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The 10 autosomal recessive limb-girdle muscular dystrophies.
Zatz M, de Paula F, Starling A, Vainzof M. Zatz M, et al. Among authors: vainzof m. Neuromuscul Disord. 2003 Sep;13(7-8):532-44. doi: 10.1016/s0960-8966(03)00100-7. Neuromuscul Disord. 2003. PMID: 12921790 Review.
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.
SJL dystrophic mice express a significant amount of human muscle proteins following systemic delivery of human adipose-derived stromal cells without immunosuppression.
Vieira NM, Bueno CR Jr, Brandalise V, Moraes LV, Zucconi E, Secco M, Suzuki MF, Camargo MM, Bartolini P, Brum PC, Vainzof M, Zatz M. Vieira NM, et al. Among authors: vainzof m. Stem Cells. 2008 Sep;26(9):2391-8. doi: 10.1634/stemcells.2008-0043. Epub 2008 Jun 26. Stem Cells. 2008. PMID: 18583542
Human adipose-derived mesenchymal stromal cells injected systemically into GRMD dogs without immunosuppression are able to reach the host muscle and express human dystrophin.
Vieira NM, Valadares M, Zucconi E, Secco M, Bueno CR Jr, Brandalise V, Assoni A, Gomes J, Landini V, Andrade T, Caetano HV, Vainzof M, Zatz M. Vieira NM, et al. Among authors: vainzof m. Cell Transplant. 2012;21(7):1407-17. doi: 10.3727/096368911X. Cell Transplant. 2012. PMID: 23168016 Free article.
190 results