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Artigo de periodico
Mining Novel Candidate Imprinted Genes Using Genome-Wide Methylation Screening and Literature Review (2017)
Bonaldi, Adriano; Kashiwabara, André; Araújo, Érica S. de; Pereira, Lygia da Veiga ; Paschoal, Alexandre R; Andozia, Mayra B; Villela, Darine; Rivas, Maria P; Suemoto, Claudia K; Pasqualucci, Carlos A; Grinberg, Lea T; Brentani, Helena; Maria-Engler, Silvya Stuchi ; Carraro, Dirce M; Vianna-Morgante, Angela M ; Rosenberg, Carla ; Vasques, Luciana R; Krepischi, Ana Cristina Victorino
Source: Epigenomes. Unidades: IB, FM, FCF
Subjects: METILAÇÃO DE DNA, GENOMAS, EXPRESSÃO GÊNICA, GENÉTICA MÉDICA, EPIGÊNESE GENÉTICA, EMBRIÃO
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ABNT
BONALDI, Adriano et al. Mining Novel Candidate Imprinted Genes Using Genome-Wide Methylation Screening and Literature Review. Epigenomes, v. 1, n. 2, p. 1-5, 2017Tradução . . Disponível em: https://doi.org/10.3390/epigenomes1020013. Acesso em: 14 nov. 2024.
APA
Bonaldi, A., Kashiwabara, A., Araújo, É. S. de, Pereira, L. da V., Paschoal, A. R., Andozia, M. B., et al. (2017). Mining Novel Candidate Imprinted Genes Using Genome-Wide Methylation Screening and Literature Review. Epigenomes, 1( 2), 1-5. doi:10.3390/epigenomes1020013
NLM
Bonaldi A, Kashiwabara A, Araújo ÉS de, Pereira L da V, Paschoal AR, Andozia MB, Villela D, Rivas MP, Suemoto CK, Pasqualucci CA, Grinberg LT, Brentani H, Maria-Engler SS, Carraro DM, Vianna-Morgante AM, Rosenberg C, Vasques LR, Krepischi ACV. Mining Novel Candidate Imprinted Genes Using Genome-Wide Methylation Screening and Literature Review [Internet]. Epigenomes. 2017 ; 1( 2): 1-5.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/epigenomes1020013
Vancouver
Bonaldi A, Kashiwabara A, Araújo ÉS de, Pereira L da V, Paschoal AR, Andozia MB, Villela D, Rivas MP, Suemoto CK, Pasqualucci CA, Grinberg LT, Brentani H, Maria-Engler SS, Carraro DM, Vianna-Morgante AM, Rosenberg C, Vasques LR, Krepischi ACV. Mining Novel Candidate Imprinted Genes Using Genome-Wide Methylation Screening and Literature Review [Internet]. Epigenomes. 2017 ; 1( 2): 1-5.[citado 2024 nov. 14 ] Available from: https://doi.org/10.3390/epigenomes1020013
Artigo de periodico
Differential DNA Methylation of MicroRNA Genes in Temporal Cortex from Alzheimer’s Disease Individuals (2016)
Villela, Darine; Ramalho, Rodrigo F.; Silva, Aderbal R. T.; Brentani, Helena; Suemoto, Claudia K.; Pasqualucci, Carlos Augusto; Grinberg, Lea T.; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla
Source: Neural Plasticity. Unidades: FM, IB
Subjects: METILAÇÃO DE DNA, CÓRTEX PRÉ-FRONTAL, CADÁVER, DOENÇA DE ALZHEIMER
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VILLELA, Darine et al. Differential DNA Methylation of MicroRNA Genes in Temporal Cortex from Alzheimer’s Disease Individuals. Neural Plasticity, v. 2016, p. 10 2016, 2016Tradução . . Disponível em: https://doi.org/10.1155/2016/2584940. Acesso em: 14 nov. 2024.
APA
Villela, D., Ramalho, R. F., Silva, A. R. T., Brentani, H., Suemoto, C. K., Pasqualucci, C. A., et al. (2016). Differential DNA Methylation of MicroRNA Genes in Temporal Cortex from Alzheimer’s Disease Individuals. Neural Plasticity, 2016, 10 2016. doi:10.1155/2016/2584940
NLM
Villela D, Ramalho RF, Silva ART, Brentani H, Suemoto CK, Pasqualucci CA, Grinberg LT, Krepischi ACV, Rosenberg C. Differential DNA Methylation of MicroRNA Genes in Temporal Cortex from Alzheimer’s Disease Individuals [Internet]. Neural Plasticity. 2016 ; 2016 10 2016.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1155/2016/2584940
Vancouver
Villela D, Ramalho RF, Silva ART, Brentani H, Suemoto CK, Pasqualucci CA, Grinberg LT, Krepischi ACV, Rosenberg C. Differential DNA Methylation of MicroRNA Genes in Temporal Cortex from Alzheimer’s Disease Individuals [Internet]. Neural Plasticity. 2016 ; 2016 10 2016.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1155/2016/2584940
Artigo de periodico
A microdeletion in Alzheimer’s disease disrupts NAMPT gene (2014)
Villela, Darine; Schlesinger, David; Suemoto, Claudia K.; Grinberg, Lea T.; Rosenberg, Carla
Source: Journal of Genetics. Unidades: FM, IB
Subjects: VARIAÇÃO GENÉTICA, GENÉTICA MÉDICA, DOENÇA DE ALZHEIMER
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VILLELA, Darine et al. A microdeletion in Alzheimer’s disease disrupts NAMPT gene. Journal of Genetics, v. 93, n. 2, p. 535-537, 2014Tradução . . Disponível em: https://doi.org/10.1007/s12041-014-0399-3. Acesso em: 14 nov. 2024.
