CLYD

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Also found in: Acronyms.

CLYD

A gene on chromosome 16q12.1 that encodes a cytoplasmic protein with deubiquitinating activity and plays a key role in regulating pathways leading to NF-kappa-B activation, which affects cell survival, proliferation and differentiation.

Molecular pathology
CLYD mutations are causatively linked to cylindromatosis, multiple familial trichoepithelioma and Brooke-Spiegler syndrome.
References in periodicals archive ?
As all steps are available onscreen, repeat users can skip this section and move to wherever they want to be in the CDMT.
As the CDMT is an instructor-led activity, the instructor can choose to spend class time going through the activities, or can give them to students to complete as homework.
A key feature of the CDMT is that it complements information and resources available through the ACRN network.
Counselors, teachers or others who use the CDMT as an instructional tool can tie it to their state CIDS to increase its relevance and usefulness for students (the "Tools by State" link in the CDMT reference menu has links to online ACRN resources in every state).