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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
Source: Pharmacogenetics and Genomics. Unidades: FCF, IDPC
Subjects: HIPERCOLESTEROLEMIA, ESTATINAS
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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: 30 jun. 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 jun. 30 ] 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 jun. 30 ] Available from: https://dx.doi.org/10.1097/FPC.0000000000000524
Artigo de periodico
Effects of LDLR variants rs5928, rs750518671 and rs879254797 on protein structure and functional activity in HepG2 cells transfected with CRISPR/ Cas9 constructs (2024)
Mori, Augusto Akira ; Malaquias, Vanessa Barbosa ; Bonjour, Kennedy ; Ferreira, Glaucio Monteiro ; Bortolin, Raul Hernandes ; Borges, Jéssica Bassani ; Oliveira, Victor Fernandes de ; Gonçalves, Rodrigo Marques; Faludi, Andre Arpad; Bastos, Gisele Monteiro; Thurow, Helena; Sampaio, Marcelo Ferraz; Ciconelli, Rozana Mesquita; Cury, Adriano Namo; Fajardo, Cristina Moreno ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Source: Gene. Unidades: FCF, ICB
Subjects: HIPERCOLESTEROLEMIA, RECEPTORES DE LDL
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MORI, Augusto Akira et al. Effects of LDLR variants rs5928, rs750518671 and rs879254797 on protein structure and functional activity in HepG2 cells transfected with CRISPR/ Cas9 constructs. Gene, v. 890, p. 1-12 art. 147821, 2024Tradução . . Disponível em: https://doi.org/10.1016/j.gene.2023.147821. Acesso em: 30 jun. 2024.
APA
Mori, A. A., Malaquias, V. B., Bonjour, K., Ferreira, G. M., Bortolin, R. H., Borges, J. B., et al. (2024). Effects of LDLR variants rs5928, rs750518671 and rs879254797 on protein structure and functional activity in HepG2 cells transfected with CRISPR/ Cas9 constructs. Gene, 890, 1-12 art. 147821. doi:10.1016/j.gene.2023.147821
NLM
Mori AA, Malaquias VB, Bonjour K, Ferreira GM, Bortolin RH, Borges JB, Oliveira VF de, Gonçalves RM, Faludi AA, Bastos GM, Thurow H, Sampaio MF, Ciconelli RM, Cury AN, Fajardo CM, Hirata RDC, Hirata MH. Effects of LDLR variants rs5928, rs750518671 and rs879254797 on protein structure and functional activity in HepG2 cells transfected with CRISPR/ Cas9 constructs [Internet]. Gene. 2024 ; 890 1-12 art. 147821.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.gene.2023.147821
Vancouver
Mori AA, Malaquias VB, Bonjour K, Ferreira GM, Bortolin RH, Borges JB, Oliveira VF de, Gonçalves RM, Faludi AA, Bastos GM, Thurow H, Sampaio MF, Ciconelli RM, Cury AN, Fajardo CM, Hirata RDC, Hirata MH. Effects of LDLR variants rs5928, rs750518671 and rs879254797 on protein structure and functional activity in HepG2 cells transfected with CRISPR/ Cas9 constructs [Internet]. Gene. 2024 ; 890 1-12 art. 147821.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.gene.2023.147821
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
Source: Gene. Unidades: FM, FCF
Subjects: HIPERCOLESTEROLEMIA, LIPOPROTEÍNAS, MODELAGEM MOLECULAR
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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: 30 jun. 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 jun. 30 ] 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 jun. 30 ] 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
Source: Gene. Unidades: FM, FCF
Subjects: HIPERCOLESTEROLEMIA, GENOMAS, BIOINFORMÁTICA, NUCLEOTÍDEOS
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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: 30 jun. 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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.1016/j.gene.2022.146908
Artigo de periodico
Identification of pathogenic variants in the Brazilian cohort with familial hypercholesterolemia using exon-targeted gene sequencing (2023)
Borges, Jéssica Bassani ; Oliveira, Victor Fernandes de ; Dagli-Hernandez, Carolina; Ferreira, Glaucio Monteiro ; Barbosa, Thais Kristini Almendros Afonso; Marçal, Elisangela da Silva Rodrigues; Los, Bruna ; Malaquias, Vanessa Barbosa ; Bortolin, Raul Hernandes ; Freitas, Renata Caroline Costa de ; Mori, Augusto Akira ; Hirata, Thiago Dominguez Crespo ; Nakaya, Helder Takashi Imoto ; Jannes, Cinthia Elim ; Pereira, Alexandre da Costa ; Wang, Jaqueline Yu Ting; Naslavsky, Michel ; Fajardo, Cristina Moreno ; Hirata, Rosario Dominguez Crespo
Source: Gene. Unidades: FCF, FM, IB, BIOINFORMÁTICA
Subjects: HIPERCOLESTEROLEMIA, GENOMAS, SEQUENCIAMENTO GENÉTICO
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BORGES, Jéssica Bassani et al. Identification of pathogenic variants in the Brazilian cohort with familial hypercholesterolemia using exon-targeted gene sequencing. Gene, v. 875, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.gene.2023.147501. Acesso em: 30 jun. 2024.
