Filtros : "2006" "Indexado no Research Alert" Removido: "Final Program" Limpar

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  • Source: Journal of Colloid and Interface Science. Unidade: IQ

    Subjects: BIOQUÍMICA, SURFACTANTES

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      SOUZA, Tereza Pereira de et al. pH at the micellar interface: Synthesis of pH probes derived from salicylic acid, acid-base dissociation in sodium dodecyl sulfate micelles, and Poisson-Boltzmann simulation. Journal of Colloid and Interface Science, v. 297, n. 1, p. 292-302, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.jcis.2005.10.008. Acesso em: 10 dez. 2025.
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      Souza, T. P. de, Zanette, D., Kawanani, A. E., Rezende, L. de, Ishiki, H. M., Amaral, A. T. do, et al. (2006). pH at the micellar interface: Synthesis of pH probes derived from salicylic acid, acid-base dissociation in sodium dodecyl sulfate micelles, and Poisson-Boltzmann simulation. Journal of Colloid and Interface Science, 297( 1), 292-302. doi:10.1016/j.jcis.2005.10.008
    • NLM

      Souza TP de, Zanette D, Kawanani AE, Rezende L de, Ishiki HM, Amaral AT do, Chaimovich Guralnik H, Neto AA, Cuccovia IM. pH at the micellar interface: Synthesis of pH probes derived from salicylic acid, acid-base dissociation in sodium dodecyl sulfate micelles, and Poisson-Boltzmann simulation [Internet]. Journal of Colloid and Interface Science. 2006 ; 297( 1): 292-302.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.jcis.2005.10.008
    • Vancouver

      Souza TP de, Zanette D, Kawanani AE, Rezende L de, Ishiki HM, Amaral AT do, Chaimovich Guralnik H, Neto AA, Cuccovia IM. pH at the micellar interface: Synthesis of pH probes derived from salicylic acid, acid-base dissociation in sodium dodecyl sulfate micelles, and Poisson-Boltzmann simulation [Internet]. Journal of Colloid and Interface Science. 2006 ; 297( 1): 292-302.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.jcis.2005.10.008
  • Source: Journal of Solid State Chemistry. Unidade: IQ

    Subjects: LUMINESCÊNCIA, TERRAS RARAS

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      STEFANI, Roberval et al. Photoluminescent behavior of Sr'B IND. 4''O IND. 7':'RE POT. 2+' (RE = Sm and Eu) prepared by Pechini, combustion and ceramic methods. Journal of Solid State Chemistry, v. 179, n. 4, p. 1086-1092, 2006Tradução . . Acesso em: 10 dez. 2025.
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      Stefani, R., Maia, A. de S., Teotonio, E. E. de S., Monteiro, M. A. F., Felinto, M. C. F. da C., & Brito, H. F. de. (2006). Photoluminescent behavior of Sr'B IND. 4''O IND. 7':'RE POT. 2+' (RE = Sm and Eu) prepared by Pechini, combustion and ceramic methods. Journal of Solid State Chemistry, 179( 4), 1086-1092.
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      Stefani R, Maia A de S, Teotonio EE de S, Monteiro MAF, Felinto MCF da C, Brito HF de. Photoluminescent behavior of Sr'B IND. 4''O IND. 7':'RE POT. 2+' (RE = Sm and Eu) prepared by Pechini, combustion and ceramic methods. Journal of Solid State Chemistry. 2006 ; 179( 4): 1086-1092.[citado 2025 dez. 10 ]
    • Vancouver

      Stefani R, Maia A de S, Teotonio EE de S, Monteiro MAF, Felinto MCF da C, Brito HF de. Photoluminescent behavior of Sr'B IND. 4''O IND. 7':'RE POT. 2+' (RE = Sm and Eu) prepared by Pechini, combustion and ceramic methods. Journal of Solid State Chemistry. 2006 ; 179( 4): 1086-1092.[citado 2025 dez. 10 ]
  • Source: Polyhedron. Unidade: IQ

