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Artigo de periodico
Induced degeneration and regeneration in aged muscle reduce tubular aggregates but not muscle function (2024)
Vasconcelos, Felipe Tadeu Galante Rocha de ; Ribeiro Junior, Antonio Fernando ; Souza, Brandow Willy ; Zogbi, Isabela de Aquino; Carvalho, Laura Machado Lara ; Feitosa, Letícia Nogueira ; Souza, Lucas Santos ; Saldys, Nathália Gagliardi ; Ferrari, Merari de Fátima Ramires ; Vainzof, Mariz
Source: Frontiers in Neurology. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MÚSCULOS, DOENÇAS NEUROMUSCULARES, ENVELHECIMENTO
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ABNT
VASCONCELOS, Felipe Tadeu Galante Rocha de et al. Induced degeneration and regeneration in aged muscle reduce tubular aggregates but not muscle function. Frontiers in Neurology, v. 15, 2024Tradução . . Disponível em: https://doi.org/10.3389/fneur.2024.1325222. Acesso em: 13 nov. 2024.
APA
Vasconcelos, F. T. G. R. de, Ribeiro Junior, A. F., Souza, B. W., Zogbi, I. de A., Carvalho, L. M. L., Feitosa, L. N., et al. (2024). Induced degeneration and regeneration in aged muscle reduce tubular aggregates but not muscle function. Frontiers in Neurology, 15. doi:10.3389/fneur.2024.1325222
NLM
Vasconcelos FTGR de, Ribeiro Junior AF, Souza BW, Zogbi I de A, Carvalho LML, Feitosa LN, Souza LS, Saldys NG, Ferrari M de FR, Vainzof M. Induced degeneration and regeneration in aged muscle reduce tubular aggregates but not muscle function [Internet]. Frontiers in Neurology. 2024 ; 15[citado 2024 nov. 13 ] Available from: https://doi.org/10.3389/fneur.2024.1325222
Vancouver
Vasconcelos FTGR de, Ribeiro Junior AF, Souza BW, Zogbi I de A, Carvalho LML, Feitosa LN, Souza LS, Saldys NG, Ferrari M de FR, Vainzof M. Induced degeneration and regeneration in aged muscle reduce tubular aggregates but not muscle function [Internet]. Frontiers in Neurology. 2024 ; 15[citado 2024 nov. 13 ] Available from: https://doi.org/10.3389/fneur.2024.1325222
Artigo de periodico
Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype (2022)
Shelton, G. Diane ; Minor, Katie M; Vieira, Natassia M; Kunkel, Louis M; Friedenberg, Steven G; Cullen, Jonah N; Guo, Ling T; Zatz, Mayana ; Mickelson, James R
Source: Neuromuscular Disorders. Unidade: IB
Subjects: DISTROFIA MUSCULAR, SEQUENCIAMENTO GENÉTICO, MIOPATIAS CONGÊNITAS ESTRUTURAIS, CÃO GOLDEN RETRIEVER
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SHELTON, G. Diane et al. Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype. Neuromuscular Disorders, v. 32, n. 10, p. 836-841, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2022.08.001. Acesso em: 13 nov. 2024.
APA
Shelton, G. D., Minor, K. M., Vieira, N. M., Kunkel, L. M., Friedenberg, S. G., Cullen, J. N., et al. (2022). Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype. Neuromuscular Disorders, 32( 10), 836-841. doi:10.1016/j.nmd.2022.08.001
NLM
Shelton GD, Minor KM, Vieira NM, Kunkel LM, Friedenberg SG, Cullen JN, Guo LT, Zatz M, Mickelson JR. Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype [Internet]. Neuromuscular Disorders. 2022 ; 32( 10): 836-841.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.nmd.2022.08.001
Vancouver
Shelton GD, Minor KM, Vieira NM, Kunkel LM, Friedenberg SG, Cullen JN, Guo LT, Zatz M, Mickelson JR. Tandem duplication within the DMD gene in Labrador retrievers with a mild clinical phenotype [Internet]. Neuromuscular Disorders. 2022 ; 32( 10): 836-841.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.nmd.2022.08.001
Artigo de periodico
Correction to: effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model (2022)
Comim, Clarissa M; Soares, Jaime A; Alberti, Adriano; Freiberger, Viviane; Ventura, Letícia; Dias, Paula; Schactae, Aryadnne L; Grigollo, Leoberto R; Steckert, Amanda V; Martins, Daniel F; Nodari Junior, Rudy J; Vainzof, Mariz ; Quevedo, João
Source: Neurological Sciences. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES, MIOPATIAS CONGÊNITAS ESTRUTURAIS
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ABNT
COMIM, Clarissa M et al. Correction to: effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model. Neurological Sciences, v. 153, 2022Tradução . . Disponível em: https://doi.org/10.1007/s10072-022-05999-9. Acesso em: 13 nov. 2024.
