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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
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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: 11 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. 11 ] 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. 11 ] Available from: https://doi.org/10.1007%2Fs10815-017-0936-0
Artigo de periodico
Bcl-2 rs956572 Polymorphism is Associated with Increased Anterior Cingulate Cortical Glutamate in Euthymic Bipolar I Disorder (2013)
Soeiro-de-Souza, Márcio Gerhardt; Salvadore, Giacomo; Moreno, Ricardo Alberto; Otaduy, Maria Concepción Garcia; Chaim, Kalil T.; Gattaz, Wagner F.; Zarate Jr., Carlos A.; Machado-Vieira, Rodrigo
Source: Neuropsychopharmacology. Unidade: FM
Subjects: TRANSTORNO BIPOLAR, POLIMORFISMO, GLUTAMATOS, CÁLCIO, DEPRESSÃO
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SOEIRO-DE-SOUZA, Márcio Gerhardt et al. Bcl-2 rs956572 Polymorphism is Associated with Increased Anterior Cingulate Cortical Glutamate in Euthymic Bipolar I Disorder. Neuropsychopharmacology, v. 38, n. 3, p. 468-475, 2013Tradução . . Disponível em: https://doi.org/10.1038/npp.2012.203. Acesso em: 11 nov. 2024.
APA
Soeiro-de-Souza, M. G., Salvadore, G., Moreno, R. A., Otaduy, M. C. G., Chaim, K. T., Gattaz, W. F., et al. (2013). Bcl-2 rs956572 Polymorphism is Associated with Increased Anterior Cingulate Cortical Glutamate in Euthymic Bipolar I Disorder. Neuropsychopharmacology, 38( 3), 468-475. doi:10.1038/npp.2012.203
NLM
Soeiro-de-Souza MG, Salvadore G, Moreno RA, Otaduy MCG, Chaim KT, Gattaz WF, Zarate Jr. CA, Machado-Vieira R. Bcl-2 rs956572 Polymorphism is Associated with Increased Anterior Cingulate Cortical Glutamate in Euthymic Bipolar I Disorder [Internet]. Neuropsychopharmacology. 2013 ; 38( 3): 468-475.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1038/npp.2012.203
Vancouver
Soeiro-de-Souza MG, Salvadore G, Moreno RA, Otaduy MCG, Chaim KT, Gattaz WF, Zarate Jr. CA, Machado-Vieira R. Bcl-2 rs956572 Polymorphism is Associated with Increased Anterior Cingulate Cortical Glutamate in Euthymic Bipolar I Disorder [Internet]. Neuropsychopharmacology. 2013 ; 38( 3): 468-475.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1038/npp.2012.203
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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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: 11 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. 11 ] 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. 11 ] Available from: https://doi.org/10.1007/s00702-012-0766-2
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: 11 nov. 2024.
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 2024 nov. 11 ] 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 2024 nov. 11 ] Available from: https://doi.org/10.1093/aje/kwr408
Artigo de periodico
Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency (2011)
França, Marcela M.; Jorge, Alexander A. L.; Alatzoglou, Kyriaki S.; Carvalho, Luciani R. S.; Mendonça, Berenice Bilharinho; Audi, Laura; Carrascosa, Antonio; Dattani, Mehul T.; Arnhold, Ivo J. P.
Source: Journal of Clinical Endocrinology and Metabolism. Unidade: FM
Subjects: MUTAÇÃO GENÉTICA, POLIMORFISMO, HORMÔNIO DO CRESCIMENTO (DEFICIÊNCIA), FENÓTIPOS, ELETROFORESE, SEGUIMENTO GENÉTICO
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FRANÇA, Marcela M. et al. Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency. Journal of Clinical Endocrinology and Metabolism, v. 96, n. 9, p. E1457-1460, 2011Tradução . . Disponível em: https://doi.org/10.1210/jc.2011-0170. Acesso em: 11 nov. 2024.
