Filtros : "Indexado na Base de dados Biological Abstracts" "IMUNOLOGIA" Removidos: "Tozzi, Claudio" "Nova Zelândia" Limpar

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  • Source: Clinical and Experimental Allergy. Unidades: ICB, FMRP, FCFRP

    Assunto: IMUNOLOGIA

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      FONSECA, Denise Morais da et al. Recombinant DNA immunotherapy ameliorate established airway allergy in a IL-10 dependent pathway. Clinical and Experimental Allergy, v. 42, n. 1, p. 131-143, 2012Tradução . . Disponível em: https://doi.org/10.1111/j.1365-2222.2011.03845.x. Acesso em: 15 nov. 2024.
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      Fonseca, D. M. da, Wowk, P. F., Paula, M. O., Campos, L. W., Gembre, A. F., Turato, W. M., et al. (2012). Recombinant DNA immunotherapy ameliorate established airway allergy in a IL-10 dependent pathway. Clinical and Experimental Allergy, 42( 1), 131-143. doi:10.1111/j.1365-2222.2011.03845.x
    • NLM

      Fonseca DM da, Wowk PF, Paula MO, Campos LW, Gembre AF, Turato WM, Ramos SG, Dias-Baruffi M, Barboza R, Gomes E, Silva CL, Russo M, Bonato VLD. Recombinant DNA immunotherapy ameliorate established airway allergy in a IL-10 dependent pathway [Internet]. Clinical and Experimental Allergy. 2012 ; 42( 1): 131-143.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1365-2222.2011.03845.x
    • Vancouver

      Fonseca DM da, Wowk PF, Paula MO, Campos LW, Gembre AF, Turato WM, Ramos SG, Dias-Baruffi M, Barboza R, Gomes E, Silva CL, Russo M, Bonato VLD. Recombinant DNA immunotherapy ameliorate established airway allergy in a IL-10 dependent pathway [Internet]. Clinical and Experimental Allergy. 2012 ; 42( 1): 131-143.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1365-2222.2011.03845.x
  • Source: The Journal Of Biological Chemistry. Unidade: ICB

    Assunto: IMUNOLOGIA

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      CALVO, Eric et al. Alboserpin, a factor Xa inhibitor from the mosquito vector of yellow fever, binds heparin and membrane phospholipids and exhibits antithrombotic activity. The Journal Of Biological Chemistry, v. 286, n. 32, p. 27998-28010, 2011Tradução . . Disponível em: https://doi.org/10.1074/jbc.M111.247924. Acesso em: 15 nov. 2024.
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      Calvo, E., Mizurini, D. M., Nunes, A. de S., Ribeiro, J. M. C., Andersen, J. F., Mans, B. J., et al. (2011). Alboserpin, a factor Xa inhibitor from the mosquito vector of yellow fever, binds heparin and membrane phospholipids and exhibits antithrombotic activity. The Journal Of Biological Chemistry, 286( 32), 27998-28010. doi:10.1074/jbc.M111.247924
    • NLM

      Calvo E, Mizurini DM, Nunes A de S, Ribeiro JMC, Andersen JF, Mans BJ, Monteiro RQ, Kotsyfakis M, Francischetti IMB. Alboserpin, a factor Xa inhibitor from the mosquito vector of yellow fever, binds heparin and membrane phospholipids and exhibits antithrombotic activity [Internet]. The Journal Of Biological Chemistry. 2011 ; 286( 32): 27998-28010.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1074/jbc.M111.247924
    • Vancouver

      Calvo E, Mizurini DM, Nunes A de S, Ribeiro JMC, Andersen JF, Mans BJ, Monteiro RQ, Kotsyfakis M, Francischetti IMB. Alboserpin, a factor Xa inhibitor from the mosquito vector of yellow fever, binds heparin and membrane phospholipids and exhibits antithrombotic activity [Internet]. The Journal Of Biological Chemistry. 2011 ; 286( 32): 27998-28010.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1074/jbc.M111.247924
  • Source: Rheumatology International. Unidade: ICB

