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| Status |
Public on Jan 20, 2015 |
| Title |
Muscle from patients with mitochondrial myopathies and congenital muscular dystrophies versus normal human muscle |
| Organism |
Homo sapiens |
| Experiment type |
Expression profiling by array
|
| Summary |
Global gene expression analysis was performed comparing human skeletal muscle samples from patients with various forms of muscular dystrophy and mitochondrial myopathies in order to identify specific gene expression changes associated with collagen VI deficiency (leading to Ullrich´s Congenital Muscular Dystrophy) and depletion of mitochondrial DNA relative to other mitochondrial myopathies
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| Overall design |
We analysed the gene expression profile of skeletal muscle from children suffering from mitochondrial myopathies and various forms of muscular dystrophy relative to skeletal muscle from healthy children using commercially available arrays that represents the complete human genome (Agilent Human SurePrintGE, 8x60K )
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| Contributor(s) |
Kalko S, Jimenez-Mallebrera C, Paco S |
| Citation(s) |
24484525 |
| Submission date |
Jan 23, 2013 |
| Last update date |
Nov 27, 2018 |
| Contact name |
Susana Kalko |
| E-mail(s) |
kalko.susana@gmail.com
|
| Organization name |
IDIBAPS
|
| Department |
Bioinformatics Platform
|
| Street address |
c/Rosello 153
|
| City |
Barcelona |
| State/province |
BARCELONA |
| ZIP/Postal code |
08036 |
| Country |
Spain |
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| Platforms (1) |
| GPL13607 |
Agilent-028004 SurePrint G3 Human GE 8x60K Microarray (Feature Number version) |
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| Samples (29)
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| Relations |
| BioProject |
PRJNA187082 |
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