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Artigo de periodico
Genome-wide and candidate genes approach for pharmacogenomics of atorvastatin (2009)
Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Source: Clinica Lipidology. Unidade: FCF
Subjects: DOENÇAS CARDIOVASCULARES, HIPERCOLESTEROLEMIA, FARMACOGENÉTICA, GENOMAS
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ABNT
HIRATA, Rosario Dominguez Crespo e HIRATA, Mario Hiroyuki. Genome-wide and candidate genes approach for pharmacogenomics of atorvastatin. Clinica Lipidology, v. 4, n. 4, p. 419-423, 2009Tradução . . Disponível em: https://doi.org/10.2217/clp.09.32. Acesso em: 18 nov. 2024.
APA
Hirata, R. D. C., & Hirata, M. H. (2009). Genome-wide and candidate genes approach for pharmacogenomics of atorvastatin. Clinica Lipidology, 4( 4), 419-423. doi:10.2217/clp.09.32
NLM
Hirata RDC, Hirata MH. Genome-wide and candidate genes approach for pharmacogenomics of atorvastatin [Internet]. Clinica Lipidology. 2009 ; 4( 4): 419-423.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2217/clp.09.32
Vancouver
Hirata RDC, Hirata MH. Genome-wide and candidate genes approach for pharmacogenomics of atorvastatin [Internet]. Clinica Lipidology. 2009 ; 4( 4): 419-423.[citado 2024 nov. 18 ] Available from: https://doi.org/10.2217/clp.09.32
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
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
Genetic population data of 12 STR loci of the PowerPlex(R) Y system in the state of Sao Paulo population (Southeast of Brazil) (2008)
Góis, Carolina Costa; Martins, Joyce Aparecida; Pereira, Gabriella Augusto; Freschi, Adriana; Paneto, Greiciane Gaburro; Alvarenga, Vera Lucy de Santi; Cicarelli, Regina Maria Barretto; Hirata, Mario Hiroyuki ; Oliveira, Rogério Nogueira de
Source: Forensic Science International. Unidades: FCF, FO
Subjects: GENÉTICA DE POPULAÇÕES, CROMOSSOMO Y
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ABNT
GÓIS, Carolina Costa et al. Genetic population data of 12 STR loci of the PowerPlex(R) Y system in the state of Sao Paulo population (Southeast of Brazil). Forensic Science International, v. 174, n. 1, p. 80-85, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.forsciint.2006.12.018. Acesso em: 18 nov. 2024.
APA
Góis, C. C., Martins, J. A., Pereira, G. A., Freschi, A., Paneto, G. G., Alvarenga, V. L. de S., et al. (2008). Genetic population data of 12 STR loci of the PowerPlex(R) Y system in the state of Sao Paulo population (Southeast of Brazil). Forensic Science International, 174( 1), 80-85. doi:10.1016/j.forsciint.2006.12.018
NLM
Góis CC, Martins JA, Pereira GA, Freschi A, Paneto GG, Alvarenga VL de S, Cicarelli RMB, Hirata MH, Oliveira RN de. Genetic population data of 12 STR loci of the PowerPlex(R) Y system in the state of Sao Paulo population (Southeast of Brazil) [Internet]. Forensic Science International. 2008 ;174( 1): 80-85.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.forsciint.2006.12.018
Vancouver
Góis CC, Martins JA, Pereira GA, Freschi A, Paneto GG, Alvarenga VL de S, Cicarelli RMB, Hirata MH, Oliveira RN de. Genetic population data of 12 STR loci of the PowerPlex(R) Y system in the state of Sao Paulo population (Southeast of Brazil) [Internet]. Forensic Science International. 2008 ;174( 1): 80-85.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.forsciint.2006.12.018
Artigo de periodico
Leptin G-2548A promoter polymorphism is assciated with increased plasma leptin and BMI in Brazilian women (2008)
Hinuy, Hamilton Massayuki; Hirata, Mario Hiroyuki ; Forti, Neusa; Diament, Jayme; Sampaio, Marcelo Ferraz; Armaganijan, Dikran; Salazar, Luís Antônio; Hirata, Rosario Dominguez Crespo
Source: Arquivos Brasileiros de Endocrinologia e Metabologia. Unidades: FCF, FM
Subjects: POLIMORFISMO, OBESIDADE, REAÇÃO EM CADEIA POR POLIMERASE
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ABNT
HINUY, Hamilton Massayuki et al. Leptin G-2548A promoter polymorphism is assciated with increased plasma leptin and BMI in Brazilian women. Arquivos Brasileiros de Endocrinologia e Metabologia, v. 52, n. 4, p. 611-616, 2008Tradução . . Disponível em: https://doi.org/10.1590/s0004-27302008000400006. Acesso em: 18 nov. 2024.
