-
1
-
-
78049447421
-
Asymmetric prefrontal cortex functions predict asymmetries in number space
-
Bachmann, V., Fischer, M. H., Landolt, H. P. and Brugger, P. (2010). Asymmetric prefrontal cortex functions predict asymmetries in number space. Brain Cogn. 74, 306-311.
-
(2010)
Brain Cogn
, vol.74
, pp. 306-311
-
-
Bachmann, V.1
Fischer, M.H.2
Landolt, H.P.3
Brugger, P.4
-
2
-
-
78049434700
-
Loss of maternal ATRX results in centromere instability and aneuploidy in the mammalian oocyte and pre-implantation embryo
-
Baumann, C., Viveiros, M. M. and De La Fuente, R. (2010). Loss of maternal ATRX results in centromere instability and aneuploidy in the mammalian oocyte and pre-implantation embryo. PLoS Genet. 6, e1001137.
-
(2010)
PLoS Genet.
, vol.6
, pp. e1001137
-
-
Baumann, C.1
Viveiros, M.M.2
De La Fuente, R.3
-
3
-
-
0342514792
-
Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association
-
Bérubé, N. G., Smeenk, C. A. and Picketts, D. J. (2000). Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association. Hum. Mol. Genet. 9, 539-547.
-
(2000)
Hum. Mol. Genet
, vol.9
, pp. 539-547
-
-
Bérubé, N.G.1
Smeenk, C.A.2
Picketts, D.J.3
-
4
-
-
14944359718
-
The chromatinremodeling protein ATRX is critical for neuronal survival during corticogenesis
-
Bérubé, N. G., Mangelsdorf, M., Jagla, M., Vanderluit, J., Garrick, D., Gibbons, R. J., Higgs, D. R., Slack, R. S. and Picketts, D. J. (2005). The chromatinremodeling protein ATRX is critical for neuronal survival during corticogenesis. J. Clin. Invest. 115, 258-267.
-
(2005)
J. Clin. Invest.
, vol.115
, pp. 258-267
-
-
Bérubé, N.G.1
Mangelsdorf, M.2
Jagla, M.3
Vanderluit, J.4
Garrick, D.5
Gibbons, R.J.6
Higgs, D.R.7
Slack, R.S.8
Picketts, D.J.9
-
5
-
-
0028983389
-
T-brain-1: A homolog of Brachyury whose expression defines molecularly distinct domains within the cerebral cortex
-
Bulfone, A., Smiga, S. M., Shimamura, K., Peterson, A., Puelles, L. and Rubenstein, J. L. (1995). T-brain-1: a homolog of Brachyury whose expression defines molecularly distinct domains within the cerebral cortex. Neuron 15, 63-78.
-
(1995)
Neuron
, vol.15
, pp. 63-78
-
-
Bulfone, A.1
Smiga, S.M.2
Shimamura, K.3
Peterson, A.4
Puelles, L.5
Rubenstein, J.L.6
-
6
-
-
18144405762
-
Cortical neuron specification: It has its time and place
-
Campbell, K. (2005). Cortical neuron specification: it has its time and place. Neuron 46, 373-376.
-
(2005)
Neuron
, vol.46
, pp. 373-376
-
-
Campbell, K.1
-
7
-
-
33645702778
-
A novel mutation in the last exon of ATRX in a patient with alpha-thalassemia myelodysplastic syndrome.
-
Costa, D. B., Fisher, C. A., Miller, K. B., Pihan, G. A., Steensma, D. P., Gibbons, R. J. and Higgs, D. R. (2006). A novel mutation in the last exon of ATRX in a patient with alpha-thalassemia myelodysplastic syndrome. Eur. J. Haematol. 76, 432-435, 453.
-
(2006)
Eur.J. Haematol.
, vol.76
, Issue.432-435
, pp. 453
-
-
Costa, D.B.1
Fisher, C.A.2
Miller, K.B.3
Pihan, G.A.4
Steensma, D.P.5
Gibbons, R.J.6
Higgs, D.R.7
-
8
-
-
3042780173
-
ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes
-
De La Fuente, R., Viveiros, M. M., Wigglesworth, K. and Eppig, J. J. (2004). ATRX, a member of the SNF2 family of helicase/ATPases, is required for chromosome alignment and meiotic spindle organization in metaphase II stage mouse oocytes. Dev. Biol. 272, 1-14.
-
(2004)
Dev. Biol.
