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Artigo de periodico
Diagnostic prediction model for levodopa-induced dyskinesia in Parkinson’s disease (2020)
Santos-Lobato, Bruno Lopes; SCHUMACHER-SCHUH, Artur F.; Rieder, Carlos R. M.; Hutz, Mara H.; Borges, Vanderci; Ferraz, Henrique Ballalai; Mata, Ignacio F.; Zabetian, Cyrus P.; Tumas, Vitor
Source: Arquivos de Neuro-Psiquiatria. Unidade: FMRP
Subjects: DISCINESIAS, DOENÇA DE PARKINSON, POLIMORFISMO
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ABNT
SANTOS-LOBATO, Bruno Lopes et al. Diagnostic prediction model for levodopa-induced dyskinesia in Parkinson’s disease. Arquivos de Neuro-Psiquiatria, v. 78, n. 4, p. 206-216, 2020Tradução . . Disponível em: https://doi.org/10.1590/0004-282X20190191. Acesso em: 10 nov. 2024.
APA
Santos-Lobato, B. L., SCHUMACHER-SCHUH, A. F., Rieder, C. R. M., Hutz, M. H., Borges, V., Ferraz, H. B., et al. (2020). Diagnostic prediction model for levodopa-induced dyskinesia in Parkinson’s disease. Arquivos de Neuro-Psiquiatria, 78( 4), 206-216. doi:10.1590/0004-282X20190191
NLM
Santos-Lobato BL, SCHUMACHER-SCHUH AF, Rieder CRM, Hutz MH, Borges V, Ferraz HB, Mata IF, Zabetian CP, Tumas V. Diagnostic prediction model for levodopa-induced dyskinesia in Parkinson’s disease [Internet]. Arquivos de Neuro-Psiquiatria. 2020 ; 78( 4): 206-216.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1590/0004-282X20190191
Vancouver
Santos-Lobato BL, SCHUMACHER-SCHUH AF, Rieder CRM, Hutz MH, Borges V, Ferraz HB, Mata IF, Zabetian CP, Tumas V. Diagnostic prediction model for levodopa-induced dyskinesia in Parkinson’s disease [Internet]. Arquivos de Neuro-Psiquiatria. 2020 ; 78( 4): 206-216.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1590/0004-282X20190191
Artigo de periodico
Appetite effects of prefrontal stimulation depend on COMT Val158Met polymorphism: a randomized clinical trial (2019)
Fassini, Priscila Giacomo ; Das, Sai Krupa; Suen, Vivian Marques Miguel; Magerowski, Greta; Marchini, Julio Sergio ; Silva Junior, Wilson Araújo da ; Changyu, Shen; Alonso-Alonso, Miguel
Source: Appetite. Unidade: FMRP
Subjects: POLIMORFISMO, NEUROTRANSMISSORES, APETITE
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ABNT
FASSINI, Priscila Giacomo et al. Appetite effects of prefrontal stimulation depend on COMT Val158Met polymorphism: a randomized clinical trial. Appetite, v. 140, p. 142-150, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.appet.2019.05.015. Acesso em: 10 nov. 2024.
APA
Fassini, P. G., Das, S. K., Suen, V. M. M., Magerowski, G., Marchini, J. S., Silva Junior, W. A. da, et al. (2019). Appetite effects of prefrontal stimulation depend on COMT Val158Met polymorphism: a randomized clinical trial. Appetite, 140, 142-150. doi:10.1016/j.appet.2019.05.015
NLM
Fassini PG, Das SK, Suen VMM, Magerowski G, Marchini JS, Silva Junior WA da, Changyu S, Alonso-Alonso M. Appetite effects of prefrontal stimulation depend on COMT Val158Met polymorphism: a randomized clinical trial [Internet]. Appetite. 2019 ; 140 142-150.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.appet.2019.05.015
Vancouver
Fassini PG, Das SK, Suen VMM, Magerowski G, Marchini JS, Silva Junior WA da, Changyu S, Alonso-Alonso M. Appetite effects of prefrontal stimulation depend on COMT Val158Met polymorphism: a randomized clinical trial [Internet]. Appetite. 2019 ; 140 142-150.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.appet.2019.05.015
Artigo de periodico
Polymorphisms in TLR4 and TNFA and risk of mycobacterium tuberculosis mnfection and development of active disease in contacts of tuberculosis cases in Brazil: a prospective cohort study (2019)
Cubillos-Angulo, Juan Manuel; Arriaga, María B.; Silva, Elisângela C.; Müller, Beatriz L. A.; Ramalho, Daniela M. P.; Fukutani, Kiyoshi F.; Miranda, Pryscila F. C.; Moreira, Adriana S. R.; Ruffino Netto, Antônio; Silva, Jose R. Lapa e; Sterling, Timothy R.; Kritski, Afrânio L.; Oliveira, Martha M.; Andrade, Bruno B.
Source: Clinical Infectious Disease. Unidade: FMRP
Subjects: POLIMORFISMO, MYCOBACTERIUM TUBERCULOSIS, NECROSE, TUBERCULOSE
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ABNT
CUBILLOS-ANGULO, Juan Manuel et al. Polymorphisms in TLR4 and TNFA and risk of mycobacterium tuberculosis mnfection and development of active disease in contacts of tuberculosis cases in Brazil: a prospective cohort study. Clinical Infectious Disease, 2019Tradução . . Disponível em: https://doi.org/10.1093/cid/ciy1001/5204461. Acesso em: 10 nov. 2024.
