124
Xenopus
nuclear export of RBP-J. EMBO J. 30, 43–56. https://doi.
org/10.1038/emboj.2010.289
Wahi, K., Bochter, M.S., Cole, S.E., 2016. The many roles of Notch
signaling during vertebrate somitogenesis. Semin. Cell Dev.
Biol. 49, 68–75. https://doi.org/10.1016/j.semcdb.2014.11.010
Wang, J., Li, S., Chen, Y., Ding, X., 2007. Wnt/β-catenin signaling
controls Mespo expression to regulate segmentation during
Xenopus somitogenesis. Dev. Biol. 304, 836–847. https://doi.
org/10.1016/j.ydbio.2006.12.034
Wardle, F.C., Smith, J.C., 2004. Refnement of gene expression
patterns in the early Xenopus embryo. Development 131,
4687–4696. https://doi.org/10.1242/dev.01340
Watanabe, M., Yasuoka, Y., Mawaribuchi, S., Kuretani, A., Ito,
M., Kondo, M., Ochi, H., Ogino, H., Fukui, A., Taira, M.,
Kinoshita, T., 2017. Conservatism and variability of gene
expression profles among homeologous transcription factors in Xenopus laevis. Dev. Biol. 426, 301–324. https://doi.
org/10.1016/j.ydbio.2016.09.017
Wessely, O., Agius, E., Oelgeschläger, M., Pera, E.M., De Robertis,
E.M., 2001. Neural induction in the absence of mesoderm:
Beta-catenin-dependent expression of secreted BMP antagonists at the blastula stage in Xenopus. Dev. Biol. 234, 161–
173. https://doi.org/10.1006/dbio.2001.0258
Wettstein, D.A., Turner, D.L., Kintner, C., 1997. The Xenopus homolog of Drosophila suppressor of Hairless mediates Notch signaling during primary neurogenesis. Development 124, 693–702.
Wittenberger, T., Steinbach, O.C., Authaler, A., Kopan, R., Rupp,
R.A., 1999. MyoD stimulates delta-1 transcription and triggers notch signaling in the Xenopus gastrula. EMBO J. 18,
1915–1922. https://doi.org/10.1093/emboj/18.7.1915
Yamaguti, M., Cho, K.W.Y., Hashimoto, C., 2005. Xenopus hairy2b
specifes anterior prechordal mesoderm identity within
Spemann’s organizer. Dev. Dyn. 234, 102–113. https://doi.
org/10.1002/dvdy.20523
Yan, B., Moody, S.A., 2007. The competence of Xenopus blastomeres to produce neural and retinal progeny is repressed by
two endo-mesoderm promoting pathways. Dev. Biol. 305,
103–119. https://doi.org/10.1016/J.YDBIO.2007.01.040
Yan, B., Neilson, K.M., Moody, S.A., 2009. Notch signaling downstream of foxD5 promotes neural ectodermal transcription
factors that inhibit neural differentiation. Dev. Dyn. 238,
1358–1365. https://doi.org/10.1002/dvdy.21885
Zhou, M., Yan, J., Ma, Z., Zhou, Y., Abbood, N.N., Liu, J., Su, L.,
Jia, H., Guo, A.-Y., 2012. Comparative and evolutionary
analysis of the HES/HEY gene family reveal exon/intron loss
and teleost specifc duplication events. PLoS One 7, e40649.
https://doi.org/10.1371/journal.pone.0040649
Zimmerman, K., Shih, J., Bars, J., Collazo, A., Anderson, D.J.,
1993. XASH-3, a novel Xenopus achaete-scute homolog,
provides an early marker of planar neural induction and
position along the mediolateral axis of the neural plate.
Development 119, 221–232.
Xenopus
nuclear export of RBP-J. EMBO J. 30, 43–56. https://doi.
org/10.1038/emboj.2010.289
Wahi, K., Bochter, M.S., Cole, S.E., 2016. The many roles of Notch
signaling during vertebrate somitogenesis. Semin. Cell Dev.
Biol. 49, 68–75. https://doi.org/10.1016/j.semcdb.2014.11.010
Wang, J., Li, S., Chen, Y., Ding, X., 2007. Wnt/β-catenin signaling
controls Mespo expression to regulate segmentation during
Xenopus somitogenesis. Dev. Biol. 304, 836–847. https://doi.
org/10.1016/j.ydbio.2006.12.034
Wardle, F.C., Smith, J.C., 2004. Refnement of gene expression
patterns in the early Xenopus embryo. Development 131,
4687–4696. https://doi.org/10.1242/dev.01340
Watanabe, M., Yasuoka, Y., Mawaribuchi, S., Kuretani, A., Ito,
M., Kondo, M., Ochi, H., Ogino, H., Fukui, A., Taira, M.,
Kinoshita, T., 2017. Conservatism and variability of gene
expression profles among homeologous transcription factors in Xenopus laevis. Dev. Biol. 426, 301–324. https://doi.
org/10.1016/j.ydbio.2016.09.017
Wessely, O., Agius, E., Oelgeschläger, M., Pera, E.M., De Robertis,
E.M., 2001. Neural induction in the absence of mesoderm:
Beta-catenin-dependent expression of secreted BMP antagonists at the blastula stage in Xenopus. Dev. Biol. 234, 161–
173. https://doi.org/10.1006/dbio.2001.0258
Wettstein, D.A., Turner, D.L., Kintner, C., 1997. The Xenopus homolog of Drosophila suppressor of Hairless mediates Notch signaling during primary neurogenesis. Development 124, 693–702.
Wittenberger, T., Steinbach, O.C., Authaler, A., Kopan, R., Rupp,
R.A., 1999. MyoD stimulates delta-1 transcription and triggers notch signaling in the Xenopus gastrula. EMBO J. 18,
1915–1922. https://doi.org/10.1093/emboj/18.7.1915
Yamaguti, M., Cho, K.W.Y., Hashimoto, C., 2005. Xenopus hairy2b
specifes anterior prechordal mesoderm identity within
Spemann’s organizer. Dev. Dyn. 234, 102–113. https://doi.
org/10.1002/dvdy.20523
Yan, B., Moody, S.A., 2007. The competence of Xenopus blastomeres to produce neural and retinal progeny is repressed by
two endo-mesoderm promoting pathways. Dev. Biol. 305,
103–119. https://doi.org/10.1016/J.YDBIO.2007.01.040
Yan, B., Neilson, K.M., Moody, S.A., 2009. Notch signaling downstream of foxD5 promotes neural ectodermal transcription
factors that inhibit neural differentiation. Dev. Dyn. 238,
1358–1365. https://doi.org/10.1002/dvdy.21885
Zhou, M., Yan, J., Ma, Z., Zhou, Y., Abbood, N.N., Liu, J., Su, L.,
Jia, H., Guo, A.-Y., 2012. Comparative and evolutionary
analysis of the HES/HEY gene family reveal exon/intron loss
and teleost specifc duplication events. PLoS One 7, e40649.
https://doi.org/10.1371/journal.pone.0040649
Zimmerman, K., Shih, J., Bars, J., Collazo, A., Anderson, D.J.,
1993. XASH-3, a novel Xenopus achaete-scute homolog,
provides an early marker of planar neural induction and
position along the mediolateral axis of the neural plate.
Development 119, 221–232.