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Results 1-10 of 16 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2017Knockout of the epilepsy gene Depdc5 in mice causes severe embryonic dysmorphology with hyperactivity of mTORC1 signallingHughes, J.; Dawson, R.; Tea, M.; McAninch, D.; Piltz, S.; Jackson, D.; Stewart, L.; Ricos, M.; Dibbens, L.; Harvey, N.; Thomas, P.
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.
2014Identification of highly conserved putative developmental enhancers bound by SOX3 in neural progenitors using ChIP-SeqMcAninch, D.; Thomas, P.; Zheng, D.
2014Dbx1 is a direct target of SOX3 in the spinal cordRogers, N.; McAninch, D.; Thomas, P.; Alsina, B.
2014SOX3 deletion in mouse and human Is associated with persistence of the craniopharyngeal canalAlatzoglou, 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.
2012PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndromeHeron, 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.
2012A new species of Asthenocotyle Robinson, 1961 (Monogenea: Microbothriidae), a skin parasite of the great lanternshark Etmopterus princeps Collett from the Azores, with a redescription of A. kaikourensis Robinson, 1961 and observations on A. taranakiensis Beverley-Burton, Klassen & Lester, 1987Kearn, G.; Whittington, I.; Thomas, P.
2012The role of zinc in genomic stabilitySharif, R.; Thomas, P.; Zalewski, P.; Fenech, M.
2011Deep sequencing analysis of the developing mouse brain reveals a novel microRNALing, K.; Brautigan, P.; Hahn, C.; Daish, T.; Rayner, J.; Cheah, P.; Raison, J.; Piltz, S.; Mann, J.; Mattiske, D.; Thomas, P.; Adelson, D.; Scott, H.
2012Congenital hydrocephalus and abnormal subcommissural organ development in Sox3 transgenic miceLee, K.; Tan, J.; Morris, M.; Rizzoti, K.; Hughes, J.; Cheah, P.; Felquer, F.; Liu, X.; Piltz, S.; Lovell-Badge, R.; Thomas, P.; Schmidt, J.V.

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