References
Papers based off of data acquired from In Situ Hybridization Core
Maynard TM, Meechan DW, Dudevoir ML, Gopalakrishna D, Peters AZ, Heindel CC, Sugimoto TJ, Wu Y, Lieberman JA, Lamantia AS. 2008. Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes. Mol Cell Neurosci. 39:439-51.
PMCID: PMC2729512
Powell AW, Sassa T, Wu Y, Tessier-Lavigne M, Polleux F. 2008. Topography of thalamic projections requires attractive and repulsive functions of Netrin-1 in the ventral telencephalon. PLoS Biol. 6:1047-68.
PMCID: PMC2584572
Tucker ES, Segall S, Gopalakrishna D, Wu Y, Vernon M, Polleux F, Lamantia AS. 2008. Molecular specification and patterning of progenitor cells in the lateral and medial ganglionic eminences. J Neurosci. 28:9504-18.
Weimer JM, Stanco A, Cheng JG, Vargo AC, Voora S, Anton ES. 2008. A BAC transgenic mouse model to analyze the function of astroglial SPARCL1 (SC1) in the central nervous system. Glia. 56:935-41.
Buhusi M, Demyanenko GP, Jannie KM, Dalal J, Darnell EP, Weiner JA, Maness PF. 2009. ALCAM Regulates Mediolateral Retinotopic Mapping in the Superior Colliculus. J Neurosci. 29(50):15630-41.
James JM, Gewolb C, Bautch VL. 2009. Neurovascular development uses VEGF-A signaling to regulate blood vessel ingression into the neural tube. Development. 136:833-41.
PMCID: PMC2685948
Kim WY, Wang X, Wu Y, Doble BW, Patel S, Woodgett JR, Snider WD. 2009. GSK-3 is a master regulator of neural progenitor homeostasis. Nat Neurosci. 12:1390-7.
Meechan DW, Tucker ES, Maynard TM, LaMantia AS. 2009. Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome. Proc Natl Acad Sci U S A. 106:16434-45.
PMCID: PMC2752572
Siesser PF, Maness PF. 2009. L1 cell adhesion molecules as regulators of tumor cell invasiveness. Cell Adh Migr. 3:275-7.
PMCID: PMC2712809
Rawson NE, Lischka FW, Yee KK, Peters AZ, Tucker ES, Meechan DW, Zirlinger M, Maynard TM, Burd GB, Dulac C, Pevny L, LaMantia AS. 2010. Specific mesenchymal/epithelial induction of olfactory receptor, vomeronasal, and gonadotrophin-releasing hormone (GnRH) neurons. Dev Dyn. 239(6): 1723-38.
Tucker ES, Lehtinen MK, Maynard T, Zirlinger M, Dulac C, Rawson N, Pevny L, Lamantia AS. 2010. Proliferative and transcriptional identity of distinct classes of neural precursors in the mammalian olfactory epithelium. Development. 137(15):2471-81.
PMCID: PMC2927697
Yu TW, Mochida GH, Tischfield DJ, Sgaier SK, Flores-Sarnat L, Sergi CM, Topçu M, McDonald MT, Barry BJ, Felie JM, Sunu C, Dobyns WB, Folkerth RD, Barkovich AJ, Walsh CA. 2010. Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture. Nature Genetics. 42(11):1015-20.
PMCID: PMC2969850
Hutton SR, Pevny LH. 2011. SOX2 expression levels distinguish between neural progenitor populations of the developing dorsal telencephalon. Dev Biol. 352(1):40-7.
Matsushima D, Heavner W, Pevny LH. 2011. Combinatorial regulation of optic cup progenitor cell fate by SOX2 and PAX6. Development. 138(3):443-54.
PMCID: PMC3014633
