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  • Source: Microbial Pathogenesis. Unidade: FM

    Subjects: GRANULOMA DE INFECÇÃO (HISTOLOGIA), TÉCNICAS BIOLÓGICAS, DOENÇAS INFECCIOSAS, PARACOCCIDIOIDES BRASILIENSIS (ETIOLOGIA), TÉCNICAS HISTOLÓGICAS

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    • ABNT

      SILVA, Aline Alves de Lima et al. Regulatory T cells in cutaneous lesions of patients with Paracoccidioidomycosis. Microbial Pathogenesis, v. 65, p. 36-40, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.micpath.2013.09.004. Acesso em: 03 ago. 2024.
    • APA

      Silva, A. A. de L., Sotto, M. N., Duarte, M. I. S., & Pagliari, C. (2013). Regulatory T cells in cutaneous lesions of patients with Paracoccidioidomycosis. Microbial Pathogenesis, 65, 36-40. doi:10.1016/j.micpath.2013.09.004
    • NLM

      Silva AA de L, Sotto MN, Duarte MIS, Pagliari C. Regulatory T cells in cutaneous lesions of patients with Paracoccidioidomycosis [Internet]. Microbial Pathogenesis. 2013 ; 65 36-40.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.micpath.2013.09.004
    • Vancouver

      Silva AA de L, Sotto MN, Duarte MIS, Pagliari C. Regulatory T cells in cutaneous lesions of patients with Paracoccidioidomycosis [Internet]. Microbial Pathogenesis. 2013 ; 65 36-40.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.micpath.2013.09.004
  • Source: Microbial Pathogenesis. Unidade: FMVZ

    Subjects: BACTÉRIAS GRAM-NEGATIVAS, LEPTOSPIROSE, METALOPROTEINASES

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      HASHIMOTO, Vivian Lika et al. Evaluation of the elastinolytic activity and protective effect of Leptallo I, a protein composed by metalloprotease and FA5/8C domains, from Leptospira interrogans Copenhageni. Microbial Pathogenesis, v. 61-62, p. 29-36, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.micpath.2013.04.011. Acesso em: 03 ago. 2024.
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      Hashimoto, V. L., Abreu, P. A. E., Carvalho, E., Gonçalves, A. P., Morais, Z. M. de, Vasconcellos, S. A., et al. (2013). Evaluation of the elastinolytic activity and protective effect of Leptallo I, a protein composed by metalloprotease and FA5/8C domains, from Leptospira interrogans Copenhageni. Microbial Pathogenesis, 61-62, 29-36. doi:10.1016/j.micpath.2013.04.011
    • NLM

      Hashimoto VL, Abreu PAE, Carvalho E, Gonçalves AP, Morais ZM de, Vasconcellos SA, Romero EC, Ho PL. Evaluation of the elastinolytic activity and protective effect of Leptallo I, a protein composed by metalloprotease and FA5/8C domains, from Leptospira interrogans Copenhageni [Internet]. Microbial Pathogenesis. 2013 ; 61-62 29-36.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.micpath.2013.04.011
    • Vancouver

      Hashimoto VL, Abreu PAE, Carvalho E, Gonçalves AP, Morais ZM de, Vasconcellos SA, Romero EC, Ho PL. Evaluation of the elastinolytic activity and protective effect of Leptallo I, a protein composed by metalloprotease and FA5/8C domains, from Leptospira interrogans Copenhageni [Internet]. Microbial Pathogenesis. 2013 ; 61-62 29-36.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.micpath.2013.04.011
  • Source: Insect Biochemistry and Molecular Biology. Unidades: FMVZ, FMRP

    Subjects: GLÂNDULAS SALIVARES, CARRAPATOS

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      RIBEIRO, José Marcos Chaves et al. The sialotranscriptome of Antricola delacruzi female ticks is compatible with non-hematophagous behavior and an alternative source of food. Insect Biochemistry and Molecular Biology, v. 42, n. 5, p. 332-342, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.ibmb.2012.01.003. Acesso em: 03 ago. 2024.
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      Ribeiro, J. M. C., Labruna, M. B., Mans, B. J., Maruyama, S. R. C., Francischetti, I. M. B., Barizon, G. C., & Santos, I. K. F. de M. (2012). The sialotranscriptome of Antricola delacruzi female ticks is compatible with non-hematophagous behavior and an alternative source of food. Insect Biochemistry and Molecular Biology, 42( 5), 332-342. doi:10.1016/j.ibmb.2012.01.003
    • NLM

