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Artigo de periodico
Predicted deleterious variants in ABCA1, LPL, LPA and KIF6 are associated with statin response and adverse events in patients with familial hypercholesterolemia and disturb protein structure and stability (2024)
Hernandez, Carolina Dagli; Ferreira, Glaucio Monteiro ; Freitas, Renata Caroline Costa de ; Borges, Jéssica Bassani ; Oliveira, Victor Fernandes de; Gonçalves, Rodrigo Marques; Faludi, Andre Arpad; Marçal, Elisangela da Silva Rodrigues; Bastos, Gisele Medeiros ; Bortolin, Raul Hernandes ; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Fonte: Pharmacogenetics and Genomics. Unidades: FCF, IDPC
Assuntos: HIPERCOLESTEROLEMIA, ESTATINAS
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ABNT
HERNANDEZ, Carolina Dagli et al. Predicted deleterious variants in ABCA1, LPL, LPA and KIF6 are associated with statin response and adverse events in patients with familial hypercholesterolemia and disturb protein structure and stability. Pharmacogenetics and Genomics, v. 34, n. 4, p. 91-104, 2024Tradução . . Disponível em: https://dx.doi.org/10.1097/FPC.0000000000000524. Acesso em: 16 nov. 2024.
APA
Hernandez, C. D., Ferreira, G. M., Freitas, R. C. C. de, Borges, J. B., Oliveira, V. F. de, Gonçalves, R. M., et al. (2024). Predicted deleterious variants in ABCA1, LPL, LPA and KIF6 are associated with statin response and adverse events in patients with familial hypercholesterolemia and disturb protein structure and stability. Pharmacogenetics and Genomics, 34( 4), 91-104. doi:10.1097/FPC.0000000000000524
NLM
Hernandez CD, Ferreira GM, Freitas RCC de, Borges JB, Oliveira VF de, Gonçalves RM, Faludi AA, Marçal E da SR, Bastos GM, Bortolin RH, Hirata MH, Hirata RDC. Predicted deleterious variants in ABCA1, LPL, LPA and KIF6 are associated with statin response and adverse events in patients with familial hypercholesterolemia and disturb protein structure and stability [Internet]. Pharmacogenetics and Genomics. 2024 ; 34( 4): 91-104.[citado 2024 nov. 16 ] Available from: https://dx.doi.org/10.1097/FPC.0000000000000524
Vancouver
Hernandez CD, Ferreira GM, Freitas RCC de, Borges JB, Oliveira VF de, Gonçalves RM, Faludi AA, Marçal E da SR, Bastos GM, Bortolin RH, Hirata MH, Hirata RDC. Predicted deleterious variants in ABCA1, LPL, LPA and KIF6 are associated with statin response and adverse events in patients with familial hypercholesterolemia and disturb protein structure and stability [Internet]. Pharmacogenetics and Genomics. 2024 ; 34( 4): 91-104.[citado 2024 nov. 16 ] Available from: https://dx.doi.org/10.1097/FPC.0000000000000524
Artigo de periodico
Increased expression of miR-320b in blood plasma of patients in response to SARS-CoV-2 infection (2024)
Nicoletti, Aline de Souza; Visacri, Marilia Berlofa ; Ronda, Carla Regina da Silva Correa da; Siguemoto, Julia Tiemi; Neri, Carolini Motta; Souza, Rafael Nogueira de ; Ventura, Deise de Souza; Eguti, Adriana; Silva, Lilian Ferreira de Souza; Perroud Junior, Mauricio Wesley ; Buosi, Keini ; Jalalizadeh, Mehrsa ; Dionato, Franciele; Col, Luciana Dal; Giacomelli, Cristiane; Leme, Patrícia; Reis, Leonardo Oliveira ; Santos, Luiz Augusto dos; Durán, Nelson; Fávaro, Wagner José ; Costa, José Luiz da ; Hernandez, Carolina Dagli ; Moriel, Patricia ; Pincinato, Eder de Carvalho
Fonte: Scientific Reports. Unidade: FCF
Assuntos: EPIGÊNESE GENÉTICA, COVID-19
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ABNT
NICOLETTI, Aline de Souza et al. Increased expression of miR-320b in blood plasma of patients in response to SARS-CoV-2 infection. Scientific Reports, v. 14, p. 1-10 art. 13702, 2024Tradução . . Disponível em: https://dx.doi.org/10.1038/s41598-024-64325-9. Acesso em: 16 nov. 2024.
APA
Nicoletti, A. de S., Visacri, M. B., Ronda, C. R. da S. C. da, Siguemoto, J. T., Neri, C. M., Souza, R. N. de, et al. (2024). Increased expression of miR-320b in blood plasma of patients in response to SARS-CoV-2 infection. Scientific Reports, 14, 1-10 art. 13702. doi:10.1038/s41598-024-64325-9
NLM
Nicoletti A de S, Visacri MB, Ronda CR da SC da, Siguemoto JT, Neri CM, Souza RN de, Ventura D de S, Eguti A, Silva LF de S, Perroud Junior MW, Buosi K, Jalalizadeh M, Dionato F, Col LD, Giacomelli C, Leme P, Reis LO, Santos LA dos, Durán N, Fávaro WJ, Costa JL da, Hernandez CD, Moriel P, Pincinato E de C. Increased expression of miR-320b in blood plasma of patients in response to SARS-CoV-2 infection [Internet]. Scientific Reports. 2024 ; 14 1-10 art. 13702.[citado 2024 nov. 16 ] Available from: https://dx.doi.org/10.1038/s41598-024-64325-9
Vancouver
Nicoletti A de S, Visacri MB, Ronda CR da SC da, Siguemoto JT, Neri CM, Souza RN de, Ventura D de S, Eguti A, Silva LF de S, Perroud Junior MW, Buosi K, Jalalizadeh M, Dionato F, Col LD, Giacomelli C, Leme P, Reis LO, Santos LA dos, Durán N, Fávaro WJ, Costa JL da, Hernandez CD, Moriel P, Pincinato E de C. Increased expression of miR-320b in blood plasma of patients in response to SARS-CoV-2 infection [Internet]. Scientific Reports. 2024 ; 14 1-10 art. 13702.[citado 2024 nov. 16 ] Available from: https://dx.doi.org/10.1038/s41598-024-64325-9
Artigo de periodico
Single-nucleotide polymorphisms related to vitamin D metabolism and severity or mortality of COVID-19: a systematic review and meta-analysis (2024)
Ronda, Carla Regina da Silva Corrêa da; Visacri, Marilia Berlofa ; Siguemoto, Júlia Tiemi; Neri, Carolini Motta; Abreu, Micaela Crispim Lopo de; Nicoletti, Aline de Souza; Rotta, Inajara ; Hernandez, Carolina Dagli ; Pincinato, Pedro Moriel; Pincinato, Eder de Carvalho; Moriel, Patricia
Fonte: Gene. Unidade: FCF
Assuntos: POLIMORFISMO, NUCLEOTÍDEOS
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ABNT
RONDA, Carla Regina da Silva Corrêa da et al. Single-nucleotide polymorphisms related to vitamin D metabolism and severity or mortality of COVID-19: a systematic review and meta-analysis. Gene, v. 906, p. 1-17 art. 148236, 2024Tradução . . Disponível em: https://dx.doi.org/10.1016/j.gene.2024.148236. Acesso em: 16 nov. 2024.