APA
Cubillos-Angulo, J. M., Arriaga, M. B., Silva, E. C., Müller, B. L. A., Ramalho, D. M. P., Fukutani, K. F., et al. (2019). Polymorphisms in TLR4 and TNFA and risk of mycobacterium tuberculosis mnfection and development of active disease in contacts of tuberculosis cases in Brazil: a prospective cohort study. Clinical Infectious Disease. doi:10.1093/cid/ciy1001/5204461
NLM
Cubillos-Angulo JM, Arriaga MB, Silva EC, Müller BLA, Ramalho DMP, Fukutani KF, Miranda PFC, Moreira ASR, Ruffino Netto A, Silva JRL e, Sterling TR, Kritski AL, Oliveira MM, Andrade BB. Polymorphisms in TLR4 and TNFA and risk of mycobacterium tuberculosis mnfection and development of active disease in contacts of tuberculosis cases in Brazil: a prospective cohort study [Internet]. Clinical Infectious Disease. 2019 ;[citado 2024 nov. 10 ] Available from: https://doi.org/10.1093/cid/ciy1001/5204461
Vancouver
Cubillos-Angulo JM, Arriaga MB, Silva EC, Müller BLA, Ramalho DMP, Fukutani KF, Miranda PFC, Moreira ASR, Ruffino Netto A, Silva JRL e, Sterling TR, Kritski AL, Oliveira MM, Andrade BB. Polymorphisms in TLR4 and TNFA and risk of mycobacterium tuberculosis mnfection and development of active disease in contacts of tuberculosis cases in Brazil: a prospective cohort study [Internet]. Clinical Infectious Disease. 2019 ;[citado 2024 nov. 10 ] Available from: https://doi.org/10.1093/cid/ciy1001/5204461
Artigo de periodico
Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study (2019)
Hoang, Thanh T.; Manso, Paulo Henrique ; Edman, Sharon; Mercer-Rosa, Laura; Mitchell, Laura E.; Sewda, Anshuman; Swartz, Michael D.; Fogel, Mark A.; Agopian, A. J.; Goldmuntz, Elizabeth
Source: Journal of Cardiovascular Magnetic Resonance. Unidade: FMRP
Subjects: RESSONÂNCIA MAGNÉTICA, CARDIOPATIAS, CARDIOPATIAS CONGÊNITAS, GENÉTICA, VENTRÍCULO CARDÍACO, POLIMORFISMO
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ABNT
HOANG, Thanh T. et al. Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study. Journal of Cardiovascular Magnetic Resonance, v. 21, n. 1, p. art. 51 [10], 2019Tradução . . Disponível em: https://doi.org/10.1186/s12968-019-0555-2. Acesso em: 10 nov. 2024.
APA
Hoang, T. T., Manso, P. H., Edman, S., Mercer-Rosa, L., Mitchell, L. E., Sewda, A., et al. (2019). Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study. Journal of Cardiovascular Magnetic Resonance, 21( 1), art. 51 [10]. doi:10.1186/s12968-019-0555-2
NLM
Hoang TT, Manso PH, Edman S, Mercer-Rosa L, Mitchell LE, Sewda A, Swartz MD, Fogel MA, Agopian AJ, Goldmuntz E. Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study [Internet]. Journal of Cardiovascular Magnetic Resonance. 2019 ; 21( 1): art. 51 [10].[citado 2024 nov. 10 ] Available from: https://doi.org/10.1186/s12968-019-0555-2
Vancouver
Hoang TT, Manso PH, Edman S, Mercer-Rosa L, Mitchell LE, Sewda A, Swartz MD, Fogel MA, Agopian AJ, Goldmuntz E. Genetic variants of HIF1α are associated with right ventricular fibrotic load in repaired tetralogy of Fallot patients: a cardiovascular magnetic resonance study [Internet]. Journal of Cardiovascular Magnetic Resonance. 2019 ; 21( 1): art. 51 [10].[citado 2024 nov. 10 ] Available from: https://doi.org/10.1186/s12968-019-0555-2
Artigo de periodico
HLA-G polymorphisms are associated with non-segmental vitiligo among Brazilians (2019)
Castelli, Luciana Caricati Veiga ; Oliveira, Maria Luiza Guimarães de ; Pereira, Álison Luís Eburnêo; Debortoli, Guilherme ; Marcorin, Letícia ; Fracasso, Nádia Carolina de Aguiar; Silva, Guilherme do Valle; Souza, Andréia da Silva; Massaro, Juliana Doblas ; Simões, Aguinaldo Luiz ; Sabbagh, Audrey; Cardili, Renata Nahas; Donadi, Eduardo Antônio ; Castelli, Erick da Cruz; Mendes-Junior, Celso Teixeira
Source: Biomolecules. Unidades: FMRP, FFCLRP
Subjects: ANTÍGENOS HLA, VITILIGO, POLIMORFISMO, SEQUÊNCIA DO DNA, AUTOIMUNIDADE, GENES
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ABNT
CASTELLI, Luciana Caricati Veiga et al. HLA-G polymorphisms are associated with non-segmental vitiligo among Brazilians. Biomolecules, v. 9, n. 9, p. [10] , 2019Tradução . . Disponível em: https://doi.org/10.3390/biom9090463. Acesso em: 10 nov. 2024.
