ReP USP - Resultado da busca

Artigo de periodico
CCDC22 gene polymorphism is associated with advanced stages of endometriosis in a sample of Brazilian women (2017)
Francisco, Daniela de Oliveira; Andres, Marina de Paula; Gueuvoghlanian-Silva, Bárbara Yasmim; Podgaec, Sergio; Fridman, Cintia
Source: Journal of Assisted Reproduction and Genetics. Unidade: FM
Subjects: ENDOMETRIOSE, TESTES SOROLÓGICOS, POLIMORFISMO, REAÇÃO EM CADEIA POR POLIMERASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FRANCISCO, Daniela de Oliveira et al. CCDC22 gene polymorphism is associated with advanced stages of endometriosis in a sample of Brazilian women. Journal of Assisted Reproduction and Genetics, v. 34, n. 7, p. 939-944, 2017Tradução . . Disponível em: https://doi.org/10.1007%2Fs10815-017-0936-0. Acesso em: 15 nov. 2024.
APA
Francisco, D. de O., Andres, M. de P., Gueuvoghlanian-Silva, B. Y., Podgaec, S., & Fridman, C. (2017). CCDC22 gene polymorphism is associated with advanced stages of endometriosis in a sample of Brazilian women. Journal of Assisted Reproduction and Genetics, 34( 7), 939-944. doi:10.1007%2Fs10815-017-0936-0
NLM
Francisco D de O, Andres M de P, Gueuvoghlanian-Silva BY, Podgaec S, Fridman C. CCDC22 gene polymorphism is associated with advanced stages of endometriosis in a sample of Brazilian women [Internet]. Journal of Assisted Reproduction and Genetics. 2017 ; 34( 7): 939-944.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007%2Fs10815-017-0936-0
Vancouver
Francisco D de O, Andres M de P, Gueuvoghlanian-Silva BY, Podgaec S, Fridman C. CCDC22 gene polymorphism is associated with advanced stages of endometriosis in a sample of Brazilian women [Internet]. Journal of Assisted Reproduction and Genetics. 2017 ; 34( 7): 939-944.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007%2Fs10815-017-0936-0
Trabalho de evento-resumo periodico
Interleukin-1 beta (IL1ß) gene polymorphisms and periapical lesion development in individuals with deep caries (2014)
Ghaneh, G.; Dill, A.; Chaves de Souza, L.; Yadlapati, M.; Vieira, A.; Garlet, Gustavo Pompermaier; Silva, R.; Letra, A.
Source: Journal of Endodontics. Conference titles: Annual Session of the American Association of Endodontists. Unidade: FOB
Subjects: INTERLEUCINA 1, POLIMORFISMO, LESÕES PERIAPICAIS, CÁRIE DENTÁRIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GHANEH, G. et al. Interleukin-1 beta (IL1ß) gene polymorphisms and periapical lesion development in individuals with deep caries. Journal of Endodontics. New York: Elsevier. Disponível em: https://doi.org/10.1016/S0099-2399(14)00129-0. Acesso em: 15 nov. 2024. , 2014
APA
Ghaneh, G., Dill, A., Chaves de Souza, L., Yadlapati, M., Vieira, A., Garlet, G. P., et al. (2014). Interleukin-1 beta (IL1ß) gene polymorphisms and periapical lesion development in individuals with deep caries. Journal of Endodontics. New York: Elsevier. doi:10.1016/S0099-2399(14)00129-0
NLM
Ghaneh G, Dill A, Chaves de Souza L, Yadlapati M, Vieira A, Garlet GP, Silva R, Letra A. Interleukin-1 beta (IL1ß) gene polymorphisms and periapical lesion development in individuals with deep caries [Internet]. Journal of Endodontics. 2014 ; 40( 3): e3.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/S0099-2399(14)00129-0
Vancouver
Ghaneh G, Dill A, Chaves de Souza L, Yadlapati M, Vieira A, Garlet GP, Silva R, Letra A. Interleukin-1 beta (IL1ß) gene polymorphisms and periapical lesion development in individuals with deep caries [Internet]. Journal of Endodontics. 2014 ; 40( 3): e3.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/S0099-2399(14)00129-0
Artigo de periodico
Polymorphisms in TREX1 and susceptibility to HIV-1 infection (2013)
Pontillo, Alessandra ; Girardelli, M.; Catamo, E.; Duarte, A. J.; Crovella, S.
Source: International Journal of Immunogenetics. Unidades: FM, ICB
Subjects: POLIMORFISMO, INFECÇÕES POR HIV, INFECÇÕES OPORTUNISTAS, SISTEMA IMUNE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PONTILLO, Alessandra et al. Polymorphisms in TREX1 and susceptibility to HIV-1 infection. International Journal of Immunogenetics, v. (online), p. 3 , 2013Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/iji.12071/pdf. Acesso em: 15 nov. 2024.
APA
Pontillo, A., Girardelli, M., Catamo, E., Duarte, A. J., & Crovella, S. (2013). Polymorphisms in TREX1 and susceptibility to HIV-1 infection. International Journal of Immunogenetics, (online), 3 . doi:10.1111/iji.12071
NLM
Pontillo A, Girardelli M, Catamo E, Duarte AJ, Crovella S. Polymorphisms in TREX1 and susceptibility to HIV-1 infection [Internet]. International Journal of Immunogenetics. 2013 ; (online) 3 .[citado 2024 nov. 15 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/iji.12071/pdf