APA
Ronda, C. R. da S. C. da, Visacri, M. B., Siguemoto, J. T., Neri, C. M., Abreu, M. C. L. de, Nicoletti, A. de S., et al. (2024). Single-nucleotide polymorphisms related to vitamin D metabolism and severity or mortality of COVID-19: a systematic review and meta-analysis. Gene, 906, 1-17 art. 148236. doi:10.1016/j.gene.2024.148236
NLM
Ronda CR da SC da, Visacri MB, Siguemoto JT, Neri CM, Abreu MCL de, Nicoletti A de S, Rotta I, Hernandez CD, Pincinato PM, Pincinato E de C, Moriel P. Single-nucleotide polymorphisms related to vitamin D metabolism and severity or mortality of COVID-19: a systematic review and meta-analysis [Internet]. Gene. 2024 ; 906 1-17 art. 148236.[citado 2024 nov. 16 ] Available from: https://dx.doi.org/10.1016/j.gene.2024.148236
Vancouver
Ronda CR da SC da, Visacri MB, Siguemoto JT, Neri CM, Abreu MCL de, Nicoletti A de S, Rotta I, Hernandez CD, Pincinato PM, Pincinato E de C, Moriel P. Single-nucleotide polymorphisms related to vitamin D metabolism and severity or mortality of COVID-19: a systematic review and meta-analysis [Internet]. Gene. 2024 ; 906 1-17 art. 148236.[citado 2024 nov. 16 ] Available from: https://dx.doi.org/10.1016/j.gene.2024.148236
Artigo de periodico
Identification of mutations in canine oral mucosal melanomas by exome sequencing and comparison with human melanomas (2024)
Dagli, Maria Lúcia Zaidan ; Lourenço, Sílvia Vanessa ; Nagamine, Márcia Kazumi ; Ikeda, Tatícia Lieh; Fonseca, Ivone Izabel Mackowiak da ; Kremer, Frederico Schmitt; Seixas, Fabiana Kommling; Hernandez, Carolina Dagli ; Leite, João Vitor Pereira; Yasumaru, Cassia Correa; Gomes, Cristina de Oliveira Massoco-Salles ; Hsieh, Ricardo; Collares, Tiago Veiras
Fonte: Scientific Reports. Unidades: FO, FMVZ, FCFRP, BIOTECNOLOGIA, FCF
Assuntos: MELANOMA, MUCOSA ORAL, DOENÇAS DAS GLÂNDULAS SALIVARES, MUTAÇÃO
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ABNT
DAGLI, Maria Lúcia Zaidan et al. Identification of mutations in canine oral mucosal melanomas by exome sequencing and comparison with human melanomas. Scientific Reports, v. 14, 2024Tradução . . Acesso em: 16 nov. 2024.
APA
Dagli, M. L. Z., Lourenço, S. V., Nagamine, M. K., Ikeda, T. L., Fonseca, I. I. M. da, Kremer, F. S., et al. (2024). Identification of mutations in canine oral mucosal melanomas by exome sequencing and comparison with human melanomas. Scientific Reports, 14.
NLM
Dagli MLZ, Lourenço SV, Nagamine MK, Ikeda TL, Fonseca IIM da, Kremer FS, Seixas FK, Hernandez CD, Leite JVP, Yasumaru CC, Gomes C de OM-S, Hsieh R, Collares TV. Identification of mutations in canine oral mucosal melanomas by exome sequencing and comparison with human melanomas. Scientific Reports. 2024 ; 14[citado 2024 nov. 16 ]
Vancouver
Dagli MLZ, Lourenço SV, Nagamine MK, Ikeda TL, Fonseca IIM da, Kremer FS, Seixas FK, Hernandez CD, Leite JVP, Yasumaru CC, Gomes C de OM-S, Hsieh R, Collares TV. Identification of mutations in canine oral mucosal melanomas by exome sequencing and comparison with human melanomas. Scientific Reports. 2024 ; 14[citado 2024 nov. 16 ]
Artigo de periodico
Effects of PCSK9 missense variants on molecular conformation and biological activity in transfected HEK293FT cells (2023)
Los, Bruna ; Ferreira, Glaucio Monteiro ; Borges, Jéssica Bassani ; Kronenberger, Thales ; Oliveira, Victor Fernandes de ; Hernandez, Carolina Dagli ; Bortolin, Raul Hernandes ; Gonçalves, Rodrigo M ; Faludi, André Arpad; Mori, Augusto Akira ; Barbosa, Thais Kristini Almendros; Freitas, Renata Caroline Costa de ; Jannes, Cinthia Elim ; Pereira, Alexandre da Costa; Bastos, Gisele Medeiros ; Poso, Antti ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Fonte: Gene. Unidades: FM, FCF
Assuntos: HIPERCOLESTEROLEMIA, LIPOPROTEÍNAS, MODELAGEM MOLECULAR
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ABNT
LOS, Bruna et al. Effects of PCSK9 missense variants on molecular conformation and biological activity in transfected HEK293FT cells. Gene, v. 851, p. 1-14 art. 146979, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.gene.2022.146979. Acesso em: 16 nov. 2024.
