2008年6月23日 · MED12-related disorders include the phenotypes of FG syndrome type 1 (FGS1), Lujan syndrome (LS), X-linked Ohdo syndrome (XLOS), Hardikar syndrome (HS), and …

2024年12月25日 · MED12 (Mediator Complex Subunit 12) is a Protein Coding gene. Diseases associated with MED12 include Opitz-Kaveggia Syndrome and Intellectual Developmental …

The MED12 gene provides instructions for making a protein called mediator complex subunit 12. As its name suggests, this protein forms one part (subunit) of the mediator complex, which is a …

MED12 is involved in a variety of cellular activities, and mutations in MED12 gene impair MED12 activities and are associated with several diseases, including Opitz-Kaveggia syndrome, Lujan …

MED12 mutation as a potential predictive biomarker for immune checkpoint inhibitors in pan-cancer. A mediator complex subunit 12 gain-of-function mutation induces partial leiomyoma …

This overview of MED12-related disorders may help to correlate clinical findings in such patients with sequence variants found in MED12. MED12 is a member of the large Mediator complex, …

Mediator complex subunit 12 (MED12) is a subunit of Mediator, a large multi-subunit protein complex that acts an important regulator of transcription. Specifically, MED12 is an integral …

MED12 is involved in a variety of cellular activities, and mutations in MED12 gene impair MED12 activities and are associated with several diseases, including Opitz-Kaveggia syndrome, Lujan …

HGNC Approved Gene Symbol: MED12. Mediator is a multiprotein complex that can function in transcriptional activation or repression depending on the factors with which it interacts. The …

2016年5月17日 · Med12-mediated suppression of NSC adhesion is a dynamically regulated process in vitro, enforced in self-renewing NSCs and alleviated during the course of neuronal …