GPL7222[Accession] - GEO DataSets

Warning: The NCBI web site requires JavaScript to function. more...

Format

Summary
Summary (text)
Unique Identifier List

Sort by

Default order
Number of Samples (High to Low)
Number of Samples (Low to High)

Send to:

Choose Destination

File
Clipboard
Collections

Search results

Items: 4

Select item 2000126031.

Impaired Cohesin Loading in Cornelia de Lange Syndrome Results in a Highly Specific Pattern of Dysregulated Genes

(Submitter supplied) Heterozygous mutations in the cohesin regulator, NIPBL, or cohesin structural components SMC1A, and SMC3, result in Cornelia de Lange Syndrome (CdLS). Genome-wide transcription assessment has identified unique profiles of genes dysregulated in CdLS that correlate with different clinical presentations. Cohesin binding analysis demonstrates a preference for intergenic regions suggesting a cis-regulatory function mimicking that of an insulator. more...

Organism:: Homo sapiens

Type:: Genome binding/occupancy profiling by genome tiling array

7 related Platforms
14 Samples

Download data: CEL, TXT

Series

Accession:: GSE12603

ID:: 200012603

PubMed Full text in PMC Similar studies

Select item 1000072222.

Affymetrix GeneChip Human Tiling 2.0R Array Set_Array 1of7 (NCBI Build 36)

(Submitter supplied) Sequences used in the design of this Human Tiling 2.0R Array Set were based on NCBI human genome assembly hg18 (Build 36). Protocol: See manufacturer's web site