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10.3390/genes6030592 http://scihub22266oqcxt.onion/10.3390/genes6030592 C4584319!4584319!26184323     free     free     free Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Genes+(Basel) 2015 ; 6 (3): 592-606 Nephropedia Template TP {{tp|p=26184323|t=2015. RNF20-SNF2H Pathway of Chromatin Relaxation in DNA Double-Strand Break Repair |pdf=|usr=}}{{26184323}} gab.com Text RNF20-SNF2H Pathway of Chromatin Relaxation in DNA Double-Strand Break Repair JO: Genes (Basel) http://www.kidney.de/pget.php?&tw=1&pmid=26184323 #FOAvip Rapid progress in the study on the association of histone modifications with chromatin remodeling factors has broadened our understanding of chromatin dynamics in DNA transactions. In DNA double-strand break (DSB) repair, the well-known mark of histones is the phosphorylation of the H2A variant, H2AX, which has been used as a surrogate marker of DSBs. The ubiquitylation of histone H2B by RNF20 E3 ligase was recently found to be a DNA damage-induced histone modification. This modification is required for DSB repair and regulated by a distinctive pathway from that of histone H2AX phosphorylation. Moreover, the connection between H2B ubiquitylation and the chromatin remodeling activity of SNF2H has been elucidated. In this review, we summarize the current knowledge of RNF20-mediated processes and the molecular link to H2AX-mediated processes during DSB repair. Twit Text FOAVip RNF20-SNF2H Pathway of Chromatin Relaxation in DNA Double-Strand Break Repair ????Genes (Basel) http://www.kidney.de/pget.php?&tw=1&pmid=26184323 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26184323 #FOAvip English Wikipedia <ref>{{Cite pmid|26184323}}</ref> RNF20-SNF2H Pathway of Chromatin Relaxation in DNA Double-Strand Break Repair #MMPMID26184323 Kato A; Komatsu K Genes (Basel) 2015[Sep]; 6 (3): 592-606 PMID26184323show ga Rapid progress in the study on the association of histone modifications with chromatin remodeling factors has broadened our understanding of chromatin dynamics in DNA transactions. In DNA double-strand break (DSB) repair, the well-known mark of histones is the phosphorylation of the H2A variant, H2AX, which has been used as a surrogate marker of DSBs. The ubiquitylation of histone H2B by RNF20 E3 ligase was recently found to be a DNA damage-induced histone modification. This modification is required for DSB repair and regulated by a distinctive pathway from that of histone H2AX phosphorylation. Moreover, the connection between H2B ubiquitylation and the chromatin remodeling activity of SNF2H has been elucidated. In this review, we summarize the current knowledge of RNF20-mediated processes and the molecular link to H2AX-mediated processes during DSB repair. äRNF20-SNF2H Pathway of Chromatin Relaxation in DNA Double-Strand Break(epmc).pdf DeepDyve Pubget Overpricing