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Artigo de periodico
Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil (2024)
Migliavacca, Michele P ; Sobreira, Joselito ; Bermeo, Diana; Gomes, Mireille; Alencar, Dayse; Sussuchi, Luciane; Souza, Camila Alves; Silva, Juliana Santos; Kroll, José Eduardo; Burger, Matheus; Sousa, Rodrigo Guarischi ; Villela, Darine ; Yamamoto, Guilherme L ; Milanezi, Fernanda ; Horigoshi, Nelson; Cesar, Regina Grigolli; Carvalho, Werther Brunow de ; Honjo, Rachel Sayuri ; Bertola, Débora Romeo ; Kim, Chong Ae ; Souza, Lucian de; Procianoy, Renato S; Silveria, Rita C; Rosenberg, Carla ; Giugliani, Roberto ; Campana, Gustavo Aguiar; Scapulatempo-Neto, Cristovam ; Sobreira, Nara
Source: American Journal of Medical Genetics. Part A. Unidades: BIOINFORMÁTICA, FM, IB
Subjects: PEDIATRIA, SEQUENCIAMENTO GENÉTICO, DOENÇAS DO RECÉM-NASCIDO
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ABNT
MIGLIAVACCA, Michele P et al. Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil. American Journal of Medical Genetics. Part A, n. ja, 2024Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.63544. Acesso em: 05 nov. 2024.
APA
Migliavacca, M. P., Sobreira, J., Bermeo, D., Gomes, M., Alencar, D., Sussuchi, L., et al. (2024). Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil. American Journal of Medical Genetics. Part A, (ja). doi:10.1002/ajmg.a.63544
NLM
Migliavacca MP, Sobreira J, Bermeo D, Gomes M, Alencar D, Sussuchi L, Souza CA, Silva JS, Kroll JE, Burger M, Sousa RG, Villela D, Yamamoto GL, Milanezi F, Horigoshi N, Cesar RG, Carvalho WB de, Honjo RS, Bertola DR, Kim CA, Souza L de, Procianoy RS, Silveria RC, Rosenberg C, Giugliani R, Campana GA, Scapulatempo-Neto C, Sobreira N. Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil [Internet]. American Journal of Medical Genetics. Part A. 2024 ;(ja):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1002/ajmg.a.63544
Vancouver
Migliavacca MP, Sobreira J, Bermeo D, Gomes M, Alencar D, Sussuchi L, Souza CA, Silva JS, Kroll JE, Burger M, Sousa RG, Villela D, Yamamoto GL, Milanezi F, Horigoshi N, Cesar RG, Carvalho WB de, Honjo RS, Bertola DR, Kim CA, Souza L de, Procianoy RS, Silveria RC, Rosenberg C, Giugliani R, Campana GA, Scapulatempo-Neto C, Sobreira N. Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: a pilot study in Brazil [Internet]. American Journal of Medical Genetics. Part A. 2024 ;(ja):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1002/ajmg.a.63544
Artigo de periodico
Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders (2024)
Tolezano, Giovanna Cantini; Bastos, Giovanna Civitate; Costa, Silvia Souza da; Scliar, Marília de Oliveira; Souza, Carolina Fischinger Moura de; Linden Jr, Hélio Van Der; Fernandes, Walter Luiz Magalhães; Otto, Paulo A ; Vianna-Morgante, Angela M ; Haddad, Luciana Amaral ; Honjo, Rachel Sayuri; Yamamoto, Guilherme Lopes; Kim, Chong Ae; Rosenberg, Carla ; Jorge, Alexander Augusto de Lima ; Bertola, Débora Romeo ; Krepischi, Ana Cristina Victorino
Source: Molecular Neurobiology. Unidades: IB, BIOINFORMÁTICA, FM
Subjects: MICROCEFALIA, NEUROLOGIA, GENÉTICA
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ABNT
TOLEZANO, Giovanna Cantini et al. Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders. Molecular Neurobiology, 2024Tradução . . Disponível em: https://doi.org/10.1007/s12035-023-03894-8. Acesso em: 05 nov. 2024.
APA
Tolezano, G. C., Bastos, G. C., Costa, S. S. da, Scliar, M. de O., Souza, C. F. M. de, Linden Jr, H. V. D., et al. (2024). Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders. Molecular Neurobiology. doi:10.1007/s12035-023-03894-8
NLM
Tolezano GC, Bastos GC, Costa SS da, Scliar M de O, Souza CFM de, Linden Jr HVD, Fernandes WLM, Otto PA, Vianna-Morgante AM, Haddad LA, Honjo RS, Yamamoto GL, Kim CA, Rosenberg C, Jorge AA de L, Bertola DR, Krepischi ACV. Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders [Internet]. Molecular Neurobiology. 2024 ;[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s12035-023-03894-8
Vancouver
Tolezano GC, Bastos GC, Costa SS da, Scliar M de O, Souza CFM de, Linden Jr HVD, Fernandes WLM, Otto PA, Vianna-Morgante AM, Haddad LA, Honjo RS, Yamamoto GL, Kim CA, Rosenberg C, Jorge AA de L, Bertola DR, Krepischi ACV. Clinical characterization and underlying genetic findings in brazilian patients with syndromic microcephaly associated with neurodevelopmental disorders [Internet]. Molecular Neurobiology. 2024 ;[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s12035-023-03894-8
Artigo de periodico
Exome Sequencing Identifies Multiple Genetic Diagnoses in Children with Syndromic Growth Disorders (2024)
Rezende, Raissa Carneiro ; Andrade, Nathalia Liberatoscioli Menezes ; Dantas, Naiara Castelo Branco ; Cellin, Laurana de Polli ; Krepischi, Ana Cristina Victorino ; Lerario, Antonio Marcondes ; Jorge, Alexander Augusto de Lima
Source: JOURNAL OF PEDIATRICS. Unidades: IB, FM
Subjects: ANÁLISE DE SEQUÊNCIA DE DNA, TRANSTORNOS DO CRESCIMENTO, CRIANÇAS
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ABNT
REZENDE, Raissa Carneiro et al. Exome Sequencing Identifies Multiple Genetic Diagnoses in Children with Syndromic Growth Disorders. JOURNAL OF PEDIATRICS, v. 265, 2024Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/58750. Acesso em: 05 nov. 2024.
