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Artigo de periodico
Linkage disequilibrium with HLA-DRB1-DQB1 haplotypes explains the association of TNF-308G>A variant with type 1 diabetes in a Brazilian cohort (2015)
Patente, Thiago A.; Monteiro, Maria B.; Vieira, Suzana M.; Silva, Maria E. Rossi da; Nery, Márcia; Queiroz, Márcia; Azevedo, Mirela J.; Canani, Luis H.; Parisi, Maria C.; Pavin, Elizabeth J.; Mainardi, Débora; Javor, Juraj; Velho, Gilberto; Coimbra, Cássio N.; Corrêa-Giannella, Maria Lúcia
Source: Gene. Unidade: FM
Subjects: POLIMORFISMO, ESTUDOS DE COORTES, DIABETES MELLITUS (FISIOPATOLOGIA), BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PATENTE, Thiago A. et al. Linkage disequilibrium with HLA-DRB1-DQB1 haplotypes explains the association of TNF-308G>A variant with type 1 diabetes in a Brazilian cohort. Gene, v. 568, n. 1, p. 50-54, 2015Tradução . . Disponível em: http://www.sciencedirect.com/science/article/pii/S0378111915005752. Acesso em: 11 nov. 2024.
APA
Patente, T. A., Monteiro, M. B., Vieira, S. M., Silva, M. E. R. da, Nery, M., Queiroz, M., et al. (2015). Linkage disequilibrium with HLA-DRB1-DQB1 haplotypes explains the association of TNF-308G>A variant with type 1 diabetes in a Brazilian cohort. Gene, 568( 1), 50-54. doi:10.1016/j.gene.2015.05.017
NLM
Patente TA, Monteiro MB, Vieira SM, Silva MER da, Nery M, Queiroz M, Azevedo MJ, Canani LH, Parisi MC, Pavin EJ, Mainardi D, Javor J, Velho G, Coimbra CN, Corrêa-Giannella ML. Linkage disequilibrium with HLA-DRB1-DQB1 haplotypes explains the association of TNF-308G>A variant with type 1 diabetes in a Brazilian cohort [Internet]. Gene. 2015 ; 568( 1): 50-54.[citado 2024 nov. 11 ] Available from: http://www.sciencedirect.com/science/article/pii/S0378111915005752
Vancouver
Patente TA, Monteiro MB, Vieira SM, Silva MER da, Nery M, Queiroz M, Azevedo MJ, Canani LH, Parisi MC, Pavin EJ, Mainardi D, Javor J, Velho G, Coimbra CN, Corrêa-Giannella ML. Linkage disequilibrium with HLA-DRB1-DQB1 haplotypes explains the association of TNF-308G>A variant with type 1 diabetes in a Brazilian cohort [Internet]. Gene. 2015 ; 568( 1): 50-54.[citado 2024 nov. 11 ] Available from: http://www.sciencedirect.com/science/article/pii/S0378111915005752
Artigo de periodico
Catalase activity, allelic variations in the catalase gene and risk of kidney complications in patients with type 1 diabetes (2013)
Mohammedi, Kamel; Patente, Thiago A.; Muñoz, Naiïma Bellili; Driss, Fathi; Monteiro, Maria Beatriz; Roussel, Ronan; Pavin, Elizabeth J.; Seta, Nathalie; Fumeron, Frédéric; Azevedo, Mirela J.; Canani, Luis H.; Hadjadj, Samy; Marre, Michel; Giannella, Maria Lúcia Cardillo Côrrea
Source: Diabetologia. Unidade: FM
Subjects: CATALASE (ATIVIDADE), GENÉTICA, FATORES DE RISCO, DIABETES MELLITUS, NEFROPATIAS, ANTIOXIDANTES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MOHAMMEDI, Kamel et al. Catalase activity, allelic variations in the catalase gene and risk of kidney complications in patients with type 1 diabetes. Diabetologia, v. 56, n. 12, p. 2733-2742, 2013Tradução . . Disponível em: https://doi.org/10.1007/s00125-013-3057-z. Acesso em: 11 nov. 2024.
