GSM1185327[Accession] - GEO DataSets

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Items: 3

Select item 2000488281.

Expression and Splicing Analysis of Myotonic Dystrophy and Other Dystrophic Muscle

(Submitter supplied) The prevailing patho-mechanistic paradigm for myotonic dystrophy (DM) is that the aberrant presence of embryonic isoforms is responsible for many, if not most, aspects of the pleiotropic disease phenotype. In order to identify such aberrantly expressed isoforms in skeletal muscle of DM type 1 (DM1) and type 2 (DM2) patients, we utilized the Affymetrix exon array to characterize the largest collection of DM samples analyzed to date, and included non-DM dystrophic muscle samples (NMD) as disease controls.

Organism:: Homo sapiens

Type:: Expression profiling by array

Platforms:: GPL5175 GPL5188
56 Samples

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Accession:: GSE48828

ID:: 200048828

PubMed Full text in PMC Similar studies Analyze with GEO2R

Select item 1000051752.

[HuEx-1_0-st] Affymetrix Human Exon 1.0 ST Array [transcript (gene) version]

(Submitter supplied) Affymetrix submissions are typically submitted to GEO using the GEOarchive method described at http://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/projects/geo/info/geo_affy.html June 03, 2009: annotation table updated with netaffx build 28 Oct 11, 2012: annotation table updated with netaffx build 32 Protocol: See manufacturer's web site