APA
Hinuy, H. M., Hirata, M. H., Forti, N., Diament, J., Sampaio, M. F., Armaganijan, D., et al. (2008). Leptin G-2548A promoter polymorphism is assciated with increased plasma leptin and BMI in Brazilian women. Arquivos Brasileiros de Endocrinologia e Metabologia, 52( 4), 611-616. doi:10.1590/s0004-27302008000400006
NLM
Hinuy HM, Hirata MH, Forti N, Diament J, Sampaio MF, Armaganijan D, Salazar LA, Hirata RDC. Leptin G-2548A promoter polymorphism is assciated with increased plasma leptin and BMI in Brazilian women [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ;52( 4): 611-616.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s0004-27302008000400006
Vancouver
Hinuy HM, Hirata MH, Forti N, Diament J, Sampaio MF, Armaganijan D, Salazar LA, Hirata RDC. Leptin G-2548A promoter polymorphism is assciated with increased plasma leptin and BMI in Brazilian women [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2008 ;52( 4): 611-616.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s0004-27302008000400006
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
Receptor ativado por proliferadores de peroxissoma gama (PPAR'gama'): estudo molecular na homeostase da glicose, metabolismo de lipideos e abordagem terapeutica (2007)
Tavares, Vladimir; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Source: Arquivos Brasileiros de Endocrinologia e Metabologia. Unidade: FCF
Subjects: LIPÍDEOS (METABOLISMO), INFLAMAÇÃO
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ABNT
TAVARES, Vladimir e HIRATA, Mario Hiroyuki e HIRATA, Rosario Dominguez Crespo. Receptor ativado por proliferadores de peroxissoma gama (PPAR'gama'): estudo molecular na homeostase da glicose, metabolismo de lipideos e abordagem terapeutica. Arquivos Brasileiros de Endocrinologia e Metabologia, v. 51, n. 4, p. 526-533, 2007Tradução . . Disponível em: https://doi.org/10.1590/s0004-27302007000400005. Acesso em: 18 nov. 2024.
APA
Tavares, V., Hirata, M. H., & Hirata, R. D. C. (2007). Receptor ativado por proliferadores de peroxissoma gama (PPAR'gama'): estudo molecular na homeostase da glicose, metabolismo de lipideos e abordagem terapeutica. Arquivos Brasileiros de Endocrinologia e Metabologia, 51( 4), 526-533. doi:10.1590/s0004-27302007000400005
NLM
Tavares V, Hirata MH, Hirata RDC. Receptor ativado por proliferadores de peroxissoma gama (PPAR'gama'): estudo molecular na homeostase da glicose, metabolismo de lipideos e abordagem terapeutica [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2007 ; 51( 4): 526-533.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s0004-27302007000400005
Vancouver
Tavares V, Hirata MH, Hirata RDC. Receptor ativado por proliferadores de peroxissoma gama (PPAR'gama'): estudo molecular na homeostase da glicose, metabolismo de lipideos e abordagem terapeutica [Internet]. Arquivos Brasileiros de Endocrinologia e Metabologia. 2007 ; 51( 4): 526-533.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s0004-27302007000400005
Artigo de periodico
Rapid identification of Fonsecaea by duplex polymerase chain reaction in isolates from patients with chromoblastomycosis (2007)
Andrade, Tânia Sueli de; Cury, Arlete Emily; Castro, Luiz Guilherme Martins de; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Source: Diagnostic Microbiology and Infectious Disease. Unidade: FCF
Subjects: CROMOBLASTOMICOSE, DNA RECOMBINANTE
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ABNT
ANDRADE, Tânia Sueli de et al. Rapid identification of Fonsecaea by duplex polymerase chain reaction in isolates from patients with chromoblastomycosis. Diagnostic Microbiology and Infectious Disease, v. 57, n. 3, p. 267-272, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.diagmicrobio.2006.08.024. Acesso em: 18 nov. 2024.