      Ribeiro JMC, Labruna MB, Mans BJ, Maruyama SRC, Francischetti IMB, Barizon GC, Santos IKF de M. The sialotranscriptome of Antricola delacruzi female ticks is compatible with non-hematophagous behavior and an alternative source of food [Internet]. Insect Biochemistry and Molecular Biology. 2012 ; 42( 5): 332-342.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.ibmb.2012.01.003
    • Vancouver

      Ribeiro JMC, Labruna MB, Mans BJ, Maruyama SRC, Francischetti IMB, Barizon GC, Santos IKF de M. The sialotranscriptome of Antricola delacruzi female ticks is compatible with non-hematophagous behavior and an alternative source of food [Internet]. Insect Biochemistry and Molecular Biology. 2012 ; 42( 5): 332-342.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.ibmb.2012.01.003
  • Source: Food and Chemical Toxicology. Unidade: FMVZ

    Subjects: TOXICOLOGIA, AROMATIZANTES, DERMATOLOGIA

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      BELSITO, D et al. A toxicologic and dermatologic assessment of cyclopentanones and cyclopentenones when used as fragrance ingredients. Food and Chemical Toxicology, v. 50, p. S517-S556, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2012.04.019. Acesso em: 03 ago. 2024.
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      Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Dekant, W., et al. (2012). A toxicologic and dermatologic assessment of cyclopentanones and cyclopentenones when used as fragrance ingredients. Food and Chemical Toxicology, 50, S517-S556. doi:10.1016/j.fct.2012.04.019
    • NLM

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Dekant W, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicologic and dermatologic assessment of cyclopentanones and cyclopentenones when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S517-S556.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.fct.2012.04.019
    • Vancouver

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Dekant W, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicologic and dermatologic assessment of cyclopentanones and cyclopentenones when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S517-S556.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.fct.2012.04.019
  • Source: Food and Chemical Toxicology. Unidade: FMVZ

    Assunto: TOXICOLOGIA

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      BELSITO, D et al. A toxicological and dermatological assessment of aryl alkyl alcohol simple acid ester derivatives when used as fragrance ingredients. Food and Chemical Toxicology, v. 50, p. S269-S313, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2012.02.091. Acesso em: 03 ago. 2024.
    • APA

      Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Fryer, A. D., et al. (2012). A toxicological and dermatological assessment of aryl alkyl alcohol simple acid ester derivatives when used as fragrance ingredients. Food and Chemical Toxicology, 50, S269-S313. doi:10.1016/j.fct.2012.02.091
    • NLM

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of aryl alkyl alcohol simple acid ester derivatives when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S269-S313.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.fct.2012.02.091
    • Vancouver

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of aryl alkyl alcohol simple acid ester derivatives when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S269-S313.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.fct.2012.02.091
  • Source: Microbial Pathogenesis. Unidade: FMVZ

    Subjects: LEPTOSPIROSE (ESTUDO CLÍNICO), SEQUENCIAMENTO GENÉTICO

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      SOUZA, N. M et al. Lsa30, a novel adhesin of Leptospira interrogans binds human plasminogen and the complement regulator C4bp. Microbial Pathogenesis, v. 53, n. 3/4, p. 125-134, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.micpath.2012.06.001. Acesso em: 03 ago. 2024.
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      Souza, N. M., Vieira, M. L., Alves, I. de J., Morais, Z. M. de, Vasconcellos, S. A., & Nascimento, A. L. T. O. do. (2012). Lsa30, a novel adhesin of Leptospira interrogans binds human plasminogen and the complement regulator C4bp. Microbial Pathogenesis, 53( 3/4), 125-134. doi:10.1016/j.micpath.2012.06.001
    • NLM

      Souza NM, Vieira ML, Alves I de J, Morais ZM de, Vasconcellos SA, Nascimento ALTO do. Lsa30, a novel adhesin of Leptospira interrogans binds human plasminogen and the complement regulator C4bp [Internet]. Microbial Pathogenesis. 2012 ; 53( 3/4): 125-134.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.micpath.2012.06.001
    • Vancouver

