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Year | Number of Results |
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2023 | 4 |
2024 | 1 |
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Page 1
FBH1 deficiency sensitizes cells to WEE1 inhibition by promoting mitotic catastrophe.
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.
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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Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease.
Claus LR, Chen C, Stallworth J, Turner JL, Slaats GG, Hawks AL, Mabillard H, Senum SR, Srikanth S, Flanagan-Steet H, Louie RJ, Silver J, Lerner-Ellis J, Morel C, Mighton C, Sleutels F, van Slegtenhorst M, van Ham T, Brooks AS, Dorresteijn EM, Barakat TS, Dahan K, Demoulin N, Goffin EJ, Olinger E; Genomics England Research Consortium; Larsen M, Hertz JM, Lilien MR, Obeidová L, Seeman T, Stone HK, Kerecuk L, Gurgu M, Yousef Yengej FA, Ammerlaan CME, Rookmaaker MB, Hanna C, Rogers RC, Duran K, Peters E, Sayer JA, van Haaften G, Harris PC, Ling K, Mason JM, van Eerde AM, Steet R.
Claus LR, et al.
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
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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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