • Vancouver

      Fonsseca EM de A, Chagas CEA, Mazzantini RP, Heidor R, Ong TP, Moreno FS. All-trans and 9-cis retinoic acids, retinol and 'beta'-carotene chemopreventive activities during the initial phases of hepatocarcinogenesis involve distinct actions on glutathione S-transferase positive preneoplastic lesions remodeling and DNA damage. Carcinogenesis. 2005 ; 26( 11): 1940-1946.[citado 2024 jul. 17 ]
  • Source: Journal of Antimicrobial Chemotherapy. Unidades: FCF, IQ

    Subjects: BIOQUÍMICA, HISTOPATOLOGIA ANIMAL

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      LINCOPAN, Nilton e MAMIZUKA, Elsa Masae e CARMONA-RIBEIRO, Ana Maria. Low nephrotoxicity of an effective amphotericin B formulation with cationic bilayer fragments. Journal of Antimicrobial Chemotherapy, v. 55, n. 5, p. 727-734, 2005Tradução . . Disponível em: https://doi.org/10.1093/jac/dki064. Acesso em: 17 jul. 2024.
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      Lincopan, N., Mamizuka, E. M., & Carmona-Ribeiro, A. M. (2005). Low nephrotoxicity of an effective amphotericin B formulation with cationic bilayer fragments. Journal of Antimicrobial Chemotherapy, 55( 5), 727-734. doi:10.1093/jac/dki064
    • NLM

      Lincopan N, Mamizuka EM, Carmona-Ribeiro AM. Low nephrotoxicity of an effective amphotericin B formulation with cationic bilayer fragments [Internet]. Journal of Antimicrobial Chemotherapy. 2005 ; 55( 5): 727-734.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/jac/dki064
    • Vancouver

      Lincopan N, Mamizuka EM, Carmona-Ribeiro AM. Low nephrotoxicity of an effective amphotericin B formulation with cationic bilayer fragments [Internet]. Journal of Antimicrobial Chemotherapy. 2005 ; 55( 5): 727-734.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/jac/dki064
  • Source: Bioinformactics. Unidade: IQ

    Subjects: BIOQUÍMICA, BIOLOGIA MOLECULAR

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      PAQUOLA, Apuã C. M. et al. ESTWeb: bioinformatics services for EST sequencing projects. Bioinformactics, v. 19, n. 12, p. 1587-1588, 2003Tradução . . Disponível em: https://doi.org/10.1093/bioinformatics/btg196. Acesso em: 17 jul. 2024.
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      Paquola, A. C. M., Nishyiama Junior, M. Y., Reis, E. M., Da Silva, A. M., & Verjovski-Almeida, S. (2003). ESTWeb: bioinformatics services for EST sequencing projects. Bioinformactics, 19( 12), 1587-1588. doi:10.1093/bioinformatics/btg196
    • NLM

      Paquola ACM, Nishyiama Junior MY, Reis EM, Da Silva AM, Verjovski-Almeida S. ESTWeb: bioinformatics services for EST sequencing projects [Internet]. Bioinformactics. 2003 ; 19( 12): 1587-1588.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/bioinformatics/btg196
    • Vancouver

      Paquola ACM, Nishyiama Junior MY, Reis EM, Da Silva AM, Verjovski-Almeida S. ESTWeb: bioinformatics services for EST sequencing projects [Internet]. Bioinformactics. 2003 ; 19( 12): 1587-1588.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/bioinformatics/btg196
  • Source: Bioinformactics. Unidade: IQ

    Subjects: BIOQUÍMICA, BIOLOGIA MOLECULAR

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      PAQUOLA, Apuã C. M. et al. Zerg: a very fast BLAST parser library. Bioinformactics, v. 19, n. 12, p. 1035-1036, 2003Tradução . . Disponível em: https://doi.org/10.1093/bioinformatics/btg122. Acesso em: 17 jul. 2024.
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      Paquola, A. C. M., Machado, A. A., Reis, E. M., Da Silva, A. M., & Verjovski-Almeida, S. (2003). Zerg: a very fast BLAST parser library. Bioinformactics, 19( 12), 1035-1036. doi:10.1093/bioinformatics/btg122
    • NLM

      Paquola ACM, Machado AA, Reis EM, Da Silva AM, Verjovski-Almeida S. Zerg: a very fast BLAST parser library [Internet]. Bioinformactics. 2003 ; 19( 12): 1035-1036.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/bioinformatics/btg122
    • Vancouver

      Paquola ACM, Machado AA, Reis EM, Da Silva AM, Verjovski-Almeida S. Zerg: a very fast BLAST parser library [Internet]. Bioinformactics. 2003 ; 19( 12): 1035-1036.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/bioinformatics/btg122
  • Source: Nucleic Acids Research. Unidade: IQ

    Subjects: BIOQUÍMICA, BIOLOGIA MOLECULAR, RNA, SACCHAROMYCES, PROTEÍNAS

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      OLIVEIRA, Carla Columbano de e GONZALES, Fernando A. e ZANCHIN, Nilson I. T. Temperature-sensitive mutants of the exosome subunit Rrp43p show a deficiency in mRNA degradation and no longer interact with the exosome. Nucleic Acids Research, v. 30, n. 19, p. 4186-4198, 2002Tradução . . Disponível em: https://doi.org/10.1093/nar/gkf545. Acesso em: 17 jul. 2024.
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      Oliveira, C. C. de, Gonzales, F. A., & Zanchin, N. I. T. (2002). Temperature-sensitive mutants of the exosome subunit Rrp43p show a deficiency in mRNA degradation and no longer interact with the exosome. Nucleic Acids Research, 30( 19), 4186-4198. doi:10.1093/nar/gkf545
    • NLM

      Oliveira CC de, Gonzales FA, Zanchin NIT. Temperature-sensitive mutants of the exosome subunit Rrp43p show a deficiency in mRNA degradation and no longer interact with the exosome [Internet]. Nucleic Acids Research. 2002 ; 30( 19): 4186-4198.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/nar/gkf545
    • Vancouver

      Oliveira CC de, Gonzales FA, Zanchin NIT. Temperature-sensitive mutants of the exosome subunit Rrp43p show a deficiency in mRNA degradation and no longer interact with the exosome [Internet]. Nucleic Acids Research. 2002 ; 30( 19): 4186-4198.[citado 2024 jul. 17 ] Available from: https://doi.org/10.1093/nar/gkf545

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