Fusser M - Search Results

1

Endonuclease G preferentially cleaves 5-hydroxymethylcytosine-modified DNA creating a substrate for recombination.

Robertson AB, Robertson J, Fusser M, Klungland A. Robertson AB, et al. Among authors: fusser m. Nucleic Acids Res. 2014 Dec 1;42(21):13280-93. doi: 10.1093/nar/gku1032. Epub 2014 Oct 29. Nucleic Acids Res. 2014. PMID: 25355512 Free PMC article.

2

Genome-wide profiling of DNA 5-hydroxymethylcytosine during rat Sertoli cell maturation.

Landfors M, Johansen J, Aronsen JM, Vågbø CB, Doré LC, He C, Sjaastad I, Sætrom P, Fedorcsák P, Dahl JA, Aanes H, Fußer M, Klungland A. Landfors M, et al. Among authors: fusser m. Cell Discov. 2017 May 9;3:17013. doi: 10.1038/celldisc.2017.13. eCollection 2017. Cell Discov. 2017. PMID: 28529766 Free PMC article.

3

ALKBH4 depletion in mice leads to spermatogenic defects.

Nilsen A, Fusser M, Greggains G, Fedorcsak P, Klungland A. Nilsen A, et al. Among authors: fusser m. PLoS One. 2014 Aug 25;9(8):e105113. doi: 10.1371/journal.pone.0105113. eCollection 2014. PLoS One. 2014. PMID: 25153837 Free PMC article.

4

Lysine Methylation of the Valosin-Containing Protein (VCP) Is Dispensable for Development and Survival of Mice.

Fusser M, Kernstock S, Aileni VK, Egge-Jacobsen W, Falnes PØ, Klungland A. Fusser M, et al. PLoS One. 2015 Nov 6;10(11):e0141472. doi: 10.1371/journal.pone.0141472. eCollection 2015. PLoS One. 2015. PMID: 26544960 Free PMC article.

5

Sequencing of FTO and ALKBH5 in men undergoing infertility work-up identifies an infertility-associated variant and two missense mutations.

Landfors M, Nakken S, Fusser M, Dahl JA, Klungland A, Fedorcsak P. Landfors M, et al. Among authors: fusser m. Fertil Steril. 2016 May;105(5):1170-1179.e5. doi: 10.1016/j.fertnstert.2016.01.002. Epub 2016 Jan 25. Fertil Steril. 2016. PMID: 26820768 Free article.

6

ALKBH4-dependent demethylation of actin regulates actomyosin dynamics.

Li MM, Nilsen A, Shi Y, Fusser M, Ding YH, Fu Y, Liu B, Niu Y, Wu YS, Huang CM, Olofsson M, Jin KX, Lv Y, Xu XZ, He C, Dong MQ, Rendtlew Danielsen JM, Klungland A, Yang YG. Li MM, et al. Among authors: fusser m. Nat Commun. 2013;4:1832. doi: 10.1038/ncomms2863. Nat Commun. 2013. PMID: 23673617 Free PMC article.

7

Spontaneous mutagenesis in Csb(m/m)Ogg1⁻(/)⁻ mice is attenuated by dietary resveratrol.

Fusser M, Nesse GJ, Khobta A, Xia N, Li H, Klungland A, Epe B. Fusser M, et al. Carcinogenesis. 2011 Jan;32(1):80-5. doi: 10.1093/carcin/bgq196. Epub 2010 Nov 9. Carcinogenesis. 2011. PMID: 21062970

8

CK2 phosphorylation-dependent interaction between aprataxin and MDC1 in the DNA damage response.

Becherel OJ, Jakob B, Cherry AL, Gueven N, Fusser M, Kijas AW, Peng C, Katyal S, McKinnon PJ, Chen J, Epe B, Smerdon SJ, Taucher-Scholz G, Lavin MF. Becherel OJ, et al. Among authors: fusser m. Nucleic Acids Res. 2010 Mar;38(5):1489-503. doi: 10.1093/nar/gkp1149. Epub 2009 Dec 14. Nucleic Acids Res. 2010. PMID: 20008512 Free PMC article.

9

Correction for: Sod2 haploinsufficiency does not accelerate aging of telomere dysfunctional mice.

Guachalla LM, Ju Z, Koziel R, von Figura G, Song Z, Fusser M, Epe B, Jansen-Dürr P, Rudolph KL. Guachalla LM, et al. Among authors: fusser m. Aging (Albany NY). 2019 Dec 6;11(23):11793-11794. doi: 10.18632/aging.102602. Epub 2019 Dec 6. Aging (Albany NY). 2019. PMID: 31879376 Free PMC article. No abstract available.

10

Senataxin, defective in ataxia oculomotor apraxia type 2, is involved in the defense against oxidative DNA damage.

Suraweera A, Becherel OJ, Chen P, Rundle N, Woods R, Nakamura J, Gatei M, Criscuolo C, Filla A, Chessa L, Fusser M, Epe B, Gueven N, Lavin MF. Suraweera A, et al. Among authors: fusser m. J Cell Biol. 2007 Jun 18;177(6):969-79. doi: 10.1083/jcb.200701042. Epub 2007 Jun 11. J Cell Biol. 2007. PMID: 17562789 Free PMC article.

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