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Items: 4

1.

Cockayne syndrome (CSB) fibroblasts

(Submitter supplied) Cockayne syndrome (CS) is an inherited neurodevelopmental disorder with progeroid features. Although the genes responsible for CS have been implicated in a variety of DNA repair- and transcription-related pathways, the nature of the molecular defect in CS remains mysterious. We sought to define this defect by expression analysis of cells lacking functional CSB, a SWI/SNF-like ATPase that is responsible for most CS cases. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Datasets:
GDS2175 GDS2176
Platforms:
GPL97 GPL96
16 Samples
Download data: CEL
Series
Accession:
GSE3407
ID:
200003407
2.
Full record GDS2175

Cockayne syndrome group B protein-null fibroblast rescue (HG-U133A)

Analysis of Cockayne syndrome group B (CSB) protein-null fibroblasts rescued by expression of CSB cDNA. CS, a neurodegenerative disorder, arises mostly from CSB defects. Results provide insight into how CSB defects cause CS.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 protocol sets
Platform:
GPL96
Series:
GSE3407
8 Samples
Download data: CEL
3.

[HG-U133A] Affymetrix Human Genome U133A Array

(Submitter supplied) Affymetrix submissions are typically submitted to GEO using the GEOarchive method described at http://www.ncbi.nlm.nih.gov/projects/geo/info/geo_affy.html June 03, 2009: annotation table updated with netaffx build 28 June 08, 2012: annotation table updated with netaffx build 32 June 24, 2016: annotation table updated with netaffx build 35 Protocol: see manufacturer's web site The U133 set includes 2 arrays with a total of 44928 entries and was indexed 29-Jan-2002. more...
Organism:
Homo sapiens
364 DataSets
1125 Series
11 Related Platforms
42430 Samples
Download data
Platform
Accession:
GPL96
ID:
100000096
4.

CSB wt-rescued replicate 3 U133A

Organism:
Homo sapiens
Source name:
human Cockayne syndrome skin fibroblasts
Platform:
GPL96
Series:
GSE3407
Dataset:
GDS2175
Download data: CEL
Sample
Accession:
GSM76878
ID:
300076878
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