APA
Borges, J. B., Oliveira, V. F. de, Dagli-Hernandez, C., Ferreira, G. M., Barbosa, T. K. A. A., Marçal, E. da S. R., et al. (2023). Identification of pathogenic variants in the Brazilian cohort with familial hypercholesterolemia using exon-targeted gene sequencing. Gene, 875. doi:10.1016/j.gene.2023.147501
NLM
Borges JB, Oliveira VF de, Dagli-Hernandez C, Ferreira GM, Barbosa TKAA, Marçal E da SR, Los B, Malaquias VB, Bortolin RH, Freitas RCC de, Mori AA, Hirata TDC, Nakaya HTI, Jannes CE, Pereira A da C, Wang JYT, Naslavsky M, Fajardo CM, Hirata RDC. Identification of pathogenic variants in the Brazilian cohort with familial hypercholesterolemia using exon-targeted gene sequencing [Internet]. Gene. 2023 ; 875[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.gene.2023.147501
Vancouver
Borges JB, Oliveira VF de, Dagli-Hernandez C, Ferreira GM, Barbosa TKAA, Marçal E da SR, Los B, Malaquias VB, Bortolin RH, Freitas RCC de, Mori AA, Hirata TDC, Nakaya HTI, Jannes CE, Pereira A da C, Wang JYT, Naslavsky M, Fajardo CM, Hirata RDC. Identification of pathogenic variants in the Brazilian cohort with familial hypercholesterolemia using exon-targeted gene sequencing [Internet]. Gene. 2023 ; 875[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.gene.2023.147501
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
Source: Gene. Unidade: FCF
Subjects: LINFÓCITOS T, HIPERCOLESTEROLEMIA
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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: 30 jun. 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 jun. 30 ] 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 jun. 30 ] 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
Source: Chemistry and Physics of Lipids. Unidades: FCF, ICB
Subjects: 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: 30 jun. 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 jun. 30 ] 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 jun. 30 ] 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
Source: Molecular Biology Reports. Unidades: IDPC, FCF
Subjects: 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: 30 jun. 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 jun. 30 ] 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 jun. 30 ] Available from: https://dx.doi.org/10.1007/s11033-023-08784-9
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
Source: Pharmaceutics. Unidade: FCF
Subjects: 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: 30 jun. 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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.3390/pharmaceutics14050944
Artigo de periodico
Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy (2021)
Mori, Augusto Akira ; Castro, Lara Reinel de; Bortolin, Raul Hernandes ; Bastos, Gisele Medeiros; Oliveira, Victor Fernandes de ; Ferreira, Glaucio Monteiro ; Hirata, Thiago Dominguez Crespo ; Fajardo, Cristina Moreno ; Sampaio, Marcelo Ferraz; Moreira, Dalmo Antonio Ribeiro ; Mateos, José Carlos Pachon; Correia, Edileide de Barros; Sousa, Amanda Guerra de Moraes Rego ; Brion, Maria ; Carracedo, Angel ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Source: Forensic Science International. Unidades: FCF, IDPC
Subjects: MORTE SÚBITA, HIPERTROFIA VENTRICULAR ESQUERDA, FATORES DE RISCO
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ABNT
MORI, Augusto Akira et al. Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy. Forensic Science International, v. 52, p. 1-10 art. 102478, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.fsigen.2021.102478. Acesso em: 30 jun. 2024.
