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Author/Creator Breslin, Kelsey

1. Setdb1-mediated H3K9 methylation is enriched on the inactive X and plays a role in its epigenetic silencing. Issue 1 (December 2016)

Authors:
Keniry, Andrew; Gearing, Linden; Jansz, Natasha; Liu, Joy; Holik, Aliaksei; Hickey, Peter; Kinkel, Sarah; Moore, Darcy; Breslin, Kelsey; Chen, Kelan; Liu, Ruijie; Phillips, Catherine; Pakusch, Miha; Biben, Christine; Sheridan, Julie; Kile, Benjamin; Carmichael, Catherine; Ritchie, Matthew; Hilton...
Journal:
Epigenetics & chromatin
Issue:
Volume 9:Issue 1(2016)
Page Start:
1
Record Type:
Journal Article
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2. Smchd1 haploinsufficiency exacerbates the phenotype of a transgenic FSHD1 mouse model. (21st December 2017)

Authors:
de Greef, Jessica C; Krom, Yvonne D; den Hamer, Bianca; Snider, Lauren; Hiramuki, Yosuke; van den Akker, Rob F P; Breslin, Kelsey; Pakusch, Miha; Salvatori, Daniela C F; Slütter, Bram; Tawil, Rabi; Blewitt, Marnie E; Tapscott, Stephen J; van der Maarel, Silvère M
Journal:
Human molecular genetics
Issue:
Volume 27:Number 4(2018:Feb. 15)
Page Start:
716
Record Type:
Journal Article
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3. The long and the short of it: unlocking nanopore long-read RNA sequencing data with short-read differential expression analysis tools. (26th April 2021)

Authors:
Dong, Xueyi; Tian, Luyi; Gouil, Quentin; Kariyawasam, Hasaru; Su, Shian; De Paoli-Iseppi, Ricardo; Prawer, Yair David Joseph; Clark, Michael B; Breslin, Kelsey; Iminitoff, Megan; Blewitt, Marnie E; Law, Charity W; Ritchie, Matthew E
Journal:
NAR genomics and bioinformatics
Issue:
Volume 3:issue 2(2021)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