ReP USP - Resultado da busca

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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 16 maio 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 maio 16 ] 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 maio 16 ] Available from: https://doi.org/10.1172/jci.insight.99357
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: 16 maio 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 maio 16 ] 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 maio 16 ] Available from: https://doi.org/10.1038/s41431-017-0017-y
Artigo de periodico
Idiopathic hyperCKemia and malignant hyperthermia susceptibility (2017)
Santos, Joilson M.; Andrade, Pamela V; Galleni, Leonardo ; Vainzof, Mariz ; Sobreira, Claudia F. R.; Schmidt, Beny ; Oliveira, Acary S. B; Amaral, José L G; Silva, Helga C.A
Source: Canadian Journal of Anesthesia/Journal canadien d'anesthésie. Unidade: IB
Subjects: DOENÇAS NEUROMUSCULARES, MUTAÇÃO GENÉTICA, HISTOQUÍMICA, ENZIMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Joilson M. et al. Idiopathic hyperCKemia and malignant hyperthermia susceptibility. Canadian Journal of Anesthesia/Journal canadien d'anesthésie, v. 64, p. 1202-1210, 2017Tradução . . Disponível em: https://doi.org/10.1007/s12630-017-0978-x. Acesso em: 16 maio 2024.
APA
Santos, J. M., Andrade, P. V., Galleni, L., Vainzof, M., Sobreira, C. F. R., Schmidt, B., et al. (2017). Idiopathic hyperCKemia and malignant hyperthermia susceptibility. Canadian Journal of Anesthesia/Journal canadien d'anesthésie, 64, 1202-1210. doi:10.1007/s12630-017-0978-x
NLM
Santos JM, Andrade PV, Galleni L, Vainzof M, Sobreira CFR, Schmidt B, Oliveira ASB, Amaral JLG, Silva HCA. Idiopathic hyperCKemia and malignant hyperthermia susceptibility [Internet]. Canadian Journal of Anesthesia/Journal canadien d'anesthésie. 2017 ; 64 1202-1210.[citado 2024 maio 16 ] Available from: https://doi.org/10.1007/s12630-017-0978-x
Vancouver
Santos JM, Andrade PV, Galleni L, Vainzof M, Sobreira CFR, Schmidt B, Oliveira ASB, Amaral JLG, Silva HCA. Idiopathic hyperCKemia and malignant hyperthermia susceptibility [Internet]. Canadian Journal of Anesthesia/Journal canadien d'anesthésie. 2017 ; 64 1202-1210.[citado 2024 maio 16 ] Available from: https://doi.org/10.1007/s12630-017-0978-x
Artigo de periodico
Muscle satellite cells: exploring the basic biology to rule them (2016)
Almeida, Camila F; Fernandes, Stephanie A; Ribeiro Junior, Antonio F ; Okamoto, Oswaldo Keith ; Vainzof, Mariz
Source: Stem Cells International. Unidade: IB
Subjects: GENÉTICA MÉDICA, MÚSCULO ESQUELÉTICO, CÉLULAS-TRONCO, BIOLOGIA CELULAR, MÚSCULOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ALMEIDA, Camila F et al. Muscle satellite cells: exploring the basic biology to rule them. Stem Cells International, p. 14 2016, 2016Tradução . . Disponível em: https://doi.org/10.1155/2016/1078686. Acesso em: 16 maio 2024.
APA
Almeida, C. F., Fernandes, S. A., Ribeiro Junior, A. F., Okamoto, O. K., & Vainzof, M. (2016). Muscle satellite cells: exploring the basic biology to rule them. Stem Cells International, 14 2016. doi:10.1155/2016/1078686
NLM
Almeida CF, Fernandes SA, Ribeiro Junior AF, Okamoto OK, Vainzof M. Muscle satellite cells: exploring the basic biology to rule them [Internet]. Stem Cells International. 2016 ; 14 2016.[citado 2024 maio 16 ] Available from: https://doi.org/10.1155/2016/1078686
Vancouver
Almeida CF, Fernandes SA, Ribeiro Junior AF, Okamoto OK, Vainzof M. Muscle satellite cells: exploring the basic biology to rule them [Internet]. Stem Cells International. 2016 ; 14 2016.[citado 2024 maio 16 ] Available from: https://doi.org/10.1155/2016/1078686