APA
Rezende, R. C., Andrade, N. L. M., Dantas, N. C. B., Cellin, L. de P., Krepischi, A. C. V., Lerario, A. M., & Jorge, A. A. de L. (2024). Exome Sequencing Identifies Multiple Genetic Diagnoses in Children with Syndromic Growth Disorders. JOURNAL OF PEDIATRICS, 265. doi:10.1016/j.jpeds.2023.113841
NLM
Rezende RC, Andrade NLM, Dantas NCB, Cellin L de P, Krepischi ACV, Lerario AM, Jorge AA de L. Exome Sequencing Identifies Multiple Genetic Diagnoses in Children with Syndromic Growth Disorders [Internet]. JOURNAL OF PEDIATRICS. 2024 ; 265[citado 2024 nov. 05 ] Available from: https://observatorio.fm.usp.br/handle/OPI/58750
Vancouver
Rezende RC, Andrade NLM, Dantas NCB, Cellin L de P, Krepischi ACV, Lerario AM, Jorge AA de L. Exome Sequencing Identifies Multiple Genetic Diagnoses in Children with Syndromic Growth Disorders [Internet]. JOURNAL OF PEDIATRICS. 2024 ; 265[citado 2024 nov. 05 ] Available from: https://observatorio.fm.usp.br/handle/OPI/58750
Artigo de periodico
A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis (2024)
Carvalho, Laura Machado Lara ; Jorge, Alexander Augusto de Lima ; Bertola, Débora Romeo ; Krepischi, Ana Cristina Victorino ; Rosenberg, Carla
Source: Current Obesity Reports. Unidades: FM, IB
Subjects: OBESIDADE, GENÉTICA
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ABNT
CARVALHO, Laura Machado Lara et al. A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis. Current Obesity Reports, n. 26 Ja 2024, 2024Tradução . . Disponível em: https://doi.org/10.1007/s13679-023-00543-y. Acesso em: 05 nov. 2024.
APA
Carvalho, L. M. L., Jorge, A. A. de L., Bertola, D. R., Krepischi, A. C. V., & Rosenberg, C. (2024). A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis. Current Obesity Reports, (26 Ja 2024). doi:10.1007/s13679-023-00543-y
NLM
Carvalho LML, Jorge AA de L, Bertola DR, Krepischi ACV, Rosenberg C. A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis [Internet]. Current Obesity Reports. 2024 ;(26 Ja 2024):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s13679-023-00543-y
Vancouver
Carvalho LML, Jorge AA de L, Bertola DR, Krepischi ACV, Rosenberg C. A comprehensive review of syndromic forms of obesity: genetic etiology, clinical features and molecular diagnosis [Internet]. Current Obesity Reports. 2024 ;(26 Ja 2024):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1007/s13679-023-00543-y
Artigo de periodico
Germline mutations in cancer predisposition genes among pediatric patients with cancer and congenital anomalies (2024)
Dangoni, Gustavo D; Teixeira, Anne Caroline B; Costa, Silvia S. da; Scliar, Marília O; Carvalho, Laura Machado Lara ; Silva, Luciana N; Novak, Estela M; Vince, Carolina S. C; Maschietto, Mariana C; Sugayama, Sofia M. M; Odone-filho, Vicente ; Krepischi, Ana Cristina Victorino
Source: Pediatric Research. Unidades: IB, FM
Subjects: NEOPLASIAS, NEUROBLASTOMA
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ABNT
DANGONI, Gustavo D et al. Germline mutations in cancer predisposition genes among pediatric patients with cancer and congenital anomalies. Pediatric Research, 2024Tradução . . Disponível em: https://doi.org/10.1038/s41390-023-03000-7. Acesso em: 05 nov. 2024.