APA
Comim, C. M., Soares, J. A., Alberti, A., Freiberger, V., Ventura, L., Dias, P., et al. (2022). Correction to: effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model. Neurological Sciences, 153. doi:10.1007/s10072-022-05999-9
NLM
Comim CM, Soares JA, Alberti A, Freiberger V, Ventura L, Dias P, Schactae AL, Grigollo LR, Steckert AV, Martins DF, Nodari Junior RJ, Vainzof M, Quevedo J. Correction to: effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model [Internet]. Neurological Sciences. 2022 ; 153[citado 2024 nov. 13 ] Available from: https://doi.org/10.1007/s10072-022-05999-9
Vancouver
Comim CM, Soares JA, Alberti A, Freiberger V, Ventura L, Dias P, Schactae AL, Grigollo LR, Steckert AV, Martins DF, Nodari Junior RJ, Vainzof M, Quevedo J. Correction to: effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model [Internet]. Neurological Sciences. 2022 ; 153[citado 2024 nov. 13 ] Available from: https://doi.org/10.1007/s10072-022-05999-9
Artigo de periodico
Effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model (2022)
Comim, Clarissa M; Soares, Jaime A; Alberti, Adriano; Freiberger, Viviane; Ventura, Letícia; Dias, Paula; Schactae, Aryadnne L; Grigollo, Leoberto R; Steckert, Amanda V; Martins, Daniel F; Nodari Junior, Rudy J; Vainzof, Mariz ; Quevedo, João
Source: Neurological Sciences. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES, MIOPATIAS CONGÊNITAS ESTRUTURAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COMIM, Clarissa M et al. Effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model. Neurological Sciences, v. 153, 2022Tradução . . Disponível em: https://doi.org/10.1007/s10072-022-05928-w. Acesso em: 13 nov. 2024.
APA
Comim, C. M., Soares, J. A., Alberti, A., Freiberger, V., Ventura, L., Dias, P., et al. (2022). Effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model. Neurological Sciences, 153. doi:10.1007/s10072-022-05928-w
NLM
Comim CM, Soares JA, Alberti A, Freiberger V, Ventura L, Dias P, Schactae AL, Grigollo LR, Steckert AV, Martins DF, Nodari Junior RJ, Vainzof M, Quevedo J. Effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model [Internet]. Neurological Sciences. 2022 ; 153[citado 2024 nov. 13 ] Available from: https://doi.org/10.1007/s10072-022-05928-w
Vancouver
Comim CM, Soares JA, Alberti A, Freiberger V, Ventura L, Dias P, Schactae AL, Grigollo LR, Steckert AV, Martins DF, Nodari Junior RJ, Vainzof M, Quevedo J. Effects of low-intensity training on the brain and muscle in the congenital muscular dystrophy 1D model [Internet]. Neurological Sciences. 2022 ; 153[citado 2024 nov. 13 ] Available from: https://doi.org/10.1007/s10072-022-05928-w
Artigo de periodico
Sarcoglycanopathies: an update (2021)
Vainzof, Mariz ; Souza, Lucas S; Gurgel-Giannetti, Juliana; Zatz, Mayana
Source: Neuromuscular Disorders. Unidade: IB
Subjects: DISTROFIA MUSCULAR, EXPRESSÃO GÊNICA, MUTAÇÃO GENÉTICA, GENES
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ABNT
VAINZOF, Mariz et al. Sarcoglycanopathies: an update. Neuromuscular Disorders, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2021.07.014. Acesso em: 13 nov. 2024.
APA
Vainzof, M., Souza, L. S., Gurgel-Giannetti, J., & Zatz, M. (2021). Sarcoglycanopathies: an update. Neuromuscular Disorders. doi:10.1016/j.nmd.2021.07.014
NLM
Vainzof M, Souza LS, Gurgel-Giannetti J, Zatz M. Sarcoglycanopathies: an update [Internet]. Neuromuscular Disorders. 2021 ;[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.nmd.2021.07.014
Vancouver
Vainzof M, Souza LS, Gurgel-Giannetti J, Zatz M. Sarcoglycanopathies: an update [Internet]. Neuromuscular Disorders. 2021 ;[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.nmd.2021.07.014
Artigo de periodico
Muscle satellite cells and impaired late stage regeneration in diferent murine models for muscular dystrophies (2019)
Ribeiro Jr., Antonio F ; Souza, Lucas S; Almeida, Camila F; Ishiba, Renata ; Fernandes, Stephanie A; Guerrieri, Danielle A; Santos, André L. F; Onofre-Oliveira, Paula C.G ; Vainzof, Mariz
Source: Scientific Reports. Unidade: IB
Subjects: DISTROFIA MUSCULAR, CÉLULAS-TRONCO, EXPRESSÃO GÊNICA, DOENÇAS DEGENERATIVAS, MÚSCULOS, MODELOS ANIMAIS DE DOENÇAS
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RIBEIRO JR., Antonio F et al. Muscle satellite cells and impaired late stage regeneration in diferent murine models for muscular dystrophies. Scientific Reports, v. 9, 2019Tradução . . Disponível em: https://doi.org/10.1038/s41598-019-48156-7. Acesso em: 13 nov. 2024.