    Subjects: IMUNOLOGIA, MICROBIOLOGIA

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      ROCHA SOBRINHO, Hermínio M. da et al. Mycoplasmal lipid-associated membrane proteins and Mycoplasma arthritidis mitogen recognition by serum antibodies from patients with rheumatoid arthritis. Rheumatology International, v. 31, n. 7, p. 951-957, 2011Tradução . . Disponível em: https://doi.org/10.1007/s00296-010-1612-1. Acesso em: 15 nov. 2024.
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      Rocha Sobrinho, H. M. da, Jarach, R., Silva, N. A. da, Shio, M. T., Jancar, S., Timenetsky, J., et al. (2011). Mycoplasmal lipid-associated membrane proteins and Mycoplasma arthritidis mitogen recognition by serum antibodies from patients with rheumatoid arthritis. Rheumatology International, 31( 7), 951-957. doi:10.1007/s00296-010-1612-1
    • NLM

      Rocha Sobrinho HM da, Jarach R, Silva NA da, Shio MT, Jancar S, Timenetsky J, Oliveira MAP, Dorta ML, Ribeiro-Dias F. Mycoplasmal lipid-associated membrane proteins and Mycoplasma arthritidis mitogen recognition by serum antibodies from patients with rheumatoid arthritis [Internet]. Rheumatology International. 2011 ; 31( 7): 951-957.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s00296-010-1612-1
    • Vancouver

      Rocha Sobrinho HM da, Jarach R, Silva NA da, Shio MT, Jancar S, Timenetsky J, Oliveira MAP, Dorta ML, Ribeiro-Dias F. Mycoplasmal lipid-associated membrane proteins and Mycoplasma arthritidis mitogen recognition by serum antibodies from patients with rheumatoid arthritis [Internet]. Rheumatology International. 2011 ; 31( 7): 951-957.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s00296-010-1612-1
  • Source: Immunology and Cell Biology. Unidades: ICB, FMRP, FCFRP

    Assunto: IMUNOLOGIA

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      FONSECA, Denise Morais da et al. IFN-'gama'-mediated efficacy of allergen-free immunotherapy using mycobacterial antigens and CpG-ODN. Immunology and Cell Biology, v. 89, n. 7, p. 777-785, 2011Tradução . . Disponível em: https://doi.org/10.1038/icb.2011.9. Acesso em: 15 nov. 2024.
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      Fonseca, D. M. da, Paula, M. O. e, Wowk, P. F., Campos, L. W., Gembre, A. F., Turato, W. M., et al. (2011). IFN-'gama'-mediated efficacy of allergen-free immunotherapy using mycobacterial antigens and CpG-ODN. Immunology and Cell Biology, 89( 7), 777-785. doi:10.1038/icb.2011.9
    • NLM

      Fonseca DM da, Paula MO e, Wowk PF, Campos LW, Gembre AF, Turato WM, Ramos SG, Dias-Baruffi M, Barboza R, Gomes E, Horn C, Marchal G, Arruda LK de P, Russo M, Bonato VLD. IFN-'gama'-mediated efficacy of allergen-free immunotherapy using mycobacterial antigens and CpG-ODN [Internet]. Immunology and Cell Biology. 2011 ; 89( 7): 777-785.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/icb.2011.9
    • Vancouver

      Fonseca DM da, Paula MO e, Wowk PF, Campos LW, Gembre AF, Turato WM, Ramos SG, Dias-Baruffi M, Barboza R, Gomes E, Horn C, Marchal G, Arruda LK de P, Russo M, Bonato VLD. IFN-'gama'-mediated efficacy of allergen-free immunotherapy using mycobacterial antigens and CpG-ODN [Internet]. Immunology and Cell Biology. 2011 ; 89( 7): 777-785.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/icb.2011.9
  • Source: FEMS Immunology and Medical Microbiology. Unidade: ICB

    Assunto: IMUNOLOGIA

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      NISHIKAKU, Angela Satie et al. Immunolocalization of IFN-gamma in the lesions of resistant and susceptible mice to Paracoccidioides brasiliensis infection. FEMS Immunology and Medical Microbiology, v. 63, n. 2, p. 281-288, 2011Tradução . . Disponível em: https://doi.org/10.1111/j.1574-695X.2011.00851.x. Acesso em: 15 nov. 2024.
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      Nishikaku, A. S., Molina, R. F. S., Albe, B. P., Cunha, C. da S., Scavone, R., Pizzo, C. R. P., et al. (2011). Immunolocalization of IFN-gamma in the lesions of resistant and susceptible mice to Paracoccidioides brasiliensis infection. FEMS Immunology and Medical Microbiology, 63( 2), 281-288. doi:10.1111/j.1574-695X.2011.00851.x
    • NLM

