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Artigo de periodico
HFE gene mutations and iron status of Brazilian blood donors (2010)
Santos, P. C. J. L; Cançado, Rodolfo Delfini; Terada, Cristiane Tie; Rostelato, Samuel; Gonzales, Iris; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki ; Chiattone, Carlos Sérgio; Guerra-Shinohara, Elvira Maria
Source: Brazilian Journal of Medical and Biological Research. Unidade: FCF
Subjects: MUTAÇÃO GENÉTICA, FERRO
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ABNT
SANTOS, P. C. J. L et al. HFE gene mutations and iron status of Brazilian blood donors. Brazilian Journal of Medical and Biological Research, v. 43, n. 1, p. 107-114, 2010Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2010000100015. Acesso em: 18 nov. 2024.
APA
Santos, P. C. J. L., Cançado, R. D., Terada, C. T., Rostelato, S., Gonzales, I., Hirata, R. D. C., et al. (2010). HFE gene mutations and iron status of Brazilian blood donors. Brazilian Journal of Medical and Biological Research, 43( 1), 107-114. doi:10.1590/s0100-879x2010000100015
NLM
Santos PCJL, Cançado RD, Terada CT, Rostelato S, Gonzales I, Hirata RDC, Hirata MH, Chiattone CS, Guerra-Shinohara EM. HFE gene mutations and iron status of Brazilian blood donors [Internet]. Brazilian Journal of Medical and Biological Research. 2010 ; 43( 1): 107-114.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s0100-879x2010000100015
Vancouver
Santos PCJL, Cançado RD, Terada CT, Rostelato S, Gonzales I, Hirata RDC, Hirata MH, Chiattone CS, Guerra-Shinohara EM. HFE gene mutations and iron status of Brazilian blood donors [Internet]. Brazilian Journal of Medical and Biological Research. 2010 ; 43( 1): 107-114.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s0100-879x2010000100015
Artigo de periodico
A novel point mutation in a class IV glucose-6-phosphate dehydrogenase variant (G6PD São Paulo) and polymorphic G6PD variants in São Paulo State, Brazil (2009)
Oliveira, Raimundo Antônio Gomes; Oshiro, Marilena; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo ; Ribeiro, Georgina Severo; Medeiros, Tereza Maria Dantas de; Barretto, Orlando César de Oliveira
Source: Genetics and Molecular Biology. Unidades: FCF, FM
Subjects: POLIMORFISMO, MUTAÇÃO GENÉTICA
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ABNT
OLIVEIRA, Raimundo Antônio Gomes et al. A novel point mutation in a class IV glucose-6-phosphate dehydrogenase variant (G6PD São Paulo) and polymorphic G6PD variants in São Paulo State, Brazil. Genetics and Molecular Biology, 2009Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572009005000033. Acesso em: 18 nov. 2024.
APA
Oliveira, R. A. G., Oshiro, M., Hirata, M. H., Hirata, R. D. C., Ribeiro, G. S., Medeiros, T. M. D. de, & Barretto, O. C. de O. (2009). A novel point mutation in a class IV glucose-6-phosphate dehydrogenase variant (G6PD São Paulo) and polymorphic G6PD variants in São Paulo State, Brazil. Genetics and Molecular Biology. doi:10.1590/s1415-47572009005000033
NLM
Oliveira RAG, Oshiro M, Hirata MH, Hirata RDC, Ribeiro GS, Medeiros TMD de, Barretto OC de O. A novel point mutation in a class IV glucose-6-phosphate dehydrogenase variant (G6PD São Paulo) and polymorphic G6PD variants in São Paulo State, Brazil [Internet]. Genetics and Molecular Biology. 2009 ;[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s1415-47572009005000033
Vancouver
Oliveira RAG, Oshiro M, Hirata MH, Hirata RDC, Ribeiro GS, Medeiros TMD de, Barretto OC de O. A novel point mutation in a class IV glucose-6-phosphate dehydrogenase variant (G6PD São Paulo) and polymorphic G6PD variants in São Paulo State, Brazil [Internet]. Genetics and Molecular Biology. 2009 ;[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s1415-47572009005000033
Artigo de periodico
Effects of APOE, APOB and LDLR variants on serum lipids and lack of association with xanthelasma in individuals from Southeastern Brazil (2009)
Nakazone, Marcelo Arruda; De Marchi, Miguel Angelo; Pinhel, Marcela Augusta de Souza; Barros, Carolina F. D. C.; Júlio, Maysa A. F.; Pinheiro, Anielli; Arazi, Simone Sorkin; Hotta, Júlia K.; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo ; Santos, José Ernesto dos; Souza, Doroteia Rossi da Silva
Source: Genetics and Molecular Biology. Unidades: FCF, FMRP
Subjects: POLIMORFISMO, APOLIPOPROTEÍNAS, LIPOPROTEÍNAS LDL
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ABNT
NAKAZONE, Marcelo Arruda et al. Effects of APOE, APOB and LDLR variants on serum lipids and lack of association with xanthelasma in individuals from Southeastern Brazil. Genetics and Molecular Biology, v. 32, n. 2, p. 227-233, 2009Tradução . . Disponível em: https://doi.org/10.1590/s1415-47572009005000028. Acesso em: 18 nov. 2024.