APA
Los, B., Ferreira, G. M., Borges, J. B., Kronenberger, T., Oliveira, V. F. de, Hernandez, C. D., et al. (2023). Effects of PCSK9 missense variants on molecular conformation and biological activity in transfected HEK293FT cells. Gene, 851, 1-14 art. 146979. doi:10.1016/j.gene.2022.146979
NLM
Los B, Ferreira GM, Borges JB, Kronenberger T, Oliveira VF de, Hernandez CD, Bortolin RH, Gonçalves RM, Faludi AA, Mori AA, Barbosa TKA, Freitas RCC de, Jannes CE, Pereira A da C, Bastos GM, Poso A, Hirata RDC, Hirata MH. Effects of PCSK9 missense variants on molecular conformation and biological activity in transfected HEK293FT cells [Internet]. Gene. 2023 ; 851 1-14 art. 146979.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.gene.2022.146979
Vancouver
Los B, Ferreira GM, Borges JB, Kronenberger T, Oliveira VF de, Hernandez CD, Bortolin RH, Gonçalves RM, Faludi AA, Mori AA, Barbosa TKA, Freitas RCC de, Jannes CE, Pereira A da C, Bastos GM, Poso A, Hirata RDC, Hirata MH. Effects of PCSK9 missense variants on molecular conformation and biological activity in transfected HEK293FT cells [Internet]. Gene. 2023 ; 851 1-14 art. 146979.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.gene.2022.146979
Artigo de periodico
In silico analysis of upstream variants in Brazilian patients with Familial hypercholesterolemia (2023)
Araújo, Jéssica Nayara Góes de ; Oliveira, Victor Fernandes de ; Borges, Jéssica Bassani ; Hernandez, Carolina Dagli ; Marçal, Elisangela da Silva Rodrigues; Freitas, Renata Caroline Costa de ; Bastos, Gisele Medeiros ; Gonçalves, Rodrigo Marques; Faludi, André Arpad; Jannes, Cinthia Elim; Pereira, Alexandre da Costa ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki ; Luchessi, André Ducati ; Silbiger, Vivian Nogueira
Fonte: Gene. Unidades: FM, FCF
Assuntos: HIPERCOLESTEROLEMIA, GENOMAS, BIOINFORMÁTICA, NUCLEOTÍDEOS
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ABNT
ARAÚJO, Jéssica Nayara Góes de et al. In silico analysis of upstream variants in Brazilian patients with Familial hypercholesterolemia. Gene, v. 849, p. 1-7 art. 146908, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.gene.2022.146908. Acesso em: 16 nov. 2024.
APA
Araújo, J. N. G. de, Oliveira, V. F. de, Borges, J. B., Hernandez, C. D., Marçal, E. da S. R., Freitas, R. C. C. de, et al. (2023). In silico analysis of upstream variants in Brazilian patients with Familial hypercholesterolemia. Gene, 849, 1-7 art. 146908. doi:10.1016/j.gene.2022.146908
NLM
Araújo JNG de, Oliveira VF de, Borges JB, Hernandez CD, Marçal E da SR, Freitas RCC de, Bastos GM, Gonçalves RM, Faludi AA, Jannes CE, Pereira A da C, Hirata RDC, Hirata MH, Luchessi AD, Silbiger VN. In silico analysis of upstream variants in Brazilian patients with Familial hypercholesterolemia [Internet]. Gene. 2023 ; 849 1-7 art. 146908.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.gene.2022.146908
Vancouver
Araújo JNG de, Oliveira VF de, Borges JB, Hernandez CD, Marçal E da SR, Freitas RCC de, Bastos GM, Gonçalves RM, Faludi AA, Jannes CE, Pereira A da C, Hirata RDC, Hirata MH, Luchessi AD, Silbiger VN. In silico analysis of upstream variants in Brazilian patients with Familial hypercholesterolemia [Internet]. Gene. 2023 ; 849 1-7 art. 146908.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.gene.2022.146908
Artigo de periodico
LDLR missense variants disturb structural conformation and LDLR activity in T-lymphocytes of Familial hypercholesterolemia patients (2023)
Barbosa, Thais Kristini Almendros; Hirata, Rosario Dominguez Crespo ; Ferreira, Glaucio Monteiro ; Borges, Jéssica Bassani ; Oliveira, Victor Fernandes de ; Gorjão, Renata ; Marçal, Elisangela Rodrigues da Silva; Gonçalves, Rodrigo Marques; Faludi, André Arpad; Freitas, Renata Caroline Costa de ; Hernandez, Carolina Dagli ; Bortolin, Raul Hernandes ; Bastos, Gisele Medeiros ; Curi, Tania Cristina Pithon ; Nader, Helena Bonciani; Hirata, Mario Hiroyuki
Fonte: Gene. Unidade: FCF
Assuntos: LINFÓCITOS T, HIPERCOLESTEROLEMIA
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ABNT
BARBOSA, Thais Kristini Almendros et al. LDLR missense variants disturb structural conformation and LDLR activity in T-lymphocytes of Familial hypercholesterolemia patients. Gene, v. 853, p. 1-14 art. 147084, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.gene.2022.147084. Acesso em: 16 nov. 2024.
APA
Barbosa, T. K. A., Hirata, R. D. C., Ferreira, G. M., Borges, J. B., Oliveira, V. F. de, Gorjão, R., et al. (2023). LDLR missense variants disturb structural conformation and LDLR activity in T-lymphocytes of Familial hypercholesterolemia patients. Gene, 853, 1-14 art. 147084. doi:10.1016/j.gene.2022.147084
NLM
Barbosa TKA, Hirata RDC, Ferreira GM, Borges JB, Oliveira VF de, Gorjão R, Marçal ER da S, Gonçalves RM, Faludi AA, Freitas RCC de, Hernandez CD, Bortolin RH, Bastos GM, Curi TCP, Nader HB, Hirata MH. LDLR missense variants disturb structural conformation and LDLR activity in T-lymphocytes of Familial hypercholesterolemia patients [Internet]. Gene. 2023 ; 853 1-14 art. 147084.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.gene.2022.147084
Vancouver
Barbosa TKA, Hirata RDC, Ferreira GM, Borges JB, Oliveira VF de, Gorjão R, Marçal ER da S, Gonçalves RM, Faludi AA, Freitas RCC de, Hernandez CD, Bortolin RH, Bastos GM, Curi TCP, Nader HB, Hirata MH. LDLR missense variants disturb structural conformation and LDLR activity in T-lymphocytes of Familial hypercholesterolemia patients [Internet]. Gene. 2023 ; 853 1-14 art. 147084.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.gene.2022.147084
Artigo de periodico
Lipidomic analysis identified potential predictive biomarkers of statin response in subjects with Familial hypercholesterolemia (2023)
Cerda, Alvaro; Bortolin, Raul Hernandes ; Yoshinaga, Marcos Yukio ; Freitas, Renata Caroline Costa de ; Hernandez, Carolina Dagli; Borges, Jessica Bassani; Oliveira, Victor Fernandes de ; Gonçalves, Rodrigo Marques; Faludi, André Arpad; Bastos, Gisele Medeiros ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Fonte: Chemistry and Physics of Lipids. Unidades: FCF, ICB
Assuntos: BIOMARCADORES, ESTATINAS, HIPERCOLESTEROLEMIA
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ABNT
CERDA, Alvaro et al. Lipidomic analysis identified potential predictive biomarkers of statin response in subjects with Familial hypercholesterolemia. Chemistry and Physics of Lipids, v. 257, p. 1-9 art. 105348, 2023Tradução . . Disponível em: https://dx.doi.org/10.1016/j.chemphyslip.2023.105348. Acesso em: 16 nov. 2024.