APA
Castelli, L. C. V., Oliveira, M. L. G. de, Pereira, Á. L. E., Debortoli, G., Marcorin, L., Fracasso, N. C. de A., et al. (2019). HLA-G polymorphisms are associated with non-segmental vitiligo among Brazilians. Biomolecules, 9( 9), [10] . doi:10.3390/biom9090463
NLM
Castelli LCV, Oliveira MLG de, Pereira ÁLE, Debortoli G, Marcorin L, Fracasso NC de A, Silva G do V, Souza A da S, Massaro JD, Simões AL, Sabbagh A, Cardili RN, Donadi EA, Castelli E da C, Mendes-Junior CT. HLA-G polymorphisms are associated with non-segmental vitiligo among Brazilians [Internet]. Biomolecules. 2019 ; 9( 9): [10] .[citado 2024 nov. 10 ] Available from: https://doi.org/10.3390/biom9090463
Vancouver
Castelli LCV, Oliveira MLG de, Pereira ÁLE, Debortoli G, Marcorin L, Fracasso NC de A, Silva G do V, Souza A da S, Massaro JD, Simões AL, Sabbagh A, Cardili RN, Donadi EA, Castelli E da C, Mendes-Junior CT. HLA-G polymorphisms are associated with non-segmental vitiligo among Brazilians [Internet]. Biomolecules. 2019 ; 9( 9): [10] .[citado 2024 nov. 10 ] Available from: https://doi.org/10.3390/biom9090463
Artigo de periodico
Pharmacogenetics-based population pharmacokinetic analysis of gabapentin in patients with chronic pain: effect of OCT2 and OCTN1 gene polymorphisms (2019)
Yamamoto, Priscila A.; Benzi, Jhohann Richard de Lima ; Azeredo, Francine J.; Dach, Fabiola; Ianhez Júnior, Edgar; Zanelli, Cleslei F.; Moraes, Natália V. de
Source: Basic and Clinical Pharmacology and Toxicology. Unidade: FMRP
Subjects: FARMACOGENÉTICA, GENÉTICA, POLIMORFISMO, FARMACOCINÉTICA
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ABNT
YAMAMOTO, Priscila A. et al. Pharmacogenetics-based population pharmacokinetic analysis of gabapentin in patients with chronic pain: effect of OCT2 and OCTN1 gene polymorphisms. Basic and Clinical Pharmacology and Toxicology, v. 124, n. 3, p. 266-272, 2019Tradução . . Disponível em: https://doi.org/10.1111/bcpt.13126. Acesso em: 10 nov. 2024.
APA
Yamamoto, P. A., Benzi, J. R. de L., Azeredo, F. J., Dach, F., Ianhez Júnior, E., Zanelli, C. F., & Moraes, N. V. de. (2019). Pharmacogenetics-based population pharmacokinetic analysis of gabapentin in patients with chronic pain: effect of OCT2 and OCTN1 gene polymorphisms. Basic and Clinical Pharmacology and Toxicology, 124( 3), 266-272. doi:10.1111/bcpt.13126
NLM
Yamamoto PA, Benzi JR de L, Azeredo FJ, Dach F, Ianhez Júnior E, Zanelli CF, Moraes NV de. Pharmacogenetics-based population pharmacokinetic analysis of gabapentin in patients with chronic pain: effect of OCT2 and OCTN1 gene polymorphisms [Internet]. Basic and Clinical Pharmacology and Toxicology. 2019 ; 124( 3): 266-272.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1111/bcpt.13126
Vancouver
Yamamoto PA, Benzi JR de L, Azeredo FJ, Dach F, Ianhez Júnior E, Zanelli CF, Moraes NV de. Pharmacogenetics-based population pharmacokinetic analysis of gabapentin in patients with chronic pain: effect of OCT2 and OCTN1 gene polymorphisms [Internet]. Basic and Clinical Pharmacology and Toxicology. 2019 ; 124( 3): 266-272.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1111/bcpt.13126
Artigo de periodico
The genetic diversity within the 1.4 kb HLA-G 5′ upstream regulatory region moderately impacts on cellular microenvironment responses (2018)
Dias, Fabrício César; Bertol, Bruna Cristina ; Poras, Isabelle; Souto, Bruno M.; Mendes Júnior, Celso Teixeira ; Castelli, Erick C.; Gineau, Laure; Sabbagh, Audrey; Rouas-Freiss, Nathalie; Carosella, Edgardo D.; Donadi, Eduardo Antônio ; Moreau, Philippe
Source: Scientific Reports. Unidades: FFCLRP, FMRP
Subjects: DIVERSIDADE GENÉTICA, POLIMORFISMO, EXPRESSÃO GÊNICA, DOENÇAS AUTOIMUNES
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ABNT
DIAS, Fabrício César et al. The genetic diversity within the 1.4 kb HLA-G 5′ upstream regulatory region moderately impacts on cellular microenvironment responses. Scientific Reports, v. 8, n. 1, 2018Tradução . . Disponível em: https://doi.org/10.1038/s41598-018-24009-7. Acesso em: 10 nov. 2024.