Vancouver
Pontillo A, Girardelli M, Catamo E, Duarte AJ, Crovella S. Polymorphisms in TREX1 and susceptibility to HIV-1 infection [Internet]. International Journal of Immunogenetics. 2013 ; (online) 3 .[citado 2024 nov. 15 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/iji.12071/pdf
Artigo de periodico
Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD (2012)
Salatino-Oliveira, Angélica; Genro, Julia P.; Guimarães, Ana P.; Chazan, Rodrigo; Zeni, Cristian; Schmitz, Marcelo; Polanczyk, Guilherme; Roman, Tatiana; Rohde, Luis A.; Hutz, Mara H.
Source: Journal of Neural Transmission. Unidade: FM
Subjects: SINAIS E SINTOMAS, CRIANÇAS, ADOLESCENTES, HIPERATIVIDADE, POLIMORFISMO, CÉREBRO (QUÍMICA), DISTÚRBIOS DO COMPORTAMENTO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SALATINO-OLIVEIRA, Angélica et al. Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD. Journal of Neural Transmission, v. 119, n. 6, p. 729-733, 2012Tradução . . Disponível em: https://doi.org/10.1007/s00702-012-0766-2. Acesso em: 15 nov. 2024.
APA
Salatino-Oliveira, A., Genro, J. P., Guimarães, A. P., Chazan, R., Zeni, C., Schmitz, M., et al. (2012). Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD. Journal of Neural Transmission, 119( 6), 729-733. doi:10.1007/s00702-012-0766-2
NLM
Salatino-Oliveira A, Genro JP, Guimarães AP, Chazan R, Zeni C, Schmitz M, Polanczyk G, Roman T, Rohde LA, Hutz MH. Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD [Internet]. Journal of Neural Transmission. 2012 ; 119( 6): 729-733.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s00702-012-0766-2
Vancouver
Salatino-Oliveira A, Genro JP, Guimarães AP, Chazan R, Zeni C, Schmitz M, Polanczyk G, Roman T, Rohde LA, Hutz MH. Cathechol-O-methyltransferase Val158Met polymorphism is associated with disruptive behavior disorders among children and adolescents with ADHD [Internet]. Journal of Neural Transmission. 2012 ; 119( 6): 729-733.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s00702-012-0766-2
Artigo de periodico
Mannose-binding lectin and MBL-associated serine protease-2 gene polymorphisms in a Brazilian population from Rio de Janeiro (2012)
Ferraroni, N. R.; Segat, L.; Guimarães, R. L.; Brandão, L. A. C.; Crovella, S.; Constantino-Silva, R. N.; Loja, C.; Duarte, A. J. da Silva; Grumach, A. S.
Source: International Journal of Immunogenetics. Unidade: FM
Subjects: POLIMORFISMO, GENÓTIPOS, TRANSFUSÃO DE SANGUE, LECTINAS, POPULAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRARONI, N. R. et al. Mannose-binding lectin and MBL-associated serine protease-2 gene polymorphisms in a Brazilian population from Rio de Janeiro. International Journal of Immunogenetics, v. 39, n. 1, p. 32-38, 2012Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/j.1744-313X.2011.01052.x/pdf. Acesso em: 15 nov. 2024.
APA
Ferraroni, N. R., Segat, L., Guimarães, R. L., Brandão, L. A. C., Crovella, S., Constantino-Silva, R. N., et al. (2012). Mannose-binding lectin and MBL-associated serine protease-2 gene polymorphisms in a Brazilian population from Rio de Janeiro. International Journal of Immunogenetics, 39( 1), 32-38. doi:10.1111/j.1744-313X.2011.01052.x
NLM
Ferraroni NR, Segat L, Guimarães RL, Brandão LAC, Crovella S, Constantino-Silva RN, Loja C, Duarte AJ da S, Grumach AS. Mannose-binding lectin and MBL-associated serine protease-2 gene polymorphisms in a Brazilian population from Rio de Janeiro [Internet]. International Journal of Immunogenetics. 2012 ; 39( 1): 32-38.[citado 2024 nov. 15 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/j.1744-313X.2011.01052.x/pdf
Vancouver
Ferraroni NR, Segat L, Guimarães RL, Brandão LAC, Crovella S, Constantino-Silva RN, Loja C, Duarte AJ da S, Grumach AS. Mannose-binding lectin and MBL-associated serine protease-2 gene polymorphisms in a Brazilian population from Rio de Janeiro [Internet]. International Journal of Immunogenetics. 2012 ; 39( 1): 32-38.[citado 2024 nov. 15 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/j.1744-313X.2011.01052.x/pdf
Artigo de periodico
Association of IL1 gene polymorphisms with chronic periodontitis in brazilians (2011)
Trevilatto, Paula C.; Pardo, Ana Paula de Souza; Scarel-Caminaga, Raquel M.; Brito Jr., Rui B. de; Alvim-Pereira, Fabiano; Alvim-Pereira, Claudia C.; Probst, Christian M.; Garlet, Gustavo Pompermaier; Sallum, Antonio W.; Line, Sergio R. P.
Source: Archives of Oral Biology. Unidade: FOB
Subjects: POLIMORFISMO, INTERLEUCINA 1, PERIODONTITE CRÔNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TREVILATTO, Paula C. et al. Association of IL1 gene polymorphisms with chronic periodontitis in brazilians. Archives of Oral Biology, v. 56, n. Ja 2011, p. 54-62, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.archoralbio.2010.09.004. Acesso em: 15 nov. 2024.
