Conserved Patterns of Cell Movements during Vertebrate Gastrulation

Rho GTPases in cell biology

Etienne‐Manneville, S., & Hall, A. (2002) · Nature · doi:10.1038/nature01148 · Cited by 4,796 · see citing works

The snail superfamily of zinc-finger transcription factors

Nieto, M. A. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm757 · Cited by 1,719 · see citing works

Embryonic Development and Induction

(1939) · Annals of the Entomological Society of America · doi:10.1093/aesa/32.3.657 · Cited by 1,148 · see citing works

Expression of a dominant negative mutant of the FGF receptor disrupts mesoderm formation in xenopus embryos

Amaya, E., Musci, T. J., & Kirschner, M. W. (1991) · Cell · doi:10.1016/0092-8674(91)90616-7 · Cited by 1,085 · see citing works

A major developmental transition in early xenopus embryos: II. control of the onset of transcription

Newport, J., & Kirschner, M. (1982) · Cell · doi:10.1016/0092-8674(82)90273-2 · Cited by 1,055 · see citing works

Silberblick/Wnt11 mediates convergent extension movements during zebrafish gastrulation

Heisenberg, C.-P., Tada, M., Rauch, G.-J., Saúde, L., Concha, M. L., Geisler, R., Stemple, D. L., Smith, J. C., & Wilson, S. W. (2000) · Nature · doi:10.1038/35011068 · Cited by 1,013 · see citing works

Zebrafish Prickle, a Modulator of Noncanonical Wnt/Fz Signaling, Regulates Gastrulation Movements

Veeman, M. T., Slusarski, D. C., Kaykas, A., Louie, S. H., & Moon, R. T. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00240-9 · Cited by 945 · see citing works

Clonal analysis of epiblast fate during germ layer formation in the mouse embryo

Lawson, K. A., Meneses, J. J., & Pedersen, R. A. (1991) · Development · doi:10.1242/dev.113.3.891 · Cited by 881 · see citing works

Wnt/Frizzled Activation of Rho Regulates Vertebrate Gastrulation and Requires a Novel Formin Homology Protein Daam1

Habas, R., Kato, Y., & He, X. (2001) · Cell · doi:10.1016/s0092-8674(01)00614-6 · Cited by 842 · see citing works

FORMATION AND FUNCTION OF SPEMANN'S ORGANIZER

Harland, R., & Gerhart, J. (1997) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.13.1.611 · Cited by 839 · see citing works

Molecular nature of Spemann's organizer: the role of the Xenopus homeobox gene goosecoid

Cho, K. W. Y., Blumberg, B., Steinbeißer, H., & Robertis, E. M. D. (1991) · Cell · doi:10.1016/0092-8674(91)90288-a · Cited by 807 · see citing works

fgfr-1 is required for embryonic growth and mesodermal patterning during mouse gastrulation.Preprint

Yamaguchi, T. P., Harpal, K., Henkemeyer, M. J., & Rossant, J. (1994) · Genes & Development · doi:10.1101/gad.8.24.3032 · Cited by 776 · see citing works

A primary requirement for nodal in the formation and maintenance of the primitive streak in the mouse

Conlon, F. L., Lyons, K. M., Takaesu, N. T., Barth, K. S., Kispert, A., Herrmann, B. G., & Robertson, E. J. (1994) · Development · doi:10.1242/dev.120.7.1919 · Cited by 772 · see citing works

Axis Development and Early Asymmetry in Mammals

Beddington, R. S. P., & Robertson, E. J. (1999) · Cell · doi:10.1016/s0092-8674(00)80560-7 · Cited by 758 · see citing works

Dishevelled controls cell polarity during Xenopus gastrulation

Wallingford, J. B., Rowning, B. A., Vogeli, K. M., Rothbächer, U., Fraser, S. E., & Harland, R. M. (2000) · Nature · doi:10.1038/35011077 · Cited by 751 · see citing works

The zebrafish midblastula transition

Kane, D. A., & Kimmel, C. B. (1993) · Development · doi:10.1242/dev.119.2.447 · Cited by 722 · see citing works

Shaping the Vertebrate Body Plan by Polarized Embryonic Cell Movements

Keller, R. E. (2002) · Science · doi:10.1126/science.1079478 · Cited by 716 · see citing works

The EGF-CFC Protein One-Eyed Pinhead Is Essential for Nodal Signaling

Gritsman, K., Zhang, J., Cheng, S. K., Heckscher, E. S., Talbot, W. S., & Schier, A. F. (1999) · Cell · doi:10.1016/s0092-8674(00)80720-5 · Cited by 713 · see citing works

Origin and organization of the zebrafish fate map

Kimmel, C. B., Warga, R. M., & Schilling, T. F. (1990) · Development · doi:10.1242/dev.108.4.581 · Cited by 698 · see citing works

FGF Signaling Regulates Mesoderm Cell Fate Specification and Morphogenetic Movement at the Primitive Streak

Ciruna, B. G., & Rossant, J. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00017-x · Cited by 695 · see citing works

Overexpression of cadherins and underexpression of β-catenin inhibit dorsal mesoderm induction in early Xenopus embryos

Heasman, J., Crawford, A., Goldstone, K., Garner-Hamrick, P., Gumbiner, B., McCrea, P., Kintner, C., Noro, C., & Wylie, C. (1994) · Cell · doi:10.1016/0092-8674(94)90069-8 · Cited by 693 · see citing works

Xwnt11is a target ofXenopusBrachyury: regulation of gastrulation movements via Dishevelled, but not through the canonical Wnt pathway

Tada, M., & Smith, J. C. (2000) · Development · doi:10.1242/dev.127.10.2227 · Cited by 675 · see citing works

Zebrafish organizer development and germ-layer formation require nodal-related signals

Feldman, B., Gates, M. A., Egan, E. S., Dougan, S. T., Rennebeck, G., Sirotkin, H. I., Schier, A. F., & Talbot, W. S. (1998) · Nature · doi:10.1038/26013 · Cited by 666 · see citing works

Targeted disruption of Fgf8 causes failure of cell migration in the gastrulating mouse embryoPreprint

Sun, X., Meyers, E. N., Lewandoski, M. B., & Martin, G. R. (1999) · Genes & Development · doi:10.1101/gad.13.14.1834 · Cited by 644 · see citing works

The Mouse Snail Gene Encodes a Key Regulator of the Epithelial-Mesenchymal Transition

Carver, E. A., Jiang, R., Lan, Y., Oram, K. F., & Gridley, T. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.23.8184-8188.2001 · Cited by 624 · see citing works

Nodal is a novel TGF-β-like gene expressed in the mouse node during gastrulation

Zhou, X., Sasaki, H., Lowe, L. A., Hogan, B. L. M., & Kuehn, M. R. (1993) · Nature · doi:10.1038/361543a0 · Cited by 615 · see citing works

Coactivation of Rac and Rho by Wnt/Frizzled signaling is required for vertebrate gastrulation

Habas, R., Dawid, I. B., & He, X. (2003) · Genes & Development · doi:10.1101/gad.1022203 · Cited by 603 · see citing works

Cell movements during epiboly and gastrulation in zebrafish

Warga, R. M., & Kimmel, C. B. (1990) · Development · doi:10.1242/dev.108.4.569 · Cited by 574 · see citing works

Drosophila Rho-Associated Kinase (Drok) Links Frizzled-Mediated Planar Cell Polarity Signaling to the Actin Cytoskeleton

Winter, C. G., Wang, B., Ballew, A. C., Royou, A., Karess, R. E., Axelrod, J. D., & Luo, L. (2001) · Cell · doi:10.1016/s0092-8674(01)00298-7 · Cited by 555 · see citing works

Anterior primitive endoderm may be responsible for patterning the anterior neural plate in the mouse embryo

Thomas, P. Q., & Beddington, R. S. P. (1996) · Current Biology · doi:10.1016/s0960-9822(96)00753-1 · Cited by 552 · see citing works

βCatenin Signaling Activity Dissected in the Early Xenopus Embryo: A Novel Antisense Approach

Heasman, J., Kofron, M. J., & Wylie, C. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9720 · Cited by 523 · see citing works

Mechanisms of convergence and extension by cell intercalation

Keller, R. E., Davidson, L. A., Edlund, A., Elul, T., Ezin, M., Shook, D. R., & Skoglund, P. (2000) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2000.0626 · Cited by 521 · see citing works

β-catenin translocation into nuclei demarcates the dorsalizing centers in frog and fish embryos

