1Kikuchi A.Roles of axin in the Wnt signaling pathway[].Cellular Signalling.1999
2Dale T C.Signal transduction by the Wnt family of ligands[].Biochemical Journal.1998
3Cadigan K M,Nusse R.Wnt signaling: a commom theme in animal development[].Genes and Development.1997
4Dann C E,Hsieh J,Rattner A,et al.Insights into Wnt binding and signaling from the structures of two frizzled cysteine-rich domains[].Nature.2001
5Tamai K,Semenov M,Kato Y,et al.LDL-receptor-related proteins in Wnt signal transduction[].Nature.2000
6Davidson G,Mao B,del Barco Barrantes I,et al.Kremen proteins interact with dickkopf 1 to regulate anteroposterior CNS patterning[].Development.2002
7Huelsken J,Birchmeier W.New aspects of Wnt signaling pathways in higher vertebrates[].Current Opinion in Genetics and Development.2001
8Seidensticker M J,Behrens J.Biochemical interactions in the Wnt pathway[].Biochimica et Biophysica Acta.2000
9Katoh M,Katoh M.Identification and characterization of human DAMM2 gene in silico[].International Journal of Oncology.2003
10Yamamoto H,Kishida S,Kishida M,et al.Phosphorylation of axin, a Wnt signal negative regulator, by glycogen synthase kinase-3beta regulates its stability[].Journal of Biological Chemistry.1999
5Flanigan KM, Coffeen CM, Sexton L, et al. Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy[J]. Neuromuscul Disord,2001,11:525-529.
6Tawil R, Van Der Maarel SM. Facioscapulohumeral muscular dystrophy[J]. Muscle Nerve,2006,34: 1- 15.
7Shields CL, Zahler J, Falk N, et al. Neovascular glaucoma from advanced Coats disease as the initial manifestation of facioscapulohumeral dystrophy in a 2-year-old child[J].Arch Ophthalmol,2007,125: 840-842.
8Coats G. Forms of retinal diseases with massive exudation[J].Roy Lond Ophthalmol Hosp Rep,1908,17:440-525.
9Adrian Bruce, Justin O' Day, Daniel McKay, et al. Coats' disease: Retinal telangiectasia[J].The Optician,2006,232:51-51.
10Black GC, Perveen R, Bonshek R, et al. Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogeuesis[J].Hum Mol Genet, 1999,8:2031-2035.