• Dent JA, Polson AG, Klymkowsky MW. 1989. A whole-mount immunocytochemical analysis of the expression of the intermediate filament protein vimentin in Xenopus. Development 105: 6174.
  • Fitzsimons RB, Gurwin EB, Bird AC. 1987. Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy. A general association with genetic and therapeutic implications. Brain 110(pt 3): 631648.
  • Gabellini D, Green MR, Tupler R. 2002. Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle. Cell 110: 339348.
  • Gabellini D, D'Antona G, Moggio M, Prelle A, Zecca C, Adami R, Angeletti B, Ciscato P, Pellegrino MA, Bottinelli R, Green MR, Tupler R. 2006. Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1. Nature 439: 973977.
  • Grewal PK, Todd LC, van der Maarel S, Frants RR, Hewitt JE. 1998. FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates. Gene 216: 1319.
  • Hamilton L. 1969. The formation of somites in Xenopus. J Embryol Exp Morphol 22: 253264.
  • Harland RM. 1991. In situ hybridization: an improved whole-mount method for Xenopus embryos. Methods Cell Biol 36: 685695.
  • Hay ED. 2005. The mesenchymal cell, its role in the embryo, and the remarkable signaling mechanisms that create it. Dev Dyn 233: 706720.
  • Hopwood ND, Pluck A, Gurdon JB. 1991. Xenopus Myf-5 marks early muscle cells and can activate muscle genes ectopically in early embryos. Development 111: 551560.
  • Jiang G, Yang F, van Overveld PG, Vedanarayanan V, van der Maarel S, Ehrlich M. 2003. Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q. Hum Mol Genet 12: 29092921.
  • Kamath RS, Ahringer J. 2003. Genome-wide RNAi screening in Caenorhabditis elegans. Methods 30: 313321.
  • Lunt PW, Jardine PE, Koch MC, Maynard J, Osborn M, Williams M, Harper PS, Upadhyaya M. 1995. Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD). Hum Mol Genet 4: 951958.
  • Nieuwkoop PD, Faber J. 1994. Normal table of Xenopus laevis (Daudin): a systematical and chronological survey of the development from the fertilized egg till the end of metamorphosis. New York: Garland Pub. 252, 210 leaves of plates pp.
  • Ori M, Nardini M, Casini P, Perris R, Nardi I. 2006. XHas2 activity is required during somitogenesis and precursor cell migration in Xenopus development. Development 133: 631640.
  • Osborne RJ, Welle S, Venance SL, Thornton CA, Tawil R. 2007. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy. Neurology 68: 569577.
  • Padberg GW, Brouwer OF, de Keizer RJ, Dijkman G, Wijmenga C, Grote JJ, Frants RR. 1995a. On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophy. Muscle Nerve 2: S73S80.
  • Padberg GW, Frants RR, Brouwer OF, Wijmenga C, Bakker E, Sandkuijl LA. 1995b. Facioscapulohumeral muscular dystrophy in the Dutch population. Muscle Nerve 2: S81S84.
  • Scaal M, Christ B. 2004. Formation and differentiation of the avian dermomyotome. Anat Embryol (Berl) 208: 411424.
  • van Deutekom JC, Lemmers RJ, Grewal PK, van Geel M, Romberg S, Dauwerse HG, Wright TJ, Padberg GW, Hofker MH, Hewitt JE, Frants RR. 1996. Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35. Hum Mol Genet 5: 581590.
  • van Koningsbruggen S, Dirks RW, Mommaas AM, Onderwater JJ, Deidda G, Padberg GW, Frants RR, van der Maarel SM. 2004. FRG1P is localised in the nucleolus, Cajal bodies, and speckles. J Med Genet 41: e46.
  • van Koningsbruggen S, Straasheijm KR, Sterrenburg E, de Graaf N, Dauwerse HG, Frants RR, van der Maarel SM. 2007. FRG1P-mediated aggregation of proteins involved in pre-mRNA processing. Chromosoma 116: 5364.
  • Winokur ST, Chen YW, Masny PS, Martin JH, Ehmsen JT, Tapscott SJ, van der Maarel SM, Hayashi Y, Flanigan KM. 2003. Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation. Hum Mol Genet 12: 28952907.