Artigo de periodico
Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy (2006)
Tonini, Maria Manuela O; Lemmers, Richard J.L.F; Pavanello, Rita C M; Cerqueira, Antonia M.P; Frants, Rune R; Maarel, Silvere M. van der ; Zatz, Mayana
Source: Human Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR, BIOLOGIA CELULAR, MÚSCULOS, SANGUE, DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TONINI, Maria Manuela O et al. Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy. Human Genetics, v. 119, p. 23-28, 2006Tradução . . Disponível em: https://doi.org/10.1007/s00439-005-0100-2. Acesso em: 16 maio 2024.
APA
Tonini, M. M. O., Lemmers, R. J. L. F., Pavanello, R. C. M., Cerqueira, A. M. P., Frants, R. R., Maarel, S. M. van der, & Zatz, M. (2006). Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy. Human Genetics, 119, 23-28. doi:10.1007/s00439-005-0100-2
NLM
Tonini MMO, Lemmers RJLF, Pavanello RCM, Cerqueira AMP, Frants RR, Maarel SM van der, Zatz M. Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy [Internet]. Human Genetics. 2006 ; 119 23-28.[citado 2024 maio 16 ] Available from: https://doi.org/10.1007/s00439-005-0100-2
Vancouver
Tonini MMO, Lemmers RJLF, Pavanello RCM, Cerqueira AMP, Frants RR, Maarel SM van der, Zatz M. Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy [Internet]. Human Genetics. 2006 ; 119 23-28.[citado 2024 maio 16 ] Available from: https://doi.org/10.1007/s00439-005-0100-2
Artigo de periodico
Prenatal diagnosis in laminin aα2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centers (2005)
Vainzof, Mariz ; Richard, Pascale; Herrmann, Ralf ; Jimenez-Mallebrera, Cecilia ; Talim, Beril ; Yamamoto, Lydia U; Ledeuil, Céline; Mein, Rachael ; Abbs, Stephen ; Brockington, Martin; Romero, Norma B; Zatz, Mayana ; Topaloglu, Haluk ; Voit, Thomas ; Sewry, Caroline ; Muntoni, Francesco ; Guicheney, Pascale ; Tomé, Fernando M.S
Source: Neuromuscular Disorders. Unidade: IB
Subjects: GENÉTICA MÉDICA, DISTROFIA MUSCULAR, PROTEÍNAS MUSCULARES, ACONSELHAMENTO GENÉTICO, DIAGNÓSTICO PRÉ-NATAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Prenatal diagnosis in laminin aα2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centers. Neuromuscular Disorders, v. 15, p. 588-594, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.nmd.2005.04.009. Acesso em: 16 maio 2024.
APA
Vainzof, M., Richard, P., Herrmann, R., Jimenez-Mallebrera, C., Talim, B., Yamamoto, L. U., et al. (2005). Prenatal diagnosis in laminin aα2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centers. Neuromuscular Disorders, 15, 588-594. doi:10.1016/j.nmd.2005.04.009
NLM
Vainzof M, Richard P, Herrmann R, Jimenez-Mallebrera C, Talim B, Yamamoto LU, Ledeuil C, Mein R, Abbs S, Brockington M, Romero NB, Zatz M, Topaloglu H, Voit T, Sewry C, Muntoni F, Guicheney P, Tomé FMS. Prenatal diagnosis in laminin aα2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centers [Internet]. Neuromuscular Disorders. 2005 ; 15 588-594.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.nmd.2005.04.009
Vancouver
Vainzof M, Richard P, Herrmann R, Jimenez-Mallebrera C, Talim B, Yamamoto LU, Ledeuil C, Mein R, Abbs S, Brockington M, Romero NB, Zatz M, Topaloglu H, Voit T, Sewry C, Muntoni F, Guicheney P, Tomé FMS. Prenatal diagnosis in laminin aα2 chain (merosin)-deficient congenital muscular dystrophy: a collective experience of five international centers [Internet]. Neuromuscular Disorders. 2005 ; 15 588-594.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.nmd.2005.04.009
