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Preview	Issue Date	Title	Author(s)
	2012	Adipokines and adipocyte function in clock mutant mice that retain melatonin rhythmicity	Kennaway, D.; Owens, J.; Voultsios, A.; Wight, N.
	2009	Grape seed polyphenols and curcumin reduce genomic instability events in a transgenic mouse model for Alzheimer's disease	Thomas, P.; Wang, Y.; Zhong, J.; Kosaraju, S.; Callaghan, N.; Zhou, X.; Fenech, M.
	2010	Disruption at the PTCHD1 locus on Xp22.11 in Autism Spectrum Disorder and intellectual disability	Gecz, J.
	2014	Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth	Homan, C.; Kumar, R.; Nguyen, L.; Haan, E.; Raymond, F.; Abidi, F.; Raynaud, M.; Schwartz, C.; Wood, S.; Gecz, J.; Jolly, L.
	2007	Transforming growth factor-β1 null mutation causes infertility in male mice associated with testosterone deficiency and sexual dysfunction	Ingram, W.; Robertson, S.
	2010	Canal cristae growth and fiber extension to the outer hair cells of the mouse ear require Prox1 activity	Fritzsch, B.; Dillard, M.; Lavado, A.; Harvey, N.; Israt, J.; Koch, K.-W.
	2018	Differential effects on gene transcription and hematopoietic differentiation correlate with GATA2 mutant disease phenotypes	Chong, C.-E.; Venugopal, P.; Stokes, P.; Lee, Y.; Brautigan, P.; Yeung, D.; Babic, M.; Engler, G.; Lane, S.; Klingler-Hoffmann, M.; Matthews, J.; D'Andrea, R.; Brown, A.; Hahn, C.; Scott, H.
	1998	PAK3 mutation in nonsyndromic X-linked mental retardation	Allen, K.; Gleeson, J.; Bagrodia, S.; Partington, M.; MacMillan, J.; Cerione, R.; Mulley, J.; Walsh, C.
	2018	Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder	Frints, S.G.M.; Ozanturk, A.; Rodríguez Criado, G.; Grasshoff, U.; de Hoon, B.; Field, M.; Manouvrier-Hanu, S.; E Hickey, S.; Kammoun, M.; Gripp, K.W.; Bauer, C.; Schroeder, C.; Toutain, A.; Mihalic Mosher, T.; Kelly, B.J.; White, P.; Dufke, A.; Rentmeester, E.; Moon, S.; Koboldt, D.C.; et al.
	2015	Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome	Walz, K.; Cohen, D.; Neilsen, P.; Foster, J.; Brancati, F.; Demir, K.; Fisher, R.; Moffat, M.; Verbeek, N.; Bjørgo, K.; Lo Castro, A.; Curatolo, P.; Novelli, G.; Abad, C.; Lei, C.; Zhang, L.; Diaz-Horta, O.; Young, J.; Callen, D.; Tekin, M.