Publications
Xu Q, Guo L, Moore H, Waclaw RR, Campbell K, Anderson SA (2010). Shh signaling confers ventral telencephalic progenitors with distinct cortical interneuron fates. Neuron. 65:328-340.
Woodruff A, Xu Q, Anderson SA, Yuste R (2009). Depolarizing effect of neocortical chandelier neurons. Frontiers in Neural Circuits. vol. 3, article 15.
Gulacsi AA, Anderson SA (2008). β-catenin-mediated Wnt signaling regulates neurogenesis in the ventral telencephalon. Nature Neuroscience. 11(12), 1383-91.
Nóbrega-Pereira S, Kessaris N, Du T, Kimura S, Anderson SA, Marín O (2008). Transcriptional regulation of cortical interneuron migration by postmitotic Nkx2-1 homeodomain function. Neuron. 59(5), 733-45.
Du T, Xu Q, Ocbina PJ, Anderson SA (2008). Nkx2.1 specifies cortical interneuron fate by direct activation of Lhx6. Development. 135(8), 1559-67.
Wonders CP, Mbata I, Anderson SA (2008). A spatial bias for the origins of interneuron subgroups within the medial ganglionic eminence. Developmental Biology. 314(1):127-36.
Xu Q, Tam M, Anderson SA (2008). Fate-mapping Nkx2.1-lineage cells in the mouse telencephalon. Journal of Comparative Neurology. 506, 16-29.
Shen L, Nam HS, Song S, Moore H, Anderson SA (2006). FoxG1 haploinsufficiency results in impaired neurogenesis in the postnatal hippocampus and contextual memory deficits. Hippocampus. 16(10), 875-90.
Wonders C, Anderson SA (2006). The origin and specification of cortical interneurons. Nature Reviews Neuroscience. 7(9):687-96.
Gulacsi A, Anderson SA (2006). Shh maintains Nkx2.1 in the MGE by a Gli3-independent mechanism. Cerebral Cortex. 16, 89-95.
Xu Q, Wonders CP, Anderson SA (2005). Sonic hedgehog maintains the identity of cortical interneuron progenitors in the ventral telencephalon. Development. 132(22), 4987-4998.
