Dataset: BCOR-regulated genes in human oculo-facio-cardio-dental syndrome

Oculo-facio-cardio-dental syndrome (OFCD) is a rare genetic disorder characterized by teeth with extremely long roots (radiculomegaly), and craniofacial, eye and cardiac abnormalities. The mutation of the transcriptional co-repressor BCOR has been identified as being responsible for oculo-facio-cardio-dental (OFCD) syndrome. Mesenchymal stem cells (MSCs) is isolated from the root apical papilla of an OFCD patient. Gene expression profiling is performed and compared between mutant MSCs and wild type MSCs. Total RNA were extracted from normal MSCs (MSCWT) and mutant MSCs (MSCO).

Species:

human

Samples:

2

Source:

E-GEOD-15214

PubMed:

19578371

Updated:

Dec.12, 2014

Registered:

Sep.12, 2014