Boyle S - Search Results

1

Low Level of Expression of C-Terminally Truncated Human FUS Causes Extensive Changes in the Spinal Cord Transcriptome of Asymptomatic Transgenic Mice.

Lysikova EA, Funikov S, Rezvykh AP, Chaprov KD, Kukharsky MS, Ustyugov A, Deykin AV, Flyamer IM, Boyle S, Bachurin SO, Ninkina N, Buchman VL. Lysikova EA, et al. Among authors: boyle s. Neurochem Res. 2020 May;45(5):1168-1179. doi: 10.1007/s11064-020-02999-z. Epub 2020 Mar 11. Neurochem Res. 2020. PMID: 32157564

2

A central role for canonical PRC1 in shaping the 3D nuclear landscape.

Boyle S, Flyamer IM, Williamson I, Sengupta D, Bickmore WA, Illingworth RS. Boyle S, et al. Genes Dev. 2020 Jul 1;34(13-14):931-949. doi: 10.1101/gad.336487.120. Epub 2020 May 21. Genes Dev. 2020. PMID: 32439634 Free PMC article.

3

Ultra-long-range interactions between active regulatory elements.

Friman ET, Flyamer IM, Marenduzzo D, Boyle S, Bickmore WA. Friman ET, et al. Among authors: boyle s. Genome Res. 2023 Aug;33(8):1269-1283. doi: 10.1101/gr.277567.122. Epub 2023 Jul 14. Genome Res. 2023. PMID: 37451823 Free PMC article.

4

Transcription decouples estrogen-dependent changes in enhancer-promoter contact frequencies and spatial proximity.

Gómez Acuña LI, Flyamer I, Boyle S, Friman ET, Bickmore WA. Gómez Acuña LI, et al. Among authors: boyle s. PLoS Genet. 2024 May 23;20(5):e1011277. doi: 10.1371/journal.pgen.1011277. eCollection 2024 May. PLoS Genet. 2024. PMID: 38781242 Free PMC article.

5

Expression of progerin does not result in an increased mutation rate.

Deniaud E, Lemaître C, Boyle S, Bickmore WA. Deniaud E, et al. Among authors: boyle s. Chromosome Res. 2017 Oct;25(3-4):227-239. doi: 10.1007/s10577-017-9556-x. Epub 2017 May 6. Chromosome Res. 2017. PMID: 28477268 Free PMC article.

6

Recruitment to the nuclear periphery can alter expression of genes in human cells.

Finlan LE, Sproul D, Thomson I, Boyle S, Kerr E, Perry P, Ylstra B, Chubb JR, Bickmore WA. Finlan LE, et al. Among authors: boyle s. PLoS Genet. 2008 Mar 21;4(3):e1000039. doi: 10.1371/journal.pgen.1000039. PLoS Genet. 2008. PMID: 18369458 Free PMC article.

7

Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype.

Fantes J, Redeker B, Breen M, Boyle S, Brown J, Fletcher J, Jones S, Bickmore W, Fukushima Y, Mannens M, et al. Fantes J, et al. Among authors: boyle s. Hum Mol Genet. 1995 Mar;4(3):415-22. doi: 10.1093/hmg/4.3.415. Hum Mol Genet. 1995. PMID: 7795596

8

The reticulocalbin gene maps to the WAGR region in human and to the Small eye Harwell deletion in mouse.

Kent J, Lee M, Schedl A, Boyle S, Fantes J, Powell M, Rushmere N, Abbott C, van Heyningen V, Bickmore WA. Kent J, et al. Among authors: boyle s. Genomics. 1997 Jun 1;42(2):260-7. doi: 10.1006/geno.1997.4706. Genomics. 1997. PMID: 9192846

9

Scaffold attachments within the human genome.

Craig JM, Boyle S, Perry P, Bickmore WA. Craig JM, et al. Among authors: boyle s. J Cell Sci. 1997 Nov;110 ( Pt 21):2673-82. doi: 10.1242/jcs.110.21.2673. J Cell Sci. 1997. PMID: 9427385

10

Differences in the localization and morphology of chromosomes in the human nucleus.

Croft JA, Bridger JM, Boyle S, Perry P, Teague P, Bickmore WA. Croft JA, et al. Among authors: boyle s. J Cell Biol. 1999 Jun 14;145(6):1119-31. doi: 10.1083/jcb.145.6.1119. J Cell Biol. 1999. PMID: 10366586 Free PMC article.

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