scholarly article | Q13442814 |
P819 | ADS bibcode | 2009PNAS..10619286B |
P356 | DOI | 10.1073/PNAS.0905469106 |
P932 | PMC publication ID | 2780808 |
P698 | PubMed publication ID | 19880750 |
P5875 | ResearchGate publication ID | 38058989 |
P50 | author | Dan Longo | Q12100062 |
Adriana De Siervi | Q61142186 | ||
Richard A Koup | Q97635775 | ||
P2093 | author name string | Kevin Gardner | |
Keiko Ozato | |||
Sven Bilke | |||
Audrey Player | |||
Constantinos Petrovas | |||
Gila Idelman | |||
Michael J Thirman | |||
Cynthia M Haggerty | |||
Jung S Byun | |||
Joseph J Kaberlein | |||
Wenwu Cui | |||
Madeline M Wong | |||
Yong Hong Wang | |||
Quentin Li | |||
P2860 | cites work | Elongation and premature termination of transcripts initiated from c-fos and c-myc promoters show dissimilar patterns | Q41379713 |
Identification of an evolutionarily conserved transcriptional signature of CD8 memory differentiation that is shared by T and B cells | Q42116867 | ||
Regulation of c-fos expression by RNA polymerase elongation competence | Q42828009 | ||
Overexpression of the MEN/ELL protein, an RNA polymerase II elongation factor, results in transformation of Rat1 cells with dependence on the lysine-rich region | Q42831594 | ||
Deacetylase activity is required for cAMP activation of a subset of CREB target genes | Q44562092 | ||
Molecular and functional profiling of memory CD8 T cell differentiation. | Q52008481 | ||
Platelet-derived growth factor induces rapid but transient expression of the c-fos gene and protein | Q59086707 | ||
Analysis of a cAMP-responsive activator reveals a two-component mechanism for transcriptional induction via signal-dependent factors | Q64382469 | ||
Cloning of ELL, a gene that fuses to MLL in a t(11;19)(q23;p13.1) in acute myeloid leukemia | Q24310726 | ||
The bromodomain protein Brd4 is a positive regulatory component of P-TEFb and stimulates RNA polymerase II-dependent transcription | Q24316236 | ||
An RNA polymerase II elongation factor encoded by the human ELL gene | Q24321774 | ||
A human RNA polymerase II complex containing factors that modify chromatin structure | Q24522669 | ||
Conditional knockout mice reveal distinct functions for the global transcriptional coactivators CBP and p300 in T-cell development | Q24537650 | ||
MAP kinase phosphorylation-dependent activation of Elk-1 leads to activation of the co-activator p300. | Q24540319 | ||
RNA polymerase stalling at developmental control genes in the Drosophila melanogaster embryo | Q24645367 | ||
Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome | Q28131828 | ||
Transcriptional coactivator complexes | Q28200751 | ||
ChIP-seq accurately predicts tissue-specific activity of enhancers | Q28235102 | ||
Controlling the elongation phase of transcription with P-TEFb | Q28255518 | ||
Nascent RNA sequencing reveals widespread pausing and divergent initiation at human promoters | Q28302903 | ||
Negative elongation factor NELF controls transcription of immediate early genes in a stimulus-specific manner | Q28578282 | ||
A chromatin landmark and transcription initiation at most promoters in human cells | Q29547180 | ||
Divergent transcription from active promoters | Q29614332 | ||
A high-resolution map of active promoters in the human genome | Q29614431 | ||
Elongation by RNA polymerase II: the short and long of it | Q29614529 | ||
RNA polymerase is poised for activation across the genome | Q29615047 | ||
CREB-binding protein and p300: molecular integrators of hematopoietic transcription. | Q33825038 | ||
Breaking barriers to transcription elongation | Q34561019 | ||
Expression of a set of growth-related immediate early genes in BALB/c 3T3 cells: coordinate regulation with c-fos or c-myc | Q34599313 | ||
Structure and mechanism of the RNA polymerase II transcription machinery | Q35758805 | ||
Regulatory diversity among metazoan co-activator complexes | Q35762480 | ||
Rapid default transition of CD4 T cell effectors to functional memory cells | Q36229656 | ||
Functional and genomic profiling of effector CD8 T cell subsets with distinct memory fates | Q36509866 | ||
Homeostasis of memory T cells | Q36528980 | ||
The bromodomain protein Brd4 stimulates G1 gene transcription and promotes progression to S phase | Q36727254 | ||
Regulation of the transcriptional activity of poised RNA polymerase II by the elongation factor ELL | Q36735223 | ||
Biphasic regulation of Il2 transcription in CD4+ T cells: roles for TNF-alpha receptor signaling and chromatin structure | Q36791858 | ||
NELF-mediated stalling of Pol II can enhance gene expression by blocking promoter-proximal nucleosome assembly | Q36802956 | ||
Kinetic profiles of p300 occupancy in vivo predict common features of promoter structure and coactivator recruitment | Q37415446 | ||
Targeting of p300 to the interleukin-2 promoter via CREB-Rel cross-talk during mitogen and oncogenic molecular signaling in activated T-cells | Q38301703 | ||
