Cyclin-dependent kinase 9: a key transcriptional regulator and potential drug target in oncology, virology and cardiology
S Wang, PM Fischer - Trends in pharmacological sciences, 2008 - cell.com
Unlike other CDKs, CDK9 does not regulate the cell cycle but promotes RNA synthesis in
genetic programmes for cell growth, differentiation and viral pathogenesis. It is becoming …
genetic programmes for cell growth, differentiation and viral pathogenesis. It is becoming …
Curcumin and its analogues: a potential natural compound against HIV infection and AIDS
No safe and effective cure currently exists for human immunodeficiency virus (HIV).
However, antiretroviral therapy can prolong the lives of HIV patients and lowers the …
However, antiretroviral therapy can prolong the lives of HIV patients and lowers the …
Meriolins (3-(pyrimidin-4-yl)-7-azaindoles): synthesis, kinase inhibitory activity, cellular effects, and structure of a CDK2/cyclin A/meriolin complex
A Echalier, K Bettayeb, Y Ferandin… - Journal of medicinal …, 2008 - ACS Publications
We report the synthesis and biological characterization of 3-(pyrimidin-4-yl)-7-azaindoles
(meriolins), a chemical hybrid between the natural products meridianins and variolins …
(meriolins), a chemical hybrid between the natural products meridianins and variolins …
Engineering and optimization of the miR-106b cluster for ectopic expression of multiplexed anti-HIV RNAs
LA Aagaard, J Zhang, KJ von Eije, H Li, P Sætrom… - Gene therapy, 2008 - nature.com
Many microRNAs (miRNAs) are encoded within the introns of RNA Pol II transcripts, often as
polycistronic precursors. Here, we demonstrate the optimization of an intron encoding three …
polycistronic precursors. Here, we demonstrate the optimization of an intron encoding three …
Pyrazolo[1,5-a]-1,3,5-triazine as a Purine Bioisostere: Access to Potent Cyclin-Dependent Kinase Inhibitor (R)-Roscovitine Analogue
Pharmacological inhibitors of cyclin-dependent kinases (CDKs) have a wide therapeutic
potential. Among the CDK inhibitors currently under clinical trials, the 2, 6, 9-trisubstituted …
potential. Among the CDK inhibitors currently under clinical trials, the 2, 6, 9-trisubstituted …
CDK13, a new potential human immunodeficiency virus type 1 inhibitory factor regulating viral mRNA splicing
The human immunodeficiency virus type 1 (HIV-1) Tat is a 14-kDa viral protein that acts as a
potent transactivator by binding to the transactivation-responsive region, a structured RNA …
potent transactivator by binding to the transactivation-responsive region, a structured RNA …
Nucleophosmin interacts with HEXIM1 and regulates RNA polymerase II transcription
Hexamethylene bis-acetamide-inducible protein 1 (HEXIM1) was identified earlier as an
inhibitor of positive transcription elongation factor b (P-TEFb), which is a key transcriptional …
inhibitor of positive transcription elongation factor b (P-TEFb), which is a key transcriptional …
HEXIM1 and the control of transcription elongation: from cancer and inflammation to AIDS and cardiac hypertrophy
Hexamethylene bis-acetamide inducible protein 1 (HEXIM1) is an inhibitor of positive
transcription elongation factor b (P-TEFb) that has recently been shown to be involved in …
transcription elongation factor b (P-TEFb) that has recently been shown to be involved in …
Strategies to block HIV transcription: focus on small molecule Tat inhibitors
G Mousseau, S Valente - Biology, 2012 - mdpi.com
After entry into the target cell, the human immunodeficiency virus type I (HIV) integrates into
the host genome and becomes a proviral eukaryotic transcriptional unit. Transcriptional …
the host genome and becomes a proviral eukaryotic transcriptional unit. Transcriptional …
Role of cellular iron and oxygen in the regulation of HIV-1 infection
Despite efficient antiretroviral therapy, eradication of HIV-1 infection is challenging and
requires novel biological insights and therapeutic strategies. Among other physiological and …
requires novel biological insights and therapeutic strategies. Among other physiological and …