APA
Andrade, T. S. de, Cury, A. E., Castro, L. G. M. de, Hirata, M. H., & Hirata, R. D. C. (2007). Rapid identification of Fonsecaea by duplex polymerase chain reaction in isolates from patients with chromoblastomycosis. Diagnostic Microbiology and Infectious Disease, 57( 3), 267-272. doi:10.1016/j.diagmicrobio.2006.08.024
NLM
Andrade TS de, Cury AE, Castro LGM de, Hirata MH, Hirata RDC. Rapid identification of Fonsecaea by duplex polymerase chain reaction in isolates from patients with chromoblastomycosis [Internet]. Diagnostic Microbiology and Infectious Disease. 2007 ; 57( 3): 267-272.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.diagmicrobio.2006.08.024
Vancouver
Andrade TS de, Cury AE, Castro LGM de, Hirata MH, Hirata RDC. Rapid identification of Fonsecaea by duplex polymerase chain reaction in isolates from patients with chromoblastomycosis [Internet]. Diagnostic Microbiology and Infectious Disease. 2007 ; 57( 3): 267-272.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.diagmicrobio.2006.08.024
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
Heteroplasmy in hair: differences among hair and blood from the same individuals are still a matter of debate (2007)
Paneto, Greiciane Gaburro; Martins, Joyce Aparecida; Longo, Larissa Valle Guilhen; Pereira, Gabriella Augusto; Freschi, Adriana; Alvarenga, Vera Lucy de Santi; Chen, Bety; Oliveira, Rogério Nogueira de; Hirata, Mario Hiroyuki ; Cicarelli, Regina Maria Barretto
Source: Forensic Science International. Unidades: FO, FCF
Subjects: DNA MITOCONDRIAL, GENÉTICA
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ABNT
PANETO, Greiciane Gaburro et al. Heteroplasmy in hair: differences among hair and blood from the same individuals are still a matter of debate. Forensic Science International, v. 173, n. 2-3, p. 117-121, 2007Tradução . . Disponível em: https://doi.org/10.1016/j.forsciint.2007.02.011. Acesso em: 18 nov. 2024.
APA
Paneto, G. G., Martins, J. A., Longo, L. V. G., Pereira, G. A., Freschi, A., Alvarenga, V. L. de S., et al. (2007). Heteroplasmy in hair: differences among hair and blood from the same individuals are still a matter of debate. Forensic Science International, 173( 2-3), 117-121. doi:10.1016/j.forsciint.2007.02.011
NLM
Paneto GG, Martins JA, Longo LVG, Pereira GA, Freschi A, Alvarenga VL de S, Chen B, Oliveira RN de, Hirata MH, Cicarelli RMB. Heteroplasmy in hair: differences among hair and blood from the same individuals are still a matter of debate [Internet]. Forensic Science International. 2007 ; 173( 2-3): 117-121.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.forsciint.2007.02.011
Vancouver
Paneto GG, Martins JA, Longo LVG, Pereira GA, Freschi A, Alvarenga VL de S, Chen B, Oliveira RN de, Hirata MH, Cicarelli RMB. Heteroplasmy in hair: differences among hair and blood from the same individuals are still a matter of debate [Internet]. Forensic Science International. 2007 ; 173( 2-3): 117-121.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.forsciint.2007.02.011
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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
PCR in the diagnosis of cutaneous tuberculosis (2003)
Ogusku, Mauricio Morishi; Sadahiro, Aya; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo ; Zaitz, Clarisse; Salem, Julia Ignez
Source: Brazilian Journal of Microbiology. Unidade: FCF
Subjects: REAÇÃO EM CADEIA POR POLIMERASE, MYCOBACTERIUM TUBERCULOSIS, TUBERCULOSE CUTÂNEA, TÉCNICAS E PROCEDIMENTOS DE LABORATÓRIO, MICROBIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OGUSKU, Mauricio Morishi et al. PCR in the diagnosis of cutaneous tuberculosis. Brazilian Journal of Microbiology, 2003Tradução . . Disponível em: https://doi.org/10.1590/s1517-83822003000200015. Acesso em: 18 nov. 2024.