APA
Nakazone, M. A., De Marchi, M. A., Pinhel, M. A. de S., Barros, C. F. D. C., Júlio, M. A. F., Pinheiro, A., et al. (2009). Effects of APOE, APOB and LDLR variants on serum lipids and lack of association with xanthelasma in individuals from Southeastern Brazil. Genetics and Molecular Biology, 32( 2), 227-233. doi:10.1590/s1415-47572009005000028
NLM
Nakazone MA, De Marchi MA, Pinhel MA de S, Barros CFDC, Júlio MAF, Pinheiro A, Arazi SS, Hotta JK, Hirata MH, Hirata RDC, Santos JE dos, Souza DR da S. Effects of APOE, APOB and LDLR variants on serum lipids and lack of association with xanthelasma in individuals from Southeastern Brazil [Internet]. Genetics and Molecular Biology. 2009 ; 32( 2): 227-233.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s1415-47572009005000028
Vancouver
Nakazone MA, De Marchi MA, Pinhel MA de S, Barros CFDC, Júlio MAF, Pinheiro A, Arazi SS, Hotta JK, Hirata MH, Hirata RDC, Santos JE dos, Souza DR da S. Effects of APOE, APOB and LDLR variants on serum lipids and lack of association with xanthelasma in individuals from Southeastern Brazil [Internet]. Genetics and Molecular Biology. 2009 ; 32( 2): 227-233.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s1415-47572009005000028
Artigo de periodico
The expression of efflux and uptake transporters are regulated by statins in Caco-2 and HepG2 cells (2009)
Rodrigues, Alice Cristina ; Curi, Rui; Genvigir, Fabiana Dalla Vecchia; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Source: Acta Pharmacologica Sinica. Unidades: ICB, FCF
Subjects: GLICOPROTEÍNAS, EXPRESSÃO GÊNICA
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ABNT
RODRIGUES, Alice Cristina et al. The expression of efflux and uptake transporters are regulated by statins in Caco-2 and HepG2 cells. Acta Pharmacologica Sinica, v. 30, n. 7, p. 956-964, 2009Tradução . . Disponível em: https://doi.org/10.1038/aps.2009.85. Acesso em: 18 nov. 2024.
APA
Rodrigues, A. C., Curi, R., Genvigir, F. D. V., Hirata, M. H., & Hirata, R. D. C. (2009). The expression of efflux and uptake transporters are regulated by statins in Caco-2 and HepG2 cells. Acta Pharmacologica Sinica, 30( 7), 956-964. doi:10.1038/aps.2009.85.
NLM
Rodrigues AC, Curi R, Genvigir FDV, Hirata MH, Hirata RDC. The expression of efflux and uptake transporters are regulated by statins in Caco-2 and HepG2 cells [Internet]. Acta Pharmacologica Sinica. 2009 ; 30( 7): 956-964.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1038/aps.2009.85.
Vancouver
Rodrigues AC, Curi R, Genvigir FDV, Hirata MH, Hirata RDC. The expression of efflux and uptake transporters are regulated by statins in Caco-2 and HepG2 cells [Internet]. Acta Pharmacologica Sinica. 2009 ; 30( 7): 956-964.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1038/aps.2009.85.