Schneider, S., Steinbeißer, H., Warga, R. M., & Hausen, P. (1996) · Mechanisms of Development · doi:10.1016/0925-4773(96)00546-1 · Cited by 515 · see citing works

Induction of muscle pioneers and floor plate is distinguished by the zebrafish no tail mutation

Halpern, M. E., Ho, R. K., Walker, C., & Kimmel, C. B. (1993) · Cell · doi:10.1016/s0092-8674(05)80087-x · Cited by 508 · see citing works

Fate map for the 32-cell stage ofXenopus laevis

Dale, L., & Slack, J. M. W. (1987) · Development · doi:10.1242/dev.99.4.527 · Cited by 507 · see citing works

Zebrafish trilobite identifies new roles for Strabismus in gastrulation and neuronal movements

Jessen, J. R., Topczewski, J., Bingham, S., Sepich, D. S., Marlow, F., Chandrasekhar, A., & Solnica-Krezel, L. (2002) · Nature Cell Biology · doi:10.1038/ncb828 · Cited by 504 · see citing works

How we are shaped: The biomechanics of gastrulation

Keller, R. E., Davidson, L. A., & Shook, D. R. (2003) · Differentiation · doi:10.1046/j.1432-0436.2003.710301.x · Cited by 495 · see citing works

A homeobox gene essential for zebrafish notochord development

Talbot, W. S., Trevarrow, B., Halpern, M. E., Melby, A. E., Farr, G., Postlethwait, J. H., Jowett, T., Kimmel, C. B., & Kimelman, D. (1995) · Nature · doi:10.1038/378150a0 · Cited by 465 · see citing works

The Zebrafish Glypican Knypek Controls Cell Polarity during Gastrulation Movements of Convergent Extension

Topczewski, J., Sepich, D. S., Myers, D. C., Walker, C., Amores, A., Lele, Z., Hammerschmidt, M., Postlethwait, J. H., & Solnica‐Krezel, L. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00005-3 · Cited by 454 · see citing works

Studies with a Xenopus BMP receptor suggest that ventral mesoderm-inducing signals override dorsal signals in vivo

Graff, J. M., Thies, R. S., Song, J. J., Celeste, A. J., & Melton, D. A. (1994) · Cell · doi:10.1016/0092-8674(94)90409-x · Cited by 451 · see citing works

The establishment of spemann's organizer and patterning of the vertebrate embryo

De Robertis, E. M., Larraín, J., Oelgeschläger, M., & Wessely, O. (2000) · Nature Reviews Genetics · doi:10.1038/35042039 · Cited by 429 · see citing works

Planar cell polarity signalling controls cell division orientation during zebrafish gastrulation

Gong, Y., Mo, C., & Fraser, S. E. (2004) · Nature · doi:10.1038/nature02796 · Cited by 420 · see citing works

Endodermal Nodal-related signals and mesoderm induction in Xenopus

Agius, E., Oelgeschläger, M., Wessely, O., Kemp, C. R., & Robertis, E. M. D. (2000) · Development · doi:10.1242/dev.127.6.1173 · Cited by 420 · see citing works

Gastrulation: from cells to embryo

(2005) · Choice Reviews Online · doi:10.5860/choice.42-4013 · Cited by 414 · see citing works

Nodal antagonists in the anterior visceral endoderm prevent the formation of multiple primitive streaks.

Perea-Gomez, A., Vella, F., Shawlot, W., Oulad-Abdelghani, M., Chazaud, C., Meno, C., Pfister, V., Chen, L., Robertson, E., Hamada, H., et al. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00321-0 · Cited by 410 · see citing works

Cell-autonomous action of zebrafish spt-1 mutation in specific mesodermal precursors

Ho, R. K., & Kane, D. A. (1990) · Nature · doi:10.1038/348728a0 · Cited by 395 · see citing works

The planar cell-polarity gene stbm regulates cell behaviour and cell fate in vertebrate embryos

Park, M., & Moon, R. T. (2002) · Nature Cell Biology · doi:10.1038/ncb716 · Cited by 381 · see citing works

Mouse Lefty2 and Zebrafish Antivin Are Feedback Inhibitors of Nodal Signaling during Vertebrate Gastrulation

Meno, C., Gritsman, K., Ohishi, S., Ohfuji, Y., Heckscher, E., Mochida, K., Shimono, A., Kondoh, H., Talbot, W. S., Robertson, E. J., et al. (1999) · Molecular Cell · doi:10.1016/s1097-2765(00)80331-7 · Cited by 374 · see citing works

Cell motility driving mediolateral intercalation in explants of Xenopus laevis

Shih, J., & Keller, R. E. (1992) · Development · doi:10.1242/dev.116.4.901 · Cited by 356 · see citing works

Origin and development of the zebrafish endoderm

Warga, R. M., & Nüsslein‐Volhard, C. (1999) · Development · doi:10.1242/dev.126.4.827 · Cited by 355 · see citing works

Zinc transporter LIVI controls epithelial-mesenchymal transition in zebrafish gastrula organizer

Yamashita, S., Miyagi, C., Fukada, T., Kagara, N., Che, Y., & Hirano, T. (2004) · Nature · doi:10.1038/nature02545 · Cited by 352 · see citing works

The zebrafish Nodal signal Squint functions as a morphogen

Chen, Y., & Schier, A. F. (2001) · Nature · doi:10.1038/35079121 · Cited by 342 · see citing works

Zebrafish Rho Kinase 2 Acts Downstream of Wnt11 to Mediate Cell Polarity and Effective Convergence and Extension Movements

Marlow, F., Topczewski, J., Sepich, D., & Solnica-Krezel, L. (2002) · Current Biology · doi:10.1016/s0960-9822(02)00864-3 · Cited by 337 · see citing works

Chimeric analysis of fibroblast growth factor receptor-1 (Fgfr1) function: a role for FGFR1 in morphogenetic movement through the primitive streak

Ciruna, B. G., Schwartz, L., Harpal, K., Yamaguchi, T. P., & Rossant, J. (1997) · Development · doi:10.1242/dev.124.14.2829 · Cited by 328 · see citing works

The role of Ppt/Wnt5 in regulating cell shape and movement during zebrafish gastrulation

Kilian, B., Mansukoski, H., Carreira-Barbosa, F., Ulrich, F., Tada, M., & Heisenberg, C. (2003) · Mechanisms of Development · doi:10.1016/s0925-4773(03)00004-2 · Cited by 327 · see citing works

Cell Movement Patterns during Gastrulation in the Chick Are Controlled by Positive and Negative Chemotaxis Mediated by FGF4 and FGF8

Yang, X., Dormann, D., Münsterberg, A., & Weijer, C. J. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00256-3 · Cited by 324 · see citing works

Mutations affecting cell fates and cellular rearrangements during gastrulation in zebrafish

Solnica‐Krezel, L., Stemple, D. L., Mountcastle-Shah, E., Rangini, Z., Neuhauss, S. C. F., Malicki, J. J., Schier, A. F., Stainier, D. Y. R., Zwartkruis, F. J. T., Abdelilah, S., et al. (1996) · Development · doi:10.1242/dev.123.1.67 · Cited by 321 · see citing works

Role of <i>frizzled 7</i> in the regulation of convergent extension movements during gastrulation in <i>Xenopus laevis</i>

Djiane, A., Riou, J.-F., Umbhauer, M., Boucaut, J.-C., & Shi, D.-L. (2000) · Development · doi:10.1242/dev.127.14.3091 · Cited by 316 · see citing works

Regionally specific induction by the Spemann–Mangold organizer

Niehrs, C. (2004) · Nature Reviews Genetics · doi:10.1038/nrg1347 · Cited by 294 · see citing works

Promotion and Attenuation of FGF Signaling Through the Ras-MAPK Pathway

Tsang, M., & Dawid, I. (2004) · Science's STKE · doi:10.1126/stke.2282004pe17 · Cited by 287 · see citing works

Mutations affecting morphogenesis during gastrulation and tail formation in the zebrafish, Danio rerio

Hammerschmidt, M., Pelegri, F. J., Mullins, M. C., Kane, D. A., Brand, M., van Eeden, F. J. M., Furutani‐Seiki, M., Granato, M., Haffter, P., Heisenberg, C., et al. (1996) · Development · doi:10.1242/dev.123.1.143 · Cited by 287 · see citing works

