A postnatal function for Nkx2-1 in basal forebrain integrity (Commentary on Magno et al.)
First published: 28 November 2011
No abstract is available for this article.
References
-
Butt, S.J.,
Sousa, V.H.,
Fuccillo, M.V.,
Hjerling-Leffler, J.,
Miyoshi, G.,
Kimura, S. &
Fishell, G. (2008) The requirement of Nkx2-1 in the temporal specification of cortical interneuron subtypes.
Neuron, 59, 722–732.
-
Kleiner-Fisman, G. &
Lang, A.E. (2007) Benign hereditary chorea revisited: a journey to understanding.
Mov. Disord., 22, 2297–2305.
-
Magno, L.,
Catanzariti, V.,
Nitsch, R.,
Krude, H. &
Naumann, T. (2009) Ongoing expression of Nkx2.1 in the postnatal mouse forebrain: potential for understanding NKX2.1 haploinsufficiency in humans?
Brain Res., 1304, 164–186.
-
Magno, L.,
Kretz, O.,
Bert, B.,
Ersözlü, S.,
Vogt, J.,
Fink, H.,
Kimura, S.,
Vogt, A.,
Monyer, H.,
Nitsch, R. &
Naumann, T. (2011) The integrity of cholinergic basal forebrain neurons depends on expression of Nkx2-1.
Eur. J. Neurosci., 34, 1767–1782.
-
Marín, O.,
Anderson, S.A. &
Rubenstein, J.L.R. (2000) Origin and molecular specification of striatal interneurons.
J. Neurosci., 20, 6063–6076.
-
Nóbrega-Pereira, S.,
Kessaris, N.,
Du, T.,
Kimura, S.,
Anderson, S.A. &
Marin, O. (2008) Postmitotic Nkx2-1 controls the migration of telencephalic interneurons by direct repression of guidance receptors.
Neuron, 59, 733–745.
-
Smeyne, R.J.,
Klein, R.,
Schnapp, A.,
Long, L.K.,
Bryant, S.,
Lewin, A.,
Lira, S.A. &
Barbacid, M. (1994) Severe sensory and sympathetic neuropathies in mice carrying a disrupted Trk/NGF receptor gene.
Nature, 368, 246–249.
-
Sussel, L.,
Marín, O.,
Kimura, S. &
Rubenstein, J.L. (1999) Loss of Nkx2.1 homeobox gene function results in a ventral to dorsal molecular respecification within the basal telencephalon: evidence for a transformation of the pallidum into the striatum.
Development, 126, 3359–3370.