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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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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: 04 jul. 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 jul. 04 ] 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 jul. 04 ] 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: 04 jul. 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 jul. 04 ] 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 jul. 04 ] Available from: https://doi.org/10.1016/j.gene.2023.147821
Artigo de periodico
Methylation status of LDLR, PCSK9 and LDLRAP1 is associated with cardiovascular events in familial hypercholesterolemia (2024)
Marçal, Elisangela da Silva Rodrigues; Borges, Jéssica Bassani ; Bastos, Gisele Medeiros ; Hirata, Thiago Dominguez Crespo ; Oliveira, Victor Fernandes de ; Gonçalves, Rodrigo M ; Faludi, André Arpad; França, Joao Italo Dias ; Silva, Daiana Vitor de Oliveira; Malaquias, Vanessa Barbosa ; Luchessi, Andre Ducati ; Silbiger, Vivian Nogueira ; Nakazone, Marcelo Arruda ; Carmo, Tayanne Silva do ; Souzai, Dorotéia Rossi Silva; Sampaio, Marcelo Ferraz; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Source: Epigenomics. Unidades: FCF, ICB
Subjects: HIPERCOLESTEROLEMIA, METILAÇÃO
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ABNT
MARÇAL, Elisangela da Silva Rodrigues et al. Methylation status of LDLR, PCSK9 and LDLRAP1 is associated with cardiovascular events in familial hypercholesterolemia. Epigenomics, 2024Tradução . . Disponível em: https://dx.doi.org/10.1080/17501911.2024.2351792. Acesso em: 04 jul. 2024.
APA
Marçal, E. da S. R., Borges, J. B., Bastos, G. M., Hirata, T. D. C., Oliveira, V. F. de, Gonçalves, R. M., et al. (2024). Methylation status of LDLR, PCSK9 and LDLRAP1 is associated with cardiovascular events in familial hypercholesterolemia. Epigenomics. doi:10.1080/17501911.2024.2351792
NLM
Marçal E da SR, Borges JB, Bastos GM, Hirata TDC, Oliveira VF de, Gonçalves RM, Faludi AA, França JID, Silva DV de O, Malaquias VB, Luchessi AD, Silbiger VN, Nakazone MA, Carmo TS do, Souzai DRS, Sampaio MF, Hirata RDC, Hirata MH. Methylation status of LDLR, PCSK9 and LDLRAP1 is associated with cardiovascular events in familial hypercholesterolemia [Internet]. Epigenomics. 2024 ;[citado 2024 jul. 04 ] Available from: https://dx.doi.org/10.1080/17501911.2024.2351792
Vancouver
Marçal E da SR, Borges JB, Bastos GM, Hirata TDC, Oliveira VF de, Gonçalves RM, Faludi AA, França JID, Silva DV de O, Malaquias VB, Luchessi AD, Silbiger VN, Nakazone MA, Carmo TS do, Souzai DRS, Sampaio MF, Hirata RDC, Hirata MH. Methylation status of LDLR, PCSK9 and LDLRAP1 is associated with cardiovascular events in familial hypercholesterolemia [Internet]. Epigenomics. 2024 ;[citado 2024 jul. 04 ] Available from: https://dx.doi.org/10.1080/17501911.2024.2351792
Artigo de periodico
Adenovirus 36 seropositivity is related to the expression of anti-adipogenic lncRNAs GAS5 and MEG3 in adipose tissue obtained from subjects with obesity (2024)
Manriquez, Victor; Brito, Roberto; Pavez, Monica; Sapunar, Jorge; Fonseca, Luis; Molina, Víctor; Ortiz, Eugenia; Baeza, Romilio; Reimer, Camila; Charles, Maria; Schneider, Constance; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo ; Cerda, Alvaro
Source: international journal of obesity. Unidade: FCF
Subjects: ADENOVÍRUS, OBESIDADE
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ABNT
MANRIQUEZ, Victor et al. Adenovirus 36 seropositivity is related to the expression of anti-adipogenic lncRNAs GAS5 and MEG3 in adipose tissue obtained from subjects with obesity. international journal of obesity, 2024Tradução . . Disponível em: https://dx.doi.org/10.1038/s41366-024-01555-x. Acesso em: 04 jul. 2024.
