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Artigo de periodico
Genetic variants in bone morphogenetic proteins signaling pathway might be involved in palatal rugae phenotype in humans (2021)
Silva-Sousa, Alice Corrêa ; Marañón-Vásquez, Guido Artemio; Stuani, Maria Bernadete Sasso ; Proff, Peter; Andrades, Kesly Mary Ribeiro; Baratto-Filho, Flares; Matsumoto, Mirian Aiko Nakane ; Paddenberg, Eva; Küchler, Erika Calvano ; Kirschneck, Christian
Source: Scientific Reports. Unidade: FORP
Subjects: ALELOS, MUCOSA ORAL, PALATO DURO, FENÓTIPOS, POLIMORFISMO, TRANSDUÇÃO DE SINAL CELULAR
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ABNT
SILVA-SOUSA, Alice Corrêa et al. Genetic variants in bone morphogenetic proteins signaling pathway might be involved in palatal rugae phenotype in humans. Scientific Reports, v. 11, n. 1, 2021Tradução . . Disponível em: https://doi.org/10.1038/s41598-021-92169-0. Acesso em: 03 jan. 2025.
APA
Silva-Sousa, A. C., Marañón-Vásquez, G. A., Stuani, M. B. S., Proff, P., Andrades, K. M. R., Baratto-Filho, F., et al. (2021). Genetic variants in bone morphogenetic proteins signaling pathway might be involved in palatal rugae phenotype in humans. Scientific Reports, 11( 1). doi:10.1038/s41598-021-92169-0
NLM
Silva-Sousa AC, Marañón-Vásquez GA, Stuani MBS, Proff P, Andrades KMR, Baratto-Filho F, Matsumoto MAN, Paddenberg E, Küchler EC, Kirschneck C. Genetic variants in bone morphogenetic proteins signaling pathway might be involved in palatal rugae phenotype in humans [Internet]. Scientific Reports. 2021 ; 11( 1):[citado 2025 jan. 03 ] Available from: https://doi.org/10.1038/s41598-021-92169-0
Vancouver
Silva-Sousa AC, Marañón-Vásquez GA, Stuani MBS, Proff P, Andrades KMR, Baratto-Filho F, Matsumoto MAN, Paddenberg E, Küchler EC, Kirschneck C. Genetic variants in bone morphogenetic proteins signaling pathway might be involved in palatal rugae phenotype in humans [Internet]. Scientific Reports. 2021 ; 11( 1):[citado 2025 jan. 03 ] Available from: https://doi.org/10.1038/s41598-021-92169-0
Artigo de periodico
Thermal behavior and polymorphism of the antioxidants: BHA, BHT and TBHQ (2020)
De Jesus, Jany Hellen Ferreira ; Ferreira, Ana Paula Garcia ; Szilágyi, I. M; Cavalheiro, Eder Tadeu Gomes
Source: Fuel: The Science and Technology of Fuel and Energy. Unidade: IQSC
Subjects: ANÁLISE TÉRMICA, COMBUSTÍVEIS, POLIMORFISMO, ANTIOXIDANTES
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ABNT
DE JESUS, Jany Hellen Ferreira et al. Thermal behavior and polymorphism of the antioxidants: BHA, BHT and TBHQ. Fuel: The Science and Technology of Fuel and Energy, v. 278, n. 118298 October 2020, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.fuel.2020.118298. Acesso em: 03 jan. 2025.
