The emerging role of lysine demethylases in DNA damage response: dissecting the recruitment mode of KDM4D/JMJD2D to DNA damage sites
about
A role of human RNase P subunits, Rpp29 and Rpp21, in homology directed-repair of double-strand breaks.Depletion of Histone Demethylase Jarid1A Resulting in Histone Hyperacetylation and Radiation Sensitivity Does Not Affect DNA Double-Strand Break Repair.Ligand Similarity Complements Sequence, Physical Interaction, and Co-Expression for Gene Function Prediction.H3K9me3 demethylase Kdm4d facilitates the formation of pre-initiative complex and regulates DNA replication.NELF-E is recruited to DNA double-strand break sites to promote transcriptional repression and repair.KDM4D crosstalks with PARP1 and RNA at DNA DSBs.CDYL1 fosters double-strand break-induced transcription silencing and promotes homology-directed repair.The JmjN domain as a dimerization interface and a targeted inhibitor of KDM4 demethylase activity.KDM5B demethylates H3K4 to recruit XRCC1 and promote chemoresistance.KDM5A Regulates a Translational Program that Controls p53 Protein Expression
P2860
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P2860
The emerging role of lysine demethylases in DNA damage response: dissecting the recruitment mode of KDM4D/JMJD2D to DNA damage sites
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The emerging role of lysine de ...... M4D/JMJD2D to DNA damage sites
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type
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The emerging role of lysine de ...... M4D/JMJD2D to DNA damage sites
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prefLabel
The emerging role of lysine de ...... M4D/JMJD2D to DNA damage sites
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P2093
P2860
P1433
P1476
The emerging role of lysine de ...... M4D/JMJD2D to DNA damage sites
@en
P2093
Hanan Khoury-Haddad
Nabieh Ayoub
Prathamesh T Nadar-Ponniah
Samah Awwad
P2860
P304
P356
10.1080/15384101.2015.1014147
P577
2015-01-01T00:00:00Z