APA
Dangoni, G. D., Teixeira, A. C. B., Costa, S. S. da, Scliar, M. O., Carvalho, L. M. L., Silva, L. N., et al. (2024). Germline mutations in cancer predisposition genes among pediatric patients with cancer and congenital anomalies. Pediatric Research. doi:10.1038/s41390-023-03000-7
NLM
Dangoni GD, Teixeira ACB, Costa SS da, Scliar MO, Carvalho LML, Silva LN, Novak EM, Vince CSC, Maschietto MC, Sugayama SMM, Odone-filho V, Krepischi ACV. Germline mutations in cancer predisposition genes among pediatric patients with cancer and congenital anomalies [Internet]. Pediatric Research. 2024 ;[citado 2024 nov. 05 ] Available from: https://doi.org/10.1038/s41390-023-03000-7
Vancouver
Dangoni GD, Teixeira ACB, Costa SS da, Scliar MO, Carvalho LML, Silva LN, Novak EM, Vince CSC, Maschietto MC, Sugayama SMM, Odone-filho V, Krepischi ACV. Germline mutations in cancer predisposition genes among pediatric patients with cancer and congenital anomalies [Internet]. Pediatric Research. 2024 ;[citado 2024 nov. 05 ] Available from: https://doi.org/10.1038/s41390-023-03000-7
Artigo de jornal-dep/entr
Novo biotério da USP criará suínos para produção de órgãos para transplante em humanos [Depoimento] (2024)
Carlotti Júnior, Carlos Gilberto ; Raia, Silvano ; Zatz, Mayana
Source: Jornal da USP. Unidades: FM, IB
Subjects: BIOTÉRIO, TRANSPLANTE HETERÓLOGO, SUÍNOS
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ABNT
CARLOTTI JÚNIOR, Carlos Gilberto e RAIA, Silvano e ZATZ, Mayana. Novo biotério da USP criará suínos para produção de órgãos para transplante em humanos [Depoimento]. Jornal da USP. São Paulo: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://jornal.usp.br/institucional/novo-bioterio-da-usp-criara-suinos-para-producao-de-orgaos-para-transplante-em-humanos/. Acesso em: 05 nov. 2024. , 2024
APA
Carlotti Júnior, C. G., Raia, S., & Zatz, M. (2024). Novo biotério da USP criará suínos para produção de órgãos para transplante em humanos [Depoimento]. Jornal da USP. São Paulo: Faculdade de Medicina, Universidade de São Paulo. Recuperado de https://jornal.usp.br/institucional/novo-bioterio-da-usp-criara-suinos-para-producao-de-orgaos-para-transplante-em-humanos/
NLM
Carlotti Júnior CG, Raia S, Zatz M. Novo biotério da USP criará suínos para produção de órgãos para transplante em humanos [Depoimento] [Internet]. Jornal da USP. 2024 ;[citado 2024 nov. 05 ] Available from: https://jornal.usp.br/institucional/novo-bioterio-da-usp-criara-suinos-para-producao-de-orgaos-para-transplante-em-humanos/
Vancouver
Carlotti Júnior CG, Raia S, Zatz M. Novo biotério da USP criará suínos para produção de órgãos para transplante em humanos [Depoimento] [Internet]. Jornal da USP. 2024 ;[citado 2024 nov. 05 ] Available from: https://jornal.usp.br/institucional/novo-bioterio-da-usp-criara-suinos-para-producao-de-orgaos-para-transplante-em-humanos/
Artigo de periodico
Anti-RBD IgG antibodies from endemic coronaviruses do not protect against the acquisition of SARS-CoV-2 infection among exposed uninfected individuals (2024)
Adami, Flávia Lopes ; Castro, Mateus Vidigal de ; Almeida, Bianca da Silva ; Daher, Isabela Pazotti ; Yamamoto, Marcio Massao ; Santos, Keity Souza ; Zatz, Mayana ; Naslavsky, Michel Satya ; Rosa, Daniela Santoro ; Cunha Neto, Edecio ; Oliveira, Vivian Leite de ; Kalil Filho, Jorge Elias ; Boscardin, Silvia Beatriz
Source: Frontiers in Immunology. Unidades: ICB, FM, IB
Subjects: PARASITOLOGIA, ANTIVIRAIS, COVID-19, CORONAVIRUS, INFECÇÕES POR CORONAVIRUS, IMUNOGLOBULINAS, GLICOPROTEÍNAS, ESTUDOS DE COORTES
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ABNT
ADAMI, Flávia Lopes et al. Anti-RBD IgG antibodies from endemic coronaviruses do not protect against the acquisition of SARS-CoV-2 infection among exposed uninfected individuals. Frontiers in Immunology, v. 15, p. 10 , 2024Tradução . . Disponível em: https://doi.org/10.3389/fimmu.2024.1396603. Acesso em: 05 nov. 2024.
APA
Adami, F. L., Castro, M. V. de, Almeida, B. da S., Daher, I. P., Yamamoto, M. M., Santos, K. S., et al. (2024). Anti-RBD IgG antibodies from endemic coronaviruses do not protect against the acquisition of SARS-CoV-2 infection among exposed uninfected individuals. Frontiers in Immunology, 15, 10 . doi:10.3389/fimmu.2024.1396603
NLM
Adami FL, Castro MV de, Almeida B da S, Daher IP, Yamamoto MM, Santos KS, Zatz M, Naslavsky MS, Rosa DS, Cunha Neto E, Oliveira VL de, Kalil Filho JE, Boscardin SB. Anti-RBD IgG antibodies from endemic coronaviruses do not protect against the acquisition of SARS-CoV-2 infection among exposed uninfected individuals [Internet]. Frontiers in Immunology. 2024 ; 15 10 .[citado 2024 nov. 05 ] Available from: https://doi.org/10.3389/fimmu.2024.1396603
Vancouver
