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Artigo de periodico
Influence of genetic polymorphisms on mechanical pain sensitivity and endogenous pain modulation of trigeminal and spinal areas (2023)
Soares, Flávia Fonseca Carvalho ; Ferreira, Dyna Mara Araújo Oliveira ; Raimundini, Amanda Ayla; Dionisio, Thiago José ; Santos, Carlos Ferreira dos ; Conti, Paulo César Rodrigues ; Costa, Yuri Martins ; Bonjardim, Leonardo Rigoldi
Source: Journal of Oral Rehabilitation. Unidade: FOB
Subjects: ODONTALGIA, POLIMORFISMO, SENSIBILIDADE DA DENTINA, DISFUNÇÃO TEMPOROMANDIBULAR
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ABNT
SOARES, Flávia Fonseca Carvalho et al. Influence of genetic polymorphisms on mechanical pain sensitivity and endogenous pain modulation of trigeminal and spinal areas. Journal of Oral Rehabilitation, v. 50, n. Ja 2023, p. 39-53, 2023Tradução . . Disponível em: https://doi.org/10.1111/joor.13384. Acesso em: 19 nov. 2024.
APA
Soares, F. F. C., Ferreira, D. M. A. O., Raimundini, A. A., Dionisio, T. J., Santos, C. F. dos, Conti, P. C. R., et al. (2023). Influence of genetic polymorphisms on mechanical pain sensitivity and endogenous pain modulation of trigeminal and spinal areas. Journal of Oral Rehabilitation, 50( Ja 2023), 39-53. doi:10.1111/joor.13384
NLM
Soares FFC, Ferreira DMAO, Raimundini AA, Dionisio TJ, Santos CF dos, Conti PCR, Costa YM, Bonjardim LR. Influence of genetic polymorphisms on mechanical pain sensitivity and endogenous pain modulation of trigeminal and spinal areas [Internet]. Journal of Oral Rehabilitation. 2023 ; 50( Ja 2023): 39-53.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1111/joor.13384
Vancouver
Soares FFC, Ferreira DMAO, Raimundini AA, Dionisio TJ, Santos CF dos, Conti PCR, Costa YM, Bonjardim LR. Influence of genetic polymorphisms on mechanical pain sensitivity and endogenous pain modulation of trigeminal and spinal areas [Internet]. Journal of Oral Rehabilitation. 2023 ; 50( Ja 2023): 39-53.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1111/joor.13384
Artigo de periodico
Clinically relevant endothelial nitric oxide synthase polymorphisms and their impact on drug response (2020)
Cotta Filho, Cezar Kayzuka; Oliveira-Paula, Gustavo Henrique; Pereira, Vitória Carolina Rondon; Lacchini, Riccardo
Source: Expert Opinion on Drug Metabolism & Toxicology. Unidades: FMRP, EERP
Subjects: ÓXIDO NÍTRICO, FARMACOGENÉTICA, POLIMORFISMO, ALELOS, PREDISPOSIÇÃO GENÉTICA PARA DOENÇA, NUCLEOTÍDEOS
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COTTA FILHO, Cezar Kayzuka et al. Clinically relevant endothelial nitric oxide synthase polymorphisms and their impact on drug response. Expert Opinion on Drug Metabolism & Toxicology, v. 16, n. 10, p. 927-951, 2020Tradução . . Disponível em: https://doi.org/10.1080/17425255.2020.1804857. Acesso em: 19 nov. 2024.
APA
Cotta Filho, C. K., Oliveira-Paula, G. H., Pereira, V. C. R., & Lacchini, R. (2020). Clinically relevant endothelial nitric oxide synthase polymorphisms and their impact on drug response. Expert Opinion on Drug Metabolism & Toxicology, 16( 10), 927-951. doi:10.1080/17425255.2020.1804857
NLM
Cotta Filho CK, Oliveira-Paula GH, Pereira VCR, Lacchini R. Clinically relevant endothelial nitric oxide synthase polymorphisms and their impact on drug response [Internet]. Expert Opinion on Drug Metabolism & Toxicology. 2020 ; 16( 10): 927-951.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1080/17425255.2020.1804857
Vancouver
Cotta Filho CK, Oliveira-Paula GH, Pereira VCR, Lacchini R. Clinically relevant endothelial nitric oxide synthase polymorphisms and their impact on drug response [Internet]. Expert Opinion on Drug Metabolism & Toxicology. 2020 ; 16( 10): 927-951.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1080/17425255.2020.1804857
Artigo de periodico
Brazilian cohort and genes encoding for drug-metabolizing enzymes and drug transporters (2020)
Kim, Vera; Wal, Thijs van der; Nishi, Miriam Yumie; Montenegro, Luciana Ribeiro; Carrilho, Flair Jose ; Hoshida, Yujin; Ono, Suzane Kioko
Source: Pharmacogenomics. Unidade: FM
Subjects: ENVELHECIMENTO, ESTUDOS DE COORTES, FARMACOGENÉTICA, FARMACOCINÉTICA, POLIMORFISMO
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KIM, Vera et al. Brazilian cohort and genes encoding for drug-metabolizing enzymes and drug transporters. Pharmacogenomics, v. 21, n. 9, p. 575-586, 2020Tradução . . Disponível em: https://doi.org/10.2217/pgs-2020-0013. Acesso em: 19 nov. 2024.