APA
Mohammedi, K., Patente, T. A., Muñoz, N. B., Driss, F., Monteiro, M. B., Roussel, R., et al. (2013). Catalase activity, allelic variations in the catalase gene and risk of kidney complications in patients with type 1 diabetes. Diabetologia, 56( 12), 2733-2742. doi:10.1007/s00125-013-3057-z
NLM
Mohammedi K, Patente TA, Muñoz NB, Driss F, Monteiro MB, Roussel R, Pavin EJ, Seta N, Fumeron F, Azevedo MJ, Canani LH, Hadjadj S, Marre M, Giannella MLCC. Catalase activity, allelic variations in the catalase gene and risk of kidney complications in patients with type 1 diabetes [Internet]. Diabetologia. 2013 ; 56( 12): 2733-2742.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s00125-013-3057-z
Vancouver
Mohammedi K, Patente TA, Muñoz NB, Driss F, Monteiro MB, Roussel R, Pavin EJ, Seta N, Fumeron F, Azevedo MJ, Canani LH, Hadjadj S, Marre M, Giannella MLCC. Catalase activity, allelic variations in the catalase gene and risk of kidney complications in patients with type 1 diabetes [Internet]. Diabetologia. 2013 ; 56( 12): 2733-2742.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s00125-013-3057-z
Artigo de periodico
Association of genetic variants in the promoter region of genes encoding p22phox (CYBA) and glutamate cysteine ligase catalytic subunit (GCLC) and renal disease in patients with type 1 diabetes mellitus (2011)
Vieira, Suzana M.; Monteiro, Maria B.; Marques, Tatiana; Luna, Ana M.; Fortes, Maria A.; Nery, Márcia; Queiroz, Márcia; Dib, Sérgio A.; Vendramini, Márcio F.; Azevedo, Mirela J.; Canani, Luis H.; Parisi, Maria C.; Pavin, Elizabeth J.; Giannella-Neto, Daniel; Corrêa-Giannella, Maria L.
Source: BMC Medical Genetics. Unidade: FM
Subjects: VARIAÇÃO GENÉTICA, GENES (ANÁLISE), NEFROPATIAS (FISIOPATOLOGIA), DIABETES MELLITUS, NEFROPATIAS (GENÉTICA), GENÓTIPOS, ESTRESSE OXIDATIVO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIEIRA, Suzana M. et al. Association of genetic variants in the promoter region of genes encoding p22phox (CYBA) and glutamate cysteine ligase catalytic subunit (GCLC) and renal disease in patients with type 1 diabetes mellitus. BMC Medical Genetics, v. 12, n. 129, p. 1-6, 2011Tradução . . Disponível em: https://doi.org/10.1186/1471-2350-12-129. Acesso em: 11 nov. 2024.
APA
Vieira, S. M., Monteiro, M. B., Marques, T., Luna, A. M., Fortes, M. A., Nery, M., et al. (2011). Association of genetic variants in the promoter region of genes encoding p22phox (CYBA) and glutamate cysteine ligase catalytic subunit (GCLC) and renal disease in patients with type 1 diabetes mellitus. BMC Medical Genetics, 12( 129), 1-6. doi:10.1186/1471-2350-12-129
NLM
Vieira SM, Monteiro MB, Marques T, Luna AM, Fortes MA, Nery M, Queiroz M, Dib SA, Vendramini MF, Azevedo MJ, Canani LH, Parisi MC, Pavin EJ, Giannella-Neto D, Corrêa-Giannella ML. Association of genetic variants in the promoter region of genes encoding p22phox (CYBA) and glutamate cysteine ligase catalytic subunit (GCLC) and renal disease in patients with type 1 diabetes mellitus [Internet]. BMC Medical Genetics. 2011 ; 12( 129): 1-6.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1186/1471-2350-12-129
Vancouver
Vieira SM, Monteiro MB, Marques T, Luna AM, Fortes MA, Nery M, Queiroz M, Dib SA, Vendramini MF, Azevedo MJ, Canani LH, Parisi MC, Pavin EJ, Giannella-Neto D, Corrêa-Giannella ML. Association of genetic variants in the promoter region of genes encoding p22phox (CYBA) and glutamate cysteine ligase catalytic subunit (GCLC) and renal disease in patients with type 1 diabetes mellitus [Internet]. BMC Medical Genetics. 2011 ; 12( 129): 1-6.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1186/1471-2350-12-129

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