Adami FL, Castro MV de, Almeida B da S, Daher IP, Yamamoto MM, Santos KS, Zatz M, Naslavsky MS, Rosa DS, Cunha Neto E, Oliveira VL de, Kalil Filho JE, Boscardin SB. Anti-RBD IgG antibodies from endemic coronaviruses do not protect against the acquisition of SARS-CoV-2 infection among exposed uninfected individuals [Internet]. Frontiers in Immunology. 2024 ; 15 10 .[citado 2024 nov. 05 ] Available from: https://doi.org/10.3389/fimmu.2024.1396603
Apresentacao sonora/cenica/entrevista
Laboratório começa a funcionar na USP com desafio de permitir transplante de órgãos entre espécies diferentes (2024)
Raia, Silvano ; Zatz, Mayana
Source: Jornal Nacional. Unidades: FM, IB
Subjects: TRANSPLANTE HETERÓLOGO, LABORATÓRIOS, BIOTÉRIO, SUÍNOS
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ABNT
RAIA, Silvano e ZATZ, Mayana. Laboratório começa a funcionar na USP com desafio de permitir transplante de órgãos entre espécies diferentes. Jornal Nacional. Rio de Janeiro: Faculdade de Medicina, Universidade de São Paulo. Disponível em: https://g1.globo.com/jornal-nacional/noticia/2024/04/22/laboratorio-comeca-a-funcionar-na-usp-com-desafio-de-permitir-transplante-de-orgaos-entre-especies-diferentes.ghtml. Acesso em: 05 nov. 2024. , 2024
APA
Raia, S., & Zatz, M. (2024). Laboratório começa a funcionar na USP com desafio de permitir transplante de órgãos entre espécies diferentes. Jornal Nacional. Rio de Janeiro: Faculdade de Medicina, Universidade de São Paulo. Recuperado de https://g1.globo.com/jornal-nacional/noticia/2024/04/22/laboratorio-comeca-a-funcionar-na-usp-com-desafio-de-permitir-transplante-de-orgaos-entre-especies-diferentes.ghtml
NLM
Raia S, Zatz M. Laboratório começa a funcionar na USP com desafio de permitir transplante de órgãos entre espécies diferentes [Internet]. Jornal Nacional. 2024 ;[citado 2024 nov. 05 ] Available from: https://g1.globo.com/jornal-nacional/noticia/2024/04/22/laboratorio-comeca-a-funcionar-na-usp-com-desafio-de-permitir-transplante-de-orgaos-entre-especies-diferentes.ghtml
Vancouver
Raia S, Zatz M. Laboratório começa a funcionar na USP com desafio de permitir transplante de órgãos entre espécies diferentes [Internet]. Jornal Nacional. 2024 ;[citado 2024 nov. 05 ] Available from: https://g1.globo.com/jornal-nacional/noticia/2024/04/22/laboratorio-comeca-a-funcionar-na-usp-com-desafio-de-permitir-transplante-de-orgaos-entre-especies-diferentes.ghtml
Artigo de periodico
The seroconversion history to SARS-CoV-2 in Indigenous people from Brazil – the interplay between exposure, vaccination, and tuberculosis (2024)
Nagai, Alice ; Lemes, Renan Barbosa ; Mill, José Geraldo ; Pereira, Alexandre Costa ; Marques, Rafael Elias ; Hünemeier, Tábita
Source: Frontiers in Immunology. Unidades: FM, IB
Subjects: COVID-19, IMUNOLOGIA, VACINAÇÃO, INDÍGENAS
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ABNT
NAGAI, Alice et al. The seroconversion history to SARS-CoV-2 in Indigenous people from Brazil – the interplay between exposure, vaccination, and tuberculosis. Frontiers in Immunology, v. 15, 2024Tradução . . Disponível em: https://doi.org/10.3389/fimmu.2024.1359066. Acesso em: 05 nov. 2024.
APA
Nagai, A., Lemes, R. B., Mill, J. G., Pereira, A. C., Marques, R. E., & Hünemeier, T. (2024). The seroconversion history to SARS-CoV-2 in Indigenous people from Brazil – the interplay between exposure, vaccination, and tuberculosis. Frontiers in Immunology, 15. doi:10.3389/fimmu.2024.1359066
NLM
Nagai A, Lemes RB, Mill JG, Pereira AC, Marques RE, Hünemeier T. The seroconversion history to SARS-CoV-2 in Indigenous people from Brazil – the interplay between exposure, vaccination, and tuberculosis [Internet]. Frontiers in Immunology. 2024 ; 15[citado 2024 nov. 05 ] Available from: https://doi.org/10.3389/fimmu.2024.1359066
Vancouver
Nagai A, Lemes RB, Mill JG, Pereira AC, Marques RE, Hünemeier T. The seroconversion history to SARS-CoV-2 in Indigenous people from Brazil – the interplay between exposure, vaccination, and tuberculosis [Internet]. Frontiers in Immunology. 2024 ; 15[citado 2024 nov. 05 ] Available from: https://doi.org/10.3389/fimmu.2024.1359066
Artigo de periodico
Early Leishmania infectivity depends on miR‐372/373/520d family‐mediated reprogramming of polyamines metabolism inTHP‐1‐derived macrophages (2024)
Fernandes, J. C. R ; Muxel, S. M ; López-Gonzálvez, M. A ; Barbas, C; Floeter-Winter, Lucile Maria
Source: Scientific Reports. Unidades: IB, FM, ICB
Subjects: METABOLÔMICA, RNA, PARASITOLOGIA, LEISHMANIA
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ABNT
FERNANDES, J. C. R et al. Early Leishmania infectivity depends on miR‐372/373/520d family‐mediated reprogramming of polyamines metabolism inTHP‐1‐derived macrophages. Scientific Reports, v. 14, n. art. 996, 2024Tradução . . Disponível em: https://doi.org/10.1038/s41598-024-51511-y. Acesso em: 05 nov. 2024.
