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Results 1-10 of 13 (Search time: 0.002 seconds).
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Issue Date
Title
Author(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.
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.
2011
Deep sequencing analysis of the developing mouse brain reveals a novel microRNA
Ling, 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.
2012
Congenital hydrocephalus and abnormal subcommissural organ development in Sox3 transgenic mice
Lee, 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.
2013
Mechanistic insight into the pathology of polyalanine expansion disorders revealed by a mouse model for x linked hypopituitarism
Hughes, J.
;
Piltz, S.
;
Rogers, N.
;
McAninch, D.
;
Rowley, L.
;
Thomas, P.
;
Camper, S.
2016
Pcdh19 loss-of-function increases neuronal migration in vitro but is dispensable for brain development in mice
Pederick, D.
;
Homan, C.
;
Jaehne, E.
;
Piltz, S.
;
Haines, B.
;
Baune, B.
;
Jolly, L.
;
Hughes, J.
;
Gecz, J.
;
Thomas, P.
2014
A reduction in Npas4 expression results in delayed neural differentiation of mouse embryonic stem cells
Klaric, T.
;
Thomas, P.
;
Dottori, M.
;
Leong, W.
;
Koblar, S.
;
Lewis, M.
Discover
Author
5
Hughes, J.
5
Piltz, S.
4
McAninch, D.
3
Rogers, N.
2
Cheah, P.
2
Gecz, J.
2
Jolly, L.
1
Adelson, D.
1
Adikusuma, F.
1
Afawi, Z.
.
next >
Subject
3
Disease Models, Animal
3
Embryo, Mammalian
3
Embryonic Development
3
Embryonic Stem Cells
2
Base Sequence
2
Binding Sites
2
Cell Line
2
Cells, Cultured
2
Child, Preschool
2
CRISPR-Cas Systems
.
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2014
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2013
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2012
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2011