Cyclin-dependent kinases and rare developmental disorders.
Ontology highlight
ABSTRACT: Extensive studies in the past 30 years have established that cyclin-dependent kinases (CDKs) exert many diverse, important functions in a number of molecular and cellular processes that are at play during development. Not surprisingly, mutations affecting CDKs or their activating cyclin subunits have been involved in a variety of rare human developmental disorders. These recent findings are reviewed herein, giving a particular attention to the discovered mutations and their demonstrated or hypothesized functional consequences, which can account for pathological human phenotypes. The review highlights novel, important CDK or cyclin functions that were unveiled by their association with human disorders, and it discusses the shortcomings of mouse models to reveal some of these functions. It e
SUBMITTER: Colas P
PROVIDER: S-EPMC7410148 | biostudies-literature | 2020 Aug
REPOSITORIES: biostudies-literature
ACCESS DATA