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Preview	Issue Date	Title	Author(s)
	1998	The identification and localisation of a human gene with sequence similarity to Polycomblike of Drosophila melanogaster	Coulson, M.; Robert, S.; Eyre, H.; Saint, R.
	2017	Mitochondrion to endoplasmic reticulum apposition length in zebrafish embryo spinal progenitors is unchanged in response to perturbations associated with Alzheimer’s disease	Newman, M.; Halter, L.; Lim, A.; Lardelli, M.; Lakshmana, M.
	2017	Phosphoenolpyruvate carboxykinase maintains glycolysis-driven growth in Drosophila tumors	Hussain, R.; Shaukat, Z.; Khan, M.; Saint, R.; Gregory, S.
	2015	Mammalian evolution: a Jurassic spark	Lee, M.S.Y.; Beck, R.M.D.
	1998	Localisation of the human NMDAR2D receptor subunit gene (GRIN2D) to 19q13.1-qter, the NMDAR2A subunit gene to 16p13.2 (GRIN2A), and the NMDAR2C subunit gene (GRIN2C) to 17q24-q25 using somatic cell hybrid and radiation hybrid mapping panels.	Kalsi, G.; Whiting, P.; Bourdelles, B.; Callen, D.; Barnard, E.; Gurling, H.
	1998	The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.	Kortschak, R.; Reimann, H.; Zimmer, M.; Eyre, H.; Saint, R.; Jenne, D.
	2015	Combining experimental evolution with next-generation sequencing: a powerful tool to study adaptation from standing genetic variation	Schlötterer, C.; Kofler, R.; Versace, E.; Tobler, R.; Franssen, S.
	2023	The impact of the cytoplasmic ubiquitin ligase TNFAIP3 gene variation on transcription factor NF-κB activation in acute kidney injury	Rogers, N.M.; Zammit, N.; Nguyen-Ngo, D.; Souilmi, Y.; Minhas, N.; Meijles, D.N.; Self, E.; Walters, S.N.; Warren, J.; Cultrone, D.; El-Rashid, M.; Li, J.; Chtanova, T.; O'Connell, P.J.; Grey, S.T.
	1995	X-Y chromosome dissociation in mice and rats exposed to increased testicular or environmental temperatures	Van Zelst, S.; Zupp, J.; Hayman, D.; Setchell, B.