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Preview	Issue Date	Title	Author(s)
	2013	Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse	Bellone, R.; Holl, H.; Sealuri, V.; Devi, S.; Maddodi, N.; Archer, S.; Sandmeyer, L.; Ludwig, A.; Foerster, D.; Pruvost, M.; Reissmann, M.; Bortfeldt, R.; Adelson, D.; Lim, S.; Nelson, J.; Haase, B.; Engensteiner, M.; Leeb, T.; Forsyth, G.; Mienaltowski, M.; et al.; Anderson, M.G.
	2013	Distinct roles for Toll and autophagy pathways in double-stranded RNA toxicity in a Drosophila model of expanded repeat neurodegenerative diseases	Samaraweera, S.; O'Keefe, L.; Price, G.; Venter, D.; Richards, R.
	2014	SOX3 deletion in mouse and human Is associated with persistence of the craniopharyngeal canal	Alatzoglou, K.; Azriyanti, A.; Rogers, N.; Ryan, F.; Curry, N.; Noakes, C.; Bignell, P.; Hall, G.; Littooij, A.; Saunders, D.; Thomas, P.; Stewart, H.; Dattani, M.
	2015	Identification of markers that functionally define a quiescent multiple myeloma cell sub-population surviving bortezomib treatment	Adomako, A.; Calvo, V.; Biran, N.; Osman, K.; Chari, A.; Paton, J.; Paton, A.; Moore, K.; Schewe, D.; Aguirre-Ghiso, J.
	2012	Unfolded protein response causes a phenotypic shift of inflamed glomerular cells toward redifferentiation through dual blockade of Akt and Smad signaling pathways	Johno, H.; Nakajima, S.; Kato, H.; Yao, J.; Paton, A.; Paton, J.; Katoh, R.; Shimizu, F.; Kitamura, M.
	2010	A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24	Bahlo, M.; Jolly, L.; Afawi, Z.; Gardner, A.; Oliver, K.; Tan, S.; Coffey, A.; Mulley, J.; Dibbens, L.; Simri, W.; Shalata, A.; Kivity, S.; Jackson, G.; Berkovic, S.; Gecz, J.; Corbett, M.
	2010	Mitochondrial uncoupler FCCP activates proton conductance but does not block store-operated Ca2+ current in liver cells	To, M.; Aromataris, E.; Castro, J.; Roberts, M.; Barritt, G.; Rychkov, G.
	2010	Functional and structural diversification of the Anguimorpha lizard venom system	Scanlon, D.
	2011	Tmprss3, a transmembrane serine protease deficient in human DFNB8/10 deafness, is critical for cochlear hair cell survival at the onset of hearing	Fasquelle, L.; Scott, H.; Lenoir, M.; Wang, J.; Rebillard, G.; Gaboyard, S.; Venteo, S.; Francois, F.; Masset-Bonnefont, A.; Antonarakis, S.; Neidhart, E.; Chabbert, C.; Puel, J.; Guipponi, M.; Delprat, B.
	2013	A heterozygous moth genome provides insights into herbivory and detoxification	You, M.; Baxter, S.