APA
Trevilatto, P. C., Pardo, A. P. de S., Scarel-Caminaga, R. M., Brito Jr., R. B. de, Alvim-Pereira, F., Alvim-Pereira, C. C., et al. (2011). Association of IL1 gene polymorphisms with chronic periodontitis in brazilians. Archives of Oral Biology, 56( Ja 2011), 54-62. doi:10.1016/j.archoralbio.2010.09.004
NLM
Trevilatto PC, Pardo AP de S, Scarel-Caminaga RM, Brito Jr. RB de, Alvim-Pereira F, Alvim-Pereira CC, Probst CM, Garlet GP, Sallum AW, Line SRP. Association of IL1 gene polymorphisms with chronic periodontitis in brazilians [Internet]. Archives of Oral Biology. 2011 ; 56( Ja 2011): 54-62.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.archoralbio.2010.09.004
Vancouver
Trevilatto PC, Pardo AP de S, Scarel-Caminaga RM, Brito Jr. RB de, Alvim-Pereira F, Alvim-Pereira CC, Probst CM, Garlet GP, Sallum AW, Line SRP. Association of IL1 gene polymorphisms with chronic periodontitis in brazilians [Internet]. Archives of Oral Biology. 2011 ; 56( Ja 2011): 54-62.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.archoralbio.2010.09.004
Artigo de periodico
Short communication: intermediate prevalence of HIV type 1 primary antiretroviral resistance in Ceará state, northeast Brazil (2011)
Arruda, Erico; Simões, Leda; Sucupira, Maria Cecília; Medeiros, Melissa; Arruda Neto, Eurico de; Diaz, Ricardo Sobhie; Lima, Aldo
Source: AIDS Research and Human Retroviruses. Unidade: FMRP
Subjects: POLIMORFISMO, ANTÍGENOS HLA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ARRUDA, Erico et al. Short communication: intermediate prevalence of HIV type 1 primary antiretroviral resistance in Ceará state, northeast Brazil. AIDS Research and Human Retroviruses, v. 27, n. 2, p. 153-156, 2011Tradução . . Acesso em: 15 nov. 2024.
APA
Arruda, E., Simões, L., Sucupira, M. C., Medeiros, M., Arruda Neto, E. de, Diaz, R. S., & Lima, A. (2011). Short communication: intermediate prevalence of HIV type 1 primary antiretroviral resistance in Ceará state, northeast Brazil. AIDS Research and Human Retroviruses, 27( 2), 153-156.
NLM
Arruda E, Simões L, Sucupira MC, Medeiros M, Arruda Neto E de, Diaz RS, Lima A. Short communication: intermediate prevalence of HIV type 1 primary antiretroviral resistance in Ceará state, northeast Brazil. AIDS Research and Human Retroviruses. 2011 ; 27( 2): 153-156.[citado 2024 nov. 15 ]
Vancouver
Arruda E, Simões L, Sucupira MC, Medeiros M, Arruda Neto E de, Diaz RS, Lima A. Short communication: intermediate prevalence of HIV type 1 primary antiretroviral resistance in Ceará state, northeast Brazil. AIDS Research and Human Retroviruses. 2011 ; 27( 2): 153-156.[citado 2024 nov. 15 ]
Artigo de periodico
GSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas (2010)
Custódio, Aline Cadurin; Almeida, Luciana Oliveira de; Pinto, Giovanny Rebouças; Santos, Marcelo José dos; Almeida, José Reynaldo Walther de; Clara, Carlos Afonso; Rey, Juan A; Casartelli, Cacilda
Source: Genetics and Molecular Research. Unidade: FMRP
Subjects: POLIMORFISMO, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CUSTÓDIO, Aline Cadurin et al. GSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas. Genetics and Molecular Research, v. 9, n. 4, p. 2328-2334, 2010Tradução . . Acesso em: 15 nov. 2024.
APA
Custódio, A. C., Almeida, L. O. de, Pinto, G. R., Santos, M. J. dos, Almeida, J. R. W. de, Clara, C. A., et al. (2010). GSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas. Genetics and Molecular Research, 9( 4), 2328-2334.
NLM
Custódio AC, Almeida LO de, Pinto GR, Santos MJ dos, Almeida JRW de, Clara CA, Rey JA, Casartelli C. GSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas. Genetics and Molecular Research. 2010 ; 9( 4): 2328-2334.[citado 2024 nov. 15 ]
Vancouver
Custódio AC, Almeida LO de, Pinto GR, Santos MJ dos, Almeida JRW de, Clara CA, Rey JA, Casartelli C. GSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas. Genetics and Molecular Research. 2010 ; 9( 4): 2328-2334.[citado 2024 nov. 15 ]
Artigo de periodico
Effects of eNOS polymorphisms on nitric oxide formation in healthy pregnancy and in pre-eclampsia (2010)
Sandrim, Valéria Cristina; Palei, Ana Carolina Taveiros; Sertorio, Jonas T.; Cavalli, Ricardo de Carvalho; Duarte, Geraldo; Tanus-Santos, José Eduardo
Source: Molecular Human Reproduction. Unidade: FMRP
Subjects: PRÉ-ECLÂMPSIA, ÓXIDO NÍTRICO, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANDRIM, Valéria Cristina et al. Effects of eNOS polymorphisms on nitric oxide formation in healthy pregnancy and in pre-eclampsia. Molecular Human Reproduction, v. 16, n. 7, p. 506-510, 2010Tradução . . Disponível em: https://doi.org/10.1093/molehr/gaq030. Acesso em: 15 nov. 2024.
