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Year | Number of Results |
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2023 | 4 |
2024 | 1 |
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Page 1
Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease.
Kidney Int. 2023 Nov;104(5):995-1007. doi: 10.1016/j.kint.2023.07.021. Epub 2023 Aug 19.
Kidney Int. 2023.
PMID: 37598857
UBC13-mediated template switching promotes replication stress resistance in FBH1-deficient cells.
Hawks AL, Bergmann A, McCraw TJ, Mason JM.
Hawks AL, et al.
bioRxiv [Preprint]. 2023 Sep 19:2023.09.04.556280. doi: 10.1101/2023.09.04.556280.
bioRxiv. 2023.
PMID: 37732269
Free PMC article.
Preprint.
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FBH1 deficiency sensitizes cells to WEE1 inhibition by promoting mitotic catastrophe.
Jennings L, Walters HA, Mason JM.
Jennings L, et al.
bioRxiv [Preprint]. 2023 May 18:2023.05.15.540841. doi: 10.1101/2023.05.15.540841.
bioRxiv. 2023.
PMID: 37292855
Free PMC article.
Updated.
Preprint.
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FBH1 deficiency sensitizes cells to WEE1 inhibition by promoting mitotic catastrophe.
Jennings L, Walters HA, McCraw TJ, Turner JL, Mason JM.
Jennings L, et al.
DNA Repair (Amst). 2024 Jan;133:103611. doi: 10.1016/j.dnarep.2023.103611. Epub 2023 Dec 5.
DNA Repair (Amst). 2024.
PMID: 38103522
Free article.
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