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  • Brand M, Heisenberg CP, Warga RM, Pelegri F, Karlstrom RO, Beuchle D, Picker A, Jiang YJ, Furutani-Seiki M, van Eeden FJ, Granato M, Haffter P, Hammerschmidt M, Kane DA, Kelsh RN, Mullins MC, Odenthal J, Nusslein-Volhard C. 1996. Mutations affecting development of the midline and general body shape during zebrafish embryogenesis. Development 123: 129142.
  • Chiotaki R, Petrou P, Giakoumaki E, Pavlakis E, Sitaru C, Chalepakis G. 2007. Spatiotemporal distribution of Fras1/Frem proteins during mouse embryonic development. Gene Expr Patterns 7: 381388.
  • Cleaver O, Krieg PA. 1998. VEGF mediates angioblast migration during development of the dorsal aorta in Xenopus. Development 125: 39053914.
  • Dane PJ, Tucker JB. 1985. Modulation of epidermal cell shaping and extracellular matrix during caudal fin morphogenesis in the zebra fish Brachydanio rerio. J Embryol Exp Morphol 87: 145161.
  • Eriksson J, Lofberg J. 2000. Development of the hypochord and dorsal aorta in the zebrafish embryo (Danio rerio). J Morphol 244: 167176.
  • Higashijima S, Nose A, Eguchi G, Hotta Y, Okamoto H. 1997. Mindin/F-spondin family: novel ECM proteins expressed in the zebrafish embryonic axis. Dev Biol 192: 211227.
  • Jadeja S, Smyth I, Pitera JE, Taylor MS, van Haelst M, Bentley E, McGregor L, Hopkins J, Chalepakis G, Philip N, Perez Aytes A, Watt FM, Darling SM, Jackson I, Woolf AS, Scambler PJ. 2005. Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs. Nat Genet 37: 520525.
  • Jowett T. 1999. Analysis of protein and gene expression. San Diego: Academic Press. p 6385.
  • Kimmel CB, Ballard WW, Kimmel SR, Ullmann B, Schilling TF. 1995. Stages of embryonic development of the zebrafish. Dev Dyn 203: 253310.
  • Kiyozumi D, Sugimoto N, Sekiguchi K. 2006. Breakdown of the reciprocal stabilization of QBRICK/Frem1, Fras1, and Frem2 at the basement membrane provokes Fraser syndrome-like defects. Proc Natl Acad Sci U S A 103: 1198111986.
  • Kiyozumi D, Sugimoto N, Nakano I, Sekiguchi K. 2007. Frem3, a member of the 12 CSPG repeats-containing extracellular matrix protein family, is a basement membrane protein with tissue distribution patterns distinct from those of Fras1, Frem2, and QBRICK/Frem1. Matrix Biol 26: 456462.
  • Kudon T, Tsang M, Hukriede NA, Chen X, Dedekian M, Clarke CJ, Kiang A, Schultz S, Epstein JA, Toyama R, Dawid IB. 2001. A gene expression screen in zebrafish embryogenesis. In: ZFIN direct data submission.
  • Latimer AJ, Dong X, Markov Y, Appel B. 2002. Delta-Notch signaling induces hypochord development in zebrafish. Development 129: 25552563.
  • McGregor L, Makela V, Darling SM, Vrontou S, Chalepakis G, Roberts C, Smart N, Rutland P, Prescott N, Hopkins J, Bentley E, Shaw A, Roberts E, Mueller R, Jadeja S, Philip N, Nelson J, Francannet C, Perez-Aytes A, Megarbane A, Kerr B, Wainwright B, Woolf AS, Winter RM, Scambler PJ. 2003. Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein. Nat Genet 34: 203208.
  • Petrou P, Chiotaki R, Dalezios Y, Chalepakis G. 2007a. Overlapping and divergent localization of Frem1 and Fras1 and its functional implications during mouse embryonic development. Exp Cell Res 313: 910920.
  • Petrou P, Pavlakis E, Dalezios Y, Chalepakis G. 2007b. Basement membrane localization of Frem3 is independent of the Fras1/Frem1/Frem2 protein complex within the sublamina densa. Matrix Biol 26: 652658.
  • Shafeghati Y, Kniepert A, Vakili G, Zenker M. 2008. Fraser syndrome due to homozygosity for a splice site mutation of FREM2. Am J Med Genet A 146: 529531.
  • Short K, Wiradjaja F, Smyth I. 2007. Let's stick together: the role of the Fras1 and Frem proteins in epidermal adhesion. IUBMB Life 59: 427435.
  • Slavotinek A, Li C, Sherr EH, Chudley AE. 2006. Mutation analysis of the FRAS1 gene demonstrates new mutations in a propositus with Fraser syndrome. Am J Med Genet A 140: 19091914.
  • Smyth I, Scambler P. 2005. The genetics of Fraser syndrome and the blebs mouse mutants. Hum Mol Genet 14 Spec No. 2: R269R274.
  • Smyth I, Du X, Taylor MS, Justice MJ, Beutler B, Jackson IJ. 2004. The extracellular matrix gene Frem1 is essential for the normal adhesion of the embryonic epidermis. Proc Natl Acad Sci U S A 101: 1356013565.
  • Staub E, Hinzmann B, Rosenthal A. 2002. A novel repeat in the melanoma-associated chondroitin sulfate proteoglycan defines a new protein family. FEBS Lett 527: 114118.
  • Takamiya K, Kostourou V, Adams S, Jadeja S, Chalepakis G, Scambler PJ, Huganir RL, Adams RH. 2004. A direct functional link between the multi-PDZ domain protein GRIP1 and the Fraser syndrome protein Fras1. Nat Genet 36: 172177.
  • Thisse B, Thisse C. 2004. Fast release clones: a high throughput expression analysis. In: ZFIN direct data submission.
  • Vrontou S, Petrou P, Meyer BI, Galanopoulos VK, Imai K, Yanagi M, Chowdhury K, Scambler PJ, Chalepakis G. 2003. Fras1 deficiency results in cryptophthalmos, renal agenesis and blebbed phenotype in mice. Nat Genet 34: 209214.
  • Winter RM. 1990. Fraser syndrome and mouse 'bleb' mutants. Clin Genet 37: 494495.
  • Yan YL, Hatta K, Riggleman B, Postlethwait JH. 1995. Expression of a type II collagen gene in the zebrafish embryonic axis. Dev Dyn 203: 363376.