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Issue Date
Title
Author(s)
2010
Genome-wide identification of human FOXP3 target genes in natural regulatory T cells
Sadlon, T.
;
Wilkinson, B.
;
Pederson, S.
;
Brown, C.
;
Bresatz, S.
;
Gargett, T.
;
Melville, E.
;
Peng, K.
;
D'Andrea, R.
;
Glonek, G.
;
Goodall, G.
;
Zola, H.
;
Shannon, F.
;
Barry, S.
2015
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.
Jolly, L.
;
Nguyen, L.
;
Domingo, D.
;
Sun, Y.
;
Barry, S.
;
Hancarova, M.
;
Plevova, P.
;
Vlckova, M.
;
Havlovicova, M.
;
Kalscheuer, V.
;
Graziano, C.
;
Pippucci, T.
;
Bonora, E.
;
Sedlacek, Z.
;
Gecz, J.
2013
The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth
Jolly, L.
;
Homan, C.
;
Jacob, R.
;
Barry, S.
;
Gecz, J.
2010
Robust, reversible gene knockdown using a single lentiviral short hairpin RNA vector
Brown, C.
;
Sadlon, T.
;
Gargett, T.
;
Melville, E.
;
Zhang, R.
;
Drabsch, Y.
;
Ling, M.
;
Strathdee, C.
;
Gonda, T.
;
Barry, S.
2017
Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis
Hinze, S.
;
Jackson, M.
;
Lie, S.
;
Jolly, L.
;
Field, M.
;
Barry, S.
;
Harvey, R.
;
Shoubridge, C.
Discover
Author
3
Jolly, L.
2
Brown, C.
2
Gargett, T.
2
Gecz, J.
2
Melville, E.
2
Sadlon, T.
1
Bonora, E.
1
Bresatz, S.
1
D'Andrea, R.
1
Domingo, D.
.
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Subject
5
Mice
4
Humans
3
Cells, Cultured
3
Female
3
Intellectual Disability
3
RNA, Small Interfering
2
Brain
2
Cell Differentiation
2
Cell Proliferation
2
Forkhead Transcription Factors
.
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Date issued
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2010