APA
Cerda, A., Bortolin, R. H., Yoshinaga, M. Y., Freitas, R. C. C. de, Hernandez, C. D., Borges, J. B., et al. (2023). Lipidomic analysis identified potential predictive biomarkers of statin response in subjects with Familial hypercholesterolemia. Chemistry and Physics of Lipids, 257, 1-9 art. 105348. doi:10.1016/j.chemphyslip.2023.105348
NLM
Cerda A, Bortolin RH, Yoshinaga MY, Freitas RCC de, Hernandez CD, Borges JB, Oliveira VF de, Gonçalves RM, Faludi AA, Bastos GM, Hirata RDC, Hirata MH. Lipidomic analysis identified potential predictive biomarkers of statin response in subjects with Familial hypercholesterolemia [Internet]. Chemistry and Physics of Lipids. 2023 ; 257 1-9 art. 105348.[citado 2024 nov. 16 ] Available from: https://dx.doi.org/10.1016/j.chemphyslip.2023.105348
Vancouver
Cerda A, Bortolin RH, Yoshinaga MY, Freitas RCC de, Hernandez CD, Borges JB, Oliveira VF de, Gonçalves RM, Faludi AA, Bastos GM, Hirata RDC, Hirata MH. Lipidomic analysis identified potential predictive biomarkers of statin response in subjects with Familial hypercholesterolemia [Internet]. Chemistry and Physics of Lipids. 2023 ; 257 1-9 art. 105348.[citado 2024 nov. 16 ] Available from: https://dx.doi.org/10.1016/j.chemphyslip.2023.105348
Artigo de periodico
LDLR and PCSK9 3´UTR variants and their putative effects on microRNA molecular interactions in familial hypercholesterolemia: a computational approach (2023)
Freitas, Renata Caroline Costa de ; Bortolin, Raul Hernandes ; Borges, Jéssica Bassani ; Oliveira, Victor Fernandes de; Hernandez, Carolina Dagli ; Marçal, Elisangela da Silva Rodrigues; Bastos, Gisele Medeiros ; Gonçalves, Rodrigo Marques; Faludi, André Arpad; Silbiger, Vivian Nogueira ; Luchessi, Andre Ducati ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Fonte: Molecular Biology Reports. Unidades: IDPC, FCF
Assuntos: MICRORNAS, HIPERCOLESTEROLEMIA, LIPOPROTEÍNAS LDL
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ABNT
FREITAS, Renata Caroline Costa de et al. LDLR and PCSK9 3´UTR variants and their putative effects on microRNA molecular interactions in familial hypercholesterolemia: a computational approach. Molecular Biology Reports, v. 50, n. 11, p. 9165-9177, 2023Tradução . . Disponível em: https://dx.doi.org/10.1007/s11033-023-08784-9. Acesso em: 16 nov. 2024.
APA
Freitas, R. C. C. de, Bortolin, R. H., Borges, J. B., Oliveira, V. F. de, Hernandez, C. D., Marçal, E. da S. R., et al. (2023). LDLR and PCSK9 3´UTR variants and their putative effects on microRNA molecular interactions in familial hypercholesterolemia: a computational approach. Molecular Biology Reports, 50( 11), 9165-9177. doi:10.1007/s11033-023-08784-9
NLM
Freitas RCC de, Bortolin RH, Borges JB, Oliveira VF de, Hernandez CD, Marçal E da SR, Bastos GM, Gonçalves RM, Faludi AA, Silbiger VN, Luchessi AD, Hirata RDC, Hirata MH. LDLR and PCSK9 3´UTR variants and their putative effects on microRNA molecular interactions in familial hypercholesterolemia: a computational approach [Internet]. Molecular Biology Reports. 2023 ; 50( 11): 9165-9177.[citado 2024 nov. 16 ] Available from: https://dx.doi.org/10.1007/s11033-023-08784-9
Vancouver
Freitas RCC de, Bortolin RH, Borges JB, Oliveira VF de, Hernandez CD, Marçal E da SR, Bastos GM, Gonçalves RM, Faludi AA, Silbiger VN, Luchessi AD, Hirata RDC, Hirata MH. LDLR and PCSK9 3´UTR variants and their putative effects on microRNA molecular interactions in familial hypercholesterolemia: a computational approach [Internet]. Molecular Biology Reports. 2023 ; 50( 11): 9165-9177.[citado 2024 nov. 16 ] Available from: https://dx.doi.org/10.1007/s11033-023-08784-9
Artigo de periodico
Pharmacogenomics of statins: lipid response and other outcomes in Brazilian cohorts (2022)
Hernandez, Carolina Dagli ; Zhou, Yitian; Lauschke, Volker Martin; Genvigir, Fabiana Dalla Vecchia ; Hirata, Thiago Dominguez Crespo ; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Fonte: Pharmacological Reports. Unidade: FCF
Assuntos: ESTATINAS, FARMACOGENÉTICA
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ABNT
HERNANDEZ, Carolina Dagli et al. Pharmacogenomics of statins: lipid response and other outcomes in Brazilian cohorts. Pharmacological Reports, v. 74, p. 47–66, 2022Tradução . . Disponível em: https://doi.org/10.1007/s43440-021-00319-y. Acesso em: 16 nov. 2024.
APA
Hernandez, C. D., Zhou, Y., Lauschke, V. M., Genvigir, F. D. V., Hirata, T. D. C., Hirata, M. H., & Hirata, R. D. C. (2022). Pharmacogenomics of statins: lipid response and other outcomes in Brazilian cohorts. Pharmacological Reports, 74, 47–66. doi:10.1007/s43440-021-00319-y
NLM
Hernandez CD, Zhou Y, Lauschke VM, Genvigir FDV, Hirata TDC, Hirata MH, Hirata RDC. Pharmacogenomics of statins: lipid response and other outcomes in Brazilian cohorts [Internet]. Pharmacological Reports. 2022 ; 74 47–66.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s43440-021-00319-y
Vancouver
Hernandez CD, Zhou Y, Lauschke VM, Genvigir FDV, Hirata TDC, Hirata MH, Hirata RDC. Pharmacogenomics of statins: lipid response and other outcomes in Brazilian cohorts [Internet]. Pharmacological Reports. 2022 ; 74 47–66.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s43440-021-00319-y
Tese (Doutorado)
Pharmacogenomic analysis in patients with familial hypercholesterolemia (2022)
Hernandez, Carolina Dagli ; Hirata, Rosario Dominguez Crespo (Orientador)
Unidade: FCF
Assuntos: FARMACOGENÉTICA, HIPERCOLESTEROLEMIA, ESTATINAS
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ABNT
HERNANDEZ, Carolina Dagli. Pharmacogenomic analysis in patients with familial hypercholesterolemia. 2022. Tese (Doutorado) – Universidade de São Paulo, São Paulo, 2022. Disponível em: https://www.teses.usp.br/teses/disponiveis/9/9142/tde-20052022-121840/. Acesso em: 16 nov. 2024.