APA
De Jesus, J. H. F., Ferreira, A. P. G., Szilágyi, I. M., & Cavalheiro, E. T. G. (2020). Thermal behavior and polymorphism of the antioxidants: BHA, BHT and TBHQ. Fuel: The Science and Technology of Fuel and Energy, 278( 118298 October 2020). doi:10.1016/j.fuel.2020.118298
NLM
De Jesus JHF, Ferreira APG, Szilágyi IM, Cavalheiro ETG. Thermal behavior and polymorphism of the antioxidants: BHA, BHT and TBHQ [Internet]. Fuel: The Science and Technology of Fuel and Energy. 2020 ; 278( 118298 October 2020):[citado 2025 jan. 03 ] Available from: https://doi.org/10.1016/j.fuel.2020.118298
Vancouver
De Jesus JHF, Ferreira APG, Szilágyi IM, Cavalheiro ETG. Thermal behavior and polymorphism of the antioxidants: BHA, BHT and TBHQ [Internet]. Fuel: The Science and Technology of Fuel and Energy. 2020 ; 278( 118298 October 2020):[citado 2025 jan. 03 ] Available from: https://doi.org/10.1016/j.fuel.2020.118298
Artigo de periodico
Polymorphism and thermal behavior of sodium cyclamate (2019)
Medina, Daniel A. V; Ferreira, A. P. G; Cavalheiro, Eder Tadeu Gomes
Source: Journal of Thermal Analysis and Calorimetry. Unidade: IQSC
Assunto: POLIMORFISMO
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ABNT
MEDINA, Daniel A. V e FERREIRA, A. P. G e CAVALHEIRO, Eder Tadeu Gomes. Polymorphism and thermal behavior of sodium cyclamate. Journal of Thermal Analysis and Calorimetry, v. 137, p. 1307–1313, 2019Tradução . . Disponível em: https://doi.org/10.1007/s10973-019-08037-7. Acesso em: 03 jan. 2025.
APA
Medina, D. A. V., Ferreira, A. P. G., & Cavalheiro, E. T. G. (2019). Polymorphism and thermal behavior of sodium cyclamate. Journal of Thermal Analysis and Calorimetry, 137, 1307–1313. doi:10.1007/s10973-019-08037-7
NLM
Medina DAV, Ferreira APG, Cavalheiro ETG. Polymorphism and thermal behavior of sodium cyclamate [Internet]. Journal of Thermal Analysis and Calorimetry. 2019 ; 137 1307–1313.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1007/s10973-019-08037-7
Vancouver
Medina DAV, Ferreira APG, Cavalheiro ETG. Polymorphism and thermal behavior of sodium cyclamate [Internet]. Journal of Thermal Analysis and Calorimetry. 2019 ; 137 1307–1313.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1007/s10973-019-08037-7
Artigo de periodico
NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children (2016)
Salatino-Oliveira, Angélica; Akutagava-Martins, Glaucia C.; Bruxel, Estela M.; Genro, Julia P.; Polanczyk, Guilherme V.; Zeni, Cristian; Kieling, Christian; Karam, Rafael G.; Rovaris, Diego Luiz ; Contini, Verônica; Cupertino, Renata B.; Mota, Nina R.; Grevet, Eugenio H.; Bau, Claiton H.; Rohde, Luis A.; Hutz, Mara H.
Source: Journal of Psychiatric Research. Unidade: FM
Subjects: SINAIS E SINTOMAS, POLIMORFISMO, CRIANÇAS, HIPERATIVIDADE
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ABNT
SALATINO-OLIVEIRA, Angélica et al. NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children. Journal of Psychiatric Research, v. 75, p. 75-81, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.jpsychires.2015.01.018. Acesso em: 03 jan. 2025.