APA
Kim, V., Wal, T. van der, Nishi, M. Y., Montenegro, L. R., Carrilho, F. J., Hoshida, Y., & Ono, S. K. (2020). Brazilian cohort and genes encoding for drug-metabolizing enzymes and drug transporters. Pharmacogenomics, 21( 9), 575-586. doi:10.2217/pgs-2020-0013
NLM
Kim V, Wal T van der, Nishi MY, Montenegro LR, Carrilho FJ, Hoshida Y, Ono SK. Brazilian cohort and genes encoding for drug-metabolizing enzymes and drug transporters [Internet]. Pharmacogenomics. 2020 ; 21( 9): 575-586.[citado 2024 nov. 19 ] Available from: https://doi.org/10.2217/pgs-2020-0013
Vancouver
Kim V, Wal T van der, Nishi MY, Montenegro LR, Carrilho FJ, Hoshida Y, Ono SK. Brazilian cohort and genes encoding for drug-metabolizing enzymes and drug transporters [Internet]. Pharmacogenomics. 2020 ; 21( 9): 575-586.[citado 2024 nov. 19 ] Available from: https://doi.org/10.2217/pgs-2020-0013
Artigo de periodico
Association of the genetic ancestry with resistant hypertension in the ReHOT (Resistant Hypertension Optimal Treatment) randomized study (2020)
Bueno, Carolina Tosin; Pereira, Alexandre Costa; Santos, Hadassa Campos; Gomez, Luz Marina Gomez; Horimoto, Andrea Roseli Vancan Russo; Krieger, Eduardo Moacyr; Krieger, Jose Eduardo ; Santos, Paulo Caleb Junior Lima
Source: Scientific reports. Unidade: FM
Subjects: HIPERTENSÃO, ÍNDIOS, MEIA IDADE, POLIMORFISMO, ESTUDOS PROSPECTIVOS, AFRICANOS
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BUENO, Carolina Tosin et al. Association of the genetic ancestry with resistant hypertension in the ReHOT (Resistant Hypertension Optimal Treatment) randomized study. Scientific reports, v. 10, n. 1, 2020Tradução . . Disponível em: https://doi.org/10.1038/s41598-020-58540-3. Acesso em: 19 nov. 2024.
APA
Bueno, C. T., Pereira, A. C., Santos, H. C., Gomez, L. M. G., Horimoto, A. R. V. R., Krieger, E. M., et al. (2020). Association of the genetic ancestry with resistant hypertension in the ReHOT (Resistant Hypertension Optimal Treatment) randomized study. Scientific reports, 10( 1). doi:10.1038/s41598-020-58540-3
NLM
Bueno CT, Pereira AC, Santos HC, Gomez LMG, Horimoto ARVR, Krieger EM, Krieger JE, Santos PCJL. Association of the genetic ancestry with resistant hypertension in the ReHOT (Resistant Hypertension Optimal Treatment) randomized study [Internet]. Scientific reports. 2020 ; 10( 1):[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41598-020-58540-3
Vancouver
Bueno CT, Pereira AC, Santos HC, Gomez LMG, Horimoto ARVR, Krieger EM, Krieger JE, Santos PCJL. Association of the genetic ancestry with resistant hypertension in the ReHOT (Resistant Hypertension Optimal Treatment) randomized study [Internet]. Scientific reports. 2020 ; 10( 1):[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/s41598-020-58540-3
Artigo de periodico
ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome (2019)
Scalco, Renata C; Trarbach, Ericka B; Albuquerque, Edoarda V. A; Homma, Thais K; Inoue-Lima, Thais H; Nishi, Mirian Y; Mendonça, Berenice Bilharinho de ; Jorge, Alexander Augusto de Lima
Source: Endocrine connections. Unidade: FM
Subjects: TRANSTORNOS DO DESENVOLVIMENTO SEXUAL, POLIMORFISMO, DENSIDADE ÓSSEA, MAMA, ÚTERO, TERAPIA DE REPOSIÇÃO DE ESTRÓGENOS, RECEPTORES DE ESTEROIDES
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ABNT
SCALCO, Renata C et al. ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome. Endocrine connections, v. 8, n. 11, p. 1513-1519, 2019Tradução . . Disponível em: https://doi.org/10.1530/EC-19-0398. Acesso em: 19 nov. 2024.
