David Szuts
Affiliations: | Institute of Enzymology | Research Centre for Natural Sciences, Budapest |
Area:
DNA repairGoogle:
"David Szuts"Mean distance: (not calculated yet)
Parents
Sign in to add mentorMariann Bienz | grad student | 1995-1999 | (FlyTree) |
Torsten Krude | post-doc | 1999-2004 | Cambridge |
Julian E. Sale | post-doc | 2004-2008 | MRC LMB |
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Publications
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Lózsa R, Németh E, Gervai JZ, et al. (2023) DNA mismatch repair protects the genome from oxygen-induced replicative mutagenesis. Nucleic Acids Research |
Gyüre Z, Póti Á, Németh E, et al. (2023) Spontaneous mutagenesis in human cells is controlled by REV1-Polymerase ζ and PRIMPOL. Cell Reports. 42: 112887 |
Póti Á, Szikriszt B, Gervai JZ, et al. (2022) Characterisation of the spectrum and genetic dependence of collateral mutations induced by translesion DNA synthesis. Plos Genetics. 18: e1010051 |
Chen D, Gervai JZ, Póti Á, et al. (2022) BRCA1 deficiency specific base substitution mutagenesis is dependent on translesion synthesis and regulated by 53BP1. Nature Communications. 13: 226 |
Szeltner Z, Póti Á, Harami GM, et al. (2021) Evaluation and modulation of DNA lesion bypass in an SV40 large T antigen-based in vitro replication system. Febs Open Bio |
Szikriszt B, Póti Á, Németh E, et al. (2021) A comparative analysis of the mutagenicity of platinum-containing chemotherapeutic agents reveals direct and indirect mutagenic mechanisms. Mutagenesis. 36: 75-86 |
Pálinkás HL, Békési A, Róna G, et al. (2020) Genome-wide alterations of uracil distribution patterns in human DNA upon chemotherapeutic treatments. Elife. 9 |
Póti Á, Gyergyák H, Németh E, et al. (2019) Correlation of homologous recombination deficiency induced mutational signatures with sensitivity to PARP inhibitors and cytotoxic agents. Genome Biology. 20: 240 |
Vető B, Szabó P, Bacquet C, et al. (2018) Inhibition of DNA methyltransferase leads to increased genomic 5-hydroxymethylcytosine levels in hematopoietic cells. Febs Open Bio. 8: 584-592 |
Gervai JZ, Gálicza J, Szeltner Z, et al. (2017) A genetic study based on PCNA-ubiquitin fusions reveals no requirement for PCNA polyubiquitylation in DNA damage tolerance. Dna Repair. 54: 46-54 |