Genome-wide screen reveals APC-associated RNAs enriched in cell protrusions. Mili S, Moissoglu K, Macara IG (2008) Nature 453: 115-9 Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome. Hinds HL, Ashley CT, Sutcliffe JS, Nelson DL, Warren ST, Housman DE, Schalling M (1993) Nat Genet 3: 36-43 Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Verkerk AJ, Pieretti M, Sutcliffe JS, Fu YH, Kuhl DP, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang FP (1991) Cell 65: 905-14 Altered Neuronal and Circuit Excitability in Fragile X Syndrome. Contractor A, Klyachko VA, Portera-Cailliau C (2015) Neuron 87: 699-715 Paternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size range. Sullivan AK, Crawford DC, Scott EH, Leslie ML, Sherman SL (2002) Am J Hum Genet 70: 1532-44 In vivo neuronal function of the fragile X mental retardation protein is regulated by phosphorylation. Coffee RL, Williamson AJ, Adkins CM, Gray MC, Page TL, Broadie K (2012) Hum Mol Genet 21: 900-15 Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1. Gunter C, Paradee W, Crawford DC, Meadows KA, Newman J, Kunst CB, Nelson DL, Schwartz C, Murray A, Macpherson JN, Sherman SL, Warren ST (1998) Hum Mol Genet 7: 1935-46 Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability. Crawford DC, Zhang F, Wilson B, Warren ST, Sherman SL (2000) Hum Mol Genet 9: 1759-69 DNA methylation represses FMR-1 transcription in fragile X syndrome. Sutcliffe JS, Nelson DL, Zhang F, Pieretti M, Caskey CT, Saxe D, Warren ST (1992) Hum Mol Genet 1: 397-400 Activity-dependent FMRP requirements in development of the neural circuitry of learning and memory. Doll CA, Broadie K (2015) Development 142: 1346-56 GABAergic circuit dysfunction in the Drosophila Fragile X syndrome model. Gatto CL, Pereira D, Broadie K (2014) Neurobiol Dis 65: 142-59 The fragile X mental retardation protein developmentally regulates the strength and fidelity of calcium signaling in Drosophila mushroom body neurons. Tessier CR, Broadie K (2011) Neurobiol Dis 41: 147-59 Neuron class-specific requirements for Fragile X Mental Retardation Protein in critical period development of calcium signaling in learning and memory circuitry. Doll CA, Broadie K (2016) Neurobiol Dis 89: 76-87 FMR1 and the fragile X syndrome: human genome epidemiology review. Crawford DC, Acuña JM, Sherman SL (2001) Genet Med 3: 359-71 Fragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2P. Coffee RL, Tessier CR, Woodruff EA, Broadie K (2010) Dis Model Mech 3: 471-85 Fragile X mental retardation protein regulates trans-synaptic signaling in Drosophila. Friedman SH, Dani N, Rushton E, Broadie K (2013) Dis Model Mech 6: 1400-13 Neural circuit architecture defects in a Drosophila model of Fragile X syndrome are alleviated by minocycline treatment and genetic removal of matrix metalloproteinase. Siller SS, Broadie K (2011) Dis Model Mech 4: 673-85 Fragile X mental retardation protein is required for programmed cell death and clearance of developmentally-transient peptidergic neurons. Gatto CL, Broadie K (2011) Dev Biol 356: 291-307 Fragile X mouse: strain effects of knockout phenotype and evidence suggesting deficient amygdala function. Paradee W, Melikian HE, Rasmussen DL, Kenneson A, Conn PJ, Warren ST (1999) Neuroscience 94: 185-92 Fragile X gene premutation in multiple system atrophy. Garland EM, Vnencak-Jones CL, Biaggioni I, Davis TL, Montine TJ, Robertson D (2004) J Neurol Sci 227: 115-8
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