APA
Dias, F. C., Bertol, B. C., Poras, I., Souto, B. M., Mendes Júnior, C. T., Castelli, E. C., et al. (2018). The genetic diversity within the 1.4 kb HLA-G 5′ upstream regulatory region moderately impacts on cellular microenvironment responses. Scientific Reports, 8( 1). doi:10.1038/s41598-018-24009-7
NLM
Dias FC, Bertol BC, Poras I, Souto BM, Mendes Júnior CT, Castelli EC, Gineau L, Sabbagh A, Rouas-Freiss N, Carosella ED, Donadi EA, Moreau P. The genetic diversity within the 1.4 kb HLA-G 5′ upstream regulatory region moderately impacts on cellular microenvironment responses [Internet]. Scientific Reports. 2018 ; 8( 1):[citado 2024 nov. 10 ] Available from: https://doi.org/10.1038/s41598-018-24009-7
Vancouver
Dias FC, Bertol BC, Poras I, Souto BM, Mendes Júnior CT, Castelli EC, Gineau L, Sabbagh A, Rouas-Freiss N, Carosella ED, Donadi EA, Moreau P. The genetic diversity within the 1.4 kb HLA-G 5′ upstream regulatory region moderately impacts on cellular microenvironment responses [Internet]. Scientific Reports. 2018 ; 8( 1):[citado 2024 nov. 10 ] Available from: https://doi.org/10.1038/s41598-018-24009-7
Artigo de periodico
Association of ACE ID and ACTN3 C>T genetic polymorphisms with response to a multicomponent training program in physical performance in women from 50 to 70 years (2018)
Moraes, Vitor Nolasco de ; Trapé, Átila Alexandre ; Ferezin, Letícia Perticarrara; Gonçalves, Thiago Correa Porto ; Monteiro, Cristina Paula ; Bueno Júnior, Carlos Roberto
Source: Science & Sports. Unidades: PUSP-RP, EEFERP, FMRP
Subjects: EXERCÍCIO FÍSICO, ENVELHECIMENTO, POLIMORFISMO
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ABNT
MORAES, Vitor Nolasco de et al. Association of ACE ID and ACTN3 C>T genetic polymorphisms with response to a multicomponent training program in physical performance in women from 50 to 70 years. Science & Sports, v. 33, n. 5, p. 282-290, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.scispo.2018.03.077. Acesso em: 10 nov. 2024.
APA
Moraes, V. N. de, Trapé, Á. A., Ferezin, L. P., Gonçalves, T. C. P., Monteiro, C. P., & Bueno Júnior, C. R. (2018). Association of ACE ID and ACTN3 C>T genetic polymorphisms with response to a multicomponent training program in physical performance in women from 50 to 70 years. Science & Sports, 33( 5), 282-290. doi:10.1016/j.scispo.2018.03.077
NLM
Moraes VN de, Trapé ÁA, Ferezin LP, Gonçalves TCP, Monteiro CP, Bueno Júnior CR. Association of ACE ID and ACTN3 C>T genetic polymorphisms with response to a multicomponent training program in physical performance in women from 50 to 70 years [Internet]. Science & Sports. 2018 ; 33( 5): 282-290.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.scispo.2018.03.077
Vancouver
Moraes VN de, Trapé ÁA, Ferezin LP, Gonçalves TCP, Monteiro CP, Bueno Júnior CR. Association of ACE ID and ACTN3 C>T genetic polymorphisms with response to a multicomponent training program in physical performance in women from 50 to 70 years [Internet]. Science & Sports. 2018 ; 33( 5): 282-290.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.scispo.2018.03.077
Artigo de periodico
Genetic association between HLA-G 14-bp polymorphism and diseases: a systematic review and meta-analysis (2018)
Almeida, Bibiana Sgorla de ; Muniz, Yara Costa Netto ; Prompt, Alice Heidrich; Castelli, Erick C. ; Mendes Júnior, Celso Teixeira ; Donadi, Eduardo Antônio
Source: Human Immunology. Unidades: FFCLRP, FMRP
Subjects: POLIMORFISMO, ALELOS, LÚPUS ERITEMATOSO SISTÊMICO, MUTAÇÃO
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ABNT
ALMEIDA, Bibiana Sgorla de et al. Genetic association between HLA-G 14-bp polymorphism and diseases: a systematic review and meta-analysis. Human Immunology, v. 79, n. 10, p. 724-735, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.humimm.2018.08.003. Acesso em: 10 nov. 2024.
APA
Almeida, B. S. de, Muniz, Y. C. N., Prompt, A. H., Castelli, E. C., Mendes Júnior, C. T., & Donadi, E. A. (2018). Genetic association between HLA-G 14-bp polymorphism and diseases: a systematic review and meta-analysis. Human Immunology, 79( 10), 724-735. doi:10.1016/j.humimm.2018.08.003
NLM
Almeida BS de, Muniz YCN, Prompt AH, Castelli EC, Mendes Júnior CT, Donadi EA. Genetic association between HLA-G 14-bp polymorphism and diseases: a systematic review and meta-analysis [Internet]. Human Immunology. 2018 ; 79( 10): 724-735.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.humimm.2018.08.003
Vancouver
Almeida BS de, Muniz YCN, Prompt AH, Castelli EC, Mendes Júnior CT, Donadi EA. Genetic association between HLA-G 14-bp polymorphism and diseases: a systematic review and meta-analysis [Internet]. Human Immunology. 2018 ; 79( 10): 724-735.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.humimm.2018.08.003
Artigo de periodico
Hla-mapper: an application to optimize the mapping of HLA sequences produced by massively parallel sequencing procedures (2018)
Castelli, Erick C. ; Paz, Michelle A.; Souza, Andréia S.; Ramalho, Jaqueline; Mendes Júnior, Celso Teixeira
Source: Human Immunology. Unidade: FFCLRP
Subjects: MAPEAMENTO GENÉTICO, SEQUENCIAMENTO GENÉTICO, POLIMORFISMO, ALGORITMOS, GENOMAS, ANÁLISE DE SEQUÊNCIA DE DNA
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ABNT
CASTELLI, Erick C. et al. Hla-mapper: an application to optimize the mapping of HLA sequences produced by massively parallel sequencing procedures. Human Immunology, v. 79, n. 9, p. 678-684, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.humimm.2018.06.010. Acesso em: 10 nov. 2024.