, vol.272
, pp. 1-14
-
-
De La Fuente, R.1
Viveiros, M.M.2
Wigglesworth, K.3
Eppig, J.J.4
-
9
-
-
77953955724
-
The death-associated protein DAXX is a novel histone chaperone involved in the replication-independent deposition of H3.3
-
Drané, P., Ouararhni, K., Depaux, A., Shuaib, M. and Hamiche, A. (2010). The death-associated protein DAXX is a novel histone chaperone involved in the replication-independent deposition of H3.3. Genes Dev. 24, 1253-1265.
-
(2010)
Genes Dev
, vol.24
, pp. 1253-1265
-
-
Drané, P.1
Ouararhni, K.2
Depaux, A.3
Shuaib, M.4
Hamiche, A.5
-
10
-
-
0028939603
-
Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)
-
Gibbons, R. J., Picketts, D. J., Villard, L. and Higgs, D. R. (1995). Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome). Cell 80, 837-845.
-
(1995)
Cell
, vol.80
, pp. 837-845
-
-
Gibbons, R.J.1
Picketts, D.J.2
Villard, L.3
Higgs, D.R.4
-
11
-
-
77649099092
-
Distinct factors control histone variant H3.3 localization at specific genomic regions
-
Goldberg, A. D., Banaszynski, L. A., Noh, K. M., Lewis, P. W., Elsaesser, S. J., Stadler, S., Dewell, S., Law, M., Guo, X., Li, X. et al. (2010). Distinct factors control histone variant H3.3 localization at specific genomic regions. Cell 140, 678-691.
-
(2010)
Cell
, vol.140
, pp. 678-691
-
-
Goldberg, A.D.1
Banaszynski, L.A.2
Noh, K.M.3
Lewis, P.W.4
Elsaesser, S.J.5
Stadler, S.6
Dewell, S.7
Law, M.8
Guo, X.9
Li, X.10
-
12
-
-
37749022460
-
Neuroepithelial progenitors undergo LGN-dependent planar divisions to maintain self-renewability during mammalian neurogenesis
-
Konno, D., Shioi, G., Shitamukai, A., Mori, A., Kiyonari, H., Miyata, T. and Matsuzaki, F. (2008). Neuroepithelial progenitors undergo LGN-dependent planar divisions to maintain self-renewability during mammalian neurogenesis. Nat. Cell Biol. 10, 93-101.
-
(2008)
Nat. Cell Biol
, vol.10
, pp. 93-101
-
-
Konno, D.1
Shioi, G.2
Shitamukai, A.3
Mori, A.4
Kiyonari, H.5
Miyata, T.6
Matsuzaki, F.7
-
13
-
-
46549089463
-
The determination of projection neuron identity in the developing cerebral cortex
-
Leone, D. P., Srinivasan, K., Chen, B., Alcamo, E. and McConnell, S. K. (2008). The determination of projection neuron identity in the developing cerebral cortex. Curr. Opin. Neurobiol. 18, 28-35.
-
(2008)
Curr. Opin. Neurobiol
, vol.18
, pp. 28-35
-
-
Leone, D.P.1
Srinivasan, K.2
Chen, B.3
Alcamo, E.4
McConnell, S.K.5
-
14
-
-
77956282773
-
Daxx is an H3.3-specific histone chaperone and cooperates with ATRX in replication-independent chromatin assembly at telomeres
-
Lewis, P. W., Elsaesser, S. J., Noh, K. M., Stadler, S. C. and Allis, C. D. (2010). Daxx is an H3.3-specific histone chaperone and cooperates with ATRX in replication-independent chromatin assembly at telomeres. Proc. Natl. Acad. Sci. USA 107, 14075-14080.
-
(2010)
Proc. Natl. Acad. Sci. USA
, vol.107
, pp. 14075-14080
-
-
Lewis, P.W.1
Elsaesser, S.J.2
Noh, K.M.3
Stadler, S.C.4
Allis, C.D.5
-
15
-
-
79958763042
-
Functional significance of mutations in the Snf2 domain of ATRX
-
Mitson, M., Kelley, L. A., Sternberg, M. J., Higgs, D. R. and Gibbons, R. J. (2011). Functional significance of mutations in the Snf2 domain of ATRX. Hum. Mol. Genet. 20, 2603-2610.
-
(2011)
Hum. Mol. Genet
, vol.20
, pp. 2603-2610
-
-
Mitson, M.1
Kelley, L.A.2
Sternberg, M.J.3
Higgs, D.R.4
Gibbons, R.J.5
-
16
-
-
80054841867
-
Mouse inscuteable induces apical-basal spindle orientation to facilitate intermediate progenitor generation in the developing neocortex
-
Postiglione, M. P., Jüschke, C., Xie, Y., Haas, G. A., Charalambous, C. and Knoblich, J. A. (2011). Mouse inscuteable induces apical-basal spindle orientation to facilitate intermediate progenitor generation in the developing neocortex. Neuron 72, 269-284.
