Evaluation of the therapeutic potential of carbonic anhydrase inhibitors in two animal models of dystrophin deficient muscular dystrophy-Reference-Cited by-同舟云学术

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Evaluation of the therapeutic potential of carbonic anhydrase inhibitors in two animal models of dystrophin deficient muscular dystrophy

Published:2009-07-31 Issue:21 Volume:18 Page:4089-4101
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Giacomotto J.,Pertl C.,Borrel C.,Walter M. C.,Bulst S.,Johnsen B.,Baillie D. L.,Lochmuller H.,Thirion C.,Segalat L.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Reference51 articles.

1. Molecular Genetics of Duchenne Muscular Dystrophy

2. Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

3. The dystrophin-glycoprotein complex, cellular signaling, and the regulation of cell survival in the muscular dystrophies

4. The WW Domain of Dystrophin Requires EF-Hands Region to Interact with β-Dystroglycan

5. Association of dystrophin and an integral membrane glycoprotein

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