Fates and migratory routes of primitive streak cells in the chick embryo

Psychoyos, D., & Stern, C. D. (1996) · Development · doi:10.1242/dev.122.5.1523 · Cited by 281 · see citing works

Prickle 1 regulates cell movements during gastrulation and neuronal migration in zebrafish

Carreira-Barbosa, F., Concha, M. L., Takeuchi, M., Ueno, N., Wilson, S. W., & Tada, M. (2003) · Development · doi:10.1242/dev.00567 · Cited by 269 · see citing works

Frizzled-7 signalling controls tissue separation during Xenopus gastrulation

Winklbauer, R., Medina, A., Swain, R. K., & Steinbeisser, H. (2001) · Nature · doi:10.1038/35101621 · Cited by 263 · see citing works

Nodal signaling patterns the organizer

Gritsman, K., Talbot, W. S., & Schier, A. F. (2000) · Development · doi:10.1242/dev.127.5.921 · Cited by 261 · see citing works

A mutation that changes cell movement and cell fate in the zebrafish embryo

Kimmel, C. B., Kane, D. A., Walker, C., Warga, R. M., & Rothman, M. B. (1989) · Nature · doi:10.1038/337358a0 · Cited by 259 · see citing works

A transient array of parallel microtubules in frog eggs: Potential tracks for a cytoplasmic rotation that specifies the dorso-ventral axis

Elinson, R. P., & Rowning, B. A. (1988) · Developmental Biology · doi:10.1016/0012-1606(88)90281-3 · Cited by 250 · see citing works

Mesoderm movement and fate during avian gastrulation and neurulation

Schoenwolf, G. C., García‐Martínez, V., & Dias, M. S. (1992) · Developmental Dynamics · doi:10.1002/aja.1001930304 · Cited by 239 · see citing works

The planar polarity gene strabismus regulates convergent extension movements in Xenopus

Darken, R. S., Scola, A. M., Rakeman, A. S., Das, G., Mlodzik, M., & Wilson, P. A. (2002) · The EMBO Journal · doi:10.1093/emboj/21.5.976 · Cited by 239 · see citing works

Induction of the Xenopus organizer: expression and regulation of Xnot, a novel FGF and activin-regulated homeo box gene.Preprint

von Dassow, G., Schmidt, J. E., & Kimelman, D. (1993) · Genes & Development · doi:10.1101/gad.7.3.355 · Cited by 236 · see citing works

The cellular basis of epiboly: An SEM study of deep-cell rearrangement during gastrulation in Xenopus laevis

Keller, R. E. (1980) · Development · doi:10.1242/dev.60.1.201 · Cited by 232 · see citing works

The Planar Cell Polarity Gene Strabismus Regulates Convergence and Extension and Neural Fold Closure in Xenopus

Goto, T., & Keller, R. E. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0673 · Cited by 229 · see citing works

Analysis of FGF function in normal and no tail zebrafish embryos reveals separate mechanisms for formation of the trunk and the tail

Griffin, K. J. P., Patient, R. K., & Holder, N. (1995) · Development · doi:10.1242/dev.121.9.2983 · Cited by 223 · see citing works

The role of Paraxial Protocadherin in selective adhesion and cell movements of the mesoderm during Xenopus gastrulation

Kim, S., Yamamoto, A., Bouwmeester, T., Agius, E., & Robertis, E. M. D. (1998) · Development · doi:10.1242/dev.125.23.4681 · Cited by 220 · see citing works

The Xenopus homeobox gene Twin mediates Wnt induction of Goosecoid in establishment of Spemann’s organizer

Laurent, M. N., Blitz, I. L., Hashimoto, C., Rothbächer, U., & Cho, K. W. Y. (1997) · Development · doi:10.1242/dev.124.23.4905 · Cited by 219 · see citing works

Zebrafish paraxial protocadherin is a downstream target of spadetail involved in morphogenesis of gastrula mesoderm

Yamamoto, A., Amacher, S. L., Kim, S., Geissert, D., Kimmel, C. B., & Robertis, E. M. D. (1998) · Development · doi:10.1242/dev.125.17.3389 · Cited by 219 · see citing works

Shaping the zebrafish notochord

Glickman, N. S., Kimmel, C. B., Jones, M. A., & Adams, R. J. (2003) · Development · doi:10.1242/dev.00314 · Cited by 216 · see citing works

The T gene is necessary for normal mesodermal morphogenetic cell movements during gastrulation

Wilson, V. A., Manson, L., Skarnes, W. C., & Beddington, R. S. P. (1995) · Development · doi:10.1242/dev.121.3.877 · Cited by 216 · see citing works

Maternally controlled β-catenin-mediated signaling is required for organizer formation in the zebrafish

Kelly, C., Chin, A. J., Leatherman, J. L., Kozlowski, D. J., & Weinberg, E. S. (2000) · Development · doi:10.1242/dev.127.18.3899 · Cited by 215 · see citing works

Activin- and Nodal-related factors control antero–posterior patterning of the zebrafish embryo

Thisse, B., Wright, C. V. E., & Thisse, C. (2000) · Nature · doi:10.1038/35000200 · Cited by 211 · see citing works

Fgf signalling controls the dorsoventral patterning of the zebrafish embryo

Fürthauer, M., van Celst, J., Thisse, C., & Thisse, B. (2004) · Development · doi:10.1242/dev.01156 · Cited by 208 · see citing works

The molecular nature of the zebrafish tail organizer

Agathon, A., Thisse, C., & Thisse, B. (2003) · Nature · doi:10.1038/nature01822 · Cited by 206 · see citing works

Wnt8 is required in lateral mesendodermal precursors for neural posteriorization in vivo

Burns, C. E., Wilm, T. P., Basler, N., Wright, C. V. E., & Solnica‐Krezel, L. (2001) · Development · doi:10.1242/dev.128.18.3571 · Cited by 205 · see citing works

Churchill, a Zinc Finger Transcriptional Activator, Regulates the Transition between Gastrulation and Neurulation

Sheng, G., dos Reis, M., & Stern, C. D. (2003) · Cell · doi:10.1016/s0092-8674(03)00927-9 · Cited by 201 · see citing works

Mutations affecting development of the notochord in zebrafish

Stemple, D. L., Solnica‐Krezel, L., Zwartkruis, F. J. T., Neuhauss, S. C. F., Schier, A. F., Malicki, J. J., Stainier, D. Y. R., Abdelilah, S., Rangini, Z., Mountcastle-Shah, E., et al. (1996) · Development · doi:10.1242/dev.123.1.117 · Cited by 198 · see citing works

Bmp Activity Gradient Regulates Convergent Extension during Zebrafish Gastrulation

Myers, D. C., Sepich, D. S., & Solnica‐Krezel, L. (2002) · Developmental Biology · doi:10.1006/dbio.2001.0523 · Cited by 193 · see citing works

Mutations inhalf baked/E-cadherin block cell behaviors that are necessary for teleost epiboly

Kane, D. A., McFarland, K. N., & Warga, R. M. (2005) · Development · doi:10.1242/dev.01668 · Cited by 189 · see citing works

Shield formation at the onset of zebrafish gastrulation

Montero, J. A., Carvalho, L., Wilsch‐Bräuninger, M., Kilian, B., Mustafa, C. A., & Heisenberg, C. (2005) · Development · doi:10.1242/dev.01667 · Cited by 186 · see citing works

Dynamic microtubules and specification of the zebrafish embryonic axis

Jesuthasan, S. J., & Strähle, U. (1997) · Current Biology · doi:10.1016/s0960-9822(06)00025-x · Cited by 185 · see citing works

Regulation of cell polarity, radial intercalation and epiboly in Xenopus : novel roles for integrin and fibronectin

Marsden, M., & DeSimone, D. W. (2001) · Development · doi:10.1242/dev.128.18.3635 · Cited by 184 · see citing works

Role of glypican 4 in the regulation of convergent extension movements during gastrulation inXenopus laevis

Ohkawara, B., Yamamoto, T. S., Tada, M., & Ueno, N. (2003) · Development · doi:10.1242/dev.00435 · Cited by 182 · see citing works

Wnt5 is required for tail formation in the zebrafish embryo.Preprint

Rauch, G.-J., Hammerschmidt, M., Blader, P., Schauerte, H. E., Strähle, U., Ingham, P. W., McMahon, A., & Haffter, P. (1997) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1997.062.01.028 · Cited by 180 · see citing works

Stat3 Controls Cell Movements during Zebrafish Gastrulation

Yamashita, S., Miyagi, C., Carmany-Rampey, A., Shimizu, T., Fujii, R., Schier, A. F., & Hirano, T. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00126-0 · Cited by 178 · see citing works

Mesodermal development in mouse embryos mutant for fibronectin

Georges‐Labouesse, E., George, E. L., Rayburn, H., & Hynes, R. O. (1996) · Developmental Dynamics · doi:10.1002/(sici)1097-0177(199610)207:2 · Cited by 174 · see citing works

Planar polarity in the Drosophila eye: a multifaceted view of signaling specificity and cross‐talk

Mlodzik, M. (1999) · The EMBO Journal · doi:10.1093/emboj/18.24.6873 · Cited by 172 · see citing works

Lefty Proteins Are Long-Range Inhibitors of Squint-Mediated Nodal Signaling

Chen, Y., & Schier, A. F. (2002) · Current Biology · doi:10.1016/s0960-9822(02)01362-3 · Cited by 171 · see citing works

Convergence and extension in vertebrate gastrulae: cell movements according to or in search of identity?