      Nishikaku AS, Molina RFS, Albe BP, Cunha C da S, Scavone R, Pizzo CRP, Camargo ZP de, Burger E. Immunolocalization of IFN-gamma in the lesions of resistant and susceptible mice to Paracoccidioides brasiliensis infection [Internet]. FEMS Immunology and Medical Microbiology. 2011 ; 63( 2): 281-288.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1574-695X.2011.00851.x
    • Vancouver

      Nishikaku AS, Molina RFS, Albe BP, Cunha C da S, Scavone R, Pizzo CRP, Camargo ZP de, Burger E. Immunolocalization of IFN-gamma in the lesions of resistant and susceptible mice to Paracoccidioides brasiliensis infection [Internet]. FEMS Immunology and Medical Microbiology. 2011 ; 63( 2): 281-288.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1574-695X.2011.00851.x
  • Source: Memórias do Instituto Oswaldo Cruz. Unidades: ICB, FCF

    Subjects: PLASMODIUM, IMUNOLOGIA, SALMONELLA TYPHIMURIUM

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      CAMACHO, Ariane Guglielmi Ariza et al. TLR5-dependent immunogenicity of a recombinant fusion protein containing an immunodominant epitope of malarial circumsporozoite protein and the FliC flagellin of Salmonella Typhimurium. Memórias do Instituto Oswaldo Cruz, v. 106, p. 167-171, 2011Tradução . . Disponível em: https://doi.org/10.1590/s0074-02762011000900021. Acesso em: 15 nov. 2024.
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      Camacho, A. G. A., Teixeira, L. H., Bargieri, D. Y., Boscardin, S. B., Soares, I. da S., Nussenzweig, R. S., et al. (2011). TLR5-dependent immunogenicity of a recombinant fusion protein containing an immunodominant epitope of malarial circumsporozoite protein and the FliC flagellin of Salmonella Typhimurium. Memórias do Instituto Oswaldo Cruz, 106, 167-171. doi:10.1590/s0074-02762011000900021
    • NLM

      Camacho AGA, Teixeira LH, Bargieri DY, Boscardin SB, Soares I da S, Nussenzweig RS, Nussenzweig V, Rodrigues MM. TLR5-dependent immunogenicity of a recombinant fusion protein containing an immunodominant epitope of malarial circumsporozoite protein and the FliC flagellin of Salmonella Typhimurium [Internet]. Memórias do Instituto Oswaldo Cruz. 2011 ; 106 167-171.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1590/s0074-02762011000900021
    • Vancouver

      Camacho AGA, Teixeira LH, Bargieri DY, Boscardin SB, Soares I da S, Nussenzweig RS, Nussenzweig V, Rodrigues MM. TLR5-dependent immunogenicity of a recombinant fusion protein containing an immunodominant epitope of malarial circumsporozoite protein and the FliC flagellin of Salmonella Typhimurium [Internet]. Memórias do Instituto Oswaldo Cruz. 2011 ; 106 167-171.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1590/s0074-02762011000900021
  • Source: Cell and Tissue Research. Unidade: ICB

    Subjects: ANATOMIA, IMUNOLOGIA

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      MATTOS, Gabriele Ebling et al. Comparative effect of FGF2, synthetic peptides 1-28 N-POMC and ACTH on proliferation in rat adrenal cell primary cultures. Cell and Tissue Research, v. 345, n. 3, p. 343-356, 2011Tradução . . Disponível em: https://doi.org/10.1007/s00441-011-1220-8. Acesso em: 15 nov. 2024.
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      Mattos, G. E., Jacysyn, J. de F., Amarante-Mendes, J. G. P., & Lotfi, C. F. P. (2011). Comparative effect of FGF2, synthetic peptides 1-28 N-POMC and ACTH on proliferation in rat adrenal cell primary cultures. Cell and Tissue Research, 345( 3), 343-356. doi:10.1007/s00441-011-1220-8
    • NLM

      Mattos GE, Jacysyn J de F, Amarante-Mendes JGP, Lotfi CFP. Comparative effect of FGF2, synthetic peptides 1-28 N-POMC and ACTH on proliferation in rat adrenal cell primary cultures [Internet]. Cell and Tissue Research. 2011 ; 345( 3): 343-356.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s00441-011-1220-8
    • Vancouver

