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Preview	Issue Date	Title	Author(s)
	2005	Development and function of the adult generation of Leydig cells in mice with sertoli cell-selective or total ablation of the androgen receptor	De Gendt, K.; Atanassova, N.; Tan, K.; de Franca, L.; Parreira, G.; McKinnell, C.; Sharpe, R.; Saunders, P.; Mason, J.; Hartung, S.; Ivell, R.; Denolet, E.; Verhoeven, G.
	2010	DNA-binding-dependent androgen receptor signaling contributes to gender differences and has physiological actions in males and females	MacLean, H.; Moore, A.; Sastra, S.; Morris, H.; Ghasem-Zadeh, A.; Rana, K.; Axell, A.; Notini, A.; Handelsman, D.; Seeman, E.; Zajac, J.; Davey, R.
	2009	Dietary zinc supplementation and methotrexate-induced small intestinal mucositis in metallothionein-knockout and wild-type mice	Tran, C.; Sundar, S.; Howarth, G.
	2016	Pcdh19 loss-of-function increases neuronal migration in vitro but is dispensable for brain development in mice	Pederick, D.; Homan, C.; Jaehne, E.; Piltz, S.; Haines, B.; Baune, B.; Jolly, L.; Hughes, J.; Gecz, J.; Thomas, P.
	2014	Comparative analyses of lung transcriptomes in patients with alveolar capillary dysplasia with misalignment of pulmonary veins and in foxf1 heterozygous knockout mice	Sen, P.; Dharmadhikari, A.; Majewski, T.; Mohammad, M.; Kalin, T.; Zabielska, J.; Ren, X.; Bray, M.; Brown, H.; Welty, S.; Thevananther, S.; Langston, C.; Szafranski, P.; Justice, M.; Kalinichenko, V.; Gambin, A.; Belmont, J.; Stankiewicz, P.; Koval, M.
	2020	SOX3 promotes generation of committed spermatogonia in postnatal mouse testes	McAninch, D.; Mäkelä, J.-A.; La, H.M.; Hughes, J.N.; Lovell-Badge, R.; Hobbs, R.M.; Thomas, P.Q.
	2009	The ion channel TRPA1 is required for normal mechanosensation and is modulated by algesic stimuli	Brierley, S.; Hughes, P.; Page, A.; Kwan, K.; Martin, C.; O'Donnell, T.; Isaacs, N.; Harrington, A.; Adam, B.; Liebregts, T.; Holtmann, G.; Corey, D.; Rychkov, G.; Blackshaw, L.
	2008	Selective role for TRPV4 ion channels in visceral sensory pathways	Brierley, S.; Page, A.; Hughes, P.; Adam, B.; Liebregts, T.; Isaacs, N.; Holtmann, G.; Liedtke, W.; Blackshaw, L.
	2017	Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis	Hinze, S.; Jackson, M.; Lie, S.; Jolly, L.; Field, M.; Barry, S.; Harvey, R.; Shoubridge, C.
	2013	Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFβ-mediated axonogenesis	Stegeman, S.; Jolly, L.; Premarathne, S.; Gecz, J.; Richards, L.; Mackay-Sim, A.; Wood, S.; Alsina, B.