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Preview	Issue Date	Title	Author(s)
	2016	TBC1D24 genotype-phenotype correlation	Balestrini, S.; Milh, M.; Castiglioni, C.; Lüthy, K.; Finelli, M.; Verstreken, P.; Cardon, A.; Stražišar, B.; Holder, J.; Lesca, G.; Mancardi, M.; Poulat, A.; Repetto, G.; Banka, S.; Bilo, L.; Birkeland, L.; Bosch, F.; Brockmann, K.; Cross, J.; Doummar, D.; et al.
	2017	ProBDNF Accelerates Brain Amyloid-β Deposition and Learning and Memory Impairment in APPswePS1dE9 Transgenic Mice	Chen, J.; Zhang, T.; Jiao, S.; Zhou, X.; Zhong, J.; Wang, Y.; Liu, J.; Deng, J.; Wang, S.; Xu, Z.
	2004	Reproductive performance in female ClockΔ19 mutant mice	Kennaway, D.; Boden, M.; Voultsios, A.
	1999	Comparative virulence of Streptococcus pneumoniae strains with insertion-duplication, point, and deletion mutations in the pneumolysin gene	Berry, A.; Ogunniyi, A.; Miller, D.; Paton, J.; Fischetti, V.A.
	2001	Bovine spongiform encephalopathy and variant Creutzfeldt-Jakob disease: implications for Australia	Goldwater, P.
	2017	Knockout of the epilepsy gene Depdc5 in mice causes severe embryonic dysmorphology with hyperactivity of mTORC1 signalling	Hughes, J.; Dawson, R.; Tea, M.; McAninch, D.; Piltz, S.; Jackson, D.; Stewart, L.; Ricos, M.; Dibbens, L.; Harvey, N.; Thomas, P.
	2017	NAD deficiency, congenital malformations, and niacin supplementation	Shi, H.; Enriquez, A.; Rapadas, M.; Martin, E.; Wang, R.; Moreau, J.; Lim, C.; Szot, J.; Ip, E.; Hughes, J.; Sugimoto, K.; Humphreys, D.; McInerney-Leo, A.; Leo, P.; Maghzal, G.; Halliday, J.; Smith, J.; Colley, A.; Mark, P.; Collins, F.; et al.
	2001	Impaired thrombin generation in b2-glycoprotein I null mice	Sheng, Y.; Reddel, S.; Herzog, H.; Wang, Y.; Brighton, T.; France, M.; Robertson, S.; Krilis, S.
	2019	International experience in the development of patient-derived xenograft models of diffuse intrinsic pontine glioma	Tsoli, M.; Shen, H.; Mayoh, C.; Franshaw, L.; Ehteda, A.; Upton, D.; Carvalho, D.; Vinci, M.; Meel, M.H.; van Vuurden, D.; Plessier, A.; Castel, D.; Drissi, R.; Farrell, M.; Cryan, J.; Crimmins, D.; Caird, J.; Pears, J.; Francis, S.; Ludlow, L.E.A.; et al.
	2021	A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouse	Houston, B.J.; Conrad, D.F.; O'Bryan, M.K.