APA
Sandrim, V. C., Palei, A. C. T., Sertorio, J. T., Cavalli, R. de C., Duarte, G., & Tanus-Santos, J. E. (2010). Effects of eNOS polymorphisms on nitric oxide formation in healthy pregnancy and in pre-eclampsia. Molecular Human Reproduction, 16( 7), 506-510. doi:10.1093/molehr/gaq030
NLM
Sandrim VC, Palei ACT, Sertorio JT, Cavalli R de C, Duarte G, Tanus-Santos JE. Effects of eNOS polymorphisms on nitric oxide formation in healthy pregnancy and in pre-eclampsia [Internet]. Molecular Human Reproduction. 2010 ; 16( 7): 506-510.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1093/molehr/gaq030
Vancouver
Sandrim VC, Palei ACT, Sertorio JT, Cavalli R de C, Duarte G, Tanus-Santos JE. Effects of eNOS polymorphisms on nitric oxide formation in healthy pregnancy and in pre-eclampsia [Internet]. Molecular Human Reproduction. 2010 ; 16( 7): 506-510.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1093/molehr/gaq030
Artigo de periodico
Role of the CYP2D6, EPHX1, MPO, and NQO1 genes in the susceptibiblity to acute lymphoblastic leukemia in Brazilian children (2010)
Silveira, Vanessa da Silva; Canalle, Renata; Scrideli, Carlos Alberto; Queiroz, Rosane Gomes de Paula; Tone, Luiz Gonzaga
Source: Environmental and molecular mutagenesis. Unidade: FMRP
Subjects: POLIMORFISMO, LEUCEMIA, CRIANÇAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVEIRA, Vanessa da Silva et al. Role of the CYP2D6, EPHX1, MPO, and NQO1 genes in the susceptibiblity to acute lymphoblastic leukemia in Brazilian children. Environmental and molecular mutagenesis, v. 51, n. 1, p. 48-56, 2010Tradução . . Disponível em: https://doi.org/10.1002/em.20510. Acesso em: 15 nov. 2024.
APA
Silveira, V. da S., Canalle, R., Scrideli, C. A., Queiroz, R. G. de P., & Tone, L. G. (2010). Role of the CYP2D6, EPHX1, MPO, and NQO1 genes in the susceptibiblity to acute lymphoblastic leukemia in Brazilian children. Environmental and molecular mutagenesis, 51( 1), 48-56. doi:10.1002/em.20510
NLM
Silveira V da S, Canalle R, Scrideli CA, Queiroz RG de P, Tone LG. Role of the CYP2D6, EPHX1, MPO, and NQO1 genes in the susceptibiblity to acute lymphoblastic leukemia in Brazilian children [Internet]. Environmental and molecular mutagenesis. 2010 ; 51( 1): 48-56.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/em.20510
Vancouver
Silveira V da S, Canalle R, Scrideli CA, Queiroz RG de P, Tone LG. Role of the CYP2D6, EPHX1, MPO, and NQO1 genes in the susceptibiblity to acute lymphoblastic leukemia in Brazilian children [Internet]. Environmental and molecular mutagenesis. 2010 ; 51( 1): 48-56.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/em.20510
Artigo de periodico
Genetic polymorphisms involved in folate metabolism and concentrations of methylmalonic acid and folate on plasma homocysteine and risk of coronary artery disease (2010)
Biselli, Patrícia Matos; Guerzoni, Alexandre Rodrigues; Godoy, Moacir Fernandes de; Eberlin, Marcos Nogueira; Haddad, Renato; Carvalho, Valdemir Melechco; Vannucchi, Hélio; Bertelli, Érika Cristina Pavarino; Goloni-Bertollo, Eny Maria
Source: Journal of Thrombosis and Thrombolysis. Unidade: FMRP
Subjects: POLIMORFISMO, VITAMINA B12 (DEFICIÊNCIA), DOENÇAS CARDIOVASCULARES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BISELLI, Patrícia Matos et al. Genetic polymorphisms involved in folate metabolism and concentrations of methylmalonic acid and folate on plasma homocysteine and risk of coronary artery disease. Journal of Thrombosis and Thrombolysis, v. 29, n. 1, p. 32-40, 2010Tradução . . Disponível em: https://doi.org/10.1007/s11239-009-0321-7. Acesso em: 15 nov. 2024.
APA
Biselli, P. M., Guerzoni, A. R., Godoy, M. F. de, Eberlin, M. N., Haddad, R., Carvalho, V. M., et al. (2010). Genetic polymorphisms involved in folate metabolism and concentrations of methylmalonic acid and folate on plasma homocysteine and risk of coronary artery disease. Journal of Thrombosis and Thrombolysis, 29( 1), 32-40. doi:10.1007/s11239-009-0321-7
NLM
Biselli PM, Guerzoni AR, Godoy MF de, Eberlin MN, Haddad R, Carvalho VM, Vannucchi H, Bertelli ÉCP, Goloni-Bertollo EM. Genetic polymorphisms involved in folate metabolism and concentrations of methylmalonic acid and folate on plasma homocysteine and risk of coronary artery disease [Internet]. Journal of Thrombosis and Thrombolysis. 2010 ; 29( 1): 32-40.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s11239-009-0321-7
Vancouver