-
(2011)
Neuron
, vol.72
, pp. 269-284
-
-
Postiglione, M.P.1
Jüschke, C.2
Xie, Y.3
Haas, G.A.4
Charalambous, C.5
Knoblich, J.A.6
-
17
-
-
0015965793
-
Neurons in rhesus monkey visual cortex: Systematic relation between time of origin and eventual disposition
-
Rakic, P. (1974). Neurons in rhesus monkey visual cortex: systematic relation between time of origin and eventual disposition. Science 183, 425-427.
-
(1974)
Science
, vol.183
, pp. 425-427
-
-
Rakic, P.1
-
18
-
-
38749117849
-
Loss of ATRX leads to chromosome cohesion and congression defects
-
Ritchie, K., Seah, C., Moulin, J., Isaac, C., Dick, F. and Bérubé, N. G. (2008). Loss of ATRX leads to chromosome cohesion and congression defects. J. Cell Biol. 180, 315-324.
-
(2008)
J. Cell Biol.
, vol.180
, pp. 315-324
-
-
Ritchie, K.1
Seah, C.2
Moulin, J.3
Isaac, C.4
Dick, F.5
Bérubé, N.G.6
-
19
-
-
58149391969
-
Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53
-
Seah, C., Levy, M. A., Jiang, Y., Mokhtarzada, S., Higgs, D. R., Gibbons, R. J. and Bérubé, N. G. (2008). Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53. J. Neurosci. 28, 12570-12580.
-
(2008)
J. Neurosci.
, vol.28
, pp. 12570-12580
-
-
Seah, C.1
Levy, M.A.2
Jiang, Y.3
Mokhtarzada, S.4
Higgs, D.R.5
Gibbons, R.J.6
Bérubé, N.G.7
-
20
-
-
79952381377
-
Oblique radial glial divisions in the developing mouse neocortex induce self-renewing progenitors outside the germinal zone that resemble primate outer subventricular zone progenitors
-
Shitamukai, A., Konno, D. and Matsuzaki, F. (2011). Oblique radial glial divisions in the developing mouse neocortex induce self-renewing progenitors outside the germinal zone that resemble primate outer subventricular zone progenitors. J. Neurosci. 31, 3683-3695.
-
(2011)
J. Neurosci.
, vol.31
, pp. 3683-3695
-
-
Shitamukai, A.1
Konno, D.2
Matsuzaki, F.3
-
21
-
-
79955455586
-
A new subtype of progenitor cell in the mouse embryonic neocortex
-
Wang, X., Tsai, J. W., LaMonica, B. and Kriegstein, A. R. (2011). A new subtype of progenitor cell in the mouse embryonic neocortex. Nat. Neurosci. 14, 555-561.
-
(2011)
Nat. Neurosci
, vol.14
, pp. 555-561
-
-
Wang, X.1
Tsai, J.W.2
LaMonica, B.3
Kriegstein, A.R.4
-
22
-
-
84877115679
-
Atrx deficiency induces telomere dysfunction, endocrine defects, and reduced life span
-
Watson, L. A., Solomon, L. A., Li, J. R., Jiang, Y., Edwards, M., Shin-ya, K., Beier, F. and Bérubé, N. G. (2013). Atrx deficiency induces telomere dysfunction, endocrine defects, and reduced life span. J. Clin. Invest. 123, 2049-2063.
-
(2013)
J. Clin. Invest.
, vol.123
, pp. 2049-2063
-
-
Watson, L.A.1
Solomon, L.A.2
Li, J.R.3
Jiang, Y.4
Edwards, M.5
Shin-Ya, K.6
Beier, F.7
Bérubé, N.G.8
-
23
-
-
0141703327
-
The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies
-
Xue, Y., Gibbons, R., Yan, Z., Yang, D., McDowell, T. L., Sechi, S., Qin, J., Zhou, S., Higgs, D. and Wang, W. (2003). The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies. Proc. Natl. Acad. Sci. USA 100, 10635-10640.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 10635-10640
-
-
Xue, Y.1
Gibbons, R.2
Yan, Z.3
Yang, D.4
McDowell, T.L.5
Sechi, S.6
Qin, J.7
Zhou, S.8
Higgs, D.9
Wang, W.10
|