Stewart GS - Search Results

1

PRMT5-Dependent Methylation of the TIP60 Coactivator RUVBL1 Is a Key Regulator of Homologous Recombination.

Clarke TL, Sanchez-Bailon MP, Chiang K, Reynolds JJ, Herrero-Ruiz J, Bandeiras TM, Matias PM, Maslen SL, Skehel JM, Stewart GS, Davies CC. Clarke TL, et al. Among authors: stewart gs. Mol Cell. 2017 Mar 2;65(5):900-916.e7. doi: 10.1016/j.molcel.2017.01.019. Epub 2017 Feb 23. Mol Cell. 2017. PMID: 28238654 Free PMC article.

2

A single strand that links multiple neuropathologies in human disease.

Reynolds JJ, Stewart GS. Reynolds JJ, et al. Among authors: stewart gs. Brain. 2013 Jan;136(Pt 1):14-27. doi: 10.1093/brain/aws310. Brain. 2013. PMID: 23365091 Review.

3

A nervous predisposition to unrepaired DNA double strand breaks.

Reynolds JJ, Stewart GS. Reynolds JJ, et al. Among authors: stewart gs. DNA Repair (Amst). 2013 Aug;12(8):588-99. doi: 10.1016/j.dnarep.2013.04.011. Epub 2013 May 17. DNA Repair (Amst). 2013. PMID: 23684796 Review.

4

Reply: A single strand that links multiple neuropathologies in human disease.

Reynolds JJ, Stewart GS. Reynolds JJ, et al. Among authors: stewart gs. Brain. 2014 Apr;137(Pt 4):e267. doi: 10.1093/brain/awt198. Epub 2013 Aug 5. Brain. 2014. PMID: 23921167 No abstract available.

5

BOD1L Is Required to Suppress Deleterious Resection of Stressed Replication Forks.

Higgs MR, Reynolds JJ, Winczura A, Blackford AN, Borel V, Miller ES, Zlatanou A, Nieminuszczy J, Ryan EL, Davies NJ, Stankovic T, Boulton SJ, Niedzwiedz W, Stewart GS. Higgs MR, et al. Among authors: stewart gs. Mol Cell. 2015 Aug 6;59(3):462-77. doi: 10.1016/j.molcel.2015.06.007. Epub 2015 Jul 9. Mol Cell. 2015. PMID: 26166705 Free article.

6

Histone Methylation by SETD1A Protects Nascent DNA through the Nucleosome Chaperone Activity of FANCD2.

Higgs MR, Sato K, Reynolds JJ, Begum S, Bayley R, Goula A, Vernet A, Paquin KL, Skalnik DG, Kobayashi W, Takata M, Howlett NG, Kurumizaka H, Kimura H, Stewart GS. Higgs MR, et al. Among authors: stewart gs. Mol Cell. 2018 Jul 5;71(1):25-41.e6. doi: 10.1016/j.molcel.2018.05.018. Epub 2018 Jun 21. Mol Cell. 2018. PMID: 29937342 Free PMC article.

7

H3K4 methylation by SETD1A/BOD1L facilitates RIF1-dependent NHEJ.

Bayley R, Borel V, Moss RJ, Sweatman E, Ruis P, Ormrod A, Goula A, Mottram RMA, Stanage T, Hewitt G, Saponaro M, Stewart GS, Boulton SJ, Higgs MR. Bayley R, et al. Among authors: stewart gs. Mol Cell. 2022 May 19;82(10):1924-1939.e10. doi: 10.1016/j.molcel.2022.03.030. Epub 2022 Apr 18. Mol Cell. 2022. PMID: 35439434 Free PMC article.

8

Regulation of DNA-end resection by hnRNPU-like proteins promotes DNA double-strand break signaling and repair.

Polo SE, Blackford AN, Chapman JR, Baskcomb L, Gravel S, Rusch A, Thomas A, Blundred R, Smith P, Kzhyshkowska J, Dobner T, Taylor AM, Turnell AS, Stewart GS, Grand RJ, Jackson SP. Polo SE, et al. Among authors: stewart gs. Mol Cell. 2012 Feb 24;45(4):505-16. doi: 10.1016/j.molcel.2011.12.035. Mol Cell. 2012. PMID: 22365830 Free PMC article.

9

Analysis of novel missense ATR mutations reveals new splicing defects underlying Seckel syndrome.

Llorens-Agost M, Luessing J, van Beneden A, Eykelenboom J, O'Reilly D, Bicknell LS, Reynolds JJ, van Koegelenberg M, Hurles ME, Brady AF, Jackson AP, Stewart GS, Lowndes NF. Llorens-Agost M, et al. Among authors: stewart gs. Hum Mutat. 2018 Dec;39(12):1847-1853. doi: 10.1002/humu.23648. Epub 2018 Sep 24. Hum Mutat. 2018. PMID: 30199583 Free PMC article.

10

Novel PNKP mutations causing defective DNA strand break repair and PARP1 hyperactivity in MCSZ.

Kalasova I, Hanzlikova H, Gupta N, Li Y, Altmüller J, Reynolds JJ, Stewart GS, Wollnik B, Yigit G, Caldecott KW. Kalasova I, et al. Among authors: stewart gs. Neurol Genet. 2019 Mar 25;5(2):e320. doi: 10.1212/NXG.0000000000000320. eCollection 2019 Apr. Neurol Genet. 2019. PMID: 31041400 Free PMC article.

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