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Preview	Issue Date	Title	Author(s)
	2014	Aberrant GDF9 expression and activation are associated with common human ovarian disorders	Simpson, C.; Robertson, D.; Al-Musawi, S.; Heath, D.; McNatty, K.; Ritter, L.; Mottershead, D.; Gilchrist, R.; Harrison, C.; Stanton, P.
	2013	Phl p 1-Specific Human Monoclonal IgE and Design of a Hypoallergenic Group 1 Grass Pollen Allergen Fragment	Levin, M.; Rydnert, F.; Kallstrom, E.; Tan, L.; Wormald, P.; Lindstedt, M.; Greiff, L.; Ohlin, M.
	2015	p84 forms a negative regulatory complex with p110γ to control PI3Kγ signalling during cell migration	Turvey, M.; Klingler-Hoffmann, M.; Hoffmann, P.; McColl, S.
	2013	The genomic landscape of hypodiploid acute lymphoblastic leukemia	To, L.
	2013	A tudor domain protein SPINDLIN1 interacts with the mRNA-binding protein SERBP1 and is involved in mouse oocyte meiotic resumption	Chew, T.; Peaston, A.; Lim, A.; Lorthongpanich, C.; Knowles, B.; Solter, D.; Sun, Q.-Y.
	2013	Yunis-Varón Syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatase	Campeau, P.; Lenk, G.; Lu, J.; Bae, Y.; Burrage, L.; Turnpenny, P.; Corona-Rivera, J.; Morandi, L.; Mora, M.; Reutter, H.; Vulto-van Silfhout, A.; Faivre, L.; Haan, E.; Gibbs, R.; Meisler, M.; Lee, B.
	2011	An MD2 hot-spot-mimicking peptide that suppresses TLR4-mediated inflammatory response in vitro and in vivo	Liu, L.; Ghosh, N.; Slivka, P.; Fiorini, Z.; Hutchinson, M.; Watkins, L.; Yin, H.
	2012	A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability	Huang, L.; Jolly, L.; Willis-Owen, S.; Gardner, A.; Sharma, R.; Douglas, E.; Shoubridge, C.; Wieczorek, D.; Tzschach, A.; Cohen, M.; Hackett, A.; Field, M.; Froyen, G.; Hu, H.; Haas, S.; Ropers, H.; Kalscheuer, V.; Corbett, M.; Gecz, J.
	2010	GM-CSF is an essential regulator of T cell activation competence in uterine dendritic cells during early pregnancy in mice	Moldenhauer, L.; Keenihan, S.; Hayball, J.; Robertson, S.
	2014	Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human disease	Newman, M.; Wilson, L.; Verdile, G.; Lim, A.; Khan, I.; Nik, S.; Pursglove, S.; Chapman, G.; Martins, R.; Lardelli, M.