      Mattos GE, Jacysyn J de F, Amarante-Mendes JGP, Lotfi CFP. Comparative effect of FGF2, synthetic peptides 1-28 N-POMC and ACTH on proliferation in rat adrenal cell primary cultures [Internet]. Cell and Tissue Research. 2011 ; 345( 3): 343-356.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s00441-011-1220-8
  • Source: Oncogene. Unidades: FMRP, ICB, FCFRP

    Assunto: IMUNOLOGIA

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      CARVALHO, Daniel Diniz de et al. BCR–ABL-mediated upregulation of PRAME is responsible for knocking down TRAIL in CML patients. Oncogene, v. 30, n. 2, p. 223-233, 2011Tradução . . Disponível em: https://doi.org/10.1038/onc.2010.409. Acesso em: 15 nov. 2024.
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      Carvalho, D. D. de, Binato, R., Pereira, W. de O., Leroy, J. M. G., Colassanti, M. D., Proto-Siqueira, R., et al. (2011). BCR–ABL-mediated upregulation of PRAME is responsible for knocking down TRAIL in CML patients. Oncogene, 30( 2), 223-233. doi:10.1038/onc.2010.409
    • NLM

      Carvalho DD de, Binato R, Pereira W de O, Leroy JMG, Colassanti MD, Proto-Siqueira R, Silva AEBB da, Zago MA, Zanichelli MA, Abdelhay E, Castro FA de, Jacysyn JF, Amarante-Mendes JGP. BCR–ABL-mediated upregulation of PRAME is responsible for knocking down TRAIL in CML patients [Internet]. Oncogene. 2011 ; 30( 2): 223-233.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/onc.2010.409
    • Vancouver

      Carvalho DD de, Binato R, Pereira W de O, Leroy JMG, Colassanti MD, Proto-Siqueira R, Silva AEBB da, Zago MA, Zanichelli MA, Abdelhay E, Castro FA de, Jacysyn JF, Amarante-Mendes JGP. BCR–ABL-mediated upregulation of PRAME is responsible for knocking down TRAIL in CML patients [Internet]. Oncogene. 2011 ; 30( 2): 223-233.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/onc.2010.409
  • Source: The Journal Of Biological Chemistry. Unidade: ICB

    Assunto: IMUNOLOGIA

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      MORATO-MARQUES, Mariana et al. Leukotrienes target F-actin/cofilin-1 to enhance alveolar macrophage anti-fungal activity. The Journal Of Biological Chemistry, v. 286, n. 33, p. 28902-28913, 2011Tradução . . Disponível em: https://doi.org/10.1074/jbc.M111.235309. Acesso em: 15 nov. 2024.
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      Morato-Marques, M., Campos, M. R., Kane, S., Rangel, A. P., Lewis, C., Ballinger, M. N., et al. (2011). Leukotrienes target F-actin/cofilin-1 to enhance alveolar macrophage anti-fungal activity. The Journal Of Biological Chemistry, 286( 33), 28902-28913. doi:10.1074/jbc.M111.235309
    • NLM

      Morato-Marques M, Campos MR, Kane S, Rangel AP, Lewis C, Ballinger MN, Kim S-H, Peters-Golden M, Jancar S, Serezani CH. Leukotrienes target F-actin/cofilin-1 to enhance alveolar macrophage anti-fungal activity [Internet]. The Journal Of Biological Chemistry. 2011 ; 286( 33): 28902-28913.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1074/jbc.M111.235309
    • Vancouver

      Morato-Marques M, Campos MR, Kane S, Rangel AP, Lewis C, Ballinger MN, Kim S-H, Peters-Golden M, Jancar S, Serezani CH. Leukotrienes target F-actin/cofilin-1 to enhance alveolar macrophage anti-fungal activity [Internet]. The Journal Of Biological Chemistry. 2011 ; 286( 33): 28902-28913.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1074/jbc.M111.235309
  • Source: Circulation. Unidade: ICB