APA
Scalco, R. C., Trarbach, E. B., Albuquerque, E. V. A., Homma, T. K., Inoue-Lima, T. H., Nishi, M. Y., et al. (2019). ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome. Endocrine connections, 8( 11), 1513-1519. doi:10.1530/EC-19-0398
NLM
Scalco RC, Trarbach EB, Albuquerque EVA, Homma TK, Inoue-Lima TH, Nishi MY, Mendonça BB de, Jorge AA de L. ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome [Internet]. Endocrine connections. 2019 ; 8( 11): 1513-1519.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1530/EC-19-0398
Vancouver
Scalco RC, Trarbach EB, Albuquerque EVA, Homma TK, Inoue-Lima TH, Nishi MY, Mendonça BB de, Jorge AA de L. ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome [Internet]. Endocrine connections. 2019 ; 8( 11): 1513-1519.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1530/EC-19-0398
Artigo de periodico
Influence of a mannose-binding lectin gene polymorphism and exposure to Chlamydia trachomatis on fallopian tube obstruction in Brazilian woman (2019)
Vinagre, Joao G; Witkin, Steven S; Ribeiro, Sergio C; Robial, Renata; I, Eiko Fukazawa; Ortolani, Carla C; Baracat, Edmund Chada ; Linhares, Iara M
Source: Archives of gynecology and obstetrics. Unidade: FM
Subjects: POLIMORFISMO, LECTINAS, CHLAMYDIA, DOENÇAS UTERINAS, MULHERES, BRASIL
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ABNT
VINAGRE, Joao G et al. Influence of a mannose-binding lectin gene polymorphism and exposure to Chlamydia trachomatis on fallopian tube obstruction in Brazilian woman. Archives of gynecology and obstetrics, v. 300, n. 3, p. 641-645, 2019Tradução . . Disponível em: https://doi.org/10.1007/s00404-019-05231-8. Acesso em: 19 nov. 2024.
APA
Vinagre, J. G., Witkin, S. S., Ribeiro, S. C., Robial, R., I, E. F., Ortolani, C. C., et al. (2019). Influence of a mannose-binding lectin gene polymorphism and exposure to Chlamydia trachomatis on fallopian tube obstruction in Brazilian woman. Archives of gynecology and obstetrics, 300( 3), 641-645. doi:10.1007/s00404-019-05231-8
NLM
Vinagre JG, Witkin SS, Ribeiro SC, Robial R, I EF, Ortolani CC, Baracat EC, Linhares IM. Influence of a mannose-binding lectin gene polymorphism and exposure to Chlamydia trachomatis on fallopian tube obstruction in Brazilian woman [Internet]. Archives of gynecology and obstetrics. 2019 ; 300( 3): 641-645.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1007/s00404-019-05231-8
Vancouver
Vinagre JG, Witkin SS, Ribeiro SC, Robial R, I EF, Ortolani CC, Baracat EC, Linhares IM. Influence of a mannose-binding lectin gene polymorphism and exposure to Chlamydia trachomatis on fallopian tube obstruction in Brazilian woman [Internet]. Archives of gynecology and obstetrics. 2019 ; 300( 3): 641-645.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1007/s00404-019-05231-8
Artigo de periodico
The ATC/TTC haplotype in the interleukin 8 gene in response to Gram-negative bacteria: a pilot study (2019)
Pigossi, Suzane Cristina ; Anovazzi, Giovana; Finoti, Lívia Sertori ; Medeiros, Marcell Costa de ; Moreira, Tatiana Maria de Souza ; Mayer, Marcia Pinto Alves ; Zanelli, Gleslei Fernando; Valentini, Sandro Roberto ; Rossa Junior, Carlos ; Caminaga, Raquel Mantuaneli Scarel
Source: Archives of Oral Biology. Unidade: ICB
Subjects: MICROBIOLOGIA, POLIMORFISMO, INTERLEUCINA 8, BACTÉRIAS GRAM-NEGATIVAS, QUIMIOCINAS, EXPRESSÃO GÊNICA, NEUTRÓFILOS, ACTINOMYCETACEAE, REAÇÃO EM CADEIA POR POLIMERASE, HAPLOTIPOS, PERIODONTITE
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ABNT
PIGOSSI, Suzane Cristina et al. The ATC/TTC haplotype in the interleukin 8 gene in response to Gram-negative bacteria: a pilot study. Archives of Oral Biology, v. 107, p. 9 , 2019Tradução . . Disponível em: https://doi.org/10.1016/j.archoralbio.2019.104508. Acesso em: 19 nov. 2024.
