Alan R. Lehmann
Affiliations: | University of Sussex, Falmer, England, United Kingdom |
Area:
DNA repairGoogle:
"Alan Lehmann"
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Giovannini S, Weibel L, Schittek B, et al. (2024) Skin cancer induction by the antimycotic drug voriconazole is caused by impaired DNA damage detection due to chromatin compaction. The Journal of Investigative Dermatology |
| Yurchenko AA, Rajabi F, Braz-Petta T, et al. (2023) Genomic mutation landscape of skin cancers from DNA repair-deficient xeroderma pigmentosum patients. Nature Communications. 14: 2561 |
| Cipolla L, Bertoletti F, Maffia A, et al. (2019) UBR5 interacts with the replication fork and protects DNA replication from DNA polymerase η toxicity. Nucleic Acids Research |
| Theil AF, Botta E, Raams A, et al. (2019) Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype. American Journal of Human Genetics. 105: 434-440 |
| Abeti R, Zeitlberger A, Peelo C, et al. (2018) Xeroderma pigmentosum: overview of pharmacology and novel therapeutic strategies for neurological symptoms. British Journal of Pharmacology |
| Bertoletti F, Cea V, Liang CC, et al. (2017) Phosphorylation regulates human polη stability and damage bypass throughout the cell cycle. Nucleic Acids Research. 45: 9441-9454 |
| Alt A, Dang HQ, Wells OS, et al. (2017) Specialized interfaces of Smc5/6 control hinge stability and DNA association. Nature Communications. 8: 14011 |
| van der Crabben SN, Hennus MP, McGregor GA, et al. (2016) Destabilized SMC5/6 complex leads to chromosome breakage syndrome with severe lung disease. The Journal of Clinical Investigation |
| Kuschal C, Botta E, Orioli D, et al. (2016) GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy. American Journal of Human Genetics |
| Fassihi H, Sethi M, Fawcett H, et al. (2016) Deep phenotyping of 89 xeroderma pigmentosum patients reveals unexpected heterogeneity dependent on the precise molecular defect. Proceedings of the National Academy of Sciences of the United States of America |