    Assunto: IMUNOLOGIA

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      KETELHUTH, Daniel F. J. et al. Identification of a danger-associated peptide from apolipoprotein B100 (ApoBDS-1) that triggers innate proatherogenic responses. Circulation, v. 124, n. 22, p. 2433-2443 supl. 1-7, 2011Tradução . . Acesso em: 15 nov. 2024.
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      Ketelhuth, D. F. J., Rios, F. J. O., Wang, Y., Liu, H., Johansson, M. E., Fredrikson, G. N., et al. (2011). Identification of a danger-associated peptide from apolipoprotein B100 (ApoBDS-1) that triggers innate proatherogenic responses. Circulation, 124( 22), 2433-2443 supl. 1-7.
    • NLM

      Ketelhuth DFJ, Rios FJO, Wang Y, Liu H, Johansson ME, Fredrikson GN, Hedin U, Gidlund MA, Nilsson J, Hansson GK, Yan Z-qun. Identification of a danger-associated peptide from apolipoprotein B100 (ApoBDS-1) that triggers innate proatherogenic responses. Circulation. 2011 ; 124( 22): 2433-2443 supl. 1-7.[citado 2024 nov. 15 ]
    • Vancouver

      Ketelhuth DFJ, Rios FJO, Wang Y, Liu H, Johansson ME, Fredrikson GN, Hedin U, Gidlund MA, Nilsson J, Hansson GK, Yan Z-qun. Identification of a danger-associated peptide from apolipoprotein B100 (ApoBDS-1) that triggers innate proatherogenic responses. Circulation. 2011 ; 124( 22): 2433-2443 supl. 1-7.[citado 2024 nov. 15 ]
  • Source: Arteriosclerosis, Thrombosis Vascular Biology. Unidades: ICB, FM, FCF

    Assunto: IMUNOLOGIA

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      RUDNICKI, Martina et al. Hypoxia inducible factor–dependent regulation of angiogenesis by nitro–fatty acids. Arteriosclerosis, Thrombosis Vascular Biology, v. 31, n. 6, p. 1360-1367, 2011Tradução . . Disponível em: https://doi.org/10.1161/ATVBAHA.111.224626. Acesso em: 15 nov. 2024.
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      Rudnicki, M., Faine, L. A., Dehne, N., Namgaladze, D., Ferderbar, S., Weinlich, R., et al. (2011). Hypoxia inducible factor–dependent regulation of angiogenesis by nitro–fatty acids. Arteriosclerosis, Thrombosis Vascular Biology, 31( 6), 1360-1367. doi:10.1161/ATVBAHA.111.224626
    • NLM

      Rudnicki M, Faine LA, Dehne N, Namgaladze D, Ferderbar S, Weinlich R, Amarante-Mendes JGP, Yan CYI, Krieger JE, Brüne B, Abdalla DSP. Hypoxia inducible factor–dependent regulation of angiogenesis by nitro–fatty acids [Internet]. Arteriosclerosis, Thrombosis Vascular Biology. 2011 ; 31( 6): 1360-1367.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1161/ATVBAHA.111.224626
    • Vancouver

      Rudnicki M, Faine LA, Dehne N, Namgaladze D, Ferderbar S, Weinlich R, Amarante-Mendes JGP, Yan CYI, Krieger JE, Brüne B, Abdalla DSP. Hypoxia inducible factor–dependent regulation of angiogenesis by nitro–fatty acids [Internet]. Arteriosclerosis, Thrombosis Vascular Biology. 2011 ; 31( 6): 1360-1367.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1161/ATVBAHA.111.224626
  • Source: American Journal of Reproductive Immunology. Unidade: ICB

    Assunto: IMUNOLOGIA

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      OLIVEIRA, Leandro de et al. Proportion of invariant NKT Cells in normal pregnant women at term: an evaluation in peripheral blood, placenta and umbilical cord blood. American Journal of Reproductive Immunology, v. 65, n. 1, p. 11-12, 2011Tradução . . Disponível em: https://doi.org/10.1111/j.1600-0897.2010.00915.x. Acesso em: 15 nov. 2024.
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      Oliveira, L. de, Larocca, R. A., Sass, N., & Câmara, N. O. S. (2011). Proportion of invariant NKT Cells in normal pregnant women at term: an evaluation in peripheral blood, placenta and umbilical cord blood. American Journal of Reproductive Immunology, 65( 1), 11-12. doi:10.1111/j.1600-0897.2010.00915.x
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      Oliveira L de, Larocca RA, Sass N, Câmara NOS. Proportion of invariant NKT Cells in normal pregnant women at term: an evaluation in peripheral blood, placenta and umbilical cord blood [Internet]. American Journal of Reproductive Immunology. 2011 ; 65( 1): 11-12.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1600-0897.2010.00915.x
    • Vancouver