APA
Ribeiro Jr., A. F., Souza, L. S., Almeida, C. F., Ishiba, R., Fernandes, S. A., Guerrieri, D. A., et al. (2019). Muscle satellite cells and impaired late stage regeneration in diferent murine models for muscular dystrophies. Scientific Reports, 9. doi:10.1038/s41598-019-48156-7
NLM
Ribeiro Jr. AF, Souza LS, Almeida CF, Ishiba R, Fernandes SA, Guerrieri DA, Santos ALF, Onofre-Oliveira PCG, Vainzof M. Muscle satellite cells and impaired late stage regeneration in diferent murine models for muscular dystrophies [Internet]. Scientific Reports. 2019 ; 9[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/s41598-019-48156-7
Vancouver
Ribeiro Jr. AF, Souza LS, Almeida CF, Ishiba R, Fernandes SA, Guerrieri DA, Santos ALF, Onofre-Oliveira PCG, Vainzof M. Muscle satellite cells and impaired late stage regeneration in diferent murine models for muscular dystrophies [Internet]. Scientific Reports. 2019 ; 9[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/s41598-019-48156-7
Artigo de periodico
Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin‐defcient mouse (2019)
Ishiba, Renata ; Santos, André Luis F.; Almeida, Camila F; Caires-Junior, Luiz Carlos ; Ribeiro Jr., Antonio F.; Ayub‐Guerrieri, Danielle ; Fernandes, Stephanie A; Souza, Lucas S; Vainzof, Mariz
Source: Journal of Molecular Histology. Unidade: IB
Subjects: DISTROFIA MUSCULAR, FIBRAS MUSCULARES, EXPRESSÃO GÊNICA, PROTEÍNAS MUSCULARES, MÚSCULOS
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ISHIBA, Renata et al. Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin‐defcient mouse. Journal of Molecular Histology, v. 50, n. 4, p. 375-387, 2019Tradução . . Disponível em: https://doi.org/10.1007/s10735-019-09834-y. Acesso em: 13 nov. 2024.
APA
Ishiba, R., Santos, A. L. F., Almeida, C. F., Caires-Junior, L. C., Ribeiro Jr., A. F., Ayub‐Guerrieri, D., et al. (2019). Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin‐defcient mouse. Journal of Molecular Histology, 50( 4), 375-387. doi:10.1007/s10735-019-09834-y
NLM
Ishiba R, Santos ALF, Almeida CF, Caires-Junior LC, Ribeiro Jr. AF, Ayub‐Guerrieri D, Fernandes SA, Souza LS, Vainzof M. Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin‐defcient mouse [Internet]. Journal of Molecular Histology. 2019 ; 50( 4): 375-387.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1007/s10735-019-09834-y
Vancouver
Ishiba R, Santos ALF, Almeida CF, Caires-Junior LC, Ribeiro Jr. AF, Ayub‐Guerrieri D, Fernandes SA, Souza LS, Vainzof M. Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin‐defcient mouse [Internet]. Journal of Molecular Histology. 2019 ; 50( 4): 375-387.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1007/s10735-019-09834-y
Artigo de periodico
Efficient exon skipping of SGCG mutations mediated by phosphorodiamidate morpholino oligomers (2018)
Wyatt, Eugene J.; Demonbreun, Alexis R; Kim, Ellis Y; Puckelwartz, Megan J; Vo, Andy H; Dellefave-Castillo, Lisa M; Gao, Quan Q; Vainzof, Mariz ; Pavanello, Rita C M; Zatz, Mayana ; McNally, Elizabeth M
Source: JCI Insight. Unidade: IB
Subjects: DOENÇAS NEUROMUSCULARES, DISTROFIA MUSCULAR, EXONS, MUTAÇÃO GENÉTICA, PROTEÍNAS
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WYATT, Eugene J. et al. Efficient exon skipping of SGCG mutations mediated by phosphorodiamidate morpholino oligomers. JCI Insight, v. 3, n. 9, 2018Tradução . . Disponível em: https://doi.org/10.1172/jci.insight.99357. Acesso em: 13 nov. 2024.
