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ABNT
FEREZIN, Letícia Perticarrara et al. The rs2682826 polymorphism of the NOS1 gene is associated with the degree of disability of erectile dysfunction. Life, v. 13, n. 5, p. 1-13, 2023Tradução . . Disponível em: https://doi.org/10.3390/life13051082. Acesso em: 08 out. 2024.
APA
Ferezin, L. P., Cotta Filho, C. K., Pereira, V. C. R., Andrade, M. F. de, Molina, C. A. F., Tucci Júnior, S., et al. (2023). The rs2682826 polymorphism of the NOS1 gene is associated with the degree of disability of erectile dysfunction. Life, 13( 5), 1-13. doi:10.3390/life13051082
NLM
Ferezin LP, Cotta Filho CK, Pereira VCR, Andrade MF de, Molina CAF, Tucci Júnior S, Tanus-Santos JE, Lacchini R. The rs2682826 polymorphism of the NOS1 gene is associated with the degree of disability of erectile dysfunction [Internet]. Life. 2023 ; 13( 5): 1-13.[citado 2024 out. 08 ] Available from: https://doi.org/10.3390/life13051082
Vancouver
Ferezin LP, Cotta Filho CK, Pereira VCR, Andrade MF de, Molina CAF, Tucci Júnior S, Tanus-Santos JE, Lacchini R. The rs2682826 polymorphism of the NOS1 gene is associated with the degree of disability of erectile dysfunction [Internet]. Life. 2023 ; 13( 5): 1-13.[citado 2024 out. 08 ] Available from: https://doi.org/10.3390/life13051082
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NUNES, Fernanda Daniela Dornelas et al. The association of biochemical and genetic biomarkers in VEGF pathway with depression. Pharmaceutics, v. 14, n. 12, p. 1-15, 2022Tradução . . Disponível em: https://doi.org/10.3390/pharmaceutics14122757. Acesso em: 08 out. 2024.
APA
Nunes, F. D. D., Ferezin, L. P., Pereira, S. C., Figaro-Drumond, F. V., Pinheiro, L. C., Menezes, I. C., et al. (2022). The association of biochemical and genetic biomarkers in VEGF pathway with depression. Pharmaceutics, 14( 12), 1-15. doi:10.3390/pharmaceutics14122757
NLM
Nunes FDD, Ferezin LP, Pereira SC, Figaro-Drumond FV, Pinheiro LC, Menezes IC, Baes CVW, Coeli-Lacchini FB, Tanus-Santos JE, Juruena MF, Lacchini R. The association of biochemical and genetic biomarkers in VEGF pathway with depression [Internet]. Pharmaceutics. 2022 ; 14( 12): 1-15.[citado 2024 out. 08 ] Available from: https://doi.org/10.3390/pharmaceutics14122757
Vancouver
Nunes FDD, Ferezin LP, Pereira SC, Figaro-Drumond FV, Pinheiro LC, Menezes IC, Baes CVW, Coeli-Lacchini FB, Tanus-Santos JE, Juruena MF, Lacchini R. The association of biochemical and genetic biomarkers in VEGF pathway with depression [Internet]. Pharmaceutics. 2022 ; 14( 12): 1-15.[citado 2024 out. 08 ] Available from: https://doi.org/10.3390/pharmaceutics14122757
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OLIVEIRA-PAULA, Gustavo Henrique et al. Arginase II polymorphisms modify the hypotensive responses to propofol by affecting nitric oxide bioavailability. European Journal of Clinical Pharmacology, v. 77, n. 6, p. 869-877, 2021Tradução . . Disponível em: https://doi.org/10.1007/s00228-020-03059-9. Acesso em: 08 out. 2024.
