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Items: 9

1.

Developmental and cancer-associated plasticity of DNA replication preferentially targets GC-poor, lowly expressed and late-replicating regions.

Wu X, Kabalane H, Kahli M, Petryk N, Laperrousaz B, Jaszczyszyn Y, Drillon G, Nicolini FE, Perot G, Robert A, Fund C, Chibon F, Xia R, Wiels J, Argoul F, Maguer-Satta V, Arneodo A, Audit B, Hyrien O.

Nucleic Acids Res. 2018 Nov 2;46(19):10532. doi: 10.1093/nar/gky849. No abstract available.

2.

Developmental and cancer-associated plasticity of DNA replication preferentially targets GC-poor, lowly expressed and late-replicating regions.

Wu X, Kabalane H, Kahli M, Petryk N, Laperrousaz B, Jaszczyszyn Y, Drillon G, Nicolini FE, Perot G, Robert A, Fund C, Chibon F, Xia R, Wiels J, Argoul F, Maguer-Satta V, Arneodo A, Audit B, Hyrien O.

Nucleic Acids Res. 2018 Nov 2;46(19):10157-10172. doi: 10.1093/nar/gky797. Erratum in: Nucleic Acids Res. 2018 Nov 2;46(19):10532.

3.

Accurate Recycling of Parental Histones Reproduces the Histone Modification Landscape during DNA Replication.

Reverón-Gómez N, González-Aguilera C, Stewart-Morgan KR, Petryk N, Flury V, Graziano S, Johansen JV, Jakobsen JS, Alabert C, Groth A.

Mol Cell. 2018 Oct 18;72(2):239-249.e5. doi: 10.1016/j.molcel.2018.08.010. Epub 2018 Aug 23.

4.

MCM2 promotes symmetric inheritance of modified histones during DNA replication.

Petryk N, Dalby M, Wenger A, Stromme CB, Strandsby A, Andersson R, Groth A.

Science. 2018 Sep 28;361(6409):1389-1392. doi: 10.1126/science.aau0294. Epub 2018 Aug 16.

PMID:
30115746
5.

Deciphering DNA replication dynamics in eukaryotic cell populations in relation with their averaged chromatin conformations.

Goldar A, Arneodo A, Audit B, Argoul F, Rappailles A, Guilbaud G, Petryk N, Kahli M, Hyrien O.

Sci Rep. 2016 Mar 3;6:22469. doi: 10.1038/srep22469.

6.

Replication landscape of the human genome.

Petryk N, Kahli M, d'Aubenton-Carafa Y, Jaszczyszyn Y, Shen Y, Silvain M, Thermes C, Chen CL, Hyrien O.

Nat Commun. 2016 Jan 11;7:10208. doi: 10.1038/ncomms10208.

7.

Functional study of the Hap4-like genes suggests that the key regulators of carbon metabolism HAP4 and oxidative stress response YAP1 in yeast diverged from a common ancestor.

Petryk N, Zhou YF, Sybirna K, Mucchielli MH, Guiard B, Bao WG, Stasyk OV, Stasyk OG, Krasovska OS, Budin K, Reymond N, Imbeaud S, Coudouel S, Delacroix H, Sibirny A, Bolotin-Fukuhara M.

PLoS One. 2014 Dec 5;9(12):e112263. doi: 10.1371/journal.pone.0112263. eCollection 2014.

8.

From simple bacterial and archaeal replicons to replication N/U-domains.

Hyrien O, Rappailles A, Guilbaud G, Baker A, Chen CL, Goldar A, Petryk N, Kahli M, Ma E, d'Aubenton-Carafa Y, Audit B, Thermes C, Arneodo A.

J Mol Biol. 2013 Nov 29;425(23):4673-89. doi: 10.1016/j.jmb.2013.09.021. Epub 2013 Oct 3. Review.

PMID:
24095859
9.

A novel Hansenula polymorpha transcriptional factor HpHAP4-B, able to functionally replace the S. cerevisiae HAP4 gene, contains an additional bZip motif.

Sybirna K, Petryk N, Zhou YF, Sibirny A, Bolotin-Fukuhara M.

Yeast. 2010 Nov;27(11):941-54. doi: 10.1002/yea.1802.

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