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Artigo de periodico
10q23.31 microduplication encompassing PTEN decreases mTOR signalling activity and is associated with autosomal dominant primary microcephaly (2018)
Oliveira, Danyllo; Leal, Gabriela Ferraz; Sertié, Andréa L; Caires Jr, Luiz Carlos; Goulart, Ernesto ; Musso, Camila Manso; Oliveira, João Ricardo Mendes de; Krepischi, Ana Cristina Victorino ; Vianna-Morgante, Angela M ; Zatz, Mayana
Source: Journal of Medical Genetics. Unidade: IB
Subjects: MICROCEFALIA, EXPRESSÃO GÊNICA, DOENÇAS GENÉTICAS, CRESCIMENTO E DESENVOLVIMENTO, PESSOAS COM DEFICIÊNCIA INTELECTUAL
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ABNT
OLIVEIRA, Danyllo et al. 10q23.31 microduplication encompassing PTEN decreases mTOR signalling activity and is associated with autosomal dominant primary microcephaly. Journal of Medical Genetics, p. 1-5, 2018Tradução . . Disponível em: https://doi.org/10.1136/jmedgenet-2018-105471. Acesso em: 01 jun. 2024.
APA
Oliveira, D., Leal, G. F., Sertié, A. L., Caires Jr, L. C., Goulart, E., Musso, C. M., et al. (2018). 10q23.31 microduplication encompassing PTEN decreases mTOR signalling activity and is associated with autosomal dominant primary microcephaly. Journal of Medical Genetics, 1-5. doi:10.1136/jmedgenet-2018-105471
NLM
Oliveira D, Leal GF, Sertié AL, Caires Jr LC, Goulart E, Musso CM, Oliveira JRM de, Krepischi ACV, Vianna-Morgante AM, Zatz M. 10q23.31 microduplication encompassing PTEN decreases mTOR signalling activity and is associated with autosomal dominant primary microcephaly [Internet]. Journal of Medical Genetics. 2018 ; 1-5.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1136/jmedgenet-2018-105471
Vancouver
Oliveira D, Leal GF, Sertié AL, Caires Jr LC, Goulart E, Musso CM, Oliveira JRM de, Krepischi ACV, Vianna-Morgante AM, Zatz M. 10q23.31 microduplication encompassing PTEN decreases mTOR signalling activity and is associated with autosomal dominant primary microcephaly [Internet]. Journal of Medical Genetics. 2018 ; 1-5.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1136/jmedgenet-2018-105471
Artigo de periodico
Zika Virus Selectively Kills Aggressive Human Embryonal CNS Tumor Cells In Vitro and In Vivo (2018)
Kaid, Carolini ; Goulart, Ernesto ; Caires-Junior, Luiz C. ; Araújo, Bruno H. S; Soares-Schanoski, Alessandra ; Bueno, Heloisa M. S; Telles-Silva, Kayque A. ; Astray, Renato Mancini ; Assoni, Amanda F ; Junior, Antonio F.R.; Monteiro, Daniella Cristina Ventini; Puglia, Ana L.P. ; Gomes, Roselane P.; Zatz, Mayana ; Okamoto, Oswaldo Keith
Source: Cancer Research. Unidade: IB
Subjects: ZIKA VÍRUS, ANORMALIDADES DO SISTEMA NERVOSO, CÉLULAS-TRONCO, TUMOR CARCINOIDE, MODELOS ANIMAIS DE DOENÇAS
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KAID, Carolini et al. Zika Virus Selectively Kills Aggressive Human Embryonal CNS Tumor Cells In Vitro and In Vivo. Cancer Research, v. 78, n. 12, p. 3363-3374, 2018Tradução . . Disponível em: https://doi.org/10.1158/0008-5472.CAN-17-3201. Acesso em: 01 jun. 2024.
