CDK9 as an Appealing Target for Therapeutic Interventions
Author:
Affiliation:
1. Molecular Medicine Research Center, Biomedicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran
2. Faculty of medicine, Tabriz University of Medical Sciences, Tabriz, Iran
Abstract
Publisher
Bentham Science Publishers Ltd.
Subject
Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Medicine
Reference123 articles.
1. Shore SM, Byers SA, Dent P, Price DH. Characterization of Cdk9 55 and differential regulation of two Cdk9 isoforms.
2. Romano G, Giordano A. Role of the cyclin-dependent kinase 9-related pathway in mammalian gene expression and human diseases.
3. De Falco G, Bagella L, Claudio PP. Physical interaction between CDK9 and B-Myb results in suppression of B-Myb gene autoregulation.
4. De Falco G, Neri LM, De Falco M. Cdk9, a member of the cdc2-like family of kinases, binds to gp130, the receptor of the IL-6 family of cytokines.
5. Eberhardy SR, Farnham PJ. c-Myc mediates activation of the cad promoter a post-RNA polymerase II recruitment mechanism.
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