Artigo de periodico
Decreased ABCB1 mRNA expression induced by atorvastatin results from enhanced mRNA degradation in HepG2 cells (2009)
Rodrigues, Alice Cristina ; Curi, Rui; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Source: European Journal of Pharmaceutical Sciences. Unidades: ICB, FCF
Subjects: EXPRESSÃO GÊNICA, FARMACOGENÉTICA
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ABNT
RODRIGUES, Alice Cristina et al. Decreased ABCB1 mRNA expression induced by atorvastatin results from enhanced mRNA degradation in HepG2 cells. European Journal of Pharmaceutical Sciences, v. 37, n. 3-4, p. 486-491, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.ejps.2009.04.006. Acesso em: 18 nov. 2024.
APA
Rodrigues, A. C., Curi, R., Hirata, M. H., & Hirata, R. D. C. (2009). Decreased ABCB1 mRNA expression induced by atorvastatin results from enhanced mRNA degradation in HepG2 cells. European Journal of Pharmaceutical Sciences, 37( 3-4), 486-491. doi:10.1016/j.ejps.2009.04.006
NLM
Rodrigues AC, Curi R, Hirata MH, Hirata RDC. Decreased ABCB1 mRNA expression induced by atorvastatin results from enhanced mRNA degradation in HepG2 cells [Internet]. European Journal of Pharmaceutical Sciences. 2009 ; 37( 3-4): 486-491.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.ejps.2009.04.006
Vancouver
Rodrigues AC, Curi R, Hirata MH, Hirata RDC. Decreased ABCB1 mRNA expression induced by atorvastatin results from enhanced mRNA degradation in HepG2 cells [Internet]. European Journal of Pharmaceutical Sciences. 2009 ; 37( 3-4): 486-491.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.ejps.2009.04.006
Artigo de periodico
Evaluation of nutritional and genetic determinants of total homocysteine, methylmalonic acid and S-adenosylmethionine/S-adenosylhomocysteine values in Brazilian childbearing-age women (2008)
Barbosa, Patrícia Roberto; Stabler, Sally P.; Trentin, Renata; Carvalho, Felipe de Rezende; Luchessi, Augusto Ducati; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki ; Allen, Robert H.; Guerra-Shinohara, Elvira Maria
Source: Clinica Chimica Acta. Unidade: FCF
Subjects: POLIMORFISMO, GRAVIDEZ
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ABNT
BARBOSA, Patrícia Roberto et al. Evaluation of nutritional and genetic determinants of total homocysteine, methylmalonic acid and S-adenosylmethionine/S-adenosylhomocysteine values in Brazilian childbearing-age women. Clinica Chimica Acta, v. 388, n. 1-2, p. 139-147, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.cca.2007.10.023. Acesso em: 18 nov. 2024.
APA
Barbosa, P. R., Stabler, S. P., Trentin, R., Carvalho, F. de R., Luchessi, A. D., Hirata, R. D. C., et al. (2008). Evaluation of nutritional and genetic determinants of total homocysteine, methylmalonic acid and S-adenosylmethionine/S-adenosylhomocysteine values in Brazilian childbearing-age women. Clinica Chimica Acta, 388( 1-2), 139-147. doi:10.1016/j.cca.2007.10.023
NLM
Barbosa PR, Stabler SP, Trentin R, Carvalho F de R, Luchessi AD, Hirata RDC, Hirata MH, Allen RH, Guerra-Shinohara EM. Evaluation of nutritional and genetic determinants of total homocysteine, methylmalonic acid and S-adenosylmethionine/S-adenosylhomocysteine values in Brazilian childbearing-age women [Internet]. Clinica Chimica Acta. 2008 ;388( 1-2): 139-147.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.cca.2007.10.023
Vancouver
Barbosa PR, Stabler SP, Trentin R, Carvalho F de R, Luchessi AD, Hirata RDC, Hirata MH, Allen RH, Guerra-Shinohara EM. Evaluation of nutritional and genetic determinants of total homocysteine, methylmalonic acid and S-adenosylmethionine/S-adenosylhomocysteine values in Brazilian childbearing-age women [Internet]. Clinica Chimica Acta. 2008 ;388( 1-2): 139-147.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.cca.2007.10.023
Artigo de periodico
Atorvastatin effects on SREBF1a and SCAP gene expression in mononuclear cells and its relation with lowering-lipids response (2008)
Arazi, Simone Sorkin; Genvigir, Fabiana Dalla Vecchia; Willrich, Maria Alice Vieira; Hirata, Mario Hiroyuki ; Dorea, Egidio Lima; Bernik, Márcia Martins Silveira; Hirata, Rosario Dominguez Crespo
Source: Clinica Chimica Acta. Unidades: FCF, HU
Subjects: EXPRESSÃO GÊNICA, FARMACOGENÉTICA
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ABNT
ARAZI, Simone Sorkin et al. Atorvastatin effects on SREBF1a and SCAP gene expression in mononuclear cells and its relation with lowering-lipids response. Clinica Chimica Acta, v. 393, n. 2, p. 119-124, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.cca.2008.03.031. Acesso em: 18 nov. 2024.