APA
Salatino-Oliveira, A., Akutagava-Martins, G. C., Bruxel, E. M., Genro, J. P., Polanczyk, G. V., Zeni, C., et al. (2016). NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children. Journal of Psychiatric Research, 75, 75-81. doi:10.1016/j.jpsychires.2015.01.018
NLM
Salatino-Oliveira A, Akutagava-Martins GC, Bruxel EM, Genro JP, Polanczyk GV, Zeni C, Kieling C, Karam RG, Rovaris DL, Contini V, Cupertino RB, Mota NR, Grevet EH, Bau CH, Rohde LA, Hutz MH. NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children [Internet]. Journal of Psychiatric Research. 2016 ; 75 75-81.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1016/j.jpsychires.2015.01.018
Vancouver
Salatino-Oliveira A, Akutagava-Martins GC, Bruxel EM, Genro JP, Polanczyk GV, Zeni C, Kieling C, Karam RG, Rovaris DL, Contini V, Cupertino RB, Mota NR, Grevet EH, Bau CH, Rohde LA, Hutz MH. NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children [Internet]. Journal of Psychiatric Research. 2016 ; 75 75-81.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1016/j.jpsychires.2015.01.018
Artigo de periodico
SLC24A5 and ASIP as phenotypic predictors in Brazilian population for forensic purposes (2015)
Lima, Felícia de Araújo; Gonçalves, Fernanda de Toledo; Fridman, Cintia
Source: Legal Medicine. Unidade: FM
Subjects: GENÉTICA FORENSE, FENÓTIPOS, BRASILEIROS, POLIMORFISMO
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ABNT
LIMA, Felícia de Araújo e GONÇALVES, Fernanda de Toledo e FRIDMAN, Cintia. SLC24A5 and ASIP as phenotypic predictors in Brazilian population for forensic purposes. Legal Medicine, v. 17, n. 4, p. 261-266, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.legalmed.2015.03.001. Acesso em: 03 jan. 2025.
APA
Lima, F. de A., Gonçalves, F. de T., & Fridman, C. (2015). SLC24A5 and ASIP as phenotypic predictors in Brazilian population for forensic purposes. Legal Medicine, 17( 4), 261-266. doi:10.1016/j.legalmed.2015.03.001
NLM
Lima F de A, Gonçalves F de T, Fridman C. SLC24A5 and ASIP as phenotypic predictors in Brazilian population for forensic purposes [Internet]. Legal Medicine. 2015 ; 17( 4): 261-266.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1016/j.legalmed.2015.03.001
Vancouver
Lima F de A, Gonçalves F de T, Fridman C. SLC24A5 and ASIP as phenotypic predictors in Brazilian population for forensic purposes [Internet]. Legal Medicine. 2015 ; 17( 4): 261-266.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1016/j.legalmed.2015.03.001
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
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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: 03 jan. 2025.
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 2025 jan. 03 ] 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 2025 jan. 03 ] 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
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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: 03 jan. 2025.
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 2025 jan. 03 ] 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 2025 jan. 03 ] 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
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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: 03 jan. 2025.
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 2025 jan. 03 ] 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 2025 jan. 03 ] Available from: http://onlinelibrary.wiley.com/doi/10.1111/j.1744-313X.2011.01052.x/pdf
Artigo de periodico
Literature Review and Practical Aspects on the Management of Oxaliplatin-Associated Toxicity (2012)
Hoff, Paulo M.; Saad, Everardo D.; Costa, Frederico; Coutinho, Anelisa K.; Caponero, Ricardo; Prolla, Gabriel; Gansl, Rene C.
Source: Clinical Colorectal Cancer. Unidade: FM
Subjects: NEOPLASIAS COLORRETAIS (TERAPIA), DROGATERAPIA (TOXIDADE), METÁSTASE NEOPLÁSICA, ANTINEOPLÁSICOS (TOXIDADE), MANIFESTAÇÕES NEUROLÓGICAS, POLIMORFISMO
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ABNT
HOFF, Paulo M. et al. Literature Review and Practical Aspects on the Management of Oxaliplatin-Associated Toxicity. Clinical Colorectal Cancer, v. 11, n. 2, p. 93-100, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.clcc.2011.10.004. Acesso em: 03 jan. 2025.