APA
Oliveira-Paula, G. H., Coeli-Lacchini, F. B., Ferezin, L. P., Ferreira, G. C., Pinheiro, L. C., Garcia, W. N. de P., et al. (2021). Arginase II polymorphisms modify the hypotensive responses to propofol by affecting nitric oxide bioavailability. European Journal of Clinical Pharmacology, 77( 6), 869-877. doi:10.1007/s00228-020-03059-9
NLM
Oliveira-Paula GH, Coeli-Lacchini FB, Ferezin LP, Ferreira GC, Pinheiro LC, Garcia WN de P, Garcia LV, Tanus-Santos JE, Lacchini R. Arginase II polymorphisms modify the hypotensive responses to propofol by affecting nitric oxide bioavailability [Internet]. European Journal of Clinical Pharmacology. 2021 ; 77( 6): 869-877.[citado 2024 out. 08 ] Available from: https://doi.org/10.1007/s00228-020-03059-9
Vancouver
Oliveira-Paula GH, Coeli-Lacchini FB, Ferezin LP, Ferreira GC, Pinheiro LC, Garcia WN de P, Garcia LV, Tanus-Santos JE, Lacchini R. Arginase II polymorphisms modify the hypotensive responses to propofol by affecting nitric oxide bioavailability [Internet]. European Journal of Clinical Pharmacology. 2021 ; 77( 6): 869-877.[citado 2024 out. 08 ] Available from: https://doi.org/10.1007/s00228-020-03059-9
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SILVA, Roberta Fernanda da et al. Association between endothelial nitric oxide synthase and the renin-angiotensin-aldosterone system polymorphisms, blood pressure and training status in normotensive/pre-hypertension and hypertensive older adults: a pilot study. Clinical and Experimental Hypertension, v. 43, n. 7, p. 661-670, 2021Tradução . . Disponível em: https://doi.org/10.1080/10641963.2021.1937202. Acesso em: 08 out. 2024.
APA
Silva, R. F. da, Lacchini, R., Pinheiro, L. C., Ferezin, L. P., Tanus-Santos, J. E., Luizon, M. R., et al. (2021). Association between endothelial nitric oxide synthase and the renin-angiotensin-aldosterone system polymorphisms, blood pressure and training status in normotensive/pre-hypertension and hypertensive older adults: a pilot study. Clinical and Experimental Hypertension, 43( 7), 661-670. doi:10.1080/10641963.2021.1937202
NLM
Silva RF da, Lacchini R, Pinheiro LC, Ferezin LP, Tanus-Santos JE, Luizon MR, Dionísio TJ, Santos CF dos, Reia TA, Jacomini AM, Moreno AMG, Zago AS. Association between endothelial nitric oxide synthase and the renin-angiotensin-aldosterone system polymorphisms, blood pressure and training status in normotensive/pre-hypertension and hypertensive older adults: a pilot study [Internet]. Clinical and Experimental Hypertension. 2021 ; 43( 7): 661-670.[citado 2024 out. 08 ] Available from: https://doi.org/10.1080/10641963.2021.1937202
Vancouver
Silva RF da, Lacchini R, Pinheiro LC, Ferezin LP, Tanus-Santos JE, Luizon MR, Dionísio TJ, Santos CF dos, Reia TA, Jacomini AM, Moreno AMG, Zago AS. Association between endothelial nitric oxide synthase and the renin-angiotensin-aldosterone system polymorphisms, blood pressure and training status in normotensive/pre-hypertension and hypertensive older adults: a pilot study [Internet]. Clinical and Experimental Hypertension. 2021 ; 43( 7): 661-670.[citado 2024 out. 08 ] Available from: https://doi.org/10.1080/10641963.2021.1937202
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PEREIRA, Daniela A. et al. NAMPT single-nucleotide polymorphism rs1319501 and visfatin/NAMPT affect nitric oxide formation, sFlt-1 and antihypertensive therapy response in preeclampsia. Pharmacogenomics, v. 22, n. 8, p. 451-464, 2021Tradução . . Disponível em: https://doi.org/10.2217/pgs-2021-0006. Acesso em: 08 out. 2024.