APA
França, M. M., Jorge, A. A. L., Alatzoglou, K. S., Carvalho, L. R. S., Mendonça, B. B., Audi, L., et al. (2011). Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency. Journal of Clinical Endocrinology and Metabolism, 96( 9), E1457-1460. doi:10.1210/jc.2011-0170
NLM
França MM, Jorge AAL, Alatzoglou KS, Carvalho LRS, Mendonça BB, Audi L, Carrascosa A, Dattani MT, Arnhold IJP. Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 9): E1457-1460.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1210/jc.2011-0170
Vancouver
França MM, Jorge AAL, Alatzoglou KS, Carvalho LRS, Mendonça BB, Audi L, Carrascosa A, Dattani MT, Arnhold IJP. Absence of GH-Releasing Hormone (GHRH) Mutations in Selected Patients with Isolated GH Deficiency [Internet]. Journal of Clinical Endocrinology and Metabolism. 2011 ; 96( 9): E1457-1460.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1210/jc.2011-0170
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
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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: 11 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. 11 ]
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. 11 ]
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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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: 11 nov. 2024.
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 2024 nov. 11 ] 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 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.jdermsci.2011.06.003
Artigo de periodico
Vitamin D receptor haplotypes affect lead levels during pregnancy (2010)
Rezende, Vania B.; Amaral, Jefferson H.; Quintana, Silvana Maria; Gerlach, Raquel Fernanda; Barbosa Júnior, Fernando; Tanus-Santos, José Eduardo
Source: Science of the Total Environment. Unidades: FMRP, FORP, FCFRP
Subjects: VITAMINA D, GRAVIDEZ, POLIMORFISMO
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ABNT
REZENDE, Vania B. et al. Vitamin D receptor haplotypes affect lead levels during pregnancy. Science of the Total Environment, v. 408, n. 21, p. 4955-4960, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.scitotenv.2010.07.039. Acesso em: 11 nov. 2024.
APA
Rezende, V. B., Amaral, J. H., Quintana, S. M., Gerlach, R. F., Barbosa Júnior, F., & Tanus-Santos, J. E. (2010). Vitamin D receptor haplotypes affect lead levels during pregnancy. Science of the Total Environment, 408( 21), 4955-4960. doi:10.1016/j.scitotenv.2010.07.039
NLM
Rezende VB, Amaral JH, Quintana SM, Gerlach RF, Barbosa Júnior F, Tanus-Santos JE. Vitamin D receptor haplotypes affect lead levels during pregnancy [Internet]. Science of the Total Environment. 2010 ; 408( 21): 4955-4960.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.scitotenv.2010.07.039
Vancouver
Rezende VB, Amaral JH, Quintana SM, Gerlach RF, Barbosa Júnior F, Tanus-Santos JE. Vitamin D receptor haplotypes affect lead levels during pregnancy [Internet]. Science of the Total Environment. 2010 ; 408( 21): 4955-4960.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.scitotenv.2010.07.039
Artigo de periodico
Mineralocorticoid receptor p.I180V polymorphism: association with body mass index and LDL-cholesterol levels (2010)
Fernandes Rosa, F. L.; Bueno, A. C.; Souza, R. Molina de; Castro, Margaret de; Santos, Jose Ernesto dos; Foss, Milton César; Zennaro, M. -C.; Bettiol, Heloisa; Barbieri, Marco Antonio; Antonini, Sonir Roberto Rauber
Source: Journal of Endocrinological Investigation. Unidade: FMRP
Subjects: HIPERTENSÃO, POLIMORFISMO
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ABNT
FERNANDES ROSA, F. L. et al. Mineralocorticoid receptor p.I180V polymorphism: association with body mass index and LDL-cholesterol levels. Journal of Endocrinological Investigation, v. 33, n. 7, p. 472-477, 2010Tradução . . Disponível em: https://doi.org/10.1007/bf03346627. Acesso em: 11 nov. 2024.
