Corrigendum to “Differential genomic destabilisation in human cells with pathogenic MSH2 mutations introduced by genome editing” [Exp. Cell Res. 377 (2019) 24–35](S0014482719300825)(10.1016/j.yexcr.2019.02.020)

Genki Hayashida, Seijiro Shioi, Kyoko Hidaka, Ryosuke Fujikane, Masumi Hidaka, Toshiki Tsurimoto, Teruhisa Tsuzuki, Shinya Oda, Yoshimichi Nakatsu

Research output: Contribution to journalComment/debate

Abstract

The authors regret that the following errors have occurred in publication of the above article. 1) In the author listing, the affiliation of the two authors, Ryosuke Fujikane and Masumi Hidaka, was incorrectly indicated. Please see above their correct affiliation.2) In Introduction, there remains a typographical error, “E. coli stains”, which is correctly “E. coli strains”. The legend of Fig. 3. Also includes another typographical error, “NMU”, which is correctly “MNU (N-methyl-N-nitrosourea)”.3) In Fig. 5., the x and y axes are reversely mentioned in its figure legend. Correctly, “The y axis indicates the quantitatively detected amount of each DNA fragment, and the x axis corresponds to its length standardised using co-electrophoresed size markers”.4) In Discussion (“4.2. Genomic instability in MSH2-mutant HeLa cells”), the flap endonucleases, RAD27 and FEN1, are incorrectly mentioned. Since they process flap structures formed at the 5′ ends of Okazaki fragments, “3’” in the corresponding parts should be replaced with “5’ ”, as follows: “ …., failure in 5’-‘flap’ processing has also been pointed out. The 5′ ends of Okazaki fragments often form flap-like structures, ….”.The authors sincerely apologise for these errors and any inconvenience that they may have caused.

Original languageEnglish
Article number111432
JournalExperimental Cell Research
Volume383
Issue number1
DOIs
Publication statusPublished - Oct 1 2019

All Science Journal Classification (ASJC) codes

  • Cell Biology

Fingerprint Dive into the research topics of 'Corrigendum to “Differential genomic destabilisation in human cells with pathogenic MSH2 mutations introduced by genome editing” [Exp. Cell Res. 377 (2019) 24–35](S0014482719300825)(10.1016/j.yexcr.2019.02.020)'. Together they form a unique fingerprint.

  • Cite this