    Subjects: LUMINESCÊNCIA, ESPECTROSCOPIA RAMAN

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      UMEDA, Kiyoe e ZUKERMAN-SCHPECTOR, Júlio e ISOLANI, Paulo Celso. Uranyl (1,3-diphenylpropane-1,3-dionato) complexes with N-adamantylacetamide and azacyclononanone. Polyhedron, v. 25, n. 12, p. 2447-2451, 2006Tradução . . Acesso em: 10 dez. 2025.
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      Umeda, K., Zukerman-Schpector, J., & Isolani, P. C. (2006). Uranyl (1,3-diphenylpropane-1,3-dionato) complexes with N-adamantylacetamide and azacyclononanone. Polyhedron, 25( 12), 2447-2451.
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      Umeda K, Zukerman-Schpector J, Isolani PC. Uranyl (1,3-diphenylpropane-1,3-dionato) complexes with N-adamantylacetamide and azacyclononanone. Polyhedron. 2006 ; 25( 12): 2447-2451.[citado 2025 dez. 10 ]
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      Umeda K, Zukerman-Schpector J, Isolani PC. Uranyl (1,3-diphenylpropane-1,3-dionato) complexes with N-adamantylacetamide and azacyclononanone. Polyhedron. 2006 ; 25( 12): 2447-2451.[citado 2025 dez. 10 ]
  • Source: Applied Catalysis B - Environmental. Unidade: IQ

    Subjects: FOTOQUÍMICA, ESPECTROSCOPIA RAMAN

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      BONANCÊA, Carlos Eduardo et al. Substrate development for surface-enhanced Raman study of photocatalytic degradation processes: congo red over silver modified titanium dioxide films. Applied Catalysis B - Environmental, v. 69, n. 1-2, p. 34-42, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.apcatb.2006.05.016. Acesso em: 10 dez. 2025.
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      Bonancêa, C. E., Do Nascimento, G. M., Souza, M. L. de, Temperini, M. L. A., & Corio, P. (2006). Substrate development for surface-enhanced Raman study of photocatalytic degradation processes: congo red over silver modified titanium dioxide films. Applied Catalysis B - Environmental, 69( 1-2), 34-42. doi:10.1016/j.apcatb.2006.05.016
    • NLM

      Bonancêa CE, Do Nascimento GM, Souza ML de, Temperini MLA, Corio P. Substrate development for surface-enhanced Raman study of photocatalytic degradation processes: congo red over silver modified titanium dioxide films [Internet]. Applied Catalysis B - Environmental. 2006 ; 69( 1-2): 34-42.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.apcatb.2006.05.016
    • Vancouver

      Bonancêa CE, Do Nascimento GM, Souza ML de, Temperini MLA, Corio P. Substrate development for surface-enhanced Raman study of photocatalytic degradation processes: congo red over silver modified titanium dioxide films [Internet]. Applied Catalysis B - Environmental. 2006 ; 69( 1-2): 34-42.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.apcatb.2006.05.016
  • Source: Journal of Organometallic Chemistry. Unidade: IQ

    Subjects: TELÚRIO, QUÍMICA ORGÂNICA

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      CUNHA, Rodrigo Luiz Oliveira Rodrigues et al. Revisiting the addition reaction of TeCl4 to alkynes: the crystal structure and docking studies of 1-chloro-2-trichlorotelluro-3-phenyl-propen-2-ol. Journal of Organometallic Chemistry, v. 691, n. 23, p. 4807-4815, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.jorganchem.2006.05.055. Acesso em: 10 dez. 2025.
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      Cunha, R. L. O. R., Zukerman-Schpector, J., Caracelli, I., & Comasseto, J. V. (2006). Revisiting the addition reaction of TeCl4 to alkynes: the crystal structure and docking studies of 1-chloro-2-trichlorotelluro-3-phenyl-propen-2-ol. Journal of Organometallic Chemistry, 691( 23), 4807-4815. doi:10.1016/j.jorganchem.2006.05.055
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      Cunha RLOR, Zukerman-Schpector J, Caracelli I, Comasseto JV. Revisiting the addition reaction of TeCl4 to alkynes: the crystal structure and docking studies of 1-chloro-2-trichlorotelluro-3-phenyl-propen-2-ol [Internet]. Journal of Organometallic Chemistry. 2006 ; 691( 23): 4807-4815.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.jorganchem.2006.05.055
    • Vancouver