APA
Castelli, E. C., Paz, M. A., Souza, A. S., Ramalho, J., & Mendes Júnior, C. T. (2018). Hla-mapper: an application to optimize the mapping of HLA sequences produced by massively parallel sequencing procedures. Human Immunology, 79( 9), 678-684. doi:10.1016/j.humimm.2018.06.010
NLM
Castelli EC, Paz MA, Souza AS, Ramalho J, Mendes Júnior CT. Hla-mapper: an application to optimize the mapping of HLA sequences produced by massively parallel sequencing procedures [Internet]. Human Immunology. 2018 ; 79( 9): 678-684.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.humimm.2018.06.010
Vancouver
Castelli EC, Paz MA, Souza AS, Ramalho J, Mendes Júnior CT. Hla-mapper: an application to optimize the mapping of HLA sequences produced by massively parallel sequencing procedures [Internet]. Human Immunology. 2018 ; 79( 9): 678-684.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.humimm.2018.06.010
Artigo de periodico
The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeries (2017)
Costa, A. C. C.; Coelho, Eduardo Barbosa; Lanchote, Vera Lúcia; Correia, B. V.; Abumansur, Juliana Trench; Lauretti, Gabriela Rocha; Moraes, N. V. de
Source: European Journal of Clinical Pharmacology. Unidades: FMRP, FCFRP
Subjects: FARMACOGENÉTICA, FARMACOCINÉTICA, POLIMORFISMO, BLOQUEIO NERVOSO
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ABNT
COSTA, A. C. C. et al. The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeries. European Journal of Clinical Pharmacology, v. 73, n. 8, p. 957-963, 2017Tradução . . Disponível em: https://doi.org/10.1007/s00228-017-2243-1. Acesso em: 10 nov. 2024.
APA
Costa, A. C. C., Coelho, E. B., Lanchote, V. L., Correia, B. V., Abumansur, J. T., Lauretti, G. R., & Moraes, N. V. de. (2017). The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeries. European Journal of Clinical Pharmacology, 73( 8), 957-963. doi:10.1007/s00228-017-2243-1
NLM
Costa ACC, Coelho EB, Lanchote VL, Correia BV, Abumansur JT, Lauretti GR, Moraes NV de. The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeries [Internet]. European Journal of Clinical Pharmacology. 2017 ; 73( 8): 957-963.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1007/s00228-017-2243-1
Vancouver
Costa ACC, Coelho EB, Lanchote VL, Correia BV, Abumansur JT, Lauretti GR, Moraes NV de. The SLCO1A2 -189_-188InsA polymorphism reduces clearance of rocuronium in patients submitted to elective surgeries [Internet]. European Journal of Clinical Pharmacology. 2017 ; 73( 8): 957-963.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1007/s00228-017-2243-1
Artigo de periodico
Relationship between asymmetric dimethylarginine, nitrite and genetic polymorphisms: impact on erectile dysfunction therapy (2017)
Azevedo, Ana Maria Milanez; Brites-Anselmi, Guilhermo; Pinheiro, Lucas Cezar; Belo, Vanessa de Almeida; Coeli-Lacchini, Fernanda Borchers; Molina, Carlos Augusto Fernandes; Andrade, Murilo Ferreira de; Tucci Júnior, Silvio; Hirsch, Emilio; Tanus-Santos, José Eduardo; Lacchini, Riccardo
Source: Nitric Oxide. Unidades: FMRP, EERP
Subjects: ARGININA, BIOMARCADORES, DISFUNÇÃO ERÉTIL, POLIMORFISMO
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ABNT
AZEVEDO, Ana Maria Milanez et al. Relationship between asymmetric dimethylarginine, nitrite and genetic polymorphisms: impact on erectile dysfunction therapy. Nitric Oxide, v. 71, p. 44-51, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.niox.2017.10.006. Acesso em: 10 nov. 2024.
APA
Azevedo, A. M. M., Brites-Anselmi, G., Pinheiro, L. C., Belo, V. de A., Coeli-Lacchini, F. B., Molina, C. A. F., et al. (2017). Relationship between asymmetric dimethylarginine, nitrite and genetic polymorphisms: impact on erectile dysfunction therapy. Nitric Oxide, 71, 44-51. doi:10.1016/j.niox.2017.10.006
NLM
Azevedo AMM, Brites-Anselmi G, Pinheiro LC, Belo V de A, Coeli-Lacchini FB, Molina CAF, Andrade MF de, Tucci Júnior S, Hirsch E, Tanus-Santos JE, Lacchini R. Relationship between asymmetric dimethylarginine, nitrite and genetic polymorphisms: impact on erectile dysfunction therapy [Internet]. Nitric Oxide. 2017 ; 71 44-51.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.niox.2017.10.006
Vancouver
Azevedo AMM, Brites-Anselmi G, Pinheiro LC, Belo V de A, Coeli-Lacchini FB, Molina CAF, Andrade MF de, Tucci Júnior S, Hirsch E, Tanus-Santos JE, Lacchini R. Relationship between asymmetric dimethylarginine, nitrite and genetic polymorphisms: impact on erectile dysfunction therapy [Internet]. Nitric Oxide. 2017 ; 71 44-51.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.niox.2017.10.006
Artigo de periodico
HLA-E regulatory and coding region variability and haplotypes in a Brazilian population sample (2017)
Ramalho, Jaqueline; Veiga-Castelli, Luciana C.; Donadi, Eduardo Antônio; Mendes Júnior, Celso Teixeira; Castelli, Erick C.