Biselli PM, Guerzoni AR, Godoy MF de, Eberlin MN, Haddad R, Carvalho VM, Vannucchi H, Bertelli ÉCP, Goloni-Bertollo EM. Genetic polymorphisms involved in folate metabolism and concentrations of methylmalonic acid and folate on plasma homocysteine and risk of coronary artery disease [Internet]. Journal of Thrombosis and Thrombolysis. 2010 ; 29( 1): 32-40.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s11239-009-0321-7
Artigo de periodico
HLA-G polymorphisms in women with squamous intraepithelial lesions harboring human papillomavirus (2009)
Simões, Renata T.; Gonçalves, Maria Alice G.; Castelli, Erick C.; M. Júnior, Celso; Bettini, Jussara de Sousa Ribeiro; Discorde, Magali L.; Duarte, Geraldo; Quintana, Silvana Maria; Simões, Aguinaldo Luiz; Moreau, Philippe; Carosella, Edgardo D.; Soares, Edson Garcia; Donadi, Eduardo Antônio
Source: Modern Pathology. Unidade: FMRP
Subjects: PAPILLOMAVIRUS, NEOPLASIAS DO COLO UTERINO, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SIMÕES, Renata T. et al. HLA-G polymorphisms in women with squamous intraepithelial lesions harboring human papillomavirus. Modern Pathology, v. 22, n. 8, p. 1075-1082, 2009Tradução . . Disponível em: https://doi.org/10.1038/modpathol.2009.67. Acesso em: 15 nov. 2024.
APA
Simões, R. T., Gonçalves, M. A. G., Castelli, E. C., M. Júnior, C., Bettini, J. de S. R., Discorde, M. L., et al. (2009). HLA-G polymorphisms in women with squamous intraepithelial lesions harboring human papillomavirus. Modern Pathology, 22( 8), 1075-1082. doi:10.1038/modpathol.2009.67
NLM
Simões RT, Gonçalves MAG, Castelli EC, M. Júnior C, Bettini J de SR, Discorde ML, Duarte G, Quintana SM, Simões AL, Moreau P, Carosella ED, Soares EG, Donadi EA. HLA-G polymorphisms in women with squamous intraepithelial lesions harboring human papillomavirus [Internet]. Modern Pathology. 2009 ; 22( 8): 1075-1082.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/modpathol.2009.67
Vancouver
Simões RT, Gonçalves MAG, Castelli EC, M. Júnior C, Bettini J de SR, Discorde ML, Duarte G, Quintana SM, Simões AL, Moreau P, Carosella ED, Soares EG, Donadi EA. HLA-G polymorphisms in women with squamous intraepithelial lesions harboring human papillomavirus [Internet]. Modern Pathology. 2009 ; 22( 8): 1075-1082.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/modpathol.2009.67
Artigo de periodico
Strong and persistent microbial and inflammatory stimuli overcome the genetic predisposition to higher matrix metalloproteinase-1 (MMP-1) expression: a mechanistic explanation for the lack of association of MMP1-1607 single-nucleotide polymorphism genotypes with MMP-1 expression in chronic periodontitis lesions (2009)
Repeke, Carlos Eduardo; Trombone, Ana Paula Fávaro; Ferreira Júnior, Samuel Barros; Cardoso, Cristina R.; Silveira, Elcia Maria; Martins Junior, Walter; Trevilatto, Paula Cristina; Silva, João Santana; Campanelli, Ana Paula; Garlet, Gustavo Pompermaier
Source: Journal of Clinical Periodontology. Unidade: FOB
Subjects: POLIMORFISMO, PERIODONTITE, METALOPROTEINASES, CITOCINAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
REPEKE, Carlos Eduardo et al. Strong and persistent microbial and inflammatory stimuli overcome the genetic predisposition to higher matrix metalloproteinase-1 (MMP-1) expression: a mechanistic explanation for the lack of association of MMP1-1607 single-nucleotide polymorphism genotypes with MMP-1 expression in chronic periodontitis lesions. Journal of Clinical Periodontology, v. 36, n. 9, p. 726-738, 2009Tradução . . Disponível em: https://doi.org/10.1111/j.1600-051X.2009.01447.x. Acesso em: 15 nov. 2024.
APA
Repeke, C. E., Trombone, A. P. F., Ferreira Júnior, S. B., Cardoso, C. R., Silveira, E. M., Martins Junior, W., et al. (2009). Strong and persistent microbial and inflammatory stimuli overcome the genetic predisposition to higher matrix metalloproteinase-1 (MMP-1) expression: a mechanistic explanation for the lack of association of MMP1-1607 single-nucleotide polymorphism genotypes with MMP-1 expression in chronic periodontitis lesions. Journal of Clinical Periodontology, 36( 9), 726-738. doi:10.1111/j.1600-051X.2009.01447.x
NLM
Repeke CE, Trombone APF, Ferreira Júnior SB, Cardoso CR, Silveira EM, Martins Junior W, Trevilatto PC, Silva JS, Campanelli AP, Garlet GP. Strong and persistent microbial and inflammatory stimuli overcome the genetic predisposition to higher matrix metalloproteinase-1 (MMP-1) expression: a mechanistic explanation for the lack of association of MMP1-1607 single-nucleotide polymorphism genotypes with MMP-1 expression in chronic periodontitis lesions [Internet]. Journal of Clinical Periodontology. 2009 ; 36( 9): 726-738.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1600-051X.2009.01447.x
Vancouver
