Filtros : "Indexado na Base de Dados MEDLINE" "Molecular and Cellular Endocrinology" Removidos: "Grupo de pesquisa: DES Collaboration" "ADMINISTRACAO" "Paquistão" Limpar

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  • Source: Molecular and Cellular Endocrinology. Unidade: ICB

    Subjects: TRIIODOTIRONINA, HORMÔNIOS TIREOIDIANOS, EXPRESSÃO GÊNICA, LINFÓCITOS T, RNA MENSAGEIRO, RIBOSSOMOS, PROTEÍNAS DA MEMBRANA

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      SOUZA, Paula Bargi de e SILVA, Francemilson Goulart da e NUNES, Maria Tereza. Posttranscriptional actions of triiodothyronine on Tshb expression in TαT1 cells: new insights into molecular mechanisms of negative feedback. Molecular and Cellular Endocrinology, v. 478, p. 45-52, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2018.07.006. Acesso em: 01 nov. 2024.
    • APA

      Souza, P. B. de, Silva, F. G. da, & Nunes, M. T. (2018). Posttranscriptional actions of triiodothyronine on Tshb expression in TαT1 cells: new insights into molecular mechanisms of negative feedback. Molecular and Cellular Endocrinology, 478, 45-52. doi:10.1016/j.mce.2018.07.006
    • NLM

      Souza PB de, Silva FG da, Nunes MT. Posttranscriptional actions of triiodothyronine on Tshb expression in TαT1 cells: new insights into molecular mechanisms of negative feedback [Internet]. Molecular and Cellular Endocrinology. 2018 ; 478 45-52.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2018.07.006
    • Vancouver

      Souza PB de, Silva FG da, Nunes MT. Posttranscriptional actions of triiodothyronine on Tshb expression in TαT1 cells: new insights into molecular mechanisms of negative feedback [Internet]. Molecular and Cellular Endocrinology. 2018 ; 478 45-52.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2018.07.006
  • Source: Molecular and Cellular Endocrinology. Unidade: ICB

    Assunto: FISIOLOGIA

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    • ABNT

      SOUZA, Arnaldo H. de et al. NADPH oxidase-2 does not contribute to β-cell glucotoxicity in cultured pancreatic islets from C57BL/6J mice. Molecular and Cellular Endocrinology, v. 439, p. 354-362, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2016.09.022. Acesso em: 01 nov. 2024.
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      Souza, A. H. de, Santos, L. R. B., Roma, L. P., Bensellam, M., Carpinelli, A. R., & Jonas, J. -C. (2017). NADPH oxidase-2 does not contribute to β-cell glucotoxicity in cultured pancreatic islets from C57BL/6J mice. Molecular and Cellular Endocrinology, 439, 354-362. doi:10.1016/j.mce.2016.09.022
    • NLM

      Souza AH de, Santos LRB, Roma LP, Bensellam M, Carpinelli AR, Jonas J-C. NADPH oxidase-2 does not contribute to β-cell glucotoxicity in cultured pancreatic islets from C57BL/6J mice [Internet]. Molecular and Cellular Endocrinology. 2017 ; 439 354-362.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2016.09.022
    • Vancouver

      Souza AH de, Santos LRB, Roma LP, Bensellam M, Carpinelli AR, Jonas J-C. NADPH oxidase-2 does not contribute to β-cell glucotoxicity in cultured pancreatic islets from C57BL/6J mice [Internet]. Molecular and Cellular Endocrinology. 2017 ; 439 354-362.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2016.09.022
  • Source: Molecular and Cellular Endocrinology. Unidade: ICB

    Assunto: HISTOLOGIA

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      FUZIWARA, Cesar Seigi e KIMURA, Edna Teruko. MicroRNAs in thyroid development, function and tumorigenesis. Molecular and Cellular Endocrinology, v. 456, p. 44-50, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2016.12.017. Acesso em: 01 nov. 2024.
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      Fuziwara, C. S., & Kimura, E. T. (2017). MicroRNAs in thyroid development, function and tumorigenesis. Molecular and Cellular Endocrinology, 456, 44-50. doi:10.1016/j.mce.2016.12.017
    • NLM

      Fuziwara CS, Kimura ET. MicroRNAs in thyroid development, function and tumorigenesis [Internet]. Molecular and Cellular Endocrinology. 2017 ; 456 44-50.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2016.12.017
    • Vancouver

      Fuziwara CS, Kimura ET. MicroRNAs in thyroid development, function and tumorigenesis [Internet]. Molecular and Cellular Endocrinology. 2017 ; 456 44-50.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2016.12.017
  • Source: Molecular and Cellular Endocrinology. Unidade: ICB