APA
Hernandez, C. D. (2022). Pharmacogenomic analysis in patients with familial hypercholesterolemia (Tese (Doutorado). Universidade de São Paulo, São Paulo. Recuperado de https://www.teses.usp.br/teses/disponiveis/9/9142/tde-20052022-121840/
NLM
Hernandez CD. Pharmacogenomic analysis in patients with familial hypercholesterolemia [Internet]. 2022 ;[citado 2024 nov. 16 ] Available from: https://www.teses.usp.br/teses/disponiveis/9/9142/tde-20052022-121840/
Vancouver
Hernandez CD. Pharmacogenomic analysis in patients with familial hypercholesterolemia [Internet]. 2022 ;[citado 2024 nov. 16 ] Available from: https://www.teses.usp.br/teses/disponiveis/9/9142/tde-20052022-121840/
Artigo de periodico
Unraveling the risk factors and etiology of the canine oral mucosal melanoma: results of an epidemiological questionnaire, oral microbiome analysis and investigation of papillomavirus infection (2022)
Carvalho, Joyce Pires de ; Carrilho, Marcella Collaneri; Anjos, Denner Santos dos ; Hernandez, Carolina Dagli ; Sichero, Laura ; Dagli, Maria Lúcia Zaidan
Fonte: Cancers. Unidades: FMVZ, FCF
Assuntos: MELANOMA ANIMAL, PAPILLOMAVIRUS, CÃES, NEOPLASIAS OROFARÍNGEAS, FATORES DE RISCO
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ABNT
CARVALHO, Joyce Pires de et al. Unraveling the risk factors and etiology of the canine oral mucosal melanoma: results of an epidemiological questionnaire, oral microbiome analysis and investigation of papillomavirus infection. Cancers, v. 14, n. 14, p. 1-15, 2022Tradução . . Disponível em: https://doi.org/10.3390/cancers14143397. Acesso em: 16 nov. 2024.
APA
Carvalho, J. P. de, Carrilho, M. C., Anjos, D. S. dos, Hernandez, C. D., Sichero, L., & Dagli, M. L. Z. (2022). Unraveling the risk factors and etiology of the canine oral mucosal melanoma: results of an epidemiological questionnaire, oral microbiome analysis and investigation of papillomavirus infection. Cancers, 14( 14), 1-15. doi:10.3390/cancers14143397
NLM
Carvalho JP de, Carrilho MC, Anjos DS dos, Hernandez CD, Sichero L, Dagli MLZ. Unraveling the risk factors and etiology of the canine oral mucosal melanoma: results of an epidemiological questionnaire, oral microbiome analysis and investigation of papillomavirus infection [Internet]. Cancers. 2022 ; 14( 14): 1-15.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/cancers14143397
Vancouver
Carvalho JP de, Carrilho MC, Anjos DS dos, Hernandez CD, Sichero L, Dagli MLZ. Unraveling the risk factors and etiology of the canine oral mucosal melanoma: results of an epidemiological questionnaire, oral microbiome analysis and investigation of papillomavirus infection [Internet]. Cancers. 2022 ; 14( 14): 1-15.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/cancers14143397
Artigo de periodico
Genetic variant ABCC1 rs45511401 is Associated with increased response to statins in patients with familial hypercholesterolemia (2022)
Hernandez, Carolina Dagli ; Borges, Jéssica Bassani ; Marçal, Elisangela da Silva Rodrigues; Freitas, Renata Caroline Costa de ; Mori, Augusto Akira ; Gonçalves, Rodrigo Marques; Faludi, André Arpad ; Oliveira, Victor Fernandes de ; Ferreira, Glaucio Monteiro ; Bastos, Gisele Medeiros ; Zhou, Yitian ; Lauschke, Volker Martin ; Cerda, Alvaro ; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Fonte: Pharmaceutics. Unidade: FCF
Assuntos: HIPERCOLESTEROLEMIA, ESTATINAS, VARIAÇÃO GENÉTICA, FARMACOGENÉTICA, MEDICAMENTO
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ABNT
HERNANDEZ, Carolina Dagli et al. Genetic variant ABCC1 rs45511401 is Associated with increased response to statins in patients with familial hypercholesterolemia. Pharmaceutics, v. 14, p. 1-20 art. 944, 2022Tradução . . Disponível em: https://doi.org/10.3390/pharmaceutics14050944. Acesso em: 16 nov. 2024.
APA
Hernandez, C. D., Borges, J. B., Marçal, E. da S. R., Freitas, R. C. C. de, Mori, A. A., Gonçalves, R. M., et al. (2022). Genetic variant ABCC1 rs45511401 is Associated with increased response to statins in patients with familial hypercholesterolemia. Pharmaceutics, 14, 1-20 art. 944. doi:10.3390/pharmaceutics14050944
NLM
Hernandez CD, Borges JB, Marçal E da SR, Freitas RCC de, Mori AA, Gonçalves RM, Faludi AA, Oliveira VF de, Ferreira GM, Bastos GM, Zhou Y, Lauschke VM, Cerda A, Hirata MH, Hirata RDC. Genetic variant ABCC1 rs45511401 is Associated with increased response to statins in patients with familial hypercholesterolemia [Internet]. Pharmaceutics. 2022 ; 14 1-20 art. 944.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/pharmaceutics14050944
Vancouver
Hernandez CD, Borges JB, Marçal E da SR, Freitas RCC de, Mori AA, Gonçalves RM, Faludi AA, Oliveira VF de, Ferreira GM, Bastos GM, Zhou Y, Lauschke VM, Cerda A, Hirata MH, Hirata RDC. Genetic variant ABCC1 rs45511401 is Associated with increased response to statins in patients with familial hypercholesterolemia [Internet]. Pharmaceutics. 2022 ; 14 1-20 art. 944.[citado 2024 nov. 16 ] Available from: https://doi.org/10.3390/pharmaceutics14050944
Artigo de periodico
Cardiovascular pharmacogenomics: an update on clinical studies of antithrombotic drugs in Brazilian patients (2021)
Hirata, Thiago Dominguez Crespo ; Hernandez, Carolina Dagli ; Genvigir, Fabiana Dalla Vecchia ; Lauschke, Volker Martin ; Zhou, Yitian ; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Fonte: Molecular Diagnosis and Therapy. Unidade: FCF
Assuntos: ANTICOAGULANTES, DOENÇAS CARDIOVASCULARES, TROMBOSE
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ABNT
HIRATA, Thiago Dominguez Crespo et al. Cardiovascular pharmacogenomics: an update on clinical studies of antithrombotic drugs in Brazilian patients. Molecular Diagnosis and Therapy, v. 25, p. 735–755, 2021Tradução . . Disponível em: https://doi.org/10.1007/s40291-021-00549-z. Acesso em: 16 nov. 2024.
