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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

A normal life without muscle dystrophin

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Author(s):
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Zatz, M. [1] ; Vieira, N. M. [1] ; Zucconi, E. [1] ; Pelatti, M. [1] ; Gomes, J. [1] ; Vainzof, M. [1] ; Martins-Bach, A. B. [1] ; Garcia Otaduy, M. C. [2] ; Bento dos Santos, G. [2] ; Amaro, Jr., E. [2] ; Landini, V. [1] ; Andrade, T. [1]
Total Authors: 12
Affiliation:
[1] Human Genome Res Ctr, Inst Biosci, Sao Paulo - Brazil
[2] Univ Sao Paulo, Fac Med, Sao Paulo - Brazil
Total Affiliations: 2
Document type: Journal article
Source: Neuromuscular Disorders; v. 25, n. 5, p. 371-374, MAY 2015.
Web of Science Citations: 11
Abstract

Here we summarize the clinical history of Ringo, a golden retriever muscular dystrophy (GRMD) dog, who had a mild phenotype despite the absence of muscle dystrophin. Ringo died of cardiac arrest at age 11 and therefore displayed a normal lifespan. One of his descendants, Suflair, born April 2006, also displays a mild course. Dystrophin analysis confirmed total absence of muscle dystrophin in both dogs. Muscle utrophin expression did not differ from severely affected GRMD dogs. Finding what protects these special dogs from the dystrophic degeneration process is now a great challenge that may open new avenues for treatment. But most importantly, the demonstration that it is possible to have a functional muscle, in a medium-large animal even in the absence of dystrophin, brings new hope for Duchenne patients. (C) 2015 Elsevier B.V. All rights reserved. (AU)

FAPESP's process: 08/57899-7 - Stem cells in human genetic diseases - CETGEN
Grantee:Mayana Zatz
Support type: Research Projects - Thematic Grants
FAPESP's process: 13/08028-1 - CEGH-CEL - Human Genome and Stem Cell Research Center
Grantee:Mayana Zatz
Support type: Research Grants - Research, Innovation and Dissemination Centers - RIDC