    Assunto: HISTOLOGIA

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      LIMA, Cilene Rebouças de e GOMES, Cibele Crastequini e SANTOS, Marinilce Fagundes dos. Role of microRNAs in endocrine cancer metastasis. Molecular and Cellular Endocrinology, v. 456, p. 62-75, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2017.03.015. Acesso em: 01 nov. 2024.
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      Lima, C. R. de, Gomes, C. C., & Santos, M. F. dos. (2017). Role of microRNAs in endocrine cancer metastasis. Molecular and Cellular Endocrinology, 456, 62-75. doi:10.1016/j.mce.2017.03.015
    • NLM

      Lima CR de, Gomes CC, Santos MF dos. Role of microRNAs in endocrine cancer metastasis [Internet]. Molecular and Cellular Endocrinology. 2017 ; 456 62-75.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2017.03.015
    • Vancouver

      Lima CR de, Gomes CC, Santos MF dos. Role of microRNAs in endocrine cancer metastasis [Internet]. Molecular and Cellular Endocrinology. 2017 ; 456 62-75.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2017.03.015
  • Source: Molecular and Cellular Endocrinology. Unidades: FM, ICB

    Subjects: FÍGADO, DOENÇA CRÔNICA, INSULINA (RESISTÊNCIA), RATOS

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      FABRE, Nelly T. et al. Hormetic modulation of hepatic insulin sensitivity by advanced glycation end products. Molecular and Cellular Endocrinology, v. 447, p. 116-124, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2017.02.035. Acesso em: 01 nov. 2024.
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      Fabre, N. T., Thieme, K., Silva, K. S., Catanozi, S., Cavaleiro, A. M., Pinto jr, D. A. C., et al. (2017). Hormetic modulation of hepatic insulin sensitivity by advanced glycation end products. Molecular and Cellular Endocrinology, 447, 116-124. doi:10.1016/j.mce.2017.02.035
    • NLM

      Fabre NT, Thieme K, Silva KS, Catanozi S, Cavaleiro AM, Pinto jr DAC, Maristela M. Okamoto, Morais MRPT, Falquetto B, Zorn TM, Machado UF, Passarelli M, Correa-Giannella ML. Hormetic modulation of hepatic insulin sensitivity by advanced glycation end products [Internet]. Molecular and Cellular Endocrinology. 2017 ; 447 116-124.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2017.02.035
    • Vancouver

      Fabre NT, Thieme K, Silva KS, Catanozi S, Cavaleiro AM, Pinto jr DAC, Maristela M. Okamoto, Morais MRPT, Falquetto B, Zorn TM, Machado UF, Passarelli M, Correa-Giannella ML. Hormetic modulation of hepatic insulin sensitivity by advanced glycation end products [Internet]. Molecular and Cellular Endocrinology. 2017 ; 447 116-124.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2017.02.035
  • Source: Molecular and Cellular Endocrinology. Unidades: FMRP, ICB

    Subjects: ANATOMIA, FISIOLOGIA

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      SILVEIRA, Marina Augusto et al. STAT5 signaling in kisspeptin cells regulates the timing of puberty. Molecular and Cellular Endocrinology, v. 448, p. 55-65, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2017.03.024. Acesso em: 01 nov. 2024.
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      Silveira, M. A., Furigo, I. C., Zampieri, T. T., Bohlen, T. M., Paula, D. G. de, Franci, C. R., et al. (2017). STAT5 signaling in kisspeptin cells regulates the timing of puberty. Molecular and Cellular Endocrinology, 448, 55-65. doi:10.1016/j.mce.2017.03.024
    • NLM

      Silveira MA, Furigo IC, Zampieri TT, Bohlen TM, Paula DG de, Franci CR, Donato Junior J, Frazão R. STAT5 signaling in kisspeptin cells regulates the timing of puberty [Internet]. Molecular and Cellular Endocrinology. 2017 ; 448 55-65.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2017.03.024
    • Vancouver

      Silveira MA, Furigo IC, Zampieri TT, Bohlen TM, Paula DG de, Franci CR, Donato Junior J, Frazão R. STAT5 signaling in kisspeptin cells regulates the timing of puberty [Internet]. Molecular and Cellular Endocrinology. 2017 ; 448 55-65.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2017.03.024
  • Source: Molecular and Cellular Endocrinology. Unidade: ICB