APA
Arazi, S. S., Genvigir, F. D. V., Willrich, M. A. V., Hirata, M. H., Dorea, E. L., Bernik, M. M. S., & Hirata, R. D. C. (2008). Atorvastatin effects on SREBF1a and SCAP gene expression in mononuclear cells and its relation with lowering-lipids response. Clinica Chimica Acta, 393( 2), 119-124. doi:10.1016/j.cca.2008.03.031
NLM
Arazi SS, Genvigir FDV, Willrich MAV, Hirata MH, Dorea EL, Bernik MMS, Hirata RDC. Atorvastatin effects on SREBF1a and SCAP gene expression in mononuclear cells and its relation with lowering-lipids response [Internet]. Clinica Chimica Acta. 2008 ; 393( 2): 119-124.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.cca.2008.03.031
Vancouver
Arazi SS, Genvigir FDV, Willrich MAV, Hirata MH, Dorea EL, Bernik MMS, Hirata RDC. Atorvastatin effects on SREBF1a and SCAP gene expression in mononuclear cells and its relation with lowering-lipids response [Internet]. Clinica Chimica Acta. 2008 ; 393( 2): 119-124.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.cca.2008.03.031
Artigo de periodico
Relationships between gene polymorphisms of folate-related proteins and vitamins and metabolites in pregnant women and neonates (2008)
Lopreato, Fernanda Roquette; Stabler, Sally P.; Carvalho, Felipe de Rezende; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki ; Robi, Debora de Lima; Sampaio Neto, Luiz Ferraz de; Allen, Robert H.; Guerra-Shinohara, Elvira Maria
Source: Clinica Chimica Acta. Unidade: FCF
Subjects: POLIMORFISMO, DEFICIÊNCIA DE PROTEÍNA
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ABNT
LOPREATO, Fernanda Roquette et al. Relationships between gene polymorphisms of folate-related proteins and vitamins and metabolites in pregnant women and neonates. Clinica Chimica Acta, v. 398, n. 1-2, p. 134-139, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.cca.2008.09.004. Acesso em: 18 nov. 2024.
APA
Lopreato, F. R., Stabler, S. P., Carvalho, F. de R., Hirata, R. D. C., Hirata, M. H., Robi, D. de L., et al. (2008). Relationships between gene polymorphisms of folate-related proteins and vitamins and metabolites in pregnant women and neonates. Clinica Chimica Acta, 398( 1-2), 134-139. doi:10.1016/j.cca.2008.09.004
NLM
Lopreato FR, Stabler SP, Carvalho F de R, Hirata RDC, Hirata MH, Robi D de L, Sampaio Neto LF de, Allen RH, Guerra-Shinohara EM. Relationships between gene polymorphisms of folate-related proteins and vitamins and metabolites in pregnant women and neonates [Internet]. Clinica Chimica Acta. 2008 ; 398( 1-2): 134-139.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.cca.2008.09.004
Vancouver
Lopreato FR, Stabler SP, Carvalho F de R, Hirata RDC, Hirata MH, Robi D de L, Sampaio Neto LF de, Allen RH, Guerra-Shinohara EM. Relationships between gene polymorphisms of folate-related proteins and vitamins and metabolites in pregnant women and neonates [Internet]. Clinica Chimica Acta. 2008 ; 398( 1-2): 134-139.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.cca.2008.09.004
Artigo de periodico
AMI is associated with polymorphisms in the NOS3 and FGB but not in PAI-1 genes in young adults (2007)
Sampaio, Marcelo Ferraz; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo ; Santos, Fabiana Cristina Pereira dos; Picciotti, Raffaella; Luchessi, André Ducati; Doi, Sonia de Quateli; Armaganijan, Dikran; Batlouni, Michel
Source: Clinica Chimica Acta. Unidade: FCF
Subjects: ÓXIDO NÍTRICO, ENDOTÉLIO, POLIMORFISMO
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ABNT
SAMPAIO, Marcelo Ferraz et al. AMI is associated with polymorphisms in the NOS3 and FGB but not in PAI-1 genes in young adults. Clinica Chimica Acta, v. 377, n. 1-2, p. 154-162, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.cca.2006.09.013. Acesso em: 18 nov. 2024.
