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What does CDKA stand for?

Cyclin Dependent Kinase


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This definition appears very rarely and is found in the following Acronym Finder categories:

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Cyclin-Dependent Kinase 2
Cyclin-Dependent Kinase 2-Associated Protein 1
Cyclin-Dependent Kinase 3
Cyclin-Dependent Kinase 4
Cyclin-Dependent Kinase 4 Inhibitor
Cyclin-Dependent Kinase 5
Cyclin Dependent Kinase 6
Cyclin-Dependent Kinase 7 (human gene)
Cyclin-Dependent Kinase 8
Cyclin Dependent Kinase 9
Chief Dull Knife College (Lame Deer, MT)
Center for Diabetic Kidney Disease (Thomas Jefferson Hospital; Philadelphia, PA)
Cyclin-Dependent Kinase D1 (genetics)
Carolinas District Kiwanis Foundation (Columbia, SC)
Central Difference Kalman Filter
Cyclin-Dependent Kinase Inhibitor
Cyclin-Dependent Kinase Inhibitor Proteins
Cyclin-Dependent Kinase Like
Cyclin-dependent Kinase-like 3
Cyclin-Dependent Kinase-Like 5 (gene)

Samples in periodicals archive:
The company is currently evaluating seliciclib (CYC202), an orally-available Cyclin Dependent Kinase inhibitor, in Phase II clinical trials for the treatment of non-small cell lung cancer and B-cell hematological malignancies.
CYC202 (R-roscovitine) is a novel cell cycle drug belonging to the Cyclin Dependent Kinase (CDK) inhibitor class.
This gene encodes a protein called cyclin dependent kinase 1, or CDK 1.
Seliciclib, Cyclacel's orally available cyclin dependent kinase (CDK) inhibitor, has shown encouraging anti-cancer activity in several Phase 1 and Phase 2 studies.
In April at the Annual Meeting of the American Association for Cancer Research Cyclacel reported preclinical results from a combination study of seliciclib, an orally-available cyclin dependent kinase (CDK) inhibitor, with epidermal growth factor receptor (EGFR) inhibitor drugs, including erlotinib (Tarceva[R]).
Seliciclib is an orally available cyclin dependent kinase (CDK) inhibitor that selectively inhibits multiple enzyme targets that are central to the process of cell division and cell cycle control.
Nasdaq: CYCC) (Nasdaq: CYCCP) announced today preclinical results from a combination study of seliciclib, an orally-available cyclin dependent kinase (CDK) inhibitor, with epidermal growth factor receptor (EGFR) inhibitor erlotinib (Tarceva[R]).
Seliciclib is the most advanced orally-available, cyclin dependent kinase (CDK) inhibitor in Phase II clinical development in patients with non-small cell lung cancer.

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