APA
Fernandes Rosa, F. L., Bueno, A. C., Souza, R. M. de, Castro, M. de, Santos, J. E. dos, Foss, M. C., et al. (2010). Mineralocorticoid receptor p.I180V polymorphism: association with body mass index and LDL-cholesterol levels. Journal of Endocrinological Investigation, 33( 7), 472-477. doi:10.1007/bf03346627
NLM
Fernandes Rosa FL, Bueno AC, Souza RM de, Castro M de, Santos JE dos, Foss MC, Zennaro M-C, Bettiol H, Barbieri MA, Antonini SRR. Mineralocorticoid receptor p.I180V polymorphism: association with body mass index and LDL-cholesterol levels [Internet]. Journal of Endocrinological Investigation. 2010 ; 33( 7): 472-477.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/bf03346627
Vancouver
Fernandes Rosa FL, Bueno AC, Souza RM de, Castro M de, Santos JE dos, Foss MC, Zennaro M-C, Bettiol H, Barbieri MA, Antonini SRR. Mineralocorticoid receptor p.I180V polymorphism: association with body mass index and LDL-cholesterol levels [Internet]. Journal of Endocrinological Investigation. 2010 ; 33( 7): 472-477.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/bf03346627
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
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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: 11 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. 11 ]
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. 11 ]
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
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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: 11 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. 11 ] 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. 11 ] Available from: https://doi.org/10.1093/molehr/gaq030
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: 11 nov. 2024.
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 2024 nov. 11 ] 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 2024 nov. 11 ] 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: 11 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. 11 ] 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. 11 ] Available from: https://doi.org/10.1002/em.20510
Artigo de periodico
The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival (2010)
Almeida, Luciana Oliveira de; Custódio, Aline Cadurin; Santos, Marcelo José dos; Almeida, José R. W.; Clara, Carlos Afonso; Pinto, Giovanny Rebouças; Rey, Juan A.; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: POLIMORFISMO, NEOPLASIAS CEREBRAIS
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ABNT
ALMEIDA, Luciana Oliveira de et al. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival. Cancer Genetics and Cytogenetics, v. 198, n. 1, p. 15-21, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2009.11.013. Acesso em: 11 nov. 2024.
APA
Almeida, L. O. de, Custódio, A. C., Santos, M. J. dos, Almeida, J. R. W., Clara, C. A., Pinto, G. R., et al. (2010). The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival. Cancer Genetics and Cytogenetics, 198( 1), 15-21. doi:10.1016/j.cancergencyto.2009.11.013
NLM
Almeida LO de, Custódio AC, Santos MJ dos, Almeida JRW, Clara CA, Pinto GR, Rey JA, Casartelli C. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 198( 1): 15-21.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.11.013
Vancouver
Almeida LO de, Custódio AC, Santos MJ dos, Almeida JRW, Clara CA, Pinto GR, Rey JA, Casartelli C. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 198( 1): 15-21.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.11.013
Artigo de periodico
Association of -308G/A polymorphism in the tumor necrosis factor-'alfa' gene promoter with susceptibility to development of hantavirus cardiopulmonary syndrome in the Ribeirão Preto region, Brazil (2010)
Borges, Alessandra Abel; Donadi, Eduardo Antônio; Campos, Gelse Mazzoni; Moreli, Marcos Lázaro; Sousa, Ricardo Luiz Moro de; Saggioro, Fabiano Pinto; Figueiredo, Glauciane Garcia de; Badra, Soraya Jabur; Deghaide, Neifi Hassan Saloum; Figueiredo, Luiz Tadeu Moraes
Source: Archives of Virology. Unidades: FMRP, FZEA
Subjects: INFECÇÕES POR HANTAVIRUS, POLIMORFISMO
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ABNT
BORGES, Alessandra Abel et al. Association of -308G/A polymorphism in the tumor necrosis factor-'alfa' gene promoter with susceptibility to development of hantavirus cardiopulmonary syndrome in the Ribeirão Preto region, Brazil. Archives of Virology, v. 155, n. 6, p. 971-975, 2010Tradução . . Disponível em: https://doi.org/10.1007/s00705-010-0655-7. Acesso em: 11 nov. 2024.