Transcriptional pausing caused by NELF plays a dual role in regulating immediate-early expression of the junB gene | Q38408801 | ||
Metabolic consequences of p300 gene deletion in human colon cancer cells | Q40248535 | ||
P433 | issue | 46 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 19286-19291 | |
P577 | publication date | 2009-10-30 | |
P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
P1476 | title | Dynamic bookmarking of primary response genes by p300 and RNA polymerase II complexes | |
P478 | volume | 106 |
Q37635773 | A dual role for the histone methyltransferase PR-SET7/SETD8 and histone H4 lysine 20 monomethylation in the local regulation of RNA polymerase II pausing |
Q34541567 | A novel form of human STAT1 deficiency impairing early but not late responses to interferons |
Q38782944 | A polymorphism in miR-1262 regulatory region confers the risk of lung cancer in Chinese population. |
Q36442907 | Activation of tachykinin, neurokinin 3 receptors affects chromatin structure and gene expression by means of histone acetylation |
Q33936571 | BET Inhibitor JQ1 Blocks Inflammation and Bone Destruction. |
Q35062754 | BTB-ZF transcriptional regulator PLZF modifies chromatin to restrain inflammatory signaling programs. |
Q36008355 | CBP30, a selective CBP/p300 bromodomain inhibitor, suppresses human Th17 responses |
Q36781101 | Cell cycle-dependent changes in H3K56ac in human cells |
Q38574884 | Cellular and chromatin dynamics of antibody-secreting plasma cells |
Q37395287 | Coordinated histone H3 methylation and acetylation regulate physiologic and pathologic fas ligand gene expression in human CD4+ T cells |
Q35458646 | Coupled pre-mRNA and mRNA dynamics unveil operational strategies underlying transcriptional responses to stimuli. |
Q55428125 | CpG island composition differences are a source of gene expression noise indicative of promoter responsiveness. |
Q34582060 | Cyclin T1 overexpression induces malignant transformation and tumor growth |
Q37769635 | Do chromatin loops provide epigenetic gene expression states? |
Q35738247 | ELL facilitates RNA polymerase II pause site entry and release |
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Q41003055 | Genome architecture and the role of transcription |
Q38058189 | Genomic occupancy of the transcriptional co-activators p300 and CBP. |
Q39703646 | HIV-1 Tat assembles a multifunctional transcription elongation complex and stably associates with the 7SK snRNP |
Q36632043 | High expression levels of COX-2 and P300 are associated with unfavorable survival in laryngeal squamous cell carcinoma |
Q24310867 | Human mediator subunit MED26 functions as a docking site for transcription elongation factors |
Q34013832 | Inactivation of a single copy of Crebbp selectively alters pre-mRNA processing in mouse hematopoietic stem cells |
Q38085375 | Lysine acetyltransferases CBP and p300 as therapeutic targets in cognitive and neurodegenerative disorders. |
Q35145001 | Perturbation of BRD4 protein function by BRD4-NUT protein abrogates cellular differentiation in NUT midline carcinoma |
Q36598963 | Polycomb inhibits histone acetylation by CBP by binding directly to its catalytic domain |
Q54723457 | Prognostic impact of p300 expression in patients with colorectal cancer. |
Q36237484 | Promoter proximal pausing and the control of gene expression |
Q33779012 | Promoter-bound p300 complexes facilitate post-mitotic transmission of transcriptional memory |
Q35540172 | Regulation of primary response genes |
Q46706123 | Short-term memory of danger signals and environmental stimuli in immune cells |
Q35617209 | Signal-induced Brd4 release from chromatin is essential for its role transition from chromatin targeting to transcriptional regulation. |
Q27664700 | Structural basis for mRNA surveillance by archaeal Pelota and GTP-bound EF1α complex |
Q42293418 | TT-seq captures enhancer landscapes immediately after T-cell stimulation. |
Q31145113 | The Clostridium small RNome that responds to stress: the paradigm and importance of toxic metabolite stress in C. acetobutylicum |
Q36490860 | The basis of antagonistic pleiotropy in hfq mutations that have opposite effects on fitness at slow and fast growth rates |
Q42264246 | The histone acetyltransferase MOF is a key regulator of the embryonic stem cell core transcriptional network |
Q31129939 | The intronic long noncoding RNA ANRASSF1 recruits PRC2 to the RASSF1A promoter, reducing the expression of RASSF1A and increasing cell proliferation. |
Q21136168 | The mechanism of release of P-TEFb and HEXIM1 from the 7SK snRNP by viral and cellular activators includes a conformational change in 7SK |
Q24307973 | Transcriptional regulation of BRCA1 expression by a metabolic switch |
Q34647687 | Transferase activity function and system development process are critical in cattle embryo development |
Q55479474 | p300 promotes proliferation, migration, and invasion via inducing epithelial-mesenchymal transition in non-small cell lung cancer cells. |
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