      Cunha RLOR, Zukerman-Schpector J, Caracelli I, Comasseto JV. Revisiting the addition reaction of TeCl4 to alkynes: the crystal structure and docking studies of 1-chloro-2-trichlorotelluro-3-phenyl-propen-2-ol [Internet]. Journal of Organometallic Chemistry. 2006 ; 691( 23): 4807-4815.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.jorganchem.2006.05.055
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: ULTRASSONOGRAFIA, QUÍMICA FARMACÊUTICA

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      GUZEN, Karla Pierdoná e CELLA, Rodrigo e STEFANI, Hélio Alexandre. Ultrasound enhanced synthesis of 1,5-benzodiazepinic heterocyclic rings. Tetrahedron Letters, v. 47, n. 46, p. 8133-8136, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2006.09.043. Acesso em: 10 dez. 2025.
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      Guzen, K. P., Cella, R., & Stefani, H. A. (2006). Ultrasound enhanced synthesis of 1,5-benzodiazepinic heterocyclic rings. Tetrahedron Letters, 47( 46), 8133-8136. doi:10.1016/j.tetlet.2006.09.043
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      Guzen KP, Cella R, Stefani HA. Ultrasound enhanced synthesis of 1,5-benzodiazepinic heterocyclic rings [Internet]. Tetrahedron Letters. 2006 ; 47( 46): 8133-8136.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2006.09.043
    • Vancouver

      Guzen KP, Cella R, Stefani HA. Ultrasound enhanced synthesis of 1,5-benzodiazepinic heterocyclic rings [Internet]. Tetrahedron Letters. 2006 ; 47( 46): 8133-8136.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2006.09.043
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: QUÍMICA ORGÂNICA, TELÚRIO, LÍTIO

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      DOS SANTOS, Alcindo Aparecido et al. Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin. Tetrahedron Letters, v. 47, n. 50, p. 8933-8935, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2006.10.039. Acesso em: 10 dez. 2025.
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      Dos Santos, A. A., Ferrarini, R. dos S., Princival, J. L., & Comasseto, J. V. (2006). Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin. Tetrahedron Letters, 47( 50), 8933-8935. doi:10.1016/j.tetlet.2006.10.039
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      Dos Santos AA, Ferrarini R dos S, Princival JL, Comasseto JV. Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin [Internet]. Tetrahedron Letters. 2006 ; 47( 50): 8933-8935.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2006.10.039
    • Vancouver

      Dos Santos AA, Ferrarini R dos S, Princival JL, Comasseto JV. Organotellurides as a source of organometallics: application in the synthesis of (+/-)-frontalin [Internet]. Tetrahedron Letters. 2006 ; 47( 50): 8933-8935.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2006.10.039
  • Source: Zeitschrift für Kristallographie - New Crystal Structures. Unidade: IQ

    Assunto: QUÍMICA ORGÂNICA

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      ZUKERMAN-SCHPECTOR, Júlio et al. Crystal structure of 2-phenylsulfinyl-cyclohexanone, 'C IND. 12''H IND. 14''O IND. 2'S. Zeitschrift für Kristallographie - New Crystal Structures, v. 221, n. 3, p. 311-312, 2006Tradução . . Acesso em: 10 dez. 2025.
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      Zukerman-Schpector, J., Silva, R. O. da, Olivato, P. R., Vinhato, E., Rodrigues, A., & Cerqueira Júnior, C. R. (2006). Crystal structure of 2-phenylsulfinyl-cyclohexanone, 'C IND. 12''H IND. 14''O IND. 2'S. Zeitschrift für Kristallographie - New Crystal Structures, 221( 3), 311-312.
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      Zukerman-Schpector J, Silva RO da, Olivato PR, Vinhato E, Rodrigues A, Cerqueira Júnior CR. Crystal structure of 2-phenylsulfinyl-cyclohexanone, 'C IND. 12''H IND. 14''O IND. 2'S. Zeitschrift für Kristallographie - New Crystal Structures. 2006 ; 221( 3): 311-312.[citado 2025 dez. 10 ]
    • Vancouver

      Zukerman-Schpector J, Silva RO da, Olivato PR, Vinhato E, Rodrigues A, Cerqueira Júnior CR. Crystal structure of 2-phenylsulfinyl-cyclohexanone, 'C IND. 12''H IND. 14''O IND. 2'S. Zeitschrift für Kristallographie - New Crystal Structures. 2006 ; 221( 3): 311-312.[citado 2025 dez. 10 ]
  • Source: Tetrahedron Letters. Unidade: FCF

