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A ubiquitous disordered protein interaction module orchestrates transcription elongation
K. Cermakova, J. Demeulemeester, V. Lux, M. Nedomova, SR. Goldman, EA. Smith, P. Srb, R. Hexnerova, M. Fabry, M. Madlikova, M. Horejsi, J. De Rijck, Z. Debyser, K. Adelman, HC. Hodges, V. Veverka
Language English Country United States
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
R35 GM137996
NIGMS NIH HHS - United States
- MeSH
- Adaptor Proteins, Signal Transducing chemistry metabolism MeSH
- DNA-Binding Proteins chemistry metabolism MeSH
- Transcription Elongation, Genetic * MeSH
- Gene Expression MeSH
- Protein Interaction Domains and Motifs genetics MeSH
- Humans MeSH
- Protein Interaction Maps MeSH
- Models, Molecular MeSH
- Mutation MeSH
- Cell Line, Tumor MeSH
- Protein Domains MeSH
- RNA-Binding Proteins chemistry genetics metabolism MeSH
- RNA Polymerase II chemistry metabolism MeSH
- Transcriptional Elongation Factors chemistry metabolism MeSH
- Transcription Factors chemistry genetics metabolism MeSH
- Protein Binding MeSH
- Intrinsically Disordered Proteins chemistry metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
[Figure: see text].
Center for Cancer Epigenetics The University of Texas MD Anderson Cancer Center Houston TX USA
Department of Bioengineering Rice University Houston TX USA
Department of Biological Chemistry and Molecular Pharmacology Harvard Medical School Boston MA USA
Department of Cell Biology Faculty of Science Charles University Prague Czech Republic
Institute of Molecular Genetics of the Czech Academy of Sciences Prague Czech Republic
Molecular Virology and Gene Therapy KU Leuven Leuven Flanders Belgium
References provided by Crossref.org
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