Myers, D. C., Sepich, D. S., & Solnica‐Krezel, L. (2002) · Trends in Genetics · doi:10.1016/s0168-9525(02)02725-7 · Cited by 169 · see citing works

Slb/Wnt11 controls hypoblast cell migration and morphogenesis at the onset of zebrafish gastrulation

Ulrich, F., Concha, M. L., Heid, P. J., Voss, E. R., Witzel, S., Roehl, H. H., Tada, M., Wilson, S. W., Adams, R. J., Soll, D. R., et al. (2003) · Development · doi:10.1242/dev.00758 · Cited by 165 · see citing works

Antero-posterior tissue polarity links mesoderm convergent extension to axial patterning

Ninomiya, H., Elinson, R. P., & Winklbauer, R. (2004) · Nature · doi:10.1038/nature02620 · Cited by 164 · see citing works

Distinct functions of Rho and Rac are required for convergent extension during Xenopus gastrulation

Tahinci, E., & Symes, K. (2003) · Developmental Biology · doi:10.1016/s0012-1606(03)00206-9 · Cited by 162 · see citing works

The Hypoblast of the Chick Embryo Positions the Primitive Streak by Antagonizing Nodal Signaling

Bertocchini, F., & Stern, C. D. (2002) · Developmental Cell · doi:10.1016/s1534-5807(02)00318-0 · Cited by 158 · see citing works

E‐cadherin regulates cell movements and tissue formation in early zebrafish embryos

Babb, S. G., & Marrs, J. A. (2004) · Developmental Dynamics · doi:10.1002/dvdy.20057 · Cited by 157 · see citing works

Xenopus Sprouty2 inhibits FGF-mediated gastrulation movements but does not affect mesoderm induction and patterningPreprint

Nutt, S. L., Dingwell, K. S., Holt, C. E., & Amaya, E. (2001) · Genes & Development · doi:10.1101/gad.191301 · Cited by 152 · see citing works

Cinephotomicrographic investigations of gastrulation in the chick blastoderm.

Vakaet, L. C. (1970) · PubMed · Cited by 151 · see citing works

A novel retrovirally induced embryonic lethal mutation in the mouse: assessment of the developmental fate of embryonic stem cells homozygous for the 413.d proviral integration

Conlon, F. L., Barth, K. S., & Robertson, E. J. (1991) · Development · doi:10.1242/dev.111.4.969 · Cited by 148 · see citing works

From cleavage to primitive streak formation: A complementary normal table and a new look at the first stages of the development of the chick

Kochav, S., Ginsburg, M., & Eyal‐Giladi, H. (1980) · Developmental Biology · doi:10.1016/0012-1606(80)90117-7 · Cited by 146 · see citing works

Mesendoderm Extension and Mantle Closure in Xenopus laevis Gastrulation: Combined Roles for Integrin α5β1, Fibronectin, and Tissue Geometry

Davidson, L. A., Hoffstrom, B. G., Keller, R. E., & DeSimone, D. W. (2002) · Developmental Biology · doi:10.1006/dbio.2002.0537 · Cited by 138 · see citing works

Has2 is required upstream of Rac1 to govern dorsal migration of lateral cells during zebrafish gastrulation

Bakkers, J., Kramer, C., Pothof, J., Quaedvlieg, N. E. M., Spaink, H. P., & Hammerschmidt, M. (2004) · Development · doi:10.1242/dev.00954 · Cited by 137 · see citing works

Directional mesoderm cell migration in the Xenopus gastrula

Winklbauer, R., & Nagel, M. (1991) · Developmental Biology · doi:10.1016/0012-1606(91)90275-8 · Cited by 137 · see citing works

Wnt4 affects morphogenesis when misexpressed in the zebrafish embryo

Ungar, A. R., Kelly, G. M., & Moon, R. T. (1995) · Mechanisms of Development · doi:10.1016/0925-4773(95)00386-f · Cited by 136 · see citing works

Phosphoinositide 3-Kinase Is Required for Process Outgrowth and Cell Polarization of Gastrulating Mesendodermal Cells

Montero, J. A., Kilian, B., Chan, J. C.-Y., Bayliss, P. E., & Heisenberg, C. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00505-0 · Cited by 125 · see citing works

Lefty-Dependent Inhibition of Nodal- and Wnt-Responsive Organizer Gene Expression Is Essential for Normal Gastrulation

Branford, W. W., & Yost, H. J. (2002) · Current Biology · doi:10.1016/s0960-9822(02)01360-x · Cited by 122 · see citing works

Cellular Mechanism Underlying Neural Convergent Extension inXenopus laevisEmbryos

Elul, T., Koehl, M. A. R., & Keller, R. E. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8711 · Cited by 115 · see citing works

Gene expression and chromatin structure in the pre-implantation embryo

Kaňka, J. (2002) · Theriogenology · doi:10.1016/s0093-691x(02)01267-0 · Cited by 113 · see citing works

Fibronectin, Mesoderm Migration, and Gastrulation in Xenopus

Winklbauer, R., & Keller, R. E. (1996) · Developmental Biology · doi:10.1006/dbio.1996.0174 · Cited by 112 · see citing works

Nodal-related signals establish mesendodermal fate and trunk neural identity in zebrafish

Feldman, B., Dougan, S. T., Schier, A. F., & Talbot, W. S. (2000) · Current Biology · doi:10.1016/s0960-9822(00)00469-3 · Cited by 112 · see citing works

Monopolar Protrusive Activity: A New Morphogenic Cell Behavior in the Neural Plate Dependent on Vertical Interactions with the Mesoderm in Xenopus

Elul, T., & Keller, R. E. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9746 · Cited by 109 · see citing works

Cell autonomous commitment to an endodermal fate and behaviour by activation of Nodal signalling

David, N. B., & Rosa, F. (2001) · Development · doi:10.1242/dev.128.20.3937 · Cited by 107 · see citing works

Insertional mutation of a gene involved in growth regulation of the early mouse embryo

Iannaccone, P. M., Zhou, X., Khokha, M. K., Boucher, D., & Kuehn, M. R. (1992) · Developmental Dynamics · doi:10.1002/aja.1001940305 · Cited by 105 · see citing works

Expression of cell adhesion molecule E-cadherin in Xenopus embryos begins at gastrulation and predominates in the ectoderm.