APA
Wyatt, E. J., Demonbreun, A. R., Kim, E. Y., Puckelwartz, M. J., Vo, A. H., Dellefave-Castillo, L. M., et al. (2018). Efficient exon skipping of SGCG mutations mediated by phosphorodiamidate morpholino oligomers. JCI Insight, 3( 9). doi:10.1172/jci.insight.99357
NLM
Wyatt EJ, Demonbreun AR, Kim EY, Puckelwartz MJ, Vo AH, Dellefave-Castillo LM, Gao QQ, Vainzof M, Pavanello RCM, Zatz M, McNally EM. Efficient exon skipping of SGCG mutations mediated by phosphorodiamidate morpholino oligomers [Internet]. JCI Insight. 2018 ; 3( 9):[citado 2024 nov. 13 ] Available from: https://doi.org/10.1172/jci.insight.99357
Vancouver
Wyatt EJ, Demonbreun AR, Kim EY, Puckelwartz MJ, Vo AH, Dellefave-Castillo LM, Gao QQ, Vainzof M, Pavanello RCM, Zatz M, McNally EM. Efficient exon skipping of SGCG mutations mediated by phosphorodiamidate morpholino oligomers [Internet]. JCI Insight. 2018 ; 3( 9):[citado 2024 nov. 13 ] Available from: https://doi.org/10.1172/jci.insight.99357
Apresentacao sonora/cenica/entrevista
Mayana Zatz, la brésilienne passée maître dans l'art de détecter les maladies rares (2017)
Zatz, Mayana
Source: FRANCE 24. Unidade: IB
Subjects: GENETICISTAS, DOENÇAS GENÉTICAS, DISTROFIA MUSCULAR, PESQUISA
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ABNT
ZATZ, Mayana. Mayana Zatz, la brésilienne passée maître dans l'art de détecter les maladies rares. FRANCE 24. Issy Les Mouleneaux: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 13 nov. 2024. , 2017
APA
Zatz, M. (2017). Mayana Zatz, la brésilienne passée maître dans l'art de détecter les maladies rares. FRANCE 24. Issy Les Mouleneaux: Instituto de Biociências, Universidade de São Paulo.
NLM
Zatz M. Mayana Zatz, la brésilienne passée maître dans l'art de détecter les maladies rares. FRANCE 24. 2017 ;[citado 2024 nov. 13 ]
Vancouver
Zatz M. Mayana Zatz, la brésilienne passée maître dans l'art de détecter les maladies rares. FRANCE 24. 2017 ;[citado 2024 nov. 13 ]
Artigo de periodico
Immunoglobulin therapy ameliorates the phenotype and increases lifespan in the severely affected dystrophin-utrophin double knockout mice (2017)
Nunes, Bruno Ghirotto ; Loures, Flavio Vieira ; Bueno, Heloisa Maria Siqueira ; Cangussu, Erica Baroni; Goulart, Ernesto ; Coatti, Giuliana Castello ; Caldini, EliaTamaso Espin Garcia ; Condino Neto, Antonio ; Zatz, Mayana
Source: European Journal of Human Genetics. Unidades: FM, ICB, IB
Subjects: IMUNOLOGIA, SISTEMA IMUNE, IMUNOGLOBULINAS, DOENÇAS AUTOIMUNES, CAMUNDONGOS, FENÓTIPOS, DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, CITOCINAS, SECREÇÃO, CÉLULAS DENDRÍTICAS, LINFÓCITOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NUNES, Bruno Ghirotto et al. Immunoglobulin therapy ameliorates the phenotype and increases lifespan in the severely affected dystrophin-utrophin double knockout mice. European Journal of Human Genetics, v. 25, n. 12, p. 1388-1396, 2017Tradução . . Disponível em: https://doi.org/10.1038/s41431-017-0017-y. Acesso em: 13 nov. 2024.