APA
Pigossi, S. C., Anovazzi, G., Finoti, L. S., Medeiros, M. C. de, Moreira, T. M. de S., Mayer, M. P. A., et al. (2019). The ATC/TTC haplotype in the interleukin 8 gene in response to Gram-negative bacteria: a pilot study. Archives of Oral Biology, 107, 9 . doi:10.1016/j.archoralbio.2019.104508
NLM
Pigossi SC, Anovazzi G, Finoti LS, Medeiros MC de, Moreira TM de S, Mayer MPA, Zanelli GF, Valentini SR, Rossa Junior C, Caminaga RMS. The ATC/TTC haplotype in the interleukin 8 gene in response to Gram-negative bacteria: a pilot study [Internet]. Archives of Oral Biology. 2019 ; 107 9 .[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.archoralbio.2019.104508
Vancouver
Pigossi SC, Anovazzi G, Finoti LS, Medeiros MC de, Moreira TM de S, Mayer MPA, Zanelli GF, Valentini SR, Rossa Junior C, Caminaga RMS. The ATC/TTC haplotype in the interleukin 8 gene in response to Gram-negative bacteria: a pilot study [Internet]. Archives of Oral Biology. 2019 ; 107 9 .[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.archoralbio.2019.104508
Artigo de periodico
The association between genetic risk score and blood pressure is modified by coffee consumption: Gene-diet interaction analysis in a population-based study (2018)
Miranda, Andreia Machado; Steluti, Josiane; Norde, Marina Maintinguer; Fisberg, Regina Mara ; Marchioni, Dirce Maria Lobo
Source: Clinical Nutrition. Unidade: FSP
Subjects: GENOMAS, CAFÉ, ESTUDOS TRANSVERSAIS, PRESSÃO SANGUÍNEA, POLIMORFISMO, AMOSTRAGEM
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MIRANDA, Andreia Machado et al. The association between genetic risk score and blood pressure is modified by coffee consumption: Gene-diet interaction analysis in a population-based study. Clinical Nutrition, v. 38, n. 4, p. 1721-1728, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.clnu.2018.07.033. Acesso em: 19 nov. 2024.
APA
Miranda, A. M., Steluti, J., Norde, M. M., Fisberg, R. M., & Marchioni, D. M. L. (2018). The association between genetic risk score and blood pressure is modified by coffee consumption: Gene-diet interaction analysis in a population-based study. Clinical Nutrition, 38( 4), 1721-1728. doi:10.1016/j.clnu.2018.07.033
NLM
Miranda AM, Steluti J, Norde MM, Fisberg RM, Marchioni DML. The association between genetic risk score and blood pressure is modified by coffee consumption: Gene-diet interaction analysis in a population-based study [Internet]. Clinical Nutrition. 2018 ;38( 4): 1721-1728.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.clnu.2018.07.033
Vancouver
Miranda AM, Steluti J, Norde MM, Fisberg RM, Marchioni DML. The association between genetic risk score and blood pressure is modified by coffee consumption: Gene-diet interaction analysis in a population-based study [Internet]. Clinical Nutrition. 2018 ;38( 4): 1721-1728.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.clnu.2018.07.033
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: 19 nov. 2024.
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 2024 nov. 19 ] 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 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.jpsychires.2015.01.018
Artigo de periodico
ACTN3 R577X polymorphism and long-term survival in patients with chronic heart failure (2014)
Bernardez-Pereira, Sabrina; Santos, Paulo Caleb Junior Lima; Krieger, Jose Eduardo; Mansur, Alfredo Jose; Pereira, Alexandre Costa
Source: BMC cardiovascular disorders. Unidade: FM
Subjects: PROGNÓSTICO, INSUFICIÊNCIA CARDÍACA (ETIOLOGIA), POLIMORFISMO
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ABNT
BERNARDEZ-PEREIRA, Sabrina et al. ACTN3 R577X polymorphism and long-term survival in patients with chronic heart failure. BMC cardiovascular disorders, v. 14, n. 90, p. 5 2014, 2014Tradução . . Disponível em: https://doi.org/10.1186/1471-2261-14-90. Acesso em: 19 nov. 2024.
APA
Bernardez-Pereira, S., Santos, P. C. J. L., Krieger, J. E., Mansur, A. J., & Pereira, A. C. (2014). ACTN3 R577X polymorphism and long-term survival in patients with chronic heart failure. BMC cardiovascular disorders, 14( 90), 5 2014. doi:10.1186/1471-2261-14-90
NLM
Bernardez-Pereira S, Santos PCJL, Krieger JE, Mansur AJ, Pereira AC. ACTN3 R577X polymorphism and long-term survival in patients with chronic heart failure [Internet]. BMC cardiovascular disorders. 2014 ; 14( 90): 5 2014.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1471-2261-14-90
Vancouver
Bernardez-Pereira S, Santos PCJL, Krieger JE, Mansur AJ, Pereira AC. ACTN3 R577X polymorphism and long-term survival in patients with chronic heart failure [Internet]. BMC cardiovascular disorders. 2014 ; 14( 90): 5 2014.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1471-2261-14-90
Artigo de periodico
Analysis of polymorphisms in Plasmodium falciparum genes related to drug resistance: a survey over four decades under different treatment policies in Brazil (2014)
Inoue, Juliana; Lopes, Dinora; Rosário, Virgílio do; Machado, Marta; Hristov, Angélica D.; Lima, Giselle F. M. C.; Costa-Nascimento, Maria J.; Segurado, Aluísio C.; Di Santi, Silvia M.