APA
Hoff, P. M., Saad, E. D., Costa, F., Coutinho, A. K., Caponero, R., Prolla, G., & Gansl, R. C. (2012). Literature Review and Practical Aspects on the Management of Oxaliplatin-Associated Toxicity. Clinical Colorectal Cancer, 11( 2), 93-100. doi:10.1016/j.clcc.2011.10.004
NLM
Hoff PM, Saad ED, Costa F, Coutinho AK, Caponero R, Prolla G, Gansl RC. Literature Review and Practical Aspects on the Management of Oxaliplatin-Associated Toxicity [Internet]. Clinical Colorectal Cancer. 2012 ; 11( 2): 93-100.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1016/j.clcc.2011.10.004
Vancouver
Hoff PM, Saad ED, Costa F, Coutinho AK, Caponero R, Prolla G, Gansl RC. Literature Review and Practical Aspects on the Management of Oxaliplatin-Associated Toxicity [Internet]. Clinical Colorectal Cancer. 2012 ; 11( 2): 93-100.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1016/j.clcc.2011.10.004
Artigo de periodico
Growth Hormone Receptor Polymorphism and Growth Hormone Therapy Response in Children: A Bayesian Meta-Analysis (2012)
Renehan, Andrew G.; Solomon, Mattea; Zwahlen, Marcel; Morjaria, Reena; Whatmore, Andrew; Audí, Laura; Binder, Gerhard; Blum, Werner; Bougnères, Pierre; Dos Santos, Christine; Carrascosa, Antonio; Hokken-Koelega, Anita; Jorge, Alexander; Mullis, Primus E.; Tauber, Maïthé; Patel, Leena; Clayton, Peter E.
Source: American Journal of Epidemiology. Unidade: FM
Subjects: HORMÔNIO DO CRESCIMENTO (APLICAÇÕES TERAPÊUTICAS), CRIANÇAS, TRANSTORNOS DO CRESCIMENTO, POLIMORFISMO, PROTEÍNAS DE TRANSPORTE, INFERÊNCIA BAYESIANA
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ABNT
RENEHAN, Andrew G. et al. Growth Hormone Receptor Polymorphism and Growth Hormone Therapy Response in Children: A Bayesian Meta-Analysis. American Journal of Epidemiology, v. 175, n. 9, p. 867-877, 2012Tradução . . Disponível em: https://doi.org/10.1093/aje/kwr408. Acesso em: 03 jan. 2025.
APA
Renehan, A. G., Solomon, M., Zwahlen, M., Morjaria, R., Whatmore, A., Audí, L., et al. (2012). Growth Hormone Receptor Polymorphism and Growth Hormone Therapy Response in Children: A Bayesian Meta-Analysis. American Journal of Epidemiology, 175( 9), 867-877. doi:10.1093/aje/kwr408
NLM
Renehan AG, Solomon M, Zwahlen M, Morjaria R, Whatmore A, Audí L, Binder G, Blum W, Bougnères P, Dos Santos C, Carrascosa A, Hokken-Koelega A, Jorge A, Mullis PE, Tauber M, Patel L, Clayton PE. Growth Hormone Receptor Polymorphism and Growth Hormone Therapy Response in Children: A Bayesian Meta-Analysis [Internet]. American Journal of Epidemiology. 2012 ; 175( 9): 867-877.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1093/aje/kwr408
Vancouver
Renehan AG, Solomon M, Zwahlen M, Morjaria R, Whatmore A, Audí L, Binder G, Blum W, Bougnères P, Dos Santos C, Carrascosa A, Hokken-Koelega A, Jorge A, Mullis PE, Tauber M, Patel L, Clayton PE. Growth Hormone Receptor Polymorphism and Growth Hormone Therapy Response in Children: A Bayesian Meta-Analysis [Internet]. American Journal of Epidemiology. 2012 ; 175( 9): 867-877.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1093/aje/kwr408
Artigo de periodico
European ancestry and polymorphisms in DNA repair genes modify the risk of melanoma: A case–control study in a high UV index region in Brazil (2011)
Gonçalves, Fernanda T.; Eluf Neto, José; Francisco, Guilherme; Souza, Sonia P. de; Luiz, Olinda C.; Festa Neto, Cyro; Sanches, José A.; Chammas, Roger; Gattas, Gilka J. F.
