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Items: 3

1.

Muscle from patients with mitochondrial myopathies and congenital muscular dystrophies versus normal human muscle

(Submitter supplied) 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
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL13607
29 Samples
Download data: TXT
Series
Accession:
GSE43698
ID:
200043698
2.

Agilent-028004 SurePrint G3 Human GE 8x60K Microarray (Feature Number version)

(Submitter supplied) SurePrint G3 Human GE 8x60K Microarray Arrays of this design have barcodes that begin with 16028004 or 2528004. Orientation: Features are numbered numbered Left-to-Right, Top-to-Bottom as scanned by an Agilent scanner (barcode on the left, DNA on the back surface, scanned through the glass), matching the FeatureNum output from Agilent's Feature Extraction software. The ID column represents the Agilent Feature Extraction feature number. more...
Organism:
Homo sapiens
233 Series
2 Related Platforms
3749 Samples
Download data: TXT
Platform
Accession:
GPL13607
ID:
100013607
3.

91B-2585

Organism:
Homo sapiens
Source name:
Pat2
Platform:
GPL13607
Series:
GSE43698
Download data: TXT
Sample
Accession:
GSM1068574
ID:
301068574
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db=gds|term=GSM1068574[Accession]|query=1|qty=2|blobid=MCID_675d16320600166e514a2422|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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