Source: Malaria Journal. Unidade: FM
Subjects: POLIMORFISMO, BIOMARCADORES, RESISTÊNCIA MICROBIANA ÀS DROGAS, PLASMODIUM
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ABNT
INOUE, Juliana et al. Analysis of polymorphisms in Plasmodium falciparum genes related to drug resistance: a survey over four decades under different treatment policies in Brazil. Malaria Journal, v. 13, n. 1, p. (online), 2014Tradução . . Disponível em: https://doi.org/10.1186/1475-2875-13-372. Acesso em: 19 nov. 2024.
APA
Inoue, J., Lopes, D., Rosário, V. do, Machado, M., Hristov, A. D., Lima, G. F. M. C., et al. (2014). Analysis of polymorphisms in Plasmodium falciparum genes related to drug resistance: a survey over four decades under different treatment policies in Brazil. Malaria Journal, 13( 1), (online). doi:10.1186/1475-2875-13-372
NLM
Inoue J, Lopes D, Rosário V do, Machado M, Hristov AD, Lima GFMC, Costa-Nascimento MJ, Segurado AC, Di Santi SM. Analysis of polymorphisms in Plasmodium falciparum genes related to drug resistance: a survey over four decades under different treatment policies in Brazil [Internet]. Malaria Journal. 2014 ; 13( 1): (online).[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1475-2875-13-372
Vancouver
Inoue J, Lopes D, Rosário V do, Machado M, Hristov AD, Lima GFMC, Costa-Nascimento MJ, Segurado AC, Di Santi SM. Analysis of polymorphisms in Plasmodium falciparum genes related to drug resistance: a survey over four decades under different treatment policies in Brazil [Internet]. Malaria Journal. 2014 ; 13( 1): (online).[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1475-2875-13-372
Artigo de periodico
Plasmatic higher levels of homocysteine in Non-alcoholic fatty liver disease (NAFLD) (2013)
Carvalho, Sylene Coutinho Rampche de; Muniz, Maria Tereza Cartaxo; Siqueira, Maria Deozete Vieira; Siqueira, Erika Rabelo Forte; Gomes, Adriana Vieira; Silva, Karina Alves; Bezerra, Laís Carvalho Luma; D’Almeida, Vânia; Oliveira, Claudia Pinto Marques Souza de; Pereira, Leila Maria M. Beltrão
Source: Nutrition Journal. Unidade: FM
Subjects: POLIMORFISMO, ESTRESSE OXIDATIVO, OBESIDADE (GENÉTICA), FÍGADO GORDUROSO, HEPATOPATIAS
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ABNT
CARVALHO, Sylene Coutinho Rampche de et al. Plasmatic higher levels of homocysteine in Non-alcoholic fatty liver disease (NAFLD). Nutrition Journal, v. 12, n. 37, p. (online), 2013Tradução . . Disponível em: https://doi.org/10.1186/1475-2891-12-37. Acesso em: 19 nov. 2024.
APA
Carvalho, S. C. R. de, Muniz, M. T. C., Siqueira, M. D. V., Siqueira, E. R. F., Gomes, A. V., Silva, K. A., et al. (2013). Plasmatic higher levels of homocysteine in Non-alcoholic fatty liver disease (NAFLD). Nutrition Journal, 12( 37), (online). doi:10.1186/1475-2891-12-37
NLM
Carvalho SCR de, Muniz MTC, Siqueira MDV, Siqueira ERF, Gomes AV, Silva KA, Bezerra LCL, D’Almeida V, Oliveira CPMS de, Pereira LMMB. Plasmatic higher levels of homocysteine in Non-alcoholic fatty liver disease (NAFLD) [Internet]. Nutrition Journal. 2013 ; 12( 37): (online).[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1475-2891-12-37
Vancouver
Carvalho SCR de, Muniz MTC, Siqueira MDV, Siqueira ERF, Gomes AV, Silva KA, Bezerra LCL, D’Almeida V, Oliveira CPMS de, Pereira LMMB. Plasmatic higher levels of homocysteine in Non-alcoholic fatty liver disease (NAFLD) [Internet]. Nutrition Journal. 2013 ; 12( 37): (online).[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1475-2891-12-37
Artigo de periodico
Lack of evidence to support the association of a single IL28B genotype SNP rs12979860 with the HTLV-1 clinical outcomes and proviral load (2012)
Sanabani, Sabri Saeed; Nukui, Youko; Pereira, Juliana; Costa, Antonio Charlys da; Oliveira, Ana Carolina Soares de; Pessôa, Rodrigo; Leal, Fabio Eudes; Segurado, Aluisio C.; Kallas, Esper Georges; Sabino, Ester Cerdeira
Source: BMC Infectious Diseases. Unidade: FM
Subjects: POLIMORFISMO, GENÓTIPOS, TRANSFUSÃO DE SANGUE, IMUNOENSAIO, LINFOMA, INFECÇÕES POR HTLV-I, TRANSMISSÃO DE DOENÇAS, INTERLEUCINAS, LEUCEMIA
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ABNT
SANABANI, Sabri Saeed et al. Lack of evidence to support the association of a single IL28B genotype SNP rs12979860 with the HTLV-1 clinical outcomes and proviral load. BMC Infectious Diseases, v. 12, n. 374, p. (online), 2012Tradução . . Disponível em: https://doi.org/10.1186/1471-2334-12-374. Acesso em: 19 nov. 2024.
