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Items: 4

1.

A Marfan syndrome gene expression phenotype in cultured skin fibroblasts

(Submitter supplied) Background: Marfan syndrome (MFS) is a heritable connective tissue disorder caused by mutations in the fibrillin-1 gene. This syndrome constitutes a significant identifiable subtype of aortic aneurysmal disease, accounting for over 5% of ascending and thoracic aortic aneurysms. Results: We used spotted membrane DNA macroarrays to identify genes whose altered expression levels may contribute to the phenotype of the disease. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS2960
Platform:
GPL538
101 Samples
Download data: TXT
Series
Accession:
GSE8759
ID:
200008759
2.
Full record GDS2960

Marfan syndrome: cultured skin fibroblasts

Analysis of cultured skin fibroblasts prepared from patients with Marfan syndrome (MFS). MFS is a heritable connective tissue disorder caused by mutations in the fibrillin-1 gene. Results provide insight into the molecular pathogenesis of MFS.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 disease state sets
Platform:
GPL538
Series:
GSE8759
101 Samples
Download data
3.

Research Genetics (Invitrogen) - GF211 Microarray Filter

(Submitter supplied) Research Genetics GF 200 nylon membrane containing 4,132 spotted cDNA clones Protocol: see manufacturer's web site
Organism:
Homo sapiens
1 DataSet
13 Series
249 Samples
Download data
Platform
Accession:
GPL538
ID:
100000538
4.

fibroblast, control subject NM9 rep 1

Organism:
Homo sapiens
Source name:
cultured skin fibroblasts from control subjects
Platform:
GPL538
Series:
GSE8759
Dataset:
GDS2960
Download data
Sample
Accession:
GSM217666
ID:
300217666
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