APA
Nunes, B. G., Loures, F. V., Bueno, H. M. S., Cangussu, E. B., Goulart, E., Coatti, G. C., et al. (2017). Immunoglobulin therapy ameliorates the phenotype and increases lifespan in the severely affected dystrophin-utrophin double knockout mice. European Journal of Human Genetics, 25( 12), 1388-1396. doi:10.1038/s41431-017-0017-y
NLM
Nunes BG, Loures FV, Bueno HMS, Cangussu EB, Goulart E, Coatti GC, Caldini ETEG, Condino Neto A, Zatz M. Immunoglobulin therapy ameliorates the phenotype and increases lifespan in the severely affected dystrophin-utrophin double knockout mice [Internet]. European Journal of Human Genetics. 2017 ; 25( 12): 1388-1396.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/s41431-017-0017-y
Vancouver
Nunes BG, Loures FV, Bueno HMS, Cangussu EB, Goulart E, Coatti GC, Caldini ETEG, Condino Neto A, Zatz M. Immunoglobulin therapy ameliorates the phenotype and increases lifespan in the severely affected dystrophin-utrophin double knockout mice [Internet]. European Journal of Human Genetics. 2017 ; 25( 12): 1388-1396.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/s41431-017-0017-y
Artigo de periodico-carta/editorial
Immune-mediated rippling muscle disease in a patient with treated hypothyroidism. [Carta] (2017)
Ducci, Renata Dal-Prá ; Scola, Rosana Herminia ; Lorenzoni, Paulo José ; Kay, Claudia Suemi Kamoi ; Blood, Marcelo Rezende Young ; Leão, Leonardo G ; Vainzof, Mariz
Source: Journal of the Neurological Sciences. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, DISTROFIA MUSCULAR, DOENÇAS AUTOIMUNES, HIPOTIREOIDISMO, BIÓPSIA, MUTAÇÃO GENÉTICA, FÁRMACOS IMUNOSSUPRESSORES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DUCCI, Renata Dal-Prá et al. Immune-mediated rippling muscle disease in a patient with treated hypothyroidism. [Carta]. Journal of the Neurological Sciences. Amsterdam: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.jns.2017.10.016. Acesso em: 13 nov. 2024. , 2017
APA
Ducci, R. D. -P., Scola, R. H., Lorenzoni, P. J., Kay, C. S. K., Blood, M. R. Y., Leão, L. G., & Vainzof, M. (2017). Immune-mediated rippling muscle disease in a patient with treated hypothyroidism. [Carta]. Journal of the Neurological Sciences. Amsterdam: Instituto de Biociências, Universidade de São Paulo. doi:10.1016/j.jns.2017.10.016
NLM
Ducci RD-P, Scola RH, Lorenzoni PJ, Kay CSK, Blood MRY, Leão LG, Vainzof M. Immune-mediated rippling muscle disease in a patient with treated hypothyroidism. [Carta] [Internet]. Journal of the Neurological Sciences. 2017 ; 383 53-55.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.jns.2017.10.016
Vancouver
Ducci RD-P, Scola RH, Lorenzoni PJ, Kay CSK, Blood MRY, Leão LG, Vainzof M. Immune-mediated rippling muscle disease in a patient with treated hypothyroidism. [Carta] [Internet]. Journal of the Neurological Sciences. 2017 ; 383 53-55.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.jns.2017.10.016
Trabalho de evento-resumo periodico
Osteopontin expression during chronic and acute muscle injury (2017)
Tasaki, L; Ishiba, R; Ayub-Guerrieri, D; Almeida, C; Fernandes, S; Ribeiro Jr., A; Galleni, L; Souza, L; Santos, A; Vainzof, Mariz
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: IB
Subjects: DOENÇAS NEUROMUSCULARES, DISTROFIA MUSCULAR, EXPRESSÃO GÊNICA, MODELOS ANIMAIS, PROTEÍNAS MUSCULARES, BIOLOGIA CELULAR, GENÉTICA MÉDICA
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ABNT
TASAKI, L et al. Osteopontin expression during chronic and acute muscle injury. Neuromuscular Disorders. London: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2017.06.360. Acesso em: 13 nov. 2024. , 2017
APA
Tasaki, L., Ishiba, R., Ayub-Guerrieri, D., Almeida, C., Fernandes, S., Ribeiro Jr., A., et al. (2017). Osteopontin expression during chronic and acute muscle injury. Neuromuscular Disorders. London: Instituto de Biociências, Universidade de São Paulo. doi:10.1016/j.nmd.2017.06.360
NLM
Tasaki L, Ishiba R, Ayub-Guerrieri D, Almeida C, Fernandes S, Ribeiro Jr. A, Galleni L, Souza L, Santos A, Vainzof M. Osteopontin expression during chronic and acute muscle injury [Internet]. Neuromuscular Disorders. 2017 ; 27 S193.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.nmd.2017.06.360
Vancouver
Tasaki L, Ishiba R, Ayub-Guerrieri D, Almeida C, Fernandes S, Ribeiro Jr. A, Galleni L, Souza L, Santos A, Vainzof M. Osteopontin expression during chronic and acute muscle injury [Internet]. Neuromuscular Disorders. 2017 ; 27 S193.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.nmd.2017.06.360
Artigo de periodico
Neuromuscular disorders: genes, genetic counseling and therapeutic trials (2016)
Zatz, Mayana ; Passos-Bueno, Maria Rita ; Vainzof, Mariz
Source: Genetics and Molecular Biology. Unidade: IB
Subjects: DOENÇAS NEUROMUSCULARES, DOENÇAS GENÉTICAS, DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, ACONSELHAMENTO GENÉTICO, CÉLULAS-TRONCO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZATZ, Mayana e PASSOS-BUENO, Maria Rita e VAINZOF, Mariz. Neuromuscular disorders: genes, genetic counseling and therapeutic trials. Genetics and Molecular Biology, v. 39, n. 3, p. 339-348, 2016Tradução . . Disponível em: https://doi.org/10.1590/1678-4685-GMB-2016-0019. Acesso em: 13 nov. 2024.