APA
Sanabani, S. S., Nukui, Y., Pereira, J., Costa, A. C. da, Oliveira, A. C. S. de, Pessôa, R., et al. (2012). Lack of evidence to support the association of a single IL28B genotype SNP rs12979860 with the HTLV-1 clinical outcomes and proviral load. BMC Infectious Diseases, 12( 374), (online). doi:10.1186/1471-2334-12-374
NLM
Sanabani SS, Nukui Y, Pereira J, Costa AC da, Oliveira ACS de, Pessôa R, Leal FE, Segurado AC, Kallas EG, Sabino EC. Lack of evidence to support the association of a single IL28B genotype SNP rs12979860 with the HTLV-1 clinical outcomes and proviral load [Internet]. BMC Infectious Diseases. 2012 ; 12( 374): (online).[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1471-2334-12-374
Vancouver
Sanabani SS, Nukui Y, Pereira J, Costa AC da, Oliveira ACS de, Pessôa R, Leal FE, Segurado AC, Kallas EG, Sabino EC. Lack of evidence to support the association of a single IL28B genotype SNP rs12979860 with the HTLV-1 clinical outcomes and proviral load [Internet]. BMC Infectious Diseases. 2012 ; 12( 374): (online).[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1471-2334-12-374
Artigo de periodico
Matrix metalloproteinase-9 genetic variations affect MMP-9 levels in obese children (2012)
Belo, V. A.; Souza-Costa, D. C.; Luizon, M. R.; Lanna, C. M. M.; Carneiro, P. C.; Izidoro-Toledo, T. C.; Ferraz, K. C.; Tanus-Santos, José Eduardo
Source: International Journal of Obesity. Unidade: FMRP
Subjects: OBESIDADE, CRIANÇAS, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BELO, V. A. et al. Matrix metalloproteinase-9 genetic variations affect MMP-9 levels in obese children. International Journal of Obesity, v. 36, n. 1, p. 69-75, 2012Tradução . . Disponível em: https://doi.org/10.1038/ijo.2011.169. Acesso em: 19 nov. 2024.
APA
Belo, V. A., Souza-Costa, D. C., Luizon, M. R., Lanna, C. M. M., Carneiro, P. C., Izidoro-Toledo, T. C., et al. (2012). Matrix metalloproteinase-9 genetic variations affect MMP-9 levels in obese children. International Journal of Obesity, 36( 1), 69-75. doi:10.1038/ijo.2011.169
NLM
Belo VA, Souza-Costa DC, Luizon MR, Lanna CMM, Carneiro PC, Izidoro-Toledo TC, Ferraz KC, Tanus-Santos JE. Matrix metalloproteinase-9 genetic variations affect MMP-9 levels in obese children [Internet]. International Journal of Obesity. 2012 ; 36( 1): 69-75.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/ijo.2011.169
Vancouver
Belo VA, Souza-Costa DC, Luizon MR, Lanna CMM, Carneiro PC, Izidoro-Toledo TC, Ferraz KC, Tanus-Santos JE. Matrix metalloproteinase-9 genetic variations affect MMP-9 levels in obese children [Internet]. International Journal of Obesity. 2012 ; 36( 1): 69-75.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/ijo.2011.169
Artigo de periodico
An ancient founder mutation in PROKR2 impairs human reproduction (2012)
Stefanija, Magdalena Avbelj; Jeanpierre, Marc; Sykiotis, Gerasimos P.; Young, Jacques; Quinton, Richard; Abreu, Ana Paula; Plummer, Lacey; Au, Margaret G.; Balasubramanian, Ravikumar; Dwyer, Andrew A.; Florez, Jose C.; Cheetham, Timothy; Pearce, Simon H.; Purushothaman, Radhika; Schinzel, Albert; Pugeat, Michel; Jacobson-Dickman, Elka E.; Ten, Svetlana; Latronico, Ana Claudia; Gusella, James F.; Dode, Catherine; Crowley Jr, William F.; Pitteloud, Nelly
Source: Human Molecular Genetics. Unidade: FM
Subjects: FENÓTIPOS, GENÓTIPOS, INFLAMAÇÃO, MUTAÇÃO GENÉTICA, POLIMORFISMO, HIPOGANADISMO (DIAGNÓSTICO), GONADOTROFINAS HIPOFISÁRIAS (DEFICIÊNCIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANIJA, Magdalena Avbelj et al. An ancient founder mutation in PROKR2 impairs human reproduction. Human Molecular Genetics, v. 21, n. 19, p. 4314-4324, 2012Tradução . . Disponível em: https://doi.org/10.1093/hmg/dds264. Acesso em: 19 nov. 2024.