APA
Manriquez, V., Brito, R., Pavez, M., Sapunar, J., Fonseca, L., Molina, V., et al. (2024). Adenovirus 36 seropositivity is related to the expression of anti-adipogenic lncRNAs GAS5 and MEG3 in adipose tissue obtained from subjects with obesity. international journal of obesity. doi:10.1038/s41366-024-01555-x
NLM
Manriquez V, Brito R, Pavez M, Sapunar J, Fonseca L, Molina V, Ortiz E, Baeza R, Reimer C, Charles M, Schneider C, Hirata MH, Hirata RDC, Cerda A. Adenovirus 36 seropositivity is related to the expression of anti-adipogenic lncRNAs GAS5 and MEG3 in adipose tissue obtained from subjects with obesity [Internet]. international journal of obesity. 2024 ;[citado 2024 jul. 04 ] Available from: https://dx.doi.org/10.1038/s41366-024-01555-x
Vancouver
Manriquez V, Brito R, Pavez M, Sapunar J, Fonseca L, Molina V, Ortiz E, Baeza R, Reimer C, Charles M, Schneider C, Hirata MH, Hirata RDC, Cerda A. Adenovirus 36 seropositivity is related to the expression of anti-adipogenic lncRNAs GAS5 and MEG3 in adipose tissue obtained from subjects with obesity [Internet]. international journal of obesity. 2024 ;[citado 2024 jul. 04 ] Available from: https://dx.doi.org/10.1038/s41366-024-01555-x
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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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: 04 jul. 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 jul. 04 ] 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 jul. 04 ] Available from: https://doi.org/10.1016/j.gene.2022.146979
Artigo de periodico
Influence of polymorphisms in IRS1, IRS2, MC3R, and MC4R on metabolic and inflammatory status and food intake in Brazilian adults: An exploratory pilot study (2023)
Fajardo, Cristina Moreno ; Cerda, Alvaro ; Bortolin, Raul Hernandes ; Oliveira, Raquel de; Stefani, Tamires Invencioni Moraes; Santos, Marina Aparecida dos; Braga, Aécio Assunção; Dorea, Egídio Lima; Bernik, Marcia Martins Silveira; Bastos, Gisele Medeiros; Sampaio, Marcelo Ferraz; Damasceno, Nágila Raquel Teixeira; Verlengia, Rozangela; Oliveira, Maria Rita Marques de; Hirata, Mario Hiroyuki ; Hirata, Rosario Dominguez Crespo
Source: Nutrition Research. Unidades: FCF, HU, FSP
Subjects: POLIMORFISMO, OBESIDADE
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ABNT
FAJARDO, Cristina Moreno et al. Influence of polymorphisms in IRS1, IRS2, MC3R, and MC4R on metabolic and inflammatory status and food intake in Brazilian adults: An exploratory pilot study. Nutrition Research, v. 119, p. 21-32, 2023Tradução . . Disponível em: https://dx.doi.org/10.1016/j.nutres.2023.08.008. Acesso em: 04 jul. 2024.
APA
Fajardo, C. M., Cerda, A., Bortolin, R. H., Oliveira, R. de, Stefani, T. I. M., Santos, M. A. dos, et al. (2023). Influence of polymorphisms in IRS1, IRS2, MC3R, and MC4R on metabolic and inflammatory status and food intake in Brazilian adults: An exploratory pilot study. Nutrition Research, 119, 21-32. doi:10.1016/j.nutres.2023.08.008
NLM
Fajardo CM, Cerda A, Bortolin RH, Oliveira R de, Stefani TIM, Santos MA dos, Braga AA, Dorea EL, Bernik MMS, Bastos GM, Sampaio MF, Damasceno NRT, Verlengia R, Oliveira MRM de, Hirata MH, Hirata RDC. Influence of polymorphisms in IRS1, IRS2, MC3R, and MC4R on metabolic and inflammatory status and food intake in Brazilian adults: An exploratory pilot study [Internet]. Nutrition Research. 2023 ; 119 21-32.[citado 2024 jul. 04 ] Available from: https://dx.doi.org/10.1016/j.nutres.2023.08.008
Vancouver
Fajardo CM, Cerda A, Bortolin RH, Oliveira R de, Stefani TIM, Santos MA dos, Braga AA, Dorea EL, Bernik MMS, Bastos GM, Sampaio MF, Damasceno NRT, Verlengia R, Oliveira MRM de, Hirata MH, Hirata RDC. Influence of polymorphisms in IRS1, IRS2, MC3R, and MC4R on metabolic and inflammatory status and food intake in Brazilian adults: An exploratory pilot study [Internet]. Nutrition Research. 2023 ; 119 21-32.[citado 2024 jul. 04 ] Available from: https://dx.doi.org/10.1016/j.nutres.2023.08.008
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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ABNT
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: 04 jul. 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 jul. 04 ] 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 jul. 04 ] 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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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: 04 jul. 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 jul. 04 ] 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 jul. 04 ] Available from: https://doi.org/10.1016/j.gene.2022.147084

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