Choi, Y. S., & Gumbiner, B. (1989) · The Journal of Cell Biology · doi:10.1083/jcb.108.6.2449 · Cited by 104 · see citing works

Gastrulation : movements, patterns, and molecules

Keller, R. E., Clark, W. H., & Griffin, F. J. (1991) · Plenum Press eBooks · Cited by 96 · see citing works

Lefty Antagonism of Squint Is Essential for Normal Gastrulation

Feldman, B., Concha, M. L., Saúde, L., Parsons, M. J., Adams, R. J., Wilson, S. W., & Stemple, D. L. (2002) · Current Biology · doi:10.1016/s0960-9822(02)01361-1 · Cited by 94 · see citing works

Overexpression of a Slit Homologue Impairs Convergent Extension of the Mesoderm and Causes Cyclopia in Embryonic Zebrafish

Yeo, S.-Y., Little, M. H., Yamada, T., Miyashita, T., Halloran, M. C., Kuwada, J. Y., Huh, T., & Okamoto, H. (2001) · Developmental Biology · doi:10.1006/dbio.2000.0105 · Cited by 91 · see citing works

A homeobox gene involved in node, notochord and neural plate formation of chick embryos

Stein, S., & Kessel, M. (1995) · Mechanisms of Development · doi:10.1016/0925-4773(94)00300-c · Cited by 84 · see citing works

Morphogenetic domains in the yolk syncytial layer of axiating zebrafish embryos

D’Amico, L., & Cooper, M. S. (2001) · Developmental Dynamics · doi:10.1002/dvdy.1216 · Cited by 81 · see citing works

Calretinin neurons in human medial prefrontal cortex (areas 24a,b,c, 32?, and 25)

Gabbott, P. L. A., Jays, P. R. L., & Bacon, S. J. (1997) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19970519)381:4 · Cited by 81 · see citing works

Single-cell internalization during zebrafish gastrulation

Carmany-Rampey, A., & Schier, A. F. (2001) · Current Biology · doi:10.1016/s0960-9822(01)00353-0 · Cited by 80 · see citing works

Different clonal dispersion in the rostral and caudal mouse central nervous system

Mathis, L., & Nicolas, J. F. (2000) · Development · doi:10.1242/dev.127.6.1277 · Cited by 80 · see citing works

Dorsoventral Patterning in the Zebrafish: Bone Morphogenetic Proteins and Beyond

Hammerschmidt, M., & Mullins, M. C. (2002) · Results and problems in cell differentiation · doi:10.1007/978-3-540-46041-1_5 · Cited by 79 · see citing works

On the convergent cell movements of gastrulation in Fundulus

Trinkaus, J. P., Trinkaus, M., & Fink, R. D. (1992) · Journal of Experimental Zoology · doi:10.1002/jez.1402610107 · Cited by 79 · see citing works

Epiblast and primitive-streak origins of the endoderm in the gastrulating chick embryo

Lawson, A., & Schoenwolf, G. C. (2003) · Development · doi:10.1242/dev.00579 · Cited by 77 · see citing works

The evolution of vertebrate gastrulation

Robertis, E. M. D., Fainsod, A., Gont, L. K., & Steinbeißer, H. (1994) · Development · doi:10.1242/dev.1994.supplement.117 · Cited by 76 · see citing works

Rethinking axial patterning in amphibians

Lane, M. C., & Sheets, M. D. (2002) · Developmental Dynamics · doi:10.1002/dvdy.10182 · Cited by 63 · see citing works

The Netrin receptor Neogenin is required for neural tube formation and somitogenesis in zebrafish

Mawdsley, D. J., Cooper, H. M., Hogan, B. M., Cody, S. H., Lieschke, G. J., & Heath, J. K. (2004) · Developmental Biology · doi:10.1016/j.ydbio.2004.02.001 · Cited by 61 · see citing works

Cell populations and morphogenetic movements underlying formation of the avian primitive streak and organizer

Lawson, A., & Schoenwolf, G. C. (2001) · genesis · doi:10.1002/gene.1023 · Cited by 60 · see citing works

Cell movements during gastrulation: Snail dependent and independent pathways

Ip, Y. T., & Gridley, T. (2002) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(02)00320-9 · Cited by 57 · see citing works

The role of the homeodomain protein Bozozok in zebrafish axis formation

Solnica‐Krezel, L., & Driever, W. (2001) · The International Journal of Developmental Biology · doi:10.1387/ijdb.11291860 · Cited by 54 · see citing works

Motile behavior and protrusive activity of migratory mesoderm cells from the Xenopus gastrula

Winklbauer, R., & Selchow, A. (1992) · Developmental Biology · doi:10.1016/0012-1606(92)90246-d · Cited by 52 · see citing works

Embryonic mesoderm cells spread in response to platelet-derived growth factor and signaling by phosphatidylinositol 3-kinase.

Symes, K., & Mercola, M. A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.18.9641 · Cited by 52 · see citing works

Cell mixing during early epiboly in the zebrafish embryo

Wilson, E. T., Cretekos, C. J., & Helde, K. A. (1995) · Developmental Genetics · doi:10.1002/dvg.1020170103 · Cited by 49 · see citing works

Zebrafish E‐cadherin: Expression during early embryogenesis and regulation during brain development

Clendenon, S. G., Barnett, J., Doedens, A. L., Cobb, N., Liu, Q., Sorkin, B. C., Yelick, P. C., Raymond, P. A., & Marrs, J. A. (2001) · Developmental Dynamics · doi:10.1002/dvdy.1132 · Cited by 48 · see citing works

A flattened mouse embryo: Leveling the playing field

Behringer, R. R., Wakamiya, M., Tsang, T. E., & Tam, P. (2000) · genesis · doi:10.1002/1526-968x(200009)28:1 · Cited by 44 · see citing works

Developmentally Restricted Actin-Regulatory Molecules Control Morphogenetic Cell Movements in the Zebrafish Gastrula

Daggett, D. F., Boyd, C. A., Gautier, P. E., Bryson‐Richardson, R. J., Thisse, C., Thisse, B., Amacher, S. L., & Currie, P. D. (2004) · Current Biology · doi:10.1016/j.cub.2004.08.024 · Cited by 43 · see citing works

Life at the Edge: Epiboly and Involution in the Zebrafish

Kane, D. O., & Adams, R. J. (2002) · Results and problems in cell differentiation · doi:10.1007/978-3-540-46041-1_7 · Cited by 42 · see citing works

Ingression during Early Gastrulation of Fundulus

Trinkaus, J. P. (1996) · Developmental Biology · doi:10.1006/dbio.1996.0169 · Cited by 40 · see citing works

Dorso-ventral polarity of the zebrafish embryo is distinguishable prior to the onset of gastrulation

Schmitz, B., & Campos-Ortega, J. A. (1994) · Development Genes and Evolution · doi:10.1007/bf00188685 · Cited by 40 · see citing works

Mapping vertebrate embryos

Tam, P., & Quinlan, G. A. (1996) · Current Biology · doi:10.1016/s0960-9822(02)00432-3 · Cited by 39 · see citing works

Genetic locus half baked is necessary for morphogenesis of the ectoderm

McFarland, K. N., Warga, R. M., & Kane, D. A. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20325 · Cited by 37 · see citing works

Embryonic mouse submandibular salivary gland morphogenesis and the TNF/TNF-R1 signal transduction pathway

Melnick, M., Chen, H., Zhou, Y., & Jaskoll, T. F. (2001) · The Anatomical Record · doi:10.1002/1097-0185(20010301)262:3 · Cited by 35 · see citing works

Changing the axis changes the perspective

Gerhart, J. C. (2002) · Developmental Dynamics · doi:10.1002/dvdy.10198 · Cited by 24 · see citing works

Gastrulation in Xenopus laevis: involution—a current view

Shih, J., & Keller, R. E. (1994) · Seminars in Developmental Biology · doi:10.1006/sedb.1994.1012 · Cited by 21 · see citing works

In vivo Analysis of Convergent Cell Movements in The Germ Ring of Fundulus

Trinkaus, J. P., Trinkaus, M., & Fink, R. D. (1991) · Springer eBooks · doi:10.1007/978-1-4684-6027-8_7 · Cited by 8 · see citing works

Hormonal and photoperiodic modulation of testicular mRNAs coding for inhibin/activin subunits and follistatin inClethrionomys glareolus, Schreber

Tähkä, K. M., Kaipia, A. J., Toppari, J., Tähkä, S., Tuuri, T., & Tuohimaa, P. (1998) · Journal of Experimental Zoology · doi:10.1002/(sici)1097-010x(19980701)281:4 · Cited by 7 · see citing works

Genetic analysis of the exed region in mouse

Kendall, S. K., Strong, S. J., Litman, R. T., Litman, G. W., & Magnuson, T. (2000) · genesis · doi:10.1002/1526-968x(200008)27:4

Reconstruction of Zebrafish Early Embryonic Development by Scanned Light Sheet Microscopy

Keller, P., Schmidt, A. D., Wittbrodt, J., & Stelzer, E. H. K. (2008) · Science · doi:10.1126/science.1162493 · Cited by 1,569 · see citing works

Wnt signal transduction pathways

Komiya, Y., & Habas, R. (2008) · Organogenesis · doi:10.4161/org.4.2.5851 · Cited by 1,528 · see citing works

Forces in Tissue Morphogenesis and Patterning

Heisenberg, C., & Bellaı̈che, Y. (2013) · Cell · doi:10.1016/j.cell.2013.05.008 · Cited by 1,222 · see citing works

Epithelial-Mesenchymal Transition in Cancer: Parallels Between Normal Development and Tumor Progression