APA
Sampaio, M. F., Hirata, M. H., Hirata, R. D. C., Santos, F. C. P. dos, Picciotti, R., Luchessi, A. D., et al. (2007). AMI is associated with polymorphisms in the NOS3 and FGB but not in PAI-1 genes in young adults. Clinica Chimica Acta, 377( 1-2), 154-162. doi:10.1016/j.cca.2006.09.013
NLM
Sampaio MF, Hirata MH, Hirata RDC, Santos FCP dos, Picciotti R, Luchessi AD, Doi S de Q, Armaganijan D, Batlouni M. AMI is associated with polymorphisms in the NOS3 and FGB but not in PAI-1 genes in young adults [Internet]. Clinica Chimica Acta. 2007 ; 377( 1-2): 154-162.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.cca.2006.09.013
Vancouver
Sampaio MF, Hirata MH, Hirata RDC, Santos FCP dos, Picciotti R, Luchessi AD, Doi S de Q, Armaganijan D, Batlouni M. AMI is associated with polymorphisms in the NOS3 and FGB but not in PAI-1 genes in young adults [Internet]. Clinica Chimica Acta. 2007 ; 377( 1-2): 154-162.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.cca.2006.09.013
Artigo de periodico
APOA1 polymorphisms are associated with variations in serum triglyceride concentrations in hypercholesterolemic individuals (2005)
Sorkin, Simone Cohen; Forestiero, Francisco José; Hirata, Mario Hiroyuki ; Guzmán, Elizabeth Cecilia Rodríguez; Cavalli, Selma Andrea; Bertolami, Marcelo Chiara; Salazar, Luís Antônio; Hirata, Rosario Dominguez Crespo
Source: Clinical Chemistry and Laboratory Medicine. Unidade: FCF
Subjects: HIPERCOLESTEROLEMIA, GENÉTICA, LIPÍDEOS, POLIMORFISMO
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ABNT
SORKIN, Simone Cohen et al. APOA1 polymorphisms are associated with variations in serum triglyceride concentrations in hypercholesterolemic individuals. Clinical Chemistry and Laboratory Medicine, v. 43, n. 12, p. 1339-1345, 2005Tradução . . Disponível em: https://doi.org/10.1515/cclm.2005.229. Acesso em: 18 nov. 2024.
