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Items: 5

1.
Full record GDS5276

Myotonic dystrophy type 2: vastus lateralis biopsies

Analysis of vastus lateralis biopsies from myotonic dystrophy type 2 (DM2) patients. DM2 is a multisystemic disorder caused by a (CCTG)n repeat expansion in intron 1 of cellular nucleic acid-binding protein. Results provide insight into molecular mechanisms underlying DM2 pathogenesis.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 disease state sets
Platform:
GPL6102
Series:
GSE45331
10 Samples
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2.

Expression array analysis of myotonic dystrophy type 2 (DM2) muscle biopsies versus controls

(Submitter supplied) The hypothesis was that different genes are abnormally expressed in DM2 biopsies compared to controls.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5276
Platform:
GPL6102
10 Samples
Download data: TXT
Series
Accession:
GSE45331
ID:
200045331
3.

Transcriptome analysis of Myotonic Dystrophy type 2 (DM2) patients.

(Submitter supplied) Myotonic Dystrophy Type-2 (DM2) is an autosomal dominant disease caused by the expansion of a CCTG tetraplet repeat. It is a multisystemic disorder, affecting skeletal muscles, the heart, the eye, the central nervous system and the endocrine system. Whole mRNAs expression was measured in the muscle of DM2 patients and compared it to controls.We identified distinct genes modulated in DM2 patients compared to controls.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL5175
20 Samples
Download data: CEL
Series
Accession:
GSE37084
ID:
200037084
4.

Expression data from DM1, DM2 and Normal Adult Skeletal Muscle Biopsies

(Submitter supplied) DM1 and DM2 biopsies from patients were compared to Normal adult individuals Keywords: 3 groups of samples
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
36 Samples
Download data: CEL
Series
Accession:
GSE7014
ID:
200007014
5.

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
Download data: CEL
Series
Accession:
GSE48828
ID:
200048828
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