APA
Zatz, M., Passos-Bueno, M. R., & Vainzof, M. (2016). Neuromuscular disorders: genes, genetic counseling and therapeutic trials. Genetics and Molecular Biology, 39( 3), 339-348. doi:10.1590/1678-4685-GMB-2016-0019
NLM
Zatz M, Passos-Bueno MR, Vainzof M. Neuromuscular disorders: genes, genetic counseling and therapeutic trials [Internet]. Genetics and Molecular Biology. 2016 ; 39( 3): 339-348.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1590/1678-4685-GMB-2016-0019
Vancouver
Zatz M, Passos-Bueno MR, Vainzof M. Neuromuscular disorders: genes, genetic counseling and therapeutic trials [Internet]. Genetics and Molecular Biology. 2016 ; 39( 3): 339-348.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1590/1678-4685-GMB-2016-0019
Artigo de periodico
Activity of Krebs cycle enzymes in mdx mice (2016)
Comim, Clarissa M ; Hoepers, Andreza; Ventura, Letícia; Freiberger, Viviane; Dominguini, Diogo; Mina, Francielle; Mendonça, Bruna P; Scaini, Giselli ; Vainzof, Mariz ; Streck, Emilio L ; Quevedo, João
Source: Muscle Nerve. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS DEGENERATIVAS, MUTAÇÃO GENÉTICA, METABOLISMO ENERGÉTICO, MÚSCULO ESQUELÉTICO, PROTEÍNAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
COMIM, Clarissa M et al. Activity of Krebs cycle enzymes in mdx mice. Muscle Nerve, v. 53, n. Ja 2016, p. 91-95, 2016Tradução . . Disponível em: https://doi.org/10.1002/mus.24704. Acesso em: 13 nov. 2024.
APA
Comim, C. M., Hoepers, A., Ventura, L., Freiberger, V., Dominguini, D., Mina, F., et al. (2016). Activity of Krebs cycle enzymes in mdx mice. Muscle Nerve, 53( Ja 2016), 91-95. doi:10.1002/mus.24704
NLM
Comim CM, Hoepers A, Ventura L, Freiberger V, Dominguini D, Mina F, Mendonça BP, Scaini G, Vainzof M, Streck EL, Quevedo J. Activity of Krebs cycle enzymes in mdx mice [Internet]. Muscle Nerve. 2016 ; 53( Ja 2016): 91-95.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/mus.24704
Vancouver
Comim CM, Hoepers A, Ventura L, Freiberger V, Dominguini D, Mina F, Mendonça BP, Scaini G, Vainzof M, Streck EL, Quevedo J. Activity of Krebs cycle enzymes in mdx mice [Internet]. Muscle Nerve. 2016 ; 53( Ja 2016): 91-95.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/mus.24704
Artigo de periodico
Comparative transcriptome analysis of muscular dystrophy models Largemyd , Dmdmdx/Largemyd and Dmdmdx: what makes them different? (2016)
Almeida, Camila F; Martins, Poliana C. M; Vainzof, Mariz
Source: European Journal of Human Genetics. Unidades: IB, IQ
Subjects: DOENÇAS GENÉTICAS, DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA, GENOMAS, PROTEÍNAS, MODELOS ANIMAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALMEIDA, Camila F e MARTINS, Poliana C. M e VAINZOF, Mariz. Comparative transcriptome analysis of muscular dystrophy models Largemyd , Dmdmdx/Largemyd and Dmdmdx: what makes them different?. European Journal of Human Genetics, v. 24, p. 1301-1309, 2016Tradução . . Disponível em: https://doi.org/10.1038/ejhg.2016.16. Acesso em: 13 nov. 2024.