APA
Sorkin, S. C., Forestiero, F. J., Hirata, M. H., Guzmán, E. C. R., Cavalli, S. A., Bertolami, M. C., et al. (2005). APOA1 polymorphisms are associated with variations in serum triglyceride concentrations in hypercholesterolemic individuals. Clinical Chemistry and Laboratory Medicine, 43( 12), 1339-1345. doi:10.1515/cclm.2005.229
NLM
Sorkin SC, Forestiero FJ, Hirata MH, Guzmán ECR, Cavalli SA, Bertolami MC, Salazar LA, Hirata RDC. APOA1 polymorphisms are associated with variations in serum triglyceride concentrations in hypercholesterolemic individuals [Internet]. Clinical Chemistry and Laboratory Medicine. 2005 ; 43( 12): 1339-1345.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1515/cclm.2005.229
Vancouver
Sorkin SC, Forestiero FJ, Hirata MH, Guzmán ECR, Cavalli SA, Bertolami MC, Salazar LA, Hirata RDC. APOA1 polymorphisms are associated with variations in serum triglyceride concentrations in hypercholesterolemic individuals [Internet]. Clinical Chemistry and Laboratory Medicine. 2005 ; 43( 12): 1339-1345.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1515/cclm.2005.229
Artigo de periodico
Growth hormone promotes glomerular lipid accumulation in bGH mice (2005)
Machado, Marcos O.; Hirata, Rosario Dominguez Crespo ; Sellitti, Donald F.; Iotti, Roberto; Iotti, Alejandro; Cusumano, Ana M.; Riordan, Gavin P.; Coschigano, Karen T.; Kopchick, John J.; Zuhl, Irina; Nguyen, Nga; Hirata, Mario Hiroyuki ; Doi, Sonia Quatelli
Source: Kidney International. Unidade: FCF
Subjects: LIPOPROTEÍNAS LDL, CITOCINAS
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ABNT
MACHADO, Marcos O. et al. Growth hormone promotes glomerular lipid accumulation in bGH mice. Kidney International, v. 68, n. 5, p. 2219-2028, 2005Tradução . . Disponível em: https://doi.org/10.1111/j.1523-1755.2005.00656.x. Acesso em: 18 nov. 2024.
APA
Machado, M. O., Hirata, R. D. C., Sellitti, D. F., Iotti, R., Iotti, A., Cusumano, A. M., et al. (2005). Growth hormone promotes glomerular lipid accumulation in bGH mice. Kidney International, 68( 5), 2219-2028. doi:10.1111/j.1523-1755.2005.00656.x
NLM
Machado MO, Hirata RDC, Sellitti DF, Iotti R, Iotti A, Cusumano AM, Riordan GP, Coschigano KT, Kopchick JJ, Zuhl I, Nguyen N, Hirata MH, Doi SQ. Growth hormone promotes glomerular lipid accumulation in bGH mice [Internet]. Kidney International. 2005 ; 68( 5): 2219-2028.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1111/j.1523-1755.2005.00656.x
Vancouver
Machado MO, Hirata RDC, Sellitti DF, Iotti R, Iotti A, Cusumano AM, Riordan GP, Coschigano KT, Kopchick JJ, Zuhl I, Nguyen N, Hirata MH, Doi SQ. Growth hormone promotes glomerular lipid accumulation in bGH mice [Internet]. Kidney International. 2005 ; 68( 5): 2219-2028.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1111/j.1523-1755.2005.00656.x
Artigo de periodico
Five polymorphisms in gene candidates for cardiovascular disease in afro-Brazilian individuals (2004)
Sakuma, Tatsuya; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Source: Journal of Clinical Laboratory Analysis. Unidade: FCF
Subjects: POLIMORFISMO, DOENÇAS CARDIOVASCULARES, HIPERTENSÃO
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ABNT
SAKUMA, Tatsuya e HIRATA, Rosario Dominguez Crespo e HIRATA, Mario Hiroyuki. Five polymorphisms in gene candidates for cardiovascular disease in afro-Brazilian individuals. Journal of Clinical Laboratory Analysis, v. 18, n. 6, p. 309-316, 2004Tradução . . Disponível em: https://doi.org/10.1002/jcla.20044. Acesso em: 18 nov. 2024.
APA
Sakuma, T., Hirata, R. D. C., & Hirata, M. H. (2004). Five polymorphisms in gene candidates for cardiovascular disease in afro-Brazilian individuals. Journal of Clinical Laboratory Analysis, 18( 6), 309-316. doi:10.1002/jcla.20044
NLM
Sakuma T, Hirata RDC, Hirata MH. Five polymorphisms in gene candidates for cardiovascular disease in afro-Brazilian individuals [Internet]. Journal of Clinical Laboratory Analysis. 2004 ; 18( 6): 309-316.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1002/jcla.20044
Vancouver
Sakuma T, Hirata RDC, Hirata MH. Five polymorphisms in gene candidates for cardiovascular disease in afro-Brazilian individuals [Internet]. Journal of Clinical Laboratory Analysis. 2004 ; 18( 6): 309-316.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1002/jcla.20044
Artigo de periodico
Molecular basis of familial hypercholesterolemia in Brazil: Identification of seven novel LDLR gene mutations (2002)
Salazar, Luís Antônio; Hirata, Mario Hiroyuki ; Cavalli, Selma Andrea; Nakandakare, Edna Regina; Forti, Neusa Assumpta; Diament, Jayme; Giannini, Sérgio Diogo; Bertolami, Marcelo Chiara; Hirata, Rosario Dominguez Crespo
Source: Human Mutation. Unidades: FCF, FM
Subjects: GENÉTICA, HIPERCOLESTEROLEMIA (AVALIAÇÃO), MUTAÇÃO GENÉTICA (IDENTIFICAÇÃO), TÉCNICAS E PROCEDIMENTOS DE LABORATÓRIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SALAZAR, Luís Antônio et al. Molecular basis of familial hypercholesterolemia in Brazil: Identification of seven novel LDLR gene mutations. Human Mutation, v. 19, n. 4, p. 462-463, 2002Tradução . . Disponível em: https://doi.org/10.1002/humu.9032. Acesso em: 18 nov. 2024.