APA
Hirata, T. D. C., Hernandez, C. D., Genvigir, F. D. V., Lauschke, V. M., Zhou, Y., Hirata, M. H., & Hirata, R. D. C. (2021). Cardiovascular pharmacogenomics: an update on clinical studies of antithrombotic drugs in Brazilian patients. Molecular Diagnosis and Therapy, 25, 735–755. doi:10.1007/s40291-021-00549-z
NLM
Hirata TDC, Hernandez CD, Genvigir FDV, Lauschke VM, Zhou Y, Hirata MH, Hirata RDC. Cardiovascular pharmacogenomics: an update on clinical studies of antithrombotic drugs in Brazilian patients [Internet]. Molecular Diagnosis and Therapy. 2021 ; 25 735–755.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s40291-021-00549-z
Vancouver
Hirata TDC, Hernandez CD, Genvigir FDV, Lauschke VM, Zhou Y, Hirata MH, Hirata RDC. Cardiovascular pharmacogenomics: an update on clinical studies of antithrombotic drugs in Brazilian patients [Internet]. Molecular Diagnosis and Therapy. 2021 ; 25 735–755.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1007/s40291-021-00549-z
Artigo de periodico
Functional analysis of PCSK9 3'UTR variants and mRNA-miRNA interactions in patients with familial hypercholesterolemia (2021)
Los, Bruna ; Borges, Jéssica Bassani ; Oliveira, Victor Fernandes de ; Freitas, Renata Caroline Costa de ; Hernandez, Carolina Dagli ; Bortolin, Raul Hernandes ; Gonçalves, Rodrigo M ; Faludi, André Arpad ; Rodrigues, Alice Cristina ; Bastos, Gisele Medeiros ; Jannes, Cinthia Elim ; Pereira , Alexandre C ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Fonte: Epigenomics. Unidades: IDPC, ICB, FCF
Assuntos: HIPERCOLESTEROLEMIA, MICRORNAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOS, Bruna et al. Functional analysis of PCSK9 3'UTR variants and mRNA-miRNA interactions in patients with familial hypercholesterolemia. Epigenomics, v. 13, n. 10, p. 779–791, 2021Tradução . . Disponível em: https://doi.org/10.2217/epi-2020-0462. Acesso em: 16 nov. 2024.
APA
Los, B., Borges, J. B., Oliveira, V. F. de, Freitas, R. C. C. de, Hernandez, C. D., Bortolin, R. H., et al. (2021). Functional analysis of PCSK9 3'UTR variants and mRNA-miRNA interactions in patients with familial hypercholesterolemia. Epigenomics, 13( 10), 779–791. doi:10.2217/epi-2020-0462
NLM
Los B, Borges JB, Oliveira VF de, Freitas RCC de, Hernandez CD, Bortolin RH, Gonçalves RM, Faludi AA, Rodrigues AC, Bastos GM, Jannes CE, Pereira AC, Hirata RDC, Hirata MH. Functional analysis of PCSK9 3'UTR variants and mRNA-miRNA interactions in patients with familial hypercholesterolemia [Internet]. Epigenomics. 2021 ; 13( 10): 779–791.[citado 2024 nov. 16 ] Available from: https://doi.org/10.2217/epi-2020-0462
Vancouver
Los B, Borges JB, Oliveira VF de, Freitas RCC de, Hernandez CD, Bortolin RH, Gonçalves RM, Faludi AA, Rodrigues AC, Bastos GM, Jannes CE, Pereira AC, Hirata RDC, Hirata MH. Functional analysis of PCSK9 3'UTR variants and mRNA-miRNA interactions in patients with familial hypercholesterolemia [Internet]. Epigenomics. 2021 ; 13( 10): 779–791.[citado 2024 nov. 16 ] Available from: https://doi.org/10.2217/epi-2020-0462
Trabalho de evento
Proposta de medicina personalizada utilizando perfil farmacogenético em pacientes idosos usuários de varfarina (2021)
Rodrigues, Vitor Pitta; Araujo, Neire Niara Ferreira de; Bastos, Gisele Medeiros ; Hernandez, Carolina Dagli ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Fonte: Posters. Nome do evento: Reunião Anual da SBPC (Virtual). Unidade: FCF
Assuntos: ANTICOAGULANTES, POLIMORFISMO, GENÉTICA, FARMACOGENÉTICA, IDOSOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RODRIGUES, Vitor Pitta et al. Proposta de medicina personalizada utilizando perfil farmacogenético em pacientes idosos usuários de varfarina. 2021, Anais.. São Paulo: SBPC, 2021. Disponível em: https://reunioes.sbpcnet.org.br/73RA/inscritos/resumos/10242_1f340f1b1f65b6df5b5e3f94d95b11daf.pdf. Acesso em: 16 nov. 2024.