APA
Kaid, C., Goulart, E., Caires-Junior, L. C., Araújo, B. H. S., Soares-Schanoski, A., Bueno, H. M. S., et al. (2018). Zika Virus Selectively Kills Aggressive Human Embryonal CNS Tumor Cells In Vitro and In Vivo. Cancer Research, 78( 12), 3363-3374. doi:10.1158/0008-5472.CAN-17-3201
NLM
Kaid C, Goulart E, Caires-Junior LC, Araújo BHS, Soares-Schanoski A, Bueno HMS, Telles-Silva KA, Astray RM, Assoni AF, Junior AFR, Monteiro DCV, Puglia ALP, Gomes RP, Zatz M, Okamoto OK. Zika Virus Selectively Kills Aggressive Human Embryonal CNS Tumor Cells In Vitro and In Vivo [Internet]. Cancer Research. 2018 ; 78( 12): 3363-3374.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1158/0008-5472.CAN-17-3201
Vancouver
Kaid C, Goulart E, Caires-Junior LC, Araújo BHS, Soares-Schanoski A, Bueno HMS, Telles-Silva KA, Astray RM, Assoni AF, Junior AFR, Monteiro DCV, Puglia ALP, Gomes RP, Zatz M, Okamoto OK. Zika Virus Selectively Kills Aggressive Human Embryonal CNS Tumor Cells In Vitro and In Vivo [Internet]. Cancer Research. 2018 ; 78( 12): 3363-3374.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1158/0008-5472.CAN-17-3201
Artigo de periodico
A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts (2018)
Melo, Uirá Souto; Leite, Felipe de Souza; Costa, Silvia; Rosenberg, Carla ; Zatz, Mayana
Source: Stem Cell Research. Unidade: IB
Subjects: CÉLULAS-TRONCO, GENÉTICA MÉDICA, CITOGENÉTICA MOLECULAR, MUTAÇÃO GENÉTICA, GENOMAS
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MELO, Uirá Souto et al. A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts. Stem Cell Research, v. 31, p. 52-54, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.scr.2018.07.002. Acesso em: 01 jun. 2024.
APA
Melo, U. S., Leite, F. de S., Costa, S., Rosenberg, C., & Zatz, M. (2018). A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts. Stem Cell Research, 31, 52-54. doi:10.1016/j.scr.2018.07.002
NLM
Melo US, Leite F de S, Costa S, Rosenberg C, Zatz M. A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts [Internet]. Stem Cell Research. 2018 ; 31 52-54.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1016/j.scr.2018.07.002
Vancouver
Melo US, Leite F de S, Costa S, Rosenberg C, Zatz M. A fast method to reprogram and CRISPR/Cas9 gene editing from erythroblasts [Internet]. Stem Cell Research. 2018 ; 31 52-54.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1016/j.scr.2018.07.002
Artigo de periodico
Deepening a Simple Question: can MSCs Be Used to Treat Cancer? (2017)
Gomes, Juliana P. A; Assoni, Amanda F ; Pelatti, Mayra ; Coatti, Giuliana ; Okamoto, Oswaldo Keith ; Zatz, Mayana
Source: Anticancer Research. Unidade: IB
Subjects: NEOPLASIAS, TUMOR CARCINOIDE, CÉLULAS-TRONCO, TERAPÊUTICA, ADJUVANTES IMUNOLÓGICOS
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ABNT
GOMES, Juliana P. A et al. Deepening a Simple Question: can MSCs Be Used to Treat Cancer?. Anticancer Research, v. 37, n. 9, p. 4747-4758, 2017Tradução . . Disponível em: https://doi.org/10.21873/anticanres.11881. Acesso em: 01 jun. 2024.
APA
Gomes, J. P. A., Assoni, A. F., Pelatti, M., Coatti, G., Okamoto, O. K., & Zatz, M. (2017). Deepening a Simple Question: can MSCs Be Used to Treat Cancer? Anticancer Research, 37( 9), 4747-4758. doi:10.21873/anticanres.11881
NLM
Gomes JPA, Assoni AF, Pelatti M, Coatti G, Okamoto OK, Zatz M. Deepening a Simple Question: can MSCs Be Used to Treat Cancer? [Internet]. Anticancer Research. 2017 ; 37( 9): 4747-4758.[citado 2024 jun. 01 ] Available from: https://doi.org/10.21873/anticanres.11881
Vancouver
Gomes JPA, Assoni AF, Pelatti M, Coatti G, Okamoto OK, Zatz M. Deepening a Simple Question: can MSCs Be Used to Treat Cancer? [Internet]. Anticancer Research. 2017 ; 37( 9): 4747-4758.[citado 2024 jun. 01 ] Available from: https://doi.org/10.21873/anticanres.11881
Artigo de periodico
Transplantation of Human Adipose Mesenchymal Stem Cells in Non-Immunosuppressed GRMD Dogs is a Safe Procedure (2016)
Pelatti, M. V ; Gomes, J. P. A; Vieira, N. M. S; Cangussu, E; Landini, V; Andrade, T; Sartori, M; Petrus, L.; Zatz, Mayana
Source: Stem Cell Reviews and Reports. Unidade: IB
Subjects: DISTROFIA MUSCULAR, CÉLULAS-TRONCO, CROMOSSOMO X, MODELOS ANIMAIS, CÃO GOLDEN RETRIEVER
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PELATTI, M. V et al. Transplantation of Human Adipose Mesenchymal Stem Cells in Non-Immunosuppressed GRMD Dogs is a Safe Procedure. Stem Cell Reviews and Reports, v. 12, p. 448-453, 2016Tradução . . Disponível em: https://doi.org/10.1007/s12015-016-9659-3. Acesso em: 01 jun. 2024.