Source: Journal of Dermatological Science. Unidade: FM
Subjects: POLIMORFISMO, RNA, GENES, MELANONA, ESTUDO DE CASO, NEOPLASIAS CUTÂNEAS
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ABNT
GONÇALVES, Fernanda T. et al. European ancestry and polymorphisms in DNA repair genes modify the risk of melanoma: A case–control study in a high UV index region in Brazil. Journal of Dermatological Science, v. 64, n. 1, p. 59-66, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.jdermsci.2011.06.003. Acesso em: 03 jan. 2025.
APA
Gonçalves, F. T., Eluf Neto, J., Francisco, G., Souza, S. P. de, Luiz, O. C., Festa Neto, C., et al. (2011). European ancestry and polymorphisms in DNA repair genes modify the risk of melanoma: A case–control study in a high UV index region in Brazil. Journal of Dermatological Science, 64( 1), 59-66. doi:10.1016/j.jdermsci.2011.06.003
NLM
Gonçalves FT, Eluf Neto J, Francisco G, Souza SP de, Luiz OC, Festa Neto C, Sanches JA, Chammas R, Gattas GJF. European ancestry and polymorphisms in DNA repair genes modify the risk of melanoma: A case–control study in a high UV index region in Brazil [Internet]. Journal of Dermatological Science. 2011 ; 64( 1): 59-66.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1016/j.jdermsci.2011.06.003
Vancouver
Gonçalves FT, Eluf Neto J, Francisco G, Souza SP de, Luiz OC, Festa Neto C, Sanches JA, Chammas R, Gattas GJF. European ancestry and polymorphisms in DNA repair genes modify the risk of melanoma: A case–control study in a high UV index region in Brazil [Internet]. Journal of Dermatological Science. 2011 ; 64( 1): 59-66.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1016/j.jdermsci.2011.06.003
Artigo de periodico
Novos conhecimentos sobre a flora bacteriana vaginal (2010)
Linhares, Iara Moreno; Giraldo, Paulo Cesar; Baracat, Edmund Chada
Source: Revista da Associação Médica Brasileira. Unidade: FM
Subjects: VAGINA (MICROBIOLOGIA), FLORA, AMPLIFICAÇÃO DE GENES, LACTOBACILLUS, CANDIDÍASE, IMUNIDADE, POLIMORFISMO
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ABNT
LINHARES, Iara Moreno e GIRALDO, Paulo Cesar e BARACAT, Edmund Chada. Novos conhecimentos sobre a flora bacteriana vaginal. Revista da Associação Médica Brasileira, v. 56, n. 3, p. 370-4, 2010Tradução . . Disponível em: https://doi.org/10.1590/s0104-42302010000300026. Acesso em: 03 jan. 2025.
APA
Linhares, I. M., Giraldo, P. C., & Baracat, E. C. (2010). Novos conhecimentos sobre a flora bacteriana vaginal. Revista da Associação Médica Brasileira, 56( 3), 370-4. doi:10.1590/s0104-42302010000300026
NLM
Linhares IM, Giraldo PC, Baracat EC. Novos conhecimentos sobre a flora bacteriana vaginal [Internet]. Revista da Associação Médica Brasileira. 2010 ; 56( 3): 370-4.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1590/s0104-42302010000300026
Vancouver
Linhares IM, Giraldo PC, Baracat EC. Novos conhecimentos sobre a flora bacteriana vaginal [Internet]. Revista da Associação Médica Brasileira. 2010 ; 56( 3): 370-4.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1590/s0104-42302010000300026
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
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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: 03 jan. 2025.