Repeke CE, Trombone APF, Ferreira Júnior SB, Cardoso CR, Silveira EM, Martins Junior W, Trevilatto PC, Silva JS, Campanelli AP, Garlet GP. Strong and persistent microbial and inflammatory stimuli overcome the genetic predisposition to higher matrix metalloproteinase-1 (MMP-1) expression: a mechanistic explanation for the lack of association of MMP1-1607 single-nucleotide polymorphism genotypes with MMP-1 expression in chronic periodontitis lesions [Internet]. Journal of Clinical Periodontology. 2009 ; 36( 9): 726-738.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1600-051X.2009.01447.x
Artigo de periodico
Polymorphisms in genes involved in neurodevelopment may be associated with altered brain morphology in schizophrenia: Preliminary evidence (2009)
Gregório, Sheila P.; Sallet, Paulo C.; Do, Kim-Anh; Lin, E.; Gattaz, Wagner F.; Dias-Neto, Emmanuel
Source: Psychiatry Research. Unidade: FM
Subjects: ESQUIZOFRENIA, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GREGÓRIO, Sheila P. et al. Polymorphisms in genes involved in neurodevelopment may be associated with altered brain morphology in schizophrenia: Preliminary evidence. Psychiatry Research, v. 165, n. 1, p. 1-9, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.psychres.2007.08.011. Acesso em: 15 nov. 2024.
APA
Gregório, S. P., Sallet, P. C., Do, K. -A., Lin, E., Gattaz, W. F., & Dias-Neto, E. (2009). Polymorphisms in genes involved in neurodevelopment may be associated with altered brain morphology in schizophrenia: Preliminary evidence. Psychiatry Research, 165( 1), 1-9. doi:10.1016/j.psychres.2007.08.011
NLM
Gregório SP, Sallet PC, Do K-A, Lin E, Gattaz WF, Dias-Neto E. Polymorphisms in genes involved in neurodevelopment may be associated with altered brain morphology in schizophrenia: Preliminary evidence [Internet]. Psychiatry Research. 2009 ; 165( 1): 1-9.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.psychres.2007.08.011
Vancouver
Gregório SP, Sallet PC, Do K-A, Lin E, Gattaz WF, Dias-Neto E. Polymorphisms in genes involved in neurodevelopment may be associated with altered brain morphology in schizophrenia: Preliminary evidence [Internet]. Psychiatry Research. 2009 ; 165( 1): 1-9.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.psychres.2007.08.011
Artigo de periodico
The CTLA4 +49 A/G polymorphism is not associated with susceptibility to type 1 diabetes mellitus in the Portuguese population (2009)
Lemos, M. C.; Segat, L.; Coutinho, E.; Gomes, L.; Bastos, M.; Fagulha, A.; Barros, L.; Carrilho, F.; Geraldes, E.; Regateiro, F. J.; Carvalheiro, M.
Source: International Journal of Immunogenetics. Unidade: FM
Subjects: POLIMORFISMO, GENÓTIPOS, DIABETES MELLITUS (GENÉTICA;EPIDEMIOLOGIA), AUTOANTICORPOS, IMUNOGLOBULINAS, ESTUDOS RETROSPECTIVOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEMOS, M. C. et al. The CTLA4 +49 A/G polymorphism is not associated with susceptibility to type 1 diabetes mellitus in the Portuguese population. International Journal of Immunogenetics, v. 36, n. 3, p. 193-195, 2009Tradução . . Disponível em: http://onlinelibrary.wiley.com/doi/10.1111/j.1744-313X.2009.00844.x/pdf. Acesso em: 15 nov. 2024.
APA
Lemos, M. C., Segat, L., Coutinho, E., Gomes, L., Bastos, M., Fagulha, A., et al. (2009). The CTLA4 +49 A/G polymorphism is not associated with susceptibility to type 1 diabetes mellitus in the Portuguese population. International Journal of Immunogenetics, 36( 3), 193-195. doi:10.1111/j.1744-313X.2009.00844.x
NLM
Lemos MC, Segat L, Coutinho E, Gomes L, Bastos M, Fagulha A, Barros L, Carrilho F, Geraldes E, Regateiro FJ, Carvalheiro M. The CTLA4 +49 A/G polymorphism is not associated with susceptibility to type 1 diabetes mellitus in the Portuguese population [Internet]. International Journal of Immunogenetics. 2009 ; 36( 3): 193-195.[citado 2024 nov. 15 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/j.1744-313X.2009.00844.x/pdf
Vancouver
Lemos MC, Segat L, Coutinho E, Gomes L, Bastos M, Fagulha A, Barros L, Carrilho F, Geraldes E, Regateiro FJ, Carvalheiro M. The CTLA4 +49 A/G polymorphism is not associated with susceptibility to type 1 diabetes mellitus in the Portuguese population [Internet]. International Journal of Immunogenetics. 2009 ; 36( 3): 193-195.[citado 2024 nov. 15 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/j.1744-313X.2009.00844.x/pdf
Artigo de periodico
Tumor necrosis factor region polymorphisms are associated with AIDS and with cytomegalovirus retinitis (2009)
Deghaide, Neifi H. S.; Rodrigues, Maria de Lourdes Veronese; Castelli, Erick C.; Mendes Júnior, Celso Teixeira; Figueiredo, José Fernando de Castro; Donadi, Eduardo Antonio
Source: AIDS. Unidades: FMRP, FFCLRP