APA
Pelatti, M. V., Gomes, J. P. A., Vieira, N. M. S., Cangussu, E., Landini, V., Andrade, T., et al. (2016). Transplantation of Human Adipose Mesenchymal Stem Cells in Non-Immunosuppressed GRMD Dogs is a Safe Procedure. Stem Cell Reviews and Reports, 12, 448-453. doi:10.1007/s12015-016-9659-3
NLM
Pelatti MV, Gomes JPA, Vieira NMS, Cangussu E, Landini V, Andrade T, Sartori M, Petrus L, Zatz M. Transplantation of Human Adipose Mesenchymal Stem Cells in Non-Immunosuppressed GRMD Dogs is a Safe Procedure [Internet]. Stem Cell Reviews and Reports. 2016 ; 12 448-453.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1007/s12015-016-9659-3
Vancouver
Pelatti MV, Gomes JPA, Vieira NMS, Cangussu E, Landini V, Andrade T, Sartori M, Petrus L, Zatz M. Transplantation of Human Adipose Mesenchymal Stem Cells in Non-Immunosuppressed GRMD Dogs is a Safe Procedure [Internet]. Stem Cell Reviews and Reports. 2016 ; 12 448-453.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1007/s12015-016-9659-3
Artigo de periodico
Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype (2015)
Vieira, Natássia M; Guo, Ling T; Estrela, Elicia; Kunkel, Louis M; Zatz, Mayana ; Shelton, G. Diane
Source: Neuromuscular Disorders. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MODELOS ANIMAIS, CÃO LABRADOR RETRIEVER, MUTAÇÃO GENÉTICA
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ABNT
VIEIRA, Natássia M et al. Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype. Neuromuscular Disorders, v. 25, p. 363-370, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2015.02.012. Acesso em: 01 jun. 2024.
APA
Vieira, N. M., Guo, L. T., Estrela, E., Kunkel, L. M., Zatz, M., & Shelton, G. D. (2015). Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype. Neuromuscular Disorders, 25, 363-370. doi:10.1016/j.nmd.2015.02.012
NLM
Vieira NM, Guo LT, Estrela E, Kunkel LM, Zatz M, Shelton GD. Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype [Internet]. Neuromuscular Disorders. 2015 ; 25 363-370.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1016/j.nmd.2015.02.012
Vancouver
Vieira NM, Guo LT, Estrela E, Kunkel LM, Zatz M, Shelton GD. Muscular dystrophy in a family of Labrador Retrievers with no muscle dystrophin and a mild phenotype [Internet]. Neuromuscular Disorders. 2015 ; 25 363-370.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1016/j.nmd.2015.02.012
Artigo de periodico
Comparison of skeletal muscle potential of mesenchymal stem- cells from different sources injected in SJL mice (2009)
Zucconi, E ; Vieira, N. M; Bueno Júnior, Carlos Roberto ; Brandalise, V; Secco, M; Suzuki, M. F; Bartolini, P; Brum, P C; Vainzof, Mariz ; Zatz, Mayana
Source: Neuromuscular Disorders. Unidades: IB, EEFERP, EEFE
Subjects: DOENÇAS GENÉTICAS, DISTROFIA MUSCULAR, CÉLULAS-TRONCO, PROTEÍNAS MUSCULARES, MODELOS ANIMAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZUCCONI, E et al. Comparison of skeletal muscle potential of mesenchymal stem- cells from different sources injected in SJL mice. Neuromuscular Disorders, v. 19, p. 533-534, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2009.06.279. Acesso em: 01 jun. 2024.
APA
Zucconi, E., Vieira, N. M., Bueno Júnior, C. R., Brandalise, V., Secco, M., Suzuki, M. F., et al. (2009). Comparison of skeletal muscle potential of mesenchymal stem- cells from different sources injected in SJL mice. Neuromuscular Disorders, 19, 533-534. doi:10.1016/j.nmd.2009.06.279
NLM
Zucconi E, Vieira NM, Bueno Júnior CR, Brandalise V, Secco M, Suzuki MF, Bartolini P, Brum PC, Vainzof M, Zatz M. Comparison of skeletal muscle potential of mesenchymal stem- cells from different sources injected in SJL mice [Internet]. Neuromuscular Disorders. 2009 ; 19 533-534.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1016/j.nmd.2009.06.279
Vancouver
Zucconi E, Vieira NM, Bueno Júnior CR, Brandalise V, Secco M, Suzuki MF, Bartolini P, Brum PC, Vainzof M, Zatz M. Comparison of skeletal muscle potential of mesenchymal stem- cells from different sources injected in SJL mice [Internet]. Neuromuscular Disorders. 2009 ; 19 533-534.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1016/j.nmd.2009.06.279

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