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Preview	Issue Date	Title	Author(s)
	2006	Persistent Expression of Notch2 Delays Gonadotrope Differentiation	Raetzman, L.; Wheeler, B.; Ross, S.; Thomas, P.; Camper, S.
	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.
	2020	The gene encoding the ketogenic enzyme HMGCS2 displays a unique expression during gonad development in mice	Bagheri-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.
	2021	The BMP antagonist Gremlin1 contributes to the development of cortical excitatory neurons, motor balance and fear responses	Suzuki, M.; Suzuki, N.; Wang, T.; Kobayashi, H.; Vrbanac, L.; Ng, J.Q.; Wright, J.A.; Lannagan, T.R.M.; Gieniec, K.A.; Lewis, M.; Ando, R.; Enomoto, A.; Koblar, S.; Thomas, P.; Worthley, D.L.; Woods, S.L.
	2014	Identification of highly conserved putative developmental enhancers bound by SOX3 in neural progenitors using ChIP-Seq	McAninch, D.; Thomas, P.; Zheng, D.
	2014	Dbx1 is a direct target of SOX3 in the spinal cord	Rogers, N.; McAninch, D.; Thomas, P.; Alsina, B.
	2014	SOX3 deletion in mouse and human Is associated with persistence of the craniopharyngeal canal	Alatzoglou, K.; Azriyanti, A.; Rogers, N.; Ryan, F.; Curry, N.; Noakes, C.; Bignell, P.; Hall, G.; Littooij, A.; Saunders, D.; Thomas, P.; Stewart, H.; Dattani, M.
	2012	PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome	Heron, S.; Grinton, B.; Kivity, S.; Afawi, Z.; Zuberi, S.; Hughes, J.; Pridmore, C.; Hodgson, B.; Iona, X.; Sadleir, L.; Pelekanos, J.; Herlenius, E.; Goldberg-Stern, H.; Bassan, H.; Haan, E.; Korczyn, A.; Gardner, A.; Corbett, M.; Gecz, J.; Thomas, P.; et al.
	2003	Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation	Burdon, K.; McKay, J.; Sale, M.; Russell-Eggitt, I.; Mackey, D.; Wirth, G.; Elder, J.; Nicoll, A.; Clarke, M.; FitzGerald, L.; Stankovich, J.; Shaw, M.; Sharma, S.; Gajovic, S.; Gruss, P.; Ross, S.; Thomas, P.; Voss, A.; Thomas, T.; Gecz, J.; et al.
	2002	Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome	Lower, K.; Turner, G.; Kerr, B.; Mathews, K.; Shaw, M.; Gedeon, A.; Schelley, S.; Hoyme, H.; White, S.; Delatycki, M.; Lampe, A.; Clayton-Smith, J.; Stewart, H.; van Ravenswaay, C.; de Vries, B.; Cox, B.; Grompe, M.; Ross, S.; Thomas, P.; Mulley, J.; et al.