APA
Mori, A. A., Castro, L. R. de, Bortolin, R. H., Bastos, G. M., Oliveira, V. F. de, Ferreira, G. M., et al. (2021). Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy. Forensic Science International, 52, 1-10 art. 102478. doi:10.1016/j.fsigen.2021.102478
NLM
Mori AA, Castro LR de, Bortolin RH, Bastos GM, Oliveira VF de, Ferreira GM, Hirata TDC, Fajardo CM, Sampaio MF, Moreira DAR, Mateos JCP, Correia E de B, Sousa AG de MR, Brion M, Carracedo A, Hirata RDC, Hirata MH. Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy [Internet]. Forensic Science International. 2021 ; 52 1-10 art. 102478.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.fsigen.2021.102478
Vancouver
Mori AA, Castro LR de, Bortolin RH, Bastos GM, Oliveira VF de, Ferreira GM, Hirata TDC, Fajardo CM, Sampaio MF, Moreira DAR, Mateos JCP, Correia E de B, Sousa AG de MR, Brion M, Carracedo A, Hirata RDC, Hirata MH. Association of variants in MYH7, MYBPC3 and TNNT2 with sudden cardiac death-related risk factors in Brazilian patients with hypertrophic cardiomyopathy [Internet]. Forensic Science International. 2021 ; 52 1-10 art. 102478.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.fsigen.2021.102478
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
Source: Epigenomics. Unidades: IDPC, ICB, FCF
Subjects: 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: 30 jun. 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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.2217/epi-2020-0462
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
Source: Epigenomics. Unidades: ICB, FCF
Subjects: 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: 30 jun. 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 jun. 30 ] 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 jun. 30 ] 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
Source: Annals of Translational Medicine. Unidades: IDPC, FCF
Subjects: 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: 30 jun. 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 jun. 30 ] 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 jun. 30 ] Available from: https://doi.org/10.21037/atm-20-5540
Trabalho de evento-resumo
Reconstrução tridimensional da PCSK9 por modelagem de homologia e novas regiões de interação com receptor de LDL (2019)
Lopes, Vitor Galvão ; Oliveira, Victor Fernandes de ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki ; Ferreira, Glaucio Monteiro
Source: Resumos. Conference titles: Simpósio Internacional de Iniciação Científica e Tecnológica da Universidade de São Paulo/SIICUSP. Unidade: FCF
Subjects: HOMEOSTASE, COLESTEROL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOPES, Vitor Galvão et al. Reconstrução tridimensional da PCSK9 por modelagem de homologia e novas regiões de interação com receptor de LDL. 2019, Anais.. São Paulo: Pró-Reitoria de Pesquisa/USP, 2019. Disponível em: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210. Acesso em: 30 jun. 2024.
APA
Lopes, V. G., Oliveira, V. F. de, Hirata, R. D. C., Hirata, M. H., & Ferreira, G. M. (2019). Reconstrução tridimensional da PCSK9 por modelagem de homologia e novas regiões de interação com receptor de LDL. In Resumos. São Paulo: Pró-Reitoria de Pesquisa/USP. Recuperado de https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
NLM
Lopes VG, Oliveira VF de, Hirata RDC, Hirata MH, Ferreira GM. Reconstrução tridimensional da PCSK9 por modelagem de homologia e novas regiões de interação com receptor de LDL [Internet]. Resumos. 2019 ;[citado 2024 jun. 30 ] Available from: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
Vancouver
Lopes VG, Oliveira VF de, Hirata RDC, Hirata MH, Ferreira GM. Reconstrução tridimensional da PCSK9 por modelagem de homologia e novas regiões de interação com receptor de LDL [Internet]. Resumos. 2019 ;[citado 2024 jun. 30 ] Available from: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
Trabalho de evento-resumo
Novel HMG-CoA reductase inhibitors development by integrating dyslipidemic patients genetic studies and molecular modelling (2019)
Ferreira, Glaucio Monteiro ; Oliveira, Victor Fernandes de ; Kronenberger, Thales ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki ; Feres, Fausto
Source: Proceedings. Conference titles: International Conference of the Brazilian Association of Bioinformatics and Computational Biology/AB3C. Unidade: FCF
Subjects: MODELAGEM MOLECULAR, DISLIPIDEMIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA, Glaucio Monteiro et al. Novel HMG-CoA reductase inhibitors development by integrating dyslipidemic patients genetic studies and molecular modelling. 2019, Anais.. Campos do Jordão: Associação Brasileira de Bioinformática e Biologia Computacional/AB3C, 2019. . Acesso em: 30 jun. 2024.
APA
Ferreira, G. M., Oliveira, V. F. de, Kronenberger, T., Hirata, R. D. C., Hirata, M. H., & Feres, F. (2019). Novel HMG-CoA reductase inhibitors development by integrating dyslipidemic patients genetic studies and molecular modelling. In Proceedings. Campos do Jordão: Associação Brasileira de Bioinformática e Biologia Computacional/AB3C.