      Oliveira L de, Larocca RA, Sass N, Câmara NOS. Proportion of invariant NKT Cells in normal pregnant women at term: an evaluation in peripheral blood, placenta and umbilical cord blood [Internet]. American Journal of Reproductive Immunology. 2011 ; 65( 1): 11-12.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1600-0897.2010.00915.x
  • Source: Journal of Immunology. Unidades: ICB, FMRP

    Assunto: IMUNOLOGIA

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      CARREGARO, Vanessa et al. Nucleosides from Phlebotomus papatasi salivary gland ameliorate murine collagen-induced arthritis by impairing dendritic cell functions. Journal of Immunology, v. 187, n. 8, p. 4347-4359, 2011Tradução . . Disponível em: https://doi.org/10.4049/jimmunol.1003404. Acesso em: 15 nov. 2024.
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      Carregaro, V., Nunes, A. de S., Cunha, T. M., Grespan, R., Oliveira, C. J. F., Lima-Junior, D. S., et al. (2011). Nucleosides from Phlebotomus papatasi salivary gland ameliorate murine collagen-induced arthritis by impairing dendritic cell functions. Journal of Immunology, 187( 8), 4347-4359. doi:10.4049/jimmunol.1003404
    • NLM

      Carregaro V, Nunes A de S, Cunha TM, Grespan R, Oliveira CJF, Lima-Junior DS, Costa DL, Verri Jr WA, Milanezi CM, Pham VM, Brand DD, Venezuela JG, Silva JS da, Ribeiro JMC, Cunha FQ. Nucleosides from Phlebotomus papatasi salivary gland ameliorate murine collagen-induced arthritis by impairing dendritic cell functions [Internet]. Journal of Immunology. 2011 ; 187( 8): 4347-4359.[citado 2024 nov. 15 ] Available from: https://doi.org/10.4049/jimmunol.1003404
    • Vancouver

      Carregaro V, Nunes A de S, Cunha TM, Grespan R, Oliveira CJF, Lima-Junior DS, Costa DL, Verri Jr WA, Milanezi CM, Pham VM, Brand DD, Venezuela JG, Silva JS da, Ribeiro JMC, Cunha FQ. Nucleosides from Phlebotomus papatasi salivary gland ameliorate murine collagen-induced arthritis by impairing dendritic cell functions [Internet]. Journal of Immunology. 2011 ; 187( 8): 4347-4359.[citado 2024 nov. 15 ] Available from: https://doi.org/10.4049/jimmunol.1003404
  • Source: Scandinavian Journal of Immunology. Unidade: ICB

    Assunto: IMUNOLOGIA

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      MACCHIAVERNI, Patrícia et al. Mother to child transfer of IgG and IgA antibodies against Dermatophagoides pteronyssinus. Scandinavian Journal of Immunology, v. 74, n. 6, p. 619-627, 2011Tradução . . Disponível em: https://doi.org/10.1111/j.1365-3083.2011.02615.x. Acesso em: 15 nov. 2024.
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      Macchiaverni, P., Arslanian, C., Frazão, J. B., Palmeira, P., Russo, M., Verhasselt, V., & Condino-Neto, A. (2011). Mother to child transfer of IgG and IgA antibodies against Dermatophagoides pteronyssinus. Scandinavian Journal of Immunology, 74( 6), 619-627. doi:10.1111/j.1365-3083.2011.02615.x
    • NLM

      Macchiaverni P, Arslanian C, Frazão JB, Palmeira P, Russo M, Verhasselt V, Condino-Neto A. Mother to child transfer of IgG and IgA antibodies against Dermatophagoides pteronyssinus [Internet]. Scandinavian Journal of Immunology. 2011 ; 74( 6): 619-627.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1365-3083.2011.02615.x
    • Vancouver

      Macchiaverni P, Arslanian C, Frazão JB, Palmeira P, Russo M, Verhasselt V, Condino-Neto A. Mother to child transfer of IgG and IgA antibodies against Dermatophagoides pteronyssinus [Internet]. Scandinavian Journal of Immunology. 2011 ; 74( 6): 619-627.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1365-3083.2011.02615.x
  • Source: Journal of Biological Chemistry. Unidades: ICB, EERP, FMRP

