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Filtros : " GRU999FBC" "ICB" Removidos: "Financiamento ANR" "Sociedade Brasileira de Microbiologia" Limpar

Filtros

USP affiliated authors
- hirata, mario hiroyuki (2)
- hirata, rosario dominguez crespo (2)
- malaquias, vanessa barbosa (2)
- oliveira, victor fernandes de (2)
- fajardo, cristina moreno (1)

Date published
- 2024 (~2)
Subjects
- hipercolesterolemia (~2)
- metilação (~1)
- receptores de ldl (~1)
Language
- inglês (~2)
Source title
- epigenomics (~1)
- gene (~1)
Publisher
Conference titles
Countries/Territories
- holanda (~1)
- reino unido (~1)
Grupo de pesquisa
- gru999fbc (~2)
- fcf002 (~2)
Funding Agencies
- financiamento capes (~2)
- financiamento cnpq (~2)
- financiamento fapesp (~1)
- fundação de amparo à pesquisa do estado de são paulo (fapesp) (~1)
Indexado em
Collaboration
Normalized affiliation
Non normalized affiliation
- hospital beneficência portuguesa de são paulo - departamento de cardiologia, são paulo, sp, brasil (2)
- instituto de cardiologia dante pazzanese - divisão de clínica médica, são paulo, sp, brasil (2)
- hospital beneficiencia portuguesa de são paulo - departamento de pesquisa, são paulo, sp, brasil (1)
- hospital beneficência portuguesa de são paulo - departamento de endocrinologia, são paulo, sp, brasil (1)
- hospital beneficência portuguesa de são paulo - departamento de pesquisa, são paulo, sp, brasil (1)

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 ; Souza, Dorotéia Rossi Silva; Sampaio, Marcelo Ferraz; Hirata, Rosario Dominguez Crespo ; Hirata, Mario Hiroyuki
Source: Epigenomics. Unidades: FCF, ICB
Subjects: HIPERCOLESTEROLEMIA, METILAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 05 nov. 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, Souza 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 nov. 05 ] 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, Souza 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 nov. 05 ] Available from: https://dx.doi.org/10.1080/17501911.2024.2351792
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 05 nov. 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 nov. 05 ] 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 nov. 05 ] Available from: https://doi.org/10.1016/j.gene.2023.147821

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