    Subjects: ANATOMIA, FISIOLOGIA

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      FURIGO, Isadora C. et al. Brain STAT5 signaling and behavioral control. Molecular and Cellular Endocrinology, v. 438, p. 70-76, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2016.04.019. Acesso em: 01 nov. 2024.
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      Furigo, I. C., Ramos-Lobo, A. M., Frazão, R., & Donato Junior, J. (2016). Brain STAT5 signaling and behavioral control. Molecular and Cellular Endocrinology, 438, 70-76. doi:10.1016/j.mce.2016.04.019
    • NLM

      Furigo IC, Ramos-Lobo AM, Frazão R, Donato Junior J. Brain STAT5 signaling and behavioral control [Internet]. Molecular and Cellular Endocrinology. 2016 ; 438 70-76.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2016.04.019
    • Vancouver

      Furigo IC, Ramos-Lobo AM, Frazão R, Donato Junior J. Brain STAT5 signaling and behavioral control [Internet]. Molecular and Cellular Endocrinology. 2016 ; 438 70-76.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2016.04.019
  • Source: Molecular and Cellular Endocrinology. Unidade: ICB

    Subjects: ANATOMIA, FISIOLOGIA

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      BOHLEN, Tabata M. et al. Fatness rather than leptin sensitivity determines the timing of puberty in female mice. Molecular and Cellular Endocrinology, v. 423, p. 11-21, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2015.12.022. Acesso em: 01 nov. 2024.
    • APA

      Bohlen, T. M., Silveira, M. A., Zampieri, T. T., Frazão, R., & Donato Junior, J. (2016). Fatness rather than leptin sensitivity determines the timing of puberty in female mice. Molecular and Cellular Endocrinology, 423, 11-21. doi:10.1016/j.mce.2015.12.022
    • NLM

      Bohlen TM, Silveira MA, Zampieri TT, Frazão R, Donato Junior J. Fatness rather than leptin sensitivity determines the timing of puberty in female mice [Internet]. Molecular and Cellular Endocrinology. 2016 ; 423 11-21.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2015.12.022
    • Vancouver

      Bohlen TM, Silveira MA, Zampieri TT, Frazão R, Donato Junior J. Fatness rather than leptin sensitivity determines the timing of puberty in female mice [Internet]. Molecular and Cellular Endocrinology. 2016 ; 423 11-21.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2015.12.022
  • Source: Molecular and Cellular Endocrinology. Unidade: ICB

    Assunto: FISIOLOGIA

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      SERRANO-NASCIMENTO, Caroline et al. Excess iodide downregulates Na(+)/I(-) symporter gene transcription through activation of PI3K/Akt pathway. Molecular and Cellular Endocrinology, v. 426, p. 73-90, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2016.02.006. Acesso em: 01 nov. 2024.
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      Serrano-Nascimento, C., Nicola, J. P., Teixeira, S. da S., Poyares, L. L., Lellis-Santos, C., Bordin, S., et al. (2016). Excess iodide downregulates Na(+)/I(-) symporter gene transcription through activation of PI3K/Akt pathway. Molecular and Cellular Endocrinology, 426, 73-90. doi:10.1016/j.mce.2016.02.006
    • NLM

      Serrano-Nascimento C, Nicola JP, Teixeira S da S, Poyares LL, Lellis-Santos C, Bordin S, Masini-Repiso AM, Nunes MT. Excess iodide downregulates Na(+)/I(-) symporter gene transcription through activation of PI3K/Akt pathway [Internet]. Molecular and Cellular Endocrinology. 2016 ; 426 73-90.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2016.02.006
    • Vancouver

      Serrano-Nascimento C, Nicola JP, Teixeira S da S, Poyares LL, Lellis-Santos C, Bordin S, Masini-Repiso AM, Nunes MT. Excess iodide downregulates Na(+)/I(-) symporter gene transcription through activation of PI3K/Akt pathway [Internet]. Molecular and Cellular Endocrinology. 2016 ; 426 73-90.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2016.02.006
  • Source: Molecular and Cellular Endocrinology. Unidade: ICB

    Subjects: FISIOLOGIA, GLICOPROTEINAS, GLÂNDULA PITUITÁRIA, RATOS, SECREÇÃO ANIMAL

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      SOUZA, Paula Bargi de et al. T(3) rapidly regulates several steps of alpha subunit glycoprotein (CGA) synthesis and secretion in the pituitary of male rats: Potential repercussions on TSH, FSH and LH secretion. Molecular and Cellular Endocrinology, v. 409, p. 73-81, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2015.04.002. Acesso em: 01 nov. 2024.
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      Souza, P. B. de, Romano, R. M., Silva, F. G. da, Brunetto, E. L., & Nunes, M. T. (2015). T(3) rapidly regulates several steps of alpha subunit glycoprotein (CGA) synthesis and secretion in the pituitary of male rats: Potential repercussions on TSH, FSH and LH secretion. Molecular and Cellular Endocrinology, 409, 73-81. doi:10.1016/j.mce.2015.04.002
    • NLM

