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Preview	Issue Date	Title	Author(s)
	2015	Alzheimer's disease-related peptide PS2V plays ancient, conserved roles in suppression of the unfolded protein response under hypoxia and stimulation of γ-secretase activity	Moussavi Nik, S.; Newman, M.; Wilson, L.; Ebrahimie, E.; Wells, S.; Musgrave, I.; Verdile, G.; Martins, R.; Lardelli, M.
	2019	DNA hypermethylation encroachment at CpG island borders in cancer is predisposed by H3K4 monomethylation patterns	Skvortsova, K.; Masle-Farquhar, E.; Luu, P.L.; Song, J.Z.; Qu, W.; Zotenko, E.; Gould, C.M.; Du, Q.; Peters, T.J.; Colino-Sanguino, Y.; Pidsley, R.; Nair, S.S.; Khoury, A.; Smith, G.C.; Miosge, L.A.; Reed, J.H.; Kench, J.G.; Rubin, M.A.; Horvath, L.; Bogdanovic, O.; et al.
	1996	Gene localisation for Sutherland-Haan syndrome (SHS:MIM 309470)	Gedeon, A.; Haan, E.; Mulley, J.
	2021	The Nestin neural enhancer is essential for normal levels of endogenous Nestin in neuroprogenitors but is not required for embryo development	Thomson, E.; Dawson, R.; H'ng, C.H.; Adikusuma, F.; Piltz, S.; Thomas, P.Q.; Varshney, G.
	1998	Analysis of a Drosophila cyclin E hypomorphic mutation suggests a novel role for Cyclin E in cell proliferation control during eye imaginal disc development.	Secombe, J.; Pispa, J.; Saint, R.; Richardson, H.
	1996	Refinement of the background genetic map of Xq26-q27 and gene localisation for Borjeson-Forssman-Lehmann syndrome	Gedeon, A.; Kozman, H.; Robinson, H.; Pilia, G.; Schlessinger, D.; Turner, G.; Mulley, J.
	1996	Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation	Gedeon, A.; Glass, I.; Connor, J.; Mulley, J.
	2022	BAF complex-mediated chromatin relaxation is required for establishment of X chromosome inactivation	Keniry, A.; Jansz, N.; Gearing, L.J.; Wanigasuriya, I.; Chen, J.; Nefzger, C.M.; Hickey, P.F.; Gouil, Q.; Liu, J.; Breslin, K.A.; Iminitoff, M.; Beck, T.; Tapia Del Fierro, A.; Whitehead, L.; Jarratt, A.; Kinkel, S.A.; Taberlay, P.C.; Willson, T.; Pakusch, M.; Ritchie, M.E.; et al.
	2022	A custom hybridisation enrichment forensic intelligence panel to infer biogeographic ancestry, hair and eye colour, and Y chromosome lineage	Bardan, F.; Higgins, D.; Austin, J.J.
	1999	Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM	Friend, K.; Crimmins, D.; Phan, T.; Sue, C.; Colley, A.; Fung, V.; Morris, J.; Sutherland, G.; Richards, R.