      Souza NM, Vieira ML, Alves I de J, Morais ZM de, Vasconcellos SA, Nascimento ALTO do. Lsa30, a novel adhesin of Leptospira interrogans binds human plasminogen and the complement regulator C4bp [Internet]. Microbial Pathogenesis. 2012 ; 53( 3/4): 125-134.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.micpath.2012.06.001
  • Source: Food and Chemical Toxicology. Unidade: FMVZ

    Subjects: QUÍMICA ORGÂNICA, DERMATOLOGIA, TOXICOLOGIA

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      BELSITO, D et al. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients. Food and Chemical Toxicology, v. 50, p. S52-S99, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2011.10.042. Acesso em: 03 ago. 2024.
    • APA

      Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Fryer, A. D., et al. (2012). A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients. Food and Chemical Toxicology, 50, S52-S99. doi:10.1016/j.fct.2011.10.042
    • NLM

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S52-S99.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.fct.2011.10.042
    • Vancouver

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of aryl alkyl alcohols when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2012 ; 50 S52-S99.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.fct.2011.10.042
  • Source: Microbial Pathogenesis. Unidades: FMVZ, ICB

    Subjects: ZOONOSES, LEPTOSPIROSE ANIMAL, INFECÇÃO EXPERIMENTAL ANIMAL, PATOGENIA ANIMAL

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      SILVA, Josefa Bezerra da et al. Induction of TNF-alfa and CXCL-2 mRNAs in different organs of mice infected with pathogenic Leptospira. Microbial Pathogenesis, v. 52, n. 4, p. 206-216, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.micpath.2012.01.002. Acesso em: 03 ago. 2024.
    • APA

      Silva, J. B. da, Carvalho, E., Covarrubias, A. E., Ching, A. T. C., Mattaraia, V. G. de M., Paiva, D., et al. (2012). Induction of TNF-alfa and CXCL-2 mRNAs in different organs of mice infected with pathogenic Leptospira. Microbial Pathogenesis, 52( 4), 206-216. doi:10.1016/j.micpath.2012.01.002
    • NLM

      Silva JB da, Carvalho E, Covarrubias AE, Ching ATC, Mattaraia VG de M, Paiva D, Franco M de, Fávaro RD, Pereira MM, Vasconcellos SA, Zorn TMT, Ho PL, Martins EAL. Induction of TNF-alfa and CXCL-2 mRNAs in different organs of mice infected with pathogenic Leptospira [Internet]. Microbial Pathogenesis. 2012 ; 52( 4): 206-216.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.micpath.2012.01.002
    • Vancouver

      Silva JB da, Carvalho E, Covarrubias AE, Ching ATC, Mattaraia VG de M, Paiva D, Franco M de, Fávaro RD, Pereira MM, Vasconcellos SA, Zorn TMT, Ho PL, Martins EAL. Induction of TNF-alfa and CXCL-2 mRNAs in different organs of mice infected with pathogenic Leptospira [Internet]. Microbial Pathogenesis. 2012 ; 52( 4): 206-216.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.micpath.2012.01.002
  • Source: Food and Chemical Toxicology. Unidade: FMVZ

    Subjects: AGENTE TÓXICO, TOXICOLOGIA, DERMATOLOGIA

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      BELSITO, D et al. A toxicological and dermatological assessment of macrocyclic ketones when used as fragrance ingredients. Food and Chemical Toxicology, v. 49, p. S126-S141, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2011.07.040. Acesso em: 03 ago. 2024.
    • APA

      Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Fryer, A. D., et al. (2011). A toxicological and dermatological assessment of macrocyclic ketones when used as fragrance ingredients. Food and Chemical Toxicology, 49, S126-S141. doi:10.1016/j.fct.2011.07.040
    • NLM

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of macrocyclic ketones when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2011 ; 49 S126-S141.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.fct.2011.07.040
    • Vancouver

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of macrocyclic ketones when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2011 ; 49 S126-S141.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.fct.2011.07.040
  • Source: Food and Chemical Toxicology. Unidade: FMVZ

    Subjects: AGENTE TÓXICO, TOXICOLOGIA, DERMATOLOGIA

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      BELSITO, D et al. A toxicological and dermatological assessment of macrocyclic lactone and lactide derivatives when used as fragrance ingredients. Food and Chemical Toxicology, v. 49, p. S219-S241, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2011.07.052. Acesso em: 03 ago. 2024.
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      Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Fryer, A. D., et al. (2011). A toxicological and dermatological assessment of macrocyclic lactone and lactide derivatives when used as fragrance ingredients. Food and Chemical Toxicology, 49, S219-S241. doi:10.1016/j.fct.2011.07.052
    • NLM