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 2025 jan. 03 ] 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 2025 jan. 03 ] Available from: https://doi.org/10.1002/em.20510
Artigo de periodico
Association of polymorphisms of glutamate-cystein ligase and microsomal triglyceride transfer protein genes in non-alcoholic fatty liver disease (2010)
Oliveira, Claudia Pinto Marques Souza; Stefano, José Tadeu; Cavaleiro, Ana Mercedes; Fortes, Maria Angela Henriques Zanella; Vieira, Suzana Maria; Lima, Vicência Mara Rodrigues; Santos, Telma Eugenio; Santos, Virginia Nascimento; Salgado, Ana Lucia Farias de Azevedo; Parise, Edson Roberto; Alves, Venâncio Avancini Ferreira; Carrilho, Flair José; Giannella, Maria Lúcia Cardillo Côrrea
Source: Journal of Gastroenterology and Hepatology. Unidade: FM
Subjects: POLIMORFISMO, FÍGADO GORDUROSO (GENÉTICA), ESTRESSE OXIDATIVO, LIPÍDEOS (ANÁLISE), GLUTAMATOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Claudia Pinto Marques Souza et al. Association of polymorphisms of glutamate-cystein ligase and microsomal triglyceride transfer protein genes in non-alcoholic fatty liver disease. Journal of Gastroenterology and Hepatology, v. 25, n. 2, p. 357-361, 2010Tradução . . Disponível em: https://doi.org/10.1111/j.1440-1746.2009.06001.x. Acesso em: 03 jan. 2025.
APA
Oliveira, C. P. M. S., Stefano, J. T., Cavaleiro, A. M., Fortes, M. A. H. Z., Vieira, S. M., Lima, V. M. R., et al. (2010). Association of polymorphisms of glutamate-cystein ligase and microsomal triglyceride transfer protein genes in non-alcoholic fatty liver disease. Journal of Gastroenterology and Hepatology, 25( 2), 357-361. doi:10.1111/j.1440-1746.2009.06001.x
NLM
Oliveira CPMS, Stefano JT, Cavaleiro AM, Fortes MAHZ, Vieira SM, Lima VMR, Santos TE, Santos VN, Salgado ALF de A, Parise ER, Alves VAF, Carrilho FJ, Giannella MLCC. Association of polymorphisms of glutamate-cystein ligase and microsomal triglyceride transfer protein genes in non-alcoholic fatty liver disease [Internet]. Journal of Gastroenterology and Hepatology. 2010 ; 25( 2): 357-361.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1111/j.1440-1746.2009.06001.x
Vancouver
Oliveira CPMS, Stefano JT, Cavaleiro AM, Fortes MAHZ, Vieira SM, Lima VMR, Santos TE, Santos VN, Salgado ALF de A, Parise ER, Alves VAF, Carrilho FJ, Giannella MLCC. Association of polymorphisms of glutamate-cystein ligase and microsomal triglyceride transfer protein genes in non-alcoholic fatty liver disease [Internet]. Journal of Gastroenterology and Hepatology. 2010 ; 25( 2): 357-361.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1111/j.1440-1746.2009.06001.x
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: 03 jan. 2025.
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 2025 jan. 03 ] 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 2025 jan. 03 ] Available from: https://doi.org/10.1007/s11239-009-0321-7
Artigo de periodico
DC-SIGN (CD209) gene promoter polymorphisms in a brazilian population and their association with human T-cell lymphotropic virus type 1 infection (2009)
Kashima, Simone; Rodrigues, Evandra Strazza; Azevedo, Rochele; Castelli, Erick da Cruz; Mendes Júnior, Celso Teixeira; Yoshioka, France Keiko Nascimento; Silva, Israel Tojal da; Takayanagui, Osvaldo Massaiti; Covas, Dimas Tadeu
Source: Journal of General Virology. Unidades: FFCLRP, FMRP
Subjects: POLIMORFISMO, RETROVIRIDAE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KASHIMA, Simone et al. DC-SIGN (CD209) gene promoter polymorphisms in a brazilian population and their association with human T-cell lymphotropic virus type 1 infection. Journal of General Virology, v. 90, p. 927-934, 2009Tradução . . Disponível em: https://doi.org/10.1099/vir.0.008367-0. Acesso em: 03 jan. 2025.