Micalizzi, D. S., Farabaugh, S. M., & Ford, H. L. (2010) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-010-9178-9 · Cited by 979 · see citing works

Multicellular Rosette Formation Links Planar Cell Polarity to Tissue Morphogenesis

Blankenship, J. T., Backovic, S. T., Sanny, J., Weitz, O., & Zallen, J. A. (2006) · Developmental Cell · doi:10.1016/j.devcel.2006.09.007 · Cited by 693 · see citing works

Collective Cell Migration

Rørth, P. (2009) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.042308.113231 · Cited by 600 · see citing works

The developmental biology of Dishevelled: an enigmatic protein governing cell fate and cell polarity

Wallingford, J. B., & Habas, R. (2005) · Development · doi:10.1242/dev.02068 · Cited by 509 · see citing works

Molecular Genetics of Axis Formation in Zebrafish

Schier, A. F., & Talbot, W. S. (2005) · Annual Review of Genetics · doi:10.1146/annurev.genet.37.110801.143752 · Cited by 489 · see citing works

Tissue Organization by Cadherin Adhesion Molecules: Dynamic Molecular and Cellular Mechanisms of Morphogenetic Regulation

Niessen, C. M., Leckband, D., & Yap, A. S. (2011) · Physiological Reviews · doi:10.1152/physrev.00004.2010 · Cited by 427 · see citing works

Gastrulation: Making and Shaping Germ Layers

Solnica‐Krezel, L., & Sepich, D. S. (2011) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-092910-154043 · Cited by 366 · see citing works

Tissue Deformation Modulates Twist Expression to Determine Anterior Midgut Differentiation in Drosophila Embryos

Desprat, N., Supatto, W., Pouille, P., Beaurepaire, E., & Farge, E. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.07.009 · Cited by 331 · see citing works

Comparative transcriptome analysis reveals vertebrate phylotypic period during organogenesis

Irie, N., & Kuratani, S. (2011) · Nature Communications · doi:10.1038/ncomms1248 · Cited by 325 · see citing works

Collective cell migration in development

Weijer, C. J. (2009) · Journal of Cell Science · doi:10.1242/jcs.036517 · Cited by 323 · see citing works

Epithelial–mesenchymal transition in lung development and disease: does it exist and is it important?

Bartis, D., Miše, N., Mahida, R. Y., Eickelberg, O., & THICKETT, D. R. (2013) · Thorax · doi:10.1136/thoraxjnl-2013-204608 · Cited by 305 · see citing works

Cell migration during morphogenesis

Aman, A. J., & Piotrowski, T. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.11.014 · Cited by 292 · see citing works

Cell shape changes indicate a role for extrinsic tensile forces in Drosophila germ-band extension

Butler, L., Blanchard, G. B., Kabla, A., Lawrence, N. J., Welchman, D. P., Mahadevan, L., Adams, R. J., & Sanson, B. (2009) · Nature Cell Biology · doi:10.1038/ncb1894 · Cited by 276 · see citing works

Rho-Kinase Directs Bazooka/Par-3 Planar Polarity during Drosophila Axis Elongation

Simões, S. D. M., Blankenship, J. T., Weitz, O., Farrell, D. L., Tamada, M., Fernández‐González, R., & Zallen, J. A. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.08.011 · Cited by 274 · see citing works

PKB/Akt-Dependent Regulation of Cell Motility

Xue, G., & Hemmings, B. A. (2013) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djs648 · Cited by 262 · see citing works

The amniote primitive streak is defined by epithelial cell intercalation before gastrulation

Voiculescu, O., Bertocchini, F., Wolpert, L., Keller, R. E., & Stern, C. D. (2007) · Nature · doi:10.1038/nature06211 · Cited by 262 · see citing works

Nodal MorphogensPreprint

Schier, A. F. (2009) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a003459 · Cited by 251 · see citing works

Epithelial-to-mesenchymal transition: What is the impact on breast cancer stem cells and drug resistance

Mallini, P., Lennard, T. W. J., Kirby, J. A., & Meeson, A. P. (2013) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2013.09.008 · Cited by 240 · see citing works

Models of Biological Pattern Formation: From Elementary Steps to the Organization of Embryonic Axes

Meinhardt, H. (2007) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(07)81001-5 · Cited by 214 · see citing works

Mechanisms of endothelial cell migration

Michaelis, U. R. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1678-0 · Cited by 191 · see citing works

Apelin and Its Receptor Control Heart Field Formation during Zebrafish Gastrulation

Zeng, X.-X. I., Wilm, T. P., Sepich, D. S., & Solnica‐Krezel, L. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.01.011 · Cited by 190 · see citing works

Epithelial to mesenchymal transition during gastrulation: An embryological view

Nakaya, Y., & Sheng, G. (2008) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.2008.01070.x · Cited by 188 · see citing works

Integrin α5β1 and Fibronectin Regulate Polarized Cell Protrusions Required for Xenopus Convergence and Extension

Davidson, L. A., Marsden, M., Keller, R. E., & DeSimone, D. W. (2006) · Current Biology · doi:10.1016/j.cub.2006.03.038 · Cited by 187 · see citing works

Sdf1/Cxcr4 signaling controls the dorsal migration of endodermal cells during zebrafish gastrulation

Mizoguchi, T., Verkade, H. M., Heath, J. K., Kuroiwa, A., & Kikuchi, Y. (2008) · Development · doi:10.1242/dev.020107 · Cited by 185 · see citing works

Evolution of the Wnt Pathways

Croce, J. C., & McClay, D. R. (2008) · Methods in molecular biology · doi:10.1007/978-1-60327-469-2_1 · Cited by 179 · see citing works

Calcium signaling in vertebrate embryonic patterning and morphogenesis

Slusarski, D. C., & Pelegri, F. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.04.043 · Cited by 178 · see citing works

Epithelial–Mesenchymal Transitions

Savagner, P. (2015) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2014.11.021 · Cited by 174 · see citing works

Developmental toxicity screening in zebrafish

McCollum, C. W., Ducharme, N. A., Bondesson, M., & Gustafsson, J.-Α. (2011) · Birth Defects Research Part C Embryo Today Reviews · doi:10.1002/bdrc.20210 · Cited by 161 · see citing works

In vivo cell biology: following the zebrafish trend

Beis, D., & Stainier, D. Y. R. (2006) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.12.001 · Cited by 160 · see citing works

A stepwise model of Reaction-Diffusion and Positional-Information governs self-organized human peri-gastrulation-like patterning

Tewary, M., Östblom, J., Prochazka, L., Zulueta-Coarasa, T., Shakiba, N., Fernández‐González, R., & Zandstra, P. W. (2017) · Development · doi:10.1242/dev.149658 · Cited by 152 · see citing works

Wnt5a is essential for intestinal elongation in mice

Cervantes, S., Yamaguchi, T. P., & Hebrok, M. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.11.020 · Cited by 155 · see citing works

Quantitative differences in tissue surface tension influence zebrafish germ layer positioning

Schötz, E., Burdine, R. D., Jülicher, F., Steinberg, M. S., Heisenberg, C., & Foty, R. A. (2008) · HFSP journal · doi:10.2976/1.2834817 · Cited by 155 · see citing works

Head-tail patterning of the vertebrate embryo: one, two or many unresolved problems?

Stern, C. D., Charité, J., Deschamps, J., Duboule, D., Durston, A. J., Kmita, M., Nicolas, J.-F., Palmeirim, I., Smith, J. C., & Wolpert, L. (2005) · The International Journal of Developmental Biology · doi:10.1387/ijdb.052095cs · Cited by 150 · see citing works

The yolk syncytial layer in early zebrafish development

Carvalho, L., & Heisenberg, C. (2010) · Trends in Cell Biology · doi:10.1016/j.tcb.2010.06.009 · Cited by 143 · see citing works

Epithelial–Mesenchymal Transition in Development and Cancer

Micalizzi, D. S., & Ford, H. L. (2009) · Future Oncology · doi:10.2217/fon.09.94 · Cited by 144 · see citing works

Syndecan-4 regulates non-canonical Wnt signalling and is essential for convergent and extension movements in Xenopus embryos

Muñoz, R., Moreno, M., Oliva, C., Orbenes, C., & Larraı́n, J. (2006) · Nature Cell Biology · doi:10.1038/ncb1399 · Cited by 144 · see citing works

Fetal alcohol exposure impairs hedgehog cholesterol modification and signaling

Li, Y., Yang, H., Zdanowicz, M., Sicklick, J. K., Qi, Y. P., Camp, T., & Diehl, A. M. (2007) · Laboratory Investigation · doi:10.1038/labinvest.3700516 · Cited by 141 · see citing works

Chemokine Signaling Controls Endodermal Migration During Zebrafish Gastrulation

Nair, S., & Schilling, T. F. (2008) · Science · doi:10.1126/science.1160038 · Cited by 127 · see citing works

Chemokine signaling in embryonic cell migration: a fisheye view

Raz, E., & Mahabaleshwar, H. (2009) · Development · doi:10.1242/dev.022418 · Cited by 125 · see citing works

Gastrulation in zebrafish — all just about adhesion?