      Souza PB de, Romano RM, Silva FG da, Brunetto EL, Nunes MT. T(3) rapidly regulates several steps of alpha subunit glycoprotein (CGA) synthesis and secretion in the pituitary of male rats: Potential repercussions on TSH, FSH and LH secretion [Internet]. Molecular and Cellular Endocrinology. 2015 ; 409 73-81.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2015.04.002
    • Vancouver

      Souza PB de, Romano RM, Silva FG da, Brunetto EL, Nunes MT. T(3) rapidly regulates several steps of alpha subunit glycoprotein (CGA) synthesis and secretion in the pituitary of male rats: Potential repercussions on TSH, FSH and LH secretion [Internet]. Molecular and Cellular Endocrinology. 2015 ; 409 73-81.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2015.04.002
  • Source: Molecular and Cellular Endocrinology. Unidades: IQ, ICB

    Subjects: CÓRTEX ADRENAL, HORMÔNIO ADRENOCORTICOTRÓFICO

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      MENDONÇA, Pedro Omori Ribeiro de et al. N-`POMC IND. 1-28´ increases cyclin D expression and inhibits `P27 POT. kip1´ in the adrenal cortex. Molecular and Cellular Endocrinology, v. 37, n. 1-2, p. 166-173, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2012.11.017. Acesso em: 01 nov. 2024.
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      Mendonça, P. O. R. de, Liria, C. W., Machini, M. T., & Lotfi, C. F. P. (2013). N-`POMC IND. 1-28´ increases cyclin D expression and inhibits `P27 POT. kip1´ in the adrenal cortex. Molecular and Cellular Endocrinology, 37( 1-2), 166-173. doi:10.1016/j.mce.2012.11.017
    • NLM

      Mendonça POR de, Liria CW, Machini MT, Lotfi CFP. N-`POMC IND. 1-28´ increases cyclin D expression and inhibits `P27 POT. kip1´ in the adrenal cortex [Internet]. Molecular and Cellular Endocrinology. 2013 ; 37( 1-2): 166-173.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2012.11.017
    • Vancouver

      Mendonça POR de, Liria CW, Machini MT, Lotfi CFP. N-`POMC IND. 1-28´ increases cyclin D expression and inhibits `P27 POT. kip1´ in the adrenal cortex [Internet]. Molecular and Cellular Endocrinology. 2013 ; 37( 1-2): 166-173.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2012.11.017
  • Source: Molecular and Cellular Endocrinology. Unidade: ICB

    Assunto: ANATOMIA

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      TAKANO, Ana Paula Cremasco e DINIZ, Gabriela Placoná e BARRETO-CHAVES, Maria Luiza Morais. AMPK signaling pathway is rapidly activated by T3 and regulates the cardiomyocyte growth. Molecular and Cellular Endocrinology, v. 376, n. 1-2, p. 43-50, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2013.05.024. Acesso em: 01 nov. 2024.
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      Takano, A. P. C., Diniz, G. P., & Barreto-Chaves, M. L. M. (2013). AMPK signaling pathway is rapidly activated by T3 and regulates the cardiomyocyte growth. Molecular and Cellular Endocrinology, 376( 1-2), 43-50. doi:10.1016/j.mce.2013.05.024
    • NLM

      Takano APC, Diniz GP, Barreto-Chaves MLM. AMPK signaling pathway is rapidly activated by T3 and regulates the cardiomyocyte growth [Internet]. Molecular and Cellular Endocrinology. 2013 ; 376( 1-2): 43-50.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2013.05.024
    • Vancouver

      Takano APC, Diniz GP, Barreto-Chaves MLM. AMPK signaling pathway is rapidly activated by T3 and regulates the cardiomyocyte growth [Internet]. Molecular and Cellular Endocrinology. 2013 ; 376( 1-2): 43-50.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2013.05.024
  • Source: Molecular and Cellular Endocrinology. Unidade: ICB

    Assunto: ANATOMIA

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      DINIZ, Gabriela Placoná e TAKANO, Ana Paula Cremasco e BARRETO-CHAVES, Maria Luiza Morais. miRNA-208a and miRNA-208b are triggered in thyroid hormone-induced cardiac hypertrophy – Role of type 1 Angiotensin II receptor (AT1R) on miRNA-208a/α-MHC modulation. Molecular and Cellular Endocrinology, v. 374, n. 1-2, p. 117-124, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2013.04.010. Acesso em: 01 nov. 2024.
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      Diniz, G. P., Takano, A. P. C., & Barreto-Chaves, M. L. M. (2013). miRNA-208a and miRNA-208b are triggered in thyroid hormone-induced cardiac hypertrophy – Role of type 1 Angiotensin II receptor (AT1R) on miRNA-208a/α-MHC modulation. Molecular and Cellular Endocrinology, 374( 1-2), 117-124. doi:10.1016/j.mce.2013.04.010
    • NLM