APA
Stefanija, M. A., Jeanpierre, M., Sykiotis, G. P., Young, J., Quinton, R., Abreu, A. P., et al. (2012). An ancient founder mutation in PROKR2 impairs human reproduction. Human Molecular Genetics, 21( 19), 4314-4324. doi:10.1093/hmg/dds264
NLM
Stefanija MA, Jeanpierre M, Sykiotis GP, Young J, Quinton R, Abreu AP, Plummer L, Au MG, Balasubramanian R, Dwyer AA, Florez JC, Cheetham T, Pearce SH, Purushothaman R, Schinzel A, Pugeat M, Jacobson-Dickman EE, Ten S, Latronico AC, Gusella JF, Dode C, Crowley Jr WF, Pitteloud N. An ancient founder mutation in PROKR2 impairs human reproduction [Internet]. Human Molecular Genetics. 2012 ; 21( 19): 4314-4324.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1093/hmg/dds264
Vancouver
Stefanija MA, Jeanpierre M, Sykiotis GP, Young J, Quinton R, Abreu AP, Plummer L, Au MG, Balasubramanian R, Dwyer AA, Florez JC, Cheetham T, Pearce SH, Purushothaman R, Schinzel A, Pugeat M, Jacobson-Dickman EE, Ten S, Latronico AC, Gusella JF, Dode C, Crowley Jr WF, Pitteloud N. An ancient founder mutation in PROKR2 impairs human reproduction [Internet]. Human Molecular Genetics. 2012 ; 21( 19): 4314-4324.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1093/hmg/dds264
Artigo de periodico
MYLIP p.N342S polymorphism is not associated with lipid profile in the Brazilian population (2012)
Santos, Paulo C J L; Oliveira, Theo G M; Lemos, Pedro A; Mill, José G; Krieger, José Eduardo; Pereira, Alexandre C
Source: Lipids in Health and Disease. Unidade: FM
Subjects: POLIMORFISMO, LIPÍDEOS, GRUPOS ÉTNICOS, COLESTEROL (ANÁLISE), BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Paulo C J L et al. MYLIP p.N342S polymorphism is not associated with lipid profile in the Brazilian population. Lipids in Health and Disease, v. 11, p. 7 , 2012Tradução . . Disponível em: https://doi.org/10.1186/1476-511x-11-83. Acesso em: 19 nov. 2024.
APA
Santos, P. C. J. L., Oliveira, T. G. M., Lemos, P. A., Mill, J. G., Krieger, J. E., & Pereira, A. C. (2012). MYLIP p.N342S polymorphism is not associated with lipid profile in the Brazilian population. Lipids in Health and Disease, 11, 7 . doi:10.1186/1476-511x-11-83
NLM
Santos PCJL, Oliveira TGM, Lemos PA, Mill JG, Krieger JE, Pereira AC. MYLIP p.N342S polymorphism is not associated with lipid profile in the Brazilian population [Internet]. Lipids in Health and Disease. 2012 ; 117 .[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1476-511x-11-83
Vancouver
Santos PCJL, Oliveira TGM, Lemos PA, Mill JG, Krieger JE, Pereira AC. MYLIP p.N342S polymorphism is not associated with lipid profile in the Brazilian population [Internet]. Lipids in Health and Disease. 2012 ; 117 .[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1476-511x-11-83
Artigo de periodico
Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21 (2012)
Gioli-Pereira, Luciana; Santos, Paulo Caleb Junior L; Ferreira, Noely Evangelista; Hueb, Whady A; Krieger, José Eduardo; Pereira, Alexandre C
Source: BMC Cardiovascular Disorders. Unidade: FM
Subjects: CORONARIOPATIA (EPIDEMIOLOGIA;MORTALIDADE;GENÉTICA), POLIMORFISMO, CROMOSSOMOS (PATOLOGIA), DOENÇAS CARDIOVASCULARES (EPIDEMIOLOGIA;MORTALIDADE)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GIOLI-PEREIRA, Luciana et al. Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21. BMC Cardiovascular Disorders, v. 12, p. 7 , 2012Tradução . . Disponível em: https://doi.org/10.1186/1471-2261-12-61. Acesso em: 19 nov. 2024.
APA
Gioli-Pereira, L., Santos, P. C. J. L., Ferreira, N. E., Hueb, W. A., Krieger, J. E., & Pereira, A. C. (2012). Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21. BMC Cardiovascular Disorders, 12, 7 . doi:10.1186/1471-2261-12-61
NLM
Gioli-Pereira L, Santos PCJL, Ferreira NE, Hueb WA, Krieger JE, Pereira AC. Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21 [Internet]. BMC Cardiovascular Disorders. 2012 ; 12 7 .[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1471-2261-12-61
Vancouver
Gioli-Pereira L, Santos PCJL, Ferreira NE, Hueb WA, Krieger JE, Pereira AC. Higher incidence of death in multi-vessel coronary artery disease patients associated with polymorphisms in chromosome 9p21 [Internet]. BMC Cardiovascular Disorders. 2012 ; 12 7 .[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1471-2261-12-61
Artigo de periodico
Factors associated with serum CA19-9 levels among healthy children: a cross-sectional study (2012)
Kawai, Sayo; Oba-Shinjo, Sueli M.; Ito, Lucy S.; Uno, Miyuki; Marie, Suely K. N.; Hamajima, Nobuyuki
Source: BMC Clinical Pathology. Unidade: FM
Subjects: CRIANÇAS (CRESCIMENTO E DESENVOLVIMENTO), POLIMORFISMO, BIOMARCADORES, GENÓTIPOS, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KAWAI, Sayo et al. Factors associated with serum CA19-9 levels among healthy children: a cross-sectional study. BMC Clinical Pathology, v. 12, n. 23, p. (online), 2012Tradução . . Disponível em: https://doi.org/10.1186/1472-6890-12-23. Acesso em: 19 nov. 2024.
