Hein te Riele
Affiliations: | Netherlands Cancer Institute |
Website:
https://www.nki.nl/people/te-riele-hein/Google:
"Hein te Riele"Parents
Sign in to add mentor| Gerard Venema | grad student | 1984 | RUG | |
| (Heterospecific transformation in Bacillus subtilis) | ||||
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Publications
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| Pai G, Roohollahi K, Rockx D, et al. (2023) Genome-wide siRNA screens identify RBBP9 function as a potential target in Fanconi anaemia-deficient head-and-neck squamous cell carcinoma. Communications Biology. 6: 37 |
| Pieters W, Hugenholtz F, Kos K, et al. (2022) Pro-mutagenic effects of the gut microbiota in a Lynch syndrome mouse model. Gut Microbes. 14: 2035660 |
| Will Castro LSEP, Pieters W, Alemdehy MF, et al. (2021) The Widely Used Antihelmintic Drug Albendazole is a Potent Inducer of Loss of Heterozygosity. Frontiers in Pharmacology. 12: 596535 |
| van Ravesteyn TW, Arranz Dols M, Pieters W, et al. (2020) Extensive trimming of short single-stranded DNA oligonucleotides during replication-coupled gene editing in mammalian cells. Plos Genetics. 16: e1009041 |
| van Schie JJM, Faramarz A, Balk JA, et al. (2020) Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion. Nature Communications. 11: 4287 |
| van de Vrugt HJ, Harmsen T, Riepsaame J, et al. (2019) Effective CRISPR/Cas9-mediated correction of a Fanconi anemia defect by error-prone end joining or templated repair. Scientific Reports. 9: 768 |
| Houlleberghs H, Goverde A, Lusseveld J, et al. (2017) Suspected Lynch syndrome associated MSH6 variants: A functional assay to determine their pathogenicity. Plos Genetics. 13: e1006765 |
| Wielders E, Delzenne-Goette E, Dekker R, et al. (2017) Truncation of the MSH2 C-terminal 60 amino acids disrupts effective DNA mismatch repair and is causative for Lynch syndrome. Familial Cancer. 16: 221-229 |
| Wojciechowicz K, Cantelli E, Van Gerwen B, et al. (2014) Temozolomide increases the number of mismatch repair-deficient intestinal crypts and accelerates tumorigenesis in a mouse model of Lynch syndrome. Gastroenterology. 147: 1064-72.e5 |
| Wielders EA, Houlleberghs H, Isik G, et al. (2013) Functional analysis in mouse embryonic stem cells reveals wild-type activity for three MSH6 variants found in suspected Lynch syndrome patients. Plos One. 8: e74766 |