Artigo de periodico
Asymptomatic carriers for homozygous novel mutations in the FKRP gene: the other end of the spectrum (2003)
Paula, Flavia de ; Vieira, Natassia ; Starling, Alessandra; Yamamoto, Lydia Uraco; Lima, Bruno; Pavanello, Rita de Cássia; Vainzof, Mariz ; Nigro, Vincenzo; Zatz, Mayana
Source: European Journal of Human Genetics. Unidade: IB
Subjects: DISTROFIA MUSCULAR, DOENÇAS GENÉTICAS, MUTAÇÃO GENÉTICA, PROTEÍNAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PAULA, Flavia de et al. Asymptomatic carriers for homozygous novel mutations in the FKRP gene: the other end of the spectrum. European Journal of Human Genetics, v. 11, p. 923-930, 2003Tradução . . Disponível em: https://doi.org/10.1038/sj.ejhg.5201066. Acesso em: 16 maio 2024.
APA
Paula, F. de, Vieira, N., Starling, A., Yamamoto, L. U., Lima, B., Pavanello, R. de C., et al. (2003). Asymptomatic carriers for homozygous novel mutations in the FKRP gene: the other end of the spectrum. European Journal of Human Genetics, 11, 923-930. doi:10.1038/sj.ejhg.5201066
NLM
Paula F de, Vieira N, Starling A, Yamamoto LU, Lima B, Pavanello R de C, Vainzof M, Nigro V, Zatz M. Asymptomatic carriers for homozygous novel mutations in the FKRP gene: the other end of the spectrum [Internet]. European Journal of Human Genetics. 2003 ; 11 923-930.[citado 2024 maio 16 ] Available from: https://doi.org/10.1038/sj.ejhg.5201066
Vancouver
Paula F de, Vieira N, Starling A, Yamamoto LU, Lima B, Pavanello R de C, Vainzof M, Nigro V, Zatz M. Asymptomatic carriers for homozygous novel mutations in the FKRP gene: the other end of the spectrum [Internet]. European Journal of Human Genetics. 2003 ; 11 923-930.[citado 2024 maio 16 ] Available from: https://doi.org/10.1038/sj.ejhg.5201066
Artigo de periodico
Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies (2001)
Vainzof, Mariz ; Anderson, Louise V. B ; McNally, Elizabeth M ; Davis, Dawn B ; Faulkner, Georgine ; Valle, Giorgio ; Moreira, Eloisa S; Pavanello, Rita C M; Passos-Bueno, Maria Rita ; Zatz, Mayana
Source: Journal of Molecular Neuroscience. Unidade: IB
Subjects: GENÉTICA MÉDICA, DISTROFIA MUSCULAR, MUTAÇÃO GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VAINZOF, Mariz et al. Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies. Journal of Molecular Neuroscience, v. 17, n. 1, p. 71-80, 2001Tradução . . Disponível em: https://doi.org/10.1385/JMN:17:1:71. Acesso em: 16 maio 2024.
APA
Vainzof, M., Anderson, L. V. B., McNally, E. M., Davis, D. B., Faulkner, G., Valle, G., et al. (2001). Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies. Journal of Molecular Neuroscience, 17( 1), 71-80. doi:10.1385/JMN:17:1:71
NLM
Vainzof M, Anderson LVB, McNally EM, Davis DB, Faulkner G, Valle G, Moreira ES, Pavanello RCM, Passos-Bueno MR, Zatz M. Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies [Internet]. Journal of Molecular Neuroscience. 2001 ; 17( 1): 71-80.[citado 2024 maio 16 ] Available from: https://doi.org/10.1385/JMN:17:1:71
Vancouver
Vainzof M, Anderson LVB, McNally EM, Davis DB, Faulkner G, Valle G, Moreira ES, Pavanello RCM, Passos-Bueno MR, Zatz M. Dysferlin Protein Analysis in Limb-Girdle Muscular Dystrophies [Internet]. Journal of Molecular Neuroscience. 2001 ; 17( 1): 71-80.[citado 2024 maio 16 ] Available from: https://doi.org/10.1385/JMN:17:1:71

USP Schools

ReP

Filtros

Authors

USP affiliated authors

Date published

Subjects

Source title

Funding Agencies

Indexado em

Non normalized affiliation

Countries of institutions of collaboration