Hans Hombauer - Publications

Affiliations: 
German Cancer Research Center (DKFZ), Germany 

16 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Reyes GX, Kolodziejczak A, Devakumar LJPS, Kubota T, Kolodner RD, Putnam CD, Hombauer H. Ligation of newly replicated DNA controls the timing of DNA mismatch repair. Current Biology : Cb. PMID 33417883 DOI: 10.1016/j.cub.2020.12.018  0.844
2020 Reyes GX, Zhao B, Schmidt TT, Gries K, Kloor M, Hombauer H. Identification of MLH2/hPMS1 dominant mutations that prevent DNA mismatch repair function. Communications Biology. 3: 751. PMID 33303966 DOI: 10.1038/s42003-020-01481-4  0.491
2019 Schmidt TT, Sharma S, Reyes GX, Kolodziejczak A, Wagner T, Luke B, Hofer A, Chabes A, Hombauer H. Inactivation of folylpolyglutamate synthetase Met7 results in genome instability driven by an increased dUTP/dTTP ratio. Nucleic Acids Research. PMID 31647103 DOI: 10.1093/Nar/Gkz1006  0.664
2018 Schmidt TT, Sharma S, Reyes GX, Gries K, Gross M, Zhao B, Yuan JH, Wade R, Chabes A, Hombauer H. A genetic screen pinpoints ribonucleotide reductase residues that sustain dNTP homeostasis and specifies a highly mutagenic type of dNTP imbalance. Nucleic Acids Research. PMID 30462295 DOI: 10.1093/Nar/Gky1154  0.631
2017 Schmidt TT, Reyes G, Gries K, Ceylan CÜ, Sharma S, Meurer M, Knop M, Chabes A, Hombauer H. Alterations in cellular metabolism triggered by URA7 or GLN3 inactivation cause imbalanced dNTP pools and increased mutagenesis. Proceedings of the National Academy of Sciences of the United States of America. PMID 28416670 DOI: 10.1073/Pnas.1618714114  0.679
2015 Schmidt TT, Hombauer H. Visualization of mismatch repair complexes using fluorescence microscopy. Dna Repair. PMID 26725956 DOI: 10.1016/J.Dnarep.2015.11.014  0.562
2015 Reyes GX, Schmidt TT, Kolodner RD, Hombauer H. New insights into the mechanism of DNA mismatch repair. Chromosoma. PMID 25862369 DOI: 10.1007/S00412-015-0514-0  0.82
2014 Goellner EM, Smith CE, Campbell CS, Hombauer H, Desai A, Putnam CD, Kolodner RD. PCNA and Msh2-Msh6 activate an Mlh1-Pms1 endonuclease pathway required for Exo1-independent mismatch repair. Molecular Cell. 55: 291-304. PMID 24981171 DOI: 10.1016/J.Molcel.2014.04.034  0.76
2014 Campbell CS, Hombauer H, Srivatsan A, Bowen N, Gries K, Desai A, Putnam CD, Kolodner RD. Mlh2 is an accessory factor for DNA mismatch repair in Saccharomyces cerevisiae. Plos Genetics. 10: e1004327. PMID 24811092 DOI: 10.1371/Journal.Pgen.1004327  0.777
2013 Smith CE, Mendillo ML, Bowen N, Hombauer H, Campbell CS, Desai A, Putnam CD, Kolodner RD. Dominant mutations in S. cerevisiae PMS1 identify the Mlh1-Pms1 endonuclease active site and an exonuclease 1-independent mismatch repair pathway. Plos Genetics. 9: e1003869. PMID 24204293 DOI: 10.1371/Journal.Pgen.1003869  0.768
2013 Jaehnig EJ, Kuo D, Hombauer H, Ideker TG, Kolodner RD. Checkpoint kinases regulate a global network of transcription factors in response to DNA damage. Cell Reports. 4: 174-88. PMID 23810556 DOI: 10.1016/J.Celrep.2013.05.041  0.685
2011 Hombauer H, Srivatsan A, Putnam CD, Kolodner RD. Mismatch repair, but not heteroduplex rejection, is temporally coupled to DNA replication. Science (New York, N.Y.). 334: 1713-6. PMID 22194578 DOI: 10.1126/Science.1210770  0.744
2011 Hombauer H, Campbell CS, Smith CE, Desai A, Kolodner RD. Visualization of eukaryotic DNA mismatch repair reveals distinct recognition and repair intermediates Cell. 147: 1040-1053. PMID 22118461 DOI: 10.1016/J.Cell.2011.10.025  0.786
2011 Hombauer H, Srivatsan A, Putnam CD, Kolodner RD. Mismatch repair, but not heteroduplex rejection, is temporally coupled to DNA replication Science. 334: 1713-1716. DOI: 10.1126/science.1210770  0.763
2010 Cantagrel V, Lefeber DJ, Ng BG, Guan Z, Silhavy JL, Bielas SL, Lehle L, Hombauer H, Adamowicz M, Swiezewska E, De Brouwer AP, Blümel P, Sykut-Cegielska J, Houliston S, Swistun D, et al. SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder. Cell. 142: 203-17. PMID 20637498 DOI: 10.1016/J.Cell.2010.06.001  0.361
2009 Enserink JM, Hombauer H, Huang ME, Kolodner RD. Cdc28/Cdk1 positively and negatively affects genome stability in S. cerevisiae Journal of Cell Biology. 185: 423-437. PMID 19398760 DOI: 10.1083/Jcb.200811083  0.795
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