APA
Pereira, D. A., Sandrim, V. C., Palei, A. C., Amaral, L. M., Belo, V. A., Lacchini, R., et al. (2021). NAMPT single-nucleotide polymorphism rs1319501 and visfatin/NAMPT affect nitric oxide formation, sFlt-1 and antihypertensive therapy response in preeclampsia. Pharmacogenomics, 22( 8), 451-464. doi:10.2217/pgs-2021-0006
NLM
Pereira DA, Sandrim VC, Palei AC, Amaral LM, Belo VA, Lacchini R, Cavalli R de C, Tanus-Santos JE, Luizon MR. NAMPT single-nucleotide polymorphism rs1319501 and visfatin/NAMPT affect nitric oxide formation, sFlt-1 and antihypertensive therapy response in preeclampsia [Internet]. Pharmacogenomics. 2021 ; 22( 8): 451-464.[citado 2024 out. 08 ] Available from: https://doi.org/10.2217/pgs-2021-0006
Vancouver
Pereira DA, Sandrim VC, Palei AC, Amaral LM, Belo VA, Lacchini R, Cavalli R de C, Tanus-Santos JE, Luizon MR. NAMPT single-nucleotide polymorphism rs1319501 and visfatin/NAMPT affect nitric oxide formation, sFlt-1 and antihypertensive therapy response in preeclampsia [Internet]. Pharmacogenomics. 2021 ; 22( 8): 451-464.[citado 2024 out. 08 ] Available from: https://doi.org/10.2217/pgs-2021-0006
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FIGARO-DRUMOND, Fernanda Viana et al. Association of 11β-hydroxysteroid dehydrogenase type1 (HSD11b1) gene polymorphisms with outcome of antidepressant therapy and suicide attempts. Behavioural Brain Research, v. 81, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bbr.2019.112343. Acesso em: 08 out. 2024.
APA
Figaro-Drumond, F. V., Pereira, S. C., Menezes, I. C., Baes, C. V. W., Coeli-Lacchini, F. B., Oliveira-Paula, G. H., et al. (2020). Association of 11β-hydroxysteroid dehydrogenase type1 (HSD11b1) gene polymorphisms with outcome of antidepressant therapy and suicide attempts. Behavioural Brain Research, 81. doi:10.1016/j.bbr.2019.112343
NLM
Figaro-Drumond FV, Pereira SC, Menezes IC, Baes CVW, Coeli-Lacchini FB, Oliveira-Paula GH, Cleare AJ, Young AH, Tanus-Santos JE, Juruena MFP, Lacchini R. Association of 11β-hydroxysteroid dehydrogenase type1 (HSD11b1) gene polymorphisms with outcome of antidepressant therapy and suicide attempts [Internet]. Behavioural Brain Research. 2020 ; 81[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.bbr.2019.112343
Vancouver
Figaro-Drumond FV, Pereira SC, Menezes IC, Baes CVW, Coeli-Lacchini FB, Oliveira-Paula GH, Cleare AJ, Young AH, Tanus-Santos JE, Juruena MFP, Lacchini R. Association of 11β-hydroxysteroid dehydrogenase type1 (HSD11b1) gene polymorphisms with outcome of antidepressant therapy and suicide attempts [Internet]. Behavioural Brain Research. 2020 ; 81[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.bbr.2019.112343
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ABNT
VALENTE, Flavia Mariana et al. Plasma levels of matrix metalloproteinase-9 are elevated in individuals with hypertensive crisis. BMC Cardiovascular Disorders, v. 20, p. 1-7, 2020Tradução . . Disponível em: https://doi.org/10.1186/s12872-020-01412-5. Acesso em: 08 out. 2024.
APA
Valente, F. M., Andrade, D. O. de, Cosenso-Martin, L. N., Cesarino, C. B., Guimarães, S. M., Guimarães, V. B., et al. (2020). Plasma levels of matrix metalloproteinase-9 are elevated in individuals with hypertensive crisis. BMC Cardiovascular Disorders, 20, 1-7. doi:10.1186/s12872-020-01412-5
NLM
Valente FM, Andrade DO de, Cosenso-Martin LN, Cesarino CB, Guimarães SM, Guimarães VB, Lacchini R, Tanus-Santos JE, Yugar-Toledo JC, Vilela-Martin JF. Plasma levels of matrix metalloproteinase-9 are elevated in individuals with hypertensive crisis [Internet]. BMC Cardiovascular Disorders. 2020 ; 20 1-7.[citado 2024 out. 08 ] Available from: https://doi.org/10.1186/s12872-020-01412-5
Vancouver
Valente FM, Andrade DO de, Cosenso-Martin LN, Cesarino CB, Guimarães SM, Guimarães VB, Lacchini R, Tanus-Santos JE, Yugar-Toledo JC, Vilela-Martin JF. Plasma levels of matrix metalloproteinase-9 are elevated in individuals with hypertensive crisis [Internet]. BMC Cardiovascular Disorders. 2020 ; 20 1-7.[citado 2024 out. 08 ] Available from: https://doi.org/10.1186/s12872-020-01412-5