NLM
Ferreira GM, Oliveira VF de, Kronenberger T, Hirata RDC, Hirata MH, Feres F. Novel HMG-CoA reductase inhibitors development by integrating dyslipidemic patients genetic studies and molecular modelling. Proceedings. 2019 ;[citado 2024 jun. 30 ]
Vancouver
Ferreira GM, Oliveira VF de, Kronenberger T, Hirata RDC, Hirata MH, Feres F. Novel HMG-CoA reductase inhibitors development by integrating dyslipidemic patients genetic studies and molecular modelling. Proceedings. 2019 ;[citado 2024 jun. 30 ]
Trabalho de evento-resumo
PCSK9 three-dimensional reconstruction by homology modelling and new LDL receptor interaction regions (2019)
Lopes, Vitor Galvão ; Oliveira, Victor Fernandes de ; Kronenberger, Thales ; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo ; Ferreira, Glaucio Monteiro
Source: Proceedings. Conference titles: International Conference of the Brazilian Association of Bioinformatics and Computational Biology/AB3C. Unidade: FCF
Subjects: DISLIPIDEMIAS, LIPOPROTEÍNAS LDL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LOPES, Vitor Galvão et al. PCSK9 three-dimensional reconstruction by homology modelling and new LDL receptor interaction regions. 2019, Anais.. Campos do Jordão: Associação Brasileira de Bioinformática e Biologia Computacional/AB3C, 2019. . Acesso em: 30 jun. 2024.
APA
Lopes, V. G., Oliveira, V. F. de, Kronenberger, T., Hirata, M. H., Hirata, R. D. C., & Ferreira, G. M. (2019). PCSK9 three-dimensional reconstruction by homology modelling and new LDL receptor interaction regions. In Proceedings. Campos do Jordão: Associação Brasileira de Bioinformática e Biologia Computacional/AB3C.
NLM
Lopes VG, Oliveira VF de, Kronenberger T, Hirata MH, Hirata RDC, Ferreira GM. PCSK9 three-dimensional reconstruction by homology modelling and new LDL receptor interaction regions. Proceedings. 2019 ;[citado 2024 jun. 30 ]
Vancouver
Lopes VG, Oliveira VF de, Kronenberger T, Hirata MH, Hirata RDC, Ferreira GM. PCSK9 three-dimensional reconstruction by homology modelling and new LDL receptor interaction regions. Proceedings. 2019 ;[citado 2024 jun. 30 ]
Trabalho de evento-resumo
Studies of LDL receptor activity in patients with familial hypercholesterolemia (2019)
Afonso, Thais Kristini Almendros; Oliveira, Victor Fernandes de ; Ferreira, Glaucio Monteiro ; Borges, Jéssica Bassani ; Bastos, Gisele Medeiros ; Pithon-Curi, Tania Cristina; Gorjão, Renata; Curi, Rui ; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Source: Proceedings. Conference titles: International Conference of the Brazilian Association of Bioinformatics and Computational Biology/AB3C. Unidades: ICB, FCF
Assunto: HIPERCOLESTEROLEMIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AFONSO, Thais Kristini Almendros et al. Studies of LDL receptor activity in patients with familial hypercholesterolemia. 2019, Anais.. Campos do Jordão: Associação Brasileira de Bioinformática e Biologia Computacional/AB3C, 2019. . Acesso em: 30 jun. 2024.
APA
Afonso, T. K. A., Oliveira, V. F. de, Ferreira, G. M., Borges, J. B., Bastos, G. M., Pithon-Curi, T. C., et al. (2019). Studies of LDL receptor activity in patients with familial hypercholesterolemia. In Proceedings. Campos do Jordão: Associação Brasileira de Bioinformática e Biologia Computacional/AB3C.
NLM
Afonso TKA, Oliveira VF de, Ferreira GM, Borges JB, Bastos GM, Pithon-Curi TC, Gorjão R, Curi R, Hirata RDC, Hirata MH. Studies of LDL receptor activity in patients with familial hypercholesterolemia. Proceedings. 2019 ;[citado 2024 jun. 30 ]
Vancouver
Afonso TKA, Oliveira VF de, Ferreira GM, Borges JB, Bastos GM, Pithon-Curi TC, Gorjão R, Curi R, Hirata RDC, Hirata MH. Studies of LDL receptor activity in patients with familial hypercholesterolemia. Proceedings. 2019 ;[citado 2024 jun. 30 ]

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