APA
Almeida, C. F., Martins, P. C. M., & Vainzof, M. (2016). Comparative transcriptome analysis of muscular dystrophy models Largemyd , Dmdmdx/Largemyd and Dmdmdx: what makes them different? European Journal of Human Genetics, 24, 1301-1309. doi:10.1038/ejhg.2016.16
NLM
Almeida CF, Martins PCM, Vainzof M. Comparative transcriptome analysis of muscular dystrophy models Largemyd , Dmdmdx/Largemyd and Dmdmdx: what makes them different? [Internet]. European Journal of Human Genetics. 2016 ; 24 1301-1309.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/ejhg.2016.16
Vancouver
Almeida CF, Martins PCM, Vainzof M. Comparative transcriptome analysis of muscular dystrophy models Largemyd , Dmdmdx/Largemyd and Dmdmdx: what makes them different? [Internet]. European Journal of Human Genetics. 2016 ; 24 1301-1309.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/ejhg.2016.16
Artigo de periodico
Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers (2016)
Vainzof, Mariz ; Feitosa, Leticia; Canovas, Marta; Ayub-Guerrieri, Danielle; Pavanello, Rita de Cássia M; Zatz, Mayana
Source: Neuromuscular Disorders. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS NEUROMUSCULARES, PROTEÍNAS MUSCULARES, MUTAÇÃO GENÉTICA, ESTUDO DE CASO, GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers. Neuromuscular Disorders, v. 26, n. 3, p. 197-200, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2016.01.001. Acesso em: 13 nov. 2024.
APA
Vainzof, M., Feitosa, L., Canovas, M., Ayub-Guerrieri, D., Pavanello, R. de C. M., & Zatz, M. (2016). Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers. Neuromuscular Disorders, 26( 3), 197-200. doi:10.1016/j.nmd.2016.01.001
NLM
Vainzof M, Feitosa L, Canovas M, Ayub-Guerrieri D, Pavanello R de CM, Zatz M. Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers [Internet]. Neuromuscular Disorders. 2016 ; 26( 3): 197-200.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.nmd.2016.01.001
Vancouver
Vainzof M, Feitosa L, Canovas M, Ayub-Guerrieri D, Pavanello R de CM, Zatz M. Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers [Internet]. Neuromuscular Disorders. 2016 ; 26( 3): 197-200.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.nmd.2016.01.001
Trabalho de evento-resumo periodico
Study of myogenic potential of extra cellular vesicles in murine models for muscular dystrophies (2016)
Ayub-Guerrieri, D; Ribeiro Junior, A; Ishiba, R; Yumi, L; Semedo-Kuriki, P; Vainzof, Mariz
Source: Neuromuscular Disorders. Conference titles: International Congress of the World Muscle Society. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, DISTROFIA MUSCULAR, DOENÇAS DEGENERATIVAS, MODELOS ANIMAIS DE DOENÇAS, CÉLULAS-TRONCO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AYUB-GUERRIERI, D et al. Study of myogenic potential of extra cellular vesicles in murine models for muscular dystrophies. Neuromuscular Disorders. London: Instituto de Biociências, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.nmd.2016.06.155. Acesso em: 13 nov. 2024. , 2016
APA
Ayub-Guerrieri, D., Ribeiro Junior, A., Ishiba, R., Yumi, L., Semedo-Kuriki, P., & Vainzof, M. (2016). Study of myogenic potential of extra cellular vesicles in murine models for muscular dystrophies. Neuromuscular Disorders. London: Instituto de Biociências, Universidade de São Paulo. doi:10.1016/j.nmd.2016.06.155
NLM
Ayub-Guerrieri D, Ribeiro Junior A, Ishiba R, Yumi L, Semedo-Kuriki P, Vainzof M. Study of myogenic potential of extra cellular vesicles in murine models for muscular dystrophies [Internet]. Neuromuscular Disorders. 2016 ; 26 S128.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.nmd.2016.06.155
Vancouver
Ayub-Guerrieri D, Ribeiro Junior A, Ishiba R, Yumi L, Semedo-Kuriki P, Vainzof M. Study of myogenic potential of extra cellular vesicles in murine models for muscular dystrophies [Internet]. Neuromuscular Disorders. 2016 ; 26 S128.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.nmd.2016.06.155
Artigo de periodico
Dystrophin is required for proper functioning of luminance and red–green cone opponent mechanisms in the human retina (2016)
Barboni, Mirella Telles Salgueiro; Martins, Cristiane Maria Gomes; Nagy, Balázs Vince; Tsai, Tina; Damico, Franscisco Max; Costa, Marcelo Fernandes da ; Pavanello, Rita de Cassia M; Lourenço, Naila Cristina Vilaça; Cerqueira, Antonia Maria Pereira de; Zatz, Mayana ; Kremers, Jan; Ventura, Dora Selma Fix
Source: Investigative Ophthalmology & Visual Science. Unidades: IP, IB
Subjects: RETINA, VISÃO, ELETRORRETINOGRAFIA, DISTROFIA MUSCULAR, DOENÇAS NEURODEGENERATIVAS, PROTEÍNAS MUSCULARES, ELETROFISIOLOGIA, PERCEPÇÃO DE COR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARBONI, Mirella Telles Salgueiro et al. Dystrophin is required for proper functioning of luminance and red–green cone opponent mechanisms in the human retina. Investigative Ophthalmology & Visual Science, v. 57, n. 8, p. 3581-3587, 2016Tradução . . Disponível em: https://doi.org/10.1167/iovs.16-19287. Acesso em: 13 nov. 2024.
