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Results 1-10 of 11 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2016
TBC1D24 genotype-phenotype correlation
Balestrini, S.
;
Milh, M.
;
Castiglioni, C.
;
Lüthy, K.
;
Finelli, M.
;
Verstreken, P.
;
Cardon, A.
;
Stražišar, B.
;
Holder, J.
;
Lesca, G.
;
Mancardi, M.
;
Poulat, A.
;
Repetto, G.
;
Banka, S.
;
Bilo, L.
;
Birkeland, L.
;
Bosch, F.
;
Brockmann, K.
;
Cross, J.
;
Doummar, D.
;
et al.
2004
Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and forebrain GABAergic neurons
Colombo, E.
;
Galli, R.
;
Cossu, G.
;
Gecz, J.
;
Broccoli, V.
2013
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity
Hirata, H.
;
McMichael, G.
;
Haan, E.
;
MacLennan, A.
;
Yap, T.
;
Nguyen, L.
;
Shaw, M.
;
Gecz, J.
2015
DAT isn’t all that: cocaine reward and reinforcement require Toll-like receptor 4 signaling
Northcutt, A.
;
Hutchinson, M.
;
Wang, X.
;
Baratta, M.
;
Hiranita, T.
;
Cochran, T.
;
Pomrenze, M.
;
Galer, E.
;
Kopajtic, T.
;
Li, C.
;
Amat, J.
;
Larson, G.
;
Cooper, D.
;
Huang, Y.
;
O'Neill, C.
;
Yin, H.
;
Zahniser, N.
;
Katz, J.
;
Rice, K.
;
Maier, S.
;
et al.
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
ER stress causes rapid loss of intestinal epithelial stemness through activation of the unfolded protein response
Heijmans, J.
;
van Lidth de Jeude, J.
;
Koo, B.
;
Rosekrans, S.
;
Wielenga, M.
;
van de Wetering, M.
;
Ferrante, M.
;
Lee, A.
;
Onderwater, J.
;
Paton, J.
;
Paton, A.
;
Mommaas, A.
;
Kodach, L.
;
Hardwick, J.
;
Hommes, D.
;
Clevers, H.
;
Muncan, V.
;
van den Brink, G.
2004
Role of N- and C-terminal residues of insulin-like growth factor (IGF)-binding protein-3 in regulating IGF complex formation and receptor activation
Yan, X.
;
Forbes, B.
;
McNeil, K.
;
Baxter, R.
;
Firth, S.
2013
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
Dibbens, L.
;
de Vries, B.
;
Donatello, S.
;
Heron, S.
;
Hodgson, B.
;
Chintawar, S.
;
Crompton, D.
;
Hughes, J.
;
Bellows, S.
;
Klein, K.
;
Callenbach, P.
;
Corbett, M.
;
Gardner, A.
;
Kivity, S.
;
Iona, X.
;
Regan, B.
;
Weller, C.
;
Crimmins, D.
;
O'Brien, T.
;
Guerrero-Lopez, R.
;
et al.
2018
Adult mouse eIF2Bϵ Arg191His astrocytes display a normal integrated stress response in vitro
Wisse, L.
;
Ter Braak, T.
;
Van De Beek, M.
;
Van Berkel, C.
;
Wortel, J.
;
Heine, V.
;
Proud, C.
;
Van Der Knaap, M.
;
Abbink, T.
2007
Aristaless-related homeobox gene, the gene responsible for west syndrome and related disorders, is a groucho/transducin-like enhancer of split dependent transcriptional repressor
McKenzie, O.
;
Ponte, I.
;
Mangelsdorf, M.
;
Finnis, M.
;
Colasante, G.
;
Shoubridge, C.
;
Stifani, S.
;
Gecz, J.
;
Broccoli, V.
Discover
Author
4
Gecz, J.
3
et al.
2
Broccoli, V.
2
Nguyen, L.
2
Paton, J.
1
Abbink, T.
1
Amat, J.
1
Balestrini, S.
1
Banka, S.
1
Baratta, M.
.
next >
Subject
11
Animals
8
Humans
5
Female
5
Male
4
Brain
3
Carrier Proteins
3
Cell Differentiation
3
In Situ Hybridization
3
Neurons
3
Pedigree
.
next >
Date issued
8
2010 - 2018
3
2004 - 2009