Reference

1. 1. Alberga A.,
   2. Boulay J. L.,
   3. Kempe E.,
   4. Dennefeld C.,
   5. Haenlin M.

   (1991) The snail gene required for mesoderm formation in Drosophila is expressed dynamically in derivatives of all three germ layers. Development 111, 983–992

   OpenUrlAbstract/FREE Full Text
2. 1. Amaya E.,
   2. Musci T. J.,
   3. Kirschner M. W.

   (1991) Expression of a dominant negative mutant of the FGF receptor disrupts mesoderm formation in Xenopus embryos. Cell 66, 257–270

   OpenUrlCrossRefPubMedWeb of Science
3. 1. Amaya E.,
   2. Stein P. A.,
   3. Musci T. J.,
   4. Kirschner M. W.

   (1993) FGF signalling in the early specification of mesoderm in Xenopus. Development 118, 477–487

   OpenUrlAbstract
4. 1. Barro O.,
   2. Joly C.,
   3. Condamine H.,
   4. Boulekbache H.

   (1994) Widespread expression of the Xenopus homeobox gene Xhox3 in zebrafish eggs causes a disruption of the anterior-posterior axis. Int. J. Dev. Biol 38, 613–622

   OpenUrlPubMed
5. 1. Beddington R. S. P.,
   2. Smith J. C.

   (1993) Control of vertebrate gastrulation: inducing signals and responding genes. Curr. Op. Genet. Dev 3, 655–661

   OpenUrlCrossRefPubMed
6. 1. Chesley P.

   (1935) Development of the short-tailed mutant in the house mouse. J. Exp. Zool 70, 429–435

   OpenUrlCrossRef
7. 1. Christian J. L.,
   2. Olson D. J.,
   3. Moon R. T.

   (1992) Xwnt-8 modifies the character of mesoderm induced by bFGF in isolated Xenopus ectoderm. EMBO J 11, 33–41

   OpenUrlPubMedWeb of Science
8. 1. Cornell R. A.,
   2. Kimelman D.

   (1994) Activin-mediated mesoderm induction requires FGF. Development 120, 453–462

   OpenUrlAbstract
9. 1. Cunliffe V.,
   2. Smith J. C.

   (1992) Ectopic mesoderm formation in Xenopus embryos caused by widespread expression of a brachyury homologue. Nature 358, 427–430

   OpenUrlCrossRefPubMed
10. 1. Driever W.,
    2. Stemple D.,
    3. Schier A.,
    4. Solnica-Krezel L.

    (1994) Zebrafish: genetic tools for studying development. Trends Genet 4, 152–159
11. 1. Halpern M. E.,
    2. Ho R. K.,
    3. Walker C.,
    4. Kimmel C. B.

    (1993) Induction of muscle pioneers and floor plate is distinguished by the zebrafish no tail mutation. Cell 75, 99–112

    OpenUrlCrossRefPubMedWeb of Science
12. 1. Hammerschmidt M.,
    2. Nusslein-Volhard C.

    (1994) The expression of a zebrafish gene homologous to Drosophila snail suggests a conserved function in invertebrate and vertebrate gastrulation. Development 119, 1107–1118

    OpenUrlAbstract
13. 1. Harding K.,
    2. Rushlow C.,
    3. Doyle H. J.,
    4. Hoey T.,
    5. Levine M.

    (1986) Cross regulatory interactions among pair rule genes in Drosophila. Science 233, 953–959

    OpenUrlAbstract/FREE Full Text
14. 1. Inoue A.,
    2. Takahashi M.,
    3. Hatta K.,
    4. Hotta Y.,
    5. Okamoto H.

    (1994) Developmental regulation of islet-1 mRNA expression during neuronal differentiation in embryonic zebrafish. Dev. Dynamics 199, 1–11

    OpenUrlPubMedWeb of Science
15. 1. Isaacs H. V.,
    2. Tannahill D.,
    3. Slack J. M. W.

