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Results 1-10 of 10 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2017
Loss of Usp9x disrupts cell adhesion, and components of the Wnt and Notch signaling pathways in neural progenitors
Premarathne, S.
;
Murtaza, M.
;
Matigian, N.
;
Jolly, L.
;
Wood, S.
2012
A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability
Huang, L.
;
Jolly, L.
;
Willis-Owen, S.
;
Gardner, A.
;
Sharma, R.
;
Douglas, E.
;
Shoubridge, C.
;
Wieczorek, D.
;
Tzschach, A.
;
Cohen, M.
;
Hackett, A.
;
Field, M.
;
Froyen, G.
;
Hu, H.
;
Haas, S.
;
Ropers, H.
;
Kalscheuer, V.
;
Corbett, M.
;
Gecz, J.
2015
Seizures are regulated by ubiquitin-specific peptidase 9 x-linked (USP9X), a de-ubiquitinase
Paemka, L.
;
Mahajan, V.
;
Ehaideb, S.
;
Skeie, J.
;
Tan, M.
;
Wu, S.
;
Cox, A.
;
Sowers, L.
;
Gecz, J.
;
Jolly, L.
;
Ferguson, P.
;
Darbro, B.
;
Schneider, A.
;
Scheffer, I.
;
Carvill, G.
;
Mefford, H.
;
El-Shanti, H.
;
Wood, S.
;
Manak, J.
;
Bassuk, A.
;
Frankel, W.
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
A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24
Bahlo, M.
;
Jolly, L.
;
Afawi, Z.
;
Gardner, A.
;
Oliver, K.
;
Tan, S.
;
Coffey, A.
;
Mulley, J.
;
Dibbens, L.
;
Simri, W.
;
Shalata, A.
;
Kivity, S.
;
Jackson, G.
;
Berkovic, S.
;
Gecz, J.
;
Corbett, M.
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.
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.
2017
Viperin is an important host restriction factor in control of Zika virus infection
Van Der Hoek, K.
;
Eyre, N.
;
Shue, B.
;
Khantisitthiporn, O.
;
Glab-Ampi, K.
;
Carr, J.
;
Gartner, M.
;
Jolly, L.
;
Thomas, P.
;
Adikusuma, F.
;
Jankovic-Karasoulos, T.
;
Roberts, C.
;
Helbig, K.
;
Beard, M.
2017
USP9X deubiquitylating enzyme maintains RAPTOR protein levels, mTORC1 signalling and proliferation in neural progenitors
Bridges, C.
;
Tan, M.
;
Premarathne, S.
;
Nanayakkara, D.
;
Bellette, B.
;
Zencak, D.
;
Domingo, D.
;
Gecz, J.
;
Murtaza, M.
;
Jolly, L.
;
Wood, S.
Discover
Author
8
Gecz, J.
4
Wood, S.
3
Homan, C.
2
Barry, S.
2
Corbett, M.
2
Domingo, D.
2
Gardner, A.
2
Kalscheuer, V.
2
Murtaza, M.
2
Nguyen, L.
.
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Subject
10
Animals
8
Female
6
Male
5
Intellectual Disability
5
Neural Stem Cells
4
Mutation
4
Neurons
4
Ubiquitin Thiolesterase
3
Amino Acid Sequence
3
Brain
.
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Date issued
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2015
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2014
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2013
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2010