    Subjects: BIOTRANSFORMAÇÃO, AMINOÁCIDOS, ASSIMETRIA (SÍNTESE)

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      MOURA, Sidnei e PINTO, Ernani. One-pot synthesis of N-CbZ-L-BMAA and derivatives from N-CbZ-L-serine. Tetrahedron Letters, v. 48, n. 13, p. 2325-2327, 2006Tradução . . Acesso em: 10 dez. 2025.
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      Moura, S., & Pinto, E. (2006). One-pot synthesis of N-CbZ-L-BMAA and derivatives from N-CbZ-L-serine. Tetrahedron Letters, 48( 13), 2325-2327.
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      Moura S, Pinto E. One-pot synthesis of N-CbZ-L-BMAA and derivatives from N-CbZ-L-serine. Tetrahedron Letters. 2006 ; 48( 13): 2325-2327.[citado 2025 dez. 10 ]
    • Vancouver

      Moura S, Pinto E. One-pot synthesis of N-CbZ-L-BMAA and derivatives from N-CbZ-L-serine. Tetrahedron Letters. 2006 ; 48( 13): 2325-2327.[citado 2025 dez. 10 ]
  • Source: Redox Report. Unidade: IQ

    Subjects: COBRE, SUPERÓXIDO DISMUTASE

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      AZZELLINI, Maria Amélia de Almeida e BAGATIN, Izilda Aparecida e FERREIRA, Ana Maria da Costa. Di-imine copper(II) complexes as redox mediator and modulator in 2-deoxy-D-ribose oxidative damage. Redox Report, v. 11, n. 1, p. 25-37, 2006Tradução . . Disponível em: https://doi.org/10.1179/135100006x100995. Acesso em: 10 dez. 2025.
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      Azzellini, M. A. de A., Bagatin, I. A., & Ferreira, A. M. da C. (2006). Di-imine copper(II) complexes as redox mediator and modulator in 2-deoxy-D-ribose oxidative damage. Redox Report, 11( 1), 25-37. doi:10.1179/135100006x100995
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      Azzellini MA de A, Bagatin IA, Ferreira AM da C. Di-imine copper(II) complexes as redox mediator and modulator in 2-deoxy-D-ribose oxidative damage [Internet]. Redox Report. 2006 ; 11( 1): 25-37.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1179/135100006x100995
    • Vancouver

      Azzellini MA de A, Bagatin IA, Ferreira AM da C. Di-imine copper(II) complexes as redox mediator and modulator in 2-deoxy-D-ribose oxidative damage [Internet]. Redox Report. 2006 ; 11( 1): 25-37.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1179/135100006x100995
  • Source: Journal of Pharmaceutical and Biomedical Analysis. Unidade: IQ

    Subjects: ELETROFORESE (MÉTODO DE SEPARAÇÃO), FITOTERAPIA, PLANTAS MEDICINAIS

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      MICKE, Gustavo Amadeu et al. Method development and validation for isoflavones in soy germ pharmaceutical capsules using micellar electrokinetic chromatography. Journal of Pharmaceutical and Biomedical Analysis, v. 41, n. 5, p. 1625-1632, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.jpba.2006.03.012. Acesso em: 10 dez. 2025.
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      Micke, G. A., Fujiya, N. M., Tonin, F. G., Costa, A. C. de O., & Tavares, M. F. M. (2006). Method development and validation for isoflavones in soy germ pharmaceutical capsules using micellar electrokinetic chromatography. Journal of Pharmaceutical and Biomedical Analysis, 41( 5), 1625-1632. doi:10.1016/j.jpba.2006.03.012
    • NLM

      Micke GA, Fujiya NM, Tonin FG, Costa AC de O, Tavares MFM. Method development and validation for isoflavones in soy germ pharmaceutical capsules using micellar electrokinetic chromatography [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2006 ; 41( 5): 1625-1632.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.jpba.2006.03.012
    • Vancouver

      Micke GA, Fujiya NM, Tonin FG, Costa AC de O, Tavares MFM. Method development and validation for isoflavones in soy germ pharmaceutical capsules using micellar electrokinetic chromatography [Internet]. Journal of Pharmaceutical and Biomedical Analysis. 2006 ; 41( 5): 1625-1632.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.jpba.2006.03.012
  • Source: Tetrahedron Letters. Unidade: IQ