APA
Fernandes, J. C. R., Muxel, S. M., López-Gonzálvez, M. A., Barbas, C., & Floeter-Winter, L. M. (2024). Early Leishmania infectivity depends on miR‐372/373/520d family‐mediated reprogramming of polyamines metabolism inTHP‐1‐derived macrophages. Scientific Reports, 14( art. 996). doi:10.1038/s41598-024-51511-y
NLM
Fernandes JCR, Muxel SM, López-Gonzálvez MA, Barbas C, Floeter-Winter LM. Early Leishmania infectivity depends on miR‐372/373/520d family‐mediated reprogramming of polyamines metabolism inTHP‐1‐derived macrophages [Internet]. Scientific Reports. 2024 ; 14( art. 996):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1038/s41598-024-51511-y
Vancouver
Fernandes JCR, Muxel SM, López-Gonzálvez MA, Barbas C, Floeter-Winter LM. Early Leishmania infectivity depends on miR‐372/373/520d family‐mediated reprogramming of polyamines metabolism inTHP‐1‐derived macrophages [Internet]. Scientific Reports. 2024 ; 14( art. 996):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1038/s41598-024-51511-y
Artigo de periodico
DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKM zeta (2023)
Pramio, Dimitrius Tansini ; Vieceli, Felipe Monteleone ; Branco, Elisa Varella ; Goes, Carolina Purcell ; Kobayashi, Gerson Shigeru ; Pelegrina, Diogo Vieira da Silva; Moraes, Beatriz Caroline de ; Allam, Aicha El ; Kumar, Bony De ; Jara, Gabriel ; Farfel, José Marcelo ; Reis, Eduardo Moraes ; Passos-Bueno, Maria Rita ; Schechtman, Deborah
Source: Biochimica et biophysica acta-gene regulatory mechanisms. Unidades: IQ, IB, FM, ESALQ
Subjects: EPIGÊNESE GENÉTICA, PROTEÍNAS QUINASES, DOENÇA DE ALZHEIMER, METILAÇÃO DE DNA
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ABNT
PRAMIO, Dimitrius Tansini et al. DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKM zeta. Biochimica et biophysica acta-gene regulatory mechanisms, v. 1866, n. 1, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/54748. Acesso em: 05 nov. 2024.
APA
Pramio, D. T., Vieceli, F. M., Branco, E. V., Goes, C. P., Kobayashi, G. S., Pelegrina, D. V. da S., et al. (2023). DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKM zeta. Biochimica et biophysica acta-gene regulatory mechanisms, 1866( 1). doi:10.1016/j.bbagrm.2023.194909
NLM
Pramio DT, Vieceli FM, Branco EV, Goes CP, Kobayashi GS, Pelegrina DV da S, Moraes BC de, Allam AE, Kumar BD, Jara G, Farfel JM, Reis EM, Passos-Bueno MR, Schechtman D. DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKM zeta [Internet]. Biochimica et biophysica acta-gene regulatory mechanisms. 2023 ; 1866( 1):[citado 2024 nov. 05 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54748
Vancouver
Pramio DT, Vieceli FM, Branco EV, Goes CP, Kobayashi GS, Pelegrina DV da S, Moraes BC de, Allam AE, Kumar BD, Jara G, Farfel JM, Reis EM, Passos-Bueno MR, Schechtman D. DNA methylation of the promoter region at the CREB1 binding site is a mechanism for the epigenetic regulation of brain-specific PKM zeta [Internet]. Biochimica et biophysica acta-gene regulatory mechanisms. 2023 ; 1866( 1):[citado 2024 nov. 05 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54748
Artigo de periodico
A rare case of hepatoblastoma in a syndromic child with a de novo germline JAG1 mutation (2023)
Dangoni, Gustavo Dib ; Teixeira, Anne Caroline Barbosa ; Aguiar, Talita Ferreira ; Sugayama, Sofia Mizuho Miura; Odone Filho, Vicente ; Bertola, Débora Romeo ; Krepischi, Ana Cristina Victorino
Source: Pediatric blood & cancer. Unidades: IB, FM
Subjects: NEOPLASIAS HEPÁTICAS, CRIANÇAS, DESENVOLVIMENTO INFANTIL, ESTUDO DE CASO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DANGONI, Gustavo Dib et al. A rare case of hepatoblastoma in a syndromic child with a de novo germline JAG1 mutation. Pediatric blood & cancer, v. 70, n. 7, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/54762. Acesso em: 05 nov. 2024.
APA
Dangoni, G. D., Teixeira, A. C. B., Aguiar, T. F., Sugayama, S. M. M., Odone Filho, V., Bertola, D. R., & Krepischi, A. C. V. (2023). A rare case of hepatoblastoma in a syndromic child with a de novo germline JAG1 mutation. Pediatric blood & cancer, 70( 7). doi:10.1002/pbc.30311
NLM
Dangoni GD, Teixeira ACB, Aguiar TF, Sugayama SMM, Odone Filho V, Bertola DR, Krepischi ACV. A rare case of hepatoblastoma in a syndromic child with a de novo germline JAG1 mutation [Internet]. Pediatric blood & cancer. 2023 ; 70( 7):[citado 2024 nov. 05 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54762
Vancouver
Dangoni GD, Teixeira ACB, Aguiar TF, Sugayama SMM, Odone Filho V, Bertola DR, Krepischi ACV. A rare case of hepatoblastoma in a syndromic child with a de novo germline JAG1 mutation [Internet]. Pediatric blood & cancer. 2023 ; 70( 7):[citado 2024 nov. 05 ] Available from: https://observatorio.fm.usp.br/handle/OPI/54762
Artigo de periodico
Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample (2023)
Paradela, Regina Silva ; Justo, Alberto Fernando Oliveira ; Paes, Vítor Ribeiro; Leite, Renata E. P ; Pasqualucci, Carlos A ; Grinberg, Lea T. ; Naslavsky, Michel Satya ; Zatz, Mayana ; Nitrini, Ricardo ; Jacob Filho, Wilson ; Suemoto, Claudia Kimie
Source: Acta Neuropathologica Communications. Unidades: FM, IB
Subjects: APOLIPOPROTEÍNAS, DOENÇAS DO SISTEMA NERVOSO, COGNIÇÃO, DEMÊNCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PARADELA, Regina Silva et al. Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample. Acta Neuropathologica Communications, v. 11, 2023Tradução . . Disponível em: https://doi.org/10.1186/s40478-023-01681-z. Acesso em: 05 nov. 2024.