Solnica‐Krezel, L. (2006) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2006.06.009 · Cited by 124 · see citing works

Mechanical regulation of early vertebrate embryogenesis

Valet, M., Siggia, E. D., & Brivanlou, A. H. (2021) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-021-00424-z · Cited by 120 · see citing works

From Zygote to Implantation: Morphological and Molecular Dynamics during Embryo Development in the Pig

Oestrup, O., Hall, V. J., Petkov, S. G., Wolf, X., Hyldig, S. M. W., & Hyttel, P. (2009) · Reproduction in Domestic Animals · doi:10.1111/j.1439-0531.2009.01482.x · Cited by 123 · see citing works

Rap1, a mercenary among the Ras-like GTPases

Frische, E. W., & Zwartkruis, F. J. T. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2009.12.043 · Cited by 113 · see citing works

Geometric control of tissue morphogenesis

Nelson, C. M. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2008.12.014 · Cited by 112 · see citing works

Developmental Constraints on Vertebrate Genome Evolution

Roux, J., & Robinson‐Rechavi, M. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000311 · Cited by 111 · see citing works

Mouse prickle1 , the homolog of a PCP gene, is essential for epiblast apical-basal polarity

Tao, H., Suzuki, M., Kiyonari, H., Abe, T., Sasaoka, T., & Ueno, N. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0901332106 · Cited by 108 · see citing works

Zebrafish Gastrulation: Cell Movements, Signals, and Mechanisms

Rohde, L. A., & Heisenberg, C. (2007) · International review of cytology · doi:10.1016/s0074-7696(07)61004-3 · Cited by 107 · see citing works

Apical and Basal Matrix Remodeling Control Epithelial Morphogenesis

Díaz-de-la-Loza, M.-D.-C., Ray, R. P., Ganguly, P. S., Alt, S., Davis, J. R., Hoppe, A., Tapon, N., Salbreux, G., & Thompson, B. J. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.06.006 · Cited by 102 · see citing works

Zebrafish epiboly: Spreading thin over the yolk

Bruce, A. E. E. (2015) · Developmental Dynamics · doi:10.1002/dvdy.24353 · Cited by 101 · see citing works

Ribosomal Proteins Rpl22 and Rpl22l1 Control Morphogenesis by Regulating Pre-mRNA Splicing

Zhang, Y., O’Leary, M. N., Peri, S., Wang, M., Zha, J., Melov, S., Kappes, D. J., Feng, Q., Rhodes, J., Amieux, P. S., et al. (2017) · Cell Reports · doi:10.1016/j.celrep.2016.12.034 · Cited by 98 · see citing works

Imaging of cell migration

Dormann, D., & Weijer, C. J. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601227 · Cited by 100 · see citing works

Epithelial morphogenesis in embryos: asymmetries, motors and brakes

Quintin, S., Gally, C., & Labouesse, M. (2008) · Trends in Genetics · doi:10.1016/j.tig.2008.02.005 · Cited by 99 · see citing works

Temporally coordinated signals progressively pattern the anteroposterior and dorsoventral body axes

Tuazon, F. B., & Mullins, M. C. (2015) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2015.06.003 · Cited by 98 · see citing works

Initiation of convergence and extension movements of lateral mesoderm during zebrafish gastrulation

Sepich, D. S., Calmelet, C., Kiskowski, M. A., & Solnica‐Krezel, L. (2005) · Developmental Dynamics · doi:10.1002/dvdy.20507 · Cited by 98 · see citing works

Chapter 7 Establishment of Hox Vertebral Identities in the Embryonic Spine Precursors

Iimura, T., Denans, N., & Pourquié, O. (2009) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(09)88007-1 · Cited by 98 · see citing works

Kinase-activating and kinase-impaired cardio-facio-cutaneous syndrome alleles have activity during zebrafish development and are sensitive to small molecule inhibitors

Anastasaki, C., Estep, A. L., Marais, R., Rauen, K. A., & Patton, E. E. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp186 · Cited by 94 · see citing works

FGF signalling through RAS/MAPK and PI3K pathways regulates cell movement and gene expression in the chicken primitive streak without affecting E-cadherin expression

Hardy, K. M., Yatskievych, T. A., Konieczka, J. H., Bobbs, A. S., & Antin, P. B. (2011) · BMC Developmental Biology · doi:10.1186/1471-213x-11-20 · Cited by 92 · see citing works

Role of the extracellular matrix in cancer‐associated epithelial to mesenchymal transition phenomenon

Tzanakakis, G. N., Kavasi, R., Voudouri, K., Berdiaki, A., Spyridaki, I., Tsatsakis, A. M., & Nikitovic, D. (2017) · Developmental Dynamics · doi:10.1002/dvdy.24557 · Cited by 88 · see citing works

Cell Sorting in Development

Krens, G., & Heisenberg, C. (2011) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-385065-2.00006-2 · Cited by 91 · see citing works

The Physical Basis of Coordinated Tissue Spreading in Zebrafish Gastrulation

Morita, H., Grigolon, S., Bock, M., Krens, G., Salbreux, G., & Heisenberg, C. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.01.010 · Cited by 91 · see citing works

Secreted inducers in vertebrate eye development: more functions for old morphogens

Esteve, P., & Bovolenta, P. (2006) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2006.01.001 · Cited by 89 · see citing works

Alterations of the cytoskeleton in all three embryonic lineages contribute to the epiboly defect of Pou5f1/Oct4 deficient MZspg zebrafish embryos

Lachnit, M., Kur, E., & Driever, W. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.10.008 · Cited by 89 · see citing works

Hand2 Regulates Extracellular Matrix Remodeling Essential for Gut-Looping Morphogenesis in Zebrafish

Yin, C., Kikuchi, K., Hochgreb, T., Poss, K. D., & Stainier, D. Y. R. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.05.009 · Cited by 87 · see citing works

Wnt5b–Ryk pathway provides directional signals to regulate gastrulation movement

Lin, S., Baye, L. M., Westfall, T. A., & Slusarski, D. C. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.200912128 · Cited by 87 · see citing works

Extracellular matrix assembly and organization during zebrafish gastrulation

Latimer, A., & Jessen, J. R. (2009) · Matrix Biology · doi:10.1016/j.matbio.2009.10.002 · Cited by 85 · see citing works

Back and forth between cell fate specification and movement during vertebrate gastrulation

Heisenberg, C., & Solnica‐Krezel, L. (2008) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2008.07.011 · Cited by 86 · see citing works

Regionalized tissue fluidization is required for epithelial gap closure during insect gastrulation

Jain, A., Ulman, V., Mukherjee, A., Prakash, M., Cuenca, M. B., Pimpale, L. G., Münster, S., Haase, R., Panfilio, K. A., Jug, F., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-19356-x · Cited by 88 · see citing works

Flamingo regulates epiboly and convergence/extension movements through cell cohesive and signalling functions during zebrafish gastrulation

Carreira-Barbosa, F., Kajita, M., Morel, V., Wada, H., Okamoto, H., Arias, A. M., Fujita, Y., Wilson, S. W., & Tada, M. (2008) · Development · doi:10.1242/dev.026542 · Cited by 85 · see citing works

Membrane-type 1 matrix metalloproteinase regulates cell migration during zebrafish gastrulation: Evidence for an interaction with non-canonical Wnt signaling

Coyle, R. C., Latimer, A. J., & Jessen, J. R. (2008) · Experimental Cell Research · doi:10.1016/j.yexcr.2008.03.010 · Cited by 84 · see citing works

Multicellular dynamics during epithelial elongation

Zallen, J. A., & Blankenship, J. T. (2008) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2008.01.005 · Cited by 83 · see citing works

Deeply-supervised density regression for automatic cell counting in microscopy images