    Subjects: IMUNOLOGIA, PROTEINAS, ADJUVANTES IMUNOLÓGICOS

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      OLIVEIRA, Carlo José Freire de et al. Deconstructing tick saliva: Non-protein molecules with potent immunomodulatory properties. Journal of Biological Chemistry, v. 286, n. 13, p. 10960-10969, 2011Tradução . . Disponível em: https://doi.org/10.1074/jbc.M110.205047. Acesso em: 15 nov. 2024.
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      Oliveira, C. J. F. de, Nunes, A. de S., Francischetti, I. M. B., Carregaro, V., Anatriello, E., Silva, J. S. da, et al. (2011). Deconstructing tick saliva: Non-protein molecules with potent immunomodulatory properties. Journal of Biological Chemistry, 286( 13), 10960-10969. doi:10.1074/jbc.M110.205047
    • NLM

      Oliveira CJF de, Nunes A de S, Francischetti IMB, Carregaro V, Anatriello E, Silva JS da, Santos IKF de M, Ribeiro JMC, Ferreira BR. Deconstructing tick saliva: Non-protein molecules with potent immunomodulatory properties [Internet]. Journal of Biological Chemistry. 2011 ; 286( 13): 10960-10969.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1074/jbc.M110.205047
    • Vancouver

      Oliveira CJF de, Nunes A de S, Francischetti IMB, Carregaro V, Anatriello E, Silva JS da, Santos IKF de M, Ribeiro JMC, Ferreira BR. Deconstructing tick saliva: Non-protein molecules with potent immunomodulatory properties [Internet]. Journal of Biological Chemistry. 2011 ; 286( 13): 10960-10969.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1074/jbc.M110.205047
  • Source: Cellular and Molecular Life Sciences. Unidade: ICB

    Assunto: IMUNOLOGIA

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      AMARANTE-MENDES, João Gustavo Pessini. Cell death and the well of the organismo. Cellular and Molecular Life Sciences, v. 67, n. 10, p. 1565-1566, 2010Tradução . . Disponível em: https://doi.org/10.1007/s00018-010-0334-6. Acesso em: 15 nov. 2024.
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      Amarante-Mendes, J. G. P. (2010). Cell death and the well of the organismo. Cellular and Molecular Life Sciences, 67( 10), 1565-1566. doi:10.1007/s00018-010-0334-6
    • NLM

      Amarante-Mendes JGP. Cell death and the well of the organismo [Internet]. Cellular and Molecular Life Sciences. 2010 ; 67( 10): 1565-1566.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s00018-010-0334-6
    • Vancouver

      Amarante-Mendes JGP. Cell death and the well of the organismo [Internet]. Cellular and Molecular Life Sciences. 2010 ; 67( 10): 1565-1566.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s00018-010-0334-6
  • Source: Shock. Unidade: ICB

    Subjects: FARMACOLOGIA, IMUNOLOGIA

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      MARTINS, Joilson de Oliveira et al. Signaling pathways and mediators in lps-induced lung inflammation in diabetic rats: role of insulin. Shock, v. 33, n. 1, p. 76-82, 2010Tradução . . Acesso em: 15 nov. 2024.
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      Martins, J. de O., Ferracini, M., Anger, D. B. C., Martins, D. O., Ribeiro Jr., L. F., Sannomiya, P., & Jancar, S. (2010). Signaling pathways and mediators in lps-induced lung inflammation in diabetic rats: role of insulin. Shock, 33( 1), 76-82.
    • NLM

      Martins J de O, Ferracini M, Anger DBC, Martins DO, Ribeiro Jr. LF, Sannomiya P, Jancar S. Signaling pathways and mediators in lps-induced lung inflammation in diabetic rats: role of insulin. Shock. 2010 ; 33( 1): 76-82.[citado 2024 nov. 15 ]
    • Vancouver

      Martins J de O, Ferracini M, Anger DBC, Martins DO, Ribeiro Jr. LF, Sannomiya P, Jancar S. Signaling pathways and mediators in lps-induced lung inflammation in diabetic rats: role of insulin. Shock. 2010 ; 33( 1): 76-82.[citado 2024 nov. 15 ]
  • Source: European Journal of Pharmacology. Unidade: ICB

