Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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Mouse Models for Muscular Dystrophy


ABSTRACT: Comparative analysis of gene expression levels from hindlimb muscle tissue from 8 week old mouse models for muscular dystrophy. We have used mouse models with dystrophin-, sarcoglycan-, sarcospan-, or dysferlin-deficiency. Keywords = muscular dystrophy

ORGANISM(S): Mus musculus

SUBMITTER: Peter 't Hoen 

PROVIDER: E-GEOD-2112 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Common pathological mechanisms in mouse models for muscular dystrophies.

Turk R R   Sterrenburg E E   van der Wees C G C CG   de Meijer E J EJ   de Menezes R X RX   Groh S S   Campbell K P KP   Noguchi S S   van Ommen G J B GJ   den Dunnen J T JT   't Hoen P A C PA  

FASEB journal : official publication of the Federation of American Societies for Experimental Biology 20051123 1


Duchenne/Becker and limb-girdle muscular dystrophies share clinical symptoms like muscle weakness and wasting but differ in clinical presentation and severity. To get a closer view on the differentiating molecular events responsible for the muscular dystrophies, we have carried out a comparative gene expression profiling of hindlimb muscles of the following mouse models: dystrophin-deficient (mdx, mdx(3cv)), sarcoglycan-deficient (Sgca null, Sgcb null, Sgcg null, Sgcd null), dysferlin-deficient  ...[more]

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