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of macrocyclic lactone and lactide derivatives when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2011 ; 49 S219-S241.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.fct.2011.07.052
    • Vancouver

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicological and dermatological assessment of macrocyclic lactone and lactide derivatives when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2011 ; 49 S219-S241.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.fct.2011.07.052
  • Source: Food and Chemical Toxicology. Unidade: FMVZ

    Subjects: AGENTE TÓXICO, TOXICOLOGIA, DERMATOLOGIA

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      BELSITO, D et al. A toxicologic and dermatologic assessment of cinnamyl phenylpropyl materials when used as fragrance ingredients. Food and Chemical Toxicology, v. 49, p. S256-S267, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.fct.2011.07.053. Acesso em: 03 ago. 2024.
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      Belsito, D., Bickers, D., Bruze, M., Calow, P., Dagli, M. L. Z., Fryer, A. D., et al. (2011). A toxicologic and dermatologic assessment of cinnamyl phenylpropyl materials when used as fragrance ingredients. Food and Chemical Toxicology, 49, S256-S267. doi:10.1016/j.fct.2011.07.053
    • NLM

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicologic and dermatologic assessment of cinnamyl phenylpropyl materials when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2011 ; 49 S256-S267.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.fct.2011.07.053
    • Vancouver

      Belsito D, Bickers D, Bruze M, Calow P, Dagli MLZ, Fryer AD, Greim H, Miyachi Y, Saurat JH, Sipes IG. A toxicologic and dermatologic assessment of cinnamyl phenylpropyl materials when used as fragrance ingredients [Internet]. Food and Chemical Toxicology. 2011 ; 49 S256-S267.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.fct.2011.07.053
  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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      SINGH, Fateh Veer e AMARAL, Mônica F. Z. J. e STEFANI, Hélio Alexandre. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides. Tetrahedron Letters, v. 50, n. 22, p. 2636-2639, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.03.078. Acesso em: 03 ago. 2024.
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      Singh, F. V., Amaral, M. F. Z. J., & Stefani, H. A. (2009). Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides. Tetrahedron Letters, 50( 22), 2636-2639. doi:10.1016/j.tetlet.2009.03.078
    • NLM

      Singh FV, Amaral MFZJ, Stefani HA. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides [Internet]. Tetrahedron Letters. 2009 ; 50( 22): 2636-2639.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.078
    • Vancouver

      Singh FV, Amaral MFZJ, Stefani HA. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides [Internet]. Tetrahedron Letters. 2009 ; 50( 22): 2636-2639.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.078
  • Source: Tetrahedron Letters. Unidades: FCF, IQ

    Subjects: SÍNTESE ORGÂNICA, TELÚRIO, PALÁDIO

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      STEFANI, Hélio Alexandre et al. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters, v. 50, n. 40, p. 5589-5595, 2009Tradução . . Acesso em: 03 ago. 2024.
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      Stefani, H. A., Pena, J. M., Gueogjian, K., Petragnani, N., Vaz, B. G., & Eberlin, M. N. (2009). Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters, 50( 40), 5589-5595.
    • NLM

      Stefani HA, Pena JM, Gueogjian K, Petragnani N, Vaz BG, Eberlin MN. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters. 2009 ; 50( 40): 5589-5595.[citado 2024 ago. 03 ]
    • Vancouver

      Stefani HA, Pena JM, Gueogjian K, Petragnani N, Vaz BG, Eberlin MN. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters. 2009 ; 50( 40): 5589-5595.[citado 2024 ago. 03 ]
  • Source: Photochemical and Photobiological Sciences. Unidades: FFCLRP, IQ

    Subjects: DEGRADAÇÃO AMBIENTAL, QUÍMICA AMBIENTAL, FOTOQUÍMICA

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      MACHULEK JUNIOR, Amilcar et al. Photolysis of ferric ions in the presence of sulfate or chloride ions: implications for the photo-Fenton process. Photochemical and Photobiological Sciences, v. 8, n. 7, p. 985-991, 2009Tradução . . Disponível em: https://doi.org/10.1039/b900553f. Acesso em: 03 ago. 2024.
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      Machulek Junior, A., Moraes, J. E. F. de, Okano, L. T., Silvério, C. A., & Quina, F. H. (2009). Photolysis of ferric ions in the presence of sulfate or chloride ions: implications for the photo-Fenton process. Photochemical and Photobiological Sciences, 8( 7), 985-991. doi:10.1039/b900553f
    • NLM