APA
Borges, A. A., Donadi, E. A., Campos, G. M., Moreli, M. L., Sousa, R. L. M. de, Saggioro, F. P., et al. (2010). Association of -308G/A polymorphism in the tumor necrosis factor-'alfa' gene promoter with susceptibility to development of hantavirus cardiopulmonary syndrome in the Ribeirão Preto region, Brazil. Archives of Virology, 155( 6), 971-975. doi:10.1007/s00705-010-0655-7
NLM
Borges AA, Donadi EA, Campos GM, Moreli ML, Sousa RLM de, Saggioro FP, Figueiredo GG de, Badra SJ, Deghaide NHS, Figueiredo LTM. Association of -308G/A polymorphism in the tumor necrosis factor-'alfa' gene promoter with susceptibility to development of hantavirus cardiopulmonary syndrome in the Ribeirão Preto region, Brazil [Internet]. Archives of Virology. 2010 ; 155( 6): 971-975.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s00705-010-0655-7
Vancouver
Borges AA, Donadi EA, Campos GM, Moreli ML, Sousa RLM de, Saggioro FP, Figueiredo GG de, Badra SJ, Deghaide NHS, Figueiredo LTM. Association of -308G/A polymorphism in the tumor necrosis factor-'alfa' gene promoter with susceptibility to development of hantavirus cardiopulmonary syndrome in the Ribeirão Preto region, Brazil [Internet]. Archives of Virology. 2010 ; 155( 6): 971-975.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s00705-010-0655-7
Artigo de periodico
Adiponectin: serum levels, promoter polymorphism, and associations with birth size and cardiometabolic outcome in young adults born large for gestational age (2010)
Bueno, Ana Carolina; Espiñeira, Aniette R.; Fernandes-Rosa, Fábio L.; Souza, Roberto Molina de; Castro, Margaret de; Moreira, Ayrton Custódio; Bettiol, Heloisa; Barbieri, Marco Antonio; Antonini, Sonir Roberto Rauber
Source: European Journal of Endocrinology. Unidade: FMRP
Subjects: POLIMORFISMO, BEBÊS, ADIPONECTINA
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ABNT
BUENO, Ana Carolina et al. Adiponectin: serum levels, promoter polymorphism, and associations with birth size and cardiometabolic outcome in young adults born large for gestational age. European Journal of Endocrinology, v. 162, n. 1, p. 53-60, 2010Tradução . . Disponível em: https://doi.org/10.1530/eje-09-0697. Acesso em: 11 nov. 2024.
APA
Bueno, A. C., Espiñeira, A. R., Fernandes-Rosa, F. L., Souza, R. M. de, Castro, M. de, Moreira, A. C., et al. (2010). Adiponectin: serum levels, promoter polymorphism, and associations with birth size and cardiometabolic outcome in young adults born large for gestational age. European Journal of Endocrinology, 162( 1), 53-60. doi:10.1530/eje-09-0697
NLM
Bueno AC, Espiñeira AR, Fernandes-Rosa FL, Souza RM de, Castro M de, Moreira AC, Bettiol H, Barbieri MA, Antonini SRR. Adiponectin: serum levels, promoter polymorphism, and associations with birth size and cardiometabolic outcome in young adults born large for gestational age [Internet]. European Journal of Endocrinology. 2010 ; 162( 1): 53-60.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1530/eje-09-0697
Vancouver
Bueno AC, Espiñeira AR, Fernandes-Rosa FL, Souza RM de, Castro M de, Moreira AC, Bettiol H, Barbieri MA, Antonini SRR. Adiponectin: serum levels, promoter polymorphism, and associations with birth size and cardiometabolic outcome in young adults born large for gestational age [Internet]. European Journal of Endocrinology. 2010 ; 162( 1): 53-60.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1530/eje-09-0697
Artigo de periodico
Correlation between beta-2-glycoprotein I gene polymorphism and anti-beta-2 glycoprotein I antibodies in patients with multibacillary leprosy (2010)
Brochado, Maria José Franco; Figueiredo, José Fernando de Castro; Mendes Júnior, Celso Teixeira; Louzada Junior, Paulo; Kim, Olivia Makiyama; Roselino, Ana Maria Ferreira
Source: Archives of Dermatological Research. Unidades: FFCLRP, FMRP
Subjects: HANSENÍASE, GLICOPROTEÍNAS, POLIMORFISMO, ANTICORPOS
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ABNT
BROCHADO, Maria José Franco et al. Correlation between beta-2-glycoprotein I gene polymorphism and anti-beta-2 glycoprotein I antibodies in patients with multibacillary leprosy. Archives of Dermatological Research, v. 302, n. 8, p. 583-591, 2010Tradução . . Disponível em: https://doi.org/10.1007/s00403-010-1032-9. Acesso em: 11 nov. 2024.