    (1992) Expression of a novel FGF in the Xenopus embryo. A new candidate inducing factor for mesoderm formation and anteroposterior specification. Development 114, 711–720

    OpenUrlAbstract
16. 1. Isaacs H. V.,
    2. Pownall M. E.,
    3. Slack J. M. W.

    (1994) eFGF regulates Xbra expression during Xenopus gastrulation. EMBO J 13, 4469–4481

    OpenUrlPubMedWeb of Science
17. 1. Joly J. S.,
    2. Maury M.,
    3. Joly C.,
    4. Duprey P.,
    5. Boulekbache H.,
    6. Condamine H.

    (1992) Expression of the zebrafish caudal homeobox gene correlates with the establishment of posterior cell lineages at gastrulation. Diff 50, 75–87

    OpenUrlCrossRefPubMed
18. 1. Joly J. S.,
    2. Joly C.,
    3. Schulte-Merker S.,
    4. Boulekbache H.,
    5. Condamine H.

    (1993) The ventral and posterior expression of the zebrafish homeobox gene eve1 is perturbed in dorsalized and mutant embryos. Development 119, 1261–1275

    OpenUrlAbstract
19. 1. Keller R.,
    2. Danilchik M.

    (1988) Regional expression, pattern and timing of convergence and extension during gastrulation of Xenopus laevis. Development 103, 193–209

    OpenUrlAbstract
20. 1. Kimelman D.,
    2. Kirschner M.

    (1987) Synergistic induction of mesoderm by FGF and TGFb and the identification of an mRNA coding for FGF in the early Xenopus embryo. Cell 51, 869–877

    OpenUrlCrossRefPubMedWeb of Science
21. 1. Krauss S.,
    2. Johansen T.,
    3. Korzh V.,
    4. Fjose A.

    (1991) Expression patternof zebrafish pax genes suggest a role in early brain regionalisation. Nature 353, 267–270

    OpenUrlCrossRefPubMed
22. 1. Krauss S.,
    2. Concordet J.-P.,
    3. Ingham P. W.

    (1993) A functionally conserved homolog of the Drosophila segment polarity gene hh is expressed in tissues with polarizing activity in zebrafish embryos. Cell 75, 1431–1444

    OpenUrlCrossRefPubMedWeb of Science
23. 1. Krieg P.,
    2. Melton D.

    (1984) Functional messenger RNAs are produced by SP6 in vitro transcription of cloned cDNAs. Nucl. Acid Res 12, 7057–7070

    OpenUrlAbstract/FREE Full Text
24. 1. Mlodzik M.,
    2. Fjose A.,
    3. Gehring W. J.

    (1985) Isolation of caudal, a Drosophila homeobox-containing gene with maternal expression, whose transcripts form a concentration gradient at the preblastoderm stage. EMBO J 4, 2961–2969

    OpenUrlPubMedWeb of Science
25. 1. Mlodzik M.,
    2. Gibson G.,
    3. Gehring W. J.

    (1990) Effects of ectopic expression of caudal during Drosophila development. Development 109, 271–277

    OpenUrlAbstract
26. 1. Mullins M. C.,
    2. Hammerschmidt M.,
    3. Haffter P.,
    4. Nusslein-Volhard C.

    (1994) Large-scale mutagenesis in the zebrafish: in search of genes controlling development in a vertebrate. Curr. Biol 4, 189–202

    OpenUrlCrossRefPubMedWeb of Science
27. 1. Oxtoby E.,
    2. Jowett T.

    (1993) Cloning of the zebrafish krox-20 gene (krx-20) and its expression during hindbrain development. Nucl. Acids Res 21, 1087–1095

    OpenUrlAbstract/FREE Full Text
28. 1. Pavlath G. K.,
    2. Rich K.,
    3. Webster S. G.,
    4. Blau H. M.

    (1989) Localization of muscle gene products in nuclear domains. Nature 337, 570–573

    OpenUrlCrossRefPubMed
29. 1. Reichman-Fried M.,
    2. Dickson B.,
    3. Hafen E.,
    4. Shilo B. Z.