    Subjects: FEROMÔNIOS, SÍNTESE ORGÂNICA, TELÚRIO

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      DIEGO, Dennis Galasso e CUNHA, Rodrigo Luiz Oliveira Rodrigues e COMASSETO, João Valdir. Tellurium in organic synthesis: an approach to the synthesis of (Z,E)-dienic precursors of insect pheromones. Tetrahedron Letters, v. 47, n. 40, p. 7147-7148, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2006.08.005. Acesso em: 10 dez. 2025.
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      Diego, D. G., Cunha, R. L. O. R., & Comasseto, J. V. (2006). Tellurium in organic synthesis: an approach to the synthesis of (Z,E)-dienic precursors of insect pheromones. Tetrahedron Letters, 47( 40), 7147-7148. doi:10.1016/j.tetlet.2006.08.005
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      Diego DG, Cunha RLOR, Comasseto JV. Tellurium in organic synthesis: an approach to the synthesis of (Z,E)-dienic precursors of insect pheromones [Internet]. Tetrahedron Letters. 2006 ; 47( 40): 7147-7148.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2006.08.005
    • Vancouver

      Diego DG, Cunha RLOR, Comasseto JV. Tellurium in organic synthesis: an approach to the synthesis of (Z,E)-dienic precursors of insect pheromones [Internet]. Tetrahedron Letters. 2006 ; 47( 40): 7147-7148.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.tetlet.2006.08.005
  • Source: Journal of Photochemistry and Photobiology A - Chemistry. Unidade: IQ

    Subjects: LUMINESCÊNCIA, RUTÊNIO

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      POLO, André Sarto e ITOKAZU, Melina Kayoko e IHA, Neyde Yukie Murakami. Photoinduced luminescence of fac-'[Re'(CO) IND. 3'(phen)(stpy)] POT. +' in 'CH IND. 3'CN and PMMA. Journal of Photochemistry and Photobiology A - Chemistry, v. 181, n. 1, p. 73-78, 2006Tradução . . Acesso em: 10 dez. 2025.
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      Polo, A. S., Itokazu, M. K., & Iha, N. Y. M. (2006). Photoinduced luminescence of fac-'[Re'(CO) IND. 3'(phen)(stpy)] POT. +' in 'CH IND. 3'CN and PMMA. Journal of Photochemistry and Photobiology A - Chemistry, 181( 1), 73-78.
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      Polo AS, Itokazu MK, Iha NYM. Photoinduced luminescence of fac-'[Re'(CO) IND. 3'(phen)(stpy)] POT. +' in 'CH IND. 3'CN and PMMA. Journal of Photochemistry and Photobiology A - Chemistry. 2006 ; 181( 1): 73-78.[citado 2025 dez. 10 ]
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      Polo AS, Itokazu MK, Iha NYM. Photoinduced luminescence of fac-'[Re'(CO) IND. 3'(phen)(stpy)] POT. +' in 'CH IND. 3'CN and PMMA. Journal of Photochemistry and Photobiology A - Chemistry. 2006 ; 181( 1): 73-78.[citado 2025 dez. 10 ]
  • Source: Solar Energy Materials & Solar Cells. Unidade: IQ

    Subjects: CÉLULAS SOLARES, FOTOQUÍMICA

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      POLO, André Sarto e IHA, Neyde Yukie Murakami. Blue sensitizers for solar cells: natural dyes from Calafate and Jaboticaba. Solar Energy Materials & Solar Cells, v. 90, n. 1-3, p. 1936-1944, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.solmat.2006.02.006. Acesso em: 10 dez. 2025.
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      Polo, A. S., & Iha, N. Y. M. (2006). Blue sensitizers for solar cells: natural dyes from Calafate and Jaboticaba. Solar Energy Materials & Solar Cells, 90( 1-3), 1936-1944. doi:10.1016/j.solmat.2006.02.006
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      Polo AS, Iha NYM. Blue sensitizers for solar cells: natural dyes from Calafate and Jaboticaba [Internet]. Solar Energy Materials & Solar Cells. 2006 ; 90( 1-3): 1936-1944.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.solmat.2006.02.006
    • Vancouver