APA
Villela, D., Schlesinger, D., Suemoto, C. K., Grinberg, L. T., & Rosenberg, C. (2014). A microdeletion in Alzheimer’s disease disrupts NAMPT gene. Journal of Genetics, 93( 2), 535-537. doi:10.1007/s12041-014-0399-3
NLM
Villela D, Schlesinger D, Suemoto CK, Grinberg LT, Rosenberg C. A microdeletion in Alzheimer’s disease disrupts NAMPT gene [Internet]. Journal of Genetics. 2014 ; 93( 2): 535-537.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s12041-014-0399-3
Vancouver
Villela D, Schlesinger D, Suemoto CK, Grinberg LT, Rosenberg C. A microdeletion in Alzheimer’s disease disrupts NAMPT gene [Internet]. Journal of Genetics. 2014 ; 93( 2): 535-537.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s12041-014-0399-3
Artigo de periodico
Germline DNA copy number variation in individuals with argyrophilic grain disease reveals CTNS as a plausible candidate gene (2013)
Vilela, Darine; Kimura, Lilian; Schlesinger, David; Gonçalves, Amanda; Pearson, Peter L.; Suemoto, Claudia Kimie; Pasqualucci, Carlos Augusto Gonçalves; Krepischi, Ana Cristina Victorino ; Grinberg, Lea Tenenholz; Rosenberg, Carla
Source: Genetics and Molecular Biology. Unidades: FM, IB
Subjects: DOENÇAS NEURODEGENERATIVAS, VARIAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VILELA, Darine et al. Germline DNA copy number variation in individuals with argyrophilic grain disease reveals CTNS as a plausible candidate gene. Genetics and Molecular Biology, v. 36, n. 4, p. 498-501, 2013Tradução . . Disponível em: https://doi.org/10.1590/S1415-47572013000400006. Acesso em: 14 nov. 2024.
APA
Vilela, D., Kimura, L., Schlesinger, D., Gonçalves, A., Pearson, P. L., Suemoto, C. K., et al. (2013). Germline DNA copy number variation in individuals with argyrophilic grain disease reveals CTNS as a plausible candidate gene. Genetics and Molecular Biology, 36( 4), 498-501. doi:10.1590/S1415-47572013000400006
NLM
Vilela D, Kimura L, Schlesinger D, Gonçalves A, Pearson PL, Suemoto CK, Pasqualucci CAG, Krepischi ACV, Grinberg LT, Rosenberg C. Germline DNA copy number variation in individuals with argyrophilic grain disease reveals CTNS as a plausible candidate gene [Internet]. Genetics and Molecular Biology. 2013 ; 36( 4): 498-501.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1590/S1415-47572013000400006
Vancouver
Vilela D, Kimura L, Schlesinger D, Gonçalves A, Pearson PL, Suemoto CK, Pasqualucci CAG, Krepischi ACV, Grinberg LT, Rosenberg C. Germline DNA copy number variation in individuals with argyrophilic grain disease reveals CTNS as a plausible candidate gene [Internet]. Genetics and Molecular Biology. 2013 ; 36( 4): 498-501.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1590/S1415-47572013000400006
Trabalho de evento-resumo
Association of rare copy number variations and risk for Alzheimer's disease (2012)
Villela, D.; Schlesinger, D.; Suemoto, Claudia Kimie; Grinberg, Lea Tenenholz; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla
Source: Posters: Cytogenetics. Conference titles: Annual Meeting of the American Society of Human Genetics. Unidades: IB, FM
Subjects: DOENÇA DE ALZHEIMER, DOENÇAS NEURODEGENERATIVAS, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VILLELA, D. et al. Association of rare copy number variations and risk for Alzheimer's disease. 2012, Anais.. São Francisco: Instituto de Biociências, Universidade de São Paulo, 2012. Disponível em: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf. Acesso em: 14 nov. 2024.
APA
Villela, D., Schlesinger, D., Suemoto, C. K., Grinberg, L. T., Krepischi, A. C. V., & Rosenberg, C. (2012). Association of rare copy number variations and risk for Alzheimer's disease. In Posters: Cytogenetics. São Francisco: Instituto de Biociências, Universidade de São Paulo. Recuperado de http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf
NLM
Villela D, Schlesinger D, Suemoto CK, Grinberg LT, Krepischi ACV, Rosenberg C. Association of rare copy number variations and risk for Alzheimer's disease [Internet]. Posters: Cytogenetics. 2012 ;[citado 2024 nov. 14 ] Available from: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf
Vancouver
Villela D, Schlesinger D, Suemoto CK, Grinberg LT, Krepischi ACV, Rosenberg C. Association of rare copy number variations and risk for Alzheimer's disease [Internet]. Posters: Cytogenetics. 2012 ;[citado 2024 nov. 14 ] Available from: http://www.ashg.org/2012meeting/pdf/38731_poster_complete.pdf

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