APA
Paradela, R. S., Justo, A. F. O., Paes, V. R., Leite, R. E. P., Pasqualucci, C. A., Grinberg, L. T., et al. (2023). Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample. Acta Neuropathologica Communications, 11. doi:10.1186/s40478-023-01681-z
NLM
Paradela RS, Justo AFO, Paes VR, Leite REP, Pasqualucci CA, Grinberg LT, Naslavsky MS, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK. Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample [Internet]. Acta Neuropathologica Communications. 2023 ; 11[citado 2024 nov. 05 ] Available from: https://doi.org/10.1186/s40478-023-01681-z
Vancouver
Paradela RS, Justo AFO, Paes VR, Leite REP, Pasqualucci CA, Grinberg LT, Naslavsky MS, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK. Association between APOE-ε4 allele and cognitive function is mediated by Alzheimer’s disease pathology: a population-based autopsy study in an admixed sample [Internet]. Acta Neuropathologica Communications. 2023 ; 11[citado 2024 nov. 05 ] Available from: https://doi.org/10.1186/s40478-023-01681-z
Artigo de periodico
Corrigendum: follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report (2023)
Castro, Mateus Vidigal de ; Silva, Monize V R ; Soares, Flávia B; Coria, Vivian R ; Naslavsky, Michel ; Scliar, Marilia O ; Castelli, Erick C; Oliveira, Jamille Ramos de ; Medeiros, Giuliana Xavier de ; Sasahara, Greyce Luri ; Santos, Keity S ; Cunha Neto, Edecio ; Kalil, Jorge ; Zatz, Mayana
Source: Frontiers in Medicine. Unidades: IB, FM
Subjects: MUTAÇÃO GENÉTICA, COVID-19, CORONAVIRUS, GÊMEOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Mateus Vidigal de et al. Corrigendum: follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report. Frontiers in Medicine, v. 10, 2023Tradução . . Disponível em: https://doi.org/10.3389/fmed.2023.1185833. Acesso em: 05 nov. 2024.
APA
Castro, M. V. de, Silva, M. V. R., Soares, F. B., Coria, V. R., Naslavsky, M., Scliar, M. O., et al. (2023). Corrigendum: follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report. Frontiers in Medicine, 10. doi:10.3389/fmed.2023.1185833
NLM
Castro MV de, Silva MVR, Soares FB, Coria VR, Naslavsky M, Scliar MO, Castelli EC, Oliveira JR de, Medeiros GX de, Sasahara GL, Santos KS, Cunha Neto E, Kalil J, Zatz M. Corrigendum: follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report [Internet]. Frontiers in Medicine. 2023 ; 10[citado 2024 nov. 05 ] Available from: https://doi.org/10.3389/fmed.2023.1185833
Vancouver
Castro MV de, Silva MVR, Soares FB, Coria VR, Naslavsky M, Scliar MO, Castelli EC, Oliveira JR de, Medeiros GX de, Sasahara GL, Santos KS, Cunha Neto E, Kalil J, Zatz M. Corrigendum: follow-up of young adult monozygotic twins after simultaneous critical coronavirus disease 2019: a case report [Internet]. Frontiers in Medicine. 2023 ; 10[citado 2024 nov. 05 ] Available from: https://doi.org/10.3389/fmed.2023.1185833
Artigo de periodico
Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A) (2023)
Kobayashi, Gerson S ; Silva, Gleiciele A. Vieira; Branco, Elisa Varella ; Moreira, Danielle P; Kitajima, João Paulo F. W; Hemza, Claudia R.M.L; Mingroni Netto, Regina Celia ; Lojudice, Fernando H ; Oiticica, Jeanne ; Bento, Ricardo F ; Batissoco, Ana C ; Lezirovitz, Karina
Source: Stem Cell Research. Unidades: IB, FM
Subjects: PERDA AUDITIVA, CÉLULAS-TRONCO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
KOBAYASHI, Gerson S et al. Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A). Stem Cell Research, v. 71, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.scr.2023.103181. Acesso em: 05 nov. 2024.
APA
Kobayashi, G. S., Silva, G. A. V., Branco, E. V., Moreira, D. P., Kitajima, J. P. F. W., Hemza, C. R. M. L., et al. (2023). Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A). Stem Cell Research, 71. doi:10.1016/j.scr.2023.103181
NLM
Kobayashi GS, Silva GAV, Branco EV, Moreira DP, Kitajima JPFW, Hemza CRML, Mingroni Netto RC, Lojudice FH, Oiticica J, Bento RF, Batissoco AC, Lezirovitz K. Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A) [Internet]. Stem Cell Research. 2023 ; 71[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.scr.2023.103181
Vancouver
Kobayashi GS, Silva GAV, Branco EV, Moreira DP, Kitajima JPFW, Hemza CRML, Mingroni Netto RC, Lojudice FH, Oiticica J, Bento RF, Batissoco AC, Lezirovitz K. Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A) [Internet]. Stem Cell Research. 2023 ; 71[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.scr.2023.103181
Artigo de periodico
Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study (2023)
Paradela, Regina Silva; Farias-Itao, Daniela Souza; Pasqualucci, Carlos A; Grinberg, Lea T; Naslavsky, Michel ; Zatz, Mayana ; Nitrini, Ricardo ; Jacob Filho, Wilson ; Suemoto, Claudia Kimie ; Leite, Renata E. P
Source: Cardiovascular Pathology. Unidades: FM, IB
Subjects: ESTUDOS TRANSVERSAIS, ARTÉRIAS CARÓTIDAS, AUTÓPSIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PARADELA, Regina Silva et al. Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study. Cardiovascular Pathology, v. Jan./Fe, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.carpath.2022.107479. Acesso em: 05 nov. 2024.
