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PreviewIssue DateTitleAuthor(s)
2021Of 'junk food' and 'brain food': how parental diet influences offspring neurobiology and behaviourBodden, C.; Hannan, A.J.; Reichelt, A.C.
2021Effect of a moderate dose of fructose in solid foods on triglyceride, glucose and uric acid before and after a one-month moderate sugar feeding periodClifton, P.M.; Keogh, J.B.
2020The gene encoding the ketogenic enzyme HMGCS2 displays a unique expression during gonad development in miceBagheri-Fam, S.; Chen, H.; Wilson, S.; Ayers, K.; Hughes, J.; Sloan-Bena, F.; Calvel, P.; Robevska, G.; Puisac, B.; Kusz-Zamelczyk, K.; Gimelli, S.; Spik, A.; Jaruzelska, J.; Warenik-Szymankiewicz, A.; Faradz, S.; Nef, S.; Pié, J.; Thomas, P.; Sinclair, A.; Wilhelm, D.; Yenugu, S.
2020Genetic history from the Middle Neolithic to present on the Mediterranean island of SardiniaMarcus, J.H.; Posth, C.; Ringbauer, H.; Lai, L.; Skeates, R.; Sidore, C.; Beckett, J.; Furtwängler, A.; Olivieri, A.; Chiang, C.W.K.; Al-Asadi, H.; Dey, K.; Joseph, T.A.; Liu, C.-C.; Der Sarkissian, C.; Radzevičiūtė, R.; Michel, M.; Gradoli, M.G.; Marongiu, P.; Rubino, S.; et al.
2020Cohort profile: the Australian genetics of depression studyByrne, E.M.; Kirk, K.M.; Medland, S.E.; McGrath, J.J.; Colodro-Conde, L.; Parker, R.; Cross, S.; Sullivan, L.; Statham, D.J.; Levinson, D.F.; Licinio, J.; Wray, N.R.; Hickie, I.B.; Martin, N.G.
2020Can we blame fathers who are obese peri-conception, for increasing chronic disease risk in children?McPherson, N.O.
2023Enhanced mitotic arrest and chromosome resolution for cytogenetic analysis in the eastern mosquitofish, Gambusia holbrookiMousavi, S.E.; Grützner, F.; Patil, J.G.
2021Toll-like receptor-4 null mutation causes fetal loss and fetal growth restriction associated with impaired maternal immune tolerance in mice.Chan, H.Y.; Moldenhauer, L.M.; Groome, H.M.; Schjenken, J.E.; Robertson, S.A.
2023The effects of age and biological sex on the association between I-wave recruitment and the response to cTBS: an exploratory studyVan Dam, J.M.; Graetz, L.; Pitcher, J.B.; Goldsworthy, M.R.
2023TP53 mutation variant allele frequency of ≥10% is associated with poor prognosis in therapy-related myeloid neoplasmsShah, M.V.; Tran, E.N.H.; Shah, S.; Chhetri, R.; Baranwal, A.; Ladon, D.; Shultz, C.; Al-Kali, A.; Brown, A.L.; Chen, D.; Scott, H.S.; Greipp, P.; Thomas, D.; Alkhateeb, H.B.; Singhal, D.; Gangat, N.; Kumar, S.; Patnaik, M.M.; Hahn, C.N.; Kok, C.H.; et al.