    (1994) Elucidation of the role of breathless, a Drosophila FGF receptor homolog, in tracheal cell migration. Genes Dev 8, 428–439

    OpenUrlAbstract/FREE Full Text
30. 1. Ruiz i Altaba A.,
    2. Melton D. A.

    (1989) Interaction between peptide growth factors and homeobox genes in the establishment of antero-posterior polarity in frog embryos. Nature 341, 33–38

    OpenUrlCrossRefPubMed
31. 1. Ruiz i Altaba A.,
    2. Melton D. A.

    (1989) Involvement of the Xenopus homeobox gene Xhox3 in pattern formation along the anterior-posterior axis. Cell 57, 317–326

    OpenUrlCrossRefPubMedWeb of Science
32. 1. Schulte-Merker S.,
    2. Ho R. K.,
    3. Nusslein-Volhard C.,
    4. Herrmann B. G.

    (1992) The protein product of the zebrafish homologue of the T gene isexpressed in nuclei of the germ ring and the notochord of the early embryo. Development 116, 1021–1032

    OpenUrlAbstract/FREE Full Text
33. 1. Schulte-Merker S.,
    2. van Eeden F.,
    3. Halpern M. E.,
    4. Kimmel C. B.,
    5. Nusslein-Volhard C.

    (1994) no tail (ntl) is the zebrafish homologue of the mouse T (brachyury) gene. Development 120, 1009–1015

    OpenUrlAbstract
34. 1. Schulte-Merker S.,
    2. Smith J. C.

    (1995) Mesoderm formation in response to Brachyury requires FGF signalling. Curr. Biol 5, 62–67

    OpenUrlCrossRefPubMedWeb of Science
35. 1. Schägger H.,
    2. Von Jagow G.

    (1987) Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa. Analyt. Biochem 166, 368–379

    OpenUrlCrossRefPubMedWeb of Science
36. 1. Shishido E.,
    2. Higashijima S. I.,
    3. Emori Y.,
    4. Saigo K.

    (1993) Tw FGF-receptor homologues of Drosophila: one is expressed in mesodermal primordium in early embryos. Development 117, 751–761

    OpenUrlAbstract
37. 1. Slack J. M. W.,
    2. Darlington B. G.,
    3. Heath J. K.,
    4. Godsave S. F.

    (1987) Mesoderm induction in early Xenopus embryos by heparin-binding growth factors. Nature 326, 197–200

    OpenUrlCrossRefPubMed
38. 1. Slack J. M. W.

    (1994) Inducing factors in Xenopus early embryos. Curr. Biol 4, 116–126

    OpenUrlCrossRefPubMedWeb of Science
39. 1. Smith J. C.,
    2. Price B. M. J.,
    3. Green J. B. A.,
    4. Weigel D.,
    5. Herrmann B. G.

    (1991) Expression of the Xenopus homologue of Brachyury (T) is an immediate-early response to mesoderm induction. Cell 67, 79–87

    OpenUrlCrossRefPubMedWeb of Science
40. 1. Stachel S. E.,
    2. Grunwald D. J.,
    3. Myers P. Z.

    (1993) Lithium perturbation and goosecoid expression identify a dorsal specification pathway in the pregastrula zebrafish. Development 117, 1261–1274

    OpenUrlAbstract
41. 1. Stott D.,
    2. Kispert A.,
    3. Herrmann B. G.

    (1993) Rescue of the tail defect of Brachyury mice. Genes Dev 7, 197–203

    OpenUrlAbstract/FREE Full Text
42. 1. Thisse C.,
    2. Thisse B.,
    3. Schilling T. F.,
    4. Postlethwait J. H.

    (1994) Structure of the zebrafish snail1 geneand its expression in wild-type, spadetail and no tail mutant embryos. Development 119, 1203–1215

    OpenUrlAbstract
43. 1. Xu Q.,
    2. Holder N. H.,
    3. Patient R.,
    4. Wilson S. W.

    (1994) Spatially regulated expression of three receptor tyrosine kinase genes during gastrulation in the zebrafish. Development 120, 287–299

    OpenUrlAbstract