      Polo AS, Iha NYM. Blue sensitizers for solar cells: natural dyes from Calafate and Jaboticaba [Internet]. Solar Energy Materials & Solar Cells. 2006 ; 90( 1-3): 1936-1944.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.solmat.2006.02.006
  • Source: Thin Solid Films. Unidade: IQ

    Subjects: ELETROQUÍMICA, VOLTAMETRIA

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      MENDES DE BARROS, Rita de Cássia et al. Morphological and electrochemical studies of spherical boron doped diamond electrodes. Thin Solid Films, v. 513, n. 1-2, p. 364-368, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.tsf.2006.01.027. Acesso em: 10 dez. 2025.
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      Mendes de Barros, R. de C., Ferreira, N. G., Azevedo, A. F., Corat, E. J., Sumodjo, P. T. A., & Serrano, S. H. P. (2006). Morphological and electrochemical studies of spherical boron doped diamond electrodes. Thin Solid Films, 513( 1-2), 364-368. doi:10.1016/j.tsf.2006.01.027
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      Mendes de Barros R de C, Ferreira NG, Azevedo AF, Corat EJ, Sumodjo PTA, Serrano SHP. Morphological and electrochemical studies of spherical boron doped diamond electrodes [Internet]. Thin Solid Films. 2006 ; 513( 1-2): 364-368.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.tsf.2006.01.027
    • Vancouver

      Mendes de Barros R de C, Ferreira NG, Azevedo AF, Corat EJ, Sumodjo PTA, Serrano SHP. Morphological and electrochemical studies of spherical boron doped diamond electrodes [Internet]. Thin Solid Films. 2006 ; 513( 1-2): 364-368.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.tsf.2006.01.027
  • Source: Journal of Colloid and Interface Science. Unidade: IQ

    Subjects: ADSORÇÃO, ATIVAÇÃO ENZIMÁTICA, ENZIMAS GLICOLÍTICAS

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      PANCERA, Sabrina Montero et al. Adsorption behavior and activity of hexokinase. Journal of Colloid and Interface Science, v. 302, n. 2, p. 417-423, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.jcis.2006.06.066. Acesso em: 10 dez. 2025.
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      Pancera, S. M., Gliemann, H., Schimmel, T., & Petri, D. F. S. (2006). Adsorption behavior and activity of hexokinase. Journal of Colloid and Interface Science, 302( 2), 417-423. doi:10.1016/j.jcis.2006.06.066
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      Pancera SM, Gliemann H, Schimmel T, Petri DFS. Adsorption behavior and activity of hexokinase [Internet]. Journal of Colloid and Interface Science. 2006 ; 302( 2): 417-423.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.jcis.2006.06.066
    • Vancouver

      Pancera SM, Gliemann H, Schimmel T, Petri DFS. Adsorption behavior and activity of hexokinase [Internet]. Journal of Colloid and Interface Science. 2006 ; 302( 2): 417-423.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.jcis.2006.06.066
  • Source: Enzyme and Microbial Technology. Unidade: FCF

    Subjects: BIOTECNOLOGIA, ENZIMAS

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    • ABNT

      GURPILHARES, Daniela de Borba et al. Optimization of glucose-6-phosphate dehydrogenase releasing from Candida guilliermondii by disruption with glass beads. Enzyme and Microbial Technology, v. 39, n. 4, p. 591-595, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.enzmictec.2005.11.018. Acesso em: 10 dez. 2025.
    • APA

      Gurpilhares, D. de B., Hasmann, F. A., Pessoa Junior, A., & Roberto, I. C. (2006). Optimization of glucose-6-phosphate dehydrogenase releasing from Candida guilliermondii by disruption with glass beads. Enzyme and Microbial Technology, 39( 4), 591-595. doi:10.1016/j.enzmictec.2005.11.018
    • NLM

      Gurpilhares D de B, Hasmann FA, Pessoa Junior A, Roberto IC. Optimization of glucose-6-phosphate dehydrogenase releasing from Candida guilliermondii by disruption with glass beads [Internet]. Enzyme and Microbial Technology. 2006 ; 39( 4): 591-595.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.enzmictec.2005.11.018
    • Vancouver

      Gurpilhares D de B, Hasmann FA, Pessoa Junior A, Roberto IC. Optimization of glucose-6-phosphate dehydrogenase releasing from Candida guilliermondii by disruption with glass beads [Internet]. Enzyme and Microbial Technology. 2006 ; 39( 4): 591-595.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.enzmictec.2005.11.018
  • Source: Insect Biochemistry and Molecular Biology. Unidade: IQ