Subjects: SÍNDROME DE IMUNODEFICIÊNCIA ADQUIRIDA, POLIMORFISMO, DOENÇAS RETINIANAS, NECROSE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DEGHAIDE, Neifi H. S. et al. Tumor necrosis factor region polymorphisms are associated with AIDS and with cytomegalovirus retinitis. AIDS, v. 23, n. 13, p. 1641-1647, 2009Tradução . . Disponível em: https://doi.org/10.1097/qad.0b013e32832e5591. Acesso em: 15 nov. 2024.
APA
Deghaide, N. H. S., Rodrigues, M. de L. V., Castelli, E. C., Mendes Júnior, C. T., Figueiredo, J. F. de C., & Donadi, E. A. (2009). Tumor necrosis factor region polymorphisms are associated with AIDS and with cytomegalovirus retinitis. AIDS, 23( 13), 1641-1647. doi:10.1097/qad.0b013e32832e5591
NLM
Deghaide NHS, Rodrigues M de LV, Castelli EC, Mendes Júnior CT, Figueiredo JF de C, Donadi EA. Tumor necrosis factor region polymorphisms are associated with AIDS and with cytomegalovirus retinitis [Internet]. AIDS. 2009 ; 23( 13): 1641-1647.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1097/qad.0b013e32832e5591
Vancouver
Deghaide NHS, Rodrigues M de LV, Castelli EC, Mendes Júnior CT, Figueiredo JF de C, Donadi EA. Tumor necrosis factor region polymorphisms are associated with AIDS and with cytomegalovirus retinitis [Internet]. AIDS. 2009 ; 23( 13): 1641-1647.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1097/qad.0b013e32832e5591
Artigo de periodico
ICAM-1 (lys469Glu) and PECAM-1 (Leu125Val) polymorhisms in diffuse astrocytomas (2009)
Burim, Regislaine Valéria; Teixeira, Silvia Aparecida; Colli, Benedicto Oscar; Peria, Fernanda Maris; Tirapelli, Luis Fernando; Marie, Suely Kazue Nagahashi; Malheiros, Suzana Marias Fleury; Oba-Shinjo, Sueli Mieko; Gabbai, Alberto Alain; Lotufo, Paulo Andrade; Carlotti Junior, Carlos Gilberto
Source: Clinical and Experimental Medicine. Unidades: FM, HU, FMRP
Subjects: POLIMORFISMO, ASTRÓCITOS (PATOLOGIA), MOLÉCULAS DE ADESÃO CELULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BURIM, Regislaine Valéria et al. ICAM-1 (lys469Glu) and PECAM-1 (Leu125Val) polymorhisms in diffuse astrocytomas. Clinical and Experimental Medicine, v. 9, n. 2, p. 157-163, 2009Tradução . . Disponível em: https://doi.org/10.1007/s10238-009-0040-6. Acesso em: 15 nov. 2024.
APA
Burim, R. V., Teixeira, S. A., Colli, B. O., Peria, F. M., Tirapelli, L. F., Marie, S. K. N., et al. (2009). ICAM-1 (lys469Glu) and PECAM-1 (Leu125Val) polymorhisms in diffuse astrocytomas. Clinical and Experimental Medicine, 9( 2), 157-163. doi:10.1007/s10238-009-0040-6
NLM
Burim RV, Teixeira SA, Colli BO, Peria FM, Tirapelli LF, Marie SKN, Malheiros SMF, Oba-Shinjo SM, Gabbai AA, Lotufo PA, Carlotti Junior CG. ICAM-1 (lys469Glu) and PECAM-1 (Leu125Val) polymorhisms in diffuse astrocytomas [Internet]. Clinical and Experimental Medicine. 2009 ; 9( 2): 157-163.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s10238-009-0040-6
Vancouver
Burim RV, Teixeira SA, Colli BO, Peria FM, Tirapelli LF, Marie SKN, Malheiros SMF, Oba-Shinjo SM, Gabbai AA, Lotufo PA, Carlotti Junior CG. ICAM-1 (lys469Glu) and PECAM-1 (Leu125Val) polymorhisms in diffuse astrocytomas [Internet]. Clinical and Experimental Medicine. 2009 ; 9( 2): 157-163.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1007/s10238-009-0040-6
Artigo de periodico
Tumor necrosis factor-alpha -308G/A single nucleotide polymorphism and red-complex periodontopathogens are independently associated with increased levels of tumor necrosis factor-alpha in diseased periodontal tissues (2009)
Trombone, Ana Paula Fávaro; Cardoso, C. R.; Repeke, Carlos Eduardo; Ferreira-Júnior, Samuel Barros; Martins Junior, W.; Campanelli, Ana Paula; Avila-Campos, Mario Julio; Trevilatto, P. C.; Silva, J. S.; Garlet, Gustavo Pompermaier
Source: Journal of Periodontal Research. Unidades: FOB, ICB
Subjects: POLIMORFISMO, CITOCINAS, DOENÇAS PERIODONTAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TROMBONE, Ana Paula Fávaro et al. Tumor necrosis factor-alpha -308G/A single nucleotide polymorphism and red-complex periodontopathogens are independently associated with increased levels of tumor necrosis factor-alpha in diseased periodontal tissues. Journal of Periodontal Research, v. 44, n. 5, p. 598-608, 2009Tradução . . Disponível em: https://doi.org/10.1111/j.1600-0765.2008.01166.x. Acesso em: 15 nov. 2024.
APA
Trombone, A. P. F., Cardoso, C. R., Repeke, C. E., Ferreira-Júnior, S. B., Martins Junior, W., Campanelli, A. P., et al. (2009). Tumor necrosis factor-alpha -308G/A single nucleotide polymorphism and red-complex periodontopathogens are independently associated with increased levels of tumor necrosis factor-alpha in diseased periodontal tissues. Journal of Periodontal Research, 44( 5), 598-608. doi:10.1111/j.1600-0765.2008.01166.x
