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Evaluation of CDK9 Inhibition by Dinaciclib in Combination with Apoptosis Modulating izTRAIL for the Treatment of Colorectal Cancer

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Pause Patrol: Negative Elongation Factor’s Role in Promoter-Proximal Pausing and Beyond

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Pcf11/Spt5 condensates stall RNA polymerase II to facilitate termination and piRNA-guided heterochromatin formation

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Nuclear Transit and HIV LTR Binding of NF-κB Subunits Held by IκB Proteins: Implications for HIV-1 Activation

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ZC3H4/Restrictor Exerts a Stranglehold on Pervasive Transcription

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Keeping the balance: The noncoding RNA 7SK as a master regulator for neuron development and function

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What's all the phos about? Insights into the phosphorylation state of the RNA polymerase II C-terminal domain via mass spectrometry

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RNA polymerase II phosphorylation at serine 2 and histone H3 tri-methylation at lysine 36 are key steps for thyroid hormone receptor β gene activation by thyroid hormone in Rana catesbeiana tadpole liver

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Evidence that Two Pcl-Like Cyclins Control Cdk9 Activity during Cell Differentiation in Aspergillus nidulans Asexual Development

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Occupancy of RNA Polymerase II Phosphorylated on Serine 5 (RNAP S5 P ) and RNAP S2 P on Varicella-Zoster Virus Genes 9, 51, and 66 Is Independent of Transcript Abundance and Polymerase Location within the Gene

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Nuclear organization of RNA polymerase II transcription

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In Vivo Run-On Assays to Monitor Nascent Precursor RNA Transcripts

Percipalle, P., & Louvet, É. (2011) · Methods in molecular biology · doi:10.1007/978-1-61779-376-9_34 · Cited by 12

CDK regulation of transcription by RNAP II: Not over ‘til it's over?

Fisher, R. P. (2016) · Transcription · doi:10.1080/21541264.2016.1268244 · Cited by 12

Promoter-proximal regulation of gene transcription: Key factors involved and emerging role of general transcription factors in assisting productive elongation

Pal, S., & Biswas, D. (2023) · Gene · doi:10.1016/j.gene.2023.147571 · Cited by 11

Retroviral Cyclin Controls Cyclin-Dependent Kinase 8-Mediated Transcription Elongation and Reinitiation

Birkenheuer, C. H., Brewster, C. D., Quackenbush, S. L., & Rovnak, J. (2015) · Journal of Virology · doi:10.1128/jvi.00464-15 · Cited by 13

A diaminocyclohexyl analog of SNS-032 with improved permeability and bioavailability properties

Choong, I., Serafimova, I. M., Fan, J., Stockett, D. E., Chan, E., Cheeti, S., Lu, Y., Fahr, B. J., Pham, P., Arkin, M. R., et al. (2008) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2008.09.073 · Cited by 11

Viral RNA capping: Mechanisms and antiviral therapy

Chen, S., Jiang, Z., Li, Q., Pan, W., Chen, Y., & Liu, J. (2024) · Journal of Medical Virology · doi:10.1002/jmv.29622 · Cited by 10

Molecular Dynamics Simulation and Experimental Verification of the Interaction between Cyclin T1 and HIV-1 Tat Proteins

Asamitsu, K., Hirokawa, T., Hibi, Y., & Okamoto, T. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119451 · Cited by 10

Inhibition of HIV-1 Transcription and Replication by a Newly Identified Cyclin T1 Splice Variant*

Gao, G., Wu, X.-Y., Zhou, J., He, M., He, J. J., & Guo, D.-Y. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.438465 · Cited by 9

The ENL YEATS epigenetic reader domain critically links MLL-ENL to leukemic stem cell frequency in t(11;19) Leukemia

Hu, H., Saha, N., Yang, Y., Ahmad, E., Lachowski, L., Shrestha, U. K., Premkumar, V., Ropa, J. P., Chen, L., Teahan, B., et al. (2022) · Leukemia · doi:10.1038/s41375-022-01765-0 · Cited by 10

Functional Characterization of Human Cyclin T1 N-Terminal Region for Human Immunodeficiency Virus-1 Tat Transcriptional Activation

Asamitsu, K., Hibi, Y., Imai, K., Victoriano, A. F. B., Kurimoto, E., Kato, K., & Okamoto, T. (2011) · Journal of Molecular Biology · doi:10.1016/j.jmb.2011.04.061 · Cited by 10

Single Cell Analysis Reveals Concomitant Transcription of Pluripotent and Lineage Markers During the Early Steps of Differentiation of Embryonic Stem Cells

Lanctôt, C. (2015) · Stem Cells · doi:10.1002/stem.2108 · Cited by 10

The potential underlying mechanism of the leukemia caused by MLL‐fusion and potential treatments

Liu, H., Lee, S., Zhang, Q., Chen, Z., & Zhang, G. (2020) · Molecular Carcinogenesis · doi:10.1002/mc.23204 · Cited by 9

Internalization of Jembrana disease virus Tat: Possible pathway and implication

Deng, G., Qiao, W., Su, Y., Sha, R., Geng, Y., & Chen, Q. (2006) · Virus Research · doi:10.1016/j.virusres.2006.01.023 · Cited by 9

The Novel Protease Activities of JMJD5–JMJD6–JMJD7 and Arginine Methylation Activities of Arginine Methyltransferases Are Likely Coupled

Liu, H., Wei, P., Zhang, Q., Chen, Z., Liu, J., & Zhang, G. (2022) · Biomolecules · doi:10.3390/biom12030347 · Cited by 8

SHP‐1 dephosphorylates histone H2B to facilitate its ubiquitination during transcription

Tathe, P., Chowdary, K. R., Murmu, K. C., Prasad, P., & Maddika, S. (2022) · The EMBO Journal · doi:10.15252/embj.2021109720 · Cited by 8

MYC promotes global transcription in part by controlling P-TEFb complex formation via DNA-binding independent inhibition of CDK9 SUMOylation

Guan, Q., Chen, Z., Yu, F., Liu, L., Huang, Y., Wei, G., Chiang, C., Wong, J., & Li, J. (2023) · Science China Life Sciences · doi:10.1007/s11427-022-2281-6 · Cited by 9

A co-localization model of paired ChIP-seq data using a large ENCODE data set enables comparison of multiple samples

Maehara, K., Odawara, J., Harada, A., Yoshimi, T., Nagao, K., Obuse, C., Akashi, K., Tachibana, T., Sakata, T., & Ohkawa, Y. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks1010 · Cited by 8

P-TEFb Is Critical for the Maturation of RNA Polymerase II into Productive Elongation In Vivo

Ni, Z., Saunders, A., Fuda, N. J., Yao, J., Suárez, J.-R., Webb, W. W., & Lis, J. T. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.01859-07 · Cited by 157

Properties of RNA Polymerase II Elongation Complexes Before and After the P-TEFb-mediated Transition into Productive Elongation

Cheng, B. W., & Price, D. H. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702936200 · Cited by 165

Control of RNA polymerase II activity by dedicated CTD kinases and phosphatases

Majello, B. (2001) · Frontiers in bioscience · doi:10.2741/a685 · Cited by 43

P-TEFb, a Cyclin-Dependent Kinase Controlling Elongation by RNA Polymerase II

Price, D. H. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.8.2629-2634.2000 · Cited by 678

Control of formation of two distinct classes of RNA polymerase II elongation complexes.

Marshall, N. F., & Price, D. H. (1992) · Molecular and Cellular Biology · doi:10.1128/mcb.12.5.2078 · Cited by 298