APA
Rodrigues, V. P., Araujo, N. N. F. de, Bastos, G. M., Hernandez, C. D., Hirata, R. D. C., & Hirata, M. H. (2021). Proposta de medicina personalizada utilizando perfil farmacogenético em pacientes idosos usuários de varfarina. In Posters. São Paulo: SBPC. Recuperado de https://reunioes.sbpcnet.org.br/73RA/inscritos/resumos/10242_1f340f1b1f65b6df5b5e3f94d95b11daf.pdf
NLM
Rodrigues VP, Araujo NNF de, Bastos GM, Hernandez CD, Hirata RDC, Hirata MH. Proposta de medicina personalizada utilizando perfil farmacogenético em pacientes idosos usuários de varfarina [Internet]. Posters. 2021 ;[citado 2024 nov. 16 ] Available from: https://reunioes.sbpcnet.org.br/73RA/inscritos/resumos/10242_1f340f1b1f65b6df5b5e3f94d95b11daf.pdf
Vancouver
Rodrigues VP, Araujo NNF de, Bastos GM, Hernandez CD, Hirata RDC, Hirata MH. Proposta de medicina personalizada utilizando perfil farmacogenético em pacientes idosos usuários de varfarina [Internet]. Posters. 2021 ;[citado 2024 nov. 16 ] Available from: https://reunioes.sbpcnet.org.br/73RA/inscritos/resumos/10242_1f340f1b1f65b6df5b5e3f94d95b11daf.pdf
Artigo de periodico
Genomics, epigenomics and pharmacogenomics of familial hypercholesterolemia (FHBGEP): a study protocol (2021)
Borges, Jéssica Bassani ; Oliveira, Victor Fernandes de ; Ferreira, Glaucio Monteiro ; Los, Bruna; Barbosa, Thais Kristini Almendros Afonso; Marçal, Elisangela da Silva Rodrigues; Hernandez, Carolina Dagli; Freitas, Renata Caroline Costa de ; Bortolin, Raul Hernandes ; Mori, Augusto Akira ; Hirata, Thiago Dominguez Crespo ; Nakaya, Helder Takashi Imoto ; Bastos, Gisele Medeiros ; Thurow, Helena Strelow ; Gonçalves, Rodrigo Marques; Araújo, Daniel Branco de; Zatz, Henry Paulo; Bertolami, Adriana; Faludi, André Arpad; Bertolami, Marcelo Chiara ; Sousa, Amanda Guerra de Moraes Rego ; França, Joao Italo Dias ; Jannes, Cinthia Elim; Pereira, Alexandre da Costa; Nakazone, Marcelo Arruda; Souza, Dorotéia Rossi Silva; Carmo, Tayanne Silva; Sampaio, Marcelo Ferraz; Gorjão, Renata ; Curi, Tania Cristina Pithon ; Moriel, Patricia; Silbiger, Vivian Nogueira ; Luchessi, André Ducati ; Araújo, Jéssica Nayara Góes de; Naslavsky, Michel ; Wang, Jaqueline Yu Ting; Kronenberger, Thales ; Cerda, Alvaro ; Wang, Hui Tzu Lin; Garofalo, Adriana Regina; Fajardo, Cristina Moreno ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Fonte: Research in Social and Administrative Pharmacy. Unidades: FCF, IDPC, FM, IB
Assuntos: GENÔMICA, HIPERCOLESTEROLEMIA, FARMACOGENÉTICA, EXONS, LINFÓCITOS, LINHAGEM CELULAR, MUTAGÊNESE, SEQUENCIAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BORGES, Jéssica Bassani et al. Genomics, epigenomics and pharmacogenomics of familial hypercholesterolemia (FHBGEP): a study protocol. Research in Social and Administrative Pharmacy, v. 17, n. 7, p. 1347-1355, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.sapharm.2020.10.007. Acesso em: 16 nov. 2024.
APA
Borges, J. B., Oliveira, V. F. de, Ferreira, G. M., Los, B., Barbosa, T. K. A. A., Marçal, E. da S. R., et al. (2021). Genomics, epigenomics and pharmacogenomics of familial hypercholesterolemia (FHBGEP): a study protocol. Research in Social and Administrative Pharmacy, 17( 7), 1347-1355. doi:10.1016/j.sapharm.2020.10.007
NLM
Borges JB, Oliveira VF de, Ferreira GM, Los B, Barbosa TKAA, Marçal E da SR, Hernandez CD, Freitas RCC de, Bortolin RH, Mori AA, Hirata TDC, Nakaya HTI, Bastos GM, Thurow HS, Gonçalves RM, Araújo DB de, Zatz HP, Bertolami A, Faludi AA, Bertolami MC, Sousa AG de MR, França JID, Jannes CE, Pereira A da C, Nakazone MA, Souza DRS, Carmo TS, Sampaio MF, Gorjão R, Curi TCP, Moriel P, Silbiger VN, Luchessi AD, Araújo JNG de, Naslavsky M, Wang JYT, Kronenberger T, Cerda A, Wang HTL, Garofalo AR, Fajardo CM, Hirata RDC, Hirata MH. Genomics, epigenomics and pharmacogenomics of familial hypercholesterolemia (FHBGEP): a study protocol [Internet]. Research in Social and Administrative Pharmacy. 2021 ; 17( 7): 1347-1355.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.sapharm.2020.10.007
Vancouver
Borges JB, Oliveira VF de, Ferreira GM, Los B, Barbosa TKAA, Marçal E da SR, Hernandez CD, Freitas RCC de, Bortolin RH, Mori AA, Hirata TDC, Nakaya HTI, Bastos GM, Thurow HS, Gonçalves RM, Araújo DB de, Zatz HP, Bertolami A, Faludi AA, Bertolami MC, Sousa AG de MR, França JID, Jannes CE, Pereira A da C, Nakazone MA, Souza DRS, Carmo TS, Sampaio MF, Gorjão R, Curi TCP, Moriel P, Silbiger VN, Luchessi AD, Araújo JNG de, Naslavsky M, Wang JYT, Kronenberger T, Cerda A, Wang HTL, Garofalo AR, Fajardo CM, Hirata RDC, Hirata MH. Genomics, epigenomics and pharmacogenomics of familial hypercholesterolemia (FHBGEP): a study protocol [Internet]. Research in Social and Administrative Pharmacy. 2021 ; 17( 7): 1347-1355.[citado 2024 nov. 16 ] Available from: https://doi.org/10.1016/j.sapharm.2020.10.007
Artigo de periodico
Functional analysis of PCSK9 3′UTR variants and mRNA–miRNA interactions in patients with familial hypercholesterolemia (2021)
Los, Bruna ; Borges, Jéssica Bassani ; Oliveira, Victor Fernandes de ; Freitas, Renata Carolina Costa de ; Hernandez, Carolina Dagli ; Bortolin, Raul Hernandes ; Gonçalves, Rodrigo M. ; Faludi, André A. ; Bastos, Gisele M. ; Jannes, Cinthia E. ; Pereira, Alexandre C. ; Rodrigues, Alice Cristina ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Fonte: Epigenomics. Unidades: ICB, FCF
Assuntos: FARMACOLOGIA, HIPERCOLESTEROLEMIA, VARIAÇÃO GENÉTICA, MICRORNAS, ENVELHECIMENTO, RNA MENSAGEIRO, EPIGÊNESE GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOS, Bruna et al. Functional analysis of PCSK9 3′UTR variants and mRNA–miRNA interactions in patients with familial hypercholesterolemia. Epigenomics, v. 13, n. 10, p. 779–791, 2021Tradução . . Disponível em: https://doi.org/10.2217/epi-2020-0462. Acesso em: 16 nov. 2024.