      Diniz GP, Takano APC, Barreto-Chaves MLM. miRNA-208a and miRNA-208b are triggered in thyroid hormone-induced cardiac hypertrophy – Role of type 1 Angiotensin II receptor (AT1R) on miRNA-208a/α-MHC modulation [Internet]. Molecular and Cellular Endocrinology. 2013 ; 374( 1-2): 117-124.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2013.04.010
    • Vancouver

      Diniz GP, Takano APC, Barreto-Chaves MLM. miRNA-208a and miRNA-208b are triggered in thyroid hormone-induced cardiac hypertrophy – Role of type 1 Angiotensin II receptor (AT1R) on miRNA-208a/α-MHC modulation [Internet]. Molecular and Cellular Endocrinology. 2013 ; 374( 1-2): 117-124.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2013.04.010
  • Source: Molecular and Cellular Endocrinology. Unidade: ICB

    Assunto: FISIOLOGIA

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      SERRANO-NASCIMENTO, Caroline et al. New insights about the posttranscriptional mechanisms triggered by iodide excess on sodium/iodide symporter (NIS) expression in PCCl3 cells. Molecular and Cellular Endocrinology, v. 349, n. 2, p. 154-161, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2011.09.036. Acesso em: 01 nov. 2024.
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      Serrano-Nascimento, C., Calil-Silveira, J., Silva, F. G. da, & Nunes, M. T. (2012). New insights about the posttranscriptional mechanisms triggered by iodide excess on sodium/iodide symporter (NIS) expression in PCCl3 cells. Molecular and Cellular Endocrinology, 349( 2), 154-161. doi:10.1016/j.mce.2011.09.036
    • NLM

      Serrano-Nascimento C, Calil-Silveira J, Silva FG da, Nunes MT. New insights about the posttranscriptional mechanisms triggered by iodide excess on sodium/iodide symporter (NIS) expression in PCCl3 cells [Internet]. Molecular and Cellular Endocrinology. 2012 ; 349( 2): 154-161.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2011.09.036
    • Vancouver

      Serrano-Nascimento C, Calil-Silveira J, Silva FG da, Nunes MT. New insights about the posttranscriptional mechanisms triggered by iodide excess on sodium/iodide symporter (NIS) expression in PCCl3 cells [Internet]. Molecular and Cellular Endocrinology. 2012 ; 349( 2): 154-161.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2011.09.036
  • Source: Molecular and Cellular Endocrinology. Unidade: ICB

    Assunto: FISIOLOGIA

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      CALIL-SILVEIRA, Jamile e SERRANO-NASCIMENTO, Caroline e NUNES, Maria Tereza. Iodide treatment acutely increases pendrin (SLC26A4) mRNA expression in the rat thyroid and the PCCl3 thyroid cell line by transcriptional mechanisms. Molecular and Cellular Endocrinology, v. 350, n. 1, p. 118-124, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.mce.2011.12.002. Acesso em: 01 nov. 2024.
    • APA

      Calil-Silveira, J., Serrano-Nascimento, C., & Nunes, M. T. (2012). Iodide treatment acutely increases pendrin (SLC26A4) mRNA expression in the rat thyroid and the PCCl3 thyroid cell line by transcriptional mechanisms. Molecular and Cellular Endocrinology, 350( 1), 118-124. doi:10.1016/j.mce.2011.12.002
    • NLM

      Calil-Silveira J, Serrano-Nascimento C, Nunes MT. Iodide treatment acutely increases pendrin (SLC26A4) mRNA expression in the rat thyroid and the PCCl3 thyroid cell line by transcriptional mechanisms [Internet]. Molecular and Cellular Endocrinology. 2012 ; 350( 1): 118-124.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2011.12.002
    • Vancouver

      Calil-Silveira J, Serrano-Nascimento C, Nunes MT. Iodide treatment acutely increases pendrin (SLC26A4) mRNA expression in the rat thyroid and the PCCl3 thyroid cell line by transcriptional mechanisms [Internet]. Molecular and Cellular Endocrinology. 2012 ; 350( 1): 118-124.[citado 2024 nov. 01 ] Available from: https://doi.org/10.1016/j.mce.2011.12.002

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