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Preview	Issue Date	Title	Author(s)
	2014	Placental restriction of fetal growth reduces cutaneous responses to antigen after sensitization in sheep	Wooldridge, A.; Bischof, R.; Meeusen, E.; Liu, H.; Heinemann, G.; Hunter, D.; Giles, L.; Kind, K.; Owens, J.; Clifton, V.; Gatford, K.
	2017	Targeted insertion of an anti-CD2 monoclonal antibody transgene into the GGTA1 locus in pigs using FokI-dCas9	Nottle, M.; Salvaris, E.; Fisicaro, N.; McIlfatrick, S.; Vassiliev, I.; Hawthorne, W.; O'Connell, P.; Brady, J.; Lew, A.; Cowan, P.
	2015	Acute inhibition of casein kinase 1δ/ε rapidly delays peripheral clock gene rhythms	Kennaway, D.; Varcoe, T.; Voultsios, A.; Salkeld, M.; Rattanatray, L.; Boden, M.
	2014	Modifications of human growth differentiation factor 9 to improve the generation of embryos from low competence oocytes	Li, J.; Sugimura, S.; Mueller, T.; White, M.; Martin, G.; Ritter, L.; Liang, X.; Gilchrist, R.; Mottershead, D.
	2016	Prenatal fish oil supplementation and allergy: 6-year follow-up of a randomized controlled trial	Best, K.P.; Sullivan, T.; Palmer, D.; Gold, M.; Kennedy, D.J.; Martin, J.; Makrides, M.
	2011	Heterologous prime-boost-boost immunisation of Chinese cynomolgus macaques using DNA and recombinant poxvirus vectors expressing HIV-1 virus-like particles	Bridge, S.; Sharpe, S.; Dennis, M.; Dowall, S.; Getty, B.; Anson, D.; Skinner, M.; Stewart, J.; Blanchard, T.
	2015	shRNA off-target effects in vivo: impaired endogenous siRNA expression and spermatogenic defects	Song, H.; Bettegowda, A.; Oliver, D.; Yan, W.; Phan, M.; De Rooij, D.; Corbett, M.; Wilkinson, M.; White-Cooper, H.
	2013	A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome	Buchovecky, C.; Turley, S.; Brown, H.; Kyle, S.; McDonald, J.; Liu, B.; Pieper, A.; Huang, W.; Katz, D.; Russell, D.; Shendure, J.; Justice, M.
	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.
	2016	X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes	Hu, H.; Haas, S.; Chelly, J.; Van Esch, H.; Raynaud, M.; De Brouwer, A.; Weinert, S.; Froyen, G.; Frints, S.; Laumonnier, F.; Zemojtel, T.; Love, M.; Richard, H.; Emde, A.; Bienek, M.; Jensen, C.; Hambrock, M.; Fischer, U.; Langnick, C.; Feldkamp, M.; et al.