      Machulek Junior A, Moraes JEF de, Okano LT, Silvério CA, Quina FH. Photolysis of ferric ions in the presence of sulfate or chloride ions: implications for the photo-Fenton process [Internet]. Photochemical and Photobiological Sciences. 2009 ; 8( 7): 985-991.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1039/b900553f
    • Vancouver

      Machulek Junior A, Moraes JEF de, Okano LT, Silvério CA, Quina FH. Photolysis of ferric ions in the presence of sulfate or chloride ions: implications for the photo-Fenton process [Internet]. Photochemical and Photobiological Sciences. 2009 ; 8( 7): 985-991.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1039/b900553f
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: SÍNTESE ORGÂNICA, POTÁSSIO, PALÁDIO

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      WEBER, Minéia et al. Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes. Tetrahedron Letters, v. 50, n. 30, p. 4324-4327, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.04.127. Acesso em: 03 ago. 2024.
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      Weber, M., Singh, F. V., Vieira, A. S., Stefani, H. A., & Paixão, M. W. (2009). Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes. Tetrahedron Letters, 50( 30), 4324-4327. doi:10.1016/j.tetlet.2009.04.127
    • NLM

      Weber M, Singh FV, Vieira AS, Stefani HA, Paixão MW. Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4324-4327.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.04.127
    • Vancouver

      Weber M, Singh FV, Vieira AS, Stefani HA, Paixão MW. Palladium-catalyzed oxidative homocoupling of potassium alkenyltrifluoroborates: synthesis of symmetrical 1,3-dienes [Internet]. Tetrahedron Letters. 2009 ; 50( 30): 4324-4327.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.04.127
  • Source: Photochemical and Photobiological Sciences. Unidades: FFCLRP, IQ

    Subjects: TERAPIA FOTODINÂMICA, MEMBRANAS CELULARES, MITOCÔNDRIAS, ZINCO

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      PAVANI, Christiane et al. Effect of zinc insertion and hydrophobicity on the membrane interactions and PDT activity of porphyrin photosensitizers. Photochemical and Photobiological Sciences, v. 8, n. 2, p. 233-240, 2009Tradução . . Disponível em: https://doi.org/10.1039/b810313e. Acesso em: 03 ago. 2024.
    • APA

      Pavani, C., Uchoa, A. F., Oliveira, C. S. de, Iamamoto, Y., & Baptista, M. da S. (2009). Effect of zinc insertion and hydrophobicity on the membrane interactions and PDT activity of porphyrin photosensitizers. Photochemical and Photobiological Sciences, 8( 2), 233-240. doi:10.1039/b810313e
    • NLM

      Pavani C, Uchoa AF, Oliveira CS de, Iamamoto Y, Baptista M da S. Effect of zinc insertion and hydrophobicity on the membrane interactions and PDT activity of porphyrin photosensitizers [Internet]. Photochemical and Photobiological Sciences. 2009 ; 8( 2): 233-240.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1039/b810313e
    • Vancouver

      Pavani C, Uchoa AF, Oliveira CS de, Iamamoto Y, Baptista M da S. Effect of zinc insertion and hydrophobicity on the membrane interactions and PDT activity of porphyrin photosensitizers [Internet]. Photochemical and Photobiological Sciences. 2009 ; 8( 2): 233-240.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1039/b810313e
  • Source: Phytomedicine. Unidade: IQ

    Subjects: ÓLEOS ESSENCIAIS, PRODUTOS NATURAIS

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      LINCK, Viviane de Moura et al. Inhaled linalool-induced sedation in mice. Phytomedicine, v. 16, n. 4, p. 303-307, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.phymed.2008.08.001. Acesso em: 03 ago. 2024.
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      Linck, V. de M., Silva, A. L. da, Figueiró, M., Piato, A. L., Herrmann, A. P., Birck, F. D., et al. (2009). Inhaled linalool-induced sedation in mice. Phytomedicine, 16( 4), 303-307. doi:10.1016/j.phymed.2008.08.001
    • NLM

      Linck V de M, Silva AL da, Figueiró M, Piato AL, Herrmann AP, Birck FD, Caramão EB, Nunes DS, Moreno PRH, Elisabetsky E. Inhaled linalool-induced sedation in mice [Internet]. Phytomedicine. 2009 ; 16( 4): 303-307.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.phymed.2008.08.001
    • Vancouver