APA
Salazar, L. A., Hirata, M. H., Cavalli, S. A., Nakandakare, E. R., Forti, N. A., Diament, J., et al. (2002). Molecular basis of familial hypercholesterolemia in Brazil: Identification of seven novel LDLR gene mutations. Human Mutation, 19( 4), 462-463. doi:10.1002/humu.9032
NLM
Salazar LA, Hirata MH, Cavalli SA, Nakandakare ER, Forti NA, Diament J, Giannini SD, Bertolami MC, Hirata RDC. Molecular basis of familial hypercholesterolemia in Brazil: Identification of seven novel LDLR gene mutations [Internet]. Human Mutation. 2002 ; 19( 4): 462-463.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1002/humu.9032
Vancouver
Salazar LA, Hirata MH, Cavalli SA, Nakandakare ER, Forti NA, Diament J, Giannini SD, Bertolami MC, Hirata RDC. Molecular basis of familial hypercholesterolemia in Brazil: Identification of seven novel LDLR gene mutations [Internet]. Human Mutation. 2002 ; 19( 4): 462-463.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1002/humu.9032
Artigo de periodico
Metabolic effects of C677T and A1298C mutations at the MTHFR gene in Brazilian children with neural tube defects (2002)
Cunha, Andréa Luciana Araújo da; Hirata, Mario Hiroyuki ; Kim, Chong A.; Guerra-Shinohara, Elvira Maria ; Nonoyama, Kymio; Hirata, Rosario Dominguez Crespo
Source: Clinica Chimica Acta. Unidade: FCF
Subjects: MALFORMAÇÕES (CONGÊNITO), GENÉTICA BIOQUÍMICA, GRAVIDEZ (DEFICIÊNCIA), VITAMINA B12 (DEFICIÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CUNHA, Andréa Luciana Araújo da et al. Metabolic effects of C677T and A1298C mutations at the MTHFR gene in Brazilian children with neural tube defects. Clinica Chimica Acta, v. 318, n. 1-2, p. 139-143, 2002Tradução . . Disponível em: https://doi.org/10.1016/s0009-8981(01)00764-1. Acesso em: 18 nov. 2024.
APA
Cunha, A. L. A. da, Hirata, M. H., Kim, C. A., Guerra-Shinohara, E. M., Nonoyama, K., & Hirata, R. D. C. (2002). Metabolic effects of C677T and A1298C mutations at the MTHFR gene in Brazilian children with neural tube defects. Clinica Chimica Acta, 318( 1-2), 139-143. doi:10.1016/s0009-8981(01)00764-1
NLM
Cunha ALA da, Hirata MH, Kim CA, Guerra-Shinohara EM, Nonoyama K, Hirata RDC. Metabolic effects of C677T and A1298C mutations at the MTHFR gene in Brazilian children with neural tube defects [Internet]. Clinica Chimica Acta. 2002 ; 318( 1-2): 139-143.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/s0009-8981(01)00764-1
Vancouver
Cunha ALA da, Hirata MH, Kim CA, Guerra-Shinohara EM, Nonoyama K, Hirata RDC. Metabolic effects of C677T and A1298C mutations at the MTHFR gene in Brazilian children with neural tube defects [Internet]. Clinica Chimica Acta. 2002 ; 318( 1-2): 139-143.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/s0009-8981(01)00764-1

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