Vainzof M - Search Results

1

Faster regeneration associated to high expression of Fam65b and Hdac6 in dysferlin-deficient mouse.

Ishiba R, Santos ALF, Almeida CF, Caires LC Jr, Ribeiro AF Jr, Ayub-Guerrieri D, Fernandes SA, Souza LS, Vainzof M. Ishiba R, et al. Among authors: vainzof m. J Mol Histol. 2019 Aug;50(4):375-387. doi: 10.1007/s10735-019-09834-y. Epub 2019 Jun 19. J Mol Histol. 2019. PMID: 31218594

2

Animal models for genetic neuromuscular diseases.

Vainzof M, Ayub-Guerrieri D, Onofre PC, Martins PC, Lopes VF, Zilberztajn D, Maia LS, Sell K, Yamamoto LU. Vainzof M, et al. J Mol Neurosci. 2008 Mar;34(3):241-8. doi: 10.1007/s12031-007-9023-9. Epub 2008 Jan 18. J Mol Neurosci. 2008. PMID: 18202836 Review.

3

Differential expression of genes involved in the degeneration and regeneration pathways in mouse models for muscular dystrophies.

Onofre-Oliveira PC, Santos AL, Martins PM, Ayub-Guerrieri D, Vainzof M. Onofre-Oliveira PC, et al. Among authors: vainzof m. Neuromolecular Med. 2012 Mar;14(1):74-83. doi: 10.1007/s12017-012-8172-3. Epub 2012 Feb 24. Neuromolecular Med. 2012. PMID: 22362587

4

Systemic delivery of human mesenchymal stromal cells combined with IGF-1 enhances muscle functional recovery in LAMA2 dy/2j dystrophic mice.

Secco M, Bueno C Jr, Vieira NM, Almeida C, Pelatti M, Zucconi E, Bartolini P, Vainzof M, Miyabara EH, Okamoto OK, Zatz M. Secco M, et al. Among authors: vainzof m. Stem Cell Rev Rep. 2013 Feb;9(1):93-109. doi: 10.1007/s12015-012-9380-9. Stem Cell Rev Rep. 2013. PMID: 22664740

5

Muscle phenotypic variability in limb girdle muscular dystrophy 2 G.

Paim JF, Cotta A, Vargas AP, Navarro MM, Valicek J, Carvalho E, da-Cunha AL Jr, Plentz E, Braz SV, Takata RI, Almeida CF, Vainzof M. Paim JF, et al. Among authors: vainzof m. J Mol Neurosci. 2013 Jun;50(2):339-44. doi: 10.1007/s12031-013-9987-6. Epub 2013 Mar 12. J Mol Neurosci. 2013. PMID: 23479141

6

Dmdmdx/Largemyd: a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies.

Martins PC, Ayub-Guerrieri D, Martins-Bach AB, Onofre-Oliveira P, Malheiros JM, Tannus A, de Sousa PL, Carlier PG, Vainzof M. Martins PC, et al. Among authors: vainzof m. Dis Model Mech. 2013 Sep;6(5):1167-74. doi: 10.1242/dmm.011700. Epub 2013 Jun 20. Dis Model Mech. 2013. PMID: 23798567 Free PMC article.

7

Silent polymorphisms in the RYR1 gene do not modify the phenotype of the p.4898 I>T pathogenic mutation in central core disease: a case report.

Cuperman T, Fernandes SA, Lourenço NC, Yamamoto LU, Silva HC, Pavanello RC, Yamamoto GL, Zatz M, Oliveira AS, Vainzof M. Cuperman T, et al. Among authors: vainzof m. BMC Res Notes. 2014 Aug 1;7:487. doi: 10.1186/1756-0500-7-487. BMC Res Notes. 2014. PMID: 25084811 Free PMC article.

8

Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image pattern.

Cotta A, Paim JF, da-Cunha-Junior AL, Neto RX, Nunes SV, Navarro MM, Valicek J, Carvalho E, Yamamoto LU, Almeida CF, Braz SV, Takata RI, Vainzof M. Cotta A, et al. Among authors: vainzof m. BMC Clin Pathol. 2014 Oct 4;14:41. doi: 10.1186/1472-6890-14-41. eCollection 2014. BMC Clin Pathol. 2014. PMID: 25298746 Free PMC article.

9

Quantitative T2 combined with texture analysis of nuclear magnetic resonance images identify different degrees of muscle involvement in three mouse models of muscle dystrophy: mdx, Largemyd and mdx/Largemyd.

Martins-Bach AB, Malheiros J, Matot B, Martins PC, Almeida CF, Caldeira W, Ribeiro AF, Loureiro de Sousa P, Azzabou N, Tannús A, Carlier PG, Vainzof M. Martins-Bach AB, et al. Among authors: vainzof m. PLoS One. 2015 Feb 24;10(2):e0117835. doi: 10.1371/journal.pone.0117835. eCollection 2015. PLoS One. 2015. PMID: 25710816 Free PMC article.

10

Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers.

Vainzof M, Feitosa L, Canovas M, Ayub-Guerrieri D, Pavanello Rde C, Zatz M. Vainzof M, et al. Neuromuscul Disord. 2016 Mar;26(3):197-200. doi: 10.1016/j.nmd.2016.01.001. Epub 2016 Jan 25. Neuromuscul Disord. 2016. PMID: 26851826

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