APA
Ogusku, M. M., Sadahiro, A., Hirata, M. H., Hirata, R. D. C., Zaitz, C., & Salem, J. I. (2003). PCR in the diagnosis of cutaneous tuberculosis. Brazilian Journal of Microbiology. doi:10.1590/s1517-83822003000200015
NLM
Ogusku MM, Sadahiro A, Hirata MH, Hirata RDC, Zaitz C, Salem JI. PCR in the diagnosis of cutaneous tuberculosis [Internet]. Brazilian Journal of Microbiology. 2003 ;[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s1517-83822003000200015
Vancouver
Ogusku MM, Sadahiro A, Hirata MH, Hirata RDC, Zaitz C, Salem JI. PCR in the diagnosis of cutaneous tuberculosis [Internet]. Brazilian Journal of Microbiology. 2003 ;[citado 2024 nov. 18 ] Available from: https://doi.org/10.1590/s1517-83822003000200015
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
A method to detect the G894T polymorphism of the NOS3 gene. Clinical validation in familial hypercholesterolemia (2002)
Hirata, Rosario Dominguez Crespo ; Salazar, Luís Antônio; Cavalli, Selma Andrea; Yoshioka, Kelson K.; Matsumoto, Leonardo O.; Santos, Silvério Teixeira dos; Giannini, Sérgio Diogo; Forti, Neusa; Diament, Jayme; Doi, Sonia Q.; Hirata, Mario Hiroyuki
Source: Clinical Chemistry and Laboratory Medicine. Unidade: FCF
Subjects: BIOQUÍMICA, HIPERCOLESTEROLEMIA (AVALIAÇÃO), DOENÇAS CARDIOVASCULARES, ÓXIDO NÍTRICO (SÍNTESE QUÍMICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HIRATA, Rosario Dominguez Crespo et al. A method to detect the G894T polymorphism of the NOS3 gene. Clinical validation in familial hypercholesterolemia. Clinical Chemistry and Laboratory Medicine, v. 40, n. 5, p. 436-440, 2002Tradução . . Acesso em: 18 nov. 2024.
APA
Hirata, R. D. C., Salazar, L. A., Cavalli, S. A., Yoshioka, K. K., Matsumoto, L. O., Santos, S. T. dos, et al. (2002). A method to detect the G894T polymorphism of the NOS3 gene. Clinical validation in familial hypercholesterolemia. Clinical Chemistry and Laboratory Medicine, 40( 5), 436-440.
NLM
Hirata RDC, Salazar LA, Cavalli SA, Yoshioka KK, Matsumoto LO, Santos ST dos, Giannini SD, Forti N, Diament J, Doi SQ, Hirata MH. A method to detect the G894T polymorphism of the NOS3 gene. Clinical validation in familial hypercholesterolemia. Clinical Chemistry and Laboratory Medicine. 2002 ; 40( 5): 436-440.[citado 2024 nov. 18 ]
Vancouver
Hirata RDC, Salazar LA, Cavalli SA, Yoshioka KK, Matsumoto LO, Santos ST dos, Giannini SD, Forti N, Diament J, Doi SQ, Hirata MH. A method to detect the G894T polymorphism of the NOS3 gene. Clinical validation in familial hypercholesterolemia. Clinical Chemistry and Laboratory Medicine. 2002 ; 40( 5): 436-440.[citado 2024 nov. 18 ]
Artigo de periodico
Increasing the sensitivity of single-strand conformation polymorphism analysis of the LDLR gene mutations in brazilian patients with familial hypercholesterolemia (2002)
Salazar, Luís Antônio; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Source: Clinical Chemistry and Laboratory Medicine. Unidade: FCF
Subjects: BIOQUÍMICA, HIPERCOLESTEROLEMIA (AVALIAÇÃO), DOENÇAS CARDIOVASCULARES (AVALIAÇÃO), MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SALAZAR, Luís Antônio e HIRATA, Mario Hiroyuki e HIRATA, Rosario Dominguez Crespo. Increasing the sensitivity of single-strand conformation polymorphism analysis of the LDLR gene mutations in brazilian patients with familial hypercholesterolemia. Clinical Chemistry and Laboratory Medicine, v. 40, n. 5, p. 441-445, 2002Tradução . . Acesso em: 18 nov. 2024.
APA
Salazar, L. A., Hirata, M. H., & Hirata, R. D. C. (2002). Increasing the sensitivity of single-strand conformation polymorphism analysis of the LDLR gene mutations in brazilian patients with familial hypercholesterolemia. Clinical Chemistry and Laboratory Medicine, 40( 5), 441-445.
NLM
Salazar LA, Hirata MH, Hirata RDC. Increasing the sensitivity of single-strand conformation polymorphism analysis of the LDLR gene mutations in brazilian patients with familial hypercholesterolemia. Clinical Chemistry and Laboratory Medicine. 2002 ; 40( 5): 441-445.[citado 2024 nov. 18 ]
Vancouver
Salazar LA, Hirata MH, Hirata RDC. Increasing the sensitivity of single-strand conformation polymorphism analysis of the LDLR gene mutations in brazilian patients with familial hypercholesterolemia. Clinical Chemistry and Laboratory Medicine. 2002 ; 40( 5): 441-445.[citado 2024 nov. 18 ]
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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