Source: Molecular Immunology. Unidades: FMRP, FFCLRP
Subjects: HAPLOTIPOS, POLIMORFISMO, ANTÍGENOS HLA, VARIAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAMALHO, Jaqueline et al. HLA-E regulatory and coding region variability and haplotypes in a Brazilian population sample. Molecular Immunology, v. 91, p. 173-184, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.molimm.2017.09.007. Acesso em: 10 nov. 2024.
APA
Ramalho, J., Veiga-Castelli, L. C., Donadi, E. A., Mendes Júnior, C. T., & Castelli, E. C. (2017). HLA-E regulatory and coding region variability and haplotypes in a Brazilian population sample. Molecular Immunology, 91, 173-184. doi:10.1016/j.molimm.2017.09.007
NLM
Ramalho J, Veiga-Castelli LC, Donadi EA, Mendes Júnior CT, Castelli EC. HLA-E regulatory and coding region variability and haplotypes in a Brazilian population sample [Internet]. Molecular Immunology. 2017 ; 91 173-184.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.molimm.2017.09.007
Vancouver
Ramalho J, Veiga-Castelli LC, Donadi EA, Mendes Júnior CT, Castelli EC. HLA-E regulatory and coding region variability and haplotypes in a Brazilian population sample [Internet]. Molecular Immunology. 2017 ; 91 173-184.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.molimm.2017.09.007
Artigo de periodico
HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus (2017)
Castelli, Erick C.; Gerasimou, Petroula; Paz, Michelle A.; Ramalho, Jaqueline; Porto, Iane O. P.; Lima, Thálitta H. A.; Souza, Andréia S.; Veiga-Castelli, Luciana C.; Collares, Cristhianna V. A.; Donadi, Eduardo Antonio; Mendes-Junior, Celso Teixeira; Paul Costeas
Source: Molecular Immunology. Unidades: FMRP, FFCLRP
Subjects: HAPLOTIPOS, POLIMORFISMO, BIOINFORMÁTICA, ANTÍGENOS HLA, REAÇÃO EM CADEIA POR POLIMERASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTELLI, Erick C. et al. HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus. Molecular Immunology, v. 83, p. 115-126, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.molimm.2017.01.020. Acesso em: 10 nov. 2024.
APA
Castelli, E. C., Gerasimou, P., Paz, M. A., Ramalho, J., Porto, I. O. P., Lima, T. H. A., et al. (2017). HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus. Molecular Immunology, 83, 115-126. doi:10.1016/j.molimm.2017.01.020
NLM
Castelli EC, Gerasimou P, Paz MA, Ramalho J, Porto IOP, Lima THA, Souza AS, Veiga-Castelli LC, Collares CVA, Donadi EA, Mendes-Junior CT, Paul Costeas. HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus [Internet]. Molecular Immunology. 2017 ; 83 115-126.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.molimm.2017.01.020
Vancouver
Castelli EC, Gerasimou P, Paz MA, Ramalho J, Porto IOP, Lima THA, Souza AS, Veiga-Castelli LC, Collares CVA, Donadi EA, Mendes-Junior CT, Paul Costeas. HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus [Internet]. Molecular Immunology. 2017 ; 83 115-126.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1016/j.molimm.2017.01.020
Artigo de periodico
Genetic polymorphism in MMP9 may be associated with anterior open bite in children (2017)
Küchler, Erika Calvano; Barreiros, Driely; Silva, Raphaela Oliveira da; Abreu, Júlia Guimarães Barcellos de; Teixeira, Ellen Cardoso; Silva, Raquel Assed Bezerra da; Silva, Léa Assed Bezerra da; Nelson Filho, Paulo; Romano, Fábio Lourenço; Granjeiro, José Mauro; Antunes, Lívia Azeredo Alves; Antunes, Leonardo Santos
Source: Brazilian Dental Journal. Unidade: FORP
Subjects: POLIMORFISMO, MALOCLUSÃO, MORDIDA ABERTA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KÜCHLER, Erika Calvano et al. Genetic polymorphism in MMP9 may be associated with anterior open bite in children. Brazilian Dental Journal, v. 28, n. 3, p. 277-280, 2017Tradução . . Disponível em: https://doi.org/10.1590/0103-6440201600992. Acesso em: 10 nov. 2024.