NLM
Trombone APF, Cardoso CR, Repeke CE, Ferreira-Júnior SB, Martins Junior W, Campanelli AP, Avila-Campos MJ, Trevilatto PC, Silva JS, Garlet GP. Tumor necrosis factor-alpha -308G/A single nucleotide polymorphism and red-complex periodontopathogens are independently associated with increased levels of tumor necrosis factor-alpha in diseased periodontal tissues [Internet]. Journal of Periodontal Research. 2009 ; 44( 5): 598-608.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1600-0765.2008.01166.x
Vancouver
Trombone APF, Cardoso CR, Repeke CE, Ferreira-Júnior SB, Martins Junior W, Campanelli AP, Avila-Campos MJ, Trevilatto PC, Silva JS, Garlet GP. Tumor necrosis factor-alpha -308G/A single nucleotide polymorphism and red-complex periodontopathogens are independently associated with increased levels of tumor necrosis factor-alpha in diseased periodontal tissues [Internet]. Journal of Periodontal Research. 2009 ; 44( 5): 598-608.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1111/j.1600-0765.2008.01166.x
Artigo de periodico
Genetic polymorphisms in TLR4, CR1 and Duffy genes are not a associated with malaria resistance in patients from Baixo Amazonas region, Brasil (2008)
Soares, Simone Cardoso; Abé-Sandes, Kiyoko; Nascimento Filho, V. B.; Nunes, F. M. F.; Silva Júnior, Wilson Araújo da
Source: Genetics and Molecular Research. Unidade: FMRP
Subjects: MALÁRIA, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOARES, Simone Cardoso et al. Genetic polymorphisms in TLR4, CR1 and Duffy genes are not a associated with malaria resistance in patients from Baixo Amazonas region, Brasil. Genetics and Molecular Research, v. 7, n. 4, p. 1011-1019, 2008Tradução . . Disponível em: https://doi.org/10.4238/vol7-4gmr439. Acesso em: 15 nov. 2024.
APA
Soares, S. C., Abé-Sandes, K., Nascimento Filho, V. B., Nunes, F. M. F., & Silva Júnior, W. A. da. (2008). Genetic polymorphisms in TLR4, CR1 and Duffy genes are not a associated with malaria resistance in patients from Baixo Amazonas region, Brasil. Genetics and Molecular Research, 7( 4), 1011-1019. doi:10.4238/vol7-4gmr439
NLM
Soares SC, Abé-Sandes K, Nascimento Filho VB, Nunes FMF, Silva Júnior WA da. Genetic polymorphisms in TLR4, CR1 and Duffy genes are not a associated with malaria resistance in patients from Baixo Amazonas region, Brasil [Internet]. Genetics and Molecular Research. 2008 ; 7( 4): 1011-1019.[citado 2024 nov. 15 ] Available from: https://doi.org/10.4238/vol7-4gmr439
Vancouver
Soares SC, Abé-Sandes K, Nascimento Filho VB, Nunes FMF, Silva Júnior WA da. Genetic polymorphisms in TLR4, CR1 and Duffy genes are not a associated with malaria resistance in patients from Baixo Amazonas region, Brasil [Internet]. Genetics and Molecular Research. 2008 ; 7( 4): 1011-1019.[citado 2024 nov. 15 ] Available from: https://doi.org/10.4238/vol7-4gmr439
Artigo de periodico
Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects (2008)
Demacq, Caroline; Vasconcellos, Vivian B.; Marcaccini, Andrea M.; Gerlach, Raquel Fernanda; Silva Júnior, Wilson Araújo da; Tanus-Santos, José Eduardo
Source: Clinical Chemistry and Laboratory Medicine. Unidades: FORP, FMRP
Subjects: POLIMORFISMO, METALOPROTEINASES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DEMACQ, Caroline et al. Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects. Clinical Chemistry and Laboratory Medicine, v. 46, n. 1, p. 57-63, 2008Tradução . . Disponível em: https://doi.org/10.1515/cclm.2008.014. Acesso em: 15 nov. 2024.
APA
Demacq, C., Vasconcellos, V. B., Marcaccini, A. M., Gerlach, R. F., Silva Júnior, W. A. da, & Tanus-Santos, J. E. (2008). Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects. Clinical Chemistry and Laboratory Medicine, 46( 1), 57-63. doi:10.1515/cclm.2008.014
NLM
Demacq C, Vasconcellos VB, Marcaccini AM, Gerlach RF, Silva Júnior WA da, Tanus-Santos JE. Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects [Internet]. Clinical Chemistry and Laboratory Medicine. 2008 ; 46( 1): 57-63.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1515/cclm.2008.014
Vancouver
Demacq C, Vasconcellos VB, Marcaccini AM, Gerlach RF, Silva Júnior WA da, Tanus-Santos JE. Functional polymorphisms in the promoter of the matrix metalloproteinase-9 (MMP-9) gene are not linked with significant plasma MMP-9 variations in healthy subjects [Internet]. Clinical Chemistry and Laboratory Medicine. 2008 ; 46( 1): 57-63.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1515/cclm.2008.014

USP Schools

ReP

Filtros

USP Schools

Departament

Authors

USP affiliated authors

Date published

Subjects

Source title

Countries/Territories

Indexado em

Normalized affiliation

Non normalized affiliation