APA
Paradela, R. S., Farias-Itao, D. S., Pasqualucci, C. A., Grinberg, L. T., Naslavsky, M., Zatz, M., et al. (2023). Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study. Cardiovascular Pathology, Jan./Fe. doi:10.1016/j.carpath.2022.107479
NLM
Paradela RS, Farias-Itao DS, Pasqualucci CA, Grinberg LT, Naslavsky M, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK, Leite REP. Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study [Internet]. Cardiovascular Pathology. 2023 ; Jan./Fe[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.carpath.2022.107479
Vancouver
Paradela RS, Farias-Itao DS, Pasqualucci CA, Grinberg LT, Naslavsky M, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK, Leite REP. Apolipoprotein e genotypes were not associated with intracranial atherosclerosis: a population-based autopsy study [Internet]. Cardiovascular Pathology. 2023 ; Jan./Fe[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.carpath.2022.107479
Artigo de periodico
Immunological evaluation of young unvaccinated patients with Turner syndrome after COVID-19 (2023)
Castro, Mateus V. de ; Silva, Monize V. R ; Oliveira, Luana de Mendonça ; Gozzi-Silva, Sarah C; Naslavsky, Michel ; Scliar, Marilia O ; Magalhães, Monize L ; Rocha, Katia M. da ; Nunes, Kelly ; Castelli, Erick C; Magawa, Jhosiene Y; Santos, Keity S ; Cunha-Neto, Edecio ; Sato, Maria N; Zatz, Mayana
Source: International Journal of Infectious Diseases. Unidades: ICB, IB, FM
Subjects: IMUNOLOGIA, VACINAS, COVID-19, CROMOSSOMO X
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASTRO, Mateus V. de et al. Immunological evaluation of young unvaccinated patients with Turner syndrome after COVID-19. International Journal of Infectious Diseases, v. 129, p. 207-215, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.ijid.2023.01.042. Acesso em: 05 nov. 2024.
APA
Castro, M. V. de, Silva, M. V. R., Oliveira, L. de M., Gozzi-Silva, S. C., Naslavsky, M., Scliar, M. O., et al. (2023). Immunological evaluation of young unvaccinated patients with Turner syndrome after COVID-19. International Journal of Infectious Diseases, 129, 207-215. doi:10.1016/j.ijid.2023.01.042
NLM
Castro MV de, Silva MVR, Oliveira L de M, Gozzi-Silva SC, Naslavsky M, Scliar MO, Magalhães ML, Rocha KM da, Nunes K, Castelli EC, Magawa JY, Santos KS, Cunha-Neto E, Sato MN, Zatz M. Immunological evaluation of young unvaccinated patients with Turner syndrome after COVID-19 [Internet]. International Journal of Infectious Diseases. 2023 ; 129 207-215.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.ijid.2023.01.042
Vancouver
Castro MV de, Silva MVR, Oliveira L de M, Gozzi-Silva SC, Naslavsky M, Scliar MO, Magalhães ML, Rocha KM da, Nunes K, Castelli EC, Magawa JY, Santos KS, Cunha-Neto E, Sato MN, Zatz M. Immunological evaluation of young unvaccinated patients with Turner syndrome after COVID-19 [Internet]. International Journal of Infectious Diseases. 2023 ; 129 207-215.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.ijid.2023.01.042
Artigo de periodico
Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study (2023)
Paradela, Regina Silva ; Itáo, Daniela Souza Farias ; Leite, Renata E.P; Pasqualucci, Carlos A; Grinberg, Lea T ; Naslavsky, Michel ; Zatz, Mayana ; Nitrini, Ricardo ; Jacob Filho, Wilson ; Suemoto, Claudia Kimie
Source: ournal of Stroke & Cerebrovascular Diseases. Unidades: IB, FM
Subjects: APOLIPOPROTEÍNAS, POLIMORFISMO, ARTERIOSCLEROSE, EPIDEMIOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PARADELA, Regina Silva et al. Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study. ournal of Stroke & Cerebrovascular Diseases, v. 32, n. art. 107229, 2023Tradução . . Disponível em: https://doi.org/10.1016/j.jstrokecerebrovasdis.2023.107229. Acesso em: 05 nov. 2024.