APA
Küchler, E. C., Barreiros, D., Silva, R. O. da, Abreu, J. G. B. de, Teixeira, E. C., Silva, R. A. B. da, et al. (2017). Genetic polymorphism in MMP9 may be associated with anterior open bite in children. Brazilian Dental Journal, 28( 3), 277-280. doi:10.1590/0103-6440201600992
NLM
Küchler EC, Barreiros D, Silva RO da, Abreu JGB de, Teixeira EC, Silva RAB da, Silva LAB da, Nelson Filho P, Romano FL, Granjeiro JM, Antunes LAA, Antunes LS. Genetic polymorphism in MMP9 may be associated with anterior open bite in children [Internet]. Brazilian Dental Journal. 2017 ; 28( 3): 277-280.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1590/0103-6440201600992
Vancouver
Küchler EC, Barreiros D, Silva RO da, Abreu JGB de, Teixeira EC, Silva RAB da, Silva LAB da, Nelson Filho P, Romano FL, Granjeiro JM, Antunes LAA, Antunes LS. Genetic polymorphism in MMP9 may be associated with anterior open bite in children [Internet]. Brazilian Dental Journal. 2017 ; 28( 3): 277-280.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1590/0103-6440201600992
Artigo de periodico
Interleukin-10 rs2227307 and CXCR2 rs1126579 polymorphisms modulate the predisposition to septic shock (2015)
Cardoso, Cristina Padre; Oliveira, Argenil José de Assis de; Botoni, Fernando Antônio; Rezende, Isabela Cristina Porto; Alves Filho, José Carlos Farias; Cunha, Fernando de Queiroz; Estanislau, Juliana de Assis Silva Gomes; Magno, Luiz Alexandre Viana; Rios-Santos, Fabricio
Source: Memórias do Instituto Oswaldo Cruz. Unidade: FMRP
Subjects: RECEPTORES IMUNOLÓGICOS, CHOQUE SÉPTICO (GENÉTICA), INTERLEUCINA 8, INTERLEUCINA-10, POLIMORFISMO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARDOSO, Cristina Padre et al. Interleukin-10 rs2227307 and CXCR2 rs1126579 polymorphisms modulate the predisposition to septic shock. Memórias do Instituto Oswaldo Cruz, v. 110, n. 4, p. 453-460, 2015Tradução . . Disponível em: https://doi.org/10.1590/0074-02760150003. Acesso em: 10 nov. 2024.
APA
Cardoso, C. P., Oliveira, A. J. de A. de, Botoni, F. A., Rezende, I. C. P., Alves Filho, J. C. F., Cunha, F. de Q., et al. (2015). Interleukin-10 rs2227307 and CXCR2 rs1126579 polymorphisms modulate the predisposition to septic shock. Memórias do Instituto Oswaldo Cruz, 110( 4), 453-460. doi:10.1590/0074-02760150003
NLM
Cardoso CP, Oliveira AJ de A de, Botoni FA, Rezende ICP, Alves Filho JCF, Cunha F de Q, Estanislau J de ASG, Magno LAV, Rios-Santos F. Interleukin-10 rs2227307 and CXCR2 rs1126579 polymorphisms modulate the predisposition to septic shock [Internet]. Memórias do Instituto Oswaldo Cruz. 2015 ; 110( 4): 453-460.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1590/0074-02760150003
Vancouver
Cardoso CP, Oliveira AJ de A de, Botoni FA, Rezende ICP, Alves Filho JCF, Cunha F de Q, Estanislau J de ASG, Magno LAV, Rios-Santos F. Interleukin-10 rs2227307 and CXCR2 rs1126579 polymorphisms modulate the predisposition to septic shock [Internet]. Memórias do Instituto Oswaldo Cruz. 2015 ; 110( 4): 453-460.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1590/0074-02760150003
Artigo de periodico
Mito-nuclear discordance with evidence of shared ancestral polymorphism and selection in cactophilic species of Drosophila (2015)
Franco, Fernando F; Lavagnini, Taís C; Sene, Fábio de Melo; Manfrin, Maura Helena
Source: Biological Journal of the Linnean Society. Unidade: FFCLRP
Subjects: DROSOPHILA, POLIMORFISMO, MARCADOR MOLECULAR
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ABNT
FRANCO, Fernando F et al. Mito-nuclear discordance with evidence of shared ancestral polymorphism and selection in cactophilic species of Drosophila. Biological Journal of the Linnean Society, v. 116, n. 1, p. 197-210, 2015Tradução . . Disponível em: https://doi.org/10.1111/bij.12554. Acesso em: 10 nov. 2024.
APA
Franco, F. F., Lavagnini, T. C., Sene, F. de M., & Manfrin, M. H. (2015). Mito-nuclear discordance with evidence of shared ancestral polymorphism and selection in cactophilic species of Drosophila. Biological Journal of the Linnean Society, 116( 1), 197-210. doi:10.1111/bij.12554
NLM
Franco FF, Lavagnini TC, Sene F de M, Manfrin MH. Mito-nuclear discordance with evidence of shared ancestral polymorphism and selection in cactophilic species of Drosophila [Internet]. Biological Journal of the Linnean Society. 2015 ; 116( 1): 197-210.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1111/bij.12554
Vancouver
Franco FF, Lavagnini TC, Sene F de M, Manfrin MH. Mito-nuclear discordance with evidence of shared ancestral polymorphism and selection in cactophilic species of Drosophila [Internet]. Biological Journal of the Linnean Society. 2015 ; 116( 1): 197-210.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1111/bij.12554
Artigo de periodico
LIG4 and RAD52 DNA repair genes polymorphisms and systemic lupus erythematosus (2014)
Silva, Jaqueline De Azevêdo; Pancotto, João Alexandre Trés; Donadi, Eduardo Antônio; Crovella, Sergio; Sandrin-Garcia, Paula
Source: Molecular Biology Reports. Unidade: FMRP
Subjects: LÚPUS ERITEMATOSO SISTÊMICO (DIAGNÓSTICO;GENÉTICA), POLIMORFISMO, REPARAÇÃO DE DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Jaqueline De Azevêdo et al. LIG4 and RAD52 DNA repair genes polymorphisms and systemic lupus erythematosus. Molecular Biology Reports, v. 41, n. 4, p. 2249-2256, 2014Tradução . . Disponível em: https://doi.org/10.1007/s11033-014-3076-y. Acesso em: 10 nov. 2024.