APA
Kawai, S., Oba-Shinjo, S. M., Ito, L. S., Uno, M., Marie, S. K. N., & Hamajima, N. (2012). Factors associated with serum CA19-9 levels among healthy children: a cross-sectional study. BMC Clinical Pathology, 12( 23), (online). doi:10.1186/1472-6890-12-23
NLM
Kawai S, Oba-Shinjo SM, Ito LS, Uno M, Marie SKN, Hamajima N. Factors associated with serum CA19-9 levels among healthy children: a cross-sectional study [Internet]. BMC Clinical Pathology. 2012 ; 12( 23): (online).[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1472-6890-12-23
Vancouver
Kawai S, Oba-Shinjo SM, Ito LS, Uno M, Marie SKN, Hamajima N. Factors associated with serum CA19-9 levels among healthy children: a cross-sectional study [Internet]. BMC Clinical Pathology. 2012 ; 12( 23): (online).[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1472-6890-12-23
Artigo de periodico
Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and high plasma homocysteine in chronic hepatitis C (CHC) infected patients from the Northeast of Brazil (2011)
Siqueira, Erika R. F.; Oliveira, Cláudia P. M. S.; Muniz, Maria T. C.; Silva, Filipe; Pereira, Leila M. M. B.; Carrilho, Flair J.
Source: Nutrition Journal. Unidade: FM
Subjects: POLIMORFISMO, FÍGADO GORDUROSO, GENÓTIPOS (ANÁLISE), REGIÃO NORDESTE, HEPATITE CRÔNICA, BRASIL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SIQUEIRA, Erika R. F. et al. Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and high plasma homocysteine in chronic hepatitis C (CHC) infected patients from the Northeast of Brazil. Nutrition Journal, v. 10, n. 86, p. 1-8 (online), 2011Tradução . . Disponível em: https://doi.org/10.1186/1475-2891-10-86. Acesso em: 19 nov. 2024.
APA
Siqueira, E. R. F., Oliveira, C. P. M. S., Muniz, M. T. C., Silva, F., Pereira, L. M. M. B., & Carrilho, F. J. (2011). Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and high plasma homocysteine in chronic hepatitis C (CHC) infected patients from the Northeast of Brazil. Nutrition Journal, 10( 86), 1-8 (online). doi:10.1186/1475-2891-10-86
NLM
Siqueira ERF, Oliveira CPMS, Muniz MTC, Silva F, Pereira LMMB, Carrilho FJ. Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and high plasma homocysteine in chronic hepatitis C (CHC) infected patients from the Northeast of Brazil [Internet]. Nutrition Journal. 2011 ; 10( 86): 1-8 (online).[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1475-2891-10-86
Vancouver
Siqueira ERF, Oliveira CPMS, Muniz MTC, Silva F, Pereira LMMB, Carrilho FJ. Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and high plasma homocysteine in chronic hepatitis C (CHC) infected patients from the Northeast of Brazil [Internet]. Nutrition Journal. 2011 ; 10( 86): 1-8 (online).[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1475-2891-10-86
Artigo de periodico
A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms (2011)
Pereira, Tiago V; Mingroni Netto, Regina Celia
Source: BMC Research Notes. Unidade: IB
Subjects: POLIMORFISMO, GENÉTICA MÉDICA, METANÁLISE, DOENÇA DE ALZHEIMER
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PEREIRA, Tiago V e MINGRONI NETTO, Regina Celia. A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms. BMC Research Notes, v. 4, p. on-line art. 172, 2011Tradução . . Disponível em: https://doi.org/10.1186/1756-0500-4-172. Acesso em: 19 nov. 2024.
APA
Pereira, T. V., & Mingroni Netto, R. C. (2011). A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms. BMC Research Notes, 4, on-line art. 172. doi:10.1186/1756-0500-4-172
NLM
Pereira TV, Mingroni Netto RC. A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms [Internet]. BMC Research Notes. 2011 ; 4 on-line art. 172.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1756-0500-4-172
Vancouver
Pereira TV, Mingroni Netto RC. A note on the use of the generalized odds ratio in meta-analysis of association studies involving bi- and tri-allelic polymorphisms [Internet]. BMC Research Notes. 2011 ; 4 on-line art. 172.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1186/1756-0500-4-172

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