APA
Paradela, R. S., Itáo, D. S. F., Leite, R. E. P., Pasqualucci, C. A., Grinberg, L. T., Naslavsky, M., et al. (2023). Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study. ournal of Stroke & Cerebrovascular Diseases, 32( art. 107229). doi:10.1016/j.jstrokecerebrovasdis.2023.107229
NLM
Paradela RS, Itáo DSF, Leite REP, Pasqualucci CA, Grinberg LT, Naslavsky M, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK. Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study [Internet]. ournal of Stroke & Cerebrovascular Diseases. 2023 ; 32( art. 107229):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.jstrokecerebrovasdis.2023.107229
Vancouver
Paradela RS, Itáo DSF, Leite REP, Pasqualucci CA, Grinberg LT, Naslavsky M, Zatz M, Nitrini R, Jacob Filho W, Suemoto CK. Apolipoprotein E ε2 allele is associated with lower risk of carotid artery obstruction in a population-based autopsy study [Internet]. ournal of Stroke & Cerebrovascular Diseases. 2023 ; 32( art. 107229):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.jstrokecerebrovasdis.2023.107229
Artigo de periodico
Cephalochromin-induced mitochondrial damage overcomes venetoclax-resistance in acute Myeloid Leukemia Models (2023)
Nascimento, Mariane Cristina do ; Martins, Diego Antonio Pereira ; Alcântara, Guilherme Augusto Sousa; Lima, Keli Cristina de ; Vicari, Hugo Passos ; Huls, Gerwin A. ; Schuringa, Jan Jacob ; Rego, Eduardo Magalhães ; Ferreira, Marcelo José Pena ; Costa-Lotufo, Letícia Veras ; Machado Neto, João Agostinho
Source: Blood. Conference titles: 65th ASH Annual Meeting Abstracts. Unidades: IB, FM, ICB, FMRP
Subjects: FARMACOLOGIA, LEUCEMIA MIELOIDE AGUDA, HEMATOLOGIA, QUIMIOTERAPIA COMBINADA, CÉLULAS CULTIVADAS DE TUMOR, PROLIFERAÇÃO CELULAR, NEOPLASIAS POR TIPO HISTOLÓGICO, APOPTOSE, DANO AO DNA, MITOCÔNDRIAS, PROTEÔMICA, ANTINEOPLÁSICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASCIMENTO, Mariane Cristina do et al. Cephalochromin-induced mitochondrial damage overcomes venetoclax-resistance in acute Myeloid Leukemia Models. Blood, v. 142, n. res. 604, p. 5751, 2023Tradução . . Disponível em: https://doi.org/10.1182/blood-2023-189814. Acesso em: 05 nov. 2024.
APA
Nascimento, M. C. do, Martins, D. A. P., Alcântara, G. A. S., Lima, K. C. de, Vicari, H. P., Huls, G. A., et al. (2023). Cephalochromin-induced mitochondrial damage overcomes venetoclax-resistance in acute Myeloid Leukemia Models. Blood, 142( res. 604), 5751. doi:10.1182/blood-2023-189814
NLM
Nascimento MC do, Martins DAP, Alcântara GAS, Lima KC de, Vicari HP, Huls GA, Schuringa JJ, Rego EM, Ferreira MJP, Costa-Lotufo LV, Machado Neto JA. Cephalochromin-induced mitochondrial damage overcomes venetoclax-resistance in acute Myeloid Leukemia Models [Internet]. Blood. 2023 ; 142( res. 604): 5751.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1182/blood-2023-189814
Vancouver
Nascimento MC do, Martins DAP, Alcântara GAS, Lima KC de, Vicari HP, Huls GA, Schuringa JJ, Rego EM, Ferreira MJP, Costa-Lotufo LV, Machado Neto JA. Cephalochromin-induced mitochondrial damage overcomes venetoclax-resistance in acute Myeloid Leukemia Models [Internet]. Blood. 2023 ; 142( res. 604): 5751.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1182/blood-2023-189814
Artigo de periodico
AMEBaS: automatic midline extraction and background subtraction of ratiometric fluorescence time-lapses of polarized single cells (2023)
Badain, Rafael ; Damineli, Daniel S. C. ; Portes, Maria Teresa ; Feijó, José ; Buratti, Stefano ; Tortora, Giorgia ; Oliveira, Hugo Neves de ; César Júnior, Roberto Marcondes
Source: Journal of Visualized Experiments. Unidades: IB, IME, PRÓ-G, FM
Assunto: PROCESSAMENTO DE IMAGENS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BADAIN, Rafael et al. AMEBaS: automatic midline extraction and background subtraction of ratiometric fluorescence time-lapses of polarized single cells. Journal of Visualized Experiments, v. 196, n. artigo e64857, p. 1-15, 2023Tradução . . Disponível em: https://doi.org/10.3791/64857. Acesso em: 05 nov. 2024.
APA
Badain, R., Damineli, D. S. C., Portes, M. T., Feijó, J., Buratti, S., Tortora, G., et al. (2023). AMEBaS: automatic midline extraction and background subtraction of ratiometric fluorescence time-lapses of polarized single cells. Journal of Visualized Experiments, 196( artigo e64857), 1-15. doi:10.3791/64857
NLM
Badain R, Damineli DSC, Portes MT, Feijó J, Buratti S, Tortora G, Oliveira HN de, César Júnior RM. AMEBaS: automatic midline extraction and background subtraction of ratiometric fluorescence time-lapses of polarized single cells [Internet]. Journal of Visualized Experiments. 2023 ; 196( artigo e64857): 1-15.[citado 2024 nov. 05 ] Available from: https://doi.org/10.3791/64857
Vancouver
Badain R, Damineli DSC, Portes MT, Feijó J, Buratti S, Tortora G, Oliveira HN de, César Júnior RM. AMEBaS: automatic midline extraction and background subtraction of ratiometric fluorescence time-lapses of polarized single cells [Internet]. Journal of Visualized Experiments. 2023 ; 196( artigo e64857): 1-15.[citado 2024 nov. 05 ] Available from: https://doi.org/10.3791/64857

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