APA
Brochado, M. J. F., Figueiredo, J. F. de C., Mendes Júnior, C. T., Louzada Junior, P., Kim, O. M., & Roselino, A. M. F. (2010). Correlation between beta-2-glycoprotein I gene polymorphism and anti-beta-2 glycoprotein I antibodies in patients with multibacillary leprosy. Archives of Dermatological Research, 302( 8), 583-591. doi:10.1007/s00403-010-1032-9
NLM
Brochado MJF, Figueiredo JF de C, Mendes Júnior CT, Louzada Junior P, Kim OM, Roselino AMF. Correlation between beta-2-glycoprotein I gene polymorphism and anti-beta-2 glycoprotein I antibodies in patients with multibacillary leprosy [Internet]. Archives of Dermatological Research. 2010 ; 302( 8): 583-591.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s00403-010-1032-9
Vancouver
Brochado MJF, Figueiredo JF de C, Mendes Júnior CT, Louzada Junior P, Kim OM, Roselino AMF. Correlation between beta-2-glycoprotein I gene polymorphism and anti-beta-2 glycoprotein I antibodies in patients with multibacillary leprosy [Internet]. Archives of Dermatological Research. 2010 ; 302( 8): 583-591.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s00403-010-1032-9
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
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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: 11 nov. 2024.
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 2024 nov. 11 ] 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 2024 nov. 11 ] 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
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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: 11 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. 11 ] 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. 11 ] Available from: https://doi.org/10.1007/s11239-009-0321-7
Artigo de periodico
A functional matrix metalloproteinase (MMP)-9 polymorphism modifies plasma MMP-9 levels in subjects environmentally exposed to mercury (2010)
Jacob-Ferreira, Anna L. B; Passos, Carlos J. S.; Gerlach, Raquel Fernanda; Barbosa Júnior, Fernando; Tanus-Santos, José Eduardo
Source: Science of the Total Environment. Unidades: FORP, FCFRP, FMRP
Subjects: MERCÚRIO (ELEMENTO QUÍMICO), POLIMORFISMO, METALOPROTEINASES
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ABNT
JACOB-FERREIRA, Anna L. B et al. A functional matrix metalloproteinase (MMP)-9 polymorphism modifies plasma MMP-9 levels in subjects environmentally exposed to mercury. Science of the Total Environment, v. 408, n. 19, p. 4085-4092, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.scitotenv.2010.05.036. Acesso em: 11 nov. 2024.
APA
Jacob-Ferreira, A. L. B., Passos, C. J. S., Gerlach, R. F., Barbosa Júnior, F., & Tanus-Santos, J. E. (2010). A functional matrix metalloproteinase (MMP)-9 polymorphism modifies plasma MMP-9 levels in subjects environmentally exposed to mercury. Science of the Total Environment, 408( 19), 4085-4092. doi:10.1016/j.scitotenv.2010.05.036
NLM
Jacob-Ferreira ALB, Passos CJS, Gerlach RF, Barbosa Júnior F, Tanus-Santos JE. A functional matrix metalloproteinase (MMP)-9 polymorphism modifies plasma MMP-9 levels in subjects environmentally exposed to mercury [Internet]. Science of the Total Environment. 2010 ; 408( 19): 4085-4092.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.scitotenv.2010.05.036
Vancouver
Jacob-Ferreira ALB, Passos CJS, Gerlach RF, Barbosa Júnior F, Tanus-Santos JE. A functional matrix metalloproteinase (MMP)-9 polymorphism modifies plasma MMP-9 levels in subjects environmentally exposed to mercury [Internet]. Science of the Total Environment. 2010 ; 408( 19): 4085-4092.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1016/j.scitotenv.2010.05.036

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