APA
Los, B., Borges, J. B., Oliveira, V. F. de, Freitas, R. C. C. de, Hernandez, C. D., Bortolin, R. H., et al. (2021). Functional analysis of PCSK9 3′UTR variants and mRNA–miRNA interactions in patients with familial hypercholesterolemia. Epigenomics, 13( 10), 779–791. doi:10.2217/epi-2020-0462
NLM
Los B, Borges JB, Oliveira VF de, Freitas RCC de, Hernandez CD, Bortolin RH, Gonçalves RM, Faludi AA, Bastos GM, Jannes CE, Pereira AC, Rodrigues AC, Hirata RDC, Hirata MH. Functional analysis of PCSK9 3′UTR variants and mRNA–miRNA interactions in patients with familial hypercholesterolemia [Internet]. Epigenomics. 2021 ; 13( 10): 779–791.[citado 2024 nov. 16 ] Available from: https://doi.org/10.2217/epi-2020-0462
Vancouver
Los B, Borges JB, Oliveira VF de, Freitas RCC de, Hernandez CD, Bortolin RH, Gonçalves RM, Faludi AA, Bastos GM, Jannes CE, Pereira AC, Rodrigues AC, Hirata RDC, Hirata MH. Functional analysis of PCSK9 3′UTR variants and mRNA–miRNA interactions in patients with familial hypercholesterolemia [Internet]. Epigenomics. 2021 ; 13( 10): 779–791.[citado 2024 nov. 16 ] Available from: https://doi.org/10.2217/epi-2020-0462
Artigo de periodico
Late response to rosuvastatin and statin-related myalgia due to SLCO1B1, SLCO1B3, ABCB11, and CYP3A5 variants in a patient with familial hypercholesterolemia: a case report (2021)
Hernandez, Carolina Dagli; Freitas, Renata Caroline Costa de ; Marçal, Elisangela da Silva Rodrigues; Gonçalves, Rodrigo Marques; Faludi, André Arpad; Borges, Jéssica Bassani ; Bastos, Gisele Medeiros ; Los, Bruna; Mori, Augusto Akira ; Bortolin, Raul Hernandes ; Ferreira, Glaucio Monteiro ; Oliveira, Victor Fernandes de ; Hirata, Thiago Dominguez Crespo ; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Fonte: Annals of Translational Medicine. Unidades: IDPC, FCF
Assuntos: HIPERCOLESTEROLEMIA, ESTATINAS, FARMACOGENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
HERNANDEZ, Carolina Dagli et al. Late response to rosuvastatin and statin-related myalgia due to SLCO1B1, SLCO1B3, ABCB11, and CYP3A5 variants in a patient with familial hypercholesterolemia: a case report. Annals of Translational Medicine, v. 9, n. 1, p. 1-8 art. 76, 2021Tradução . . Disponível em: https://doi.org/10.21037/atm-20-5540. Acesso em: 16 nov. 2024.
APA
Hernandez, C. D., Freitas, R. C. C. de, Marçal, E. da S. R., Gonçalves, R. M., Faludi, A. A., Borges, J. B., et al. (2021). Late response to rosuvastatin and statin-related myalgia due to SLCO1B1, SLCO1B3, ABCB11, and CYP3A5 variants in a patient with familial hypercholesterolemia: a case report. Annals of Translational Medicine, 9( 1), 1-8 art. 76. doi:10.21037/atm-20-5540
NLM
Hernandez CD, Freitas RCC de, Marçal E da SR, Gonçalves RM, Faludi AA, Borges JB, Bastos GM, Los B, Mori AA, Bortolin RH, Ferreira GM, Oliveira VF de, Hirata TDC, Hirata MH, Hirata RDC. Late response to rosuvastatin and statin-related myalgia due to SLCO1B1, SLCO1B3, ABCB11, and CYP3A5 variants in a patient with familial hypercholesterolemia: a case report [Internet]. Annals of Translational Medicine. 2021 ; 9( 1): 1-8 art. 76.[citado 2024 nov. 16 ] Available from: https://doi.org/10.21037/atm-20-5540
Vancouver
Hernandez CD, Freitas RCC de, Marçal E da SR, Gonçalves RM, Faludi AA, Borges JB, Bastos GM, Los B, Mori AA, Bortolin RH, Ferreira GM, Oliveira VF de, Hirata TDC, Hirata MH, Hirata RDC. Late response to rosuvastatin and statin-related myalgia due to SLCO1B1, SLCO1B3, ABCB11, and CYP3A5 variants in a patient with familial hypercholesterolemia: a case report [Internet]. Annals of Translational Medicine. 2021 ; 9( 1): 1-8 art. 76.[citado 2024 nov. 16 ] Available from: https://doi.org/10.21037/atm-20-5540
Trabalho de evento-resumo
miRNA predictive profile based on , and 3'UTR variants as potential biomarker for familial hypercholesterolemia (2019)
Freitas, Renata Caroline Costa de ; Bortolin, Raul Hernandes ; Borges, Jéssica Bassani; Los, Bruna; Hernandez, Carolina Dagli; Mori, Augusto Akira ; Oliveira, V. F; Ferreira, Glaucio Monteiro; Marçal, Elisangela da Silva Rodrigues; Bastos, G. M.; Fajardo, Cristina Moreno ; Gonçalves, R. M; Faludi, André Arpad; Luchessi, André Ducati; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Fonte: Abstracts. Nome do evento: American Association for Clinical Chemistry/AACC. Unidade: FCF
Assuntos: HIPERCOLESTEROLEMIA, BIOMARCADORES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FREITAS, Renata Caroline Costa de et al. miRNA predictive profile based on , and 3'UTR variants as potential biomarker for familial hypercholesterolemia. 2019, Anais.. Washington: AACC, 2019. . Acesso em: 16 nov. 2024.
APA
Freitas, R. C. C. de, Bortolin, R. H., Borges, J. B., Los, B., Hernandez, C. D., Mori, A. A., et al. (2019). miRNA predictive profile based on , and 3'UTR variants as potential biomarker for familial hypercholesterolemia. In Abstracts. Washington: AACC.
NLM
Freitas RCC de, Bortolin RH, Borges JB, Los B, Hernandez CD, Mori AA, Oliveira VF, Ferreira GM, Marçal E da SR, Bastos GM, Fajardo CM, Gonçalves RM, Faludi AA, Luchessi AD, Hirata RDC, Hirata MH. miRNA predictive profile based on , and 3'UTR variants as potential biomarker for familial hypercholesterolemia. Abstracts. 2019 ;[citado 2024 nov. 16 ]
Vancouver
Freitas RCC de, Bortolin RH, Borges JB, Los B, Hernandez CD, Mori AA, Oliveira VF, Ferreira GM, Marçal E da SR, Bastos GM, Fajardo CM, Gonçalves RM, Faludi AA, Luchessi AD, Hirata RDC, Hirata MH. miRNA predictive profile based on , and 3'UTR variants as potential biomarker for familial hypercholesterolemia. Abstracts. 2019 ;[citado 2024 nov. 16 ]

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