APA
Barboni, M. T. S., Martins, C. M. G., Nagy, B. V., Tsai, T., Damico, F. M., Costa, M. F. da, et al. (2016). Dystrophin is required for proper functioning of luminance and red–green cone opponent mechanisms in the human retina. Investigative Ophthalmology & Visual Science, 57( 8), 3581-3587. doi:10.1167/iovs.16-19287
NLM
Barboni MTS, Martins CMG, Nagy BV, Tsai T, Damico FM, Costa MF da, Pavanello R de CM, Lourenço NCV, Cerqueira AMP de, Zatz M, Kremers J, Ventura DSF. Dystrophin is required for proper functioning of luminance and red–green cone opponent mechanisms in the human retina [Internet]. Investigative Ophthalmology & Visual Science. 2016 ;57( 8): 3581-3587.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1167/iovs.16-19287
Vancouver
Barboni MTS, Martins CMG, Nagy BV, Tsai T, Damico FM, Costa MF da, Pavanello R de CM, Lourenço NCV, Cerqueira AMP de, Zatz M, Kremers J, Ventura DSF. Dystrophin is required for proper functioning of luminance and red–green cone opponent mechanisms in the human retina [Internet]. Investigative Ophthalmology & Visual Science. 2016 ;57( 8): 3581-3587.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1167/iovs.16-19287
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 13 nov. 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 nov. 13 ] 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 nov. 13 ] Available from: https://doi.org/10.1007/s12015-016-9659-3
Artigo de periodico
The mdx Mutation in the 129/Sv Background Results in a Milder Phenotype (2016)
Calyjur, Priscila Clara; Almeida, Camila de Freitas; Ayub-Guerrieri, Danielle; Ribeiro Junior, Antonio Fernando; Fernandes, Stephanie de Alcântara; Ishiba, Renata; Santos, André Luís Fernandes dos; Onofre-Oliveira, Paula; Vainzof, Mariz
Source: PLOS ONE. Unidade: IB
Subjects: DISTROFIA MUSCULAR, MUTAÇÃO, FENÓTIPOS, GENÉTICA MOLECULAR, EXPRESSÃO GÊNICA, MODELOS ANIMAIS (TESTES;TERAPIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CALYJUR, Priscila Clara et al. The mdx Mutation in the 129/Sv Background Results in a Milder Phenotype. PLOS ONE, v. 11, n. 3, 2016Tradução . . Disponível em: https://doi.org/10.1371/journal.pone.0150748. Acesso em: 13 nov. 2024.
APA
Calyjur, P. C., Almeida, C. de F., Ayub-Guerrieri, D., Ribeiro Junior, A. F., Fernandes, S. de A., Ishiba, R., et al. (2016). The mdx Mutation in the 129/Sv Background Results in a Milder Phenotype. PLOS ONE, 11( 3). doi:10.1371/journal.pone.0150748
NLM
Calyjur PC, Almeida C de F, Ayub-Guerrieri D, Ribeiro Junior AF, Fernandes S de A, Ishiba R, Santos ALF dos, Onofre-Oliveira P, Vainzof M. The mdx Mutation in the 129/Sv Background Results in a Milder Phenotype [Internet]. PLOS ONE. 2016 ; 11( 3):[citado 2024 nov. 13 ] Available from: https://doi.org/10.1371/journal.pone.0150748
Vancouver
Calyjur PC, Almeida C de F, Ayub-Guerrieri D, Ribeiro Junior AF, Fernandes S de A, Ishiba R, Santos ALF dos, Onofre-Oliveira P, Vainzof M. The mdx Mutation in the 129/Sv Background Results in a Milder Phenotype [Internet]. PLOS ONE. 2016 ; 11( 3):[citado 2024 nov. 13 ] Available from: https://doi.org/10.1371/journal.pone.0150748

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