APA
Kashima, S., Rodrigues, E. S., Azevedo, R., Castelli, E. da C., Mendes Júnior, C. T., Yoshioka, F. K. N., et al. (2009). DC-SIGN (CD209) gene promoter polymorphisms in a brazilian population and their association with human T-cell lymphotropic virus type 1 infection. Journal of General Virology, 90, 927-934. doi:10.1099/vir.0.008367-0
NLM
Kashima S, Rodrigues ES, Azevedo R, Castelli E da C, Mendes Júnior CT, Yoshioka FKN, Silva IT da, Takayanagui OM, Covas DT. DC-SIGN (CD209) gene promoter polymorphisms in a brazilian population and their association with human T-cell lymphotropic virus type 1 infection [Internet]. Journal of General Virology. 2009 ; 90 927-934.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1099/vir.0.008367-0
Vancouver
Kashima S, Rodrigues ES, Azevedo R, Castelli E da C, Mendes Júnior CT, Yoshioka FKN, Silva IT da, Takayanagui OM, Covas DT. DC-SIGN (CD209) gene promoter polymorphisms in a brazilian population and their association with human T-cell lymphotropic virus type 1 infection [Internet]. Journal of General Virology. 2009 ; 90 927-934.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1099/vir.0.008367-0
Artigo de periodico
CXCL12 rs1801157 polymorphism in patients with breast cancer, hodgkin's lymphoma, and non-hodgkin's lymphoma (2009)
Oliveira, Karen Brajão de; Oda, Julie Massayo Maeda; Voltarelli, Julio Cesar; Nasser, Thiago Franco; Ono, Mario Augusto; Fujita, Thiago Cezar; Matsuo, Tiemi; Watanabe, Maria Angélica Ehara
Source: Journal of Clinical Laboratory Analysis. Unidade: FMRP
Subjects: POLIMORFISMO, NEOPLASIAS MAMÁRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Karen Brajão de et al. CXCL12 rs1801157 polymorphism in patients with breast cancer, hodgkin's lymphoma, and non-hodgkin's lymphoma. Journal of Clinical Laboratory Analysis, v. 23, n. 6, p. 387-393, 2009Tradução . . Disponível em: https://doi.org/10.1002/jcla.20346. Acesso em: 03 jan. 2025.
APA
Oliveira, K. B. de, Oda, J. M. M., Voltarelli, J. C., Nasser, T. F., Ono, M. A., Fujita, T. C., et al. (2009). CXCL12 rs1801157 polymorphism in patients with breast cancer, hodgkin's lymphoma, and non-hodgkin's lymphoma. Journal of Clinical Laboratory Analysis, 23( 6), 387-393. doi:10.1002/jcla.20346
NLM
Oliveira KB de, Oda JMM, Voltarelli JC, Nasser TF, Ono MA, Fujita TC, Matsuo T, Watanabe MAE. CXCL12 rs1801157 polymorphism in patients with breast cancer, hodgkin's lymphoma, and non-hodgkin's lymphoma [Internet]. Journal of Clinical Laboratory Analysis. 2009 ; 23( 6): 387-393.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1002/jcla.20346
Vancouver
Oliveira KB de, Oda JMM, Voltarelli JC, Nasser TF, Ono MA, Fujita TC, Matsuo T, Watanabe MAE. CXCL12 rs1801157 polymorphism in patients with breast cancer, hodgkin's lymphoma, and non-hodgkin's lymphoma [Internet]. Journal of Clinical Laboratory Analysis. 2009 ; 23( 6): 387-393.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1002/jcla.20346
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: 03 jan. 2025.
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 2025 jan. 03 ] 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 2025 jan. 03 ] Available from: https://doi.org/10.1590/s1415-47572009005000033
Artigo de periodico
Polymorphisms at GLUT1 gene are not associated with the development of TSP/HAM in brazilian HTLV-1 infected individuals and the discovery of a new polymorphism at GLUT1 gene (2009)
Costa, Giselle Calasans Souza; Azevedo, Rochele; Gadelha, Sandra Rocha; Kashima, Simone Haddak; Muricy, Gabriel; Olavarria, Viviana Nila; Covas, Dimas Tadeu; Takayanagui, Osvaldo Massaiti; Galvão-Castro, Bernardo; Alcantara, Luiz Carlos Júnior
Source: Journal of Medical Virology. Unidade: FMRP
Subjects: POLIMORFISMO, RETROVIRIDAE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COSTA, Giselle Calasans Souza et al. Polymorphisms at GLUT1 gene are not associated with the development of TSP/HAM in brazilian HTLV-1 infected individuals and the discovery of a new polymorphism at GLUT1 gene. Journal of Medical Virology, v. 81, n. 3, p. 552-557, 2009Tradução . . Disponível em: https://doi.org/10.1002/jmv.21421. Acesso em: 03 jan. 2025.