      Linck V de M, Silva AL da, Figueiró M, Piato AL, Herrmann AP, Birck FD, Caramão EB, Nunes DS, Moreno PRH, Elisabetsky E. Inhaled linalool-induced sedation in mice [Internet]. Phytomedicine. 2009 ; 16( 4): 303-307.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.phymed.2008.08.001
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: NUCLEOSÍDEOS, SELÊNIO (SÍNTESE), TELÚRIO (SÍNTESE)

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      BRAGA, Antonio Luiz et al. Synthesis of selenium- and tellurium-containing nucleosides derived from uridine. Tetrahedron Letters, v. 50, n. 25, p. 3005-3007, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.03.164. Acesso em: 03 ago. 2024.
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      Braga, A. L., Severo Filho, W. A., Schwab, R. S., Rodrigues, O. E. D., Dornelles, L., Braga, H. C., & Lüdtke, D. (2009). Synthesis of selenium- and tellurium-containing nucleosides derived from uridine. Tetrahedron Letters, 50( 25), 3005-3007. doi:10.1016/j.tetlet.2009.03.164
    • NLM

      Braga AL, Severo Filho WA, Schwab RS, Rodrigues OED, Dornelles L, Braga HC, Lüdtke D. Synthesis of selenium- and tellurium-containing nucleosides derived from uridine [Internet]. Tetrahedron Letters. 2009 ; 50( 25): 3005-3007.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.164
    • Vancouver

      Braga AL, Severo Filho WA, Schwab RS, Rodrigues OED, Dornelles L, Braga HC, Lüdtke D. Synthesis of selenium- and tellurium-containing nucleosides derived from uridine [Internet]. Tetrahedron Letters. 2009 ; 50( 25): 3005-3007.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.164
  • Source: Tetrahedron Letters. Unidade: FCF

    Assunto: SÍNTESE ORGÂNICA

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      SINGH, Fateh Veer et al. Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid. Tetrahedron Letters, v. 50, n. 20, p. 2312-2316, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.02.164. Acesso em: 03 ago. 2024.
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      Singh, F. V., Milagre, H. M. S., Eberlin, M. N., & Stefani, H. A. (2009). Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid. Tetrahedron Letters, 50( 20), 2312-2316. doi:10.1016/j.tetlet.2009.02.164
    • NLM

      Singh FV, Milagre HMS, Eberlin MN, Stefani HA. Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid [Internet]. Tetrahedron Letters. 2009 ; 50( 20): 2312-2316.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
    • Vancouver

      Singh FV, Milagre HMS, Eberlin MN, Stefani HA. Synthesis of benzophenones from geminal biaryl ethenes using m-chloroperbenzoic acid [Internet]. Tetrahedron Letters. 2009 ; 50( 20): 2312-2316.[citado 2024 ago. 03 ] Available from: https://doi.org/10.1016/j.tetlet.2009.02.164
  • Source: Toxicon. Unidade: FCF

    Subjects: APOPTOSE, CITOCINAS, ÓXIDO NÍTRICO

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      WAISMAN, Kaline et al. LOPAP: a non-inflammatory and cytoprotective molecule in neutrophils and endothelial cells. Toxicon, v. 53, n. 6, p. 652-659, 2009Tradução . . Acesso em: 03 ago. 2024.
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      Waisman, K., Chudzinski-Tavassi, A. M., Carvalho, L. C. C., Pacheco, M. T. F., & Farsky, S. H. P. (2009). LOPAP: a non-inflammatory and cytoprotective molecule in neutrophils and endothelial cells. Toxicon, 53( 6), 652-659.
    • NLM

      Waisman K, Chudzinski-Tavassi AM, Carvalho LCC, Pacheco MTF, Farsky SHP. LOPAP: a non-inflammatory and cytoprotective molecule in neutrophils and endothelial cells. Toxicon. 2009 ; 53( 6): 652-659.[citado 2024 ago. 03 ]
    • Vancouver

      Waisman K, Chudzinski-Tavassi AM, Carvalho LCC, Pacheco MTF, Farsky SHP. LOPAP: a non-inflammatory and cytoprotective molecule in neutrophils and endothelial cells. Toxicon. 2009 ; 53( 6): 652-659.[citado 2024 ago. 03 ]

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