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Selected Publications

  • Jeong SJ, Luo R, Li S, Strokes N, Piao X. (2012) Characterization of G protein-coupled receptor 56 protein expression in the mouse developing neocortex. J Comp Neurol 520(13):2930-40. doi: 10.1002/cne.23076.

  • Luo, R., Z. Jin, Y. Deng, N. Strokes, X. Piao (2012) Disease-Associated Mutations Prevent GPR56-Collagen III Interaction. PLoS One 7: e29818. doi:10.1371/journal.pone.0029818PONE-D-11-17966 [pii]

  • Jeong, S.J., S. Li, R. Luo, N. Strokes, X. Piao (2012) Loss of Col3a1, the Gene for Ehlers-Danlos Syndrome Type IV, Results in Neocortical Dyslamination. PLoS One 7: e29767. doi:10.1371/journal.pone.0029767PONE-D-11-21822 [pii]

  • Luo, R., S.J. Jeong, Z. Jin, N. Strokes, S. Li, X. Piao (2011) G protein-coupled receptor 56 and collagen III, a receptor-ligand pair, regulates cortical development and lamination. Proc Natl Acad Sci U S Adoi:1104821108 [pii]10.1073/pnas.1104821108

  • Luo, R., H.M. Yang, Z. Jin, D.J. Halley, B.S. Chang, L. Macpherson, et al. (2011) A Novel GPR56 Mutation Causes Bilateral Frontoparietal Polymicrogyria. Pediatr Neurol 45: 49-53. doi:S0887-8994(11)00100-7 [pii]10.1016/j.pediatrneurol.2011.02.004

  • Strokes, N., X. Piao (2011) Adhesion-GPCRs in the CNS. Adv Exp Med Biol 706: 87-97. doi:10.1007/978-1-4419-7913-1_7

  • Koirala S, Jin Z, Piao X, Corfas G. (2009) GPR56-regulated granule cell adhesion is essential for rostral cerebellar development. J Neurosci 29(23):7439-49.

  • Jin Z, Luo R, Piao X. (2009) GPR56 and its related diseases. Prog Mol Biol Transl Sci 89:1-13. Epub 2009 Oct 7. Review.

  • Li, S., Z. Jin, S. Koirala, L. Bu, L. Xu, R.O. Hynes, et al. (2008) GPR56 regulates pial basement membrane integrity and cortical lamination. J Neurosci 28: 5817-26.

  • Jin, Z., I. Tietjen, L. Bu, L. Liu-Yesucevitz, S.K. Gaur, C.A. Walsh, et al. (2007) Disease-associated mutations affect GPR56 protein trafficking and cell surface expression. Hum Mol Genet 16: 1972-85.

  • Piao, X., B.S. Chang, A. Bodell, K. Woods, B. Benzeev, M. Topcu, et al. (2005) Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes. Ann Neurol 58: 680-7.

  • Piao X, Walsh CA. (2004) A novel signaling mechanism in brain development. Pediatr Res. 56(3):309-10. Epub 2004 Jul 21. No abstract available.

  • Piao, X., R.S. Hill, A. Bodell, B.S. Chang, L. Basel-Vanagaite, R. Straussberg, et al. (2004) G protein-coupled receptor-dependent development of human frontal cortex. Science 303: 2033-6.

  • Chang, B.S., X. Piao, A. Bodell, L. Basel-Vanagaite, R. Straussberg, W.B. Dobyns, et al. (2003) Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16. Ann Neurol 53: 596-606.

  • Piao, X., L. Basel-Vanagaite, R. Straussberg, P.E. Grant, E.W. Pugh, K. Doheny, et al. (2002) An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21. Am J Hum Genet 70: 1028-33.
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