He, S., Minn, K. T., Solnica‐Krezel, L., Anastasio, M. A., & Li, H. (2020) · Medical Image Analysis · doi:10.1016/j.media.2020.101892 · Cited by 80 · see citing works

Wnt/PCP signaling controls intracellular position of MTOCs during gastrulation convergence and extension movements

Sepich, D. S., Usmani, M., Pawlicki, S., & Solnica‐Krezel, L. (2011) · Development · doi:10.1242/dev.053959 · Cited by 80 · see citing works

Chemotactic cell movement during Dictyostelium development and gastrulation

Dormann, D., & Weijer, C. J. (2006) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2006.06.003 · Cited by 79 · see citing works

Live Analysis of Endodermal Layer Formation Identifies Random Walk as a Novel Gastrulation Movement

Pézeron, G., Mourrain, P., Courty, S., Ghislain, J. J., Becker, T. S., Rosa, F., & David, N. B. (2008) · Current Biology · doi:10.1016/j.cub.2008.01.028 · Cited by 76 · see citing works

Why does Jack, and not Jill, break his crown? Sex disparity in brain tumors

Sun, T., Warrington, N. M., & Rubin, J. B. (2012) · Biology of Sex Differences · doi:10.1186/2042-6410-3-3 · Cited by 75 · see citing works

Chapter 7 Ciliary Function and Wnt Signal Modulation

Gerdes, J. M., & Katsanis, N. (2008) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(08)00807-7 · Cited by 73 · see citing works

Rack1 is required for Vangl2 membrane localization and planar cell polarity signaling while attenuating canonical Wnt activity

Li, S., Esterberg, R., Lachance, V., Ren, D., Radde‐Gallwitz, K., Chi, F., Parent, J., Fritz, A., & Chen, P. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013170108 · Cited by 74 · see citing works

Gpr125 modulates Dishevelled distribution and planar cell polarity signaling

Li, X., Roszko, I., Sepich, D. S., Ni, M., Hamm, H. E., Marlow, F. L., & Solnica‐Krezel, L. (2013) · Development · doi:10.1242/dev.094839 · Cited by 74 · see citing works

Context-Dependent Regulation of Wnt Signaling through the Primary Cilium

Oh, E. C., & Katsanis, N. (2013) · Journal of the American Society of Nephrology · doi:10.1681/asn.2012050526 · Cited by 73 · see citing works

Developmental diversity of amphibians

Elinson, R. P., & del Pino, E. M. (2011) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.23 · Cited by 73 · see citing works

Identification and Regulation of a Molecular Module for Bleb-Based Cell Motility

Goudarzi, M., Banisch, T. U., Mobin, M. B., Maghelli, N., Tarbashevich, K., Strate, I., van den Berg, J., Blaser, H., Bandemer, S., Paluch, E. K., et al. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.05.007 · Cited by 73 · see citing works

Anteroposterior and dorsoventral patterning are coordinated by an identical patterning clock

Hashiguchi, M., & Mullins, M. C. (2013) · Development · doi:10.1242/dev.088104 · Cited by 70 · see citing works

Identification of regulators of germ layer morphogenesis using proteomics in zebrafish

Link, V., Carvalho, L., Castanon, I., Stockinger, P., Shevchenko, A., & Heisenberg, C. (2006) · Journal of Cell Science · doi:10.1242/jcs.02928 · Cited by 69 · see citing works

Hydrogel-based biomimetic environment for in vitro modulation of branching morphogenesis

Miyajima, H., Matsumoto, T., Sakai, T., Yamaguchi, S., An, S., Abe, M., Wakisaka, S., Lee, K. Y., Egusa, H., & Imazato, S. (2011) · Biomaterials · doi:10.1016/j.biomaterials.2011.05.072 · Cited by 68 · see citing works

Regulated adhesion as a driving force of gastrulation movements

Hammerschmidt, M., & Wedlich, D. (2008) · Development · doi:10.1242/dev.015701 · Cited by 67 · see citing works

Role of G12 proteins in oncogenesis and metastasis

Juneja, J., & Casey, P. J. (2009) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2009.00180.x · Cited by 68 · see citing works

A Wnt-CKIɛ-Rap1 Pathway Regulates Gastrulation by Modulating SIPA1L1, a Rap GTPase Activating Protein

Tsai, I.-C., Amack, J. D., Gao, Z.-H., Band, V., Yost, H. J., & Virshup, D. M. (2007) · Developmental Cell · doi:10.1016/j.devcel.2007.02.009 · Cited by 67 · see citing works

Chapter 7 Convergence and Extension Movements During Vertebrate Gastrulation

Yin, C., Ciruna, B. G., & Solnica‐Krezel, L. (2009) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(09)89007-8 · Cited by 67 · see citing works

Tissue engineering using a combined cell sheet technology and scaffolding approach

Михайловна, З. И., Presniakova, V. S., Butnaru, D. V., Svistunov, A. А., Timashev, P. S., & Rochev, Y. A. (2020) · Acta Biomaterialia · doi:10.1016/j.actbio.2020.06.016 · Cited by 66 · see citing works

Gα12/13 regulate epiboly by inhibiting E-cadherin activity and modulating the actin cytoskeleton

Lin, F. H., Chen, S., Sepich, D. S., Panizzi, J. R., Clendenon, S. G., Marrs, J. A., Hamm, H. E., & Solnica‐Krezel, L. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200805148 · Cited by 65 · see citing works

Distinct Xenopus Nodal ligands sequentially induce mesendoderm and control gastrulation movements in parallel to the Wnt/PCP pathway

Luxardi, G., Marchal, L., Thomé, V., & Kodjabachian, L. (2010) · Development · doi:10.1242/dev.039735 · Cited by 65 · see citing works

Cell migration that orients the dorsoventral axis is coordinated with anteroposterior patterning mediated by Hedgehog signaling in the early spider embryo

Akiyama‐Oda, Y., & Oda, H. (2010) · Development · doi:10.1242/dev.045625 · Cited by 62 · see citing works

p120‐catenin regulates microtubule dynamics and cell migration in a cadherin‐independent manner

Ichii, T., & Takeichi, M. (2007) · Genes to Cells · doi:10.1111/j.1365-2443.2007.01095.x · Cited by 62 · see citing works

Recent advances in the study of zebrafish extracellular matrix proteins

Jessen, J. R. (2014) · Developmental Biology · doi:10.1016/j.ydbio.2014.12.022 · Cited by 61 · see citing works

Emergent morphogenesis: Elastic mechanics of a self-deforming tissue

Davidson, L. A., Joshi, S. D., Kim, H. Y., von Dassow, M., Zhang, L., & Zhou, J. (2009) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2009.09.010 · Cited by 61 · see citing works

Amotl2 is essential for cell movements in zebrafish embryo and regulates c-Src translocation

Huang, H., Lu, F., Jia, S., Meng, S., Cao, Y., Wang, Y., Ma, W., Yin, K., Wen, Z., Peng, J., et al. (2007) · Development · doi:10.1242/dev.02782 · Cited by 60 · see citing works

Selective neuronal requirement for huntingtin in the developing zebrafish

Henshall, T. L., Tucker, B., Lumsden, A. L., Nornes, S., Lardelli, M. T., & Richards, R. I. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp455 · Cited by 59 · see citing works

Gastrulation dynamics: cells move into focus

Montero, J. A., & Heisenberg, C. (2004) · Trends in Cell Biology · doi:10.1016/j.tcb.2004.09.008 · Cited by 68 · see citing works

Gastrulation: Making and Shaping Germ Layers

Solnica‐Krezel, L., & Sepich, D. S. (2011) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-092910-154043 · Cited by 366 · see citing works

Gastrulation Movements: the Logic and the Nuts and Bolts

Leptin, M. (2005) · Developmental Cell · doi:10.1016/j.devcel.2005.02.007 · Cited by 201 · see citing works

Morphogenetic cell movements shaping the zebrafish gastrula

Jessen, J. R., & Solnica‐Krezel, L. (2005) · Advances in developmental biology · doi:10.1016/s1574-3349(05)14007-1 · Cited by 14 · see citing works

Amphibian Gastrulation: The Molecular Bases of Mesodermal Cell Migration in Urodele Embryos

Boucaut, J., Darribère, T., Shi, D. L., Riou, J., Johnson, K. E., & Delarue, M. (1991) · Springer eBooks · doi:10.1007/978-1-4684-6027-8_10 · Cited by 8 · see citing works