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Artigo de periodico
Influence of Human Bone Marrow Mesenchymal Stem Cells Secretome from Acute Myeloid Leukemia Patients on the Proliferation and Death of K562 and K562-Lucena Leukemia Cell Lineages (2024)
Freitas, Fabio Alessandro de ; Levy, Débora ; Reichert, Cadiele Oliana ; Sampaio-Silva, Juliana ; Giglio, Pedro Nogueira; Lage, Luís Alberto de Pádua Covas ; Demange, Marco Kawamura ; Pereira, Juliana; Bydlowski, Sérgio Paulo
Fonte: International Journal of Molecular Sciences. Unidade: FM
Assuntos: LEUCEMIA, MEDULA ÓSSEA, CÉLULAS-TRONCO, CITOCININAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FREITAS, Fabio Alessandro de et al. Influence of Human Bone Marrow Mesenchymal Stem Cells Secretome from Acute Myeloid Leukemia Patients on the Proliferation and Death of K562 and K562-Lucena Leukemia Cell Lineages. International Journal of Molecular Sciences, p. 4748/1-4748/14, 2024Tradução . . Disponível em: https://doi.org/10.3390/ijms25094748. Acesso em: 01 nov. 2025.
APA
Freitas, F. A. de, Levy, D., Reichert, C. O., Sampaio-Silva, J., Giglio, P. N., Lage, L. A. de P. C., et al. (2024). Influence of Human Bone Marrow Mesenchymal Stem Cells Secretome from Acute Myeloid Leukemia Patients on the Proliferation and Death of K562 and K562-Lucena Leukemia Cell Lineages. International Journal of Molecular Sciences, 4748/1-4748/14. doi:10.3390/ijms25094748
NLM
Freitas FA de, Levy D, Reichert CO, Sampaio-Silva J, Giglio PN, Lage LA de PC, Demange MK, Pereira J, Bydlowski SP. Influence of Human Bone Marrow Mesenchymal Stem Cells Secretome from Acute Myeloid Leukemia Patients on the Proliferation and Death of K562 and K562-Lucena Leukemia Cell Lineages [Internet]. International Journal of Molecular Sciences. 2024 ; 4748/1-4748/14.[citado 2025 nov. 01 ] Available from: https://doi.org/10.3390/ijms25094748
Vancouver
Freitas FA de, Levy D, Reichert CO, Sampaio-Silva J, Giglio PN, Lage LA de PC, Demange MK, Pereira J, Bydlowski SP. Influence of Human Bone Marrow Mesenchymal Stem Cells Secretome from Acute Myeloid Leukemia Patients on the Proliferation and Death of K562 and K562-Lucena Leukemia Cell Lineages [Internet]. International Journal of Molecular Sciences. 2024 ; 4748/1-4748/14.[citado 2025 nov. 01 ] Available from: https://doi.org/10.3390/ijms25094748
Artigo de periodico
Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss (2022)
Schmitt, Ana Carolina Basso ; Pedroso-Campos, Vinicius; Pardono, Eliete; Sampaio-Silva, Juliana; Sonoda, Cindy Yukimi; Vieira-Silva, Gleiciele Alice; Longati, Estefany Uchoa da Silva de Oliveira; Mariano, Diego; Hoshino, Ana Cristina Hiromi; Bento, Ricardo Ferreira
Fonte: Human genetics. Unidade: FM
Assuntos: PERDA AUDITIVA, GENÉTICA MÉDICA, ESTUDOS DE COORTES, BRASILEIROS, PREVALÊNCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SCHMITT, Ana Carolina Basso et al. Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss. Human genetics, v. 141, n. 3/Abr, p. 519-538, 2022Tradução . . Disponível em: https://doi.org/10.1007/s00439-021-02372-2. Acesso em: 01 nov. 2025.
APA
Schmitt, A. C. B., Pedroso-Campos, V., Pardono, E., Sampaio-Silva, J., Sonoda, C. Y., Vieira-Silva, G. A., et al. (2022). Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss. Human genetics, 141( 3/Abr), 519-538. doi:10.1007/s00439-021-02372-2
NLM
Schmitt ACB, Pedroso-Campos V, Pardono E, Sampaio-Silva J, Sonoda CY, Vieira-Silva GA, Longati EU da S de O, Mariano D, Hoshino ACH, Bento RF. Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss [Internet]. Human genetics. 2022 ; 141( 3/Abr): 519-538.[citado 2025 nov. 01 ] Available from: https://doi.org/10.1007/s00439-021-02372-2
Vancouver
Schmitt ACB, Pedroso-Campos V, Pardono E, Sampaio-Silva J, Sonoda CY, Vieira-Silva GA, Longati EU da S de O, Mariano D, Hoshino ACH, Bento RF. Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss [Internet]. Human genetics. 2022 ; 141( 3/Abr): 519-538.[citado 2025 nov. 01 ] Available from: https://doi.org/10.1007/s00439-021-02372-2
Artigo de periodico
A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58 (2020)
Lezirovitz, Karina; Vieira-silva, Gleiciele A; Batissoco, Ana C; Levy, Debora; Kitajima, Joao P; Trouillet, Alix; Ouyang, Ellen; Zebarjadi, Navid; Sampaio-Silva, Juliana; Bento, Ricardo Ferreira
Fonte: Human molecular genetics. Unidade: FM
Assuntos: GENES, PERDA AUDITIVA, SURDEZ, NEURÔNIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEZIROVITZ, Karina et al. A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58. Human molecular genetics, v. 29, n. 9, p. 1520-1536, 2020Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddaa075. Acesso em: 01 nov. 2025.
APA
Lezirovitz, K., Vieira-silva, G. A., Batissoco, A. C., Levy, D., Kitajima, J. P., Trouillet, A., et al. (2020). A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58. Human molecular genetics, 29( 9), 1520-1536. doi:10.1093/hmg/ddaa075
NLM
Lezirovitz K, Vieira-silva GA, Batissoco AC, Levy D, Kitajima JP, Trouillet A, Ouyang E, Zebarjadi N, Sampaio-Silva J, Bento RF. A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58 [Internet]. Human molecular genetics. 2020 ; 29( 9): 1520-1536.[citado 2025 nov. 01 ] Available from: https://doi.org/10.1093/hmg/ddaa075
Vancouver
Lezirovitz K, Vieira-silva GA, Batissoco AC, Levy D, Kitajima JP, Trouillet A, Ouyang E, Zebarjadi N, Sampaio-Silva J, Bento RF. A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58 [Internet]. Human molecular genetics. 2020 ; 29( 9): 1520-1536.[citado 2025 nov. 01 ] Available from: https://doi.org/10.1093/hmg/ddaa075

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