    Subjects: BIOQUÍMICA, LEPIDOPTERA

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      LOPES, Adriano Rios et al. Substrate specificity of insect trypsins and the role of their subsites in catalysis. Insect Biochemistry and Molecular Biology, v. 36, n. 2, p. 130-140, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.ibmb.2005.11.006. Acesso em: 10 dez. 2025.
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      Lopes, A. R., Juliano, M. A., Marana, S. R., Juliano, L., & Terra, W. R. (2006). Substrate specificity of insect trypsins and the role of their subsites in catalysis. Insect Biochemistry and Molecular Biology, 36( 2), 130-140. doi:10.1016/j.ibmb.2005.11.006
    • NLM

      Lopes AR, Juliano MA, Marana SR, Juliano L, Terra WR. Substrate specificity of insect trypsins and the role of their subsites in catalysis [Internet]. Insect Biochemistry and Molecular Biology. 2006 ; 36( 2): 130-140.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.ibmb.2005.11.006
    • Vancouver

      Lopes AR, Juliano MA, Marana SR, Juliano L, Terra WR. Substrate specificity of insect trypsins and the role of their subsites in catalysis [Internet]. Insect Biochemistry and Molecular Biology. 2006 ; 36( 2): 130-140.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.ibmb.2005.11.006
  • Source: Journal of Insect Physiology. Unidade: IQ

    Subjects: ENZIMAS, PROTEÍNAS, FEROMÔNIOS

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      GENTA, Fernando Ariel et al. Potential role for gut microbiota in cell wall digestion and glucoside detoxification in Tenebrio molitor larvae. Journal of Insect Physiology, v. 52, n. 6, p. 593-601, 2006Tradução . . Disponível em: https://doi.org/10.1016/j.jinsphys.2006.02.007. Acesso em: 10 dez. 2025.
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      Genta, F. A., Dillon, R. J., Terra, W. R., & Ferreira, C. (2006). Potential role for gut microbiota in cell wall digestion and glucoside detoxification in Tenebrio molitor larvae. Journal of Insect Physiology, 52( 6), 593-601. doi:10.1016/j.jinsphys.2006.02.007
    • NLM

      Genta FA, Dillon RJ, Terra WR, Ferreira C. Potential role for gut microbiota in cell wall digestion and glucoside detoxification in Tenebrio molitor larvae [Internet]. Journal of Insect Physiology. 2006 ; 52( 6): 593-601.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.jinsphys.2006.02.007
    • Vancouver

      Genta FA, Dillon RJ, Terra WR, Ferreira C. Potential role for gut microbiota in cell wall digestion and glucoside detoxification in Tenebrio molitor larvae [Internet]. Journal of Insect Physiology. 2006 ; 52( 6): 593-601.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1016/j.jinsphys.2006.02.007
  • Source: IUBMB Life (International Union of Biochemistry and Molecular Biology: Life). Unidade: IQ

    Subjects: STREPTOMYCES, BIOQUÍMICA

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      MARANA, Sandro Roberto. Molecular basis of substrate specificity in family 1 glycoside hydrolases. IUBMB Life (International Union of Biochemistry and Molecular Biology: Life), v. 58, n. 2, p. 63-73, 2006Tradução . . Disponível em: https://doi.org/10.1080/15216540600617156. Acesso em: 10 dez. 2025.
    • APA

      Marana, S. R. (2006). Molecular basis of substrate specificity in family 1 glycoside hydrolases. IUBMB Life (International Union of Biochemistry and Molecular Biology: Life), 58( 2), 63-73. doi:10.1080/15216540600617156
    • NLM

      Marana SR. Molecular basis of substrate specificity in family 1 glycoside hydrolases [Internet]. IUBMB Life (International Union of Biochemistry and Molecular Biology: Life). 2006 ; 58( 2): 63-73.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1080/15216540600617156
    • Vancouver

      Marana SR. Molecular basis of substrate specificity in family 1 glycoside hydrolases [Internet]. IUBMB Life (International Union of Biochemistry and Molecular Biology: Life). 2006 ; 58( 2): 63-73.[citado 2025 dez. 10 ] Available from: https://doi.org/10.1080/15216540600617156

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