APA
Silva, J. D. A., Pancotto, J. A. T., Donadi, E. A., Crovella, S., & Sandrin-Garcia, P. (2014). LIG4 and RAD52 DNA repair genes polymorphisms and systemic lupus erythematosus. Molecular Biology Reports, 41( 4), 2249-2256. doi:10.1007/s11033-014-3076-y
NLM
Silva JDA, Pancotto JAT, Donadi EA, Crovella S, Sandrin-Garcia P. LIG4 and RAD52 DNA repair genes polymorphisms and systemic lupus erythematosus [Internet]. Molecular Biology Reports. 2014 ; 41( 4): 2249-2256.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1007/s11033-014-3076-y
Vancouver
Silva JDA, Pancotto JAT, Donadi EA, Crovella S, Sandrin-Garcia P. LIG4 and RAD52 DNA repair genes polymorphisms and systemic lupus erythematosus [Internet]. Molecular Biology Reports. 2014 ; 41( 4): 2249-2256.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1007/s11033-014-3076-y
Artigo de periodico
Genetic identification of ricketsial isolates from fatal cases of Brazilian spotted fever, and comparison with Rickettsia rickettsii isolates from the American continent (2014)
Labruna, Marcelo Bahia ; Santos, Fabiana Cristina Pereira dos; Ogrzewalska, Maria; Nascimento, Elvira M. M.; Colombo, Silvia; Marcili, Arlei; Angerami, Rodrigo Nogueira
Source: Journal of Clinical Microbiology. Unidade: FMVZ
Subjects: FEBRE MACULOSA, GENÉTICA BACTERIANA, POLIMORFISMO, RICKETTSIALES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LABRUNA, Marcelo Bahia et al. Genetic identification of ricketsial isolates from fatal cases of Brazilian spotted fever, and comparison with Rickettsia rickettsii isolates from the American continent. Journal of Clinical Microbiology, v. 52, n. 10, p. 3788-3791, 2014Tradução . . Disponível em: https://doi.org/10.1128/JCM.01914-14. Acesso em: 10 nov. 2024.
APA
Labruna, M. B., Santos, F. C. P. dos, Ogrzewalska, M., Nascimento, E. M. M., Colombo, S., Marcili, A., & Angerami, R. N. (2014). Genetic identification of ricketsial isolates from fatal cases of Brazilian spotted fever, and comparison with Rickettsia rickettsii isolates from the American continent. Journal of Clinical Microbiology, 52( 10), 3788-3791. doi:10.1128/JCM.01914-14
NLM
Labruna MB, Santos FCP dos, Ogrzewalska M, Nascimento EMM, Colombo S, Marcili A, Angerami RN. Genetic identification of ricketsial isolates from fatal cases of Brazilian spotted fever, and comparison with Rickettsia rickettsii isolates from the American continent [Internet]. Journal of Clinical Microbiology. 2014 ; 52( 10): 3788-3791.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1128/JCM.01914-14
Vancouver
Labruna MB, Santos FCP dos, Ogrzewalska M, Nascimento EMM, Colombo S, Marcili A, Angerami RN. Genetic identification of ricketsial isolates from fatal cases of Brazilian spotted fever, and comparison with Rickettsia rickettsii isolates from the American continent [Internet]. Journal of Clinical Microbiology. 2014 ; 52( 10): 3788-3791.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1128/JCM.01914-14
Artigo de periodico
Role of RET genetic variants in MEN2-associated pheochromocytoma (2014)
Siqueira, Débora Rodrigues; Ceolin, Luciele; Ferreira, Carla Vaz; Romitti, Mírian; Maia, Silvana Cavalcante; Maciel, Léa Maria Zanini; Maia, Ana Luiza
Source: European Journal of Endocrinology. Unidade: FMRP
Subjects: NEOPLASIAS EPITELIAIS E GLANDULARES, NEOPLASIA ENDÓCRINA MÚLTIPLA, FEOCROMOCITOMA, POLIMORFISMO, PROTEÍNAS PROTO-ONCOGÊNICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SIQUEIRA, Débora Rodrigues et al. Role of RET genetic variants in MEN2-associated pheochromocytoma. European Journal of Endocrinology, v. 170, n. 6, p. 821-828, 2014Tradução . . Disponível em: https://doi.org/10.1530/EJE-14-0084. Acesso em: 10 nov. 2024.
APA
Siqueira, D. R., Ceolin, L., Ferreira, C. V., Romitti, M., Maia, S. C., Maciel, L. M. Z., & Maia, A. L. (2014). Role of RET genetic variants in MEN2-associated pheochromocytoma. European Journal of Endocrinology, 170( 6), 821-828. doi:10.1530/EJE-14-0084
NLM
Siqueira DR, Ceolin L, Ferreira CV, Romitti M, Maia SC, Maciel LMZ, Maia AL. Role of RET genetic variants in MEN2-associated pheochromocytoma [Internet]. European Journal of Endocrinology. 2014 ; 170( 6): 821-828.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1530/EJE-14-0084
Vancouver
Siqueira DR, Ceolin L, Ferreira CV, Romitti M, Maia SC, Maciel LMZ, Maia AL. Role of RET genetic variants in MEN2-associated pheochromocytoma [Internet]. European Journal of Endocrinology. 2014 ; 170( 6): 821-828.[citado 2024 nov. 10 ] Available from: https://doi.org/10.1530/EJE-14-0084

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