    Assunto: IMUNOLOGIA

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      CAMPANHOLE, Gabriela et al. Bradykinin inducible receptor is essential to lipopolysaccharide-induced acute lung injury in mice. European Journal of Pharmacology, v. 634, n. 1/3, p. 132-7, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.ejphar.2010.02.002. Acesso em: 15 nov. 2024.
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      Campanhole, G., Landgraf, R. G., Borducchi, E. N., Semedo, P., Wang, P. H. M., Amano, M. T., et al. (2010). Bradykinin inducible receptor is essential to lipopolysaccharide-induced acute lung injury in mice. European Journal of Pharmacology, 634( 1/3), 132-7. doi:10.1016/j.ejphar.2010.02.002
    • NLM

      Campanhole G, Landgraf RG, Borducchi EN, Semedo P, Wang PHM, Amano MT, Russo M, Pacheco-Silva A, Jancar S, Câmara NOS. Bradykinin inducible receptor is essential to lipopolysaccharide-induced acute lung injury in mice [Internet]. European Journal of Pharmacology. 2010 ; 634( 1/3): 132-7.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ejphar.2010.02.002
    • Vancouver

      Campanhole G, Landgraf RG, Borducchi EN, Semedo P, Wang PHM, Amano MT, Russo M, Pacheco-Silva A, Jancar S, Câmara NOS. Bradykinin inducible receptor is essential to lipopolysaccharide-induced acute lung injury in mice [Internet]. European Journal of Pharmacology. 2010 ; 634( 1/3): 132-7.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ejphar.2010.02.002
  • Source: European Journal of Immunology. Unidade: ICB

    Assunto: IMUNOLOGIA

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      SINGH, Satya P. et al. Changes in histone acetylation and methylation that are important for persistent but not transient expression. of CCR4 in human CD4+ T cells. European Journal of Immunology, v. 40, n. 11, p. 3183-3197, 2010Tradução . . Disponível em: https://doi.org/10.1002/eji.201040443. Acesso em: 15 nov. 2024.
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      Singh, S. P., Camargo, M. M. de, Zhang, H. H., Foley, J. F., Hedrick, M. N., & Farber, J. M. (2010). Changes in histone acetylation and methylation that are important for persistent but not transient expression. of CCR4 in human CD4+ T cells. European Journal of Immunology, 40( 11), 3183-3197. doi:10.1002/eji.201040443
    • NLM

      Singh SP, Camargo MM de, Zhang HH, Foley JF, Hedrick MN, Farber JM. Changes in histone acetylation and methylation that are important for persistent but not transient expression. of CCR4 in human CD4+ T cells [Internet]. European Journal of Immunology. 2010 ; 40( 11): 3183-3197.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/eji.201040443
    • Vancouver

      Singh SP, Camargo MM de, Zhang HH, Foley JF, Hedrick MN, Farber JM. Changes in histone acetylation and methylation that are important for persistent but not transient expression. of CCR4 in human CD4+ T cells [Internet]. European Journal of Immunology. 2010 ; 40( 11): 3183-3197.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/eji.201040443
  • Source: Cellular and Molecular Life Sciences. Unidade: ICB

    Assunto: IMUNOLOGIA

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      WEINLICH, Ricardo e BRUNNER, T. e AMARANTE-MENDES, João Gustavo Pessini. Control of death receptor ligand activity by posttranslational modifications. Cellular and Molecular Life Sciences, v. 67, n. 10, p. 1631-1642, 2010Tradução . . Disponível em: https://doi.org/10.1007/s00018-010-0289-7. Acesso em: 15 nov. 2024.
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      Weinlich, R., Brunner, T., & Amarante-Mendes, J. G. P. (2010). Control of death receptor ligand activity by posttranslational modifications. Cellular and Molecular Life Sciences, 67( 10), 1631-1642. doi:10.1007/s00018-010-0289-7
    • NLM

      Weinlich R, Brunner T, Amarante-Mendes JGP. Control of death receptor ligand activity by posttranslational modifications [Internet]. Cellular and Molecular Life Sciences. 2010 ; 67( 10): 1631-1642.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s00018-010-0289-7
    • Vancouver

      Weinlich R, Brunner T, Amarante-Mendes JGP. Control of death receptor ligand activity by posttranslational modifications [Internet]. Cellular and Molecular Life Sciences. 2010 ; 67( 10): 1631-1642.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s00018-010-0289-7

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