APA
Costa, G. C. S., Azevedo, R., Gadelha, S. R., Kashima, S. H., Muricy, G., Olavarria, V. N., et al. (2009). Polymorphisms at GLUT1 gene are not associated with the development of TSP/HAM in brazilian HTLV-1 infected individuals and the discovery of a new polymorphism at GLUT1 gene. Journal of Medical Virology, 81( 3), 552-557. doi:10.1002/jmv.21421
NLM
Costa GCS, Azevedo R, Gadelha SR, Kashima SH, Muricy G, Olavarria VN, Covas DT, Takayanagui OM, Galvão-Castro B, Alcantara LCJ. Polymorphisms at GLUT1 gene are not associated with the development of TSP/HAM in brazilian HTLV-1 infected individuals and the discovery of a new polymorphism at GLUT1 gene [Internet]. Journal of Medical Virology. 2009 ; 81( 3): 552-557.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1002/jmv.21421
Vancouver
Costa GCS, Azevedo R, Gadelha SR, Kashima SH, Muricy G, Olavarria VN, Covas DT, Takayanagui OM, Galvão-Castro B, Alcantara LCJ. Polymorphisms at GLUT1 gene are not associated with the development of TSP/HAM in brazilian HTLV-1 infected individuals and the discovery of a new polymorphism at GLUT1 gene [Internet]. Journal of Medical Virology. 2009 ; 81( 3): 552-557.[citado 2025 jan. 03 ] Available from: https://doi.org/10.1002/jmv.21421
Artigo de periodico-carta/editorial
Extensive genetic polymorphism in the haplotype STR-TNF and HLA class I with the onset and evolution of psoriasis vulgaris.[Carta] (2009)
Biral, A. C.; Magalhães, R. F.; Wastowski, I. J.; Simões, R.; Donadi, Eduardo Antônio; Simões, Aguinaldo Luiz; Mendes Júnior, Celso Teixeira; Kraemer, M. H. S.
Source: Journal of Dermatological Science. Unidades: FMRP, FFCLRP
Subjects: PSORÍASE, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BIRAL, A. C. et al. Extensive genetic polymorphism in the haplotype STR-TNF and HLA class I with the onset and evolution of psoriasis vulgaris.[Carta]. Journal of Dermatological Science. Shannon: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 03 jan. 2025. , 2009
APA
Biral, A. C., Magalhães, R. F., Wastowski, I. J., Simões, R., Donadi, E. A., Simões, A. L., et al. (2009). Extensive genetic polymorphism in the haplotype STR-TNF and HLA class I with the onset and evolution of psoriasis vulgaris.[Carta]. Journal of Dermatological Science. Shannon: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Biral AC, Magalhães RF, Wastowski IJ, Simões R, Donadi EA, Simões AL, Mendes Júnior CT, Kraemer MHS. Extensive genetic polymorphism in the haplotype STR-TNF and HLA class I with the onset and evolution of psoriasis vulgaris.[Carta]. Journal of Dermatological Science. 2009 ; 55( 2): 137-138.[citado 2025 jan. 03 ]
Vancouver
Biral AC, Magalhães RF, Wastowski IJ, Simões R, Donadi EA, Simões AL, Mendes Júnior CT, Kraemer MHS. Extensive genetic polymorphism in the haplotype STR-TNF and HLA class I with the onset and evolution of psoriasis vulgaris.[Carta]. Journal of Dermatological Science. 2009 ; 55( 2): 137-138.[citado 2025 jan. 03 ]

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